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
_Talc and Serpentine_, Hydrous silicates of magnesia, are extensive
rock-materials in some regions, and as such require mention as
soil-formers also. Serpentine usually forms blackish-green rock-masses,
that although soft disintegrate very slowly in the absence of definite
structure, and are attacked with some energy only when charged—as is
frequently the case—with ferrous oxide. The conversion of this into
ferric hydrate, so common in nature, here also serves as the point of
attack on a rock otherwise very stable; causing it to crumble, even
though slowly.
_Talc_ (the true “soapstone”) being usually free from iron, would be
even more slow than serpentine to yield to weathering, but that its
extreme softness and ready cleavage greatly facilitate its abrasion.
Thus talc schist, which is usually a mixture of talc with more or less
quartz, undergoes mechanical disintegration quite readily.
But the soils formed from either serpentine or talcose rocks are
almost always very poor in plant food, and sometimes totally sterile.
Magnesia, though an indispensable ingredient of plant food, is rarely
deficient in soils and unlike lime does not influence in any sensible
degree the process of soil formation. Magnesian rocks as a whole are
practically found to be not specially desirable soil-formers, even in
the form of magnesian limestones. They do not even, as a rule, contain
as many useful accessory minerals as are commonly found in limestones.
Moreover, an excess of magnesia over lime is injurious to most crops,
as is shown later (chapt. 18).
_The Zeolites._—Zeolites may be defined as hydro-silicates containing
as bases chiefly lime and alumina, commonly together with more or
less of potash and soda, more rarely magnesia and baryta. The water
is easily expelled by heating, but is present in the basic form, not
merely as water of crystallization. All zeolites are readily decomposed
by chlorhydric and other stronger acids.
The zeolites proper are not original rock ingredients,
but are formed in the course of rock decomposition by
atmospheric agencies, heated water, and other processes not
fully understood. They are therefore usually found in the
cavities and crevices of rocks that have been subject to the
influence of atmospheric or thermal waters, most frequently
in eruptive rocks, particularly in the vesicular cavities
characterizing what is known as amygdaloids. They are also
found in the crevices of sandstones and shales percolated
by water, as well as in nodules of infiltration (geodes),
in which they are frequently associated with quartz. Those
found in the cavities of rocks are usually well crystallized
wherever room is afforded, and are readily recognized by
their crystalline form; they are mostly colorless, sometimes
yellow or reddish.
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