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Adjective
- Of or pertaining to geochemistry
Derived terms
Extensive Definition
The field of geochemistry involves study of the
chemical composition
of the Earth
and other planets,
chemical processes and reactions that govern the composition of
rocks and
soils, and the cycles of
matter and energy that transport the Earth's chemical components in
time and space, and their interaction with the hydrosphere and the atmosphere.
The most important fields of geochemistry are:
- Isotope geochemistry: Determination of the relative and absolute concentrations of the elements and their isotopes in the earth and on earth's surface.
- Examination of the distribution and movements of elements in different parts of the earth (crust, mantle, hydrosphere etc.) and in minerals with the goal to determine the underlying system of distribution and movement.
- Cosmochemistry: Analysis of the distribution of elements and their isotopes in the cosmos .
- Organic geochemistry: A study of the role of processes and compounds that are derived from living or once-living organisms.
- Regional, environmental and exploration geochemistry: Applications to environmental, hydrological and mineral exploration studies.
The man considered by most to be the father of
modern geochemistry was Victor
Goldschmidt, and the ideas of the subject were formed by him in
a series of publications from 1922 under the title ‘Geochemische
Verteilungsgesetze der Elemente’.
See also: Petrology,
Important publications in geochemistry
Chemical characteristics
The more common rock constituents are nearly all
oxides; chlorine, sulfur and fluorine are the only important
exceptions to this and their total amount in any rock is usually
much less than 1%. F. W.
Clarke has calculated that a little more than 47% of the
earth's crust consists of oxygen. It occurs principally in
combination as oxides, of which the chief are silica, alumina, iron oxides,
lime, magnesia, potash and soda. The silica functions
principally as an acid, forming silicates, and all the commonest
minerals of igneous rocks are of this nature. From a computation
based on 1672 analyses of all kinds of rocks Clarke arrived at the
following as the average percentage composition: SiO2=59.71,
Al2O3=15.41, Fe2O3=2.63, FeO=3.52, MgO=4.36, CaO=4.90, Na2O=3.55,
K2O=2.80, H2O=1.52, TiO2=0.60, P2O5=0.22, total 99.22%). All the
other constituents occur only in very small quantities, usually
much less than 1%.
These oxides combine in a haphazard way. The
potash and soda, for example, combine to produce feldspars. In some cases they
may take other forms, such as nepheline, leucite and muscovite, but in the great
majority of instances they are found as felspar. The phosphoric
acid with lime forms apatite. The titanium dioxide with ferrous
oxide gives rise to ilmenite. Part of the lime forms lime felspar.
Magnesia and iron oxides with silica crystallize as olivine or enstatite, or with alumina and
lime form the complex ferro-magnesian silicates of which the
pyroxenes, amphiboles and biotites are the chief. Any
excess of silica above what is required to neutralize the bases
will separate out as quartz; excess of alumina crystallizes as
corundum. These must be
regarded only as general tendencies. It is possible by inspection
of a rock analysis to say approximately what minerals the rock will
contain, but there are numerous exceptions to any rule which can be
laid down.
Mineral constitution
Hence we may say that except in acid or siliceous
rocks containing 66% of silica and over, quartz will not be
abundant. In basic rocks (containing 60% of silica or less) it is
rare and accidental. If magnesia and iron be above the average
while silica is low olivine may be expected; where silica is
present in greater quantity over ferro-magnesian minerals, such as
augite, hornblende, enstatite or biotite, occur rather than
olivine. Unless potash is high and silica relatively low leucite
will not be present, for leucite does not occur with free quartz.
Nepheline, likewise, is usually found in rocks with much soda and
comparatively little silica. With high alcalis soda-bearing
pyroxenes and amphiboles may be present. The lower the percentage
of silica and the alkalis the greater is the prevalence of t lime
felspar as contracted with soda or potash felspar. Clarke has
calculated the relative abundance of the principal rock-forming
minerals with the following results: Apatite=0.6, titanium
minerals=1.5, quartz=12.0, felspars=59.5, biotite=3.8, hornblende
and pyroxene=16.8, total=94.2%. This, however, can only be a rough
approximation. The other determining factor, namely the physical
conditions attending consolidation, plays on the whole a smaller
part, yet is by no means negligible, as a few instances will prove.
There are certain minerals which are practically confined to
deep-seated intrusive rocks, e.g. microcline, muscovite, diallage.
Leucite is very rare in plutonic masses; many minerals have special
peculiarities in microscopic character according to whether they
crystallized in depth or near the surface, e.g. hypersthene,
orthoclase, quartz. There are some curious instances of rocks
having the same chemical composition but consisting of entirely
different minerals, e.g. the hornblendite of Gran, in Norway,
containing only hornblende, has the same composition as some of the
camptonites of the same locality which contain felspar and
hornblende of a different variety. In this connection we may repeat
what has been said above about the corrosion of porphyritic
minerals in igneous rocks. In rhyolites and trachytes early
crystals of hornblende and biotite may be found in great numbers
partially converted into augite and magnetite. The hornblende and
biotite were stable under the pressures and other conditions which
obtained below the surface, but unstable at higher levels. In the
ground-mass of these rocks augite is almost universally present.
But the plutonic representatives of the same magma, granite and
syenite contain biotite and hornblende far more commonly than
augite.
Acid, intermediate and basic igneous rocks
Those rocks which contain most silica and on
crystallizing yield free quartz are erected into a group generally
designated the "acid" rocks. Those again which contain least silica
and most magnesia and iron, so that quartz is absent while olivine is usually abundant,
form the "basic" group. The "intermediate" rocks include those
which are characterized by the general absence of both quartz and
olivine. An important subdivision of these contains a very high
percentage of alkalis, especially soda, and consequently has
minerals such as nepheline and leucite not common in other
rocks. It is often separated from the others as the "alkali" or
"soda" rocks, and there is a corresponding series of basic rocks.
Lastly a small sub-group rich in olivine and without felspar has
been called the "ultrabasic" rocks. They have very low percentages
of silica but much iron and magnesia.
Except these last practically all rocks contain
felspars or felspathoid minerals. In the acid rocks the common
felspars are orthoclase, which perthite, microcline, oligoclase,
all having much silica and alkalis. In the basic rocks labradorite,
anorthite and bytownite prevail, being rich in lime and poor in
silica, potash and soda. Augite is the commonest ferro-magnesian of
the basic rocks, but biotite and hornblende are on the whole more
frequent in the acid.
The rocks which contain leucite or nepheline,
either partly or wholly replacing felspar are not included in this
table. They are essentially of intermediate or of basic character.
We might in consequence regard them as varieties of syenite,
diorite, gabbro, etc., in which felspathoid minerals occur, and
indeed there are many transitions between syenites of ordinary type
and nepheline — or leucite — syenite, and between gabbro or
dolerite and theralite or essexite. But as many minerals develop in
these "alcali" rocks which are uncommon elsewhere, it is convenient
in a purely formal classification like that which is outlined here
to treat the whole assemblage as a distinct series.
This classification is based essentially on the
mineralogical constitution of the igneous rocks. Any chemical
distinctions between the different groups, though implied, are
relegated to a subordinate position. It is admittedly artificial by
it has grown up with the grown of the science and is still adopted
as the basis on which more minute subdivisions are erected. The
subdivisions are by no means of equal value. The syenites, for
example, and the peridotites, are far less important than the
granites, diorites and gabbros. Moreover, the effusive andesites do
not always correspond to the plutonic diorites but partly also to
the gabbros. As the different kinds of rock, regarded as aggregates
of minerals, pass gradually into one another, transitional types
are very common and are often so important as to receive special
names. The quartz-syenites and nordmarkites may be interposed
between granite and syenite, the tonalites and adamellites between
granite and diorite, the monzoaites between syenite and diorite,
norites and hyperites between diorite and gabbro, and so on..
See also
- Fred Meissner, World Renowned Petroleum Geologist, Author, Professor at Colorado School of Mines
- Petroleum geology
References
Further reading
- Holland, H.D., & Turekian, K.K. (2004). Treatise on Geochemistry. 9 Volumes. Elsevier
- Marshall, C., & Fairbridge, R. (2006). Encyclopedia of Geochemistry. ISBN 1-4020-4496-8. Berlin: Springer.
- Bernard Gunn: The Geochemistry of Igneous Rocks
- Gunter Faure: Principles of Isotope Geochemistry., ISBN 0-471-86412-9
- Cl.J. Allègre, G. Michard, R.N. Varney, Introduction to Geochemistry, ISBN 90-277-0497-X
- W.M. White: Geochemistry (Free Download)
- A.A. Levinson: Introduction to Exploration Geochemistry, ISBN: 0915834049
- Victor Moritz Goldschmidt: Father of Modern Geochemistry by Brian Mason (ISBN 0-941809-03-X)
- Essays on Geochemistry & the Biosphere, tr. Olga Barash, Santa Fe, NM, Synergetic Press, ISBN 0-907791-36-0, 2006
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