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The field of '''geochemistry''' involves study of the [[chemistry|chemical]] composition of the [[Earth]] and other [[planet]]s, chemical processes and reactions that govern the composition of [[Rock (geology)|rock]]s and [[soil]]s, 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]].
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[[Image:The Earth seen from Apollo 17.jpg|thumb|300px|Geochemists study the [[chemistry|chemical]] composition of [[Earth]] and other [[planet]]s.]]
  
The most important fields of geochemistry are:
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The field of '''geochemistry''' involves study of the [[chemistry|chemical]] composition of [[Earth]] and extraterrestrial bodies and systems, and the chemical processes and reactions that take place within them. It also involves investigation of the cycles of [[matter]] and [[energy]] that transport the Earth's chemical constituents through time and space.
#[[Isotope geochemistry]]: Determination of the relative and absolute concentrations of the [[chemical element|element]]s and their [[isotope]]s 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 [[universe|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’.
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Scientific studies in geochemistry provide knowledge about Earth and its history, and they help us understand some of the processes involved in the formation of valuable [[mineral]] deposits and in changing the [[planet]]'s climate. Geochemical knowledge is also useful when making plans to dispose of [[toxic waste]]s in a manner that causes least harm to humans and the environment.
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{{toc}}
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Mineralogists [[Victor Goldschmidt]] and [[Vladimir Vernadsky]] are generally considered the founders of modern geochemistry. Goldschmidt enunciated many of the ideas in this field in a series of publications (from 1922) under the title ''Geochemische Verteilungsgesetze der Elemente''. Vernadsky's book on geochemistry was published in Russian in 1924.
  
''See also:'' [[Petrology]], [[List of publications in geology#Geochemistry|Important publications in geochemistry]]
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== Subfields ==
 +
[[Image:MET00506.jpg|thumb|200px|[[Meteorite]]s may be studied as part of cosmochemistry.]]
  
==Chemical characteristics==
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Geochemistry includes the following major subfields and areas of study.
  
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 oxide | 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: SiO<sub>2</sub>=59.71, Al<sub>2</sub>O<sub>3</sub>=15.41, Fe<sub>2</sub>O<sub>3</sub>=2.63, FeO=3.52, MgO=4.36, CaO=4.90, Na<sub>2</sub>O=3.55, K<sub>2</sub>O=2.80, H<sub>2</sub>O=1.52, TiO<sub>2</sub>=0.60, P<sub>2</sub>O<sub>5</sub>=0.22, total 99.22%). All the other constituents occur only in very small quantities, usually much less than 1%.
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* [[Cosmochemistry]]: It deals with analysis of the distribution of [[chemical element|element]]s and their [[isotope]]s in extraterrestrial bodies and systems. Studies in cosmochemistry include attempts to understand the formation of and chemical processes within the [[Solar System]], the origin of [[meteorite]]s, and the formation of elements in [[star]]s.
  
These oxides  combine in a haphazard way. The potash and soda, for example, combine to produce [[feldspar|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 [[pyroxene|pyroxenes]], [[amphibole|amphiboles]] and [[biotite|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.
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* Examination of the distribution and movements of elements in different parts of [[Earth]] (the crust, mantle, hydrosphere, and so forth) and in minerals, with the goal of determining the underlying systems of distribution and transport.
  
===Mineral constitution===
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* [[Isotope geochemistry]]: It involves determining the distribution and concentrations of the isotopes of elements in terrestrial and extraterrestrial materials. The knowledge gained may be used to determine the age of these materials and the historical changes they have gone through.
  
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.
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* [[Organic geochemistry]]: This area involves studying the role of [[carbon]]-containing compounds and processes derived from living or once-living organisms. This area of geochemistry helps us understand how living things affect chemical cycles, and the formation of [[petroleum]], [[coal]], [[natural gas]], and [[ore]]s.
  
===Acid, intermediate and basic igneous rocks===
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* [[Regional, environmental and exploration geochemistry]]: It involves studies related to environmental, hydrological, and mineral exploration.
  
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.
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==Chemical characteristics of rocks==
  
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.
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The more common constituents of [[rock (geology)|rock]]s on [[Earth]] are [[oxide]]s. The main exceptions to oxides are compounds of [[chlorine]], [[sulfur]], and [[fluorine]].
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According to calculations by [[F. W. Clarke]], a little more than 47 percent of Earth's crust consists of [[oxygen]]. It occurs mainly in the form of oxides, particularly [[silica]], [[alumina]], [[iron oxide]]s, [[lime]], [[magnesia]], [[potash]], and [[soda]]. Silica functions principally as an acid, forming silicates, and the most common minerals of igneous rocks are silicates. From a computation based on 1,672 analyses of all kinds of rocks, Clarke arrived at the following values for the average percentage composition: SiO<sub>2</sub>=59.71; Al<sub>2</sub>O<sub>3</sub>=15.41; Fe<sub>2</sub>O<sub>3</sub>=2.63; FeO=3.52; MgO=4.36; CaO=4.90; Na<sub>2</sub>O=3.55; K<sub>2</sub>O=2.80; H<sub>2</sub>O=1.52; TiO<sub>2</sub>=0.60; and P<sub>2</sub>O<sub>5</sub>=0.22. (The total of these is 99.22 percent). All other constituents occur in very small quantities, usually much less than one percent.
 +
 
 +
The oxides combine in various ways. Some examples are given below.
 +
* Potash and soda combine to produce mostly [[feldspar]]s, but may also produce [[nepheline]], [[leucite]], and [[muscovite]].
 +
* Phosphoric acid with lime forms apatite.
 +
* Titanium dioxide with ferrous oxide gives rise to ilmenite.
 +
* Magnesia and iron oxides with silica crystallize as [[olivine]] or [[enstatite]], or with alumina and lime form the complex ferro-magnesian silicates (such as the [[pyroxene]]s, [[amphibole]]s, and [[biotite]]s).
 +
* Any silica in excess of that required to neutralize the bases separates out as quartz; excess alumina crystallizes as [[corundum]].
 +
These combinations must be regarded only as general tendencies, for there are numerous exceptions to the rules. The prevalent physical conditions also play a role in the formation of rocks.
 +
 
 +
Clarke also calculated the relative abundances of the principal rock-forming minerals and obtained the following results: apatite=0.6 percent, titanium minerals=1.5 percent, quartz=12.0 percent, feldspars=59.5 percent, biotite=3.8 percent, hornblende and pyroxene=16.8 percent, for a total of 94.2 percent. These figures, however, can only be considered rough approximations.
 +
 
 +
===Acid, intermediate, basic, and ultrabasic igneous rocks===
 +
 
 +
Rocks that contain the highest levels of silica and on crystallization yield free quartz are placed in a group generally designated "acid" rocks. Rocks that contain lowest levels of silica and most magnesia and iron, so that quartz is absent while [[olivine]] is usually abundant, form the "basic" group. The "intermediate" group includes rocks 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 group rich in olivine and without feldspar has been called "ultrabasic" rocks. They have very low percentages of silica but high proportions of iron and magnesia.
 +
 
 +
Except for the last group, practically all rocks contain feldspars or feldspathoid minerals. In acid rocks, the common feldspars are orthoclase, with perthite, microcline, oligoclase, all having much silica. In the basic rocks, labradorite, anorthite, and bytownite prevail, being rich in lime and poor in silica, potash and soda. Augite is the most common ferro-magnesian of the basic rocks, while biotite and hornblende are usually more frequent in acid rocks.
  
 
{| class="wikitable"
 
{| class="wikitable"
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! Ultrabasic
 
! Ultrabasic
 
|-
 
|-
! Quartz <br> Orthoclase (and Oligoclase), Mica, Hornblende, Augite
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! Quartz <br/> Orthoclase (and Oligoclase), Mica, Hornblende, Augite
! Little or no Quartz: <br> Orthoclase hornblende, Augite, Biotite
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! Little or no Quartz: <br/> Orthoclase hornblende, Augite, Biotite
! Little or no Quartz: <br> Plagioclase Hornblende, Augite, Biotite
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! Little or no Quartz: <br/> Plagioclase Hornblende, Augite, Biotite
! No Quartz <br> Plagioclase Augite, Olivine
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! No Quartz <br/> Plagioclase Augite, Olivine
! No Felspar <br> Augite, Hornblende, Olivine
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! No Felspar <br/> Augite, Hornblende, Olivine
 
|-
 
|-
 
| Plutonic or Abyssal type
 
| Plutonic or Abyssal type
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|}
 
|}
  
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.
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Rocks that contain leucite or nepheline, either partly or wholly replacing feldspar, are not included in the above table. They are essentially of intermediate or basic character. They may be regarded as varieties of syenite, diorite, gabbro, and so forth, in which feldspathoid minerals occur. Indeed there are many transitions between ordinary syenites and nepheline (or leucite) syenite, and between gabbro or dolerite and theralite or essexite. But because many minerals that develop in these "alkali" rocks are uncommon elsewhere, it is convenient in a purely formal classification like that outlined here to treat the whole assemblage as a distinct series.
  
 
{| class="wikitable"
 
{| class="wikitable"
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|-
 
|-
 
! Commonest Minerals
 
! Commonest Minerals
! Alkali Felspar, Nepheline or Leucite, Augite, Hornblend, Biotite
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! Alkali Feldspar, Nepheline or Leucite, Augite, Hornblend, Biotite
! Soda Lime Felspar, Nepheline or Leucite, Augite, Hornblende (Olivine)
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! Soda Lime Feldspar, Nepheline or Leucite, Augite, Hornblende (Olivine)
 
! Nepheline or Leucite, Augite, Hornblende, Olivine
 
! Nepheline or Leucite, Augite, Hornblende, Olivine
 
|-
 
|-
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|}
 
|}
  
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.<ref name=EB1911>{{1911|article=Petrology}}</ref>.
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The above classification is based essentially on the mineralogical constitution of igneous rocks. Any chemical distinctions between the different groups, though implied, are relegated to a subordinate position. It is admittedly artificial, but it has developed with the growth of the science and is still adopted as the basis on which smaller subdivisions have been set up.
 +
 
 +
The subdivisions are by no means of equal value. For example, the syenites 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.
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 +
As the different types of rock, regarded as aggregates of minerals, pass gradually from one to another, transitional types are very common and are often so important as to receive special names. For example, 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, and the norites and hyperites between diorite and gabbro.
  
 
==See also==
 
==See also==
* [[Fred Meissner]], World Renowned Petroleum Geologist, Author, Professor at Colorado School of Mines
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*[[Petroleum geology]]
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* [[Astrochemistry]]
 +
* [[Earth]]
 +
* [[Geology]]
 +
* [[Petroleum geology]]
 +
* [[Petrology]]
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* [[Rock (geology)]]
  
 
== References ==
 
== References ==
<references />
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This article incorporates text from the ''Encyclopædia Britannica Eleventh Edition'', a publication now in the public domain.
  
== Further reading ==
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* Allègre, Claude J., and Gil Michard. 1974. ''Introduction to Geochemistry''. Geophysics and Astrophysics Monographs, v. 10. Dordrecht: D. Reidel Pub. Co. ISBN 902770497X
* Holland, H.D., & Turekian, K.K. (2004). [http://www.sciencedirect.com/science/referenceworks/9780080437514 ''Treatise on Geochemistry'']. 9 Volumes. Elsevier
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* Faure, Gunter. 1986. ''Principles of Isotope Geology'', 2nd ed. New York: Wiley. ISBN 0471864129
* Marshall, C., & Fairbridge, R. (2006). [http://www.springer.com/east/home/generic/search/results?SGWID=5-40109-22-33650945-0 ''Encyclopedia of Geochemistry'']. ISBN 1-4020-4496-8. Berlin: Springer.
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* Holland, H.D., and K.K. Turekian (eds.). 2003. ''Treatise on Geochemistry''. 10-volume set. New York: Elsevier. ISBN 978-0080437514
* Bernard Gunn: [http://www.Geokem.com ''The Geochemistry of Igneous Rocks'']
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* Levinson, A.A. 1980. ''Introduction to Exploration Geochemistry'', 2nd ed. Wilmette, IL: Applied Pub. ISBN 0915834014
* Gunter Faure: ''Principles of Isotope Geochemistry.'', ISBN 0-471-86412-9
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* Marshall, Clare P., and Rhodes W. Fairbridge (eds.). 2006. ''Encyclopedia of Geochemistry''. Encyclopedia of Earth Sciences Series. Berlin: Springer. ISBN 978-1402044960
* Cl.J. [[Claude Allègre|Allègre]], G. Michard, R.N. Varney, ''Introduction to Geochemistry'', ISBN 90-277-0497-X
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* Mason, Brian Harold. 1992. ''Victor Moritz Goldschmidt: Father of Modern Geochemistry.'' San Antonio, TX: Geochemical Society. ISBN 094180903X
* W.M. White: ''Geochemistry'' ([http://www.imwa.info/geochemistry Free Download])
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* Vernadsky, Vladimir. 2007. ''Geochemistry and the Biosphere''. Edited by Frank B. Salisbury, translated by Olga Barash. Santa Fe: Synergetic Press. ISBN 0907791360
* 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
 
  
[[Category:Geochemistry| ]]
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[[Category:Physical sciences]]
 
[[Category:Earth sciences]]
 
[[Category:Earth sciences]]
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[[et:Geokeemia]]
 
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Latest revision as of 16:34, 26 May 2017

Geochemists study the chemical composition of Earth and other planets.

The field of geochemistry involves study of the chemical composition of Earth and extraterrestrial bodies and systems, and the chemical processes and reactions that take place within them. It also involves investigation of the cycles of matter and energy that transport the Earth's chemical constituents through time and space.

Scientific studies in geochemistry provide knowledge about Earth and its history, and they help us understand some of the processes involved in the formation of valuable mineral deposits and in changing the planet's climate. Geochemical knowledge is also useful when making plans to dispose of toxic wastes in a manner that causes least harm to humans and the environment.

Mineralogists Victor Goldschmidt and Vladimir Vernadsky are generally considered the founders of modern geochemistry. Goldschmidt enunciated many of the ideas in this field in a series of publications (from 1922) under the title Geochemische Verteilungsgesetze der Elemente. Vernadsky's book on geochemistry was published in Russian in 1924.

Subfields

Meteorites may be studied as part of cosmochemistry.

Geochemistry includes the following major subfields and areas of study.

  • Cosmochemistry: It deals with analysis of the distribution of elements and their isotopes in extraterrestrial bodies and systems. Studies in cosmochemistry include attempts to understand the formation of and chemical processes within the Solar System, the origin of meteorites, and the formation of elements in stars.
  • Examination of the distribution and movements of elements in different parts of Earth (the crust, mantle, hydrosphere, and so forth) and in minerals, with the goal of determining the underlying systems of distribution and transport.
  • Isotope geochemistry: It involves determining the distribution and concentrations of the isotopes of elements in terrestrial and extraterrestrial materials. The knowledge gained may be used to determine the age of these materials and the historical changes they have gone through.
  • Organic geochemistry: This area involves studying the role of carbon-containing compounds and processes derived from living or once-living organisms. This area of geochemistry helps us understand how living things affect chemical cycles, and the formation of petroleum, coal, natural gas, and ores.
  • Regional, environmental and exploration geochemistry: It involves studies related to environmental, hydrological, and mineral exploration.

Chemical characteristics of rocks

The more common constituents of rocks on Earth are oxides. The main exceptions to oxides are compounds of chlorine, sulfur, and fluorine.

According to calculations by F. W. Clarke, a little more than 47 percent of Earth's crust consists of oxygen. It occurs mainly in the form of oxides, particularly silica, alumina, iron oxides, lime, magnesia, potash, and soda. Silica functions principally as an acid, forming silicates, and the most common minerals of igneous rocks are silicates. From a computation based on 1,672 analyses of all kinds of rocks, Clarke arrived at the following values for 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; and P2O5=0.22. (The total of these is 99.22 percent). All other constituents occur in very small quantities, usually much less than one percent.

The oxides combine in various ways. Some examples are given below.

  • Potash and soda combine to produce mostly feldspars, but may also produce nepheline, leucite, and muscovite.
  • Phosphoric acid with lime forms apatite.
  • Titanium dioxide with ferrous oxide gives rise to ilmenite.
  • Magnesia and iron oxides with silica crystallize as olivine or enstatite, or with alumina and lime form the complex ferro-magnesian silicates (such as the pyroxenes, amphiboles, and biotites).
  • Any silica in excess of that required to neutralize the bases separates out as quartz; excess alumina crystallizes as corundum.

These combinations must be regarded only as general tendencies, for there are numerous exceptions to the rules. The prevalent physical conditions also play a role in the formation of rocks.

Clarke also calculated the relative abundances of the principal rock-forming minerals and obtained the following results: apatite=0.6 percent, titanium minerals=1.5 percent, quartz=12.0 percent, feldspars=59.5 percent, biotite=3.8 percent, hornblende and pyroxene=16.8 percent, for a total of 94.2 percent. These figures, however, can only be considered rough approximations.

Acid, intermediate, basic, and ultrabasic igneous rocks

Rocks that contain the highest levels of silica and on crystallization yield free quartz are placed in a group generally designated "acid" rocks. Rocks that contain lowest levels of silica and most magnesia and iron, so that quartz is absent while olivine is usually abundant, form the "basic" group. The "intermediate" group includes rocks 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 group rich in olivine and without feldspar has been called "ultrabasic" rocks. They have very low percentages of silica but high proportions of iron and magnesia.

Except for the last group, practically all rocks contain feldspars or feldspathoid minerals. In acid rocks, the common feldspars are orthoclase, with perthite, microcline, oligoclase, all having much silica. In the basic rocks, labradorite, anorthite, and bytownite prevail, being rich in lime and poor in silica, potash and soda. Augite is the most common ferro-magnesian of the basic rocks, while biotite and hornblende are usually more frequent in acid rocks.

Commonest Minerals Acid Intermediate Basic Ultrabasic
Quartz
Orthoclase (and Oligoclase), Mica, Hornblende, Augite
Little or no Quartz:
Orthoclase hornblende, Augite, Biotite
Little or no Quartz:
Plagioclase Hornblende, Augite, Biotite
No Quartz
Plagioclase Augite, Olivine
No Felspar
Augite, Hornblende, Olivine
Plutonic or Abyssal type Granite Syenite Diorite Gabbro Peridotite
Intrusive or Hypabyssal type Quartz-porphyry Orthoclase-porphyry Porphyrite Dolerite Picrite
Lavas or Effusive type Rhyolite, Obsidian Trachyte Andesite Basalt Limburgite

Rocks that contain leucite or nepheline, either partly or wholly replacing feldspar, are not included in the above table. They are essentially of intermediate or basic character. They may be regarded as varieties of syenite, diorite, gabbro, and so forth, in which feldspathoid minerals occur. Indeed there are many transitions between ordinary syenites and nepheline (or leucite) syenite, and between gabbro or dolerite and theralite or essexite. But because many minerals that develop in these "alkali" rocks are uncommon elsewhere, it is convenient in a purely formal classification like that outlined here to treat the whole assemblage as a distinct series.

Nepheline and Leucite-bearing Rocks
Commonest Minerals Alkali Feldspar, Nepheline or Leucite, Augite, Hornblend, Biotite Soda Lime Feldspar, Nepheline or Leucite, Augite, Hornblende (Olivine) Nepheline or Leucite, Augite, Hornblende, Olivine
Plutonic type Nepheline-syenite, Leucite-syenite, Nepheline-porphyry Essexite and Theralite Ijolite and Missourite
Effusive type or Lavas Phonolite, Leucitophyre Tephrite and Basanite Nepheline-basalt, Leucite-basalt

The above classification is based essentially on the mineralogical constitution of igneous rocks. Any chemical distinctions between the different groups, though implied, are relegated to a subordinate position. It is admittedly artificial, but it has developed with the growth of the science and is still adopted as the basis on which smaller subdivisions have been set up.

The subdivisions are by no means of equal value. For example, the syenites 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 types of rock, regarded as aggregates of minerals, pass gradually from one to another, transitional types are very common and are often so important as to receive special names. For example, 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, and the norites and hyperites between diorite and gabbro.

See also

References
ISBN links support NWE through referral fees

This article incorporates text from the Encyclopædia Britannica Eleventh Edition, a publication now in the public domain.

  • Allègre, Claude J., and Gil Michard. 1974. Introduction to Geochemistry. Geophysics and Astrophysics Monographs, v. 10. Dordrecht: D. Reidel Pub. Co. ISBN 902770497X
  • Faure, Gunter. 1986. Principles of Isotope Geology, 2nd ed. New York: Wiley. ISBN 0471864129
  • Holland, H.D., and K.K. Turekian (eds.). 2003. Treatise on Geochemistry. 10-volume set. New York: Elsevier. ISBN 978-0080437514
  • Levinson, A.A. 1980. Introduction to Exploration Geochemistry, 2nd ed. Wilmette, IL: Applied Pub. ISBN 0915834014
  • Marshall, Clare P., and Rhodes W. Fairbridge (eds.). 2006. Encyclopedia of Geochemistry. Encyclopedia of Earth Sciences Series. Berlin: Springer. ISBN 978-1402044960
  • Mason, Brian Harold. 1992. Victor Moritz Goldschmidt: Father of Modern Geochemistry. San Antonio, TX: Geochemical Society. ISBN 094180903X
  • Vernadsky, Vladimir. 2007. Geochemistry and the Biosphere. Edited by Frank B. Salisbury, translated by Olga Barash. Santa Fe: Synergetic Press. ISBN 0907791360

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