Ore genesis
Information about Ore genesis
The various theories of ore genesis explain how the various types of mineral deposits form within the Earth's crust. Ore genesis theories are very dependent on the mineral or commodity.
Ore genesis theories generally involve three components: source, transport or conduit, and trap. This also applies to the petroleum industry, which was first to use this methodology.
Sources of hydrothermal solutions include seawater, formational brines (water trapped within sediments at deposition) and metamorphic fluids created by dehydration of hydrous minerals during metamorphism.
Metal sources may include a plethora of rocks. However most metals of economic importance are carried as trace elements within rock-forming minerals, and so may be liberated by hydrothermal processes. This happens because of
This process is especially well understood in gold metallogeny where various thiosulfate, chloride and other gold-carrying chemical complexes (notably tellurium-chloride/sulfate or antimony-chloride/sulfate). The majority of metal deposits formed by hydrothermal processes include sulfide minerals, indicating sulfur is an important metal-carrying complex.
Sulfide deposition:
Sulfide deposition within the trap zone occurs when metal-carrying sulfate, sulfide or other complexes become chemically unstable due to one or more of the following processes;
Ore deposits formed by lateral secretion are formed by metamorphic reactions during shearing, which liberate mineral constituents such as quartz, sulfides, gold, carbonates and oxides from deforming rocks and focus these constituents into zones of reduced pressure or dilation such as faults. This may occur without much hydrothermal fluid flow, and this is typical of podiform chromite deposits.
Metamorphic processes also control many physical processes which form the source of hydrothermal fluids, outlined above.
Ore deposits rarely fit snugly into the boxes in which geologists wish to place them. Many may be formed by one or more of the basic genesis processes above, creating ambiguous classifications and much argument and conjecture. Often ore deposits are classified after examples of their type, for instance Broken Hill Type lead-zinc-silver deposits or Carlin-type Gold deposits.
Classification of hydrothermal ore deposits is also achieved by classifying according to the temperature of formation, which roughly also correlates with particular mineralising fluids, mneral associations and structural styles. This scheme, proposed by Waldemar Lindgren (1933) classified hydrothermal deposits as hypothermal, mesothermal, epithermal and telethermal.
Often, more recent weathering during the Tertiary or Eocene is required to convert the usual magnetite minerals into more easily processed hematite. Some iron deposits within the Pilbara of West Australia are placer deposits, formed by accumulation of hematite gravels called pisolites which form channel-iron deposits. These are preferred because they are cheap to mine.
Lead and zinc deposits are formed by discharge of deep sedimentary brine onto the sea floor (termed sedimentary exhalative or SEDEX), or by replacement of limestone, in skarn deposits, some associated with submarine volcanoes (called volcanogenic massive sulfide ore deposits or VMS) or in the aureole of subvolcanic intrusions of granite. The vast majority of SEDEX lead and zinc deposits are Proterozoic in age, although there are significant Jurassic examples in Canada and Alaska.
The carbonate replacement type deposit is exemplified by the Mississippi valley type (MVT) ore deposits. MVT and similar styles occur by replacement and degradation of carbonate sequences by hydrocarbons, which are thought important for transporting lead.
Plate tectonics is the underlying mechanism for generating gold deposits. The majority of primary gold deposits fall into two main categories: lode gold deposits or intrusion-related deposits.
Lode gold deposits are generally high-grade, thin, vein and fault hosted. They are comprised primarily of quartz veins also known as lodes or reefs, which contain either native gold or gold sulfides and tellurides. Lode gold deposits are usually hosted in basalt or in sediments known as turbidite, although when in faults, they may occupy intrusive igneous rocks such as granite.
Lode-gold deposits are intimately associated with orogeny and other plate collision events within geologic history. Most lode gold deposits sourced from metamorphic rocks because it is thought that the majority are formed by dehydration of basalt during metamorphism. The gold is transported up faults by hydrothermal waters and deposited when the water cools too much to retain gold in solution.
Intrusive related gold (Lang & Baker, 2001) is generally hosted in granites, porphyry or rarely dikes. Intrusive related gold usually also contains copper, and is often associated with tin and tungsten, and rarely molybdenum, antimony and uranium. Intrusive-related gold deposits rely on gold existing in the fluids associated with the magma (White, 2001), and the inevitable discharge of these hydrothermal fluids into the wall-rocks (Lowenstern, 2001). Skarn deposits are another manifestation of intrusive-related deposits.
Placer deposits are sourced from pre-existing gold deposits and are secondary deposits. Placer deposits are formed by alluvial processes within rivers, streams and on beaches. Placer gold deposits form via gravity, with the density of gold causing it to sink into trap sites within the river bed, or where water velocity drops, such as bends in rivers and behind boulders. Often placer deposits are found within sedimentary rocks and can be billions of years old, for instance the Witwatersrand deposits in South Africa. Sedimentary placer deposits are known as 'leads' or 'deep leads'.
Placer deposits are often worked by fossicking, and panning for gold is a popular pastime.
Laterite gold deposits are formed from pre-existing gold deposits (including some placer deposits) during prolonged weathering of the bedrock. Gold is deposited within iron oxides in the weathered rock or regolith, and may be further enriched by reworking by erosion. Some laterite deposits are formed by wind erosion of the bedrock leaving a residuum of native gold metal at surface.
Sulfide phases only form in ultramafic magmas when the magma reaches sulfur saturation. This is generally thought to be nearly impossible by pure fractional crystallisation, so other processes are usually required in ore genesis models to explain sulfur saturation. These include contamination of the magma with crustal material, especially sulfur-rich wall-rocks or sediments; magma mixing; volatile gain or loss.
Often platinum is associated with nickel, copper, chromium, and cobalt deposits.
Nickel deposits are generally found in two forms, either as sulfide or laterite.
Sulfide type nickel deposits are formed in essentially the same manner as platinum deposits. Nickel is a chalcophile element which prefers sulfides, so an ultramafic or mafic rock which has a sulfide phase in the magma may form nickel sulfides. The best nickel deposits are formed where sulfide accumulates in the base of lava tubes or volcanic flows — especially komatiite lavas.
Komatiitic nikel-copper sulfide deposits are considered to be formed by a mixture of sulfide segregation, immiscibility, and thermal erosion of sulfidic sediments. The sediments are considered to be necessary to promote sulfur saturation.
Some subvolcanic sills in the Thompson Belt of Canada host nickel sulfide deposits formed by deposition of sulfides near the feeder vent. Sulfide was accumulated near the vent due to the loss of magma velocity at the vent interface. The massive Voisey's Bay nickel deposit is considered to have formed via a similar process.
The process of forming nickel laterite deposits is essentially similar to the formation of gold laterite deposits, except that ultramafic or mafic rocks are required. Generally nickel laterites require very large olivine-bearing ultramafic intrusions. Minerals formed in laterite nickel deposits include gibbsite.
The world's major copper deposits are formed within the granitic porphyry copper style. Copper is enriched by processes during crystallisation of the granite and forms as chalcopyrite — a sulfide mineral, which is carried up with the granite.
Sometimes granites erupt to suface as volcanoes, and copper mineralisation forms during this phase when the granite and volcanic rocks cool via hydrothermal circulation.
Sedimentary copper forms within ocean basins in sedimentary rocks. Generally this forms by brine from deeply buried sediments discharging into the deep sea, and precipitating copper and often lead and zinc sulfides directly onto the sea floor. This is then buried by further sediment.
Often copper is associated with gold, lead, zinc and nickel deposits.
Uranium deposits are usually sourced from radioactive granites, where certain minerals such as monazite are leached during hydrothermal activity or during circulation of groundwater. The uranium is brought into solution by acidic conditions and is deposited when this acidity is neutralised. Generally this occurs in certain carbon-bearing sediments, within an unconformity in sedimentary strata. The majority of the world's nuclear power is sourced from uranium in such deposits.
Uranium is also found in nearly all coal at several parts per million, and in all granites. Radon is a common problem during mining of uranium as it is a radioactive gas.
Uranium is also found associated with certain igenous rocks, such as granite and porphyry. The Olympic Dam deposit in Australia is an example of this type of uranium deposit. It contains 70% of Australia's share of 40% of the known global low-cost recoverable uranium inventory.
Mineral sands are the predominant type of titanium, zirconium and thorium deposit. They are formed by accumulation of such heavy minerals within beach systems, and are a type of placer deposits. The minerals which contain titanium are ilmenite, rutile and leucoxene, zirconium is contained within zircon, and thorium is generally contained within monazite. These minerals are sourced from primarily granite bedrock by erosion and transported to the sea by rivers where they accumulate within beach sands. Rarely, but importantly, gold, tin and platinum deposits can form in beach placer deposits.
Greisen granite is another related tin-molybdenum and topaz mineralisation style.
Carbonatite intrusions are an important source of these elements. Ore minerals are essentially part of the unusual mineralogy of carbonatite.
Phosphate deposits are also formed from alkaline igneous rocks such as nepheline syenites, carbonatites and associated rock types. The phosphate is, in this case, contained within magmatic apatite, monazite or other rare-earth phosphates.
Ore genesis theories generally involve three components: source, transport or conduit, and trap. This also applies to the petroleum industry, which was first to use this methodology.
- Source is required because metal must come from somewhere, and be liberated by some process
- Transport is required first to move the metal bearing fluids or solid minerals into the right position, and refers to the act of physically moving the metal, as well as chemical or physical phenomenon which encourage movement
- Trapping is required to concentrate the metal via some physical, chemical or geological mechanism into a concentration which forms mineable ore
Ore genesis processes
Evans (1993) divides ore genesis into the following main categories based on physical process. These are internal processes, hydrothermal processes, metamorphic processes and surficial processes.Internal processes
These processes are integral physical phenomena and chemical reactions internal to magmas, generally in plutonic or volcanic rocks. These include;- Fractional crystallization, either creating monominerallic cumulate ores or contributing to the enrichment of ore minerals and metals
- Liquation, or liquid immiscibility between melts of differing composition, usually sulfide segregations of nickel-copper-platinoid sulfides and silicates.
Hydrothermal processes
These processes are the physico-chemical phenomena and reactions caused by movement of hydrothermal waters within the crust, often as a consequence of magmatic intrusion or tectonic upheavals. The foundations of hydrothermal processes are the source-transport-trap mechanism.Sources of hydrothermal solutions include seawater, formational brines (water trapped within sediments at deposition) and metamorphic fluids created by dehydration of hydrous minerals during metamorphism.
Metal sources may include a plethora of rocks. However most metals of economic importance are carried as trace elements within rock-forming minerals, and so may be liberated by hydrothermal processes. This happens because of
- incompatibility of the metal with its host mineral, for example zinc in calcite, which favours aqueous fluids in contact with the host mineral under diagenesis.
- solubility of the host mineral within nascent hydrothermal solutions in the source rocks, for example mineral salts (halite), carbonates (cerussite), phosphates (monazite and thorianite) and sulfates (barite)
- elevated temperatures causing decomposition reactions of minerals
This process is especially well understood in gold metallogeny where various thiosulfate, chloride and other gold-carrying chemical complexes (notably tellurium-chloride/sulfate or antimony-chloride/sulfate). The majority of metal deposits formed by hydrothermal processes include sulfide minerals, indicating sulfur is an important metal-carrying complex.
Sulfide deposition:
Sulfide deposition within the trap zone occurs when metal-carrying sulfate, sulfide or other complexes become chemically unstable due to one or more of the following processes;
- falling temperature, which renders the complex unstable or metal insoluble
- loss of pressure, which has the same effect
- reaction with chemically reactive wall rocks, usually of reduced oxidation state, such as iron bearing rocks, mafic or ultramafic rocks or carbonate rocks
- degassing of the hydrothermal fluid into a gas and water system, or boiling, which alters the metal carrying capacity of the solution and even destroys metal-carrying chemical complexes
Metamorphic processes
Lateral secretion:Ore deposits formed by lateral secretion are formed by metamorphic reactions during shearing, which liberate mineral constituents such as quartz, sulfides, gold, carbonates and oxides from deforming rocks and focus these constituents into zones of reduced pressure or dilation such as faults. This may occur without much hydrothermal fluid flow, and this is typical of podiform chromite deposits.
Metamorphic processes also control many physical processes which form the source of hydrothermal fluids, outlined above.
Surficial processes
Surficial processes are the physical and chemical phenomena which cause concentration of ore material within the regolith, generally by the action of the environment. This includes placer deposits, laterite deposits and residual or eluvial deposits. The physical processes of ore deposit formation in the surficial realm include;- erosion
- deposition by sedimentary processes, including winnowing, density separation (eg; gold placers)
- weathering via oxidation or chemical attack of a rock, either liberating rock fragments or creating chemically deposited clays, laterites or manto ore deposits
- Deposition in low-energy environments in beach environments
Classification of ore deposits
Ore deposits are usually classified by ore formation processes and geological setting. For example, SEDEX deposits, literally meaning "sedimentary exhalative" are a class of ore deposit formed on the sea floor (sedimentary) by exhalation of brines into seawater (exhalative), causing chemical precipitation of ore minerals when the brine cools, mixes with sea water and loses its metal carrying capacity.Ore deposits rarely fit snugly into the boxes in which geologists wish to place them. Many may be formed by one or more of the basic genesis processes above, creating ambiguous classifications and much argument and conjecture. Often ore deposits are classified after examples of their type, for instance Broken Hill Type lead-zinc-silver deposits or Carlin-type Gold deposits.
Classification of hydrothermal ore deposits is also achieved by classifying according to the temperature of formation, which roughly also correlates with particular mineralising fluids, mneral associations and structural styles. This scheme, proposed by Waldemar Lindgren (1933) classified hydrothermal deposits as hypothermal, mesothermal, epithermal and telethermal.
Genesis of common ores
This page has been organised by metal commodity; it is also possible to organise theories according to geological criteria of formation, as well as by metal association. Often ores of the same metal can be formed by multiple processes, and this is described by commodity.Iron
Often, more recent weathering during the Tertiary or Eocene is required to convert the usual magnetite minerals into more easily processed hematite. Some iron deposits within the Pilbara of West Australia are placer deposits, formed by accumulation of hematite gravels called pisolites which form channel-iron deposits. These are preferred because they are cheap to mine.
Lead zinc silver
Lead and zinc deposits are formed by discharge of deep sedimentary brine onto the sea floor (termed sedimentary exhalative or SEDEX), or by replacement of limestone, in skarn deposits, some associated with submarine volcanoes (called volcanogenic massive sulfide ore deposits or VMS) or in the aureole of subvolcanic intrusions of granite. The vast majority of SEDEX lead and zinc deposits are Proterozoic in age, although there are significant Jurassic examples in Canada and Alaska.
The carbonate replacement type deposit is exemplified by the Mississippi valley type (MVT) ore deposits. MVT and similar styles occur by replacement and degradation of carbonate sequences by hydrocarbons, which are thought important for transporting lead.
Gold
Gold deposits are formed via a very wide variety of geological processes. Deposits are classified as primary, alluvial or placer deposits, or residual or laterite deposits. Often a deposit will contain a mixture of all three types of ore.Plate tectonics is the underlying mechanism for generating gold deposits. The majority of primary gold deposits fall into two main categories: lode gold deposits or intrusion-related deposits.
Lode gold deposits are generally high-grade, thin, vein and fault hosted. They are comprised primarily of quartz veins also known as lodes or reefs, which contain either native gold or gold sulfides and tellurides. Lode gold deposits are usually hosted in basalt or in sediments known as turbidite, although when in faults, they may occupy intrusive igneous rocks such as granite.
Lode-gold deposits are intimately associated with orogeny and other plate collision events within geologic history. Most lode gold deposits sourced from metamorphic rocks because it is thought that the majority are formed by dehydration of basalt during metamorphism. The gold is transported up faults by hydrothermal waters and deposited when the water cools too much to retain gold in solution.
Intrusive related gold (Lang & Baker, 2001) is generally hosted in granites, porphyry or rarely dikes. Intrusive related gold usually also contains copper, and is often associated with tin and tungsten, and rarely molybdenum, antimony and uranium. Intrusive-related gold deposits rely on gold existing in the fluids associated with the magma (White, 2001), and the inevitable discharge of these hydrothermal fluids into the wall-rocks (Lowenstern, 2001). Skarn deposits are another manifestation of intrusive-related deposits.
Placer deposits are sourced from pre-existing gold deposits and are secondary deposits. Placer deposits are formed by alluvial processes within rivers, streams and on beaches. Placer gold deposits form via gravity, with the density of gold causing it to sink into trap sites within the river bed, or where water velocity drops, such as bends in rivers and behind boulders. Often placer deposits are found within sedimentary rocks and can be billions of years old, for instance the Witwatersrand deposits in South Africa. Sedimentary placer deposits are known as 'leads' or 'deep leads'.
Placer deposits are often worked by fossicking, and panning for gold is a popular pastime.
Laterite gold deposits are formed from pre-existing gold deposits (including some placer deposits) during prolonged weathering of the bedrock. Gold is deposited within iron oxides in the weathered rock or regolith, and may be further enriched by reworking by erosion. Some laterite deposits are formed by wind erosion of the bedrock leaving a residuum of native gold metal at surface.
Platinum
Platinum and palladium are precious metals generally found in ultramafic rocks. The source of platinum and palladium deposits is ultramafic rocks which have enough sulfur to form a sulfide mineral while the magma is still liquid. This sulfide mineral (usually pentlandite, pyrite, chalcopyrite or pyrrhotite) gains platinum by mixing with the bulk of the magma because platinum is chalcophile and is concentrated in sulfides. Alternatively, platinum occurs in association with chromite either within the chromite mineral itself or within sulfides associated with it.Sulfide phases only form in ultramafic magmas when the magma reaches sulfur saturation. This is generally thought to be nearly impossible by pure fractional crystallisation, so other processes are usually required in ore genesis models to explain sulfur saturation. These include contamination of the magma with crustal material, especially sulfur-rich wall-rocks or sediments; magma mixing; volatile gain or loss.
Often platinum is associated with nickel, copper, chromium, and cobalt deposits.
Nickel
Nickel deposits are generally found in two forms, either as sulfide or laterite.
Sulfide type nickel deposits are formed in essentially the same manner as platinum deposits. Nickel is a chalcophile element which prefers sulfides, so an ultramafic or mafic rock which has a sulfide phase in the magma may form nickel sulfides. The best nickel deposits are formed where sulfide accumulates in the base of lava tubes or volcanic flows — especially komatiite lavas.
Komatiitic nikel-copper sulfide deposits are considered to be formed by a mixture of sulfide segregation, immiscibility, and thermal erosion of sulfidic sediments. The sediments are considered to be necessary to promote sulfur saturation.
Some subvolcanic sills in the Thompson Belt of Canada host nickel sulfide deposits formed by deposition of sulfides near the feeder vent. Sulfide was accumulated near the vent due to the loss of magma velocity at the vent interface. The massive Voisey's Bay nickel deposit is considered to have formed via a similar process.
The process of forming nickel laterite deposits is essentially similar to the formation of gold laterite deposits, except that ultramafic or mafic rocks are required. Generally nickel laterites require very large olivine-bearing ultramafic intrusions. Minerals formed in laterite nickel deposits include gibbsite.
Copper
The world's major copper deposits are formed within the granitic porphyry copper style. Copper is enriched by processes during crystallisation of the granite and forms as chalcopyrite — a sulfide mineral, which is carried up with the granite.
Sometimes granites erupt to suface as volcanoes, and copper mineralisation forms during this phase when the granite and volcanic rocks cool via hydrothermal circulation.
Sedimentary copper forms within ocean basins in sedimentary rocks. Generally this forms by brine from deeply buried sediments discharging into the deep sea, and precipitating copper and often lead and zinc sulfides directly onto the sea floor. This is then buried by further sediment.
Often copper is associated with gold, lead, zinc and nickel deposits.
Uranium
Uranium deposits are usually sourced from radioactive granites, where certain minerals such as monazite are leached during hydrothermal activity or during circulation of groundwater. The uranium is brought into solution by acidic conditions and is deposited when this acidity is neutralised. Generally this occurs in certain carbon-bearing sediments, within an unconformity in sedimentary strata. The majority of the world's nuclear power is sourced from uranium in such deposits.
Uranium is also found in nearly all coal at several parts per million, and in all granites. Radon is a common problem during mining of uranium as it is a radioactive gas.
Uranium is also found associated with certain igenous rocks, such as granite and porphyry. The Olympic Dam deposit in Australia is an example of this type of uranium deposit. It contains 70% of Australia's share of 40% of the known global low-cost recoverable uranium inventory.
Titanium and zirconium
Mineral sands are the predominant type of titanium, zirconium and thorium deposit. They are formed by accumulation of such heavy minerals within beach systems, and are a type of placer deposits. The minerals which contain titanium are ilmenite, rutile and leucoxene, zirconium is contained within zircon, and thorium is generally contained within monazite. These minerals are sourced from primarily granite bedrock by erosion and transported to the sea by rivers where they accumulate within beach sands. Rarely, but importantly, gold, tin and platinum deposits can form in beach placer deposits.
Tin, tungsten, and molybdenum
These three metals generally form in a certain type of granite, via a similar mechanism to intrusive-related gold and copper. They are considered together because the process of forming these deposits is essentially the same. Skarn type mineralisation related to these granites is a very important type of tin, tungsten and molybdenum deposit. Skarn deposits form by reaction of mineralised fluids from the granite reacting with wall rocks such as limestone. Skarn mineralisation is also important in lead, zinc, copper, gold and occasionally uranium mineralisation.Greisen granite is another related tin-molybdenum and topaz mineralisation style.
Rare earth elements, niobium, tantalum, lithium
The overwhelming majority of rare earth elements, tantalum and lithium are found within pegmatite. Ore genesis theories for these ores are wide and varied, but most involve metamorphism and igneous activity. Lithium is present as spodumene or lepidolite within pegmatite.Carbonatite intrusions are an important source of these elements. Ore minerals are essentially part of the unusual mineralogy of carbonatite.
Phosphate
Phosphate is used in fertilisers. Immense quantities of phosphate rock occur in older sedimentary basin, generally formed in the Proterozoic. Phosphate deposits are thought to be sourced from the skeletons of dead sea creatures which accumulated on the seafloor. Similar to iron ore deposits and oil, particular conditions in the ocean and environment are thought to have contributed to these deposits within the geological past.Phosphate deposits are also formed from alkaline igneous rocks such as nepheline syenites, carbonatites and associated rock types. The phosphate is, in this case, contained within magmatic apatite, monazite or other rare-earth phosphates.
See also
- Mineral exploration
- Copper extraction
- Hydrothermal circulation
- Economic geology
- Mineral redox buffer
- Metasomatism
- Igneous differentiation
References
- Arne, D.C.; Bierlein, F.P.; Morgan, J.W. & Stein, H.J., 2001. Re-Os Dating of Sulfides Associated With Gold Mineralisation in Central Victoria, Australia. Economic Geology, 96, pp1455-1459, 2001.
- Elder, D. & Cashman, S. Tectonic Control and Fluid Evolution in the Quartz Hill, California, Lode-gold Deposits. Economic Geology, 87, pp1795-1812, 1992.
- Evans, A.M., 1993. Ore Geology and Industrial Minerals, An Introduction., Blackwell Science, ISBN 0-632-02953-6
- Groves, D.I. 1993. The Crustal Continuum Model for late-Archaean lode-gold deposits of the Yilgran Block, Western Australia. Mineralium Deposita 28, pp366-374, 1993.
- Lang, J.R. & Baker, T., 2001. Intrusion-related gold systems: the present level of understanding. Mineralium Deposita, 36, pp477-489, 2001.
- Lindberg, W., 1922. A suggestion for the terminology of certain mineral deposits. Economic Geology, '17, pp. 292-294.
- Lindgren, Waldemar, 1933. Mineral Deposits, 4th ed., McGraw-Hill
- Lowenstern, J.B., 2001. Carbon dioxide in magmas and implications for hydrothermal systems. Mineralium Deposita, 36, pp490-502, 2001.
- Pettke, T; Frei, R.; Kramers J.D. & Villa, I. M. 1997. Isotope systematics in vein gold from Brusson, Val d'Ayas (NW Italy); (U+Th)/He and K/Ar in native Au and its fluid inclusions. Chemical Geology, 135, pp173-187, 1997.
- White, A.J.R, 2001. Water, restite and granite mineralisation. Australian Journal of Earth Sciences, 48, pp551-555 2001.
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crust is the outermost layer of a planet.
The crust of the Earth is composed of a great variety of igneous, metamorphic, and sedimentary rocks. The crust is underlain by the mantle.
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The crust of the Earth is composed of a great variety of igneous, metamorphic, and sedimentary rocks. The crust is underlain by the mantle.
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A mineral is a naturally occurring substance formed through geological processes that has a characteristic chemical composition, a highly ordered atomic structure and specific physical properties.
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Petroleum (Latin Petroleum derived from Greek πέτρα (Latin petra) - rock + έλαιον (Latin oleum) - oil) or crude oil
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ore is a volume of rock containing components or minerals in a mode of occurrence that renders it valuable for mining. An ore must contain materials that are
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Igneous rocks (etymology from latin ignis, fire) are rocks formed by solidification of cooled magma (molten rock), with or without crystallization, either below the surface as intrusive (plutonic) rocks or on the surface as extrusive (volcanic) rocks.
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Igneous rocks (etymology from latin ignis, fire) are rocks formed by solidification of cooled magma (molten rock), with or without crystallization, either below the surface as intrusive (plutonic) rocks or on the surface as extrusive (volcanic) rocks.
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Fractional crystallization may refer to:
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- Fractional crystallization (chemistry), a process to separate different solutes from a solution
- Fractional crystallization (geology), a natural process occurring in igneous rocks during which precipitation of minerals takes place
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Cumulate rocks are igneous rocks formed by the accumulation of crystals from a magma either by settling or floating.
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Formation
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Miscibility is a term in chemistry that refers to the property of liquids to mix in all proportions, forming a homogeneous solution. In principle, the term applies also to other phases (solids and gases), but the main focus on the solubility of one liquid in another.
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Hydrothermal circulation in its most general sense is the circulation of hot water; 'hydros' in the Greek meaning water and 'thermos' meaning heat. Hydrothermal circulation occurs most often in the vicinity of sources of heat within the Earth's crust.
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Brine is water saturated or nearly saturated with salt (NaCl). It is used (now less popular than historically) to preserve vegetables, fish, and meat. Brine is also commonly used to age Feta cheese.
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Metamorphism can be defined as the solid state recrystallisation of pre-existing rocks due to changes in heat and/or pressure and/or introduction of fluids i.e without melting. There will be mineralogical, chemical and crystallographic changes.
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Zinc (IPA: /ˈzɪŋk/, from German: Zink) is a chemical element in the periodic table that has the symbol Zn and atomic number 30.
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calcite]] The carbonate mineral, calcite, is a chemical or biochemical calcium carbonate corresponding to the formula CaCO3 and is one of the most widely distributed minerals on the Earth's surface.
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In geology and oceanography, diagenesis is any chemical, physical, or biological change undergone by a sediment after its initial deposition and during and after its lithification, exclusive of surface alteration (weathering) and metamorphism.
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Halite is the mineral form of sodium chloride, NaCl, commonly known as rock salt. Halite forms isometric crystals. The mineral is typically colourless to yellow, but may also be light blue, dark blue, and pink.
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Cerussite (also known as lead carbonate or white lead ore) is a mineral consisting of lead carbonate (PbCO3), and an important ore of lead. The name is from the Latin cerussa, white lead.
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In geology, the mineral monazite is a reddish-brown phosphate containing rare earth metals and an important source of thorium, lanthanum, and cerium. It occurs usually in small isolated crystals.
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Thorianite is a rare mineral,[1] originally discovered by Ananda Coomaraswamy in 1904 as uraninite,[2] but recognized as a new species by W. R. Dunston.
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Barite (BaSO4) is a mineral consisting of barium sulfate. It is generally white or colorless, and is the main source of barium. Baryte is the British spelling, and the mineral is also called heavy spar.
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Chelation (from Greek χηλή, chelè, meaning claw; pronounced [ˌki:ˈleɪʃən]) is the binding or complexation of a bi- or multidentate ligand.
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4, 6
(mildly acidic oxide)
Electronegativity 2.1 (scale Pauling)
Ionization energies
(more) 1st: 869.3 kJmol−1
2nd: 1790 kJmol−1
3rd: 2698 kJmol−1
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(mildly acidic oxide)
Electronegativity 2.1 (scale Pauling)
Ionization energies
(more) 1st: 869.3 kJmol−1
2nd: 1790 kJmol−1
3rd: 2698 kJmol−1
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The term sulfide (also spelled sulphide, see spelling) refers to several types of chemical compounds containing sulfur in its lowest oxidation number of −2.
Formally, "sulfide" is the dianion, S2−
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Formally, "sulfide" is the dianion, S2−
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Redox (shorthand for reduction/oxidation reaction) describes all chemical reactions in which atoms have their oxidation number (oxidation state) changed.
This can be either a simple redox process such as the oxidation of carbon to yield carbon dioxide, or the
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This can be either a simple redox process such as the oxidation of carbon to yield carbon dioxide, or the
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In chemistry, the oxidation state is an indicator of the degree of oxidation of an atom in a chemical compound. The formal oxidation state is the hypothetical charge that an atom would have if all bonds to atoms of different elements were 100% ionic.
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Rock Texture Name of Mafic Rock
Pegmatitic Gabbro pegmatite
Coarse grained (phaneritic) Gabbro
Coarse grained and porphyritic Porphyritic gabbro
Fine grained (aphanitic) Basalt
Fine grained and porphyritic Porphyritic basalt
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Pegmatitic Gabbro pegmatite
Coarse grained (phaneritic) Gabbro
Coarse grained and porphyritic Porphyritic gabbro
Fine grained (aphanitic) Basalt
Fine grained and porphyritic Porphyritic basalt
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Ultramafic (or ultrabasic) rocks are igneous and meta-igneous rocks with very low silica content (less than 45%), generally >18% MgO, high FeO, low potassium, and are composed of usually greater than 90% mafic minerals (dark colored, high magnesium and iron content).
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carbonate is a salt or ester of carbonic acid.
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Applications
Soda water (also known as Seltzer water) is water with CO2 dissolved under pressure. The taste of soda water was discovered by the 18th century chemist Joseph Priestley...... Click the link for more information.
Fugacity is a measure of chemical potential in the form of 'adjusted pressure.' It directly relates to the tendency of a substance to prefer one phase (liquid, solid, gas) over another. At a fixed temperature and pressure, water will have a different fugacity for each phase.
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sinistral shear sense. Starlight Pit, Fortnum Gold Mine, Western Australia.]] Study of geological shear is related to the study of structural geology, rock microstructure or rock texture and fault mechanics.
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