Geothermobarometry

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Geothermobarometry is the methodology for estimating the pressure and temperature history of rocks (metamorphic, igneous or sedimentary). Geothermobarometry is a combination of geobarometry, where the pressure attained (and retained) by a mineral assemblage is estimated, and geothermometry where the temperature attained (and retained) by a mineral assemblage is estimated.

Contents

An illustration of geothermobarometry. A line of temperature equilibrium (orange) and a line of pressure equilibrium (blue) of selected mineral assemblages found in the specimen are plotted on the P-T diagram. The intersection represents the likely P-T condition experienced by rock in its metamorphic history. Geothermobarometry1.png
An illustration of geothermobarometry. A line of temperature equilibrium (orange) and a line of pressure equilibrium (blue) of selected mineral assemblages found in the specimen are plotted on the P-T diagram. The intersection represents the likely P-T condition experienced by rock in its metamorphic history.

Methodology

Geothermobarometry relies upon understanding the temperature and pressure of the formation of minerals within rocks. [1] There are several methods of measuring the temperature or pressure of mineral formation or re-equilibration relying for example on chemical equilibrium between minerals [1] [2] [3] or by measuring the chemical composition [4] and/or the crystal-chemical state of order [5] of individual minerals or by measuring the residual stresses on solid inclusions [6] or densities in fluid inclusions. [7]

"Classic" (thermodynamic) thermobarometry [8] relies upon the attainment of thermodynamic equilibrium between mineral pairs/assemblages that vary their compositions as a function of temperature and pressure. The distribution of component elements between the mineral assemblages is then analysed using a variety of analytical techniques as for example electron microprobe (EM), scanning electron microscope (SEM), Mass Spectrometry (MS). There are numerous extra factors to consider such as oxygen fugacity and water activity (roughly, the same as concentration) that must be accounted for using the appropriate methodological and analytical approach (e.g. Mössbauer spectroscopy, micro-raman spectroscopy, infrared spectroscopy etc...) Geobarometers are typically net-transfer reactions, which are sensitive to pressure but have little change with temperature, such as garnet-plagioclase-muscovite-biotite reaction that involves a significant volume reduction upon high pressure: [1]

Since mineral assemblages at equilibrium are dependent on pressures and temperatures, by measuring the composition of the coexisting minerals, together with using suitable activity models, the P-T conditions experienced by the rock can be determined. [1]

After one equilibrium constant is found, a line would be plotted on the P-T diagram.[ citation needed ] As different equilibrium constants of mineral assemblages would occur as lines with different slopes in the P-T diagram, therefore, by finding the intersection of at least two lines in the P-T diagram, the P-T condition of the specimen can be obtained. [1]

Despite the usefulness of geothermobarometry, special attention should be paid to whether the mineral assemblages represent an equilibrium, any occurrence of retrograde equilibrium in the rock, and appropriateness of calibration of the results. [1]

Elastic thermobarometry is a method of determining the equilibrium pressure and temperature attained by the host mineral and its inclusion on the rock history from the excess pressures exhibited by mineral inclusions trapped inside host minerals. Upon exhumation and cooling, contrasting compressibilities and thermal expansivities induce differential strains (volume mismatches) between a host crystal and its inclusions. These strains can be quantified in situ using Raman spectroscopy or X-ray diffraction. Knowing equations of state and elastic properties of minerals, elastic thermobarometry inverts measured strains to calculate the pressure-temperature conditions under which the stress state was uniform in the host and inclusion. [6] These are commonly interpreted to represent the conditions of inclusion entrapment or the last elastic equilibration of the pair.

Data on the geothermometers and geobarometers is derived from both laboratory studies on synthetic (artificial) mineral assemblages and from natural systems for which other constraints are available.

For example, one of the best known and most widely applicable geothermometers is the garnet-biotite relationship where the relative proportions of Fe and Mg in garnet and biotite change with increasing temperature, so measurement of the compositions of these minerals to give the Fe-Mg distribution between them allows the temperature of crystallization to be calculated, given some assumptions.

Assumptions in thermodynamic thermobarometry

In natural systems, the chemical reactions occur in open systems with unknown geological and chemical histories, and application of geothermobarometers relies on several assumptions that must hold in order for the laboratory data and natural compositions to relate in a valid fashion:

Assumptions in elastic thermobarometry

In natural systems elastic behaviour of minerals can be easily perturbed by high temperature re-equilibration, plastic or brittle deformation, leading to an irreversible change beyond the elastic regime that will prevent reconstructing the "elastic history" of the pair.

Techniques

Some techniques include:

Geothermometers

Note that the Fe-Mg exchange thermometers are empirical (laboratory tested and calibrated) as well as calculated based on a theoretical thermodynamic understanding of the components and phases involved. The Ti-in-biotite thermometer is solely empirical and not well understood thermodynamically.

Geobarometers

Various mineral assemblages rely more upon pressure than temperature; for example reactions which involve a large volume change. At high pressure, specific minerals assume lower volumes (therefore density increases, as the mass does not change) - it is these minerals which are good indicators of paleo-pressure.

Software

Software for "classic" thermobarometry includes:

Software for elastic thermobarometry includes:

Clinopyroxene thermobarometry

The mineral clinopyroxene is used for temperature and pressure calculations of the magma that produced igneous rock containing this mineral.

See also

Related Research Articles

<span class="mw-page-title-main">Biotite</span> Group of phyllosilicate minerals within the mica group

Biotite is a common group of phyllosilicate minerals within the mica group, with the approximate chemical formula K(Mg,Fe)3AlSi3O10(F,OH)2. It is primarily a solid-solution series between the iron-endmember annite, and the magnesium-endmember phlogopite; more aluminous end-members include siderophyllite and eastonite. Biotite was regarded as a mineral species by the International Mineralogical Association until 1998, when its status was changed to a mineral group. The term biotite is still used to describe unanalysed dark micas in the field. Biotite was named by J.F.L. Hausmann in 1847 in honor of the French physicist Jean-Baptiste Biot, who performed early research into the many optical properties of mica.

<span class="mw-page-title-main">Metamorphism</span> Change of minerals in pre-existing rocks without melting into liquid magma

Metamorphism is the transformation of existing rock to rock with a different mineral composition or texture. Metamorphism takes place at temperatures in excess of 150 °C (300 °F), and often also at elevated pressure or in the presence of chemically active fluids, but the rock remains mostly solid during the transformation. Metamorphism is distinct from weathering or diagenesis, which are changes that take place at or just beneath Earth's surface.

<span class="mw-page-title-main">Amphibolite</span> Metamorphic rock type

Amphibolite is a metamorphic rock that contains amphibole, especially hornblende and actinolite, as well as plagioclase feldspar, but with little or no quartz. It is typically dark-colored and dense, with a weakly foliated or schistose (flaky) structure. The small flakes of black and white in the rock often give it a salt-and-pepper appearance.

<span class="mw-page-title-main">Granulite</span> Class of high-grade medium to coarse grained metamorphic rocks

Granulites are a class of high-grade metamorphic rocks of the granulite facies that have experienced high-temperature and moderate-pressure metamorphism. They are medium to coarse–grained and mainly composed of feldspars sometimes associated with quartz and anhydrous ferromagnesian minerals, with granoblastic texture and gneissose to massive structure. They are of particular interest to geologists because many granulites represent samples of the deep continental crust. Some granulites experienced decompression from deep in the Earth to shallower crustal levels at high temperature; others cooled while remaining at depth in the Earth.

<span class="mw-page-title-main">Hornfels</span>

Hornfels is the group name for a set of contact metamorphic rocks that have been baked and hardened by the heat of intrusive igneous masses and have been rendered massive, hard, splintery, and in some cases exceedingly tough and durable. These properties are caused by fine grained non-aligned crystals with platy or prismatic habits, characteristic of metamorphism at high temperature but without accompanying deformation. The term is derived from the German word Hornfels, meaning "hornstone", because of its exceptional toughness and texture both reminiscent of animal horns. These rocks were referred to by miners in northern England as whetstones.

<span class="mw-page-title-main">Chlorite group</span> Type of mineral

The chlorites are the group of phyllosilicate minerals common in low-grade metamorphic rocks and in altered igneous rocks. Greenschist, formed by metamorphism of basalt or other low-silica volcanic rock, typically contains significant amounts of chlorite.

<span class="mw-page-title-main">Greenschist</span> Metamorphic rock

Greenschists are metamorphic rocks that formed under the lowest temperatures and pressures usually produced by regional metamorphism, typically 300–450 °C (570–840 °F) and 2–10 kilobars (29,000–145,000 psi). Greenschists commonly have an abundance of green minerals such as chlorite, serpentine, and epidote, and platy minerals such as muscovite and platy serpentine. The platiness gives the rock schistosity. Other common minerals include quartz, orthoclase, talc, carbonate minerals and amphibole (actinolite).

<span class="mw-page-title-main">Omphacite</span> Member of the clinopyroxene group of silicate minerals

Omphacite is a member of the clinopyroxene group of silicate minerals with formula: (Ca, Na)(Mg, Fe2+, Al)Si2O6. It is a variably deep to pale green or nearly colorless variety of clinopyroxene. It normally appears in eclogite, which is the high-pressure metamorphic rock of basalt. Omphacite is the solid solution of Fe-bearing diopside and jadeite. It crystallizes in the monoclinic system with prismatic, typically twinned forms, though usually anhedral. Its space group can be P2/n or C2/c depending on the thermal history. It exhibits the typical near 90° pyroxene cleavage. It is brittle with specific gravity of 3.29 to 3.39 and a Mohs hardness of 5 to 6.

Restite is the residual material left at the site of melting during the in place production of magma.

<span class="mw-page-title-main">Index mineral</span>

An index mineral is used in geology to determine the degree of metamorphism a rock has experienced. Depending on the original composition of and the pressure and temperature experienced by the protolith, chemical reactions between minerals in the solid state produce new minerals. When an index mineral is found in a metamorphosed rock, it indicates the minimum pressure and temperature the protolith must have achieved in order for that mineral to form. The higher the pressure and temperature in which the rock formed, the higher the grade of the rock.

<span class="mw-page-title-main">Metamorphic facies</span> Set of mineral assemblages in metamorphic rocks formed under similar pressures and temperatures

A metamorphic facies is a set of mineral assemblages in metamorphic rocks formed under similar pressures and temperatures. The assemblage is typical of what is formed in conditions corresponding to an area on the two dimensional graph of temperature vs. pressure. Rocks which contain certain minerals can therefore be linked to certain tectonic settings, times and places in the geological history of the area. The boundaries between facies are wide because they are gradational and approximate. The area on the graph corresponding to rock formation at the lowest values of temperature and pressure is the range of formation of sedimentary rocks, as opposed to metamorphic rocks, in a process called diagenesis.

In geology ultrahigh-temperature metamorphism (UHT) is extreme crustal metamorphism with metamorphic temperatures exceeding 900 °C. Granulite-facies rocks metamorphosed at very high temperatures were identified in the early 1980s, although it took another decade for the geoscience community to recognize UHT metamorphism as a common regional phenomenon. Petrological evidence based on characteristic mineral assemblages backed by experimental and thermodynamic relations demonstrated that Earth's crust can attain and withstand very high temperatures (900–1000 °C) with or without partial melting.

<span class="mw-page-title-main">Clinopyroxene thermobarometry</span>

Clinopyroxene thermobarometry is a scientific method that uses the mineral clinopyroxene to determine the temperature and pressure of the magma when the mineral crystalized. Clinopyroxene is found in many igneous rocks, so the method can be used to determine information about the entire rock. Many different minerals can be used for geothermobarometry, but clinopyroxene is especially useful because it's a common phenocryst in igneous rocks and easy to identify, and the crystallization of jadeite, a type of clinopyroxene, implies a growth in molar volume, making it a good indicator of pressure.

<span class="mw-page-title-main">Timothy Holland</span> British scientist

Timothy John Barrington Holland is a petrologist and Emeritus Professor in the Department of Earth Sciences at the University of Cambridge.

Roger Powell FRS, is a British-born Australian based educator and academic. He is Emeritus professor in the School of Geography, Earth and Atmospheric Sciences at the University of Melbourne.

<span class="mw-page-title-main">Pressure-temperature-time path</span>

The Pressure-Temperature-time path is a record of the pressure and temperature (P-T) conditions that a rock experienced in a metamorphic cycle from burial and heating to uplift and exhumation to the surface. Metamorphism is a dynamic process which involves the changes in minerals and textures of the pre-existing rocks (protoliths) under different P-T conditions in solid state. The changes in pressures and temperatures with time experienced by the metamorphic rocks are often investigated by petrological methods, radiometric dating techniques and thermodynamic modeling.

<span class="mw-page-title-main">Petrogenetic grid</span> Pressure-temperature diagram of mineral stability ranges

A petrogenetic grid is a geological phase diagram that connects the stability ranges or metastability ranges of metamorphic minerals or mineral assemblages to the conditions of metamorphism. Experimentally determined mineral or mineral-assemblage stability ranges are plotted as metamorphic reaction boundaries in a pressure–temperature cartesian coordinate system to produce a petrogenetic grid for a particular rock composition. The regions of overlap of the stability fields of minerals form equilibrium mineral assemblages used to determine the pressure–temperature conditions of metamorphism. This is particularly useful in geothermobarometry.

Garnet-Biotite Geothermometry is a method used to evaluate the peak temperature at which metamorphic rocks have formed. Geothermometry makes up one component of geothermobarometry, which also includes the evaluation of pressure (geobarometry). There are many geothermometers, but garnet-biotite is particularly useful because of the frequent occurrence of biotite and garnet together in medium grade metamorphic rocks. The garnet biotite thermometer correlates temperature with the partitioning of Fe and Mg in coinciding garnet and biotite. The garnet-biotite thermometer has been "calibrated" many times since the 70's by both experimental and empirical methods, however Ferry and Spear's 1978 experimental calibration study is reported thoroughly and commonly cited. Given a rock containing both garnet and biotite, an equilibrium constant (KD) can be found simply by using microprobe analysis. Then, by comparing the found KD value to the calculated garnet-biotite geothermometer, the peak temperature of rock formation can be determined.

<span class="mw-page-title-main">Gore Mountain Garnet</span> Rock formation in New York

Gore Mountain Garnet, found in the Adirondack Mountains in New York, contains the world's largest garnets. The rock that holds these garnets, garnet amphibolite, is sometimes referred to as 'black ore' or 'dark ore.' This rock formation formed during metamorphism during the Ottawan phase of the Grenvillian orogeny, and extremely high temperatures combined with introduction of fluids is what most likely contributed to the unusual size of the megacrystic garnets.

<span class="mw-page-title-main">Compatibility diagram</span> Depicts coexisting mineral phases in a metamorphic rock

In metamorphic geology, a compatibility diagram shows how the mineral assemblage of a metamorphic rock in thermodynamic equilibrium varies with composition at a fixed temperature and pressure. Compatibility diagrams provide an excellent way to analyze how variations in the rock's composition affect the mineral paragenesis that develops in a rock at particular pressure and temperature conditions. Because of the difficulty of depicting more than three components, usually only the three most important components are plotted, though occasionally a compatibility diagram for four components is plotted as a projected tetrahedron.

References

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