View source for Earth:Metamorphism

{{Short description|Change of minerals in pre-existing rocks without melting into liquid magma}}
[[Image:Metamorphic reaction EN.svg|thumb|upright=1.35|Schematic representation of a metamorphic reaction. Abbreviations of minerals: act = actinolite; chl = chlorite; ep = epidote; gt = garnet; hbl = hornblende; plag = plagioclase. Two minerals represented in the figure do not participate in the reaction, they can be quartz and K-feldspar. This reaction takes place in nature when a mafic rock goes from amphibolite facies to greenschist facies.]]

[[File:Thin section of garnet-mica-schist.jpg|thumb|upright=1.35| A [[Physics:Polarized light microscopy|cross-polarized]] thin section image of a garnet-mica-schist from Salangen, Norway showing the strong strain fabric of schists. The black crystal is garnet, the pink-orange-yellow  colored strands are muscovite mica, and the brown crystals are biotite mica. The grey and white crystals are quartz and (limited) feldspar.]]

'''Metamorphism''' is the transformation of existing [[Earth:Rock (geology)|rock]] (the [[Earth:Protolith|protolith]]) to rock with a different [[Earth:Mineral|mineral]] composition or [[Earth:Texture (geology)|texture]]. Metamorphism takes place at temperatures in excess of {{cvt|150|C||sigfig=1}}, and often also at elevated pressure or in the presence of chemically active fluids, but the rock remains mostly solid during the transformation.{{sfn|Marshak|2009|p=177}} Metamorphism is distinct from [[Earth:Weathering|weathering]] or [[Earth:Diagenesis|diagenesis]], which are changes that take place at or just beneath Earth's surface.{{sfn|Vernon|2008|p=1}}

Various forms of metamorphism exist, including regional, contact, hydrothermal, [[Earth:Shock metamorphism|shock]], and dynamic metamorphism. These differ in the characteristic temperatures, pressures, and rate at which they take place and in the extent to which reactive fluids are involved. Metamorphism occurring at increasing pressure and temperature conditions is known as ''prograde metamorphism'', while decreasing temperature and pressure characterize ''retrograde metamorphism''.

Metamorphic petrology is the study of metamorphism. Metamorphic petrologists rely heavily on [[Physics:Statistical mechanics|statistical mechanics]] and [[Earth:Experimental petrology|experimental petrology]] to understand metamorphic processes.

==Metamorphic processes==
[[File:Metamorphic Pressure alignment-white.png|thumb|upright=1.2|(Left) Randomly-orientated grains in a rock before metamorphism. (Right) Grains align orthogonal to the applied stress if a rock is subjected to stress during metamorphism]]

Metamorphism is the set of processes by which existing rock is transformed physically or chemically at elevated temperature, without actually melting to any great degree. The importance of heating in the formation of [[Earth:Metamorphic rock|metamorphic rock]] was first recognized by the pioneering Scottish naturalist, James Hutton, who is often described as the father of modern geology. Hutton wrote in 1795 that some rock beds of the Scottish Highlands had originally been [[Earth:Sedimentary rock|sedimentary rock]], but had been transformed by great heat.{{sfn|Yardley|1989|pp=1–5}}

Hutton also speculated that pressure was important in metamorphism. This hypothesis was tested by his friend, James Hall, who sealed [[Earth:Chalk|chalk]] into a makeshift [[Physics:Pressure vessel|pressure vessel]] constructed from a cannon barrel and heated it in an iron foundry furnace. Hall found that this produced a material strongly resembling [[Chemistry:Marble|marble]], rather than the usual quicklime produced by heating of chalk in the open air. French geologists subsequently added [[Earth:Metasomatism|metasomatism]], the circulation of fluids through buried rock, to the list of processes that help bring about metamorphism. However, metamorphism can take place without metasomatism (isochemical metamorphism) or at depths of just a few hundred meters where pressures are relatively low (for example, in contact metamorphism).{{sfn|Yardley|1989|pp=1–5}}

Rock can be transformed without melting because heat causes atomic bonds to break, freeing the atoms to move and form new bonds with other [[Physics:Atom|atom]]s. Pore fluid present between mineral grains is an important medium through which atoms are exchanged.{{sfn|Yardley|1989|page=5}} This permits [[Earth:Recrystallization (geology)|recrystallization]] of existing minerals or crystallization of new minerals with different crystalline structures or chemical compositions (neocrystallization).{{sfn|Marshak|2009|p=177}} The transformation converts the minerals in the protolith into forms that are more stable (closer to [[Chemistry:Chemical equilibrium|chemical equilibrium]]) under the conditions of pressure and temperature at which metamorphism takes place.{{sfn|Yardley|1989|pp=29–30}}{{sfn|Philpotts|Ague|2009|pp=149, 420–425}}

Metamorphism is generally regarded to begin at temperatures of {{convert|100 to 200|C||sp=us}}. This excludes [[Earth:Diagenesis|diagenetic]] changes due to [[Earth:Compaction (geology)|compaction]] and [[Earth:Lithification|lithification]], which result in the formation of sedimentary rocks.{{sfn|Bucher|2002|p=4}} The upper boundary of metamorphic conditions lies at the [[Chemistry:Solidus|solidus]] of the rock, which is the temperature at which the rock begins to melt. At this point, the process becomes an igneous process.{{sfn|Nelson|2022}} The solidus temperature depends on the composition of the rock, the pressure, and whether the rock is saturated with water. Typical solidus temperatures range from {{convert|650|C||sp=us}} for wet granite at a few hundred megapascals (MPa) of pressure{{sfn|Holland|Powell|2001}} to about {{convert|1080|C||sp=us}} for wet basalt at atmospheric pressure.{{sfn|Philpotts|Ague|2009|p=252}} [[Earth:Migmatite|Migmatite]]s are rocks formed at this upper limit, which contains pods and veins of material that has started to melt but has not fully segregated from the refractory residue.{{sfn|Philpotts|Ague|2009|p=44}}

The metamorphic process can occur at almost any pressure, from near surface pressure (for contact metamorphism) to pressures in excess of 16 kbar (1600 MPa).{{sfn|Yardley|1989|pp=49–51}}

===Recrystallization===
[[File:Basalt-hand-sample.tif|thumb|upright=1.35|Basalt hand sample showing fine texture]]
[[File:Amphibolite (Archean, 3.1-3.2 Ga; Norris South roadcut, Madison County, Montana, USA) 1 (45574881922).jpg|thumb|upright=1.35|Amphibolite formed by metamorphism of basalt showing coarse texture]]
The change in the grain size and orientation in the rock during the process of metamorphism is called [[Earth:Recrystallization (geology)|recrystallization]]. For instance, the small [[Chemistry:Calcite|calcite]] crystals in the sedimentary rocks [[Earth:Limestone|limestone]] and [[Earth:Chalk|chalk]] change into larger crystals in the metamorphic rock [[Chemistry:Marble|marble]].{{sfn|Yardley|1989|pp=127, 154}} In metamorphosed [[Earth:Sandstone|sandstone]], recrystallization of the original [[Chemistry:Quartz|quartz]] sand grains results in very compact [[Earth:Quartzite|quartzite]], also known as metaquartzite, in which the often larger quartz crystals are interlocked.{{sfn|Jackson|1997|loc="metaquartzite"}} Both high temperatures and pressures contribute to recrystallization. High temperatures allow the [[Physics:Atom|atom]]s and [[Physics:Ion|ion]]s in solid crystals to migrate, thus reorganizing the crystals, while high pressures cause solution of the crystals within the rock at their points of contact (''[[Earth:Pressure solution|pressure solution]]'') and redeposition in pore space.{{sfn|Yardley|1989|pp=154–158}}

During recrystallization, the identity of the mineral does not change, only its texture. Recrystallization generally begins when temperatures reach above half the melting point of the mineral on the [[Kelvin]] scale.{{sfn|Gillen|1982|p=31}}

Pressure solution begins during diagenesis (the process of lithification of sediments into sedimentary rock) but is completed during early stages of metamorphism. For a sandstone protolith, the dividing line between diagenesis and metamorphism can be placed at the point where strained quartz grains begin to be replaced by new, unstrained, small quartz grains, producing a ''mortar texture'' that can be identified in [[Earth:Thin section|thin section]]s under a polarizing microscope. With increasing grade of metamorphism, further recrystallization produces ''foam texture'', characterized by polygonal grains meeting at triple junctions, and then ''porphyroblastic texture'', characterized by coarse, irregular grains, including some larger grains (porphyroblasts.){{sfn|Howard|2005}}

[[File:Mylonite Strona.jpg|thumb|upright=1.35|A mylonite (through a [[Earth:Petrographic microscope|petrographic microscope]])]]
Metamorphic rocks are typically more coarsely crystalline than the protolith from which they formed. Atoms in the interior of a crystal are surrounded by a stable arrangement of neighboring atoms. This is partially missing at the surface of the crystal, producing a ''[[Physics:Surface energy|surface energy]]'' that makes the surface thermodynamically unstable. Recrystallization to coarser crystals reduces the surface area and so minimizes the surface energy.{{sfn|Yardley|1989|pp=148–158}}

Although grain coarsening is a common result of metamorphism, rock that is intensely deformed may eliminate [[Strain energy|strain energy]] by recrystallizing as a fine-grained rock called ''[[Earth:Mylonite|mylonite]]''. Certain kinds of rock, such as those rich in quartz, [[Chemistry:Carbonate mineral|carbonate mineral]]s, or olivine, are particularly prone to form mylonites, while feldspar and garnet are resistant to mylonitization.{{sfn|Yardley|1989|p=158}}
{{clear}}

===Phase change===
{{Annotated image
| image = Al2SiO5 phase diagram.svg
| image-width=210
| height=250
| caption = Phase diagram of Al<sub>2</sub>SiO<sub>5</sub>
 <br />(nesosilicates)

|annotations = 
{{annotation|040|100|[[Chemistry:Kyanite|Kyanite]]}}
{{annotation|070|170|[[Chemistry:Andalusite|Andalusite]]}}
{{annotation|130|120|[[Chemistry:Sillimanite|Sillimanite]]}}
}}

Phase change metamorphism is the creating of a new mineral with the same chemical formula as a mineral of the protolith. This involves a rearrangement of the atoms in the crystals. An example is provided by the [[Chemistry:Aluminium silicate|aluminium silicate]] minerals, [[Chemistry:Kyanite|kyanite]], [[Chemistry:Andalusite|andalusite]], and [[Chemistry:Sillimanite|sillimanite]]. All three have the identical composition, {{chem2|Al2SiO5}}. Kyanite is stable at surface conditions. However, at atmospheric pressure, kyanite transforms to [[Chemistry:Andalusite|andalusite]] at a temperature of about {{cvt|190|C||}}. Andalusite, in turn, transforms to [[Chemistry:Sillimanite|sillimanite]] when the temperature reaches about {{cvt|800|C||}}. At pressures above about 4 kbar (400 MPa), kyanite transforms directly to sillimanite as the temperature increases.{{sfn|Yardley|1989|pp=32–33, 110, 130–131}} A similar phase change is sometimes seen between [[Chemistry:Calcite|calcite]] and [[Chemistry:Aragonite|aragonite]], with calcite transforming to aragonite at elevated pressure and relatively low temperature.{{sfn|Yardley|1989|pp=183–183}}

===Neocrystallization===
Neocrystallization involves the creation of new mineral crystals different from the protolith. [[Chemistry:Chemical reaction|Chemical reaction]]s digest the minerals of the protolith which yields new minerals. This is a very slow process as it can also involve the diffusion of atoms through solid crystals.{{sfn|Vernon|1976|p=149}}

An example of a neocrystallization reaction is the reaction of [[Chemistry:Fayalite|fayalite]] with [[Chemistry:Plagioclase|plagioclase]] at elevated pressure and temperature to form [[Chemistry:Garnet|garnet]]. The reaction is:{{sfn|Yardley|1989|pp=110, 130–131}}

{{NumBlk|:
|{{overset|fayalite|3 {{chem|Fe|2|SiO|4}}}} + {{overset|plagioclase|{{chem|CaAl|2|Si|2|O|8}}}} → {{overset|garnet|2 {{chem|CaFe|2|Al|2|Si|3|O|12}}}}
|{{EquationRef|Reaction 1}}}}

Many complex high-temperature reactions may take place between minerals without them melting, and each mineral assemblage produced provides us with a clue as to the temperatures and pressures at the time of metamorphism. These reactions are possible because of rapid diffusion of atoms at elevated temperature. Pore fluid between mineral grains can be an important medium through which atoms are exchanged.{{sfn|Yardley|1989|page=5}}

A particularly important group of neocrystallization reactions are those that release [[Earth:Volatile (astrogeology)|volatiles]] such as water and [[Chemistry:Carbon dioxide|carbon dioxide]]. During metamorphism of [[Earth:Basalt|basalt]] to [[Earth:Eclogite|eclogite]] in subduction zones, hydrous minerals break down, producing copious quantities of water.{{sfn|Stern|2002|pp=6–10}} The water rises into the overlying mantle, where it lowers the melting temperature of the mantle rock, generating [[Biology:Magma|magma]] via [[Earth:Flux melting|flux melting]].{{sfn|Schmincke|2003|pp=18, 113–126}} The mantle-derived magmas can ultimately reach the Earth's surface, resulting in volcanic eruptions. The resulting [[Earth:Volcanic arc|arc volcanoes]] tend to produce dangerous eruptions, because their high water content makes them extremely explosive.{{sfn|Stern|2002|pp=27–28}}

Examples of ''dehydration reactions'' that release water include:{{sfn|Yardley|1989|pp=75,102}}

{{NumBlk|:
|{{overset|[[Chemistry:Hornblende|hornblende]]|7{{chem2|Ca2Mg3Al4Si6O22(OH)2}}}} + {{overset|quartz|10{{chem2|SiO2}}}} → {{overset|[[Chemistry:Cummingtonite|cummingtonite]]|3{{chem2|Mg7Si8O22(OH)2}}}} + {{overset|[[Chemistry:Anorthite|anorthite]]|14{{chem2|CaAl2Si2O8}}}} + {{overset|water|4{{chem2|H2O}}}}
|{{EquationRef|Reaction 2}}}}

{{NumBlk|:
|{{overset|[[Chemistry:Muscovite|muscovite]]|2{{chem2|KAl2(AlSi3O10)(OH)2}}}} + {{overset|quartz|2{{chem2|SiO2}}}} → {{overset|sillimanite|2{{chem2|Al2SiO5}}}} + {{overset|[[Chemistry:Potassium feldspar|potassium feldspar]]|2{{chem2|KAlSi3O8}}}} + {{overset|water|2{{chem2|H2O}}}}
|{{EquationRef|Reaction 3}}}}

An example of a decarbonation reaction is:{{sfn|Yardley|1989|p=127}}

{{NumBlk|:
|{{overset|calcite|{{chem2|CaCO3}}}} + {{overset|quartz|{{chem2|SiO2}}}} → {{overset|[[Chemistry:Wollastonite|wollastonite]]|{{chem2|CaSiO3}}}} + {{overset|carbon dioxide|{{chem2|CO2}}}}
|{{EquationRef|Reaction 4}}}}

===Plastic deformation===
In plastic deformation pressure is applied to the [[Earth:Protolith|protolith]], which causes it to shear or bend, but not break. In order for this to happen temperatures must be high enough that brittle fractures do not occur, but not so high that diffusion of crystals takes place.{{sfn|Vernon|1976|p=149}}
As with pressure solution, the early stages of plastic deformation begin during diagenesis.{{sfn|Boggs|2006|pp=147–154}}

==Types==

===Regional===
''Regional metamorphism'' is a general term for metamorphism that affects entire regions of the Earth's crust.{{sfn|Jackson|1997|loc="regional metamorphism"}} It most often refers to ''dynamothermal metamorphism'', which takes place in ''orogenic belts'' (regions where mountain building is taking place),{{sfn|Jackson|1997|loc="dynamothermal metamorphism"}} but also includes ''burial metamorphism'', which results simply from rock being buried to great depths below the Earth's surface in a subsiding basin.{{sfn|Jackson|1997|loc="burial metamorphism"}}{{sfn|Yardley|1989|p=12}}

====Dynamothermal====
[[File:The stones of the Dutch - Lleida Pyrenees 04.JPG|thumb|A metamorphic rock, deformed during the Variscan orogeny, at Vall de Cardós, Lérida, {{wipe|Spain}}]]
To many geologists, regional metamorphism is practically synonymous with dynamothermal metamorphism.{{sfn|Jackson|1997|loc="regional metamorphism"}} This form of metamorphism takes place at convergent plate boundaries, where two continental plates or a continental plate and an [[Earth:Island arc|island arc]] collide. The collision zone becomes a belt of [[Earth:Mountain formation|mountain formation]] called an ''[[Physics:Orogeny|orogeny]]''. The orogenic belt is characterized by thickening of the Earth's crust, during which the deeply buried crustal rock is subjected to high temperatures and pressures and is intensely deformed.{{sfn|Yardley|1989|p=12}}{{sfn|Kearey|Klepeis|Vine|2009|pp=275–279}} Subsequent [[Earth:Erosion|erosion]] of the mountains exposes the roots of the orogenic belt as extensive outcrops of metamorphic rock,{{sfn|Levin|2010|pp=76–77, 82–83}} characteristic of mountain chains.{{sfn|Yardley|1989|p=12}}

Metamorphic rock formed in these settings tends to shown well-developed [[Earth:Foliation (geology)|foliation]].{{sfn|Yardley|1989|p=12}} Foliation develops when a rock is being shortened along one axis during metamorphism. This causes crystals of platy minerals, such as [[Chemistry:Mica|mica]] and [[Chemistry:Chlorite group|chlorite]], to become rotated such that their short axes are parallel to the direction of shortening. This results in a banded, or foliated, rock, with the bands showing the colors of the minerals that formed them. Foliated rock often develops planes of [[Earth:Cleavage (geology)|cleavage]].  [[Chemistry:Slate|Slate]] is an example of a foliated metamorphic rock, originating from [[Chemistry:Shale|shale]], and it typically shows well-developed cleavage that allows slate to be split into thin plates.{{sfn|Yardley|1989|p=22, 168–170}}

The type of foliation that develops depends on the metamorphic grade. For instance, starting with a mudstone, the following sequence develops with increasing temperature: The mudstone is first converted to slate, which is a very fine-grained, foliated metamorphic rock, characteristic of very low grade metamorphism. Slate in turn is converted to [[Chemistry:Phyllite|phyllite]], which is fine-grained and found in areas of low grade metamorphism. [[Chemistry:Schist|Schist]] is medium to coarse-grained and found in areas of medium grade metamorphism. High-grade metamorphism transforms the rock to [[Earth:Gneiss|gneiss]], which is coarse to very coarse-grained.{{sfn|Wicander|Munroe |2005|pp=174–77}}

Rocks that were subjected to uniform pressure from all sides, or those that lack minerals with distinctive growth habits, will not be foliated. Marble lacks platy minerals and is generally not foliated, which allows its use as a material for sculpture and architecture.

Collisional orogenies are preceded by [[Earth:Subduction|subduction]] of oceanic crust.{{sfn|Yuan|Pan|Wang |Jiang|2009|pp=31–48}} The conditions within the subducting slab as it plunges toward the [[Earth:Mantle (geology)|mantle]] in a subduction zone produce [[Earth:Subduction zone metamorphism|their own distinctive regional metamorphic effects]], characterized by [[Earth:Paired metamorphic belts|paired metamorphic belts]].{{sfn|Miyashiro|1973|pp=368–369}}

The pioneering work of George Barrow on regional metamorphism in the Scottish Highlands showed that some regional metamorphism produces well-defined, mappable zones of increasing metamorphic grade. This ''Barrovian metamorphism'' is the most recognized [[Earth:Metamorphic series|metamorphic series]] in the world. However, Barrovian metamorphism is specific to pelitic rock, formed from mudstone or [[Earth:Siltstone|siltstone]], and it is not unique even in pelitic rock. A different sequence in the northeast of Scotland defines ''Buchan metamorphism'', which took place at lower pressure than the Barrovian.{{sfn|Philpotts|Ague|2009|p=417}}

====Burial====
[[File:Sioux Quartzite (Paleoproterozoic, 1.65 to 1.70 Ga; Transcontinental Arch, USA) 4.jpg|thumb|Sioux Quartzite, a product of burial metamorphism]]
Burial metamorphism takes place simply through rock being buried to great depths below the Earth's surface in a subsiding basin.{{sfn|Yardley|1989|p=12}} Here the rock is subjected to high temperatures and the great pressure caused by the immense weight of the rock layers above. Burial metamorphism tends to produced low-grade metamorphic rock. This shows none of the effects of deformation and folding so characteristic of dynamothermal metamorphism.{{sfn|Robinson|Bevins|Aguirre|Vergara|2004 |pp=513–528}}

Examples of metamorphic rocks formed by burial metamorphism include some of the rocks of the Midcontinent Rift System of North America, such as the [[Earth:Sioux Quartzite|Sioux Quartzite]],{{sfn|Denison|Bickford|Lidiak|Kisvarsanyi|1987}} and in the Hamersley Basin of Australia.{{sfn|Smith|Perdrix |Parks |1982}}

===Contact===
[[File: Metamorphic Aureole in the Henry Mountains.JPG|thumb|A metamorphic aureole in the Henry Mountains, Utah. The greyish rock on top is the igneous intrusion, consisting of porphyritic granodiorite from the Henry Mountains laccolith, and the pinkish rock on the bottom is the sedimentary country rock, a siltstone. In between, the metamorphosed siltstone is visible as both the dark layer (~5&nbsp; cm thick) and the pale layer below it.]]

[[File:Rock contact metamorphism eng big text.jpg|thumbnail]]

''Contact metamorphism'' occurs typically around intrusive [[Earth:Igneous rock|igneous rock]]s as a result of the temperature increase caused by the intrusion of [[Biology:Magma|magma]] into cooler [[Earth:Country rock (geology)|country rock]]. The area surrounding the intrusion where the contact metamorphism effects are present is called the '''metamorphic aureole''',{{sfn|Marshak|2009||p=187}} the '''contact aureole''', or simply the aureole.{{sfn|Jackson|1997|loc="aureole"}} Contact metamorphic rocks are usually known as [[Chemistry:Hornfels|hornfels]]. Rocks formed by contact metamorphism may not present signs of strong deformation and are often fine-grained{{sfn|Yardley|1989|pp=12, 26}}{{sfn|Blatt|Tracy|1996|pp=367, 512}} and extremely tough.{{sfn|Philpotts|Ague|2009|pp=422, 428}}

Contact metamorphism is greater adjacent to the intrusion and dissipates with distance from the contact.{{sfn|Yardley|1989|pp=10–11}} The size of the aureole depends on the heat of the intrusion, its size, and the temperature difference with the wall rocks. Dikes generally have small aureoles with minimal metamorphism, extending not more than one or two dike thicknesses into the surrounding rock,{{sfn|Barker|Bone|Lewan|1998}} whereas the aureoles around batholiths can be up to several kilometers wide.{{sfn|Yardley|1989|p=43}}{{sfn|Philpotts|Ague|2009|p=427}}

The metamorphic grade of an aureole is measured by the peak metamorphic mineral which forms in the aureole. This is usually related to the metamorphic temperatures of [[Earth:Pelite|pelitic]] or aluminosilicate rocks and the minerals they form. The metamorphic grades of aureoles at shallow depth are [[Chemistry:Albite|albite]]-[[Chemistry:Epidote|epidote]] hornfels, hornblende hornfels, [[Chemistry:Pyroxene|pyroxene]] hornfels, and sillimanite hornfels, in increasing order of temperature of formation. However, the albite-epidote hornfels is often not formed, even though it is the lowest temperature grade.{{sfn|Philpotts|Ague|2009|p=422}}

Magmatic fluids coming from the intrusive rock may also take part in the [[Earth:Metamorphic reaction|metamorphic reaction]]s. An extensive addition of magmatic fluids can significantly modify the chemistry of the affected rocks. In this case the metamorphism grades into [[Earth:Metasomatism|metasomatism]]. If the intruded rock is rich in [[Chemistry:Carbonate|carbonate]] the result is a [[Chemistry:Skarn|skarn]].{{sfn|Yardley|1989|p=126}} [[Chemistry:Fluorine|Fluorine]]-rich magmatic waters which leave a cooling granite may often form [[Earth:Greisen|greisen]]s within and adjacent to the contact of the granite.{{sfn|Rakovan|2007}} Metasomatic altered aureoles can localize the deposition of metallic [[Earth:Ore|ore]] minerals and thus are of economic interest.{{sfn|Buseck|1967}}{{sfn|Cooper|Lee|Fortey|Cooper|1988}}

''Fenitization'', or ''Na-metasomatism'', is a distinctive form of contact metamorphism accompanied by metasomatism. It takes place around intrusions of a rare type of magma called a ''carbonatite'' that is highly enriched in [[Chemistry:Carbonate|carbonate]]s and low in [[Chemistry:Silica|silica]]. Cooling bodies of carbonatite magma give off highly alkaline fluids rich in sodium as they solidify, and the hot, reactive fluid replaces much of the mineral content in the aureole with sodium-rich minerals.{{sfn|Philpotts|Ague|2009|pp=396–397}}

A special type of contact metamorphism, associated with fossil fuel fires, is known as [[Earth:Pyrometamorphism|pyrometamorphism]].{{sfn|Grapes|2011}}{{sfn|Sokol|Maksimova|Nigmatulina|Sharygin|2005}}

===Hydrothermal===
''[[Earth:Hydrothermal circulation|Hydrothermal]] metamorphism'' is the result of the interaction of a rock with a high-temperature fluid of variable composition. The difference in composition between an existing rock and the invading fluid triggers a set of metamorphic and [[Earth:Metasomatism|metasomatic]] reactions. The hydrothermal fluid may be magmatic (originate in an intruding magma), circulating [[Earth:Groundwater|groundwater]], or ocean water.{{sfn|Yardley|1989|p=12}} Convective circulation of hydrothermal fluids in the ocean floor [[Earth:Basalt|basalt]]s produces extensive hydrothermal metamorphism adjacent to spreading centers and other submarine volcanic areas. The fluids eventually escape through vents on the ocean floor known as black smokers.{{sfn|Marshak|2009|p=190}} The patterns of this hydrothermal alteration are used as a guide in the search for deposits of valuable metal ores.{{sfn|Philpotts|Ague|2009|pp=70, 243, 346}}

===Shock===
{{Main|Earth:Shock metamorphism}}
''Shock metamorphism'' occurs when an extraterrestrial object (a [[Astronomy:Meteorite|meteorite]] for instance) collides with the Earth's surface. Impact metamorphism is, therefore, characterized by ultrahigh pressure conditions and low temperature. The resulting minerals (such as SiO<sub>2</sub> [[Physics:Polymorphism (materials science)|polymorphs]] [[Chemistry:Coesite|coesite]] and [[Chemistry:Stishovite|stishovite]]) and textures are characteristic of these conditions.{{sfn|Yardley|1989|p=13}}

===Dynamic===
''Dynamic metamorphism'' is associated with zones of high strain such as [[Earth:Fault (geology)|fault]] zones.{{sfn|Yardley|1989|p=12}} In these environments, mechanical deformation is more important than chemical reactions in transforming the rock. The minerals present in the rock often do not reflect conditions of chemical equilibrium, and the textures produced by dynamic metamorphism are more significant than the mineral makeup.{{sfn|Mason|1990|pp=94–106}}

There are three [[Physics:Deformation mechanism|deformation mechanism]]s by which rock is mechanically deformed. These are ''[[Earth:Cataclastic rock|cataclasis]]'', the deformation of rock via the fracture and rotation of mineral grains;{{sfn|Jackson|1997|loc="cataclasis"}} plastic deformation of individual mineral crystals; and movement of individual atoms by diffusive processes.{{sfn|Brodie|Rutter|1985}} The textures of dynamic metamorphic zones are dependent on the depth at which they were formed, as the temperature and confining pressure determine the deformation mechanisms which predominate.{{sfn|Fossen|2016|p=185}}

At the shallowest depths, a fault zone will be filled with various kinds of unconsolidated [[Earth:Cataclastic rock|cataclastic rock]], such as ''[[Earth:Fault gouge|fault gouge]]'' or ''[[Earth:Fault breccia|fault breccia]]''. At greater depths, these are replaced by consolidated cataclastic rock, such as ''crush breccia'', in which the larger rock fragments are cemented together by calcite or quartz. At depths greater than about {{convert|5|km||sp=us}}, ''[[Earth:Cataclasite|cataclasite]]s'' appear; these are quite hard rocks consist of crushed rock fragments in a flinty matrix, which forms only at elevated temperature. At still greater depths, where temperatures exceed {{convert|300|C||sp=us}}, plastic deformation takes over, and the fault zone is composed of mylonite. Mylonite is distinguished by its strong foliation, which is absent in most cataclastic rock.{{sfn|Fossen|2016|pp=184–186}} It is distinguished from the surrounding rock by its finer grain size.{{sfn|Fossen|2016|p=341}}

There is considerable evidence that cataclasites form as much through plastic deformation and recrystallization as brittle fracture of grains, and that the rock may never fully lose cohesion during the process. Different minerals become ductile at different temperatures, with quartz being among the first to become ductile, and sheared rock composed of different minerals may simultaneously show both plastic deformation and brittle fracture.{{sfn|Philpotts|Ague|2009|p=441}}

The strain rate also affects the way in which rocks deform. Ductile deformation is more likely at low strain rates (less than 10<sup>−14</sup> sec<sup>−1</sup>) in the middle and lower crust, but high strain rates can cause brittle deformation. At the highest strain rates, the rock may be so strongly heated that it briefly melts, forming a glassy rock called ''[[Astronomy:Pseudotachylite|pseudotachylite]]''.{{sfn|Philpotts|Ague|2009|p=443}}{{sfn|Fossen|2016|p=184}} Pseudotachylites seem to be restricted to dry rock, such as granulite.{{sfn|Yardley|1989|p=26}}

==Classification of metamorphic rocks==
Metamorphic rocks are classified by their protolith, if this can be determined from the properties of the rock itself. For example, if examination of a metamorphic rock shows that its protolith was basalt, it will be described as a metabasalt. When the protolith cannot be determined, the rock is classified by its mineral composition or its degree of foliation.{{sfn|Yardley|1989|pp=21–27}}{{sfn|Robertson|1999}}{{sfn|Schmid|Fettes|Harte|Davis|2007}}

===Metamorphic grades===
'''Metamorphic grade''' is an informal indication of the amount or degree of metamorphism.{{sfn|Marshak|2009|p=183}}

In the Barrovian sequence (described by George Barrow in zones of progressive metamorphism in Scotland), metamorphic grades are also classified by mineral assemblage based on the appearance of key minerals in rocks of pelitic (shaly, aluminous) origin:

Low grade ------------------- Intermediate --------------------- High grade
:Greenschist ------------- Amphibolite ----------------------- Granulite
:[[Chemistry:Slate|Slate]] --- [[Chemistry:Phyllite|Phyllite]] ---------- [[Chemistry:Schist|Schist]] ---------------------- [[Earth:Gneiss|Gneiss]] --- [[Earth:Migmatite|Migmatite]]
:[[Chemistry:Chlorite group|Chlorite]] zone
::::[[Chemistry:Biotite|Biotite]] zone
:::::::[[Chemistry:Garnet|Garnet]] zone
::::::::::[[Chemistry:Staurolite|Staurolite]] zone
:::::::::::::[[Chemistry:Kyanite|Kyanite]] zone
::::::::::::::::[[Chemistry:Sillimanite|Sillimanite]] zone

A more complete indication of this intensity or degree is provided by the concept of [[Earth:Metamorphic facies|metamorphic facies]].{{sfn|Marshak|2009|p=183}}

===Metamorphic facies===
{{main|Earth:Metamorphic facies}}
Metamorphic facies are recognizable terranes or zones with an assemblage of key minerals that were in equilibrium under specific range of temperature and pressure during a metamorphic event. The facies are named after the metamorphic rock formed under those facies conditions from [[Earth:Basalt|basalt]].{{sfn|Ghent|2020}}

The particular mineral assemblage is somewhat dependent on the composition of that protolith, so that (for example) the amphibolite facies of a marble will not be identical with the amphibolite facies of a pellite. However, the facies are defined such that metamorphic rock with as broad a range of compositions as is practical can be assigned to a particular facies. The present definition of metamorphic facies is largely based on the work of the Finnish geologist, Pentti Eskola in 1921, with refinements based on subsequent experimental work. Eskola drew upon the zonal schemes, based on index minerals, that were pioneered by the British geologist, George Barrow.{{sfn|Yardley|1989|pp=49–51}}

The metamorphic facies is not usually considered when classifying metamorphic rock based on protolith, mineral mode, or texture. However, a few metamorphic facies produce rock of such distinctive character that the facies name is used for the rock when more precise classification is not possible. The chief examples are [[Earth:Amphibolite|amphibolite]] and [[Earth:Eclogite|eclogite]]. The British Geological Survey strongly discourages use of ''[[Earth:Granulite|granulite]]'' as a classification for rock metamorphosed to the granulite facies. Instead, such rock will often be classified as a granofels.{{sfn|Robertson|1999}} However, this is not universally accepted.{{sfn|Schmid|Fettes|Harte|Davis|2007}}

[[File:Metamorphic Facies.jpg|thumb|upright=1.5|Temperatures and pressures of metamorphic facies]]

{| class="wikitable"
!Temperature !!Pressure !!Facies
|-
|Low ||Low ||[[Physics:Zeolite facies|Zeolite]]
|-
|Lower Moderate ||Lower Moderate ||[[Earth:Prehnite-pumpellyite facies|Prehnite-Pumpellyite]]
|-
|Moderate to High ||Low ||[[Chemistry:Hornfels|Hornfels]]
|-
|Low to Moderate ||Moderate to High ||[[Earth:Blueschist|Blueschist]]
|-
|Moderate → High ||Moderate ||[[Earth:Greenschist|Greenschist]]→[[Earth:Amphibolite|Amphibolite]]→[[Earth:Granulite|Granulite]]
|-
|Moderate to High ||High ||[[Earth:Eclogite|Eclogite]]
|}
See diagram for more detail.

===Prograde and retrograde===
Metamorphism is further divided into '''prograde''' and '''retrograde metamorphism'''. Prograde metamorphism involves the change of mineral assemblages ([[Earth:Paragenesis|paragenesis]]) with increasing temperature and (usually) pressure conditions. These are solid state dehydration reactions, and involve the loss of volatiles such as water or carbon dioxide. Prograde metamorphism results in rock characteristic of the maximum pressure and temperature experienced. Metamorphic rocks usually do not undergo further change when they are brought back to the surface.{{sfn|Blatt|Tracy|1996|p=399}}

Retrograde metamorphism involves the reconstitution of a rock via revolatisation under decreasing temperatures (and usually pressures), allowing the mineral assemblages formed in prograde metamorphism to revert to those more stable at less extreme conditions. This is a relatively uncommon process, because volatiles produced during prograde metamorphism usually migrate out of the rock and are not available to recombine with the rock during cooling. Localized retrograde metamorphism can take place when fractures in the rock provide a pathway for groundwater to enter the cooling rock.{{sfn|Blatt|Tracy|1996|p=399}}

==Equilibrium mineral assemblages==
[[File:P-T diagram showing aluminium silicate-muscovite-quartz-K feldspar phases.png|thumb|Petrogenetic grid showing aluminium silicate-muscovite-quartz-K feldspar phase boundaries]]

[[File:ACF triangles EN.svg|thumb| ACF [[Earth:Compatibility diagram|compatibility diagram]]s (aluminium-calcium-iron) showing phase equilibria in metamorphic mafic rocks at different P-T circumstances (metamorphic facies). Dots represent mineral phases, thin grey lines are equilibria between two phases. Mineral abbreviations: act = actinolite; cc = calcite; chl = chlorite; di = diopside; ep = epidote; glau = glaucophane; gt = garnet; hbl = hornblende; ky = kyanite; law = lawsonite; plag = plagioclase; om = omphacite; opx = orthopyroxene; zo = zoisite ]]
Metamorphic processes act to bring the protolith closer to [[Physics:Thermodynamic equilibrium|thermodynamic equilibrium]], which is its state of maximum stability. For example, shear stress (nonhydrodynamic stress) is incompatible with thermodynamic equilibrium, so sheared rock will tend to deform in ways that relieve the shear stress.{{sfn|Mitra|2004}} The most stable assemblage of minerals for a rock of a given composition is that which minimizes the [[Physics:Gibbs free energy|Gibbs free energy]]{{sfn|Philpotts|Ague|2009|p=159}}

<math display="block">G(p,T) = U + pV - TS</math>

where:
*''U'' is the [[Physics:Internal energy|internal energy]] (SI unit: [[Joule|joule]]),
* ''p'' is [[Physics:Pressure|pressure]] (SI unit: [[Pascal (unit)|pascal]]),
* ''V'' is [[Physics:Volume (thermodynamics)|volume]] (SI unit: m<sup>3</sup>),
* ''T'' is the [[Physics:Temperature|temperature]] (SI unit: [[Kelvin|kelvin]]),
* ''S'' is the [[Physics:Entropy|entropy]] (SI unit: joule per kelvin),

In other words, a metamorphic reaction will take place only if it lowers the total Gibbs free energy of the protolith. Recrystallization to coarser crystals lowers the Gibbs free energy by reducing surface energy,{{sfn|Yardley|1989|pp=148–158}} while phase changes and neocrystallization reduce the bulk Gibbs free energy. A reaction will begin at the temperature and pressure where the Gibbs free energy of the reagents becomes greater than that of the products.{{sfn|Philpotts|Ague|2009|pp=159–160}}

A  mineral phase will generally be more stable if it has a lower internal energy, reflecting tighter binding between its atoms. Phases with a higher density (expressed as a lower molar volume ''V'') are more stable at higher pressure, while minerals with a less ordered structure (expressed as a higher entropy ''S'') are favored at high temperature. Thus andalusite is stable only at low pressure, since it has the lowest density of any aluminium silicate polymorph, while sillimanite is the stable form at higher temperatures, since it has the least ordered structure.{{sfn|Whitney|2002}}

The Gibbs free energy of a particular mineral at a specified temperature and pressure can be expressed by various analytic formulas. These are calibrated against experimentally measured properties and phase boundaries of mineral assemblages. The equilibrium mineral assemblage for a given bulk composition of rock at a specified temperature and pressure can then be calculated on a computer.{{sfn|Holland|Powell|1998}}{{sfn|Philpotts|Ague|2009|pp=161–162}}

However, it is often very useful to represent equilibrium mineral assemblages using various kinds of diagrams.{{sfn|Philpotts|Ague|2009|pp=447–470}} These include petrogenetic grids{{sfn|Yardley|1989|pp=32–33, 52–55}}{{sfn|Philpotts|Ague|2009|pp=424–425}} and compatibility diagrams (compositional phase diagrams.){{sfn|Yardley|1989|pp=32–33}}{{sfn|Philpotts|Ague|2009|p=447}}

=== Petrogenetic grids ===
{{Main|Earth:Petrogenetic grid}}

A [[Earth:Petrogenetic grid|petrogenetic grid]] is a geologic [[Phase diagram|phase diagram]] that plots experimentally derived metamorphic reactions at their pressure and temperature conditions for a given rock composition. This allows metamorphic petrologists to determine the pressure and temperature conditions under which rocks metamorphose.{{sfn|Yardley|1989|pp=32–33, 52–55}}{{sfn|Philpotts|Ague|2009|pp=424–425}} The Al<sub>2</sub>SiO<sub>5</sub> nesosilicate phase diagram shown is a very simple petrogenetic grid for rocks that only have a composition consisting of [[Chemistry:Aluminum|aluminum]] (Al), [[Chemistry:Silicon|silicon]] (Si), and [[Chemistry:Oxygen|oxygen]] (O). As the rock undergoes different temperatures and pressure, it could be any of the three given  [[Physics:Polymorphism (materials science)|polymorphic]] minerals.{{sfn|Whitney|2002}} For a rock that contains multiple phases, the boundaries between many phase transformations may be plotted, though the petrogenetic grid quickly becomes complicated. For example, a petrogenetic grid might show both the aluminium silicate phase transitions and the transition from aluminum silicate plus potassium feldspar to muscovite plus quartz.{{sfn|Philpotts|Ague|2009|p=453}}

=== Compatibility diagrams ===
{{Main|Earth:Compatibility diagram}}
Whereas a petrogenetic grid shows phases for a single composition over a range of temperature and pressure, a ''compatibility diagram'' shows how the mineral assemblage 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 [[Earth:Paragenesis|paragenesis]] that develops in a rock at particular pressure and temperature conditions.{{sfn|Yardley|1989|pp=32–33}}{{sfn|Philpotts|Ague|2009|p=447}} Because of the difficulty of depicting more than three components (as a ternary diagram), usually only the three most important components are plotted, though occasionally a compatibility diagram for four components is plotted as a [[Orthographic projection|projected]] [[Tetrahedron|tetrahedron]].{{sfn|Philpotts|Ague|2009|p=454-455}}

==See also==
* {{annotated link|Geothermobarometry}}
* [[Physics:Snow#Metamorphosis|Metamorphosis of snow]]
* {{annotated link|Earth:Ultra-high-temperature metamorphism}}

==Footnotes==
{{Reflist|25em}}

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==Further reading==
* Winter J.D., 2001, ''An Introduction to Igneous and Metamorphic Petrology'', Prentice-Hall {{ISBN|0-13-240342-0}}.

==External links==
* [http://www.bgs.ac.uk/scmr/docs/papers/paper_1.pdf Recommendations by the IUGS Subcommission on the Systematics of Metamorphic Rocks, 1. How to Name a Metamorphic Rock]
* [http://www.bgs.ac.uk/scmr/docs/papers/paper_2.pdf Recommendations by the IUGS Subcommission on the Systematics of Metamorphic Rocks, 2. Types, Grade, and Facies of Metamorphism]
* [http://www.bgs.ac.uk/scmr/docs/papers/paper_3.pdf Recommendations by the IUGS Subcommission on the Systematics of Metamorphic Rocks, 3. Structural terms including fault rock terms]
* [http://www.bgs.ac.uk/scmr/docs/papers/paper_4.pdf Recommendations by the IUGS Subcommission on the Systematics of Metamorphic Rocks, 4. High P/T Metamorphic Rocks]
* [http://csmres.jmu.edu/geollab/Fichter/MetaRx/MetaKind.html James Madison University: Metamorphism] {{Webarchive|url=https://web.archive.org/web/20110304124837/http://csmres.jmu.edu/geollab/fichter/MetaRx/MetaKind.html |date=2011-03-04 }}
* [http://www.brocku.ca/earthsciences/people/gfinn/petrology/barrow1.htm Barrovian Metamorphism: Brock Univ.]
* [https://web.archive.org/web/20160304194845/http://www.uwgb.edu/dutchs/petrolgy/barrcarb.htm Metamorphism of Carbonate Rocks: University of Wisconsin – Green Bay]
* [https://web.archive.org/web/20110720035915/http://metpetdb.rpi.edu/ Metamorphic Petrology Database] ([[Chemistry:MetPetDB|MetPetDB]]) – Department of Earth and Environmental Sciences, [[Organization:Rensselaer Polytechnic Institute|Rensselaer Polytechnic Institute]]

{{Geologic Principles}}


[[Category:Geological processes]]
[[Category:Metamorphic petrology]]

{{Sourceattribution|Metamorphism}}