Metamorphic rocks arise from the transformation of existing rock to new types of rock in a process called metamorphism. The original rock (protolith) is subjected to temperatures greater than 150 to 200 °C and, often, elevated pressure of 100 megapascals (1,000 bar) or more, causing profound physical or chemical changes. During this process, the rock remains mostly in the solid state, but gradually recrystallizes to a new texture or mineral composition. The protolith may be an igneous, sedimentary, or existing metamorphic rock.
Skarns or tactites are coarse-grained metamorphic rocks that form by replacement of carbonate-bearing rocks during regional or contact metamorphism and metasomatism. Skarns may form by metamorphic recrystallization of impure carbonate protoliths, bimetasomatic reaction of different lithologies, and infiltration metasomatism by magmatic-hydrothermal fluids. Skarns tend to be rich in calcium-magnesium-iron-manganese-aluminium silicate minerals, which are also referred to as calc-silicate minerals. These minerals form as a result of alteration which occurs when hydrothermal fluids interact with a protolith of either igneous or sedimentary origin. In many cases, skarns are associated with the intrusion of a granitic pluton found in and around faults or shear zones that commonly intrude into a carbonate layer composed of either dolomite or limestone. Skarns can form by regional or contact metamorphism and therefore form in relatively high temperature environments. The hydrothermal fluids associated with the metasomatic processes can originate from a variety of sources; magmatic, metamorphic, meteoric, marine, or even a mix of these. The resulting skarn may consist of a variety of different minerals which are highly dependent on both the original composition of the hydrothermal fluid and the original composition of the protolith.
Phlogopite is a yellow, greenish, or reddish-brown member of the mica family of phyllosilicates. It is also known as magnesium mica.
Metasomatism is the chemical alteration of a rock by hydrothermal and other fluids. It is the replacement of one rock by another of different mineralogical and chemical composition. The minerals which compose the rocks are dissolved and new mineral formations are deposited in their place. Dissolution and deposition occur simultaneously and the rock remains solid.
Ultramafic rocks are igneous and meta-igneous rocks with a very low silica content, generally >18% MgO, high FeO, low potassium, and are composed of usually greater than 90% mafic minerals. The Earth's mantle is composed of ultramafic rocks. Ultrabasic is a more inclusive term that includes igneous rocks with low silica content that may not be extremely enriched in Fe and Mg, such as carbonatites and ultrapotassic igneous rocks.
Serpentinization is a hydration and metamorphic transformation of ferromagnesian minerals, such as olivine and pyroxene, in mafic and ultramafic rock to produce serpentinite. Minerals formed by serpentinization include the serpentine group minerals, brucite, talc, Ni-Fe alloys, and magnetite. The mineral alteration is particularly important at the sea floor at tectonic plate boundaries.
Carbonatite is a type of intrusive or extrusive igneous rock defined by mineralogic composition consisting of greater than 50% carbonate minerals. Carbonatites may be confused with marble and may require geochemical verification.
Volcanogenic massive sulfide ore deposits, also known as VMS ore deposits, are a type of metal sulfide ore deposit, mainly copper-zinc which are associated with and created by volcanic-associated hydrothermal events in submarine environments.
Komatiite is a type of ultramafic mantle-derived volcanic rock defined as having crystallised from a lava of at least 18 wt% magnesium oxide (MgO). It is classified as a 'picritic rock'. Komatiites have low silicon, potassium and aluminium, and high to extremely high magnesium content. Komatiite was named for its type locality along the Komati River in South Africa, and frequently displays spinifex texture composed of large dendritic plates of olivine and pyroxene.
Various theories of ore genesis explain how the various types of mineral deposits form within Earth's crust. Ore-genesis theories vary depending on the mineral or commodity examined.
Sedimentary exhalative deposits are zinc-lead deposits originally interpreted to have been formed by discharge of metal-bearing basinal fluids onto the seafloor resulting in the precipitation of mainly stratiform ore, often with thin laminations of sulphide minerals. SEDEX deposits are hosted largely by clastic rocks deposited in intracontinental rifts or failed rift basins and passive continental margins. Since these ore deposits frequently form massive sulfide lenses, they are also named sediment-hosted massive sulfide (SHMS) deposits, as opposed to volcanic-hosted massive sulfide (VHMS) deposits. The sedimentary appearance of the thin laminations led to early interpretations that the deposits formed exclusively or mainly by exhalative processes onto the seafloor, hence the term SEDEX. However, recent study of numerous deposits indicates that shallow subsurface replacement is also an important process, in several deposits the predominant one, with only local if any exhalations onto the seafloor. For this reason, some authors prefer the term "Clastic-dominated zinc-lead deposits". As used today, therefore, the term SEDEX is not to be taken to mean that hydrothermal fluids actually vented into the overlying water column, although this may have occurred in some cases.
The Gawler Craton covers approximately 440,000 square kilometres of central South Australia. Its Precambrian crystalline basement crustal block was cratonised ca. 1550–1450 Ma. Prior to 1550 Ma the craton comprised a number of active Proterozoic orogenic belts extending back in time to at least 2450 Ma.
Kambalda type komatiitic nickel ore deposits are a class of magmatic iron-nickel-copper-platinum-group element ore deposit in which the physical processes of komatiite volcanology serve to deposit, concentrate and enrich a Fe-Ni-Cu-(PGE) sulfide melt within the lava flow environment of an erupting komatiite volcano.
Talc carbonates are a suite of rock and mineral compositions found in metamorphosed ultramafic rocks.
Carbonate-hosted lead-zinc ore deposits are important and highly valuable concentrations of lead and zinc sulfide ores hosted within carbonate formations and which share a common genetic origin.
The Temagami Greenstone Belt (TGB) is a small 2.7 billion year old greenstone belt in the Temagami region of Northeastern Ontario, Canada. It represents a feature of the Superior craton, an ancient and stable part of the Earth's lithosphere that forms the core of the North American continent and Canadian Shield. The belt is composed of metamorphosed volcanic rocks that range in composition from basalt to rhyolite. These form the east-northeast trend of the belt and are overlain by metamorphosed sedimentary rocks. They were created during several volcanic episodes involving a variety of eruptive styles ranging from passive lava eruptions to viscous explosive eruptions.
Listwanite (also sometimes spelled listvenite, listvanite, or listwaenite) is a rock type that forms when the groundmass of ultramafic rocks, most commonly mantle peridotites, is partially altered to carbonate minerals and cut by ubiquitous carbonate veins containing one or more of magnesite, calcite, dolomite, ankerite, and/or siderite. Original pyroxene and olivine in the peridotite are commonly altered to Mg- or Ca-carbonate and hydrous Mg-silicates, such as serpentine and talc. Complete carbonation of peridotite means that every single atom of magnesium and calcium as well as some of the iron atoms have combined with CO2 to form secondary carbonate minerals such a magnesite, calcite, and siderite, while the remaining silica atoms, formerly found in pyroxene and olivine (prior to alteration), are found in quartz, serpentine, and talc. Thus, in terms of bulk mineralogy, listwanites consist primarily of quartz (often of a rusty red colour), carbonate, serpentine, talc, ± mariposite/fuchsite (i.e., Cr-muscovite) ± gold.
The geology of Nevada began to form in the Proterozoic at the western margin of North America. Terranes accreted to the continent as a marine environment dominated the area through the Paleozoic and Mesozoic periods. Intense volcanism, the horst and graben landscape of the Basin and Range Province originating from the Farallon Plate, and both glaciers and valley lakes have played important roles in the region throughout the past 66 million years.
In geology, silicification is a petrification process in which silica-rich fluids seep into the voids of Earth materials, e.g., rocks, wood, bones, shells, and replace the original materials with silica (SiO2). Silica is a naturally existing and abundant compound found in organic and inorganic materials, including Earth's crust and mantle. There are a variety of silicification mechanisms. In silicification of wood, silica permeates into and occupies cracks and voids in wood such as vessels and cell walls. The original organic matter is retained throughout the process and will gradually decay through time. In the silicification of carbonates, silica replaces carbonates by the same volume. Replacement is accomplished through the dissolution of original rock minerals and the precipitation of silica. This leads to a removal of original materials out of the system. Depending on the structures and composition of the original rock, silica might replace only specific mineral components of the rock. Silicic acid (H4SiO4) in the silica-enriched fluids forms lenticular, nodular, fibrous, or aggregated quartz, opal, or chalcedony that grows within the rock. Silicification happens when rocks or organic materials are in contact with silica-rich surface water, buried under sediments and susceptible to groundwater flow, or buried under volcanic ashes. Silicification is often associated with hydrothermal processes. Temperature for silicification ranges in various conditions: in burial or surface water conditions, temperature for silicification can be around 25°−50°; whereas temperatures for siliceous fluid inclusions can be up to 150°−190°. Silicification could occur during a syn-depositional or a post-depositional stage, commonly along layers marking changes in sedimentation such as unconformities or bedding planes.
