Коматиит: ультрамафическая порода архейского периода.

Magnesium rich igneous rock

Komatiite /k//oʊ/'/m//ɑː//t//i/,/aɪ//t/ 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. Komatiites are rare rocks; almost all komatiites were formed during the Archaean Eon (4.03–2.5 billion years ago), with few younger (Proterozoic or Phanerozoic) examples known. This restriction in age is thought to be due to cooling of the mantle, which may have been hotter during the Archaean. The early Earth had much higher heat production, due to the residual heat from planetary accretion, as well as the greater abundance of radioactive isotopes, particularly shorter lived ones like uranium 235 which produce more decay heat. Lower temperature mantle melts such as basalt and picrite have essentially replaced komatiites as an eruptive lava on the Earth's surface. Geographically, komatiites are predominantly restricted in distribution to the Archaean shield areas, and occur with other ultramafic and high magnesian mafic volcanic rocks in Archaean greenstone belts. The youngest komatiites are from the island of Gorgona on the Caribbean oceanic plateau off the Pacific coast of Colombia, and a rare example of Proterozoic komatiite is found in the Winnipegosis komatiite belt in Manitoba, Canada.

Magmas of komatiitic compositions have a very high melting point, with calculated eruption temperatures up to, and possibly in excess of 1600 °C. Basaltic lavas normally have eruption temperatures of about 1100 to 1250 °C. The higher melting temperatures required to produce komatiite have been attributed to the presumed higher geothermal gradients in the Archaean Earth. Komatiitic lava was extremely fluid when it erupted (possessing the viscosity close to that of water but with the density of rock). Compared to the basaltic lava of the Hawaiian plume basalts at ~1200 °C, which flows the way treacle or honey does, the komatiitic lava would have flowed swiftly across the surface, leaving extremely thin lava flows (down to 10 mm thick). The major komatiitic sequences preserved in Archaean rocks are thus considered to be lava tubes, ponds of lava etc., where the komatiitic lava accumulated. Komatiite chemistry is different from that of basaltic and other common mantle produced magmas, because of differences in degrees of partial melting. Komatiites are considered to have been formed by high degrees of partial melting, usually greater than 50%, and hence have high MgO with low K2O and other incompatible elements. There are two geochemical classes of komatiite; aluminium undepleted komatiite (AUDK) (also known as Group I komatiites) and aluminium depleted komatiite (ADK) (also known as Group II komatiites), defined by their Al2O3/TiO2 ratios. These two classes of komatiite are often assumed to represent a real petrological source difference between the two types related to depth of melt generation. Al depleted komatiites have been modeled by melting experiments as being produced by high degrees of partial melting at high pressure where garnet in the source is not melted, whereas Al undepleted komatiites are produced by high degrees of partial melts at lesser depth. However, recent studies of fluid inclusions in chrome spinels from the cumulate zones of komatiite flows have shown that a single komatiite flow can be derived from the mixing of parental magmas with a range of Al2O3/TiO2 ratios, calling into question this interpretation of the formations of the different komatiite groups. Komatiites probably form in extremely hot mantle plumes or in Archaean subduction zones. Boninite magmatism is similar to komatiite magmatism but is produced by fluid fluxed melting above a subduction zone. Boninites with 10–18% MgO tend to have higher large ion lithophile elements (LILE: Ba, Rb, Sr) than komatiites.

The pristine volcanic mineralogy of komatiites is composed of forsteritic olivine (Fo90 and upwards), calcic and often chromian pyroxene, anorthite (An85 and upwards) and chromite. A considerable population of komatiite examples show a cumulate texture and morphology. The usual cumulate mineralogy is highly magnesium rich forsterite olivine, though chromian pyroxene cumulates are also possible (though rarer). Volcanic rocks rich in magnesium may be produced by accumulation of olivine phenocrysts in basalt melts of normal chemistry: an example is picrite. Part of the evidence that komatiites are not magnesium rich simply because of cumulate olivine is textural: some contain spinifex texture, a texture attributable to rapid crystallization of the olivine in a thermal gradient in the upper part of a lava flow. "Spinifex" texture is named after the common name for the Australian grass Triodia, which grows in clumps with similar shapes. Another line of evidence is that the MgO content of olivines formed in komatiites is toward the nearly pure MgO forsterite composition, which can only be achieved in bulk by crystallisation of olivine from a highly magnesian melt. The rarely preserved flow top breccia and pillow margin zones in some komatiite flows are essentially volcanic glass, quenched in contact with overlying water or air. Because they are rapidly cooled, they represent the liquid composition of the komatiites, and thus record an anhydrous MgO content of up to 32% MgO. Some of the highest magnesian komatiites with clear textural preservation are those of the Barberton belt in South Africa, where liquids with up to 34% MgO can be inferred using bulk rock and olivine compositions. The mineralogy of a komatiite varies systematically through the typical stratigraphic section of a komatiite flow and reflects magmatic processes which komatiites are susceptible to during their eruption and cooling. The typical mineralogical variation is from a flow base composed of olivine cumulate, to a spinifex textured zone composed of bladed olivine and ideally a pyroxene spinifex zone and olivine rich chill zone on the upper eruptive rind of the flow unit. Primary (magmatic) mineral species also encountered in komatiites include olivine, the pyroxenes augite, pigeonite and bronzite, plagioclase, chromite, ilmenite and rarely pargasitic amphibole. Secondary (metamorphic) minerals include serpentine, chlorite, amphibole, sodic plagioclase, quartz, iron oxides and rarely phlogopite, baddeleyite, and pyrope or hydrogrossular garnet.

All known komatiites have been metamorphosed, therefore should technically be termed 'metakomatiite' though the prefix meta is inevitably assumed. Many komatiites are highly altered and serpentinized or carbonated from metamorphism and metasomatism. This results in significant changes to the mineralogy and the texture.

The metamorphic mineralogy of ultramafic rocks, particularly komatiites, is only partially controlled by composition. The character of the connate fluids which are present during low temperature metamorphism whether prograde or retrograde control the metamorphic assemblage of a metakomatiite (hereafter the prefix meta is assumed). The factor controlling the mineral assemblage is the partial pressure of carbon dioxide within the metamorphic fluid, called the XCO2. If XCO2 is above 0.5, the metamorphic reactions favor formation of talc, magnesite (magnesium carbonate), and tremolite amphibole. These are classed as talc carbonation reactions. Below XCO2 of 0.5, metamorphic reactions in the presence of water favor production of serpentinite. There are thus two main classes of metamorphic komatiite; carbonated and hydrated. Carbonated komatiites and peridotites form a series of rocks dominated by the minerals chlorite, talc, magnesite or dolomite and tremolite. Hydrated metamorphic rock assemblages are dominated by the minerals chlorite, serpentine antigorite and brucite. Traces of talc, tremolite and dolomite may be present, as it is very rare that no carbon dioxide is present in metamorphic fluids. At higher metamorphic grades, anthophyllite, enstatite, olivine and diopside dominate as the rock mass dehydrates.

Komatiites often show pillow lava structure, autobrecciated upper margins consistent with underwater eruption forming a rigid upper skin to the lava flows. Proximal volcanic facies are thinner and interleaved with sulfidic sediments, black shales, cherts and tholeiitic basalts. Komatiites were produced from a relatively wet mantle. Evidence of this is from their association with felsics, occurrences of komatiitic tuffs, niobium anomalies and by S and H2O borne rich mineralizations.

A common and distinctive texture is known as spinifex texture and consists of long acicular phenocrysts of olivine (or pseudomorphs of alteration minerals after olivine) or pyroxene which give the rock a bladed appearance especially on a weathered surface. Spinifex texture is the result of rapid crystallization of highly magnesian liquid in the thermal gradient at the margin of the flow or sill. Harrisite texture, first described from intrusive rocks (not komatiites) at Harris Bay on the island of Rùm in Scotland, is formed by nucleation of crystals on the floor of a magma chamber. Harrisites are known to form megacrystal aggregates of pyroxene and olivine up to 1 metre in length. Harrisite texture is found in some very thick lava flows of komatiite, for example in the Norseman Wiluna Greenstone Belt of Western Australia, in which crystallization of cumulates has occurred.

Komatiite magma is extremely dense and unlikely to reach the surface, being more likely to pool lower within the crust. Modern (post 2004) interpretations of some of the larger olivine adcumulate bodies in the Yilgarn craton have revealed that the majority of komatiite olivine adcumulate occurrences are likely to be subvolcanic to intrusive in nature. This is recognised at the Mt Keith nickel deposit where wall rock intrusive textures and xenoliths of felsic country rocks have been recognised within the low strain contacts. The previous interpretations of these large komatiite bodies was that they were "super channels" or reactivated channels, which grew to over 500 m in stratigraphic thickness during prolonged volcanism. These intrusions are considered to be channelised sills, formed by injection of komatiitic magma into the stratigraphy, and inflation of the magma chamber. Economic nickel mineralised olivine adcumulate bodies may represent a form of sill like conduit, where magma pools in a staging chamber before erupting onto the surface.

The economic importance of komatiite was first widely recognised in the early 1960s with the discovery of massive nickel sulfide mineralisation at Kambalda, Western Australia. Komatiite hosted nickel copper sulfide mineralisation today accounts for about 14% of the world's nickel production, mostly from Australia, Canada and South Africa. Komatiites are associated with nickel and gold deposits in Australia, Canada, South Africa and most recently in the Guiana shield of South America.