| Ringwoodite | |
|---|---|
 Crystal (~150 micrometers across) of Fo90 composition blue ringwoodite synthesized at 20 GPa and 1200 °C. | |
| General | |
| Category | Nesosilicates Spinel group |
| Formula | Magnesium silicate (Mg2SiO4) |
| IMA symbol | Rgd[1] |
| Strunz classification | 9.AC.15 |
| Crystal system | Cubic |
| Crystal class | Hexoctahedral (m3m) H-M symbol: (4/m3 2/m) |
| Space group | Fd3m |
| Unit cell | a = 8.113 Å; Z = 8 |
| Identification | |
| Colour | Deep blue, also red, violet, or colourless (pure Mg2SiO4) |
| Crystal habit | Microcrystalline aggregates |
| Diaphaneity | Semitransparent |
| Specific gravity | 3.90 (Mg2SiO4); 4.13 ((Mg0.91,Fe0.09)2SiO4); 4.85 (Fe2SiO4) |
| Optical properties | Isotropic |
| Refractive index | n = 1.8 |
| Birefringence | none |
| Pleochroism | none |
| References | [2][3][4] |
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Ringwoodite is a high-pressure phase of Mg2SiO4 (magnesium silicate) formed at high temperatures and pressures of theEarth's mantle between 525 and 660 km (326 and 410 mi) depth. It may also containiron andhydrogen. It ispolymorphous with theolivine phaseforsterite (amagnesiumironsilicate).
Ringwoodite is notable for being able to containhydroxide ions within its structure. In this case two hydroxide ions usually take the place of a magnesium ion and two oxideions.[5]
Combined with evidence of its occurrence deep in the Earth's mantle, this suggests that there is from one to three times theworld ocean's equivalent ofwater in themantle transition zone from 410 to 660 km deep.[6][7]
This mineral was first identified in theTenham meteorite in 1969,[8] and is inferred to be present in large quantities in the Earth's mantle.
Olivine,wadsleyite, and ringwoodite are polymorphs found in theupper mantle of the earth. At depths greater than about 660 kilometres (410 mi), other minerals, including some with theperovskite structure, are stable. The properties of these minerals determine many of the properties of the mantle.
Ringwoodite was named after theAustralianearth scientistTed Ringwood (1930–1993), who studied polymorphic phase transitions in the common mantle minerals olivine andpyroxene at pressures equivalent to depths as great as about 600 km.
Ringwoodite is polymorphous with forsterite, Mg2SiO4, and has aspinel structure. Spinel group minerals crystallize in the isometric system with an octahedral habit. Olivine is most abundant in the upper mantle, above about 410 km (250 mi); the olivine polymorphs wadsleyite and ringwoodite are thought to dominate thetransition zone of the mantle, a zone present from about 410 to 660 km depth.
Ringwoodite is thought to be the most abundant mineral phase in the lower part of Earth's transition zone. The physical and chemical property of this mineral partly determine properties of the mantle at those depths. The pressure range for stability of ringwoodite lies in the approximate range from 18 to 23 GPa.
Natural ringwoodite has been found in many shockedchondritic meteorites, in which the ringwoodite occurs as fine-grained polycrystallineaggregates.[9]
Natural ringwoodite generally contains much more magnesium than iron and can form a gapless solid solution series from the pure magnesiumendmember to the pure iron endmember[citation needed]. The latter, the iron-rich endmember of the γ-olivine solid solution series, γ-Fe2SiO4, was named ahrensite in honor of US mineral physicistThomas J. Ahrens (1936–2010).[10]
In meteorites, ringwoodite occurs in theveinlets of quenched shock-melt cutting the matrix and replacing olivine probably produced duringshock metamorphism.[9]
In Earth's interior, olivine occurs in the upper mantle at depths less than about 410 km, and ringwoodite is inferred to be present within thetransition zone from about 520 to 660 km depth.Seismic activity discontinuities at about 410 km, 520 km, and at 660 km depth have been attributed tophase changes involving olivine and itspolymorphs.
The 520-km depth discontinuity is generally believed to be caused by the transition of the olivine polymorphwadsleyite (beta-phase) to ringwoodite (gamma-phase), while the 660-km depth discontinuity by the phase transformation of ringwoodite (gamma-phase) to asilicate perovskite plusmagnesiowüstite.[11][12]
Ringwoodite in the lower half of the transition zone is inferred to play a pivotal role in mantle dynamics, and the plastic properties of ringwoodite are thought to be critical in determining flow of material in this part of the mantle. The ability of ringwoodite to incorporatehydroxide is important because of its effect onrheology.
Ringwoodite has been synthesized at conditions appropriate to the transition zone, containing up to 2.6 weight percent water.[13][14]
Because the transition zone between the Earth's upper and lower mantle helps govern the scale of mass and heat transport throughout the Earth, the presence of water within this region, whether global or localized, may have a significant effect on mantle rheology and therefore mantle circulation.[15] In subduction zones, the ringwoodite stability field hosts high levels of seismicity.[16]
An "ultradeep"diamond (one that has risen from a great depth) found inJuína in western Brazil contained an inclusion of ringwoodite — at the time the only known sample of natural terrestrial origin — thus providing evidence of significant amounts of water ashydroxide in the Earth's mantle.[6][17][18][19] The gemstone, about 5mm long,[19] was brought up by adiatreme eruption.[20] The ringwoodite inclusion is too small to see with the naked eye.[19] A second such diamond was later found.[21]
The mantle reservoir could contain about three times more water, in the form of hydroxide contained within the wadsleyite and ringwoodite crystal structure, than the Earth's oceans combined.[7]
For experiments, hydrous ringwoodite has been synthesized by mixing powders offorsterite (Mg
2SiO
4),brucite (Mg(OH)
2), andsilica (SiO
2) so as to give the desired final elemental composition. Putting this under 20gigapascals of pressure at 1,523 K (1,250 °C; 2,282 °F) for three or four hours turns this into ringwoodite, which can then be cooled and depressurized.[5]
Ringwoodite has thespinel structure, in theisometric crystal system withspace groupFd3m (orF43m[22]). On an atomic scale, magnesium and silicon are in octahedral and tetrahedral coordination with oxygen, respectively. The Si-O and Mg-O bonds have mixed ionic and covalent character.[23] The cubic unit cell parameter is 8.063 Å for pure Mg2SiO4 and 8.234 Å for pure Fe2SiO4.[24]
Ringwoodite compositions range from pure Mg2SiO4 to Fe2SiO4 in synthesis experiments. Ringwoodite can incorporate up to 2.6 percent by weight H2O.[5]
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The physical properties of ringwoodite are affected by pressure and temperature. At the pressure and temperature condition of the Mantle Transition Zone, the calculated density value of ringwoodite is 3.90 g/cm3 for pure Mg2SiO4;[25] 4.13 g/cm3 for (Mg0.91,Fe0.09)2SiO4[26] of pyrolitic mantle; and 4.85 g/cm3 for Fe2SiO4.[27] It is an isotropic mineral with anindex of refraction n = 1.768.
The colour of ringwoodite varies between the meteorites, between different ringwoodite bearing aggregates, and even in one single aggregate. The ringwoodite aggregates can show every shade of blue, purple, grey and green, or have no colour at all.
A closer look at coloured aggregates shows that the colour is not homogeneous, but seems to originate from something with a size similar to the ringwoodite crystallites.[28] In synthetic samples, pure Mg ringwoodite is colourless, whereas samples containing more than one mole percent Fe2SiO4 are deep blue in colour. The colour is thought to be due to Fe2+–Fe3+ charge transfer.[29]
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