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The Sheahan Diamond Literature Reference Compilation - Scientific and Media Articles based on Major Keyword - Water
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcements called the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Keyword Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In an effort to make it easier for users to track down articles related to a specific topic, KRO has extracted these key words and developed a list of major key words presented in this Key Word Index to which individual key words used in the article reference have been assigned. In most of the individual Key Word Reports the references are in crhonological order, though in some such as Deposits the order is first by key word and then chronological. Only articles classified as "technical" (mainly scientific journal articles) and "media" (independent media articles) are included in the Key Word Index. References that were added in the most recent monthly update are highlighted in yellow.
Articles with the keyword water tend to be about the presence of water within the mantle, how it affects mantle behavior, and how water ended up in the mantle. The general theory is that oceanic slabs containing hydrous minerals that were subducted are the source of water within the mantle. The dehydration of subducting slabs contributes to magmatic fluids which can play a major role in forming ore deposits, though none containing diamonds. Meteoric Water, in contrast, involves rainwater that has worked its way back into the crust where it is otherwise known as "groundwater". Hydrothermal ore genesis models usually involve a magmatic intrusion as a heat engine that drives the circulation of meteoric water which harvests metals from the rocks through which it flows. None of this has anything to do with diamonds. Fluid Inclusion studies are used extensively in the investigation of hydrothermal systems which formed orebodies at the earth's surface, but in the context of diamonds it is tiny bubbles of water within diamonds that provide clues about the mantle's history.
Song, S., Zhang, L., Chen, J., Liou, J.G., Niu, Y.
Sodic amphibole exsolutions in garnet from garnet-peridotite, North Qaidam UHP belt, NW China: implications for ultradeep origin and hydroxyl defects in mantle garnets.
Sano, A., Ohtani, E., Litasov, K., Kubo, T., Hosoya, T., Funakoshi, K., Kikegawa, T.
In situ x-ray diffraction study of the effect of water on the garnet perovksite transformation in MORB and implications for the penetration of oceanic crust...
Physics of the Earth and Planetary Interiors, Vol. 159, 1-2, pp. 118-126.
Ecologite and carpholite bearing metasedimentary rocks in the North Qilian suture zone, NW China: implications for Early Paleozoic cold oceanic subduction and water transport into
Journal of Metamorphic Geology, Vol. 25, 5, pp. 547-563.
Li, ZX., Lee, C-T.A, Peslier, A.H., Lenardic, A., Mackwell, S.J.
Water contents in mantle xeonoliths from the Colorado Plateau and vicinity: implications for the mantle rheology and hydration induced thinking of lithosphere
Journal of Geophysical Research, Vol. 113, B9, B09210.
Water storage capacity in olivine and pyroxene to 14 Gpa: implications for the water content of the Earth's upper mantle and nature of seismic discontinuities.
Earth and Planetary Science Letters, Vol. 349-350, pp. 218-230.
Water storage capacity in olivine and pyroxene to 14 Gpa as implications for the water content of the Earth's upper mantle and nature of seismic discontinuities.
Earth and Planetary Science Letters, Vol. 349-350 pp. 218-230.
Martirosyan, N., Yoshino, T., Shatskiy, A., Chanyshev, A., Litasov, K.
Effect of water on the stability of magnesite in the mantle under reduced conditions.
V.S. Sobolev Institute of Geology and Mineralogy Siberian Branch Russian Academy of Sciences International Symposium Advances in high pressure research: breaking scales and horizons ( Courtesy of N. Poikilenko), Held Sept. 22-26, 2p. Abstract
Abstract: To test if hydrogen incorporation by ionic diffusion can occur between a volatile-rich kimberlitic liquid and forsterite, results of high-pressure and high-temperature experiments using a piston-cylinder apparatus at 1200–1300 °C and 1 GPa for durations of 1 min, 5 h, and 23 h, are reported here. Kim-berlitic liquid in the system CaO-MgO-Al 2 O 3-SiO 2-CO 2-H 2 O and synthetic forsterite single crystals were chosen as a first simplification of the complex natural kimberlite composition. Unpolarized Fourier transform infrared spectroscopy was used to quantify the concentrations of OH in the crystallographically oriented forsterite. Scanning electron microscopy, electron backscattered diffraction, electron microprobe analyses, and transmission electron microscopy were performed to identify the run products. After 5 and 23 h, a forsterite overgrowth crystallized with the same orientation as the initial forsterite single crystal. The kimberlitic liquid has crystallized as micrometer-scale euhedral forsterite neocrystals with random crystallographic orientations, as well as a nanoscale aluminous phase and a calcic phase. Despite theoretical water-saturation of the system and long duration, none of the initial forsterite single crystals display signs of hydration such as hydrogen diffusion profile from the border toward the center of the crystal. Most likely, the presence of CO 2 in the system has lowered the H 2 O fugacity to such an extent that there is no significant hydration of the starting forsterite single crystal or its overgrowth. Also, the presence of CO 2 enhances rapid forsterite crystal growth. Forsterite growth rate is around 2 × 10 8 mm 3 /h at 1250 °C. These experimental results suggest a deep mantle origin of the high OH content found in natural mantle-derived xenoliths transported in kimberlites, as reported from the Kaapvaal craton. In agreement with previous studies, it also points out to the fact that significant hydration must take place in a CO 2-poor environment.
Abstract: Water is transported into the deep mantle via hydrous minerals in subducting slabs. During subduction, a series of minerals in these slabs such as serpentine or chlorite, Mg-sursassite and/or the 10 Å phase, and phase A can be stable at different pressures within the slab geotherms, and may transport significant amount of water into the Earth's interior. The transition zone has a large water storage capacity because of the high solubility of water in wadsleyite and ringwoodite. The recent discovery of hydrous ringwoodite and phase Egg as inclusions in ultra deep diamonds from Juina, Brazil suggests that the transition zone may indeed contain water. Seismic tomographic studies and electrical conductivity observations suggest that the transition zone may contain large amount of water, at least locally, beneath the subduction zones. The discovery of a new hydrous phase H, MgSiO2(OH)2, and its solid solution with isostructural phase ?-AlOOH, suggests that a significant amount of water could be stored in this hydrous magnesium silicate phase which is stable down to the lower mantle. Water may be transported into the bottom of the lower mantle via phase H–? solid solution in descending slabs. This new high pressure hydrous phase solid solution has a high bulk modulus and sound velocity owing to strong O-H bonding due to hydrogen bond symmetrization in the lower mantle. Therefore, water stored in this hydrous phase would not reduce the seismic wave velocity in the lower mantle, and is seismically invisible. Dehydration melting could then occur at the base of the lower mantle, providing a potential explanation for the ultralow-velocity zone at the core-mantle boundary. When this hydrous magnesium silicate phase or hydrous melt makes contact with the metallic outer core at the core-mantle boundary, then hydrogen is likely to dissolve into the core.
Abstract: The hydrogen-isotope [deuterium/hydrogen (D/H)] ratio of Earth can be used to constrain the origin of its water. However, the most accessible reservoir, Earth’s oceans, may no longer represent the original (primordial) D/H ratio, owing to changes caused by water cycling between the surface and the interior. Thus, a reservoir completely isolated from surface processes is required to define Earth’s original D/H signature. Here we present data for Baffin Island and Icelandic lavas, which suggest that the deep mantle has a low D/H ratio (?D more negative than -218 per mil). Such strongly negative values indicate the existence of a component within Earth’s interior that inherited its D/H ratio directly from the protosolar nebula.
Abstract: For decades, geologists have debated the geodynamic processes that operated in the young Earth. In the Archean, 4 and 2.5 billion years ago, the interior of the planet was much hotter which led to more rapid convection and, according to some authors, to an absence of plate tectonics. Komatiites (Fig. 1) - volcanic rocks with abnormal, olivine-enriched compositions - are thought to result from high-degrees of partial melting of extremely hot parts of the Earth’s mantle. This interpretation is blurred, however, by uncertainty as to the water content of komatiitic magmas. There are two schools of thought on this question: the first proposes that the magmas were dry (<0.1% water) and very hot (> 1600°C), and were produced in mantle plumes from the base of the mantle; the second suggests that the magmas were hydrated, with lower melting temperatures, and had formed in subduction settings. The analysed komatiite melt contained 30% magnesium oxide and 0.6% water and began to crystallize at a relatively low temperature of 1530°C. The chemical composition of the magma and low oxygen fugacity are inconsistent with a subduction setting. he mantle plume (orange) traverses the transition zone, which contains excess H2O, F and Cl in ringwoodite and/or wadsleyite (high pressure polymorphs of olivine).The plume is hot enough to be partially molten near the top of the transition zone (small black dots) and entrains hydrous melt (blue shapes) either from the layer at the upper boundary of the transition zone or from the hot boundary between the plume and the transition zone. Alternatively or additionally, the plume may entrain solid wadsleyite from the transition zone (green shapes). All these hydrous materials introduce H2O and possibly F and Cl into the plume and accelerate its melting (larger black dots). Further ascent of the plume generates more melt during decompression (large black dots), which then separates from the source and ascends to the surface without reaction with peridotite (purple stripes). Instead, the authors suggest that the magmas were generated in a deep mantle plume and that the water and other volatile components, especially the halogens (F, Cl), were entrained into the komatiitic magma as it passed through the transition zone between the upper and lower mantle, at a depth below 410 km (Fig. 3). This implies the existence of a deep reservoir of water in the mantle: a portion of the mantle containing a few thausends of parts per million of water in high pressure polymorphs of olivine wadsleyite, ringwoodite. This water may have accumulated during the primordial accretion of the Earth or by the unexpectedly early subduction of hydrated slabs that became trapped in the transition zone. Finally, the authors propose that modern mantle plumes do not extract water from the transition zone because they are colder and therefore entirely solid when they crossed the transition zone.
Earth and Planetary Science Letters, Vol. 447, pp. 1-9.
Mantle
Water content
Abstract: The electrical conductivity of San Carlos clinopyroxene aggregates with various water contents were measured under Ni -NiO buffer at 1.5 GPa and 600 -1200 K in a DIA-type apparatus. The conductivity increases with increasing water content in clinopyroxene. Hidden conduction mechanism was detected because of the much smaller iron content in clinopyroxene, which was usually covered by small polaron conduction in other nominally anhydrous minerals. The identified activation enthalpies ranged from 0.70 -0.75 eV to 1.23 -1.37 eV. Our result reveals that the dominant charge-carrying species in electrical conductivity could change with temperature and water content. At high temperatures relevant to asthenospheric condition, activation enthalpy for the conductivity agrees well with that for the hydrogen self-diffusion. The dominant charge carrier therefore might be M site vacancy. However, contrary to previous view that all hydrogens contribute to increasing conductivity equally, our result shows that only a limited amount (20% -40%) of hydrogen acts as effective charge carrier in clinopyroxene. On the other hand, the activation enthalpy for the conductivity at low temperatures is significantly lower than that for the hydrogen self-diffusion, similar to what has been observed in olivine and orthopyroxene. This type of conduction is probably caused by fast diffusion of specific hydrogen or fast hydrogen grain boundary diffusion. At low temperatures, the proton conduction of clinopyroxene is nearly one order and two orders of magnitude lower than those of olivine and orthopyroxene, respectively, and tends to converge at high temperatures. Using the present data combined with conductivity of olivine and orthopyroxene, a laboratory-based conductivity-depth profile in the uppermost mantle shows that hydrous clinopyroxene cannot account for the high conductive regions observed beneath the ocean floor near Eastern Pacific Rise. The presence of partial melt would be unavoidable.
Physics of the Earth and Planetary Interiors, Vol. 250, pp. 46-63.
Mantle
Water
Abstract: Although water has a major influence on tectonic and other geodynamic processes, little is known about its quantity and distribution within the deep Earth. In the last few decades, laboratory experiments on nominally anhydrous minerals (NAMs) of the transition zone have shown that these minerals can contain significant amounts of water, up to 3.3 wt%. In this study, we investigate if it is possible to use seismic observations to distinguish between a hydrous and anhydrous transition zone. We perform an extensive literature search of mineral experimental data, to generate a compilation of the water storage capacities, elastic parameters and phase boundary data for potentially hydrous minerals in the transition zone, and use thermodynamic modelling to compute synthetic seismic profiles of density, VP and VS at transition zone temperatures and pressures. We find that large uncertainties on the mineral phase equilibria (ca. 2 GPa) and elastic properties produce a wide range of seismic profiles. In particular, there is a lack of data at temperatures corresponding to those along a 1300 °C adiabat or hotter, which may be expected at transition zone pressures. Comparing our hydrous transition zone models with equivalent profiles at anhydrous conditions, we see that the depths of the 410 and 660 discontinuities cannot at present be used to map the water content of the transition zone due to these uncertainties. Further, while average velocities and densities inside the transition zone clearly decrease with increasing water content, there is a near-perfect trade-off with increases in temperature. It is therefore difficult to distinguish thermal from water effects, and the conventional view of a slow and thick transition zone for water and slow and thin transition zone for high temperature should be regarded with caution. A better diagnostic for water may be given by the average velocity gradients of the transition zone, which increase with increasing water content (but decrease for increasing temperature). However the significance of this effect depends on the degree of water saturation and partitioning between the NAMs. Since seismology is better able to constrain the thickness of the transition zone than velocity gradients, our study indicates that the most useful input from future mineral physics experiments would be to better constrain the phase relations between hydrous olivine and its high-pressure polymorphs, especially at high temperatures. Additionally, the uncertainties on the mineral seismic properties could be reduced significantly if the experimentally-observable correlations between bulk and shear moduli and their corresponding pressure derivatives would be published.
Abstract: This position statement sets out ICMM members’ approach to water stewardship. Water stewardship is the use of water in ways that are socially equitable, environmentally sustainable, and economically beneficial.1 Effective stewardship requires collaboration and concerted action from all parties, including government, civil society, business and local communities through inclusive stakeholder engagement.
Earth and Planetary Science Letters, Vol. 464, pp. 189-199.
Mantle
Water
Abstract: We investigate the influence of the mantle water content in the early Earth on that in the present mantle using numerical convection simulations that include three processes for redistribution of water: dehydration, partitioning of water into partially molten mantle, and regassing assuming an infinite water reservoir at the surface. These models suggest that the water content of the present mantle is insensitive to that of the early Earth. The initial water stored during planetary formation is regulated up to 1.2 OMs (OM = Ocean Mass; 1.4×1021 kg1.4×1021 kg), which is reasonable for early Earth. However, the mantle water content is sensitive to the rheological dependence on the water content and can range from 1.2 to 3 OMs at the present day. To explain the evolution of mantle water content, we computed water fluxes due to subducting plates (regassing), degassing and dehydration. For weakly water dependent viscosity, the net water flux is almost balanced with those three fluxes but, for strongly water dependent viscosity, the regassing dominates the water cycle system because the surface plate activity is more vigorous. The increased convection is due to enhanced lubrication of the plates caused by a weak hydrous crust for strongly water dependent viscosity. The degassing history is insensitive to the initial water content of the early Earth as well as rheological strength. The degassing flux from Earth's surface is calculated to be approximately O(1013) kg/yrO(1013) kg/yr, consistent with a coupled model of climate evolution and mantle thermal evolution.
Earth and Planetary Science Letters, Vol. 471, pp. 65-73.
Mantle
geochemistry, water cycle
Abstract: Subduction of hydrous and carbonated oceanic lithosphere replenishes the mantle volatile inventory. Substantial uncertainties exist on the magnitudes of the recycled volatile fluxes and it is unclear whether Earth surface reservoirs are undergoing net-loss or net-gain of H2O and CO2. Here, we use noble gases as tracers for deep volatile cycling. Specifically, we construct and apply a kinetic model to estimate the effect of subduction zone metamorphism on the elemental composition of noble gases in amphibole - a common constituent of altered oceanic crust. We show that progressive dehydration of the slab leads to the extraction of noble gases, linking noble gas recycling to H2O. Noble gases are strongly fractionated within hot subduction zones, whereas minimal fractionation occurs along colder subduction geotherms. In the context of our modelling, this implies that the mantle heavy noble gas inventory is dominated by the injection of noble gases through cold subduction zones. For cold subduction zones, we estimate a present-day bulk recycling efficiency, past the depth of amphibole breakdown, of 5-35% and 60-80% for 36Ar and H2O bound within oceanic crust, respectively. Given that hotter subduction dominates over geologic history, this result highlights the importance of cooler subduction zones in regassing the mantle and in affecting the modern volatile budget of Earth's interior.
Abstract: An open question for solid-earth scientists is the amount of water in Earth’s interior. The uppermost mantle and lower mantle contain little water because their dominant minerals, olivine and bridgmanite, have limited water storage capacity. In contrast, the mantle transition zone (MTZ) at a depth of 410 to 660 km is considered to be a potential water reservoir because its dominant minerals, wadsleyite and ringwoodite, can contain large amounts of water [up to 3 weight % (wt %)]. However, the actual amount of water in the MTZ is unknown. Given that water incorporated into mantle minerals can lower their viscosity, we evaluate the water content of the MTZ by measuring dislocation mobility, a property that is inversely proportional to viscosity, as a function of temperature and water content in ringwoodite and bridgmanite. We find that dislocation mobility in bridgmanite is faster by two orders of magnitude than in anhydrous ringwoodite but 1.5 orders of magnitude slower than in water-saturated ringwoodite. To fit the observed mantle viscosity profiles, ringwoodite in the MTZ should contain 1 to 2 wt % water. The MTZ should thus be nearly water-saturated globally.
Hydration of the lithospheric mantle in the northern Slave craton ( Canada): constraints from combined FTIR and ESRD measurements on peridotite xenoliths.
Earth and Planetary Science Letters, Vol. 494, 1, pp. 92-98.
Mantle
water
Abstract: In this study, we present new experimental constraints on the phase stability and thermal equation of state of an important hydrous phase, ?-AlOOH, using synchrotron X-ray diffraction up to 142 GPa and 2500 K. Our experimental results have shown that ?-AlOOH remains stable at the whole mantle pressure-temperature conditions above the D? layer yet will decompose at the core-mantle boundary because of a dramatic increase in temperature from the silicate mantle to the metallic outer core. At the bottom transition zone and top lower mantle, the formation of ?-AlOOH by the decomposition of phase Egg is associated with a ?2.1-2.5% increase in density (?) and a ?19.7-20.4% increase in bulk sound velocity (V?). The increase in ? across the phase Egg to ?-AlOOH phase transition can facilitate the subduction of ?-AlOOH to the lower mantle. Compared to major lower-mantle phases, ?-AlOOH has the lowest ? but greatest V?, leading to an anomalous low ? /V? ratio which can help to identify the potential presence of ?-AlOOH in the region. More importantly, water released from the breakdown of ?-AlOOH at the core-mantle boundary could lower the solidus of the pyrolitic mantle to cause partial melting and/or react with Fe in the region to form the low-velocity FeO2Hx phase. The presence of partial melting and/or the accumulation of FeO2Hx phase at the CMB could be the cause for the ultra-low velocity zone. ?-AlOOH is thus an important phase to transport water to the lowermost mantle and helps to understand the origin of the ultra-low velocity zone.
Abstract: Incorporation of hydrogen into metamorphic olivine during dehydration reactions in the subducting oceanic lithosphere provides a mechanism to replenish the deep mantle with water. Fourier transform infrared spectroscopy of metamorphic olivines formed at 2.5 GPa and 550 °C through the reaction antigorite + brucite = olivine + chlorite + water shows water contents between 100 and 140 ppm H2O associated exclusively with silicon vacancies, similar to the highest values found in peridotite xenoliths. Brucite involvement in the olivine-forming reaction ensures H2O saturation and a low Si activity, favoring hydrogen incorporation into Si vacancies. The mapped water distribution in olivine is consistent with growth zoning and there is no evidence of water gain or loss. Thus, even for metamorphic timescales of several million years at 550 °C, no ionic diffusion modification is observed, in agreement with recent experimental findings. Metamorphic olivines formed by this dehydration reaction may contribute considerable amounts of water to the deep water cycle. Additionally, olivine with abundant H in Si vacancies are expected to be rheologically weaker than anyhdrous mantle olivine, and might provide a weak interface between slabs and mantle wedges in subduction zones at conditions beyond the stability of hydrous phases.
Abstract: How water cycles through the Earth's interior, presumably is of fundamental importance for understanding the evolution of our planet. The presence of even trace amounts of water (or hydrogen) can dramatically affect many physical and chemical properties of Earth materials, such as phase stability conditions, viscosity, thermal conductivity, etc. Here, we report that the reaction between water and iron to form a pyrite-structured hydrogen-bearing iron peroxide, FeO2Hx (with x = 0 to 1), under the pressure-temperature conditions relevant to the Earth’s deep lower mantle. Combined with theoretical calculations and high-pressure experiments using laser-heated diamond anvil cells coupled with a suite of insitu and characterization techniques (e.g. nuclear resonant inelastic X-ray scattering spectroscopy, X-ray absorption spectroscopy, and X-ray diffraction), we find that this extremely oxygen-rich form of iron peroxide has properties consistent with ultralow velocity zones that are seismically observed at the core-mantle boundary. This phase may also have implications for deep volatile cycling and mantle redox.
Progress in Earth and Planetary Science, doi.org/10.1186/ s40645-018-0198-1 10p.
Mantle
water
Abstract: Aqueous fluids in the Earth’s interior are multicomponent systems with silicate solubility and solution mechanisms strongly dependent on other dissolved components. Here, solution mechanisms that describe the interaction between dissolved silicate and other solutes were determined experimentally to 825 °C and above 1 GPa with in situ vibrational spectroscopy of aqueous fluid while these were at high temperature and pressure. The silicate content in Na-bearing, silicate-saturated aqueous fluid exceeds that in pure SiO2 at high temperature and pressure. Silicate species were of Q0 (isolated SiO4 tetrahedra) and Q1 (dimers, Si2O7) type. The temperature dependence of its equilibrium constant, K?=?XQ1/(XQo)2, yields enthalpies of 22?±?12 and 51?±?17 kJ/mol for the SiO2-H2O and Na-bearing fluids. In contrast, in Ca-bearing fluids, the solubility is more than an order of magnitude lower, and only Q0 species are present. The present data together with other published experimental information lead to the conclusion that the silicate solubility in aqueous fluids in equilibrium with mafic rocks such as amphibolite and peridotite is an order of magnitude lower than the solubility in fluids in equilibrium with felsic rocks such as andesite and rhyolite compositions (felsic gneiss) under similar temperature and pressure conditions. The silicate speciation also is more polymerized in the felsic systems. This difference is also why second critical end-points in the Earth are at lower temperature and pressure in felsic compared with mafic systems. Alkali-rich fluids formed by dehydration of felsic rocks also show enhanced high field strength element (HFSE) solubility because alkalis in such solution form oxy complexes with the HFSE cations. Fluids formed by dehydration of felsic rocks in the Earth’s interior are, therefore, more efficient transport agents of silicate materials than fluids formed by dehydration of mafic and ultramafic rocks, whether for major, minor, or trace elements.
Earth and Planetary Science Letters, Vol. 498, pp. 9-16.
Mantle
water
Abstract: Ringwoodite, the dominant mineral at depths between 520 km and 660 km, can store up to 2-3 wt.% of water in its crystal structure, making the Earth's transition zone a plausible water reservoir that plays a central role in Earth's deep water cycle. Experiments show that hydration of ringwoodite significantly reduces elastic wave velocities at room pressure, but the effect of pressure remains poorly constrained. Here, a novel experimental setup enables a direct quantification of the effect of hydration on ringwoodite single-crystal elasticity and density at pressures of the Earth's transition zone and high temperatures. Our data show that the hydration-induced reduction of seismic velocities almost vanishes at conditions of the transition zone. Seismic data thus agree with a wide range of water contents in the transition zone.
Abstract: While mineral phases stable in the mantle transition zone (such as wadsleyite and ringwoodite) can store up to 3 wt% H2O, those in the lower mantle such as bridgmanite and ferropericlase can contain a very small amount (<50 ppm). While such dramatic differences can lead to dehydration/hydration and hydrous melting at 660-km depth in the mantle [1,2] it is uncertain how much water can be transported and stored at these depths. In order to answer this question, we have conducted a series of high pressure experiments in laser-heated diamondanvil cell and multi-anvil press combined with X-ray diffraction, infrared spectroscopy, laser Raman spectroscopy, and secondary ion mass spectrometry. Initially we examined the water storage capacity of dense (Al free) silica polymorphs at high pressure and temperature. We found that water can dramatically reduce the rutile-type to CaCl2-type phase transition from 55 GPa to 25 GPa and stabilize a new "disordered inverse" inverse NiAs-type phase at pressures above 50 GPa, which is not stable in dry SiO2 system. The CaCl2-type and NiAs-type silica polymorphs contain up to 8 wt% of H2O at 1400-2100 K up to at least 110 GPa. We next explored the effects of water on the mineralogy of the lower mantle and found that hydrous Mg2SiO4 ringwoodite (1 wt% H2O) breaks down to silica + bridgmanite + ferropericlase at pressures up to 60 GPa and 2100 K. The recovered silica samples contain 0.3-1.1 wt% H2O, suggesting that water stabilizes silica even under Si-undersaturated systems because of their large water storage capacity. Therefore, our observations support the stability of silica in hydrous regions in the pyrolitic lower mantle. In the subducting oceanic crust (basalt and sediment), silica represents 20-80% of the mineralogy. Because its stability range spans the mantle transition zone to the deep mantle, hydrous silica is expected to play a major role in the transport and storage of water in the deep mantle.
Abstract: Water is carried down into Earth at subduction zones by the process of plate tectonics. Much of the water escapes close behind the subduction zone, promoting melting of the mantle and giving rise to the volcanic chains in the Pacific Ocean basin known as the Ring of Fire, and many other volcanoes elsewhere. But can water be carried even further into the mantle? How would we even know? Why is it important, and what are the effects of such deep water storage? Diamonds can give us the answers to these questions. Recent discoveries of water-containing mineral inclusions and even free water held at high pressures in diamonds tell us that water is carried into Earth’s deep interior—perhaps as deep as 700 km.
Abstract: The transition zone (TZ) is believed to be the primary destination of subducted water [1], with the main TZ minerals (wadsleyite and ringwoodite) capable of holding up to ~ 3 wt.% H2O in their structures’. Observations of high attenuation and elevated conductivity suggest some areas of the transition zone are hydrated [2,3]. Combined with the observation of ~ 1.4 wt% H2O in a diamond-hosted ringwoodite inclusion [4], it is probable that the transition zone is at least regionally, if not globally, “wet”. The presence of water can induce partial melting, alter chemical partitioning and drastically change the strength of rocks. The detailed effect of water’s presence in the TZ will strongly depend on hydrogen’s incorporation mechanism, i.e. exchange with Si4+, Mg2+, Fe2+ cations or coupled substitution with Fe3+ in ringwoodite. Recent developments in neutron single-crystal Laue diffraction now allow measurements on crystals smaller than 0.1 mm3 [5]. Here we quantitatively study the incorporation of hydrogen in a synthetic iron-bearing ringwoodite. A multi-technique approach, with independent determination of chemistry, ferric iron content, water content and structure via x-ray and neutron diffraction allows a detailed study of the hydrous ringwoodite structure and the incorporation mechanism of water throughout Earth’s TZ.
Progress in Earth and Planetary Science, Vol. 5, pp. 51- 16p.
Mantle
water
Abstract: Here, we investigate a possible scenario of surface seawater evolution in the numerical simulations of surface plate motion driven by mantle dynamics, including thermo-chemical convection and water migration, from the early to present-day Earth to constrain the total amount of water in the planetary system. To assess the validity of two hypotheses of the total amount of water inferred from early planetary formation processes and mineral physics, we examine the model sensitivity to the total water in the planetary system (both surface and deep interior) up to 15 ocean masses. To explain the current size of the reservoir of surface seawater, the predictions based on the numerical simulations of hydrous mantle convection suggest that the total amount of water should range from 9 to 12 ocean masses. Incorporating the dense hydrous magnesium silicate (DHMS) with a recently discovered hydrous mineral at lower mantle pressures (phase H) indicates that the physical mechanism of the mantle water cycle would not be significantly influenced, but the water storage region would be expanded in addition to the mantle transition zone. The DHMS solubility field may have a limited impact on the partitioning of water in the Earth’s deep mantle.
Journal of Geophysical Research: Planets, doei:10.1029/ 2018JE005698
Mantle
water
Abstract: People have long had curiosity in the origin of Earth's water (equivalently hydrogen). Solar nebula has been given the least attention among existing theories, although it was the predominating reservoir of hydrogen in our early solar system. Here we present a first model for Earth's water origin that quantifies contribution from the solar nebula in addition to that from chondrites, the primary building blocks of Earth. The model considers dissolution of nebular hydrogen into the early Earth's magma oceans and reaction between hydrogen and iron droplets within the magma ocean. Such processes not only delivered countless hydrogen atoms from the mantle to the core but also generated an appreciable difference in hydrogen isotopic composition (2H/1H ratio) between the mantle and core. Fitting the model to current knowledge about Earth's hydrogen produces best combinations of nebular and chondritic contributions to Earth's water. We find that nearly one out of every 100 water molecules on Earth came from the solar nebula. Our planet hides majority of its water inside, with roughly two oceans in the mantle and four to five oceans in the core. These results suggest inevitable formation of water on sufficiently large rocky planets in extrasolar systems.
Rendiconti Lincei. Scienze Fisische e Naturali *** In Eng, 8p. Pdf
Mantle
water
Abstract: This contribution deals with two different hypotheses on the origin of superficial water on the Earth: the Endogenous hypothesis and the Exogenous one. They proposed that water either was brought to the surface of the Earth from the deep interior of the Earth or would have come to the Earth from celestial bodies that bombarded the planet billions of years ago. The evidence from recent astronomical and geological findings supporting the two alternative hypotheses will be discussed.
Journal of Metamorphic Geology, Vol. 37, 3, pp. 339-358.
Mantle
water
Abstract: Partial melting of continental crust and evolution of granitic magmas are inseparably linked to the availability of H2O. In the absence of a free aqueous fluid, melting takes place at relatively high temperatures by dehydration of hydrous minerals, whereas in its presence, melting temperatures are lowered, and melting need not involve hydrous minerals. With the exception of anatexis in water?saturated environments where anhydrous peritectic minerals are absent, there is no reliable indicator that clearly identifies the presence of a free aqueous fluid during anatexis. Production of Ab?rich magmas or changes in LILE ratios, such as an increase in Sr and decrease in Rb indicating increased involvement of plagioclase, are rough guidelines to the presence of aqueous fluids. Nevertheless, all indicators have caveats and cannot be unequivocally applied, allowing for the persistence of a bias in the literature towards dehydration melting. Investigation of mineral equilibria modelling of three metasedimentary protoliths of the Kangaroo Island migmatites in South Australia, shows that the main indicator for the presence of small volumes of excess water under upper amphibolite to lower granulite facies conditions (660-750°C) is the melt volume produced. Melt composition, modal content or chemical composition of peritectic minerals such as cordierite, sillimanite or garnet are relatively insensitive to the presence of free water. However, the mobility of melt during open system behaviour makes it difficult to determine the melt volume produced. We therefore argue that the presence of small volumes of excess water might be much more common than so far inferred, with large impact on the buffering of crustal temperatures and fertility, and therefore rheology of the continental crust.
Abstract: H2O strongly influences physical properties of the mantle and its ability to melt or convect and can trace recycling of surface reservoirs down to the deep mantle1,2. This makes knowledge of water content in the Earth's interior and its evolution through time crucial to understanding global geodynamics. Komatiites (MgO-rich ultramafic magmas) result from high-degree mantle melting at high pressures3 and thus are excellent probes of H2O contents in the deep mantle. A significant excess of H2O over elements of similar geochemical behavior during mantle melting (e.g. Ce) was recently found in melt inclusions in the most Mg-rich olivine in 2.7 Ga old komatiites from Canada4 and Zimbabwe5. These data were taken as evidence for a deep hydrated mantle reservoir, probably the transition zone, in the Neoarchean time. In this paper we confirm the mantle source of this H2O by measurement of deuterium to hydrogen ratios in these melt inclusions and present similar data for 3.3 Ga old komatiites from the Barberton Greenstone Belt. Using hydrogen isotopes, we show that the mantle sources of these melts contained excess H2O which implies that a deep mantle hydrated reservoir has been present in the Earth's interior at least since the Paleoarchean. The reconstructed initial hydrogen isotope composition of komatiites is significantly more depleted in deuterium than all surface reservoirs and typical mantle but resembles that in dehydrated subducted slabs. Together with a significant excess of chlorine and a temporal trend of Pb/Ce in the mantle sources of komatiites, these results argue that lithosphere recycling into the deep mantle, arguably via subduction, started before 3.3 Ga. (a un-reviewed version of the manuscript accepted for publication in Nature magazine).
Geophysical Research Letters, Vol. 46, 16, pp. 9466-9473.
Mantle
water
Abstract: Planetary-scale melting is ubiquitous after energetic impacts early in Earth's history. Therefore, determining key melt properties, such as density, is of great significance to better understand Earth's formation and subsequent evolution. In this study, we performed state-of-art first-principles molecular dynamics simulations to examine the density of deep mantle melts, namely, hydrous Fe-rich silicate melts. We find that such hydrous melts can be gravitationally stable near Earth's core-mantle boundary given their likely high iron content. This has great implications for Earth's thermochemical evolution, as well as Earth's volatile cycle.
European Journal of Mineralogy, Vol. 31, pp. 715-730.
Europe, Germany
water
Abstract: Data on water in nominally anhydrous minerals (NAMs) of orogenic garnet-bearing ultramafic rocks (GBU) are extremely rare. In this study, garnet of peridotite and pyroxenite from Erzgebirge (EG), Germany, and two peridotite samples from Alpe Arami (AA), Switzerland, were analyzed by infrared (IR) spectroscopy. Garnet from EG peridotite and pyroxenite yielded IR absorption bands at 3650 ± 10 cm?1 (type I) and in the wavenumber range of 3570-3630 cm?1 (type II) that are ascribed to structural hydroxyl (colloquially “water”). Additional broad band’s centered at <3460 cm?1, present in about half of the samples, are related to molecular water (MW). The content of structural H2O defined by band types I + II is low (3-68 ppm) in all EG samples. Structural water is negatively correlated to Mg and Ti and positively to Y and HREE in EG garnet. Including molecular water, a pronounced positive correlation between H2O and Li is observed. Because the intensity of the type II band is enhanced in domains with molecular water, the primary, peak metamorphic H2O content in EG garnet was probably as low as 0-11 ppm. Equally low contents of structural water are present in AA garnet (10-13 ppm) in which molecular water is negligible. Such concentrations are distinctly lower than the water storage capacity of garnet at the relevant pressure. Water loss upon decompression cannot serve as an explanation for the low contents because, on the contrary, post-peak-metamorphic influx of H2O led garnet to take up secondary structural water. Hence, the results are interpreted as an indication of severe water deficiency at peak metamorphism. Notably, the obtained data agree with the H2O content of 6 ppm reported in garnet from Cima di Gagnone peridotite, which originated as abyssal peridotite. It remains unknown if these low contents are typical for an abyssal, low-pressure protolith but, if the rocks were part of the lowermost, most hydrated portion of the mantle wedge, they are expected to contain much more water. Given that garnet in basaltic coesite eclogite from the Erzgebirge is equally water-deficient as the GBU samples from the same unit, it is at least a possibility that both rock types share a low-pressure origin in an oceanic setting.
Geochemistry, Geophysics, Geosystems, Vol. 20, 9, pp. 4382-4389.
Mantle
water
Abstract: We investigated the stability of the Al?rich dense hydrous magnesium silicate Phase D (PhD) in a MgO?Al2O3?SiO2?H2O system between 14 and 25 GPa at 900-1,500 °C. Al?rich PhD has a very wide stability region from 900 °C and 14 GPa to at least 1,500 °C and 25 GPa, showing strong temperature stability with increasing pressure. Al?rich PhD decomposes to Phase Egg at pressure of the mantle transition zone, whereas it decomposes to ??AlOOH phase with a temperature increase at pressure of the uppermost lower mantle. X?ray diffraction and Raman spectroscopy measurements of Al?rich PhD show that the unit?cell volume is slightly larger, but the Raman spectra resemble that of Al?free PhD. The wide stability region of Al?bearing PhD would contribute an important storage site for water in the mantle transition zone, suggesting that it can deliver a certain amount of water into the lower mantle along hot subduction and even at the normal mantle geothermal P?T condition. Furthermore, the dehydration of Al?bearing PhD might be responsible for a series of observed seismic discontinuities from the transition zone to the uppermost lower mantle and even for deep earthquakes in some typical locations.
Annual Review of Earth and Planetary Sciences, Vol. 47, pp. 41-66.
Mantle
subduction, water
Abstract: In this review, we address the current status of numerical modeling of the mantle transition zone and uppermost lower mantle, focusing on the hydration mechanism in these areas. The main points are as follows: (a) Slab stagnation and penetration may play significant roles in transporting the water in the whole mantle, and (b) a huge amount of water could be absorbed into the deep mantle to preserve the surface seawater over the geologic timescale. However, for further understanding of water circulation in the deep planetary interior, more mineral physics investigations are required to reveal the mechanism of water absorption in the lower mantle and thermochemical interaction across the core-mantle boundary region, which can provide information on material properties to the geodynamics community. Moreover, future investigations should focus on determining the amount of water in the early planetary interior, as suggested by the planetary formation theory of rocky planets. Moreover, the supplying mechanism of water during planetary formation and its evolution caused by plate tectonics are still essential issues because, in geodynamics modeling, a huge amount of water seems to be required to preserve the surface seawater in the present day and to not be dependent on an initial amount of water in Earth's system.
Abstract: The origin and evolution of Earth’s biosphere were shaped by the physical and chemical histories of the oceans. Marine chemical sediments and altered oceanic crust preserve a geochemical record of these histories. Marine chemical sediments, for example, exhibit an increase in their 18O/16O ratio through time. The implications of this signal are ambiguous but are typically cast in terms of two endmember (but not mutually exclusive) scenarios. The oceans may have been much warmer in the deep past if they had an oxygen isotope composition similar to that of today. Alternatively, the nature of fluid-rock interactions (including the weathering processes associated with continental emergence) may have been different in the past, leading to an evolving oceanic oxygen isotope composition. Here we examine approximately 3.24-billion-year-old hydrothermally altered oceanic crust from the Panorama district in the Pilbara Craton of Western Australia as an alternative oxygen isotope archive to marine chemical sediments. We find that, at that time, seawater at Panorama had an oxygen isotope composition enriched in 18O relative to the modern ocean with a ?18O of 3.3?±?0.1‰ VSMOW. We suggest that seawater ?18O may have decreased through time, in contrast to the large increases seen in marine chemical sediments. To explain this possibility, we construct an oxygen isotope exchange model of the geologic water cycle, which suggests that the initiation of continental weathering in the late Archaean, between 3 and 2.5 billion years ago, would have drawn down an 18O-enriched early Archaean ocean to ?18O values similar to those of modern seawater. We conclude that Earth’s water cycle may have gone through two separate phases of steady-state behaviour, before and after the emergence of the continents.
Annual Review of Earth and Planetary Sciences, Vol. 47, pp. 41-66. pdf
Mantle
water, subduction
Abstract: In this review, we address the current status of numerical modeling of the mantle transition zone and uppermost lower mantle, focusing on the hydration mechanism in these areas. The main points are as follows: (a) Slab stagnation and penetration may play significant roles in transporting the water in the whole mantle, and (b) a huge amount of water could be absorbed into the deep mantle to preserve the surface seawater over the geologic timescale. However, for further understanding of water circulation in the deep planetary interior, more mineral physics investigations are required to reveal the mechanism of water absorption in the lower mantle and thermochemical interaction across the core-mantle boundary region, which can provide information on material properties to the geodynamics community. Moreover, future investigations should focus on determining the amount of water in the early planetary interior, as suggested by the planetary formation theory of rocky planets. Moreover, the supplying mechanism of water during planetary formation and its evolution caused by plate tectonics are still essential issues because, in geodynamics modeling, a huge amount of water seems to be required to preserve the surface seawater in the present day and to not be dependent on an initial amount of water in Earth's system. 1) Slab stagnation and penetration of the hydrous lithosphere are essential for understanding the global-scale material circulation. 2) Thermal feedback caused by water-dependent viscosity is a main driving mechanism of water absorption in the mantle transition zone and uppermost lower mantle. 3) The hydrous state in the early rocky planets remains to be determined from cosmo- and geochemistry and planetary formation theory. 4) Volatile cycles in the deep planetary interior may affect the evolution of the surface environment.
Abstract: Most magmatism occurring on Earth is conventionally attributed to passive mantle upwelling at mid-ocean ridges, to slab devolatilization at subduction zones, or to mantle plumes. However, the widespread Cenozoic intraplate volcanism in northeast China1,2,3 and the young petit-spot volcanoes4,5,6,7 offshore of the Japan Trench cannot readily be associated with any of these mechanisms. In addition, the mantle beneath these types of volcanism is characterized by zones of anomalously low seismic velocity above and below the transition zone8,9,10,11,12 (a mantle level located at depths between 410 and 660 kilometres). A comprehensive interpretation of these phenomena is lacking. Here we show that most (or possibly all) of the intraplate and petit-spot volcanism and low-velocity zones around the Japanese subduction zone can be explained by the Cenozoic interaction of the subducting Pacific slab with a hydrous mantle transition zone. Numerical modelling indicates that 0.2 to 0.3 weight per cent of water dissolved in mantle minerals that are driven out from the transition zone in response to subduction and retreat of a tectonic plate is sufficient to reproduce the observations. This suggests that a critical amount of water may have accumulated in the transition zone around this subduction zone, as well as in others of the Tethyan tectonic belt13 that are characterized by intraplate or petit-spot volcanism and low-velocity zones in the underlying mantle.
Journal of Geophysical Letters, Vol. 47, e2020GL087222
Mantle
water
Abstract: The amount of water trapped in the Earth's interior has a strong effect on the evolution and dynamics of the planet, which ultimately controls the occurrence of earthquakes and volcanic eruptions. However, the distribution of water inside the Earth is not yet well understood. To study the Earth's deep interior, we make use of changes in the Earth's magnetic field to detect variations in electrical conductivity inside the planet. Electrical conductivity is a characteristic of a rock that varies with temperature and water content. Here, we present a novel methodology to estimate the amount of water in different regions of Earth's mantle. Our analysis suggests the presence of small amounts of water in the mantle underneath Europe, whereas larger amounts are expected beneath North America and northern Asia.
Nature Communications, doi:.org/10.1038/ s41467-020-17442 -8 11p. Pdf
Africa, South Africa, Russia, Siberia
water
Abstract: Trace amounts of water dissolved in minerals affect density, viscosity and melting behaviour of the Earth’s mantle and play an important role in global tectonics, magmatism and volatile cycle. Water concentrations and the ratios of hydrogen isotopes in the mantle give insight into these processes, as well as into the origin of terrestrial water. Here we show the presence of molecular H2 in minerals (omphacites) from eclogites from the Kaapvaal and Siberian cratons. These omphacites contain both high amounts of H2 (70 to 460 wt. ppm) and OH. Furthermore, their ?D values increase with dehydration, suggesting a positive H isotope fractionation factor between minerals and H2-bearing fluid, contrary to what is expected in case of isotopic exchange between minerals and H2O-fluids. The possibility of incorporation of large quantities of H as H2 in nominally anhydrous minerals implies that the storage capacity of H in the mantle may have been underestimated, and sheds new light on H isotope variations in mantle magmas and minerals.
Science, Vol. 369, 6507, pp. 110-1113. doi. 10.1126/ science.aba.1948
Mantle
water
Abstract: The abundances of Earth's chemical elements and their isotopic ratios can indicate which materials formed Earth. Enstatite chondrite (EC) meteorites provide a good isotopic match for many elements but are expected to contain no water because they formed in the hot inner Solar System. This would require Earth's water to be from a different source, such as comets. Piani et al. measured hydrogen contents and deuterium/hydrogen ratios (D/H) in 13 EC meteorites (see the Perspective by Peslier). They found far more hydrogen than is commonly assumed, with D/H close to that of Earth's mantle. Combining these data with cosmochemical models, they show that most of Earth's water could have formed from hydrogen delivered by EC meteorites.
Progress in Earth and Planetary Science, Vol. 7, 76 25p. Doi.org/10.1186 /s40645-020-00379-3 pdf
Mantle
water
Abstract: Oceans on Earth are present as a result of dynamic equilibrium between degassing and regassing through the interaction with Earth’s interior. We review mineral physics, geophysical, and geochemical studies related to the global water circulation and conclude that the water content has a peak in the mantle transition zone (MTZ) with a value of 0.1-1 wt% (with large regional variations). When water-rich MTZ materials are transported out of the MTZ, partial melting occurs. Vertical direction of melt migration is determined by the density contrast between the melts and coexisting minerals. Because a density change associated with a phase transformation occurs sharply for a solid but more gradually for a melt, melts formed above the phase transformation depth are generally heavier than solids, whereas melts formed below the transformation depth are lighter than solids. Consequently, hydrous melts formed either above or below the MTZ return to the MTZ, maintaining its high water content. However, the MTZ water content cannot increase without limit. The melt-solid density contrast above the 410 km depends on the temperature. In cooler regions, melting will occur only in the presence of very water-rich materials. Melts produced in these regions have high water content and hence can be buoyant above the 410 km, removing water from the MTZ. Consequently, cooler regions of melting act as a water valve to maintain the water content of the MTZ near its threshold level (~?0.1-1.0 wt%). Mass-balance considerations explain the observed near-constant sea-level despite large fluctuations over Earth history. Observations suggesting deep-mantle melting are reviewed including the presence of low-velocity anomalies just above and below the MTZ and geochemical evidence for hydrous melts formed in the MTZ. However, the interpretation of long-term sea-level change and the role of deep mantle melting in the global water circulation are non-unique and alternative models are reviewed. Possible future directions of studies on the global water circulation are proposed including geodynamic modeling, mineral physics and observational studies, and studies integrating results from different disciplines.
Earth and Planetary Science Letters, Vol. 554, doi:10.1016/ j.epsl.2020. 116626 12p. Pdf
Mantle
water
Abstract: The mantle transition zone (MTZ) is potentially a geochemical water reservoir because of the high H2O solubility in its dominant minerals, wadsleyite and ringwoodite. Whether the MTZ is wet or dry fundamentally impacts our understanding of the deep-water distribution, geochemical recycling, and the pattern of mantle convection. However, the water content in the MTZ inferred from previous studies remains disputed. Seismic observations such as velocity anomalies were used to evaluate the water content in the MTZ, but the hydration effect on the velocities of MTZ minerals under appropriate pressure (P) and temperature (T) conditions is poorly constrained. Here we investigated the elastic properties and velocities of hydrous ringwoodite at high P-T conditions using first-principles calculations. Our results show that the hydration effects on elastic moduli and velocities of ringwoodite are significantly reduced by pressure but strongly enhanced by temperature. The incorporation of 1.0 wt% water into ringwoodite decreases the compressional and shear velocities of the pyrolitic mantle by ?1.0% and ?1.4% at the conditions of MTZ, respectively. Using results from seismic tomography and together with the topography of the 660-km discontinuity, we evaluate the global distribution of water in the lower MTZ. We find that about 80% of the MTZ can be explained by varying water content and temperature, however, the remaining 20% requires the presence of high-velocity heterogeneities such as harzburgite. Our models suggest an average water concentration of ?0.2 wt% in the lower MTZ, with an interregional variation from 0 to 0.9 wt%. Together with our previous work, we conclude that the water concentration in the MTZ likely decreases with depth globally and the whole MTZ contains the equivalent of about one ocean mass of water.
Abstract: At the Earth's surface, the majority of water resides in the oceans, while in the interior, major rock?forming minerals can incorporate significant amounts of water as hydroxyl groups (OH), likely forming another reservoir of water inside the planet. The amount of water that can be dissolved in Earth's mantle minerals, called its water storage capacity, generally decreases at higher temperatures. Over billion?year timescales, the exchange of water between Earth's interior and surface may control the surface oceans' volume change. Here, we calculated the water storage capacity in Earth's solid mantle as a function of mantle temperature. We find that water storage capacity in a hot, early mantle may have been smaller than the amount of water Earth's mantle currently holds, so the additional water in the mantle today would have resided on the surface of the early Earth and formed bigger oceans. Our results suggest that the long?held assumption that the surface oceans' volume remained nearly constant through geologic time may need to be reassessed.
Abstract: Fluids are essential to the physical and chemical processes in subduction zones. Two types of subduction-zone fluids can be distinguished. First, shallow fluids, which are relatively dilute and water rich and that have properties that vary between subduction zones depending on the local thermal regime. Second, deep fluids, which possess higher proportions of dissolved silicate, salts and non-polar gases relative to water content, and have properties that are broadly similar in most subduction systems, regardless of the local thermal structure. We review key physical and chemical properties of fluids in two key subduction-zone contexts-along the slab top and beneath the volcanic front-to illustrate the distinct properties of shallow and deep subduction-zone fluids.
Abstract: Aqueous fluids are critical agents in the geochemical evolution of Earth’s interior. Fluid circulation and fluid-rock reactions in the Earth take place at temperatures ranging from ambient to magmatic, at pressures from ambient to extreme, and involve fluids that range from nearly pure H2O through to complex, multicomponent solutions. Consequently, the physical and chemical properties of hydrothermal fluids vary widely as functions of geologic setting; this variation strongly impacts fluid-driven processes. This issue will focus on the nature of geologic fluids at hydrothermal conditions and how such fluids affect geologic processes in some major settings.
Annual Review of Earth Planetary Sciences, Vol. 49, pp. 253-278.
Mantle
water
Abstract: Hydrogen and deuterium isotopic evidence indicates that the source of terrestrial water was mostly meteorites, with additional influx from nebula gas during accretion. There are two Earth models, with large (7-12 ocean masses) and small (1-4 ocean masses) water budgets that can explain the geochemical, cosmochemical, and geological observations. Geophysical and mineral physics data indicate that the upper and lower mantles are generally dry, whereas the mantle transition zone is wetter, with heterogeneous water distribution. Subducting slabs are a source of water influx, and there are three major sites of deep dehydration: the base of the upper mantle, and the top and bottom of the lower mantle in addition to slabs in the shallow upper mantle. Hydrated regions surround these dehydration sites. The core may be a hidden reservoir of hydrogen under the large water budget model.
Annual Review of Earth and Planetary Sciences, Vol. 49, pp. 253-278.
Mantle
water
Abstract: Hydrogen and deuterium isotopic evidence indicates that the source of terrestrial water was mostly meteorites, with additional influx from nebula gas during accretion. There are two Earth models, with large (7-12 ocean masses) and small (1-4 ocean masses) water budgets that can explain the geochemical, cosmochemical, and geological observations. Geophysical and mineral physics data indicate that the upper and lower mantles are generally dry, whereas the mantle transition zone is wetter, with heterogeneous water distribution. Subducting slabs are a source of water influx, and there are three major sites of deep dehydration: the base of the upper mantle, and the top and bottom of the lower mantle in addition to slabs in the shallow upper mantle. Hydrated regions surround these dehydration sites. The core may be a hidden reservoir of hydrogen under the large water budget model.
Abstract: Constraining deep-water recycling along subduction zones is a first-order problem to understand how Earth has maintained a hydrosphere over billions of years that created conditions for a habitable planet. The pressure-temperature stability of hydrous phases in conjunction with slab geotherms determines how much H2O leaves the slab or is transported to the deep mantle. Chlorite-rich, metasomatic rocks that form at the slab-mantle interface at 50-100 km depth represent an unaccounted, H2O-rich reservoir in subduction processes. Through a series of high-pressure experiments, we investigated the fate of such chlorite-rich rocks at the most critical conditions for subduction water recycling (5-6.2 GPa, 620-800 °C) using two different natural ultramafic compositions. Up to 5.7 GPa, 740 °C, chlorite breaks down to an anhydrous peridotite assemblage, and H2O is released. However, at higher pressures and lower temperatures, a hydrous Al-rich silicate (11.5 Å phase) is an important carrier to enable water transfer to the deep mantle for cold subduction zones. Based on the new phase diagrams, it is suggested that the deep-water cycle might not be in secular equilibrium.
Physics and Chemistry of Minerals, Vol. 48, 31, 10p. Pdf
Mantle
water
Abstract: We have systematically investigated the high-pressure and high-temperature stability of Al-bearing dense hydrous magnesium silicate phases (DHMSs) in natural chlorite compositions containing?~?16 wt% H2O and?~?14 wt% Al2O3 between 14 and 25 GPa at 800-1600 °C by an MA8-type multi-anvil apparatus. A chemical mixture similar to Fe-free chlorite was also investigated for comparison. Following the pressure-temperature (P-T) path of cold subduction, the phase assemblage of phase E?+?phase D is stable at 14-25 GPa. Superhydrous phase B is observed between 16 and 22 GPa coexisting with phase E?+?phase D. Following the P-T path of hot subduction, the phase assemblage of phase E?+?garnet is identified at 14-18 GPa coexisting with the melt. The phase assemblage of superhydrous phase B?+?phase D was found at 18-25 GPa, which is expected to survive at higher P-T conditions. We have confirmed that the presence of Al could enhance the stability of DHMSs. Our results indicate that, after chlorite decomposition at the shallow region of the subduction zone, the wide stability field of Al-bearing DHMSs can increase the possibility of water transportation into the deep lower mantle.
Contributions to Mineralogy and Petrology, Vol. 177, 4. 10.1007/s00410-022-01910-z
Mantle
water
Abstract: Oxidized fluids in the subduction zone may convert polyvalent elements in the mantle to their higher valence states. The most abundant polyvalent element in the mantle is Fe, a significant part of which is contained in olivine as Fe2+. Results of the study of arc mantle xenoliths, in lab high-pressure-high-temperature experiments, and thermodynamic modeling have shown that at pressures of?~?50-2000 MPa and temperatures of 1000-1250 °C, well above the serpentine stability field, Fe2+ from olivine reacts with free aqueous fluid according to the following simplified reaction: 3Fe2SiO4?+?2H2O???3SiO2?+?2Fe3O4?+?2H2. The resulting ferric iron is preserved in spinel of a certain composition, (Mg,Fe2+)Fe3+2O4, whereas new high-Mg olivine, with magnesium number up to 96 in natural samples and 99.9 in experiments, forms in the reaction zone. SiO2 produced in the reaction either dissolves in the fluid or, with a small amount of water, reacts with olivine to form orthopyroxene as follows: (Mg,Fe)2SiO4?+?SiO2?=?(Mg,Fe)2Si2O6. The released H2 may decrease the oxidation state of polyvalent elements present in the fluid (e.g., S4+, S6+). Traces of high-temperature water-olivine interaction appear as swarms of fluid-spinel inclusions and are ubiquitous in olivine from ultramafic arc xenoliths. The described process is similar to serpentinization but occurs at higher pressure and temperature conditions and yields different reaction products. The reducing capacity of olivine is relatively low; however, given the large volume of mantle (and crustal) peridotites, the overall effect may be significant.
