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1.
Diamonds containing ferropericlase (Mg,Fe)O and other silicate (enstatite [(Mg,Fe)SiO3], in particular) assemblages are generally believed to be derived from the Earth's lower mantle. On the basis of the observed ratio between ferropericlase and enstatite inclusions and the FeO content of these ferropericlases, it is concluded that most of these minerals entrapped in diamonds may not represent the lithology of the lower mantle itself as has been suggested by many investigators. Instead, ferropericlases in these diamonds represent most likely the disproportionate product of ferromagnesite [(Mg,Fe)CO3], which underwent a decarbonation reaction to form both diamond and ferropericlase simultaneously in the lower mantle. The wide variation in the Mg# of ferropericlase inclusions in diamonds is attributed to the decarbonation "loop" of the MgCO3-FeCO3 solid solutions. Some of the enstatite inclusions coexisting with these ferropericlases in the same diamond may represent the most abundant mineral species of (Mg,Fe)SiO3-perovskite in the lower mantle. The latter mineral phase experienced a retrogressive transition into enstatite during the transport of diamonds to the Earth's surface.  相似文献   

2.
The ultrabasic–basic magmatic evolution of the lower mantle material includes important physicochemical phenomena, such as the stishovite paradox and the genesis of superdeep diamonds. Stishovite SiO2 and periclase–wüstite solid solutions, (MgO · FeO)ss, associate paradoxically in primary inclusions of superdeep lower mantle diamonds. Under the conditions of the Earth’s crust and upper mantle, such oxide assemblages are chemically impossible (forbidden), because the oxides MgO and FeO and SiO2 react to produce intermediate silicate compounds, enstatite and ferrosilite. Experimental and physicochemical investigations of melting phase relations in the MgO–FeO–SiO2–CaSiO3 system at 24 GPa revealed a peritectic mechanism of the stishovite paradox, (Mg, Fe)SiO3 (bridgmanite) + L = SiO2 + (Mg, Fe)O during the ultrabasic–basic magmatic evolution of the primitive oxide–silicate lower mantle material. Experiments at 26 GPa with oxide–silicate–carbonate–carbon melts, parental for diamonds and primary inclusions in them, demonstrated the equilibrium formation of superdeep diamonds in association with ultrabasic, (Mg, Fe)SiO3 (bridgmanite) + (MgO · FeO)ss (ferropericlase), and basic minerals, (FeO · MgO)ss (magnesiowüstite) + SiO2 (stishovite). This leads to the conclusion that a peritectic mechanism, similar to that responsible for the stishovite paradox in the pristine lower mantle material, operates also in the parental media of superdeep diamonds. Thus, this mechanism promotes both the ultrabasic–basic evolution of primitive oxide–silicate magmas in the lower mantle and oxide–silicate–carbonate melts parental for superdeep diamonds and their paradoxical primary inclusions.  相似文献   

3.
We report cloudy micro- and nano-inclusions in a superdeep diamond from São-Luiz, Brazil which contains inclusions of ferropericlase (Mg, Fe)O and former bridgmanite (Mg, Fe)SiO3 and ringwoodite (Mg, Fe)2SiO4. Field emission-SEM and TEM observations showed that the cloudy inclusions were composed of euhedral micro-inclusions with grain sizes ranging from tens nanometers to submicrometers. Infrared absorption spectra of the cloudy inclusions showed that water, carbonate, and silicates were not major components of these micro- and nano-inclusions and suggested that the main constituent of the inclusions was infrared-inactive. Some inclusions were suggested to contain material with lower atomic numbers than that of carbon. Mineral phase of nano- and micro-inclusions is unclear at present. Microbeam X-ray fluorescence analysis clarified that the micro-inclusions contained transition metals (Cr, Mn, Fe, Co, Ni, Cu, Zn) possibly as metallic or sulfide phases. The cloudy inclusions provide an important information on the growth environment of superdeep diamonds in the transition zone or the lower mantle.  相似文献   

4.
Superdeep diamonds from the Juina area, Mato Grosso State, Brazil   总被引：4，自引：1，他引：3  
Alluvial diamonds from the Juina area in Mato Grosso, Brazil, have been characterized in terms of their morphology, syngenetic mineral inclusions, carbon isotopes and nitrogen contents. Morphologically, they are similar to other Brazilian diamonds, showing a strong predominance of rounded dodecahedral crystals. However, other characteristics of the Juina diamonds make them unique. The inclusion parageneses of Juina diamonds are dominated by ultra-high-pressure ("superdeep") phases that differ both from "traditional" syngenetic minerals associated with diamonds and, in detail, from most other superdeep assemblages. Ferropericlase is the dominant inclusion in the Juina diamonds. It coexists with ilmenite, Cr-Ti spinel, a phase with the major-element composition of olivine, and SiO2. CaSi-perovskite inclusions coexist with titanite (sphene), "olivine" and native Ni. MgSi-perovskite coexists with TAPP (tetragonal almandine-pyrope phase). Majoritic garnet occurs in one diamond, associated with CaTi-perovskite, Mn-ilmenite and an unidentified Si-Mg phase. Neither Cr-pyrope nor Mg-chromite was found as inclusions. The spinel inclusions are low in Cr and Mg, and high in Ti (Cr2O3<36.5 wt%, and TiO2>10 wt%). Most ilmenite inclusions have low MgO contents, and some have very high (up to 11.5 wt%) MnO contents. The rare "olivine" inclusions coexisting with ferropericlase have low Mg# (87-89), and higher Ca, Cr and Zn contents than typical diamond-inclusion olivines. They are interpreted as inverted from spinel-structured (Mg, Fe)2Si2O4. This suite of inclusions is consistent with derivation of most of the diamonds from depths near 670 km, and adds ilmenite and relatively low-Cr, high-Ti spinel to the known phases of the superdeep paragenesis. Diamonds from the Juina area are characterized by a narrow range of carbon isotopic composition ('13C=-7.8 to -2.5‰), except for the one majorite-bearing diamond ('13C=-11.4‰). There are high proportions of nitrogen-free and low-nitrogen diamonds, and the aggregated B center is predominant in nitrogen-containing diamonds. These observations have practical consequences for diamond exploration: Low-Mg olivine, low-Mg and high-Mn ilmenite, and low-Cr spinel should be included in the list of diamond indicator minerals, and the role of high-Cr, low-Ti spinel as the only spinel associated with diamond, and hence as a criterion of diamond grade in kimberlites, should be reconsidered.  相似文献   

5.
Kankan diamonds (Guinea) II: lower mantle inclusion parageneses   总被引：3，自引：2，他引：1  
Frequent inclusions of ferropericlase, some coexisting with phases of MgSiO3, CaSiO3 and SiO2 composition, suggest that a large proportion of diamonds from Guinea are derived from the lower mantle. Low aluminium contents in MgSiO3 inclusions indicate derivation from the uppermost lower mantle, where Al solubility in perovskite is low. Trace element analyses (SIMS) of CaSiO3 inclusions reveal extreme degrees of LREE (200–2000 times chondritic) and Sr enrichment (70–1000 times chondritic) together with negative and positive Eu anomalies. This implies a highly enriched lower mantle source, possibly a product of a subducted oceanic slab. A number of phases that are only stable in the upper mantle are found to coexist with lower mantle phases and thereby indicate retrograde equilibration during slow exhumation within a rising plume or convection cell. In one case, however, an inclusion paragenesis of ferropericlase and olivine can be shown to have formed within the upper mantle, indicating that the occurrence of ferropericlase inclusions alone is an unreliable indicator of lower mantle origin. Received: 26 January 2000 / Accepted: 18 May 2000  相似文献   

6.
Bridgmanite (Mg,Fe)SiO3 and ferropericlase (Mg,Fe)O are the most abundant phases in the lower mantle and localized regions of the D″ layer just above the core mantle boundary. Seismic anisotropy is observed near subduction zones at the top of the lower mantle and in the D″ region. One source of anisotropy is dislocation glide and associated texture (crystallographic preferred orientation) development. Thus, in order to interpret seismic anisotropy, it is important to understand texture development and slip system activities in bridgmanite and bridgmanite + ferropericlase aggregates. Here we report on in situ texture development in bridgmanite and bridgmanite + ferropericlase aggregates deformed in the diamond anvil cell up to 61 GPa. When bridgmanite is synthesized from enstatite, it exhibits a strong (4.2 m.r.d.) 001 transformation texture due to a structural relationship with the precursor enstatite phase. When bridgmanite + ferropericlase are synthesized from olivine or ringwoodite, bridgmanite exhibits a relatively weak 100 transformation texture (1.2 and 1.6 m.r.d., respectively). This is likely due to minimization of elastic strain energy as a result of Young’s modulus anisotropy. In bridgmanite, 001 deformation textures are observed at pressures <55 GPa. The 001 texture is likely due to slip on (001) planes in the [100], [010] and \(\left\langle {110} \right\rangle\) directions. Stress relaxation by laser annealing to 1500–1600 K does not result in a change in this texture type. However, at pressures >55 GPa a change in texture to a 100 maximum is observed, consistent with slip on the (100) plane. Ferropericlase, when deformed with bridgmanite, does not develop a coherent texture. This is likely due to strain heterogeneity within the softer ferropericlase grains. Thus, it is plausible that ferropericlase is not a significant source of anisotropy in the lower mantle.  相似文献   

7.
Felix Kaminsky 《Earth》2012,110(1-4):127-147
Starting from the late 1980s, several groups of lower-mantle mineral inclusions in diamond have been found. Three associations were established among them: juvenile ultramafic, analogous to eclogitic, and carbonatitic. The juvenile ultramafic association strongly predominates, and it is composed of ferropericlase, MgSi-, CaSi- and CaTi-perovskites, stishovite, tetragonal almandine-pyrope phase (TAPP), and some others. The association analogous to the upper-mantle eclogitic association, formed from subducting lithosphere, comprises: majorite, CaSi-perovskite bearing compositional Eu anomalies, phase ‘Egg’ with a tetragonal structure, and stishovite. The carbonatitic association is represented by various carbonates, halides, and associated minerals. Some mineral associations (wüstite + periclase and native iron + iron carbides) are, possibly, related to the D″ layer at the core/mantle boundary. The mineralogical composition of the lower mantle is now understood to be more complex than had been suggested in theoretic and experimental works. The proportion of ferropericlase in the lower mantle is higher than it was suggested before, and its composition is more iron-rich (mg = 0.36–0.90) as compared to experimental and theoretical data. Free silica (stishovite) is always present in lower-mantle associations, and a separate aluminous phase (TAPP) has been identified in several areas. These discrepancies suggest that the composition of the lower mantle differs to that of the upper-mantle, and experiments based solely on ‘pyrolitic’ compositions are not, therefore, applicable to the lower mantle. These data indicate a probability of an alternative to the CI-chondrite model of the Earth's formation, for example, an enstatite-chondrite model.  相似文献   

8.
The carbon isotopic composition of 66 inclusion-containing diamonds from the Premier kimberlite, South Africa, 93 inclusion-containing diamonds and four diamonds of two diamond-bearing peridotite xenoliths from the Finsch kimberlite, South Africa was measured. The data suggest a relationship between the carbon isotopic composition of the diamonds and the chemical composition of the associated silicates. For both kimberlites similar trends are noted for diamonds containing peridotite-suite inclusions (P-type) and for diamonds containing eclogite-suite inclusions (E-type): Higher δ13C P-type diamonds tend to have inclusions lower in SiO2 (ol), Al2O3 (opx, gt), Cr2O3, MgO, Mg(Mg + Fe) (ol, opx, gt) and higher in FeO (ol, opx, gt) and CaO (gt). Higher δ13C E-type diamonds tend to have inclusions lower in SiO2, Al2O3 (gt, cpx), MgO, Mg(Mg + Fe) (gt), Na2O, K2O, TiO2 (cpx) and higher in CaO, Ca(Ca + Mg) (gt, cpx).Consideration of a number of different models that have been proposed for the genesis of kimberlites, their xenoliths and diamonds shows that they are all consistent with the conclusion that in the mantle, regions exist that are characterized by different mean carbon isotopic compositions.  相似文献   

9.
Experimental studies of phase relations in the oxide–silicate system MgO–FeO–SiO2 at 24 GPa show that the peritectic reaction of bridgmanite controls the formation of stishovite as a primary in situ mineral of the lower mantle and as an effect of the stishovite paradox. The stishovite paradox is registered in the diamond-forming system MgO–FeO–SiO2–(Mg–Fe–Ca–Na carbonate)–carbon in experiments at 26 GPa as well. The physicochemical mechanisms of the ultrabasic–basic evolution of deep magmas and diamondforming media, as well as their role in the origin of the lower mantle minerals and genesis of ultradeep diamonds, are studied.  相似文献   

10.
Mineral inclusions of corundum are reported from diamonds from alluvial deposits of tributaries of the Rio Aripuanã, Juina, Brazil. We present the first recorded occurrence of sapphire as an inclusion in diamond and expand on the database of ruby and white corundum inclusions. Ruby inclusions are found to occur both as isolated and touching grains with aluminous pyroxene and associated with ferropericlase. Mineral chemistry and phase relations place the origin of such ruby-bearing diamonds within the lower mantle at 770 km. Mineral associations indaving other corundum inclusions were not observed; hence, their depth of origin is less certain.

Compositions of corundum samples were characterised by electron and ion microprobe. Given the scarcity of literature data, corundum samples from a variety of other geological settings were also analysed. Samples comprised corundums associated with granitic emplacement, metasomatism, amphibolite-facies and granulite-facies rocks, gem and industrial synthetic origins and carmine-coloured corundums recovered from kimberlite drill cores.

In addition to variable amounts of Cr, Fe, Ti, Mg and Si, measurable quantities of other transition elements and high field strength elements were also detected. Corundums from similar geological settings show very similar compositions and are easily distinguishable from other settings. Irrespective of locality, rubies from Norwegian, Tanzanian and Kenyan amphibolite-facies rocks are compositionally indistinguishable. Additionally, corundums from metasomatised zones associated with contact metamorphism from Arizona and Japan were very similar, particularly characterised by unusually high abundance of mobile Zr and Nb (tens of ppm). All Juina inclusions are particularly distinguishable from other corundums by high concentrations of Ni (18–171 ppm weight), typically at least an order of magnitude enriched over the same corundum varietal types from elsewhere. Furthermore, the sapphire inclusion exhibited much larger ratios of Ga and Ge to HFSE elements compared to otherwise similar samples, and ruby inclusions are distinguished by high Mg/Fe ratios (0.27–1.56 by weight). Compositional differences between inclusions in diamonds and corundums from other settings in addition to corundum's physical and chemical durability suggest that with the employment of rapid identification tools such as energy dispersive spectrometry (EDS) and laser-ICPMS, corundum has promise as an indicator of diamond prospectivity.  相似文献   


11.
The increment method is adopted to calculate oxygen isotope fractionation factors for mantle minerals, particularly for the polymorphic phases of MgSiO3 and Mg2SiO4. The results predict the following sequence of 18O-enrichment: pyroxene (Mg,Fe,Ca)2Si2O6>olivine (Mg,Fe)2SiO4>spinel (Mg,Fe)2SiO4>ilmenite (Mg,Fe, Ca)SiO3>perovskite (Mg,Fe,Ca)SiO3. The calculated fractionations for the calcite-perovskite (CaTiO3) system are in excellent agreement with experimental calibrations. If there would be complete isotopic equilibration in the mantle, the spinel-structured silicates in the transition zone are predicted to be enriched in 18O relative to the perovskite-structured silicates in the lower mantle but depleted in 18O relative to olivines and pyroxenes in the upper mantle. The oxygen isotope layering of the mantle would essentially result from differences in the chemical composition and crystal structure of mineral phases at different mantle depths. Assuming isotopic equilibrium on a whole earth scale, the chemical structure of the Earth's interior can be described by the following sequence of 18O-enrichment: uppr crust>lower crust>upper mantle>transition zone>lower mantle >core.  相似文献   

12.
Lower mantle diamonds from Rio Soriso (Juina area,Mato Grosso,Brazil)   总被引：4，自引：2，他引：2  
The morphology, colour, fluorescence, cathodoluminescence, nitrogen content and aggregation state, internal structure and mineral inclusions have been studied for 69 alluvial diamonds from the Rio Soriso (Juina area, Mato Grosso State, Brazil). Nitrogen in most diamonds (53%) is fully aggregated as B centres, but there is also a large proportion of N-free stones (38%). A strong positive correlation between nitrogen and IR-active hydrogen concentrations is observed. The diamonds contain (in order of decreasing abundance) ferropericlase, CaSi-perovskite, magnetite, MgSi-perovskite, pyrrhotite, olivine, SiO2, perovskite, tetragonal almandine-pyrope phase and some other minerals represented by single grains. The Rio Soriso diamond suite is subdivided into several subpopulations that originated in upper and lower mantle of ultramafic and mafic compositions, with the largest subgroup forming in the ultramafic lower mantle. Analysed ferropericlase grains are enriched in Fe (Mg#=0.43–0.89), which is ascribed to their origin in the lowermost mantle. The Juina kimberlites may be unique in sampling the material from depths below 1,700 km that ascended in a plume formed at the core–mantle boundary.Electronic Supplementary Material  Supplementary material is available for this article at
Maya G. KopylovaEmail: Phone: +1-604-8220865Fax: +1-604-8226088
  相似文献   

13.
Partitioning of oxygen and silicon between molten iron and (Mg,Fe)SiO3 perovskite was investigated by a combination of laser-heated diamond-anvil cell (LHDAC) and analytical transmission electron microscope (TEM) to 146 GPa and 3,500 K. The chemical compositions of co-existing quenched molten iron and perovskite were determined quantitatively with energy-dispersive X-ray spectrometry (EDS) and electron energy loss spectroscopy (EELS). The results demonstrate that the quenched liquid iron in contact with perovskite contained substantial amounts of oxygen and silicon at such high pressure and temperature (P–T). The chemical equilibrium between perovskite, ferropericlase, and molten iron at the P–T conditions of the core–mantle boundary (CMB) was calculated in Mg–Fe–Si–O system from these experimental results and previous data on partitioning of oxygen between molten iron and ferropericlase. We found that molten iron should include oxygen and silicon more than required to account for the core density deficit (<10%) when co-existing with both perovskite and ferropericlase at the CMB. This suggests that the very bottom of the mantle may consist of either one of perovskite or ferropericlase. Alternatively, it is also possible that the bulk outer core liquid is not in direct contact with the mantle. Seismological observations of a small P-wave velocity reduction in the topmost core suggest the presence of chemically-distinct buoyant liquid layer. Such layer physically separates the mantle from the bulk outer core liquid, hindering the chemical reaction between them.  相似文献   

14.
Genesis of diamonds in the lower mantle   总被引：3，自引：0，他引：3  
The “forbidden” assemblage (ferropericlase + enstatite) as inclusions in diamonds has been taken as evidence to imply that these inclusions and their host diamonds formed initially in the lower mantle. Magnesite is probably the only stable carbonate at depths greater than ∼220 km. Like dehydration reactions, the reaction boundary for the decarbonation of magnesite has a positive dT/dP slope at lower pressures, which becomes negative at higher pressures, if no other phase intervenes. This reaction boundary probably intersects the geotherm between ∼900 and ∼1100 km, below which magnesite decomposes into an assemblage periclase + diamond + oxygen. Thus, ferropericlase is the most likely inclusion in diamond formed in the lower mantle. The high frequency of sole occurrence of ferropericlase in diamonds from Sao Luiz, Brazil seems to substantiate the present speculation. Received: 8 June 1998 / Accepted: 28 September 1998  相似文献   

15.
Modal mantle metasomatism, involving the re-enrichment of depletedmantle by the introduction or production of new hydrous phases,apatite and other minerals, has been proposed as a criticalprecursor to alkaline volcanism. The merits of the modal metasomatismmodel are evaluated by examining whole-rock 100 Mg/(Mg+Fe2+)ratios and the abundances of TiO2, K2O and P2O5 in mafic volcanicsspanning the mafic alkaline-subalkaline compositional spectrum.Upper mantle amphiboles and micas are also discussed becausethey would be major donors of Ti, Fe, and K to melts duringanatexis of either modally metasomatized depleted mantle orundepleted mantle. Compared with tholeiitic and calc-alkaline basalts and andesites,basanites and alkali basalts and alkali andesites are neitherdistinctive nor unique by virtue of persistant or well-definedhigher abundances of TiO2, K2O, and P2O5 or lower 100 Mg/(Mg+Fe2+)ratios, features which might reflect precursor modal metasomatismof the alkaline sources. Some basanites and alkali basalts dohave higher abundances of TiO2, K2O, and P2O5 than some tholeiitesbut these abundances may be the result of lower degrees of meltingof similar undepleted mantle sources for both magma types. The most widespread mantle phases of inferred metasomatic originare interstitial amphiboles and micas in Group I spinel peridotitexenoliths. These have high 100 Mg/(Mg+Fe) ratios ({small tilde}90) and high Cr2O3 and low TiO2 abundances, and the K2O/Na2Oratios of the amphiboles (chromian pargasites) are low, generallyless than 0?3. Interstitial amphiboles and micas developed asa result of near-isochemical hydration reactions which largelyinvolved Cr-spinel and Cr-diopside. Their formation was probablyinduced in many instances by fluids derived from crystallizingmafic magmas. Metasomatized Group I xenoliths with interstitialhydrous phases remain depleted in TiO2, K2O, and P2O5, and theyretain the high 100 Mg/(Mg+Fe) ratios characterizing depletedGroup I xenoliths. Together with the low K2O/Na2O ratios, thesefeatures preclude such peridotites as suitable sources of mostalkaline (and subalkaline) volcanics. It is suggested that modalmetasomatism plays an insignificant role in the genesis of mostmantle-derived mafic volcanics. Compared with the interstitial phases, kaersutitic amphibolesand titaniferous micas from vein, Group II inclusion and megacrystupper mantle parageneses have lower 100 Mg/(Mg+Fe) ratios andCr2O3 contents, and much higher TiO2 abundances. K2O/Na2O ratiosof the Ti-amphiboles are also much more wide-ranging (0?3 togreater than 1?0). These Fe, Ti-rich amphiboles and micas areneither widespread nor pervasive phases in metasomatized mantle.They are directly related to alkaline magmatism in the uppermantle where they may be associated with incompatible elementenrichment of peridotite wallrocks in the immediate vicinityof frozen conduits of alkaline mafic magmas. The varying K2O/Na2O ratios of mafic volcanics (MORB constitutea major exception) indicate that the principal K-bearing phasesin undepleted mantle are kaersutitic amphibole and titaniferousmica, in varying proportions. The former is probably the majorsource of Ti and K for low K/Na volcanics (K2O/Na2O < 0?5)and also many medium K/Na types (0?5 < K2O/Na2O < 1?0),whereas mica is more likely to be the major K-bearing phasein the source regions of high K/Na extrusives (K2O/Na2 >1?0). Experimental data indicate that kaersutitic amphibole,mica and apatite probably coexist in undepleted spinel- andgarnet lherzolites at pressures up to 25 kb, with mica persistingto pressures as high as 50 kb. It is proposed that undepleted asthenospheric mantle is heterogeneouswith respect to its amphibole, mica, and apatite contents (andhence TiO2, K2O, and P2O5 abundances and K2O/Na2O ratios), andalso with respect to 100 Mg/(Mg+Fe2+ ) ratios which may be significantlyless than the ratios generally assigned to undepleted mantle,namely 88–90.  相似文献   

16.
Silicate perovskites((Mg, Fe)SiO 3 and CaS iO 3) are believed to be the major constituent minerals in the lower mantle. The phase relation, solid solution, spin state of iron and water solubility related to the lower mantle perovskite are of great effect on the geodynamics of the Earth's interior and on ore mineralization. Previous studies indicate that a large amount of iron coupled with aluminum can incorporate into magnesium perovskite, but this is discordant with the disproportionation of(Mg,Fe)SiO 3 perovskite into iron-free MgS i O3 perovskite and hexagonal phase(Mg0.6Fe0.4)SiO 3 in the Earth's lower mantle. MnS iO 3 is the first chemical component confirmed to form wide range solid solution with Ca SiO 3 perovskite and complete solid solution with MgS i O3 perovskite at the P-T conditions in the lower mantle, and addition of Mn Si O3 will strongly affects the mutual solubility between Mg Si O3 and CaS iO 3. The spin state of iron is deeply depends on the site occupation of the Fe3+or Fe2+, the synthesis and the annealing conditions of the sample. It seems that the spin state of Fe2+ in the lower mantle perovskite can be settled as high spin, however, the existence of intermediate spin or low spin state of Fe2+ in perovskite has not been clarified. Moreover, different results have also been reported for the spin state of Fe3+ in perovskite. The water solubility of the lower mantle perovskite is related with its composition. In pure Mg SiO 3 perovskite, only less than 500 ppm water was reported. Al–Mg Si O3 perovskite or Al–Fe–MgS iO 3 perovskite in the lower mantle accommodates water of 1100 to 1800 ppm. Further experiments are necessary to clarify the detailed conditions for perovskite solid solution, to reliably analyze the valence and spin states of iron in the coexisting iron-bearing phases, and to compare the water solubility of different phases at different layers for deeply understanding the geodynamics of the Earth's interior and ore mineralization.  相似文献   

17.
Thermodynamic analysis of equilibria involving minerals of the lower mantle of pyrolite composition and crystalline carbon-bearing compounds indicates that the range of oxygen fugacity values at which diamond can be formed is separated from the region in which Fe-rich metallic alloy is generated by a field in which Fe carbides are stable. This implies that diamond can be formed in the lower mantle under more oxidizing conditions than those thought to be dominant in this geosphere. The absence of a metallic phase from the lower-mantle diamond-bearing mineral assemblage is consistent with the high (approximately 1%) Ni concentration in the ferropericlase found as inclusions in diamonds (Fe-rich metallic alloy is able to intensely extract Ni). An elevated redox potential also follows from the occurrence of carbonate phases found among mineral inclusions in lower-mantle diamonds. The main reason for a local increase in oxygen fugacity in the lower mantle may be shifts of redox equilibria toward a decrease in the amount, and then the disappearance of the Fe-Ni alloy with increasing temperature. An important role in the formation of diamond may be played by the generation of carbonate-phosphate and silicate melts in high-temperature zones and the migration of these melts and their interaction with wall rocks.  相似文献   

18.
Analyses of mineral inclusions, carbon isotopes, nitrogen contents and nitrogen aggregation states in 29 diamonds from two Buffalo Hills kimberlites in northern Alberta, Canada were conducted. From 25 inclusion bearing diamonds, the following paragenetic abundances were found: peridotitic (48%), eclogitic (32%), eclogitic/websteritic (8%), websteritic (4%), ultradeep? (4%) and unknown (4%). Diamonds containing mineral inclusions of ferropericlase, and mixed eclogitic-asthenospheric-websteritic and eclogitic-websteritic mineral associations suggests the possibility of diamond growth over a range of depths and in a variety of mantle environments (lithosphere, asthenosphere and possibly lower mantle).

Eclogitic diamonds have a broad range of C-isotopic composition (δ13C=−21‰ to −5‰). Peridotitic, websteritic and ultradeep diamonds have typical mantle C-isotope values (δ13C=−4.9‰ av.), except for two 13C-depleted peridotitic (δ13C=−11.8‰, −14.6‰) and one 13C-depleted websteritic diamond (δ13C=−11.9‰). Infrared spectra from 29 diamonds identified two diamond groups: 75% are nitrogen-free (Type II) or have fully aggregated nitrogen defects (Type IaB) with platelet degradation and low to moderate nitrogen contents (av. 330 ppm-N); 25% have lower nitrogen aggregation states and higher nitrogen contents (30% IaB; <1600 ppm-N).

The combined evidence suggests two generations of diamond growth. Type II and Type IaB diamonds with ultradeep, peridotitic, eclogitic and websteritic inclusions crystallised from eclogitic and peridotitic rocks while moving in a dynamic environment from the asthenosphere and possibly the lower mantle to the base of the lithosphere. Mechanisms for diamond movement through the mantle could be by mantle convection, or an ascending plume. The interaction of partial melts with eclogitic and peridotitic lithologies may have produced the intermediate websteritic inclusion compositions, and can explain diamonds of mixed parageneses, and the overlap in C-isotope values between parageneses. Strong deformation and extremely high nitrogen aggregation states in some diamonds may indicate high mantle storage temperatures and strain in the diamond growth environment. A second diamond group, with Type IaA–IaB nitrogen aggregation and peridotitic inclusions, crystallised at the base of the cratonic lithosphere. All diamonds were subsequently sampled by kimberlites and transported to the Earth's surface.  相似文献   


19.
Fluids and melts have been trapped and analysed in high pressure experiments in the model mantle system MgO-SiO2-H2O at 6 to 10.5 GPa and 900 to 1,200 °C. The fluid/melt traps consisted of a diamond layer that was added to the experimental charge and was separate from the silicate phases. The recovered diamond traps were analysed by laser ablation - ICP - MS. Starting materials were synthetic mixtures of brucite, talc and silica with variable Mg/Si containing 11-31 wt% H2O. Experiments on a serpentine starting composition [Mg3Si2O5(OH)4] result in MgO/SiO2 weight ratios in the subsolidus fluids close to 1 at 6 GPa and close to 2 at 9 GPa. Melt compositions at 6 and 9 GPa have MgO/SiO2 ratios close to that of forsterite. At a single pressure the amount of dissolved silicate in the fluid increases steadily with increasing temperature up to 1,150 °C, where a sudden increase of both SiO2 and MgO is observed. This discrete step marks the solidus, which is more clearly developed at 6 than at 9 GPa. Thus, hydrous melts within the model mantle subsystem Mg2SiO4-Mg2Si2O6-H2O are chemically distinct from aqueous fluids up to at least 9 GPa, corresponding to 300 km depth. Extrapolation of the current data set implies that total convergence between fluid and melt along the solidus probably occurs at 12-13 GPa (~400 km), i.e. close to the Earth's mantle transition zone. Beneath cratons, interactions of hydrous fluids with upper mantle lithologies cause relative silica depletion (olivine enrichment) at depths greater than 200 km and silica (orthopyroxene) enrichment at shallower depths.  相似文献   

20.
The system peridotite-H2O-CO2 serves as a simplified model forthe phase relations of mantle peridotite involving more thanone volatile component. Run products obtained in a study ofphase relations of four mantle peridotites in the presence ofH2O- and (H2O+CO2)-bearing vapors and with controlled hydrogenfugacity (fH2) at high pressures and temperatures have beensubjected to a detailed chemical investigation, principallyby the electron microprobe. Mg/(Mg+Fe) of all phases generally increases with increasingtemperature and with increasing Mg/(Mg+Fe) of the starting material.This ratio appears to decrease with increasing pressure forolivine, and for amphibole coexisting with garnet. DecreasingfH2from that of IW buffer to that of MH buffer decreases Mg/(Mg+Fe)of the partial melt from approximately 0?85 to approximately0?50, whereas the Fo content of coexisting olivine increasesslightly less than 3 per cent and the Mg/(Mg+Fe) of clinopyroxeneincreases about 4 per cent. However, the variations in Fo contentof olivines are within those observed in olivines from naturalmantle peridotite. The chemistry of other silicate mineralsdoes not significantly reflect variations of fH2. Consequently,the peridotite mineralogy and/or chemistry is not a good indicatorfor the fH2 conditions during crystallization. All crystalline phases, except amphibole, and to some extentgarnet, show increasing Cr content with increasing temperatureand increasing Cr content of the starting material, resultingin a positive correlation with Mg/(Mg+Fe). Partial melts aredepleted in Cr2O3 relative to the crystalline phases. High Mg/(Mg+Fe)and Cr2O3 are thus expected in crystal residues after partialmelting. The absolute values depend on degree of melting andthe composition of the parent peridotite.  相似文献   

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