Geobarometry for Peridotites: Experiments in Simple and Natural Systems from 6 to 10 GPa   总被引：3，自引：0，他引：3  

Brey  Gerhard P.; Bulatov  Vadim K.; Girnis  Andrei V. 《Journal of Petrology》2008,49(1):3-24

Experiments with peridotite minerals in simple (MgO–Al₂O₃–SiO₂,CaO–MgO–SiO₂ and CaO–MgO–Al₂O₃–SiO₂)and natural systems were conducted at 1300–1500°Cand 6–10 GPa using a multi-anvil apparatus. The experimentsin simple systems demonstrated consistency with previous lowerpressure experiments in belt and piston–cylinder set-ups.The analysis of spatial variations in pyroxene compositionswithin experimental samples was used to demonstrate that pressureand temperature variations within the samples were less than0·4 GPa and 50°C. Olivine capsules were used in natural-systemexperiments with two mineral mixtures: SC1 (olivine + high-Alorthopyroxene + high-Al clinopyroxene + spinel) and J4 (olivine+ low-Al orthopyroxene + low-Al clinopyroxene + garnet). Theexperiments produced olivine + orthopyroxene + garnet ±clinopyroxene assemblages, occasionally with magnesite and carbonate-richmelt. Equilibrium compositions were derived by the analysisof grain rims and evaluation of mineral zoning. They were comparedwith our previous experiments with the same starting mixturesat 2·8–6·0 GPa and the results from simplesystems. The compositions of minerals from experiments withnatural mixtures show smooth pressure and temperature dependencesup to a pressure of 8 GPa. The experiments at 9 and 10 GPa producedandradite-rich garnets and pyroxene compositions deviating fromthe trends defined by the lower pressure experiments (e.g. higherAl in orthopyroxene and Ca in clinopyroxene). This discrepancyis attributed to a higher degree of oxidation in the high-pressureexperiments and an orthopyroxene–high-P clinopyroxenephase transition at 9 GPa. Based on new and previous resultsin simple and natural systems, a new version of the Al-in-orthopyroxenebarometer is presented. The new barometer adequately reproducesexperimental pressures up to 8 GPa. KEY WORDS: garnet; mineral equilibrium; multi-anvil apparatus; orthopyroxene; geobarometry  相似文献   

In situ LA-ICPMS Isotopic and Geochronological Studies on Carbonatites and Phoscorites from the Guli Massif,Maymecha-Kotuy,Polar Siberia     

Mahdi Ghobadi  Axel Gerdes  Lia Kogarko  Heidi Hoefer  Gerhard Brey 《Geochemistry International》2018,56(8):766-783

In this study we present a fresh isotopic data, as well as U–Pb ages from different REE-minerals in carbonatites and phoscorites of Guli massif using in situ LA-ICPMS technique. The analyses were conducted on apatites and perovskites from calcio-carbonatite and phoscorite units, as well as on pyrochlores and baddeleyites from the carbonatites. The ⁸⁷Sr/⁸⁶Sr ratios obtained from apatites and perovskites from the phoscorites are 0.70308–0.70314 and 0.70306–0.70313, respectively; and 0.70310–0.70325 and 0.70314–0.70327, for the pyrochlores and apatites from the carbonatites, respectively.Furthermore, the in situ laser ablation analyses of apatites and perovskites from the phoscorite yield εNd from 3.6 (±1) to 5.1 (±0.5) and from 3.8 (±0.5) to 4.9 (±0.5), respectively; εNd of apatites, perovskites and pyrochlores from carbonatite ranges from 3.2 (±0.7) to 4.9 (±0.9), 3.9 (±0.6) to 4.5 (±0.8) and 3.2 (±0.4) to 4.4 (±0.8), respectively. Laser ablation analyses of baddeleyites yielded an eHf(t)d of +8.5 (± 0.18); prior to this study Hf isotopic characteristic of Guli massif was not known. Our new in situ εNd, ⁸⁷Sr/⁸⁶Sr and eHf data on minerals in the Guli carbonatites imply a depleted source with a long time integrated high Lu/Hf, Sm/Nd, Sr/Rb ratios.In situ U–Pb age determination was performed on perovskites from the carbonatites and phoscorites and also on pyrochlores and baddeleyites from carbonatites. The co-existing pyrochlores, perovskites and baddeleyites in carbonatites yielded ages of 252.3 ± 1.9, 252.5 ± 1.5 and 250.8 ± 1.4 Ma, respectively. The perovskites from the phoscorites yielded an age of 253.8 ± 1.9 Ma. The obtained age for Guli carbonatites and phoscorites lies within the range of ages previously reported for the Siberian Flood Basalts and suggest essentially synchronous emplacement with the Permian-Triassic boundary.  相似文献   

Orthopyroxene-clinopyroxene equilibria in the system CaO-MgO-Al2O3-SiO2 (CMAS): new experimental results and implications for two-pyroxene thermometry     

K. G. Nickel  G. P. Brey  L. Kogarko 《Contributions to Mineralogy and Petrology》1985,91(1):44-53

A new set of reversal experiments for coexisting ortho- and clinopyroxenes in the system CMAS at conditions between 1,000–1,570° C and 30 to 50 kb is presented and combined with literature data. Pyroxene behaviour, particularly that of clinopyroxene, is very complicated and different styles of Al incorporation into the pyroxene structure for low and high concentrations of Al are indicated, strongly influencing the exchange of the enstatite component between ortho- and clinopyroxene. Thermodynamic modelling of this exchange is problematic because of the large number of unknown coefficients compared to the number of experiments. Thermometry based on such models becomes very dependent on accuracy of experimental data and analyses of small quantities of elements. Despite this complexity very simple empirical thermometric equations are capable of reproducing experimental conditions in the systems CMS and CMAS over a wide range of P, T conditions. We derived the equation which gives a mean error of estimate of 25° C when applied to CMS and CMAS data.Abbreviations Used in the Text cpx clinopyroxene - di diopside, CaMgSi₂O₆ - en enstatite, Mg₂Si₂O₆ - opx orthopyroxene - px Pyroxene - py pyrope - a _i ^j activity of component i in phase j - activity coefficient - G _P,T (A) molar Gibbs free energy difference of reaction (A) at P, T - X _i ^j mole fraction of component i in phase j  相似文献   

The determination of the oxidation state of iron in synthetic garnets by X-ray spectroscopy with the electron microprobe     

H. E. Höfer  G. P. Brey  R. Oberhänsli 《Physics and Chemistry of Minerals》1996,23(4-5):241-241

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Partitioning of trace elements between carbonate-silicate melts and mantle minerals: Experiment and petrological consequences     

A. V. Girnis  V. K. Bulatov  Y. Lahaye  G. P. Brey 《Petrology》2006,14(5):492-514

The partitioning of a number of trace elements (Ba, Nb, Zr, Y, REE, etc.) between orthopyroxene, garnet, and carbonate-silicate melt was experimentally studied using a belt apparatus at pressures of 3.5–4.2 GPa and temperatures of 1300–1500°C. The experimental products were investigated by electron microprobe analysis and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The experimental melts varied from carbonatitic (～5 wt % SiO₂) at low temperatures (1300–1350°C) to kimberlitic compositions (30 wt % SiO₂) at high temperatures (1500°C). The partition coefficients of most elements between orthopyroxene and melt (D _i ^Opx/L ) and garnet and melt (D _i ^Grt/L ) were almost independent of melt composition (temperature). The D _i ^Opx/L values ranged from <0.01 for the most incompatible Ba and light REE to 0.02–0.08 for moderately incompatible Zr, Y, and heavy REE. The D _i ^Grt/L values were approximately an order of magnitude higher, ～0.07 for light REE, 0.7 for Y, and 1.5 for Yb. The character of D _i ^Grt/L variations in the systems studied is in general similar to that established for silicate melts without volatile components. However, the differences in the behavior of moderately incompatible and compatible elements (e.g., light and heavy REE) in the experimental systems are less pronounced compared with CO₂-free systems. Considering carbonate-silicate and silicate melts as possible agents of mantle metasomatism, it can be concluded that the former can efficiently transport heavy REE, and the latter have a greater affinity for Nb, Ba, and light REE. A characteristic feature of mantle rocks enriched by carbonate-silicate melts is high Ba/La ratio coupled with relatively weakly fractionated REE distribution patterns. It was shown that the high degrees of enrichment observed in natural kimberlites can be explained by a two-stage scenario, including a preliminary invasion of carbonate-silicate melt into depleted harzburgites in the lower parts of the lithosphere and subsequent very low degree melting.  相似文献   

Plume-related mantle source of super-large rare metal deposits from the Lovozero and Khibina massifs on the Kola Peninsula, Eastern part of Baltic Shield: Sr, Nd and Hf isotope systematics     

L. N. Kogarko  Y. Lahaye  G. P. Brey 《Mineralogy and Petrology》2010,98(1-4):197-208

The two world’s largest complexes of highly alkaline nepheline syenites and related rare metal loparite and eudialyte deposits, the Khibina and Lovozero massifs, occur in the central part of the Kola Peninsula. We measured for the first time in situ the trace element concentrations and the Sr, Nd and Hf isotope ratios by LA-ICP-MS (laser ablation inductively coupled plasma mass spectrometer) in loparite, eudialyte an in some other pegmatitic minerals. The results are in aggreement with the whole rock Sr and Nd isotope which suggests the formation of these superlarge rare metal deposits in a magmatic closed system. The initial Hf, Sr, Nd isotope ratios are similar to the isotopic signatures of OIB indicating depleted mantle as a source. This leads to the suggestion that the origin of these gigantic alkaline intrusions is connected to a deep seated mantle source—possibly to a lower mantle plume. The required combination of a depleted mantle and high rare metal enrichment in the source can be explained by the input of incompatible elements by metasomatising melts/fluids into the zones of alkaline magma generation shortly before the partial melting event (to avoid ingrowth of radiogenic isotopes). The minerals belovite and pyrochlore from the pegmatites are abnormally high in ⁸⁷Sr /⁸⁶Sr ratios. This may be explained by closed system isotope evolution as a result of a significant increase in Rb/Sr during the evolution of the peralkaline magma.  相似文献   

CO2 solubility and solubility mechanisms in silicate melts at high pressures     

G. Brey 《Contributions to Mineralogy and Petrology》1976,57(2):215-221

CO₂ solubility has a slight negative temperature dependence in olivine melilitite at 30 kb with 9% CO₂ dissolved at 1,450 °C, 8.5% at 1,550 °C and 8.3% at 1,650° C. CO₂ is dissolved as the carbonate molecule (CO ₃ ^2– ) only. Feldspar melts (albite-anorthite) dissolve much less CO₂ at 30 kb (around 2%) with a slight increase with increasing anorthite content. A CO₂ absorption peak in infrared spectra of albite-rich glasses diappears in favour of the CO ₃ ^2– peak with increasing anorthite content. It is inferred that CO₂ was present as CO ₃ ^2– in albite-rich melts also, but reverts to CO₂ during quenching because of bonding differences related to Ca²⁺ and Na⁺ in the melts.  相似文献   

The role of CO2 in the genesis of olivine melilitite     

Gerhard Brey  David H. Green 《Contributions to Mineralogy and Petrology》1975,49(2):93-103

The nature of the near-liquidus phases for a mantle-derived olivine melilitite composition have been determined at high pressure under dry conditions and with various water contents. Olivine and clinopyroxene occur on or near the liquidus and there are no conditions where orthopyroxene crystallizes in equilibrium with the olivine melilitite. We have determined the effect on the liquidus temperature and liquidus phases of substituting CO₂ for H₂O on a mole for mole basis at 30 kb, using olivine melilitite + 20 wt% H₂O at = 0 and = (CO₂)/(H₂+CO₂) (mole fraction) = 0.25, 0.5, 0.75 and 1.0 (i.e. olivine melilitite + 38 wt% CO₂). Experiments were buffered by the MH or NNO buffers. At 30 kb, CO₂ is only slightly less soluble than water for <0.5 as judged by the slight increase in liquidus temperature on mole-for-mole substitution of CO₂ for H₂O and at 30 kb, 1200° C, = = 0.5 the olivine melilitite contains 8.8 wt% H₂O and 21 wt% CO₂ in solution. For 1 the CO₂ saturated liquidus is depressed 70 ° C below the anhydrous liquidus and the magma dissolves approx. 17% CO₂ at 30kb, 1400 ° C, 1, 0. Infrared spectra of quenched glasses have absorption bands characteristic of CO ₃ ⁼ and OH- molecules and no evidence for HCO ₃ ^- . The effect of CO ₃ ⁼ molecules dissolved in the olivine melilitite at high pressure is to suppress the near-liquidus crystallization of olivine and clinopyroxene and bring orthopyroxene and garnet on to the liquidus. We infer that olivine melilitite magmas may be derived by equilibrium partial melting (<5%) of pyrolite at 30 kb, 1150–1200 ° C, provided that both H₂O and CO₂ are present in the source region in minor amounts. Preferred conditions are 0< <0.5, 0.5< <1, and at low oxygen fugacities (相似文献   

Rare and unusual mineral inclusions in diamonds from Mwadui, Tanzania   总被引：9，自引：3，他引：6  

Thomas Stachel  Jeff W. Harris  Gerhard P. Brey 《Contributions to Mineralogy and Petrology》1998,132(1):34-47

Syngenetic diamond inclusions from the Mwadui kimberlite reveal that an unusually fertile section of lithospheric mantle beneath the Central African Craton was sampled. This is shown by a very high ratio of lherzolitic to harzburgitic garnet inclusions (1:2) and low Mg/Fe-ratios in olivine and orthopyroxene. Geothermometry applied to the peridotitic inclusions indicates disequilibrium between non-touching inclusion pairs to be common. Disequilibrium between garnet-olivine and garnet-orthopyroxene pairs suggests successive iron enrichment during diamond formation, e.g. leading to the presence of harzburgitic garnet and lherzolitic olivine in the same diamond. Apart from the dominant peridotitic inclusion suite (88%), rare eclogitic inclusions occur (2%) and a number of uncertain paragenesis. Two diamonds, one with eclogitic garnets with moderate pyroxene solid solution and the other with a single ferro-periclase inclusion, suggest the contribution of a small sub-lithospheric component. The finding of the association Fe-FeO-Fe₃O₄ in one single diamond indicates diamond formation over a large range of f _O2 conditions, possibly along redox fronts. Steep compositional gradients may also be reflected by the joint occurrence of harzburgitic garnet and a SiO₂-phase in the same diamond. Alternatively the formation of the SiO₂-phase may be due to extreme carbonation of the peridotitic source. Further unusual findings include the exsolution of a silicate phase from magnetite inclusions, (i.e. primary solution of γ-olivine) and an ilmenite inclusion with an eskolaite (Cr₂O₃) component of 14.5 mol%, the latter together with harzburgitic paragenesis silicate inclusions. Received: 23 August 1997 / Accepted: 7 January 1998  相似文献   

Ferropericlase—a lower mantle phase in the upper mantle     

Gerhard P. Brey  Vadim Bulatov  Andrei Girnis  Jeff W. Harris  Thomas Stachel   《Lithos》2004,77(1-4):655-663

Experiments on compositions along the join MgO–NaA³⁺Si₂O₆ (A=Al, Cr, Fe³⁺) show that sodium can be incorporated into ferropericlase at upper mantle pressures in amounts commonly found in natural diamond inclusions. These results, combined with the observed mineral parageneses of several diamond inclusion suites, establish firmly that ferropericlase exists in the upper mantle in regions with low silica activity. Such regions may be carbonated dunite or stalled and degassed carbonatitic melts. Ferropericlase as an inclusion in diamond on its own is not indicative of a lower mantle origin or of a deep mantle plume. Coexisting phases have to be taken into consideration to decide on the depth of origin. The composition of olivine will indicate an origin from the upper mantle or border of the transition zone to the lower mantle and whether it coexisted with ferropericlase in the upper mantle or as ringwoodite. The narrow and flat three phase loop at the border transition zone—lower mantle together with hybrid peridotite plus eclogite/sediments provides an explanation for the varying and Fe-rich nature of the diamond inclusion suite from Sao Luiz, Brazil.  相似文献