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1.
Abstract A Hercynian charnockite occurs within high-grade gneisses in the Agly Massif, French Pyrenees. Its thermal history has been evaluated using the Fe-Mg distribution coefticient ( K D) between garnet and biotite. These minerals have different origins but similar compositions in the charnockites and host gneisses. In the charnockite, the Bi–Ga pairs are the retrograde products of Opx alteration. This Opx reaction with feldspar can be written. Opx + PI + Fluid 1(H2O + Al + K + Fe + Ti) = Bi + Ga + Q + Fluid 2(H2O + Na). The garnets are relatively Ca poor (4–2.5% grossular); they are automorphic and zoned in the gneisses and poikiloblastic in the charnockites. Both types show a retrograde rim (of few hundred microns'width) across which Fe and Mn increase as Mg decreases. The biotites show a good correlation between the octahedral cations (Ti4++ Fe2+) and (Mg2++ Al3+VI); Ti and Fe both increase, whereas Mg and AlVI decrease. There is an inverse linear correlation between Fe2+ and Mg2+ and the Fe/Mg ratio increases as Ti increases. The relation between Ti and K Ga-BiDFe-Mg is less clear: it seems that K D slightly decreases as Ti increases. The equilibration temperatures of Ga–Bi pairs are discussed: the charnockite Ga-Bi pairs have equilibrated between 550°C and 600°C; whereas those of the gneisses have equilibrated between 550°C and 650°C. Two main thermal steps appear: one in the gneisses between 600-650°C and a second one in both the gneisses and the charnockites between 550°C and 600°C.  相似文献   

2.
The proposed geothermobarometer is based on an empirical calibration which takes account of two equilibria involving the tremolite, edenite, pargasite and hastingsite components in amphiboles. It has applications to assemblages found in metabasic rocks of widely different chemical compositions (magnesian to Fe-rich metabasalts), and for metamorphism ranging from lower greenschist to highest amphibolite facies. Knowing the Si(T1), Aliv, Alvi, Fe3+, Fe2+, Mg, Ca, NaM4, NaA and A vacancy in an amphibole, and the Al3+ and X Mg in coexisting epidote and chlorite, it is possible to calculate two values of In K d for this assemblage. These equilibria involve edenite-tremolite and (pargasite/hastingsite)-tremolite end-members in amphibole (the calculation program is given). For these equilibria, the isopleths (iso-values of K d) have been calculated for 0.27 < X Mg < 0.75 and 0 < X Fe3+= Fe3+/(Fe3++ Alvi) < 0.8. It is then possible to determine pressure and temperature directly when X Mg, X Fe3+, In K d for tremoliteedenite and In K d for (pargasite/hastingsite)-tremolite are known. Application of this geothermobarometer is limited to Ca-free plagioclase assemblages, and complete P–T paths can be drawn only if all the minerals are considered together. Phase relations at successive stages of crystallization can be constrained by studying the relationships between the coexisting minerals, their zoning and the metamorphic fabrics.  相似文献   

3.
ABSTRACT
The mineralogy and isotope geochemistry of carbonate minerals in the Coorong area are determined by the water chemistry of different depositional environments ranging from seawater to evaporitically modified continental water. The different isotopic compositions of coexisting calcite and dolomite suggest that each of the above two minerals was formed from water of composition and origin unique to that specific mineral. In addition, the dolomite was not formed by simple solid state cation exchange.
The occurrence of two types of dolomite was shown by isotope analysis and SEM observations. The dolomite, which is isotopically light (δ13C = -1 to -2% 0 ; δ18O=+3 to +5%0) and of fine grain size (˜ 0·5 μm) probably precipitated under the influence of evaporitically modified continental water. Coarser grained dolomite (up to 4 μm) is isotopically heavier (δ13C=+3 to +4%0; δ18O=+5 to + 6%0) contains Mg in excess of Ca and was formed in or close to equilibrium with atmospheric CO2 probably by the dolomitization of aragonite.  相似文献   

4.
Diffusion modelling is applied to layered garnet–pyroxene–quartz coronas, formed by a pressure-induced reaction between plagioclase and primary pyroxene in a metabasic granulite. The reconstructed reaction involves some change in composition of reactant minerals. The distribution of minerals between layers is satisfactorily explained by diffusion-controlled reaction with local equilibrium, in which the diffusion coefficient for Al was smaller than those for Fe, Mg and Ca by a factor of approximately four. Diffusion of Mg towards plagioclase implies a chemical-potential gradient for MgO component in a direction opposite to the changing Mg content of garnet; this is explained by the influence of Al2O3 on the chemical potential of the pyrope end-member. Grain-boundary diffusion is suggested to have operated, possibly with composition gradients different from those in the bulk minerals. Chemical-potential differences across the corona are estimated from the variation in garnet composition, enabling affinity (the free energy change driving the reaction) to be estimated as 6.9±1.8  kJ per 24-oxygen mole of garnet produced. This implies that the pressure for equilibrium among the minerals was overstepped by 1.4±0.4  kbar. The probable P–T conditions of reaction were in the range 650–790  °C, 8–10  kbar. Assuming a timescale of reaction between 106 and 108 years, estimated diffusion coefficients for Fe, Mg and Ca are in the range 9×10−23 to 5×10−20 m2 s−1. These are consistent with experimental values in the literature for solid-state diffusion, including grain-boundary diffusion.  相似文献   

5.
A method for the selective separation of Ag, Cd, Cr, Cu, Ni, Pb and Zn in traces from solutions of calcite (CaCO3), dolomite (CaMg(CO3)2) and gypsum (CaSO4.2H2O) before their determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES) is presented. The expected interferences of Ca and Mg on intensities of trace analytes were removed by collecting the elements of interest with cobalt(III) hexamethylenedithiocar-bamate, Co(HMDTC)3. The flotation of aqueous solutions (1 l) of calcite, dolomite and gypsum was performed at pH 6.0, by 1.5 mg l−1 Co and 0.6 mmol l−1 HMDTC−. To minimise the effect of the reaction between Ca/Mg, which restrains the function of the surfactant, careful selection of the most suitable foaming reagent was necessary. The accuracy of the method was established by analysing natural alkaline-earth minerals by the standard addition method as well as using the dolomite reference materials GBW 07114 and GSJ JDo-1. The ICP-AES limits of detection following flotation on different minerals were found to be 0.080 μg g−1 for Cd, 0.105 μg g−1 for Ag, 0.142 μg g−1 for Cu, 0.195 μg g−1 for Cr, 0.212 μg g−1 for Ni, 0.235 μg g−1 for Zn and 0.450 μg g−1 for Pb.  相似文献   

6.
Abstract Compositions of actinolite, hornblende and cummingtonite, together with pyroxene and plagioclase, are studied in basic intrusions in the Dalradian of north-east Scotland, and the Glen Scaddle complex in the West Moine. Amphibolitization is due to influx of water from the country rocks. Pyroxene compositions are found to have adjusted to the regional metamorphic environment. Owing to the difficulty of diffusion of Al and Si, calcic amphiboles are zoned and commonly contain quartz blebs. Discontinuities in zoning give rise to actinolite-hornblende pairs. Compared with north-east Scotland, disequilibrium is less strong in the Glen Scaddle area: in the latter, plagioclase compositions have been greatly changed, Na partition between hornblende and plagioclase is close to equilibrium, the maximum Al content of hornblende is lower and zoning patterns are more consistent. The Fe/Mg ratio in calcic amphiboles varies with Al content, while approaching equilibrium partition with other minerals. Both zoning patterns and Fe/Mg partition with cummingtonite suggest that Fe/Mg of the calcic amphiboles increases more strongly with increasing (Alvi+Fe3+) than can be explained simply by substitution of Al,Fe3+ for Mg on M2. Model reactions for amphibole formation are constructed. Cummingtonite formed at lower chemical potential of CaO than actinolite: Ca was exchanged for Mg,Fe between orthopyroxene-derived and clinopyroxene-derived local systems. Both cummingtonite and actinolite were formed because of kinetic constraints, as intermediate reaction products: actinolite-hornblende pairs represent disequilibrium. This work suggests that many occurrences of actinolite with hornblende, where the minerals are zoned, may also be due to diffusion kinetics.  相似文献   

7.
Cordierite samples from pegmatites and metamorphic rocks have been analysed for major [electron microprobe analysis (EMPA)] and trace elements [inductively coupled plasma mass spectrometry (ICP-MS), secondary ion mass spectrometry analyses (SIMS)] as well as for H2O and CO2 (coulometric titration), and the results evaluated in conjunction with published data in order to determine which exchange mechanisms are significant. Apart from the homovalent substitutions FeMg−1 and MnMg−1 on the octahedral site, some minor KNa−1 on the Ch0 channel site, and Fe3+Al−1 on the T11 tetrahedral site, the three most important substitution mechanisms are those for the incorporation of Li on the octahedral sites (NaLi□−1Mg−1), and of Be and other divalent cations on the tetrahedral T11 site (NaBe□−1Al−1 and Na(Mg,Fe2+)□−1Al−1). The dominant role of the last vector is clearly demonstrated. We propose a new generalized formula for cordierite: Ch(Na,K)0–1 VI(Mg,Fe2+,Mn,Li)2 IVSi5 IVAl3 IV(Al, Be, Mg, Fe2+, Fe3+)O18 *xCh(H2O, CO2…). Our results show that the population of (Mg, Fe2+) on the T11-site is limited to about 0.08 a.p.f.u. Other exchange mechanisms that were encountered in experiments operate only under P–T conditions or in bulk compositions that are rarely realized in nature. Routine analyses by electron microprobe in which Li and Be are not determined can be plotted as (Mg+Fe+Mn) versus (Si+Al) to assess whether significant amounts of Li and Be could be present. These amounts can be calculated as Li (a.p.f.u.)=Al+Na–4 and Be (a.p.f.u.)=10–2Al–M2+–Na.  相似文献   

8.
Abstract The hornblende-bearing basic gneisses in the Uvete area, central Kenya, were metamorphosed under a narrow range of P and T (6.5 ± 0.5kbar and 530 ± 40°C) of the staurolitekyanite zone in the Mozambique metamorphic belt. They show a wide variety of divariant and trivariant mineral assemblages consisting of hornblende, cumminatonite, gedrite, anthophyllite, chlorite, garnet, epidote, clinopyroxene, plagio-clase and quartz. The bulk and mineral chemistries and the graphical representation of phase relations show that each mineral assemblage approaches chemical equilibrium and defines a unique composition volume in the A'(Al + Fe3+− (13/7)Na)-F(Fe2+)-M'(Mg)-C'(Ca-(3/7)Na) tetrahedron. The composition volumes are distributed quite regularly and do not overlap each other.
The phase relations in the Uvete area are in contrast with those in the staurolite-kyanite zone amphibolites in the Mt. Cube quadrangle, Vermont. The amphibolites there contain low-variance mineral assemblages formed under different values of μH2O and μCO2. These assemblages define overlapping composition volumes in the A'-F'-M'-C'tetrahedron.
The mineral assemblages in the Uvete area are interpreted as having formed in equilibrium with fluid at a high and nearly constant μH2O value. Such a fluid composition was externally controlled by the supply of H2O-rich fluid expelled from the surrounding pelitic and psammitic rocks. The body size of the basic gneisses in the Uvete area (less than 400m in thickness) was small enough for the fluid to migrate completely.  相似文献   

9.
Abstract: Systematic measurements of magnetic susceptibility were carried out at the outcrops of the Uchiyama granitic pluton, Tsushima Islands. The pluton consists of hornblende-biotite granodiorite and biotite granite. It intrudes concordantly along an anticline axis of the Taishu Group in middle Miocene (16. 10. 5 Ma), and crops out in five areas. The results show that the low magnetic susceptibility facies (LM–facies, <100A-10-6 emu/g) always occurs in the peripheral part of the pluton, while the high magnetic susceptibility facies (HM–facies, > 250 A 10-6 emu/g) occupies the core through the medium magnetic susceptibility zone (MM–facies). It is pointed out that the pluton forms a magnetic zoning within a single plutonic body.
Chemical compositions of the granitoids show no conspicuous differences in major elements among the LM–, MM–, and HM–facies. Biotites from the LM–, MM–, and HM-facies also indicate uniform compositions with Fe/(Fe+Mg)=0. 6.
The pluton is principally surrounded by black mudstones of the Lower Formation of the Taishu Group, which is deltaic to shallow sea sediments of the Eocene to early Miocene age, and the carbon contents in them were analyzed. The analyses show that carbon was mostly decomposed and lost in the hornfels zone, while mudstones in the non-hornfels zone usually contain 0. 5 to 0. 7 % C.
From these facts, it is concluded that the magnetically zoned pluton at Tsushima was formed by an external volatile buffer system such as CH4–CO2 during the solidifying magma process.  相似文献   

10.
束今赋 《地学前缘》2020,27(3):133-153
上天、入地、下海,进行极端条件下的矿物学研究,研究微矿物,发现新矿物。主要利用金刚石压机,结合使用国内外同步辐射X-光源、中子源,以及其他多种物理的、化学的、光学的测试手段(如岩石矿物化学分析,光薄片测定,电子探针,离子探针,扫描电镜,透射电镜,红外、紫外、拉曼光谱,激光加热等),对来自天外的陨石、陨石坑样品、地球深处地幔源矿物以及海底甲烷水合物进行了一些研究。模拟不同温度和压力下各种不同成分的矿物材料的晶体结构、物理和化学性质。文章着重研究从地球内核到地壳海底的各种不同组分在不同温度、压力极端环境下形成的各种各样的典型矿物:从金属固体内核和金属液体外核中的ε-Fe到核幔边界(CMB)地球D″层的后钙钛矿(Post-Perovskite)结构(ppv)镁铁硅酸盐(Mg,Fe)SiO3,从下地幔中的铁磁性钙钛矿(Perovskite)结构(pv)镁铁硅酸盐布里奇曼石(Bridgmanite)(Mg,Fe)SiO3、镁铁氧化物(Fe,Mg)O和后尖晶石(Post-Spinel)结构的含Fe3+毛河光矿(Maohokite)(HP-Mg$Fe^{3+}_{2}O_{4}$)到过渡带、上地幔和地壳中的镁铁硅酸盐、硅氧化物、铬铁氧化物和金刚石及其内含物以及甲烷水合物(CH4·H2O)等。进行高温高压极端条件下的矿物学研究,为探索地球结构性质、形成动力和发展历史提供了新的窗口。  相似文献   

11.
A series of granitoids from Proterozoic to Cenozoic age occurred in the western Kunlun orogenic belt, Xinjiang, northwestern China. Several intrusions such as the West Datong (Middle Caledonian age), North Kuda (Late Caledonian age) and Kuzigan, Karibasheng, Zankan (Himalayan age) plutons have shoshonitic affinity. Their rock assemblages include (quartz) monzodiorite–(quartz) monzonite–quartz syenite (Middle Caledonian) or monzonitic granite–granite (Late Caledonian) or biotite (monzonitic) granite–diopside granite–diopside syenite (Himalayan). Generally, biotite is iron–phlogopite, with some eastonite and high Mg/(Mg+FeT) and Fe3+/Fe2+ ratio. Amphibole is mainly edenitic hornblende and magnesian hastingsitic hornblende, with some edenite and higher Mg/(Mg+FeT) and Fe3+/Fe2+ ratio. The rocks show SiO2 contents of 52.77–71.85% and high K2O+Na2O (mostly >8%, average 9.14%), K2O/Na2O (mostly >1, average 1.50) and Fe2O3/FeO (0.85–1.51, average 1.01) and low TiO2 contents (0.15–1.12%, average 0.57%). Al2O3 contents (13.01–19.20%) are high but variable. The granitoids are prominently enriched in LILE, LREE and volatiles such as F. However, the studied shoshonitic granitoids among the three intrusive periods also show differences in isotopic compositions and trace element concentrations, suggesting their different geneses: the origin of the West Datong pluton is probably related to the involvement of subducted oceanic crust sediments into the mantle source; the North Kuda and Himalayan plutons could have been generated by partial melting of subducted oceanic crust sediments or metasediments of thickened continental lower crust in the process of late-orogenic slab break-off or lithospheric thinning.  相似文献   

12.
We present boron isotope and concentration data from magmatic (komatiitic to rhyolitic) and sedimentary geological silicate and artificial glass reference materials that cover a wide spectrum of boron isotope compositions and boron concentrations. Boron isotope compositions were determined by TIMS (Cs2BO2+ -graphite and BO2- method) and boron concentrations by ICP-AES. Boron concentrations ranged from 7 to 159μ g-1 and agree within 14% with published values. Based on replicate analyses of individually prepared sample aliquots an overall external reproducibility of better than 10% was determined. The obtained δ11B values ranged from -12.6 to +13.6% and were reproducible within 1.1 % (2 RSD; excluding NTIMS) on the basis of individually prepared sample aliquots. The δ11B values of JA-1 (+5.3%), JB-3 (+5.9%) and JR-2 (+2.9%) overlap the published data within analytical uncertainty. For the first time δ11B values for the TB (-12.6%) and the MPI-DING glasses GOR-128-G (+13.6%), GOR-132-G (+7.1 %) and StHs6/80-G (-4.5%) are reported. The δ11B values obtained by the Cs2BO2+ -graphite and the BO2- method as well as the majority of δ11B values obtained using different sample preparation methods agree within analytical uncertainty. Therefore, we conclude that none of these analytical methods introduce any systematic error on the obtained δ11B values.  相似文献   

13.
Abstract Microprobe analysis of the continuous chemical evolution of coexisting biotite-garnet and biotite-garnet-staurolite has been undertaken from interbedded micaschists of the volcanodetrital group of the Vilaine. A thermobarometric study using pertinent mineralogical equilibria reveals a complex P-T evolution, continuous throughout time, from high pressure, medium temperature (kyanite zone) to medium pressure, high temperature (sillimanite zone), then low pressure, medium temperature (andalusite zone). The T, P, fH2o and XH2o variations have been calculated from coexisting biotite-garnet pairs, and from the equilibria: paragonite (in white mica) + quartz ± albite (in plagioclase) + Al silicate + H2O; and, 3 anorthite ± grossular + 2 Alsilicate + quartz. The P-T evolution is correlated with the continuous change in composition of minerals (using P–XMg and T–XMg diagrams) and with the evolution of assemblages. This continuous P-T-time evolution, correlated with the successive formation of S1-S2 foliations, allows us to propose a P-T-time-deformation path for the micaschists and to relate the growth of its mineral components to tectonic processes.  相似文献   

14.
Abstract Spinel-quartz-cordierite and spinel-quartz are found as relic prograde assemblages in Fe-rich granulites from the Araku area, Eastern Ghats belt, India. Subsequent reactions produced orthopyroxene + sillimanite in the former association and garnet + sillimanite in the latter. The first reaction is univariant in the FMAS system, but is trivariant in the present case because of the presence of Zn and Fe3+ in spinel. The second reaction also has high variance because of Zn and Fe3+, but also because of the presence of Ca in garnet. Thermobarometry shows that the metamorphic conditions were approximately 950° C and 8.5 kbar and the fo 2 was near the NNO buffer. In Fe-rich bulk compositions and low- P -high- T conditions of metamorphism, two of the univariant reactions around the invariant point [Sa], namely (Sa, Hy) and (Sa, Cd), change topology due to reverse partitioning of Fe-Mg between coexisting garnet and spinel. An alternative partial petrogenetic grid in the system FMAS is constructed for such conditions and is applied satisfactorily to several sapphirine-free spinel granulites. It is shown that bulk composition ( X Fe and Zn) exerts greater control on the stability of spinel + quartz than fo 2. The effect of the presence of Zn and Fe3+ in spinel on the proposed grid is evaluated. Reaction textures in the Araku spinel granulites can be explained from the petrogenetic grid as due to near-isobaric cooling.  相似文献   

15.
Oxygen isotope geothermometers for metamorphic rocks   总被引：10，自引：1，他引：10  
The Chicago mineral-carbonate oxygen isotope fractionation curves have been combined with mineral-water fractionation data for jadeite, zoisite and rutile and new data for grossular-water to provide a set of self-consistent mineral-pair calibrations. The A coefficients in the equation 1000 In α= A × 106T-2 of the new mineral-pair fractionations are
Jadeite Zoisite Grossular Rutile
Quartz 1.69 2.00 3.03 5.02
Jadeite 0.31 1.34 3.33
Zoisite 1.03 3.02
Grossular 1.99
The isotopic fractionation properties of natural pyralspite garnet [(Ca, Fe, Mg, Mn)3Al2Si3O12] can be approximated by those of the grossular end-member. Appropriate substitutions also yield coefficients for the solid-solution minerals: sodic pyroxene and epidote, e.g.
A quartz-sodic pyroxene= 2.75 - 1.06Xjd,
A quartz-epidote= 2.00 + 0.75Xps
where X Jd and X Ps are the mole fractions of the jadeite and pistacite components, respectively.
The new data set is particularly suitable for the geothermometry of metamorphic rocks. δ18O data from minerals of the high-pressure metamorphic rocks of the Sesia Zone of Italy and Cyclades Complex of Greece yield well-constrained mean temperatures of 572 and 478 C, respectively. Type III blueschist metabasalts of the Franciscan Formation of California give mean quartz-garnet temperatures of 354 C.  相似文献   

16.
Abstract. Vein type tungsten mineralization at Degana is genetically and spatially associated with the Degana Granite. The deposit is characterized by pervasive wall rock alteration around the mineralized quartz veins. Laterally three different alteration zones, greisen, silicification and potassic zones, are marked based on the field features, mineral assemblages and geo-chemical characteristics. In the present paper, systematic mineralogical and chemical variation in these alteration zones is reported. Thick mono-mineralic (zinnwaldite) selvages around the veins characterize the deposit. Plagioclase and alkali feldspar are low in the greisen zones while K-feldspar shows more increase than plagioclase in the potassic zone. Quartz is uniformly high in all the alteration zones, but it shows an anomalous value in the silicification zone. Al2O3 concentration shows initial depletion in greisen zone with gradual increase away from the contact. MgO and FeO are higher in greisen zone than silicification and potassic zones. The potassic zone is characterized by the depletion of Na2O and higher value of K2O.
The common presence of topaz and fluorite as both primary and secondary minerals and fluorine-bearing micas suggest fluorine partitioning in substantial amount between granitic melt and coexisting aqueous fluid phase and higher HF activity during the evolution of hydrothermal fluid. The mutual relationship of the fluorine minerals (topaz and fluorite) in the different alteration zones suggests an increase in the Ca2+ activity and decrease of H+ activity during the fluid evolution from greisenization towards alkali-metasomatised granite and the fluid is assumed to change from low to high activity ratio of Ca2+/H+.  相似文献   

17.
Phosphorus-rich alkali feldspars were found in three peraluminous highly differentiated albite-topaz-Li-mica granites in the W and S parts of the Bohemian Massif. The average contents of P2O5 in K-feldspars (Křížovy kámen 0.57 wt%, Homolka 0.77 wt%, and Podlesí 0.83 wt%) are higher than the average contents of P2O5 in albites (Křížovy kámen 0.23 wt%, Homolka 0.23 wt%, and Podlesí 0.39 wt%). The analyses of feldspars indicate that partition coefficient of phosphorus between K-feldspar and albite range from 1.5 to 2.5. Measured data in K-feldspars suggest a statistically significant difference from the Al3++P5+=2 Si4+ substitution mechanism for higher phosphorus concentration. The P-content in K-feldspars from the Podlesí-granite represent the highest P-content in natural feldspar known to date (up to 2.5 wt% of P2O5)- It is suggested that all studied granites retained nearly all phosphorus of granitic melts and that their alkali feldspars represent major reservoirs of phosphorus.  相似文献   

18.
Abstract. Fluid inclusion and oxygen isotope studies are performed to obtain temperatures and oxygen isotopic compositions of hydrothermal fluids for the vein-type tungsten-copper deposit at Takatori in Ibaraki Prefecture, Japan. Temperatures of the hydrothermal fluids are calculated from fluid inclusion data. The calculation incorporates the effects of the salinity, gas concentration, and fluid pressure. The fluid temperatures range from 370 to 460C. For these calculations, this study obtains a density equation for H2O-NaCl-CO2 solution at the vapor-liquid two-phase boundary. Then the present study combines the obtained equation with the equation of state by Bowers and Helgeson (1983).
The fluid temperatures determined in this study are applied to the calculation of oxygen isotopic compositions of the hydrothermal fluids. The calculation of the oxygen isotopic compositions is based on the oxygen isotope analyses of vein quartz. The oxygen isotopic compositions of vein quartz range from +13.5 to +14.4 % relative to SMOW. Then, the oxygen isotopic compositions of the hydrothermal fluids in equilibrium with the vein quartz are calculated to be from +9.7 to +10.5 %. These δ18Ofluid values agree with those of magmatic fluids derived from the ilmenite-series granitic rock, which is related to the mineralization. Keywords: Takatori tungsten-copper deposit, fluid inclusion, oxygen isotope, vein quartz, H2O-NaCl-CO2 solution, density  相似文献   

19.
Calcium hydroxyapatite and calcite precipitates around bacteria were observed in 2-week-old alluvial topsoil (Roussillon area, SE France). This observation prompted a laboratory study of Ca2+ and PO43− incorporation into hydroxyapatite and Ca2+ into calcite mediated by bacteria using similar topsoil material, but free from apatite and calcite. Subsamples were prepared using three different grain sizes, and experiments were undertaken using sucrose and different contents of Ca2+ and PO43−. Mineralization experiments proceeded over 5 days. Calcium and PO43− sorption onto clay influenced the Ca/P ratio in the solutions. Hydroxyapatite and calcite precipitation only occurred in unsterilized samples. The presence of clay minerals promoted biomineralization.  相似文献   

20.
The central trough of the Bolivian Altiplano is occupied by two wide salt crusts: the salar of Uyuni, which is probably the largest salt pan in the world (10,000 km2) and the salar of Coipasa (2,500 km2). Both crusts are essentially made of porous halite filled with an interstitial brine very rich in Li, K, Mg, B (up to 4.7 g/l Li, 4.3 g/l B, 30 g/l K and 75 g/l Mg). Lithium reserves are the highest known in the world, around 9 × 106 tons. Potassium, magnesium and boron reserves in brines are also important (around 194 × 106 tons K, 8 × 106 tons B and 211 × 106 tons Mg).

The crusts are the remnant of saline Lake Tauca (13,000–10,000 yr BP). Its salinity was estimated approximately at 80 g/l. Its paleochemistry was derived in two ways: (1) by dissolving the present amounts of all chemical components in the former lake volume, and (2) by simulating the evaporation of the major inflows to the basin. The resulting chemical compositions are quite different. The dissolution-derived one is 5 to 50 times less concentrated in Li, K, Mg, B than the evaporation-simulated ones. However all compositions present the same Na and Cl contents. This suggests either a removal of bittern salts or an enrichment of the former lake water in Na and Cl.

The most probable interpretation is that Lake Tauca redissolved a salt crust akin to that existing today. Several older lakes have been detected on the Altiplano. Nevertheless, such an explanation only pushes the problem back. It is likely that the anomaly was transferred from one lake to an other. Three hypotheses may be put forward: (1) bittern seepage through bottom sediments, (2) uptake of the missing components by minerals, and (3) leaching of ancient evaporites from the catchment area at the beginning of the lacustrine history of the basin. The excess halite could have been recycled from lake to lake. This latter process seems to be the most effective to explain the large excess of Na and Cl over the bittern solutes — Li, K, Mg and B. The occurrence of almost pure Na/1bCl saline springs flowing out from a gypsum diapir in the northern Altiplano gives substantial support to this hypothesis.  相似文献   


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