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1.
Reactions of CO2 with carbonate and silicate minerals in continental sediments and upper part of the crystalline crust produce HCO3− in river and ground waters. H2SO4 formed by the oxidation of pyrite and reacting with carbonates may produce CO2 or HCO3−. The ratio, ψ, of atmospheric or soil CO2 consumed in weathering to HCO3− produced depends on the mix of CO2 and H2SO4, and the proportions of the carbonates and silicates in the source rock. An average sediment has a CO2 uptake potential of ψ = 0.61. The potential increases by inclusion of the crystalline crust in the weathering source rock. A mineral dissolution model for an average river gives ψ = 0.68 to 0.72 that is within the range of ψ = 0.63 to 0.75, reported by other investigators using other methods. These results translate into the CO2 weathering flux of 20 to 24 × 1012mol/yr.  相似文献   

2.
New major, trace and isotopic geochemical results from a regional study of springs discharging from the major carbonate rock aquifer in the Interlake Region of Manitoba, Canada, are used to understand water–rock reactions, timing of recharge/discharge, tufa formation processes, and as baseline data. Spring waters are fresh with total dissolved solids (TDS) concentrations ranging from 150 to 880 mg/L. Waters discharging in the northern part of the study area have lower TDS, are dominantly Ca–Mg–HCO3 waters with low SO4 concentrations (<< 50 mg/L), and appear to have interacted primarily with Silurian carbonate lithologies. In contrast, waters in the southeastern part of the study area have higher TDS and have elevated SO4 concentrations (up to 210 mg/L). Spring waters have elevated Mg/Camolar (1.23 ± 0.23), typically greater than congruent dissolution of dolomite. Ca and Mg concentrations and Mg/Camolar indicate that groundwater residence times were sufficient to allow equilibration with bedrock dolomite lithologies; elevated tritium in northern waters indicates a significant recharge component in the 1960's and 1970's. Tufa precipitates that have formed from many of the spring waters are low-Mg calcite (MgO = 1.70 to 5.80 wt.%). Sr concentrations are variable (57 to 657 ppm) and tufa Sr/Camolar ratios appear to be entirely controlled by spring water Sr/Camolar. Empirically determined Sr distribution coefficients (DSr = 0.389 ± 0.083) indicate rapid crystallization following CO2 degassing, consistent with heavier δ13CVPDB compared to spring waters. Sulfate concentrations are generally too low for calcitization (dedolomitization) reactions driven by anhydrite dissolution to be the dominant control on the elevated groundwater Mg/Camolar, implying either extensive sulfate reduction along the flow paths (however, δ13CDIC suggests the elevated SO4 is more consistent with Fe-sulfide oxidation), or that other processes are involved. Major ion ratios suggest that the waters in the southern part of the study area are more consistent with interaction with siliciclastic rocks than with anhydrite dissolution. We suggest that calcitization (dedolomitization) reactions driven by anhydrite dissolution may not dominate all carbonate aquifers and that mixing of waters in karst conduits combined with ion exchange reactions are important controls on water chemistry in these systems.  相似文献   

3.
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4.
Groundwaters in the confined aquifers of the Chianan and Ilan coastal plains of Taiwan are rich in dissolved methane (CH4). Serious endemic “blackfoot disease”, which occurred in the Chianan plain, especially during AD1950-1970, has been demonstrated to have arisen from drinking highly reducing groundwater with abnormal arsenic and humic substance levels. In order to explore the origin of CH4 and its hydrological implications, stable carbon isotope ratios (δ13C) and radiocarbon (14C) ages of exsolved CH4, dissolved inorganic carbon (DIC), and sedimentary biogenic sediments from a total of 34 newly completed water wells at 16 sites were determined. The main results obtained are as follows: (1) The δ13CCH4 (−65‰ to −75‰) values indicate that, except for one thermogenic sample (δ13CCH4=38.2‰) from the Ilan plain, all CH4 samples analyzed were produced via microbially mediated CO2 reduction. Many δ13CDIC values are considerably greater than −10‰ and even up to 10‰ due to Rayleigh enrichment during CO2 reduction. (2) Almost all the 14C ages of CH4 samples from the shallow aquifer (I) (<60 m depth) are greater than the 14C ages of coexisting DIC and sediments, suggesting the presence of CH4 from underlying aquifers. (3) The 14C ages of coexisting CH4, DIC and sediments from aquifer (II) of the Chianan plain are essentially equal, reflecting in-situ generation of CH4 and DIC from decomposition of sedimentary organic matter and sluggishness of the groundwater flow. On the other hand, both CH4 and DIC from each individual well of the relatively deep aquifers (III) and (IV) in the Chianan plain are remarkably younger than the deposition of their coexisting sediments, indicating that current groundwaters entered these two aquifers much later than the deposition of aquifer sediments. (4) Each CH4 sample collected from the Ilan plain is older than coexisting DIC, which in turn is distinctly older than the deposition of respective aquifer sediments, demonstrating the presence of much older CO2 and CH4 from underlying strata.  相似文献   

5.
Lime mortar and plaster were sampled from Roman, medieval and early modern buildings in Styria. The historical lime mortar and plaster consist of calcite formed in the matrix during setting and various aggregates. The stable C and O isotopic composition of the calcite matrix was analyzed to get knowledge about the environmental conditions during calcite formation. The δ13Cmatrix and δ18Omatrix values range from −31 to 0‰ and −26 to −3‰(VPDB), respectively. Obviously, such a range of isotope values does not represent the local natural limestone assumed to be used for producing the mortar and plaster. In an ideal case, the calcite matrix in lime mortar and plaster is isotopically lighter in the exterior vs. the interior mortar layer according to the relationship δ18Omatrix = 0.61 · δ13Cmatrix − 3.3 (VPDB). Calcite precipitation by uptake of gaseous CO2 into alkaline Ca(OH)2 solutions shows a similar relationship, δ18Ocalcite = 0.67 · δ13Ccalcite − 6.4 (VPDB). Both relationships indicate that the 13C/12C and 18O/16O values of the calcite reflect the setting behaviour of the lime mortar and plaster. Initially, CO2 from the atmosphere is fixed as calcite, which is accompanied by kinetic isotope fractionation mostly due to the hydroxylation of CO2 (δ13Cmatrix ≈  −25‰ and δ18Omatrix ≈ −20‰). As calcite formation continued the remaining gaseous CO2 is subsequently enriched in 13C and 18O causing later formed calcite to be isotopically heavier along the setting path in the matrix. Deviations from such an ideal isotopic behaviour may be due to the evolution of H2O, e.g. evaporation, the source of CO2, e.g. from biogenic origin, relicts of the natural limestone, and secondary effects, such as recrystallization of calcite. The results of the field and experimental study suggest that isotope values can be used as overall proxies to decipher the origin of carbonate and the formation conditions of calcite in the matrix of ancient and recent lime mortar and plaster. Moreover, these proxies can be used to select calcite matrix from historical lime mortar and plaster for 14C dating.  相似文献   

6.
We revised an equation for estimating palaeostress magnitude using the microboudin technique by incorporating the influence of time on the fracture strength of minerals. The equation was used to estimate triaxial palaeostresses from a rare sample of metachert from Turkey that contains microboudinaged, columnar tourmaline grains in a wide range of orientations within the foliation plane. The estimated principal palaeostresses are σ1 = 605 MPa, σ2 = 598 MPa, and σ3 = 597 MPa. As the microboudinage is considered to have occurred immediately before the rock encountered the brittle-plastic transition during exhumation, these stress values correspond to conditions at approximately 18 km depth and 300 °C within a Cretaceous orogenic belt.  相似文献   

7.
Dissolution of the synthetic hydroxylapatite (HAP) and fluorapatite (FAP) in pure water was studied at 25 °C and 45 °C in a series of batch experiments. The XRD, FT-IR and SEM analyses indicated that the synthetic, microcrystalline HAP and FAP with apatite structure used in the experiments were found to have no obvious variation after dissolution except that the existence of OH groups in FT-IR spectra for FAP after 2880 h dissolution was observed. During the HAP dissolution (0–4320 h), the aqueous calcium and phosphate concentrations reached the maxima after 120 h and then decreased slowly with time. For the FAP dissolution in pure water, after a transient time of 1440 h (< 60 d), element concentrations and pH became constant suggesting attainment of a steady-state between the solution and solid. During early stages of the FAP dissolution reaction (< 72–120 h), mineral components were released in non-stoichiometric ratios with reacted solution ratios of dissolved Ca:P, Ca:F and P:F being lower than mineral stoichiometric ratios of Ca5(PO4)3F, i.e., 1.67, 5.0 and 3.0, respectively. This indicated that F were preferentially released compared to Ca from the mineral structure. The mean Ksp values were calculated by using PHREEQC for HAP of 10− 53.28 (10− 53.02–10− 53.51) and for FAP of 10− 55.71 (10− 55.18–10− 56.13) at 25 °C, the free energies of formation ΔGfo[HAP] and ΔGfo[FAP] were calculated to be − 6282.82 kJ/mol and − 6415.87 kJ/mol, respectively.  相似文献   

8.
Groundwaters and surface water in the Shihongtan sandstone-hosted U ore district, Xinjiang, NW China, were sampled and analyzed for their major-, and trace element concentrations and oxygen, hydrogen, boron and strontium isotope compositions in order to assess the possible origins of the waters and water–rock interactions that occurred in the deep aquifer system. The waters in the study district have been grouped into three hydrochemical facies: Facies 1, potable spring-water, is a pH neutral (7.0), Na–Ca–HCO3 type water with low total dissolved solids (TDS; 0.2 g/l, fresh) and has δ18O of − 8.3‰, δD of − 48.2‰,δ11B of 1.5‰, and 87Sr/86Sr of 0.70627. Facies 2 groundwaters are mildly acidic to mildly alkaline (pH of 6.5–8.0, mean 7.3), Na–Ca–Mg–Cl–SO4 type waters with moderate TDS (8.2 g/l–17.2 g/l, mean 9.3 g/l, brackish) and haveδ18O values in the − 5.8‰ to − 9.3‰ range (mean − 8.1‰), δD values in the − 20.8‰ to − 85.5‰ range (mean − 47.0‰),δ11B values in the + 9.5‰ to + 39.1‰ range (mean + 17.1‰), and 87Sr/86Sr values in the 0.70595 to 0.70975 range (mean 0.70826). Facies 3, Aiting Lake water, is a mildly alkaline (pH = 7.4), Na–Ca–Mg–Cl–SO4 type water with the highest TDS (249.1 g/l, brine) and has δ18O of − 2.8‰, δD of − 45.8‰,δ11B of 21.2‰, and 87Sr/86Sr of 0.70840. The waters from the study district show a systematic increase in major, trace element and TDS concentrations and δ11B values along the pathway of groundwater migration which can only be interpreted in terms of water–rock interaction at depth and strong surface evaporation. The hydrochemical and isotopic data presented here confirm that the groundwaters in the Shihongtan ore district are the combined result of migration, water–rock interaction and mixing of meteoric water with connate waters contained in sediments.  相似文献   

9.
Fault slip analysis of Quaternary faults in southeastern Korea   总被引：1，自引：0，他引：1  
The Quaternary stress field has been reconstructed for southeast Korea using sets of fault data. The subhorizontal direction of the maximum principal stress (σ1) trended ENE and the direction of the minimum principal stress (σ3) was nearly vertical. The stress ratio (Φ = (σ2 − σ3) / (σ1 − σ3)) value was 0.65. Two possible interpretations for the stress field can be made in the framework of eastern Asian tectonics; (1) The σHmax trajectory for southeast Korea fits well with the fan-shaped radial pattern of maximum principal stress induced by the India–Eurasia collision. Thus, we suggest that the main source for this recent stress field in southeast Korea is related to the remote India–Eurasia continental collision. (2) The stress field in Korea shows a pattern similar to that in southwestern Japan. The origin for the E–W trending σHmax in Japan is known to be related to the mantle upwelling in the East China Sea. Thus, it is possible that Quaternary stress field in Korea has evolved synchronously with that in Japan. We suggest further studies (GPS and in situ stress measurement) to test these hypotheses.  相似文献   

10.
Mercury contents in Precambrian banded iron formation-hosted hematite ores are virtually unknown. In an attempt to provide information on the abundance and distribution of Hg in Fe ore, we present analyses for Hg in samples of high-grade soft hematite ore from Gongo Soco, Minas Gerais, Brazil. Bulk samples contain from <  5 to 25  ppb Hg without obvious correlation with major elements. Granulometric fractions of follow-up samples have amounts of Hg from 6 to 48  ppb and display positive linear correlations with total Mn as MnO (r = 0.87), LOI (r = 0.87) and SiO2 (r = 0.76), as well as a negative linear correlation with total Fe as Fe2O3 (r = −  0.87). The correlations suggest that Hg is associated with a hydrated ferruginous groundmass bearing residual Mn, Al and Si, which replaced gangue minerals in itabirite in the process of formation of the Gongo Soco soft hematite ore.  相似文献   

11.
Sulfur and O isotope analyses of dissolved SO4 were used to constrain a hydrogeological model for the area overlying the Gorleben–Rambow Salt Structure, Northern Germany. Samples were collected from 80 wells screened at different depth-intervals. The study area consists of a set of two vertically stacked aquifer systems. Generally, the isotope data show a good spatial correlation, outlining well-defined groundwater zones containing SO4 of characteristic isotopic composition. Highly saline waters from deeper parts of the lower aquifer system are characterized by rather constant SO4 isotopic compositions, which are typical of Permian Zechstein evaporites (δ34S=9.6–11.9‰; δ18O=9.5–12.1‰). Above this is a transition zone containing ground waters of intermediate salinity and slightly higher isotopic values (average δ34S=16.6‰; δ18O=15.3‰). The confined groundwater horizon on the top of the lower aquifer system below the low permeable Hamburg Clays is low in total dissolved solids and is characterized by an extreme 34S enrichment (average δ34S=39.1‰; δ18O=18.4‰), suggesting that bacterially mediated SO4 reduction is a dominant geochemical process in this zone. Two areas of distinct isotopic composition can be identified in the shallow ground water horizons of the upper hydrogeological system. Sulfate in groundwaters adjacent to the river Elbe and Löcknitz has a typical meteoric isotopic signature (δ34S=5.2‰; δ18O=8.2‰), whereas the central part of the area is characterized by more elevated isotopic ratios (δ34S=12.7‰; δ18O=15.6‰). The two major SO4 pools in the area are represented by Permian seawater SO4 and a SO4 of meteoric origin that has been mixed with SO4 resulting from the oxidation of pyrite. It is suggested that the S-isotope compositions observed reflect the nature of the SO4 source that have been modified to various extent by bacterial SO4 reduction. Groundwaters with transitional salinity have resulted from mixing between brines and low-mineralized waters affected by bacterial SO4 reduction.  相似文献   

12.
Ordos Basin, the second largest sedimentary basin in China, contains enormous natural gas resources. Each of the four giant gas fields discovered so far in this basin (i.e., Sulige, Yulin, Wushenqi and Jingbian) has over 100 billion cubic meters (bcm) or 3.53 trillion cubic feet (tcf) of proven gas reserves. This study examines the stable carbon isotope data of 125 gas samples collected from the four giant gas fields in the Ordos Basin. Source rocks in the Upper Paleozoic coal measures are suggested by the generally high δ13C values of C1–C4 gaseous hydrocarbons in the gases from the Sulige, Yulin and Wushenqi gas fields. While the δ13CiC4 value is higher than that of the δ13CnC4, the dominant ranges for the δ13C1, δ13C2, and δ13C3 values in these Upper Paleozoic reservoired gases are −34 to −32‰, −27 to −23‰, and −25 to −24‰, respectively. The δ13C values of methane, benzene and toluene in gases from the Lower Paleozoic reservoirs of the Jingbian field indicate a significant contribution from humic source rocks, as they are similar to those in the Upper Paleozoic reservoirs of the Sulige, Yulin and Wushenqi gas fields. However, the wide variation and reversal in the δ13C1, δ13C2 and δ13C3 values in the Jinbian gases cannot be explained using a single source scenario, thus the gases were likely derived dominantly from the Carboniferous-Permian coal measures with some contribution from the carbonates in the Lower Permian Taiyuan Formation. The gas isotope data and extremely low total organic carbon contents (<0.2% TOC) suggest that the Ordovician Majiagou Formation carbonates are unlikely to be a significant gas source rock, thus almost all of the economic gas accumulations in the Ordos Basin were derived from Upper Paleozoic source rocks.  相似文献   

13.
Tourmalinites that are distally associated with tungsten deposits of the Pampa del Tamboreo area, San Luis, Argentina, contain tourmalines retaining evidence for its origin and evolution. Tourmaline grains uncommonly contain small grains of detrital tourmaline. Analysis of a single detrital tourmaline grain reveals that it is a Ca-rich “oxy-dravite”. Proximal to the detrital cores there are inner domains of asymmetric tourmaline overgrowths that developed during low grade metamorphism. Volumetrically dominant tourmaline overgrowths in the outer domain are concentrically zoned aluminous dravite and “oxy-dravite” with Al/(Al + Fe + Mg) = 0.71–0.74 and Mg/(Mg + Fe) = 0.64–0.71. Variability of Al is primarily controlled by the deprotonation substitution R + OH− = Al + O2− (where R = Fe + Mg), and is a function of the activity of H2O. A likely evolutionary scenario is one in which volcanogenic material is altered by hydrothermal fluids in the sea floor resulting in an aluminous and magnesian residuum. With further hydrothermal circulation and incipient metamorphism, boron-rich fluids are expelled from metasedimentary and metavolcanic basement rocks and develop Mg-rich tourmalinites in the aluminous, magnesian host rocks. The tourmalinization process occurs over a range of metamorphic conditions and with fluids of variable activity of H2O.  相似文献   

14.
Bonini (2009, Structural controls on a carbon dioxide-driven mud volcano field in the Northern Apennines (Pieve Santo Stefano, Italy): relations with pre-existing steep discontinuities and seismicity. Journal of Structural Geology 31, 44–54) presents a 2D mechanical analysis to infer the failure conditions responsible for the seismicity distribution during an Mw = 4.6 seismic sequence nucleating during 2001 in the Northern Apennines. In my view the mechanical analysis presented in this paper has some weakness or is not well constrained, in particular: 1) the assumption of a dip angle of 50°, is not consistent with the activated structures; 2) the Pf = σ3 condition, difficult to be attained along a cohesionless fault dipping at 50°; 3) the isotropic stress state, i.e. σ2 = σ3, that is not consistent with the active or recent stress field in the area.  相似文献   

15.
Stable oxygen isotopic fractionation during inorganic calcite precipitation was experimentally studied by spontaneous precipitation at various pH (8.3 < pH < 10.5), precipitation rates (1.8 < log R < 4.4 μmol m− 2 h− 1) and temperatures (5, 25, and 40 °C) using the CO2 diffusion technique.The results show that the apparent stable oxygen isotopic fractionation factor between calcite and water (αcalcite–water) is affected by temperature, the pH of the solution, and the precipitation rate of calcite. Isotopic equilibrium is not maintained during spontaneous precipitation from the solution. Under isotopic non-equilibrium conditions, at a constant temperature and precipitation rate, apparent 1000lnαcalcite–water decreases with increasing pH of the solution. If the temperature and pH are held constant, apparent 1000lnαcalcite–water values decrease with elevated precipitation rates of calcite. At pH = 8.3, oxygen isotopic fractionation between inorganically precipitated calcite and water as a function of the precipitation rate (R) can be described by the expressions
at 5, 25, and 40 °C, respectively.The impact of precipitation rate on 1000lnαcalcite–water value in our experiments clearly indicates a kinetic effect on oxygen isotopic fractionation during calcite precipitation from aqueous solution, even if calcite precipitated slowly from aqueous solution at the given temperature range. Our results support Coplen's work [Coplen T. B. (2007) Calibration of the calcite–water oxygen isotope geothermometer at Devils Hole, Nevada, a natural laboratory. Geochim. Cosmochim. Acta 71, 3948–3957], which indicates that the equilibrium oxygen isotopic fractionation factor might be greater than the commonly accepted value.  相似文献   

16.
Voluminous granitic intrusions are distributed in the West Junggar, NW China, and they can be classified as the dioritic rocks, charnockite and alkali-feldspar granite groups. The dioritic rocks (SiO2 = 50.4–63.8 wt.%) are calc-alkaline and Mg enriched (average MgO = 4.54 wt.%, Mg# = 0.39–0.64), with high Sr/Y ratios (average = 21.2), weak negative Eu (average Eu/Eu = 0.80) and pronounced negative Nb–Ta anomalies. Their Sr–Nd and zircon Hf isotopic compositions ((87Sr/86Sr)i = 0.7035–0.7042, εNd(t) = 4.5–7.9, εHf(t) = 14.1–14.5) show a depleted mantle-like signature. These features are compatible with adakites derived from partial melting of subducted oceanic crust that interacted with mantle materials. The charnockites (SiO2 = 60.0–65.3 wt.%) show transitional geochemical characteristics from calc-alkaline to alkaline, with weak negative Eu (average Eu/Eu = 0.75) but pronounced negative Nb–Ta anomalies. Sr–Nd and zircon Hf isotopic compositions ((87Sr/86Sr)i = 0.7037–0.7039, εNd(t) = 5.2–8.0, εHf(t) = 13.9–14.7) also indicate a depleted source, suggesting melts from a hot, juvenile lower crust. Alkali-feldspar granites (SiO2 = 70.0–78.4 wt.%) are alkali and Fe-enriched, and have distinct negative Eu and Nb–Ta anomalies (average Eu/Eu = 0.26), low Sr/Y ratios (average = 2.11), and depleted Sr–Nd and zircon Hf isotopic compositions ((87Sr/86Sr)i = 0.7024–0.7045, εNd(t) = 5.1–8.9, εHf(t) = 13.7–14.2). These characteristics are also comparable with those of rocks derived from juvenile lower crust. Despite of the differences in petrology, geochemistry and possibly different origins, zircon ages indicate that these three groups of rocks were coevally emplaced at ~ 305 Ma.A ridge subduction model can account for the geochemical characteristics of these granitoids and coeval mafic rocks. As the “slab window” opened, upwelling asthenosphere provided enhanced heat flux and triggered voluminous magmatisms: partial melting of the subducting slab formed the dioritic rocks; partial melting of the hot juvenile lower crust produced charnockite and alkali-feldspar granite, and partial melting in the mantle wedge generated mafic rocks in the region. These results suggest that subduction was ongoing in the Late Carboniferous and, thus support that the accretion and collision in the Central Asian Orogenic Belt took place in North Xinjiang after 305 Ma, and possibly in the Permian.  相似文献   

17.
This study provides evidence for the existence of halite and sylvite solid inclusions in igneous quartz and feldspars, the first to be reported in intrusive rocks, and to partially constrain the physicochemical environment that lets halides crystallize under magmatic conditions.Halite and sylvite solid inclusions were found included in quartz and feldspars from a micrographic–granophyric assemblage in a miarolitic aplite and, rarer, in alkali-feldspar from a miarolitic monzogranite. Monzogranite and aplite represent I-type, K-enriched postcollisional rocks of the Late Cambrian–Early Ordovician Sierra Norte–Ambargasta batholith in the Eastern Sierras Pampeanas. Both granitoids fall among the most evolved felsic rocks of the batholith, with aplite approaching haplogranitic compositions. Halite is far more common than sylvite and the presence and distribution of one or both halides are erratic within the felsic intrusive bodies. Halides occur as small skeletal grains, commonly in cross-shaped aggregates of less than 50 μm. No K or Na was found at the detection limits of EDS in either halite or sylvite respectively. Textural relationships suggest that the alkali-chlorides separated from the melt near the minima along the quartz–feldspar cotectics of PH2O > 160 < 200 MPa in a silica-, and potassium-rich magmatic system at approximately 750–700 °C, prior to the H2O-vapor saturated miarole-forming stage.Computed ratios for the magmatic volatile phase (MVP) coexisting with melt at the early stage of aplite crystallization are: NaCl/HCl = 0.11–0.97 and KCl/HCl = 0.24–1.62, being the highest range of values (0.79–0.97 and 1.45–1.62, respectively) found in those alkali-chloride-bearing samples. Maximum HCl/ΣCl(MVP) (0.28 to 0.31) indicates higher total Cl concentration in the MVP of alkali-chloride-bearing aplites, which is much higher in the halite-free aplite samples (HCl/ΣCl(MVP) = 0.59 to 0.74). One miarolitic monzogranite sample, where halite solid inclusions are present, also yielded the highest ratios for NaCl/HCl(MVP) (0.91) and KCl/HCl(MVP) (1.46), and the HCl/ΣCl(MVP) is 0.30. A high HCl concentration in the fluid phase is suggested by the log f(HF)/f(H2O) = − 4.75 to − 4.95, log f(HCl)/f(H2O) = − 3.73 to − 3.86, and log f(HF)/f(HCl) = − 0.88 to − 1.22, computed at 750 °C after biotite composition. The Cl concentrations at 800 °C, computed with a Dv/lCl = 0.84 + 26.6P (P at 200 MPa), yielded values within the range of  70 to 700 ppm Cl in the melt and  4000 to 40 000 ppm Cl in the coexisting MVP. The preferential partitioning of Cl in the vapor phase is controlled by the Dv/lCl; however, the low concentration of Cl in the melt suggests that high concentrations of Cl are not necessary to saturate the melt in NaCl or KCl.Cl-saturation of the melt and coexisting MVP might have been produced by a drop in Cl solubility due to the near-haplogranitic composition of the granitoids after extreme fractionation, probably enhanced by fluctuating reductions of the emplacement pressure in the brittle monzogranite host. Liquid immiscibility, based in the differential viscosity and density among alkali-chloride saturated hydrosaline melt, aluminosilicate felsic melt, and H2O-rich volatiles is likely to have crystallized halite and sylvite from exsolved hydrosaline melt. High degrees of undercooling might have been important at the time of alkali-chloride exsolution. The effectiveness of alkali-chloride separation from the melt at magmatic temperatures is in line with the interpretation of “halite subtraction” as a necessary process to understand the origin of the “halite trend” in highly saline fluid inclusions from porphyry copper and other hydrothermal mineralizations, despite the absence of the latter in the Cerro Baritina aplites, where this process preceded the exsolution of halite-undersaturated fluids.Pervasive alteration of the monzogranite country rock as alkali-metasomatic mineral assemblages, the mineral chemistry of some species, and the association of weak molybdenite mineralization are compatible with the activity of alkaline hypersaline fluids, most likely exsolved during the earliest stages of aplite consolidation.  相似文献   

18.
Stable (δ13C and δ18O) and radiogenic 87Sr/86Sr isotopic data have been used to investigate the origin of cleat dawsonite (NaAlCO3(OH)2) in the Late Permian Wittingham Coal Measures of the Upper Hunter region in the Sydney Basin, New South Wales. The δ13CPDB values have a narrow range (− 1.7‰ to + 2.4‰), with an average of + 0.3‰, suggesting a magmatic source for the carbon. In contrast, δ18OSMOW values have a wide range (+ 13.6‰ to + 19.8‰), and decrease systematically with decreasing distance from a major intrusion. This systematic variation reflects establishment of localised hydrothermal cells. Water–rock interaction between fluids associated with these hydrothermal cells, and Rb-poor volcaniclastic detritus in the coal measures, produced mantle-like 87Sr/86Sr (0.705032 to 0.706464) in the dawsonite.  相似文献   

19.
The Temaguessine high-level subcircular pluton is intrusive into the LATEA metacraton (Central Hoggar) Eburnian (2 Ga) basement and in the Pan-African (615 Ma) granitic batholiths along a major NW–SE oriented major shear zone. It is dated here (SHRIMP U–Pb on zircon) at 582 ± 5 Ma. Composed of amphibole–biotite granite and biotite syenogranite, it comprises abundant enclaves: mafic magmatic enclaves, country-rock xenoliths and remarkable Fe-cordierite (#Fe = 0.87) orbicules. The orbicules have a core rich in cordierite (40%) and a leucocratic quartz–feldspar rim. They are interpreted as resulting from the incongruent melting of the meta-wacke xenoliths collapsed into the magma: the breakdown of the biotite + quartz assemblage produced the cordierite and a quartz–feldspar minimum melt that is expelled, forming the leucocratic rim. The orbicule generation occurred at T < 850° and P < 0.3 GPa. The Fe-rich character of the cordierite resulted from the Fe-rich protolith (wacke with 4% Fe2O3 for 72% SiO2). Strongly negative εNd (−9.6 to −11.2), Nd TDM model ages between 1.64 and 1.92 Ga, inherited zircons between 1.76 and 2.04 Ga and low to moderately high ISr (0.704–0.710) indicate a Rb-depleted lower continental crust source for the Temaguessine pluton; regional considerations impose however also the participation of asthenospheric material. The Temaguessine pluton, together with other high-level subcircular pluton, is considered as marking the end of the Pan-African magma generation in the LATEA metacraton, resulting from the linear delamination along mega-shear zones, allowing asthenospheric uprise and melting of the lower continental crust. This implies that the younger Taourirt granitic province (535–520 Ma) should be considered as a Cambrian intraplate anorogenic event and not as a very late Pan-African event.  相似文献   

20.
We report for the first time the evidence for prograde high-pressure (HP) metamorphism preceding a peak ultrahigh-temperature (UHT) event in the northernmost part of the Madurai Block in southern India. Mg–Al-rich Grt–Ged rocks from Komateri in Karur district contain poikiloblastic garnet with numerous multi-phase inclusions. Although most of the inclusion assemblages are composed of gedrite, quartz, and secondary biotite, rare staurolite + sapphirine and spinel + quartz are also present. The XMg (=Mg/[Fe+Mg]) of staurolite (0.45–0.49) is almost consistent with that reported previously from Namakkal district in the Palghat–Cauvery Shear Zone system (XMg = 0.51–0.52), north of the Madurai Block. The HP event was followed by peak UHT metamorphism at T = 880–1040 °C and P = 9.8–12.5 kbar as indicated by thermobarometric computations in the Grt–Ged rock and associated mafic granulite. Symplectic intergrowth of spinel (XMg = 0.50–0.59, ZnO < 1.7 wt.%) and quartz, a diagnostic indicator of UHT metamorphism, probably formed by decompression at UHT conditions. The rocks subsequently underwent retrograde metamorphism at T = 720–760 °C and P = 4.2–5.1 kbar. The P–T conditions and clockwise exhumation trajectory of the Komateri rocks, comparable to similar features recorded from the Palghat–Cauvery Shear Zone system, suggest that the Madurai Block and the Palghat–Cauvery Shear Zone system underwent similar HP and UHT metamorphic history probably related to the continent–continent collision during the final stage of amalgamation of Gondwana supercontinent.  相似文献   

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