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1.
This study was aimed to test a new methodological approach to carry out measurements of gaseous elemental mercury (GEM) diffusively emitted from soils in hydrothermal-volcanic environments. This method was based on the use of a static closed-chamber (SCC) in combination with a Lumex® RA-915M analyzer that provides GEM measurements in a wide range of concentrations (from 2 to 50,000 ng m−3). Gas samples were collected at fixed time intervals from the SCC positioned on the ground (time-series samples). The Lumex® inlet port was equipped with a three-way Teflon valve allowing the free entrance of air through a carbon trap, in order to: (i) prevent disturbance to the Lumex® operative flow rate (10 L min−1) during the injection of the gas samples from the SCC and (ii) minimize the instability of the baseline signal induced by possible variations of GEM concentrations in air. In the lab, known amounts of GEM, pipetted from a vessel containing an Hg-saturated air in equilibrium with liquid mercury at 27 °C, were injected in the Lumex® via the modified inlet port to construct a calibration curve. The latter was used to calculate the amount of GEM in the SCC (KSCC) from the corresponding GEM concentrations measured by the Lumex® analyzer. The KSCC values of the time-series samples were proportionally increasing with the GEM fluxes (ϕGEM), thus ϕGEM values were computed according to the following equation: ϕGEM = (dKSCC/dt)/A, where A is the basal area of the SCC and dt is the time interval of the time-series sampling. Up to 214 ϕGEM measurements were carried out at Solfatara crater (Campi Flegrei, southern Italy), a hydrothermally altered tuff cone characterized by an anomalous diffuse soil emission of GEM-rich geogenic gases. The measured ϕGEM values varied up to 4 orders of magnitude, from 1,296, corresponding to the sensitivity of the method at the selected sampling time interval (1 min), to 1,957,500 ng m−2 day−1, and were consistent with those recently measured in this crater using a different method. In the field, 10 replicates were carried out in 5 selected sites, allowing to demonstrate that the proposed method has a high reproducibility (RDS < 4%). The ϕGEM and ϕCO2 values, the latter being measured in the same 214 sites by using the accumulation chamber method, showed a low correlation, although both gases were originated from the same deep source. This suggests that GEM and CO2 soil fluxes are differently affected by environmental parameters, such as soil humidity and temperature, which have a strong effect on the release of GEM from the soil, whereas they do not play a significant role in the diffuse degassing of CO2. The measured fluxes were used to compute the CO2 and GEM total outputs (402 and 5.41 × 10−6 t day−1, respectively) from the study area (92,000 m2) and to construct contour maps showing the spatial distribution of the ϕCO2 and ϕGEM values. By modifying the geometry of SCC and the time interval of the sampling series, the proposed method can be applied to the measurements of GEM soil fluxes in other geological systems and man-made environments.  相似文献   

2.
《Chemical Geology》2007,236(3-4):228-246
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3.
Sulfide Inhibition of Nitrate Removal in Coastal Sediments   总被引：1，自引：0，他引：1  
Microbial nitrate (NO3−) removal via denitrification (DNF) at high sulfide (H2S) concentrations was compared in sediment from a coastal freshwater pond in a developed area that receives salt-water influx during storm events, and a saline pond proximal to an undeveloped estuary. Sediments were incubated with added SO42− (1,000 μg per gram dry weight basis (gdw)) to determine whether acid volatile sulfides (AVS) were formed. DNF in the sediments was measured with NO3–N (300 μg gdw−1) alone, and with NO3–N and H2S (1,000 μg S2− gdw−1). SO42− addition to the freshwater sediments resulted in AVS formation (970 ± 307 μg S gdw−1) similar to the wetland with no added SO42− (986 ± 156 μg S gdw−1). DNF rates measured with no added H2S were greater in the freshwater than the wetland site (10.6 ± 0.6 vs. 6.4 ± 0.1 μg N2O–N gdw−1 h−1, respectively). High H2S concentrations retained NH4–N in the undeveloped wetland and retained NO3–N in the developed freshwater site, suggesting that potential salt-water influx may reduce the ability of the freshwater sediments to remove NO3–N.  相似文献   

4.
Volcanic and geothermal areas are one of the major natural sources of H2S to the atmosphere. Its environmental impact is often the main cause of the opposition to the development of geothermal energy exploitation programs. In this paper, we analyze the air concentrations and dispersion pattern of naturally emitted H2S at the geothermal area of Sousaki (Corinthia, Greece). Measurements, made with a network of passive samplers, evidence a rapid decrease of concentration values away from the emission points. The fact that the decrease is more pronounced in the summer with respect to the winter indicates that it is not only due to a dilution effect, but also to redox reactions favored by higher temperatures and intense sunlight typical of the summer period.  相似文献   

5.
Pore waters of natural clays, which are investigated as potential host rock formations for high-level nuclear waste, are known to contain large amounts of low-molecular weight organic compounds. These small organic ligands might impact the aqueous geochemistry of the stored radionuclides and, thus, their migration behavior. In the present work, the complexation of Cm(III) with formate in aqueous NaCl solution is investigated by time-resolved laser fluorescence spectroscopy (TRLFS) as a function of the ionic strength (0.5–3.0 mol/kg), the ligand concentration (0–0.2 mol/kg) and the temperature (20–90 °C). The Cm(III) speciation is determined by deconvolution of the emission spectra. The obtained distribution of Cm(III) species is used to calculate the conditional stability constants (log K′(T)) at a given temperature and ionic strength which are extrapolated to zero ionic strength by using the specific ion interaction theory (SIT). Thus, the thermodynamic log K0n(T) values for the formation of [Cm(Form)n](3−n)+ (n = 1, 2) and the ion interaction coefficients (ε(i,k)) for [Cm(Form)n](3−n)+ (n = 1, 2) with Cl− are obtained. The log K01(T) (2.11 (20 °C)–2.49 (90 °C)) and log K02(T) values (1.17 (30 °C–2.01 (90 °C)) increase continuously with increasing temperature. The log K0n(T) values are used to derive the standard reaction enthalpies and entropies (ΔrH0m, ΔrS0m) of the respective complexation reactions according to the Van’t Hoff equation. In all cases, positive ΔrH0m and ΔrS0m values are obtained. Thus, both complexation steps are endothermic and entropy-driven.  相似文献   

6.
Based on electromagnetic measurements we determined the current stress directions in the uppermost continental crust of Patagonia between the active plate margin of the Chilean Pacific coast and the Argentinean passive Atlantic margin. Regional variations of the observed stress pattern are giving details onto the acting tectonic processes. We distinguish five regional stress domains with different prevailing horizontal stress directions (SH): 1. Southern Coastal Cordillera and Longitudinal Valley (SH = SSW–NNE), 2. Chiloé Island (SH = SW–NE), 3. Northern Patagonian Andes (SH = WSW–ENE), 4. Argentinean Pampa and Atlantic margin (SH = WNW–ESE) and 5. Southern Patagonian Andes (SH = WNW–ESE). These stress regimes can be related to the geometry of the subducting Nazca- and Antarctic plates, to the transform fault between the South America and Scotia plates and to passive margin processes along the Atlantic coast. Absolute plate motion and rapid relative plate convergence control the subduction geometry and therefore the stress directions along the convergent margin of the South America Plate and the structural style within and landward of the Magmatic Arc. The knowledge of current local stress directions permits the characterisation of potential fault kinematics. By in situ measuring of electromagnetic emissions from rocks we determined the maximum horizontal stress orientation in the uppermost crust using a new geophysical tool. Our investigations on the orientation of the stress regimes also allow conclusions about the causative forces of either tectonic or gravitational origin in this part of the South-America Plate.  相似文献   

7.
Thermodynamic properties of several TeO2 polymorphs and metal tellurites were measured by a combination of calorimetric techniques. The most stable TeO2 polymorph is α-TeO2, with its enthalpy of formation (ΔfHo) selected from literature data as ?322.0 ± 1.3 kJ·mol?1. β-TeO2 is metastable (in enthalpy) with respect to α-TeO2 by +1.40 ± 0.07 kJ·mol?1, TeO2 glass by a larger amount of +14.09 ± 0.11 kJ·mol?1. >200 experimental runs and post-synthesis treatments were performed in order to produce phase-pure samples of Co, Cu, Mg, Mn, Ni, Zn tellurites. The results of the hydrothermal and solid-state syntheses are described in detail and the products were characterized by powder X-ray diffraction. The standard thermodynamic data for the Te(IV) phases are (standard enthalpy of formation from the elements, ΔfHo in kJ·mol?1, standard third-law entropy So in J·mol?1·K?1): Co2Te3O8: ΔfHo = ?1514.2 ± 6.0, So = 319.2 ± 2.2; CoTe6O13: ΔfHo = ?2212.5 ± 8.1, So = 471.7 ± 3.3; MgTe6O13: ΔfHo = ?2525.8 ± 7.9, So = 509.2 ± 3.6; Ni2Te3O8: ΔfHo not measured, So = 293.3 ± 2.1; NiTe6O13: ΔfHo = ?2198.7 ± 8.2, So = 466.5 (estimated); CuTe2O5: ΔfHo = ?820.2 ± 3.3, So = 187.2 ± 1.3; Zn2Te3O8: ΔfHo = ?1722.5 ± 4.0, So = 299.3 ± 2.1. The solubility calculations show that the Te(IV) concentration in an aqueous phase, needed to produce such phases, must be at least 3–5 orders of magnitude higher than the natural Te background concentrations. The occurrence of these minerals, as expected, are restricted to hotspots of Te concentrations. In order to produce more reliable phase diagrams, more work needs to be done on the thermodynamics of potential competing phases in these systems, including Te(VI) phases.  相似文献   

8.
Reports of the high ion content of steam and low-density supercritical fluids date back to the work of Carlon [Carlon H. R. (1980) Ion content of air humidified by boiling water.J. Appl.Phys.51, 171-173], who invoked ion and neutral-water clustering as mechanism to explain why ions partition into the low-density aqueous phase. Mass spectrometric, vibrational spectroscopic measurements and quantum chemical calculations have refined this concept by proposing strongly bound ion-solvent aggregates and water clusters such as Eigen- and Zundel-type proton clusters H3O+·(H2O)m and the more weakly bound water oligomers (H2O)m. The extent to which these clusters affect fluid chemistry is determined by their abundance, however, little is known regarding the stability of such moieties in natural low-density high-temperature fluids. Here we report results from quantum chemical calculations using chemical-accuracy multi-level G3 (Curtiss-Pople) and CBS-Q theory (Peterson) to address this question. In particular, we have investigated the cluster structures and clustering equilibria for the ions and H3S+·(H2O)m(H2S)n, where m ? 6 and n ? 4, at 300-1000 K and 1 bar as well as under vapor-liquid equilibrium conditions between 300 and 646 K. We find that incremental hydration enthalpies and entropies derived from van’t Hoff analyses for the attachment of H2O and H2S onto H3O+, and H3S+ are in excellent agreement with experimental values and that the addition of water to all three ions is energetically more favorable than solvation by H2S. As clusters grow in size, the energetic trends of cluster hydration begin to reflect those for bulk H2O liquids, i.e. calculated hydration enthalpies and entropies approach values characteristic of the condensation of bulk water (ΔHo = −44.0 kJ mol−1, ΔSo = −118.8 J K mol−1). Water and hydrogen sulfide cluster calculations at higher temperatures indicate that a significant fraction of H3O+, and H3S+ ions exists as solvated moieties.  相似文献   

9.
The Milin Kamak gold-silver deposit is located in Western Srednogorie zone, 50 km west of Sofia, Bulgaria. This zone belongs to the Late Cretaceous Apuseni-Banat-Timok-Srednogorie magmatic and metallogenic belt. The deposit is hosted by altered trachybasalt to andesitic trachybasalt volcanic and volcanoclastic rocks with Upper Cretaceous age, which are considered to be products of the Breznik paleovolcano. Milin Kamak is the first gold-silver intermediate sulfidation type epithermal deposit recognized in Srednogorie zone in Bulgaria. It consists of eight ore zones with lengths ranging from 400 to 1000 m, widths from several cm to 3–4 m, rarely to 10–15 m, an average of 80–90 m depth (a maximum of 200 m) and dip steeply to the south. The average content of gold is 5.04 g/t and silver – 13.01 g/t. The styles of alteration are propylitic, sericite, argillic, and advanced argillic. Ore mineralization consists of three stages. Quartz-pyrite stage I is dominated by quartz, euhedral to subhedral pyrite, trace pyrrhotite and hematite in the upper levels of the deposit. Quartz-polymetallic stage II is represented by major anhedral pyrite, galena, Fe-poor sphalerite; minor chalcopyrite, tennantite, bournonite, tellurides and electrum; and trace pyrrhotite, arsenopyrite, marcasite. Gangue minerals are quartz and carbonates. The carbonate-gold stage III is defined by deposition of carbonate minerals and barite with native gold and stibnite.Fluid inclusions in quartz are liquid H2O-rich with homogenization temperature (Th) ranging from 238 to 345 °C as the majority of the measurements are in the range 238–273 °C. Ice-melting temperatures (Tm) range from −2.2 to −4.1 °C, salinity – from 3.7 to 6.6 wt.% NaCl equiv. These measurements imply an epithermal environment and low- to moderate salinity of the ore-forming fluids.δ34S values of pyrite range from −0.49 to +2.44‰. The average calculated δ34S values are 1.35‰. The total range of δ34S values for pyrite are close to zero suggesting a magmatic source for the sulfur.  相似文献   

10.
Several occurrences of gold-bearing quartz veins are situated along the east–northeast-trending Barramiya–Um Salatit ophiolitic belt in the central Eastern Desert of Egypt. In the Barramiya mine, gold mineralization within carbonaceous, listvenized serpentinite and adjacent to post-tectonic granite stocks points toward a significant role of listvenitization in the ore genesis. The mineralization is related to quartz and quartz–carbonate lodes in silicified/carbonatized wallrocks. Ore minerals, disseminated in the quartz veins and adjacent wallrocks are mainly arsenopyrite, pyrite and trace amounts of chalcopyrite, sphalerite, tetrahedrite, pyrrhotite, galena, gersdorffite and gold. Partial to complete replacement of arsenopyrite by pyrite and/or marcasite is common. Other secondary phases include covellite and goethite. Native gold and gold–silver alloy occur as tiny grains along micro-fractures in the quartz veins. However, the bulk mineralization can be attributed to auriferous arsenopyrite and arsenic-bearing pyrite (with hundreds of ppms of refractory Au), as evident by electron microprobe and LA-ICP-MS analyses.The mineralized quartz veins are characterized by abundant carbonic (CO2 ± CH4 ± H2O) and aqueous-carbonic (H2O–NaCl–CO2 ± CH4) inclusions along intragranular trails, whereas aqueous inclusions (H2O–NaCl ± CO2) are common in secondary sites. Based on the fluid inclusions data combined with thermometry of the auriferous arsenopyrite, the pressure–temperature conditions of the Barramiya gold mineralization range from 1.3 to 2.4 kbar at 325–370 °C, consistent with mesothermal conditions. Based on the measured δ34S values of pyrite and arsenopyrite intimately associated with gold, the calculated δ34SΣs values suggest that circulating magmatic, dilute aqueous-carbonic fluids leached gold and isotopically light sulfur from the ophiolitic sequence. As the ore fluids infiltrated into the sheared listvenite rocks, a sharp decrease in the fluid fO2 via interaction with the carbonaceous wallrocks triggered gold deposition in structurally favorable sites.  相似文献   

11.
Boom Clay is studied as a potential host formation for the disposal of high-and intermediate level long-lived radioactive waste in Belgium. In such a geological repository, generation of gases (mainly H2 from anaerobic corrosion) will be unavoidable. In order to make a good evaluation of the balance between gas generation vs. gas dissipation for a particular waste form and/or disposal concept, good estimates for gas diffusion coefficients of dissolved gases are essential. In order to obtain an accurate diffusion coefficient for dissolved hydrogen in saturated Boom Clay, diffusion experiments were performed with a recently developed through-diffusion set-up for dissolved gases. Due to microbial activity in the test set-up, conversion of hydrogen into methane was observed within several experiments. A complex sterilisation procedure was therefore developed in order to eliminate microbiological disturbances. Only by a combination of heat sterilisation, gamma irradiation and the use of a microbial inhibitor, reliable, reproducible and accurate H2(g) diffusion coefficients (measured at 21 °C) for samples oriented parallel (Deff = 7.25 × 10−10 m2/s and Deff = 5.51 × 10−10 m2/s) and perpendicular (Deff = 2.64 × 10−10 m2/s) to the bedding plane were obtained.  相似文献   

12.
In the Alban Hills area, strong areally diffuse and localised spot degassing processes occur (Tivoli, Cava dei Selci, Solforata, Tor Caldara). The gas comprises a large proportion of CO2, with minor CH4, H2S and Rn. These advective features are generated by fluid leakage from buried reservoirs hosted in the structural highs of the Mesozoic carbonate basement. Gas migration towards the surface is controlled by fault and fracture systems bordering the structural highs of the carbonate formations (e.g. Ciampino high). His release is triggered when the total pressure of the fluid phase exceeds the hydrostatic pressure, thus forming a free gas phase. Furthermore, both the sudden and catastrophic, and slow and continuous gas release at surface, of naturally occurring toxic species (CO2, H2S and Rn) poses a serious health risk to people living in this geologically active area.This paper presents data obtained from soil gas and gas flux surveys, as well as gas isotopes analyses, which suggest the presence of a deep origin gas flux enriched in carbon dioxide and minor species (CH4 and H2S), as well as a channelled migration of geogas mixtures having a Rn component which is not produced in situ.In regards to the health risk to local inhabitants, it was found that some anomalous areas had been zoned as parkland while others had been heavily developed for residential purposes. For example, many new houses were found to have been built on ground which has soil gas CO2 concentrations of over 70% and a CO2 flux of about 0.7 kg m−2 day−1, as well as radon values of more than 250 kBq/m3. In addition, an indoor radon survey has been conducted in selected houses in the town of Cava dei Selci to search for a possible correlation between the local geology and the radon concentration in indoor air. Preliminary results indicate high indoor values at ground floor levels (up to 1000 Bq/m3) and very high values in the cellars (up to 250.000 Bq/m3). It is recommended that land-use planners incorporate soil gas and/or gas flux measurements in the environmental assessment of areas of possible risk (i.e. volcanic or structurally active areas).  相似文献   

13.
Chromophoric dissolved organic matter (CDOM) is an important component in the aquatic environment and plays a key role in light attenuation and in carbon biogeochemical cycles. We examined CDOM production in each of two laboratory experiments in which phytoplankton and macrophyte degradation were monitored using absorption and excitation–emission matrix fluorescence spectroscopy (EEMs). During the incubation period, CDOM was produced from phytoplankton and macrophytes, and partly decomposed by microorganisms. The absorption spectra of the phytoplankton derived and the macrophyte derived CDOM were distinct and characterized by peaks and shoulders in the UV bands. Production of CDOM absorption at 350 nm, a(350), was 0.0125 m2/g per unit of chlorophyll a from phytoplankton CDOM from 0–3 d. Meanwhile a(350) production was 2.708 × 10−4 m2/g per unit of wet biomass from macrophytes CDOM from 1–7 d. Despite the high production of CDOM by phytoplankton and macrophytes, extrapolation of these values to the field indicated that about 15% of total CDOM was produced from phytoplankton during algal blooms in Meiliang Bay in summer and about 8% of total CDOM was produced from macrophytes in the macrophyte dominated littorals. The mean value of the spectral slope (S) describing the exponential decrease of the absorption spectrum, which was strongly correlated to an optical index of molecular size, for the phytoplankton derived CDOM was 10.26 ± 2.05 μm−1, which was significantly lower than the mean S of 14.47 ± 2.88 μm−1 for the macrophyte derived CDOM (t-test, p < 0.001). The mean value of the spectral slope ratio (SR) for the phytoplankton derived CDOM was 1.79 ± 0.52, which was significantly higher than that of 0.35 ± 0.58 for the macrophyte derived CDOM (t-test, p < 0.001). Three fluorescent components were validated in parallel factor analysis (PARAFAC) models calculated separately for phytoplankton derived and macrophyte derived CDOM, each CDOM source resulting in distinct excitation and emission maxima for each component. The significant differences in CDOM absorption spectra, S, SR and PARAFAC fluorescence component characteristics, all showed that phytoplankton derived CDOM was compositionally distinct from macrophyte derived CDOM. Overall both sources were important to the CDOM pool in the shallow temperate lake.  相似文献   

14.
The solubility of gold in aqueous sulphide solutions has been determined from pH20°C ≈ 4 to pH20°C ≈ 9.5 in the presence of a pyrite-pyrrhotite redox buffer at temperatures from 160 to 300°C and 1000 bar pressure. Maximum solubilities were obtained in the neutral region of pH as, for example, with mNaHS = 0.15 m, pH20°C = 5.96, T = 309°C, P = 1000 bar where a gold solubility of 225 mg/kg was obtained. It was concluded that three thio gold complexes contributed to the solubility. The complex Au2(HS)2S2? predominated in alkaline solution, the Au(HS)2? complex occurred in the neutral pH region, and in the acid pH region, it was concluded with less certainty that the Au(HS)° complex was present. Formation constants calculated forAu2(HS)2S2? and Au (HS)2? emphasize their high stability. In the temperature range from 175 to 250°C, values of pβ for Au2(HS)2S2? vary from ?53.0 to 47.9 (±1.6) and from ?23.1 to ?19.5 ( ± 1.5) for Au(HS)2?. Equilibrium constante for the dissolution reactions, Au° + H2S + HS? ? Au(HS)2? + 12H2 and 2Au° + H2S + 2H8? ? Au(HS)2? + H2 vary from pKm = +2.4 to +2.55 (±0.10) for Au2(HS)2S2? and from pKn = + 1.29 to + 1.19 (±0.10) for Au(HS)2? over the temperature range 175 to 250°C. Enthalpies of these dissolution reactions were calculated to be ΔHm° = ?5.2 ±2.0 kcal/mol and ΔHn° = +1.7 ±2.0 kcal/mol respectively. It was concluded that gold is probably transported in hydrothermal ore solutions as both thio and chloro complexes and may be deposited in response to changes in temperature, pressure, pH, oxidation potential of the system and total sulphur concentration.  相似文献   

15.
Five new natural white mica reference materials (RMs) were developed for in situ H2O content analyses by secondary ion mass spectrometry at the SwissSIMS laboratory of Lausanne University, Switzerland. The white mica reference materials cover a large part of the natural muscovite–phengite compositional range and are therefore suitable as reference materials for the analysis of natural rocks as well as individual minerals. The independent H2O content of the reference materials UNIL_WM1 to UNIL_WM5 was obtained by thermal conversion elemental analyser and corresponds to 4.35 ± 0.02, 4.33 ± 0.03, 4.30 ± 0.07, 4.50 ± 0.02 and 4.42 ± 0.11 (% m/m, ± 1s), respectively. SIMS determinations of H2O content revealed a matrix effect correlated to the FeO content of white mica. The compositional range in FeO of the reference materials that were calibrated for H2O determination is from 1.13% to 3.67% m/m. No crystallographic orientation dependency was observed at the level of homogeneity of these reference materials. An analytical precision of 0.02% to 0.08% m/m (1SE) is expected for the final uncertainty on measurements of unknown white micas in natural samples.  相似文献   

16.
The black limestone widely used in Slovenian monuments, particularly in the baroque architecture, is deteriorating extensively due to salt crystallization. Samples of soluble salts from two important historical monuments (in Ljubljana, Slovenia) were investigated in terms of their mineral and isotopic (S and O) compositions. Results revealed the presence of gypsum and soluble salts of the MgSO4·nH2O series, such as starkeyite (MgSO4·4H2O), pentahydrite (MgSO4·5H2O) and hexahydrite (MgSO4·6H2O). Whereas black crusts and subflorescences consisted of gypsum, efflorescences appeared to be an assemblage of gypsum and MgSO4 hydrates. Sample δ18Osulfate values varied from ?1.9‰ to +5.5‰ vs. V-SMOW and δ34Ssulfate values from ?19.8‰ to +3.2‰ vs. V-CDT. The respective isotopic composition of analysed outdoor and indoor monument samples indicated different sources of contamination.  相似文献   

17.
The Mazhuangshan area is located in the east of the Aqikekuduke Island Arc, where there are distributed intermediate-acid magmatic rocks emplaced during the Middle-Late Carboniferous. There are more than 20 orebodies in the area with an average gold grade 6.4 × 10−6 at present. The dominant metallic minerals are natural gold, auriferous silver, natural silver, pyrite and galena. Pyrite is the key gold carrier, high in Fe and low in S. Wall-rock alterations mainly include pyritization, silicification, and sericitization. Carbonation alteration was extensive at the late stage, often resulting in a high-grade orebody. Three mineralization stages may be distinguished. The peak homogenization temperatures of primary fluid inclusions range from 240 to 260°C. Mineralization pressures and depths are 47.2–68.8 MPa and 1.6–2.3 km respectively, showing the ore-forming features of hypergene gold deposit. The average salinity is 15 wt% NaCl equivalent. Fluid inclusion geochemistry data show that Ca2+ is far higher than Mg2+, and mK +/mNa +, mNa2 +/mCa 2+ (0.001∼0.338), mΣCl/mΣS and mΣC/mΣS ratios change with the reduction parameter [R = (CO + CH4)/CO2] and temperature. And the gold contents of ores and gangues are positively correlated withR.  相似文献   

18.
The Córrego do Sítio lineament is defined as a 16-km long, NE-SW-trending ductile shear zones, which controls fourteen gold deposits, including the Carvoaria Velha deposit. The dominant lithotypes of this deposit are metagrewackes with subordinate carbonaceous phyllites lenses of the Archean Rio das Velhas greenstone belt, which host gold mineralization. Metamafic dikes and sills are parallel and crosscut the host metasedimentary sequence. All these rocks exhibit alteration to quartz, carbonate and sericite, besides sulfides and sulfosalts. The main gold mineralization styles at the Carvoaria Velha deposit, and at Córrego do Sítio as a whole, are quartz-carbonate-sulfide ± sulfosalt veins of varied distribution. The veins are classified as: V1 veins – quartz-ankerite-pyrite-berthierite-gold – parallel to the main regional foliation Sn,; V2 veins – quartz-ankerite-pyrite – developed at extensional crenulation cleavage Sn + 1, and rarely gold mineralized; V3 veins – quartz-ankerite – filling Sn + 3 fractures, usually free of sulfides and sulfosalts; V4 veins – quartz-calcite – of restricted occurrence in metamafic dikes and sills. The latter crosscut the metasedimentary sequence, are extensional and display no preferential orientation. The most common ore minerals in all vein types are arsenopyrite, pyrite, berthierite, and pyrrhotite. Microprobe analyses reveal the presence of metallic phases rich in Sb, Pb and Co, such as stibnite, ullmanite, tetrahedrite, galena, cobaltite, which commonly overgrow the sulfides. Fluid inclusion studies trapped in quartz from V1, V2 and V4 veins have identified a H2O-CO2 ± CH4-NaCl mineralizing fluid that may contain KCl, MgCl2 e FeCl2. The presence of CH4 in fluid inclusions of the V1 and V2 veins reflect interaction of the fluid with the Córrego do Sítio and Santa Quitéria carbon-bearing metapelitic host units.Based on the microthermometric data, the hydrothermal fluid is interpreted to have evolved in at least two stages: i) an early fluid stage, trapped in smoky quartz, of moderate salinity (~ 8.5 eq. wt% NaCl), and minimal trapping temperature of 330 ± 17 °C; and ii) a late-stage fluid trapped in recrystallized quartz with lower salinity (~ 4.6 eq. wt% NaCl), and a minimal trapping temperature of 365 ± 33 °C. Isotopic values of δ18Ofluid (+ 7.9 and + 13.0‰), Δ33S (+ 0.3 to + 3.5‰) and δ34S (− 2.9 to + 6.1‰) suggest that indeed the hydrothermal fluid responsible for the gold mineralization at the Carvoaria Velha deposit must have had a metamorphic origin, and interacted with metasedimentary sequences during its ascending path. The addition of CH4 during fluid-rock interaction may have caused some decrease in ƒO2 of the fluid which, as a consequence, destabilized gold-bearing sulfur complexes, liberating S− 2 for the formation of Fe sulfides and sulfosalts (arsenopyrite, pyrite, pyrrothite and berthierite, etc.), and outcome gold deposition.  相似文献   

19.
A simple and inexpensive sampler to measure bedload sediment transport in shallow subtidal or intertidal areas is described. The cylindrical sub-sediment trap with an aspect ratio of 20 (height: diameter) is an improvement over conventional bedload samplers which are difficult to use in shallow areas or fail to collect the biological material associated with bedload. Traps deployed on a low-energy intertidal sandflat for six months provided daily estimates of bedload transport (quartz grains: 0.001–40 kg m?1 d?1), passive infaunal transport (e.g., the bivalveMya arenaria, max: 800 ind m?1 d?1), and organic detrital flux (e.g., macrophyte fragments, max: 400 g dry wt m?1 d?1). Bedload rates estimated with traps were compared to predictions from a numerical bedload model to evaluate the trap’s collection and retention efficiency. A significant linear regression between observed (trap) and predicted (model) rates (r2=0.65, p<0.001, n=97) indicated that the traps were useful for the measurement of high- and low-frequency variability in bedload transport. Potential applications of the traps in benthic oceanography include recruitment and recolonization studies.  相似文献   

20.
Quantifying mercury (Hg) emissions from active volcanoes is of particular interest for better constraining the global cycle and environmental impact of this highly toxic element. Here we report on the abundance of total gaseous (TGM = Hg0(g) + HgII(g)) and particulate (Hg(p)) mercury in the summit gas emissions of La Soufrière andesitic volcano (Guadeloupe island, Lesser Antilles), where enhanced degassing of mixed hydrothermal-magmatic volatiles has been occurring since 1992 from the Southern summit crater. We demonstrate that Hg in volcanic plume occurs predominantly as gaseous mercury, with a mean TGM/Hg(p) mass ratio of ~ 63. Combining the mean TGM/H2S mass ratio of the volcanic plume (~ 3.2 × 10− 6), measured close to the source vent, with the H2S plume flux (~ 0.7 t d− 1), determined simultaneously, allows us to estimate a gaseous mercury emission rate of 0.8 kg yr− 1 from La Soufrière summit dome. Somewhat lower TGM/Stot mass ratio in fumarolic gases from the source vent (4.4 × 10− 7) suggests that plume chemical composition is not well represented by the emission source (fumaroles) due to chemical processes prior to (or upon) discharge. Current mercury emission from La Soufrìere volcano represents a very small contribution to the estimated global volcanic budget for this element.  相似文献   

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