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1.
In the Youngcheon Diversion Tunnel area, South Korea, 46 samples of tunnel seepage water (TSW) and borehole groundwater were collected from areas with sedimentary rocks (mainly sandstone and shale) and were examined for hydrogeochemical characteristics. The measured SO4 concentrations range widely from 7·7 to 942·0 mg/l, and exceed the Korean Drinking Water Standard (200 mg/l) in about half the samples. The TDS (total dissolved solid) content generally is high (171–1461 mg/l) from more shale‐rich formations and also reflects varying degrees of water–rock interaction. The water is classified into three groups: Ca? SO4 type (61% of the samples collected), Ca? SO4? HCO3 type (15%) and Ca? HCO3 type (24%). The Ca? HCO3 type water (mean concentrations=369 mg/l Ca, 148 mg/l HCO3 and 23 mg/l SO4) reflected the simple reaction between CO2‐recharged water and calcite, whereas the more SO4‐rich nature of Ca? SO4 type water (mean concentrations=153 mg/l Ca, 66 mg/l HCO3 and 416 mg/l SO4) reflected the oxidation of pyrite in sedimentary rocks and fracture zones. Pyrite oxidation resulted in precipitation of amorphous iron hydroxide locally within the tunnel as well as in high concentrations of Ca (mean 153 mg/l) and Na (mean 49 mg/l) for TSW, and is associated with calcite dissolution resulting in pH buffering. The pyrite oxidation required for the formation of Ca? SO4 type water was enhanced by the diffusion of oxygenated air through the fractures related to the tunnel's construction. The subsequent outgassing of CO2 into the tunnel resulted in precipitation of iron‐bearing carbonate. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   

2.
Recent models of chemical weathering in alpine glacial meltwaters suggest that sulphide oxidation is a major source of solute in the distributed component of the subglacial hydrological system. This reaction requires O2, and may lower dissolved oxygen levels to below saturation with respect to the atmosphere. This should result in an inverse association between SO72- and dissolved oxygen saturation. However, measurements of O2 saturation in bulk meltwaters draining the Haut Glacier d'Arolla, Switzerland, show that there is a positive association between SO42- and O2 saturation. The O2 content of glacial meltwaters depends on the initial content of snow and icemelt, which may be controlled by the rate of melting, and the kinetic balance between O2 losses (e.g. sulphide oxidation, microbial respiration) and gains (e.g. diffusion of O2 into solution).  相似文献   

3.
莼菜(Brasenia schreberi)冬芽对Cr6+污染的抗性反应   总被引：3，自引：0，他引：3  
研究了Cr^6 污染对Shun菜冬芽外部形态及过氧化物酶、硝酸还原酶活性,叶绿素、O^-2、MDA的含量等生理指标的影响,结果显示：Cr^6 对Shun菜毒害机制在于 制酶活性和损害细胞膜系统,在培养第三天时叶绿素的含量随着Cr^6 浓度的增加而降低;过化物酶的活性在10mg/L中最高;硝酸还原酶活性除在5mg/L中的略微升高外,在10－40mg/L之间随着Cr^6 培养浓度的升高而降低;O^-2的含量在5mg/L中的最高,在10mg/L中略高于对照,在随后培养中承学度的升高而降低,MDA的含量变化趋势和O^-2相似。  相似文献   

4.
Stemflow of beech (Fagus sylvatica L.) represents a significant input of water and elements to the soil and might influence the spatial patterns and the rate of seepage fluxes at the stand scale. We investigated the soil solution chemistry at different depths and distances from the stem and the element fluxes with stemflow, throughfall and seepage in proximal and distal stem areas of a 130‐year‐old beech/oak forest in Steigerwald (northern Bavaria, Germany). The proximal stem area (in total 286 m2 ha−1) was defined as a 1 m2, 60 cm deep cylinder around the beech stem. Seepage fluxes were calculated by a soil hydrological model for 1996 using measured soil matrix potentials and tree xylem flow data for calibration. Stemflow represented 6·6% of the annual soil water input. With the exception of H+ fluxes, less than 10% of the total element fluxes with throughfall and stemflow reached the soil via stemflow. The volume‐weighted concentrations of H+, K+ and SO42− in stemflow were higher than those in throughfall, while other elements had similar concentrations. Soil solution K+ concentrations decreased with stem distance, but the Na+, Mg2+, Cl− and SO42− concentrations increased. Gradients for other elements were not statistically significant. Stemflow had a strong influence on the spatial patterns of element fluxes with seepage. The water fluxes through the soil of the proximal stem areas at a depth of 60 cm contributed 13·5% to the total seepage at the stand scale. Proximal to the stems about 20% of total seepage for K+, Mn2+, Aln+, dissolved organic N and dissolved organic C were concentrated, but only 8–10% for Na+, Mg2+ and Ca2+. The loss of acid‐neutralizing capacity calculated from the flux balance was about four times higher proximal to the stems compared with distal areas, indicating high rates of soil acidification proximal to the stems. Our results confirm the concept of a microsite around beech stems, characterized by high element and water fluxes in comparison with distal stem areas. Calculations of seepage fluxes and element budgets in beech stands have to consider the spatial heterogeneity of fluxes induced by stemflow. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

5.
Samples from the surface of lava flows discharged by the 2012–2013 Tolbachik Fissure Eruption were found to contain oxysulfates of copper, sodium, and potassium: K2Cu3O(SO4)2 (fedotovite), NaKCu2O(SO4)2, and Na3K5Cu8O4(SO4)8. The last two phases have no naturally occurring or synthetic analogues that we are aware of. They form flattened crystals of prismatic to long-prismatic habits. The crystals of Na3K5Cu8O4(SO4)8 have a chemical composition corresponding to the empirical formula Na2.22K5.47Cu8.02S8.05O36. An X-ray analysis of this compound showed that it has a monoclinic symmetry, P2/c, a = 13.909(4), b = 4.977(1), c = 23.525(6) Å, β = 90.021(5)°, V = 1628.3(7) Å3. The crystal structure was determined by direct techniques and refined to yield R 1 for 3955 reflexes//web// with F 2 > 4σF. The compound NaKCu2O(SO4)2 also belongs to the monoclinic system, P2/c, a = 14.111(4), b = 4.946(1), c = 23.673(6) Å, β = 92.052(6)°, V = 1651.1(8) Å3. The structure was determined by direct techniques to yield a tentative structural model that has been refined up to R 1 = 0.135 for 4088 reflexes with F 2 > 4σF. The crystal structure of Na3K5Cu8O4(SO4)8 is based on chains of [O2Cu4]4+ consisting of rib-coupled oxy-centered tetrahedrons of (OCu4)6+. The chains are surrounded by sulfate radicals, resulting in columns of {[O2Cu4](SO4)4}4? aligned along the b axis. The interchain space contains completely ordered positions of Na+ and K+ cations. The principle underlying the connection of NaKCu2O(SO4)2 columns in the crystal structure of {[O2Cu4](SO4)4}4? is different, in view of the relation Na:K = 1 as contrasted with 3:5 for the compound Na3K5Cu8O4(SO4)8. The presence of oxy-centered tetrahedrons in the structure of these new compounds furnishes an indirect hint at the importance of polynuclear copper-oxygen radicals with centering oxygen atoms as forms of transport of copper by volcanic gases.  相似文献   

6.
Surface waters associated with peatlands, supersaturated with CO2 and CH4 with respect to the atmosphere, act as important pathways linking a large and potentially unstable global repository of C to the atmosphere. Understanding the drivers and mechanisms which control C release from peatland systems to the atmosphere will contribute to better management and modelling of terrestrial C pools. We used non‐dispersive infra‐red (NDIR) CO2 sensors to continuously measure gas concentrations in a beaver pond at Mer Bleue peatland (Canada); measurements were made between July and August 2007. Concentrations of CO2 in the surface water (10 cm) reached 13 mg C l?1 (epCO2 72), and 26 mg C l?1 (epCO2 133) at depth (60 cm). The study also showed large diurnal fluctuations in dissolved CO2 which ranged in amplitude from ～1·6 mg C l?1 at 10 cm to ～0·2 mg C l?1 at 60 cm depth. CH4 concentration and supersaturation (epCH4) measured using headspace analysis averaged 1·47 mg C l?1 and 3252, respectively; diurnal cycling was also evident in CH4 concentrations. Mean estimated evasion rates of CO2 and CH4 over the summer period were 44·92 ± 7·86 and 0·44 ± 0·25 µg C m?2s?1, respectively. Open water at Mer Bleue is a significant summer hotspot for greenhouse gas emissions within the catchment. Our results suggest that CO2 concentrations during the summer in beaver ponds at Mer Bleue are strongly influenced by biological processes within the water column involving aquatic plants and algae (in situ photosynthesis and respiration). In terms of carbon cycling, soil‐stream connectivity at this time of year is therefore relatively weak. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

7.
The trajectory of the North Atlantic Deep Water is traced from 65°N to 20°N latitude. Along this track the dissolved O2 decreases, theδ18O of the dissolved O2 increases, and the14C content of the water decreases. From these observations the rate of in-situ O2 utilization in the deep water is calculated to be 0.10 μmol kg?1 yr?1. As was observed previously in the Pacific, theδ18O data presented here indicate that the utilization is probably caused by bacterial respiration. Carbon dioxide is being added to the water at the rate of 0.07 μmol kg?1 yr?1 from the oxidation of this organic matter. An additional 0.12 μmol kg?1 yr?1 of CO2 is derived from the dissolution of particles of CaCO3.  相似文献   

8.
The conductivity of four igneous rocks with, 49, 65, 77, and 84% SiO2 was measured as a function of temperature in the interval from 20° to 1280°C; measurements were made in a vacuum of 10?3 torr. No simple relationships were found between conductivity and SiO2 content or versus major element groupings such as Na2O=K2O=CaO and TiO2=Cr2O3=Al2O3=Fe2O3=FeO. An analytical expression was obtained between conductivity and the albite-quartz ratio, valid for temperatures between 300° and 1200°C. It was necessary to compute the CIPW norm in order to obtain the albite and quartz percentages. The onset of melting apparently occurred between 600° and 700°C. Petrography performed on two samples after cooling showed 70 and 85% partial melting. Three conduction regions were identified: 1) below 300°C, 2) between 300°C and 600°C, and 3) above 600°C. Different activation energies obtained for the heating and cooling intervals confirm that the sample undergoes textural changes in the heating-cooling cycle. Activation energy increments of 0.1 and 0.2 eV per decade of albite-quartz ratio were obtained.  相似文献   

9.
Permian coal measure sandstone fissure water (referred to as “coal measure water,” that is, water in coal measures) is one of the important water sources for industrial and agricultural activities in mining areas. However, the regional high-pressure grouting, one of the most widely used floor control methods, may affect the coal measure water which is connected with limestone aquifer. This study used Taoyuan mine, a typical coal mine in Huaibei coalfield, as the research area to study the influencing mechanism of a grouting treatment on the hydrogeochemical evolution of coal measure water. The hydrogeochemical characteristics and water-rock interaction mechanism of the coal measure water before and during the treatment were evaluated using a Piper trigram, ion combination ratio, and hydrogen-oxygen stable isotope. The anions and cations in the coal measure water before and during the treatment had the same trends at SO42− > HCO3− > Cl− and Na+ > Ca2+ > Mg2+, respectively. Hydrochemical types of coal measure water before treatment were mainly SO4·Cl-Ca·Mg, SO4·Cl-Na, and HCO3-Na, and during treatment they were mainly SO4·Cl-Na and HCO3-Na. The formation of chemical components of coal measure water before treatment was mainly caused by carbonate dissolution, sulfate dissolution, and pyrite oxidation. During the treatment, sulfate dissolution and pyrite oxidation were the main geochemical processes, and ion exchange was enhanced. Atmospheric precipitation was the source of all water samples, and all showed an obvious 18O drift.  相似文献   

10.
Concerns related to climate change have resulted in an increasing interest in the importance of hydrological events such as droughts in affecting biogeochemical responses of watersheds. The effects of an unusually dry summer in 2002 had a marked impact on the biogeochemistry of three watersheds in the north‐eastern USA. Chemical, isotopic and hydrological responses with particular emphasis on S dynamics were evaluated for Archer Creek (New York), Sleepers River (Vermont) and Cone Pond (New Hampshire) watersheds. From 1 August to 14 September 2002, all three watersheds had very low precipitation (48 to 69 mm) resulting in either very low or no discharge (mean 0·015, 0·15 and 0·000 mm day?1 for Archer Creek, Sleepers River and Cone Pond, respectively). From 15 September to 31 October 2002, there was a substantial increase in precipitation totals (212, 246 and 198 mm, respectively) with increased discharge. Archer Creek was characterized by a large range of SO42? concentrations (152 to 389 µeq L?1, mean = 273 µeq L?1) and also exhibited the greatest range in δ34S values of SO42? (?1·4 to 8·8 ‰ ). Sleepers River's SO42? concentrations ranged from 136 to 243 µeq L?1 (mean = 167 µeq L?1) and δ34S values of SO42? ranged from 4·0 to 9·0 ‰ . Cone Pond's SO42? concentrations (126–187 µeq L?1, mean = 154 µeq L?1) and δ34S values (2·4 to 4·3 ‰ ) had the smallest ranges of the three watersheds. The range and mean of δ18O‐SO42? values for Archer Creek and Cone Pond were similar (3·0 to 8·9 ‰ , mean = 4·5 ‰ ; 3·9 to 6·3 ‰ , mean = 4·9 ‰ ; respectively) while δ18O‐SO42? values for Sleepers River covered a larger range with a lower mean (1·2 to 10·0 ‰ , mean = 2·5). The difference in Sleepers River chemical and isotopic responses was attributed to weathering reactions contributing SO42?. For Archer Creek wetland areas containing previously reduced S compounds that were reoxidized to SO42? probably provided a substantial source of S. Cone Pond had limited internal S sources and less chemical or isotopic response to storms. Differences among the three watersheds in S biogeochemical responses during these storm events were attributed to differences in S mineral weathering contributions, hydrological pathways and landscape features. Further evaluations of differences and similarities in biogeochemical and hydrological responses among watersheds are needed to predict the impacts of climate change. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

11.
Solute concentrations and fluxes in rainfall, throughfall and stemflow in two forest types, and stream flow in a 90 ha catchment in southern Chile (39°44′S, 73°10′W) were measured. Bulk precipitation pH was 6·1 and conductivity was low. Cation concentrations in rainfall were low (0·58 mg Ca2+ l?1, 0·13 mg K+ l?1, 0·11 mg Mg2+ l?1 and <0·08 mg NH4–N l?1), except for sodium (1·10 mg l?1). Unexpected high levels of nitrate deposition in rainfall (mean concentration 0·38 mg NO3–N l?1, total flux 6·3 kg NO3–N ha?1) were measured. Concentrations of soluble phosphorous in bulk precipitation and stream flow were below detection limits (<0·09 mg l?1) for all events. Stream‐flow pH was 6·3 and conductivity was 28·3 μs. Stream‐water chemistry was also dominated by sodium (2·70 mg l?1) followed by Ca, Mg and K (1·31, 0·70 and 0·36 mg l?1). The solute budget indicated a net loss of 3·8 kg Na+ ha?1 year?1, 5·4 kg Mg2+ ha?1 year?1, 1·5 kg Ca2+ ha?1 year?1 and 0·9 kg K+ ha?1 year?1, while 4·9 kg NO3–N ha?1 year?1 was retained by the ecosystem. Stream water is not suitable for domestic use owing to high manganese and, especially, iron concentrations. Throughfall and stemflow chemistry at a pine stand (Pinus radiata D. Don) and a native forest site (Siempreverde type), both located within the catchment, were compared. Nitrate fluxes within both forest sites were similar (1·3 kg NO3–N ha?1 year?1 as throughfall). Cation fluxes in net rainfall (throughfall plus stemflow) at the pine stand generally were higher (34·8 kg Na+ ha?1 year?1, 21·5 kg K+ ha?1 year?1, 5·1 kg Mg2+ ha?1 year?1) compared with the secondary native forest site (24·7 kg Na+ ha?1 year?1, 18·9 kg K+ ha?1 year?1 and 4·4 kg Mg2+ ha?1 year?1). However, calcium deposition beneath the native forest stand was higher (15·9 kg Ca2+ ha?1 year?1) compared with the pine stand (12·6 kg Ca2+ ha?1 year?1). Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

12.
Zoned spinel of unusual composition and morphology has been found in massive pyrrhotite-chalcopyrite-pent-landite ore from the La Perouse layered gabbro intrusion in the Fairweather Range, southeastern Alaska. The spinel grains show continuous zoning from cores with up to 53 wt.% Cr2O3 to rims with less than 11 wt.% Cr2O3. Their composition is exceptional because they contain less than 0.32 wt.% MgO and less than 0.10 wt.% Al2O3 and TiO2. Also notable are the concentrations of MnO and V2O3, which reach 4.73 and 4.50 wt.%, respectively, in the cores. The spinel is thought to have crystallized at low oxygen fugacity and at temperatures above 900°C, directly from a sulfide melt that separated by immiscibility from the gabbroic parental magma.  相似文献   

13.
This review summarizes direct and indirect analytical methods for the detection and quantification of the reactive oxygen species (ROS): 1O2, O 2 ·? /HOO·, H2O2, HO·, and CO 3 ·? in aqueous solution. Each section briefly describes the chemical properties of a specific ROS followed by a table (organized alphabetically by detection method, i.e., absorbance, chemiluminescence, etc.) summarizing the nature of the observable (associated analytical signal) for each method, limit of detection, application notes, and reaction of the probe molecule with the particular ROS.  相似文献   

14.
The use of loose spoils on steep slopes for surface coal mining reclamation sites has been promoted by the US Department of Interior, Office of Surface Mining for the establishment of native forest, as prescribed by the Forest Reclamation Approach (FRA). Although low‐compaction spoils improve tree survival and growth, erodibility on steep slopes was suspected to increase. This study quantified a combined KC factor (combining the effects of the soil erodibility K factor and cover management C) for low compaction, steep‐sloped (>20°) reclaimed mine lands in the Appalachian region, USA. The combined KC factor was used because standard Unit Plot conditions required to separate these factors, per Revised Universal Soil Loss Equation (RUSLE) experimental protocols, were not followed explicitly. Three active coal mining sites in the Appalachian region of East Tennessee, each containing four replicate field plots, were monitored for rainfall and sediment yields during a 14‐month period beginning June 2009. Average cumulative erosivity for the study sites during the monitoring period was measured as 5248.9 MJ·mm·ha?1·h?1. The KC ranged between 0.001 and 0.05 t·ha·h·ha?1·MJ?1·mm?1, with the highest values occurring immediately following reclamation site construction as rills developed (June – August 2009). The KC for two study sites with about an 18–20 mm spoil D84 were above 0.01 t·ha·h·ha?1·MJ?1·mm?1 during rill development, and below 0.003 t·ha·h·ha?1·MJ?1·mm?1 after August 2009 for the post‐rill development period. The KC values for one site with a 40 mm spoil D84 were never above 0.008 t·ha·h·ha?1·MJ?1·mm?1 and also on average were lower, being more similar to the other two sites after the rill development period. Based on an initial KC factor (Ke) measured during the first few storm events, the average C factor (Ce) was estimated as 0.58 for the rill development period and 0.13 for the post‐rill development period. It appears that larger size fractions of spoils influence KC and Ce factors on low‐compaction steep slopes reclamation sites. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

15.
The contents of Ni and Cr in sewage sludge with high and low amounts of heavy metals were investigated by polarography. The DIN-digestion (aqua regia) was used, and the resulting solution was treated with H2O2/UV (90 °C, 60 min) for further destroying of the organic material. Besides, the solution of the DIN-digestion was examined with AAS (flame) and ICP-OES. With the determination of Ni it was shown that after digestion with aqua regia no further treatment with H2O2/UV is necessary. Contrariwise it was found that for the determination of Cr a H2O2/UV photolysis is necessary followed by further steps to get good agreement with AAS and ICP results as well as with the certified values of a sludge of the Community Bureau of Standards.  相似文献   

16.
G. Stamatis  E. Gartzos 《水文研究》1999,13(17):2833-2845
The area of north Evia and eastern central Greece is characterized by strong geomorphological contrast and is built up mainly of consolidated rocks. Unconsolidated young sediments of Pleistocene to Holocene age cover the valley and basin flats, forming the most productive aquifers in this area. However, two more types of aquifers can be distinguished within the consolidated rock area. The first one is associated with karstified limestones and the second with strongly tectonized ultramafic rocks. The schist–chert formation, with intercalations of shales and cherts, seals the ultramafic masses underneath. Surface and spring waters associated with ultramafic rocks in north Evia and eastern central Greece were studied. Two types of water can be distinguished: (1) high Mg2+ and SiO2 , bicarbonate as the dominant anion, pH 7·4–9·2, temperature 9·5–16·3 °C, low TDS (total dissolved solutes) (459–1037 mg/l), found both in peridotite and serpentinite areas, classified as Mg–HCO3 type; (2) high Ca2+, low Mg2+ and SiO2 , hydroxyl ion as the major anion, pH 11·2, temperature 28 °C, very low TDS (122 mg/l), found in peridotite areas, classified as Ca–OH type. The studied waters are highly supersaturated with respect to quartz, amorphous silica, brucite and most low temperature magnesium silicates (antigorite, sepiolite, talc, etc.). These waters show relatively narrow SiO2 concentration ranges and a trend parallel to the amorphous silica saturation surface. The silica supersaturated waters have the potential to precipitate silica and consequently could affect the people of the local communities that use it as drinking water, causing health problems (kidney stones). Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

17.
Atmospheres of different oxidation potentials were used to equilibriate samples at 1300°C starting with a stoichiometric composition xFe2TiO4·(1 ? x) Fe3O4 where x = 0.3 and 0.6. Samples were selected which appeared homogeneous in polished section and gave only spinel-type X-ray reflections. All specimens were found to have small amounts of included material of higher Curie point than the bulk material. Specimens were made by dispersing grains of known size in a non-magnetic matrix and the hysteresis properties were measured for these speciméns.  相似文献   

18.
Fred Worrall  Tim Burt 《水文研究》2005,19(9):1791-1806
The dissolved CO2 concentration of stream waters is an important component of the terrestrial carbon cycle. This study reconstructs long‐term records of dissolved CO2 concentration for the outlets of two large catchments (818 and 586 km2) in northern England. The study shows that:
  • 1. The flux of dissolved CO2 from the catchments (as carbon per catchment area), when adjusted for that which would be carried by the river water at equilibrium with the atmosphere, is between 0 and 0·39 t km−2 year−1 for the River Tees and between 0 and 0·65 t km−2 year−1 for the River Coquet.
  • 2. The flux of dissolved CO2 is closely correlated with dissolved organic carbon (DOC) export and is unrelated to dissolved CO2 export from the headwaters of the study catchments.
  • 3. The evasion rate of CO2 from the rivers (as carbon per stream area) is between 0·0 and 1·49 kg m−2 year−1, and calculated in‐stream productions of CO2 are estimated as between 0·5 and 2·5% of the stream evasion rate.
  • 4. By mass balance, it is estimated that 8% of the annual flux of DOC is lost within the streams of the catchment.
The study shows that the loss of CO2 from the streams of the Tees catchment is between 3·1 and 7·5 kt year−1 (as carbon) for the River Tees, which is the same order as annual CH4 flux from peats within the catchment and approximately 50% of the net CO2 exchange to the peats of the catchment. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

19.
Samples from Kawah Ijen crater lake, spring and fumarole discharges were collected between 1990 and 1996 for chemical and isotopic analysis. An extremely low pH (<0.3) lake contains SO4–Cl waters produced during absorption of magmatic volatiles into shallow ground water. The acidic waters dissolve the rock isochemically to produce “immature” solutions. The strong D and 18O enrichment of the lake is mainly due to enhanced evaporation at elevated temperature, but involvement of a magmatic component with heavy isotopic ratios also modifies the lake D and 18O content. The large ΔSO4–S0 (23.8–26.4‰) measured in the lake suggest that dissolved SO4 forms during disproportionation of magmatic SO2 in the hydrothermal conduit at temperatures of 250280°C. The lake δ18OSO4 and δ18OH2O values may reflect equilibration during subsurface circulation of the water at temperatures near 150°C. Significant variations in the lake's bulk composition from 1990 to 1996 were not detected. However, we interpret a change in the distribution and concentration of polythionate species in 1996 as a result of increased SO2-rich gas input to the lake system.Thermal springs at Kawah Ijen consist of acidic SO4–Cl waters on the lakeshore and neutral pH HCO3–SO4–Cl–Na waters in Blawan village, 17 km from the crater. The cation contents of these discharges are diluted compared to the crater lake but still do not represent equilibrium with the rock. The SO4/Cl ratios and water and sulfur isotopic compositions support the idea that these springs are mixtures of summit acidic SO4–Cl water and ground water.The lakeshore fumarole discharges (T=170245°C) have both a magmatic and a hydrothermal component and are supersaturated with respect to elemental sulfur. The apparent equilibrium temperature of the gas is 260°C. The proportions of the oxidized, SO2-dominated magmatic vapor and of the reduced, H2S-dominated hydrothermal vapor in the fumaroles varied between 1979 and 1996. This may be the result of interaction of SO2-bearing magmatic vapors with the summit acidic hydrothermal reservoir. This idea is supported by the lower H2S/SO2 ratio deduced for the gas producing the SO4–Cl reservoir feeding the lake compared with that observed in the subaerial gas discharges. The condensing gas may have equilibrated in a liquid–vapor zone at about 350°C.Elemental sulfur occurs in the crater lake environment as banded sediments exposed on the lakeshore and as a subaqueous molten body on the crater floor. The sediments were precipitated in the past during inorganic oxidation of H2S in the lake water. This process was not continuous, but was interrupted by periods of massive silica (poorly crystallized) precipitation, similar to the present-day lake conditions. We suggest that the factor controlling the type of deposition is related to whether H2S- or silica-rich volcanic discharges enter the lake. This could depend on the efficiency with which the lake water circulates in the hydrothermal cell beneath the crater. Quenched liquid sulfur products show δ34S values similar to those found in the banded deposits, suggesting that the subaqueous molten body simply consists of melted sediments previously accumulated at the lake bottom.  相似文献   

20.
Pore water has been extracted from Boom Clay by mechanical squeezing. Clay cores were obtained from various boreholes, all drilled at the SCK·CEN domain (Mol, Belgium).In contrast to pore water collected from piezometers, high sulphate concentrations are measured in the squeezed pore water. The lowest sulphate concentrations (<60 mg/l) were measured in pore waters squeezed immediately after drilling. Higher sulphate concentrations were often measured in the pore water when the clay cores were preserved for some time (generally <500 mg/l SO42−, but sometimes up to 20,000 mg/l SO42−). Nevertheless, a relation between preservation time and sulphate content could not be retrieved. However, major ion concentrations were obviously correlated with the sulphate content in the squeezed waters. The observed evolution in chemical composition were explained by water–rock interactions considering the pyrite oxidation and the subsequent ion exchange and mineral dissolution reactions.  相似文献   

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