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1.
《Acta Geochimica》2017,(4)
While it is critical to accurately understand the sources and transformation of sulfate based on time-series analysis, there are limited studies on temporal variation of sulfate in rivers and on rock weathering by sulfuric acids.We conducted a monthly sampling campaign in the Beipan, Nanpan, and Hongshui Rivers over the course of one hydrological year. This study examined seasonal variations in riverine sulfate impacted by the monsoon climate in the upper reaches of the Xijiang River basin. In general, the SO_4~(2-) contents in these rivers dropped from relatively high levels to low values during the high-flow season, in response to increasing discharge. The sulfate was generally enriched in heavy isotopes during the low-flow season compared to the high-flow season. The calculated results indicate that the riverine sulfate was mainly derived from sulfide oxidation, but that evaporite dissolution could be an important source during the low-flow season, based on isotopic evidence. Mine drainage is likely an important source of sulfate to these rivers during the high-flow season due to contributions from fast surface flow, which responds to frequent heavy rain in monsoonal climate regions. Arelatively high proportion of HCO_3~- was found to be derived from rock weathering by sulfuric acid during the high-flow season when compared to that observed during the low-flow season. The results suggest that approximately one quarter of the HCO_3~- in the Hongshui River originated from carbonate weathering by sulfuric acid derived from the oxidation of sulfide. Such information on the specific dual isotopic characteristics of riverine sulfate throughout a hydrological year can provide unique evidence for understanding the temporal variability of sulfate concentrations and weathering processes in rivers. 相似文献
2.
Sulphur isotopic compositions of pyrite, anhydrite and native sulphur in volcanic ashes discharged by the 1979 eruption of Ontake volcano, Nagano, Japan were determined. The isotopic data indicate that sulphate in anhydrite and a part of native sulphur were produced by the disproportionation reaction of sulphite formed by dissolution of SO2 in volcanic gases into water which filled a mud reservoir probably located just below the crater zone. Some part of H2S in volcanic gases was fixed as pyrite and some was oxidised to form native sulphur. Hydrothermal alteration of country rocks to form pyrite, anhydrite and clay minerals had proceeded in the mud reservoir before eruption at temperatures ranging from 110° to 185°C which were estimated by oxygen isotopic fractionation between anhydrite and water.
相似文献3.
Mass balance studies in forested catchments in the northeastern USA show that S losses via streamwater SO42? exceed measured atmospheric S inputs. Possible sources of the excess S loss include underestimated dry deposition, mineralization of organic S in soils, desorption of soil sulphate, oxidation of recently formed sulphides and mineral weathering. Evaluating the relative contribution of these sources and processes to SO42? export is important to our understanding of S cycling as well as to policy makers in their evaluation of the efficacy of S emission controls. In order to evaluate the potential for mineral weathering contributions to SO42? export, we measured concentration and isotopic composition (δ34S and δ18O) of SO42? in stream water, and concentration and δ34S values of four S fractions in bedrock and soil parent material in catchments of varying geological composition. Geological substrates with low S concentrations were represented by catchments underlain by quartzite and granite, whereas geological substrates with high S concentrations were represented by catchments underlain by sulphidic slate, schist and metavolcanic rocks. Catchments with S‐poor bedrock had stream‐water SO42? concentrations <100 µeq L?1 and isotopic values consistent with those of atmospheric SO42? that had been cycled through the organic soil pool. Catchments with S‐rich bedrock had stream‐water SO42? concentrations ranging from 56 to 229 µeq L?1. Isotopic values deviated from those of SO42? in atmospheric deposition, clearly indicating a mineral weathering source in some cases, whereas in others spatial variability of mineral δ34S values precluded the isotopic detection of a weathering contribution. These results, along with evidence suggesting formation of secondary sulphate minerals in bedrock weathering rinds, indicate that mineral weathering may be an important source of S in the surface waters of some forested catchments in the northeastern USA. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
4.
藏南羊卓雍错流域水化学主离子特征及其控制因素 总被引：14，自引：1，他引：13
水化学主离子特征是流域湖泊的一个重要特征,对气候以及河流所经地区的环境具有指示作用.本文对藏南羊卓雍错流域水化学主离子组成特征及其控制因素进行分析,结果显示流域内不同水体(湖水、河水、地下水)之间的主离子组成以及水化学类型差异显著.其中,羊卓雍错的水化学类型为SO24--HCO3--Mg2+-Na+,巴纠错为SO24--Mg2+-Na+,沉错为SO24--Na+-Mg2+-Ca2+,普莫雍错为HCO3--SO24--Mg2+-Ca2+,空姆错为HCO3--SO24--Ca2+;流域河水中主要阴离子为HCO3-和SO24-,Ca2+为绝对优势阳离子;流域地下水化学类型则为HCO3--Ca2+.究其原因,流域水体化学组成主要受岩石风化作用控制;除此,羊卓雍错、巴纠错和沉错水化学组成亦受自身蒸发-结晶作用的影响.就入湖河水而言,羊卓雍错入湖河水整体受碳酸盐岩石风化的影响较大,蒸发岩溶解的影响次之;沉错和空姆错入湖河流(卡鲁雄曲)的蒸发岩来源则略大于碳酸盐岩来源;而硅酸盐对流域内河水的水化学性质影响较小.与入湖河水相比,羊卓雍错和沉错湖水的Mg2+、Na+和SO24-含量较高,而Ca2+和HCO3-含量较低.这应该与湖水蒸发强烈使得湖水中Ca2+和HCO3-析出并沉积到湖底有关.而空姆错由于湖泊面积小、入湖河水流量大,致使其湖水与入湖河水的主离子组成差异不显著. 相似文献
5.
A reaction set of possible mineral weathering reactions is proposed to explain observed cation and silica export for the Emerald Lake watershed, a small Sierra Nevada, California catchment. The reaction set was calculated through a stoichiometric mole‐balance method, using a multiyear record of stream flow and snowpack chemical analyses and site‐specific mineral compositions. Reaction‐set calculations were intended to explore how the processes controlling stream cation and silica export depend on differing bedrock mineralogy across the catchment as snowmelt and runoff patterns change over the year. Different regions within the watershed can be differentiated by lake inflow subdrainages, each exhibiting different stream‐flow chemistry and calculated weathering stoichiometry, indicating that different silica and cation generation processes are dominant in wet steep portions of the catchment. Short‐term differences in stream concentrations were assumed to reflect ion exchange equilibria and rapid biological processes, whereas long‐term persistent stream concentration differences in different areas of the catchment were assumed to reflect spatial variability in mineral weathering stoichiometry. Mineralogical analyses of rock samples from the watershed provided site‐specific chemical compositions of major mineral species for reaction calculations. Reaction sets were evaluated by linear regression of calculated versus observed differences between snowmelt and stream‐flow chemistry and by a combined measure. Initially, single weathering reactions were balanced and evaluated to determine the reactions that best explained observed stream chemical export. Next, reactions were combined, using mineral compositions from different rock types to estimate the dependence of ion fluxes on lithology. The seasonal variability of major solute calculated fluxes is low, approximately one order of magnitude, relative to the observed three orders of magnitude variability in basin discharge. Reaction sets using basin‐averaged lithology and Aplite lithologies gave superior explanations of stream chemical composition. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
6.
Within the hydrologic balance of the River Arno catchment (northern Tuscany), the Rivers Elsa and Era are important tributaries entering the main river from the left bank in the lower part of the watershed. Waters and bed sediments were sampled in June 2000 during low discharges in the Rivers Elsa and Era, as well as in major tributary streams. Water samples were analysed for major chemistry and sulphur isotope composition of sulphate, and sediment samples were analysed for major composition and selected trace elements of environmental concern (Zn, Cu, Pb, Cr and Ni). The main results for the waters are: (1) Na and Cl in solution show consistent downstream positive trends in the main rivers, thus supporting progressive contributions of anthropogenic salts; the highest concentration values are observed in tributaries; (2) as shown by sulphur isotopes, sulphate in solution is mainly controlled by dissolution of evaporites (Elsa basin) or oxidation of reduced organic/biogenic sulphur (Era basin), with anthropogenic contributions in most streams not higher than 10% in both the basins. A δ34S signature in the range ?2 to +3‰ is estimated for pollutant sulphate in the basins studied. The main results for the sediments are: (1) major chemistry is essentially controlled by the lithotypes drained by the waters; (2) pollution by heavy metals does not reach high levels; (3) compared with local fine‐grained rocks, copper is more frequently anomalous, whereas lead and zinc show only occasional anomalies; (4) local high concentrations of chromium and nickel can be attributed to upstream occurrences of ophiolites. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
7.
Abstract The variation of sulphur isotopic composition during the 2000 eruption of the Miyakejima Volcano was examined in order to monitor the temporal change of the volcanic activity. The δ34 S values of water-soluble sulphate leached from volcanic ash effused during intermittent eruptions from July to September 2005 range from +5 to +11‰ with a fluctuation of ca 3‰ within a single eruption. The δ34 S value of sulphuric acid mist collected with 'Cu-metal trap' placed on the flank of the volcano from December 2000 to January 2001 is +6.2‰. These sulphur isotopic compositions of sulphate, which were isotopically equilibrated in the subvolcanic hydrothermal system, indicate that the temperature of the hydrothermal system beneath the caldera increased after the period of intermittent phreatic and phreatomagmatic eruptions. Then, the δ34 S value of sulphuric acid trapped from January to March 2001 was +9.0‰ and the δ34 S value of water-soluble sulphate on volcanic ash emitted with minor eruption in May 2001 was +11.0‰, suggesting a decrease in temperature of the subvolcanic hydrothermal system. 相似文献
8.
87Sr/86Sr ratios of ground waters in the Bighorn and Laramie basins' carbonate and carbonate-cemented aquifer systems, Wyoming, United States, reflect the distinctive strontium isotope signatures of the minerals in their respective aquifers. Well water samples from the Madison Aquifer (Bighorn Basin) have strontium isotopic ratios that match their carbonate host rocks. Casper Aquifer ground waters (Laramie Basin) have strontium isotopic ratios that differ from the bulk host rock; however, stepwise leaching of Casper Sandstone indicates that most of the strontium in Casper Aquifer ground waters is acquired from preferential dissolution of carbonate cement. Strontium isotope data from both Bighorn and Laramie basins, along with dye tracing experiments in the Bighorn Basin and tritium data from the Laramie Basin, suggest that waters in carbonate or carbonate-cemented aquifers acquire their strontium isotope composition very quickly--on the order of decades. Strontium isotopes were also used successfully to verify previously identified mixed Redbeds-Casper ground waters in the Laramie Basin. The strontium isotopic compositions of ground waters near Precambrian outcrops also suggest previously unrecognized mixing between Casper and Precambrian aquifers. These results demonstrate the utility of strontium isotopic ratio data in identifying ground water sources and aquifer interactions. 相似文献
9.
Abstract In the temperate and semiarid environment the salinity of both surface and subsurface (meteoric) waters is dominated by the weathering products of soil and aquifer minerals, since even surface waters have a history of subsurface flow. In the desert environment, in contrast, surface flows are more superficial and their chemistry dominated by the aeolian salinity. This has both a marine input and a contribution from recycled salinity from surface accumulation of evaporitic minerals. Both these sources have chloride (and to a lesser extent sulphate) as the dominant anion. 相似文献
10.
Strontium (Sr) concentrations and isotopic ratios have been measured in a series of water and rock samples from most of the major tributaries of the Lake Qinghai basin on the north‐eastern Tibetan Plateau. Dissolved Sr and 87Sr/86Sr show ranges of 488–12 240 nmol/l and 0·710497–0·716977, respectively. These data, together with measurements of major cations and anions in rivers and their tributaries and various lithologies of the catchment, were used to determine the contributions of Sr and its isotopic expense to rivers and lakes. Our results demonstrate that the chemical components and 87Sr/86Sr ratios of the alkaline waters are derived from mixing of carbonate and silicate sources, with the former contributing 72 ± 18% dissolved Sr to rivers. The difference in tributary compositions stems from the lithology of different river systems and low weathering intensity under a semi‐arid condition. Variation in 87Sr/86Sr ratios places constraint on the Sr‐isotopic compositions of the main tributaries surrounding Lake Qinghai. The water chemistry of the Buha River, the largest river within the catchment underlain by the late Paleozoic marine limestone and sandstones, dominates Sr isotopic composition of the lake water, being buffered by the waters from the other rivers and probably by groundwater. However, the characteristic chemical composition of the lake itself differs remarkably from the rivers, which can be attributed to precipitation of authigenic carbonates (low‐magnesium calcite, aragonite, and dolomite), though this does not impact the Sr isotope signature, which may remain a faithful indicator in paleo‐records. Regarding the potential role of groundwater input within the Lake Qinghai systems in the water budget and water chemistry, we have also determined the Sr concentration and 87Sr/S6Sr ratio of groundwater from diverse environments. This has allowed us to further constrain the Sr isotope systematic of this source. A steady‐state calculation gives an estimate for the groundwater flux of 0·19 ± 0·03 × 108 m3/yr, accounting for about 8% of contemporary lake Sr budget. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
11.
12.
Ekaterina Bazilevskaya Marina Lebedeva Milan Pavich Gernot Rother Dilworth Y. Parkinson David Cole Susan L. Brantley 《地球表面变化过程与地形》2013,38(8):847-858
Weathering disaggregates rock into regolith – the fractured or granular earth material that sustains life on the continental land surface. Here, we investigate what controls the depth of regolith formed on ridges of two rock compositions with similar initial porosities in Virginia (USA). A priori, we predicted that the regolith on diabase would be thicker than on granite because the dominant mineral (feldspar) in the diabase weathers faster than its granitic counterpart. However, weathering advanced 20× deeper into the granite than the diabase. The 20 × ‐thicker regolith is attributed mainly to connected micron‐sized pores, microfractures formed around oxidizing biotite at 20 m depth, and the lower iron (Fe) content in the felsic rock. Such porosity allows pervasive advection and deep oxidation in the granite. These observations may explain why regolith worldwide is thicker on felsic compared to mafic rock under similar conditions. To understand regolith formation will require better understanding of such deep oxidation reactions and how they impact fluid flow during weathering. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
13.
Oxygen isotopic data are presented for bulk glacial meltwaters draining the Haut Glacier d'Arolla, Valais, Switzerland and for the sulphate contained within them in an attempt to assess the redox status of the subglacial chemical weathering environment. The sulphate derived from subglacial chemical weathering is so depleted in 18O that it must have formed, at least partially, in an anoxic environment. Under these conditions, Fe3+ can act as an oxidizing agent and oxygen atoms incorporated into sulphate are derived from 18O‐depleted water molecules (by contrast, dissolved O2 is strongly enriched in 18O). These data therefore support the hypothesis that sectors of the glacier bed are anoxic and that Fe3+ may act as a significant oxidizing agent under these conditions. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
14.
Implications of EU-Water Framework Directive for the East German Postmining Landscape Lausitz: Coping with a sparse knowledge of the underground 总被引：1，自引：0，他引：1
Bastian Johannes Graupner Friedrich-Carl Benthaus Stephan Bürger Florian Werner 《Limnologica》2005,35(3):199-205
Mining dumps are major sources of pollutants within the mining area of Lausitz, especially sulphate and iron. Their existence in catchment areas comprising groundwater bodies or lakes often imposes negative effects on the water quality. The European Union Water Framework Directive [EU-WFD, 2000. Directive 2000/60/EC of the European Parliament and of the Council of 23 October 2000 establishing a framework for Community action in the field of water policy. The European Parliament and Council, L327/1, p. 72] aims to achieve ‘good quality’ status for all water bodies across Europe by 2015. Consequently, predicting the development of ground and lake water quality is necessary and must be based on the geochemical composition of the mining dumps. Therefore, the dumps need to be quantified as pollutant sources.A method to calculate the amount of sulphate in mine dumps is presented. It is based on historic geological and geochemical data characterising the pre-mining situation. Additional information on the dump body, derived from the vertical extension of mining activities and the current Digital Elevation Model (DEM), allows the composition of the dump to be determined. This procedure is demonstrated for the Bärwalde site. An average total sulphur content of 0.62% (5.9 million tonnes) was calculated for the Bärwalde dump. About 40% of it is estimated to be pyrite sulphur. Applying an average pyrite oxidation rate for the whole dump body of 7% led to an additional water-soluble mass of 0.18 million tonnes of sulphate sulphur.Applying this technique to all mine dumps managed by the postmining administration company LMBV, will improve our knowledge of the catchment area for the different lakes of Lausitz and will form an essential basis for reactive transport calculations. 相似文献
15.
Groundwater flow-paths through shallow-perch and deep-regional basaltic aquifers at the Golan Heights, Israel, are reconstructed by using groundwater chemical and isotopic compositions. Groundwater chemical composition, which changes gradually along flow-paths due to mineral dissolution and water–rock interaction, is used to distinguish between shallow-perched and deep-regional aquifers. Groundwater replenishment areas of several springs are identified based on the regional depletion in rainwater δ18O values as a function of elevation (−0.25‰ per 100 m). Tritium concentrations assist in distinguishing between pre-bomb and post-bomb recharged rainwater.
It was found that waters emerging through the larger springs are lower in δ18O than surrounding meteoric water and poor in tritium; thus, they are inferred to originate in high-elevation regions up to 20 km away from their discharge points and at least several decades ago. These results verify the numerically simulated groundwater flow field proposed in a previous study, which considered the geological configuration, water mass balance and hydraulic head spatial distribution. 相似文献
16.
Stein-Erik Lauritzen 《地球表面变化过程与地形》1990,15(2):157-167
In carbonate karst basins, adequate denudation rates are difficult to estimate when there are allogenic inputs. It is shown that the common practice of correcting for allogenic input by Corbel's modified formula leads to erroneous results unless the karst ratio is very high. When choosing small basins that are subsets of each other, assumptions of hydrologic and lithologic uniformity may be satisfied. Then the autogenic and allogenic components of the denudation may be calculated by a linear model of uniform mixing. The model was tested in a subarctic stripe karst in North Norway, yielding an autogenic denudation rate of 32.5 ± 10.2 mm ka?1. The mean annual runoff is 2600 mm. The result is supported by independent denudation rates from comparable areas, micro-erosion meter data as well as the total post-glacial corrosion deduced from pedestal and vein heights. 相似文献
17.
Surface pelagic tar concentrations in the equatorial South Atlantic Ocean were low (< 0.001 to 14.6 mg m?2). With one exception, concentrations were less than 0.5 mg m?2. The tars were characterized by gravimetry, carbon isotopic composition, molecular compositions (gas chromatographically), sulphur content, total fluorescence spectra, and biological marker fingerprints. Most tars exhibited significant amounts of degradation. A total fluorescence technique was used to group the tars into two basic types. One type occurred at low concentrations and appeared to be due to chronic long-term oil pollution in the South Atlantic Ocean. The second group occurred at much higher concentrations and was associated with more coastal-influenced waters. Biological marker (triterpanes and steranes) fingerprints confirmed the fluorescence groupings. Carbon isotopic composition and pristane/phytane ratios exhibited few geographical trends. 相似文献
18.
Spatial,seasonal, and source variability in the stable oxygen and hydrogen isotopic composition of tap waters throughout the USA 
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下载免费PDF全文 To assess spatial, seasonal, and source variability in stable isotopic composition of human drinking waters throughout the entire USA, we have constructed a database of δ18O and δ2H of US tap waters. An additional purpose was to create a publicly available dataset useful for evaluating the forensic applicability of these isotopes for human tissue source geolocation. Samples were obtained at 349 sites, from diverse population centres, grouped by surface hydrologic units for regional comparisons. Samples were taken concurrently during two contrasting seasons, summer and winter. Source supply (surface, groundwater, mixed, and cistern) and system (public and private) types were noted. The isotopic composition of tap waters exhibits large spatial and regional variation within each season as well as significant at‐site differences between seasons at many locations, consistent with patterns found in environmental (river and precipitation) waters deriving from hydrologic processes influenced by geographic factors. However, anthropogenic factors, such as the population of a tap's surrounding community and local availability from diverse sources, also influence the isotopic composition of tap waters. Even within a locale as small as a single metropolitan area, tap waters with greatly differing isotopic compositions can be found, so that tap water within a region may not exhibit the spatial or temporal coherence predicted for environmental water. Such heterogeneities can be confounding factors when attempting forensic inference of source water location, and they underscore the necessity of measurements, not just predictions, with which to characterize the isotopic composition of regional tap waters. Published 2013. This article is a U.S. Government work and is in the public domain in the USA. 相似文献
19.
Mohammad Nuruzzama Waliur Rahaman Gyana R. Tripathy Rahul Mohan Shramik Patil 《水文研究》2020,34(11):2351-2364
Dissolved major ions, Sr concentrations and 87Sr/86Sr ratios of 10 coastal lakes from the Larsemann Hills, East Antarctica have been studied to constrain their solute sources, transport and glacial weathering patterns in their catchments. In absence of perennial river/streams, lakes serve as only reliable archive to study land surface processes in these low-temperature regions. The lake water chemistry is mostly Na-Cl type and it does not show any significant depth variations. Sr isotope compositions of these lakes vary from 0.7110 to 0.7211 with an average value of 0.7145, which is higher than modern seawater value. In addition to oceanic sources, major ions and Sr isotopic data show appreciable amount of solute supply from chemical weathering of silicate rocks in lake catchments and dissolution of Ca-Mg rich salts produced during the freezing of seawaters. The role of sulphide oxidation and carbonate weathering are found to be minimal on lake hydro-chemistry in this part of Antarctica. Inverse model calculations using this chemical dataset provide first-order estimates of dissolved cations and Sr; they are mostly derived from oceanic (seawater + snow) sources (cations approximately 76%) and (Sr approximately 92%) with minimal supplies from weathering of silicates (cations approximately 15%); (Sr approximately 2%) and Ca-rich minerals (cations approximately 9%); (Sr approximately 7%). The silicate weathering rate and its corresponding atmospheric CO2 consumption rate estimates for Scandrett lake catchment (3.6 ± 0.3 tons/km2/year and 0.5 × 105 moles/km2/year), are lower than that of reported values for the average global river basins (5.4 tons/km2/year and 0.9 × 105 tons/km2/year) respectively. The present study provides a comprehensive report of chemical weathering intensity and its role in atmospheric CO2 consumption in low-temperature pristine environment of Antarctica. These estimates underscore the importance of Antarctica weathering on atmospheric CO2 budget, particularly during the past warmer periods when the large area was exposed and available for intense chemical weathering. 相似文献
20.
D. C. McDonald 《Bulletin of Volcanology》1966,29(1):691-707
The ratios of D/H and O18/O16 in natural waters from streams, boreholes, soda springs, hot pools, ponds and larger bodies of water in the Ngawha hydrothermal area were determined. The results are considered in relation to the isotopic changes known to occur in water subjected to evaporation. Where applicable chemical and other work was also considered. It is assumed that stream water isotope composition is the mean value for the isotopic composition of meteoric waters. Measurements on waters taken from boreholes drilled to 65 feet and 350 feet and from the other water sources mentioned, indicate that they were of meteoric origin as judged by stream isotope composition. The waters from the soda springs appeared to be isotopically the same as the stream water, a finding consistent with the absence of evaporative surface. These borehole waters were similar but slightly different in O18 due probably to exchange between rock and water. Heavy isotope enrichment of the ponds and larger bodies of water appeared to be due to non-equilibrium evaporation at ambient temperature. The hot pools in the Ngawha springs area proper were enriched in the heavier isotopes probably due to non-equilibrium evaporation at the usual hot pool temperature of about 40°C and also to exchange of O18 between water and rock. The water from a further borehole drilled to approximately 2,000 feet appeared also to be of meteoric origin but was changed in O18 content to an extent consistent with the assumption that oxygen isotope exchange with rock had taken place at approximately 230°C. The results are used to illustrate possibilities for the use of oxygen and hydrogen isotope measurements in hydrothermal investigations. 相似文献