Influence of ion exchange on dissolved load of alpine meltwaters

Meltwaters were collected in Switzerland at the border of two alpine glaciers, the Tsanfleuron glacier resting on limestones and the Tsijiore Nouve glacier flowing over gneissic rocks. Waters were analysed by atomic absorption spectrophotometry for the four major cations. Cation exchange appears to be an essential mechanism in the explanation of the dissolved cationic content of meltwaters in the frontal zone of glaciers. This is indicated by a study of the rate and characteristics of water enrichment. The rate-determining step in the process seems to be film diffusion. The influence of this diffusion is put forward in an analysis of the rates of change in concentration of the four major cations with discharge. Glacier grinding is considered as a factor favouring cation exchange in a proglacial environment.     

Charakterisierung von Al(III)-Spezies in basischen Aluminiumchlorid-Flockungsmitteln mittels Ferronreaktion bzw. 27Al-Kernresonanzspektroskopie Characterization of Al(III) Species in Basic Aluminium Chloride Flocculants by Means of Ferron Method and 27 Al Nuclear Magnetic Resonance

Flocculant processes as a treatment step in water and wastewater purification technology are of increasing importance. Partially neutralized aqueous aluminium chloride solutions — the basic aluminium chlorides — are often used as flocculants in water conditioning. The present paper describes the reactions which appear in these solutions by their dilution, the identification of occurring cationic aluminium species, and the relations between the composition of the solutions and their efficiency as flocculants. The solutions were quantitatively analyzed using ²⁷Al NMR and the ferron method; the latter method offers a simple and inexpensive alternative for identification and quantification of aluminium cations and can facilitate investigations of the Al speciation at concentrations too low for analysis by NMR. The distribution of aluminium cations in basic aluminium chloride solutions changes drastically by the dilution while applied as flocculants because the equilibrium strongly depends on the concentration. The dynamic changes following the dilution of partially neutralized solutions were investigated simply by mixing a solution with water and immediate analysis by the ferron method. It could be shown that rearrangement reactions occur in the system, partially overlapping each other, the oligomeric cations seem to be especially instable. Furthermore, a partial change from octahedral to tetrahedral coordination of the aluminium in the species can be observed. At extremely low aluminium concentration as in the case of application of the basic aluminium chloride solutions for flocculation, monomeric and especially transition polymeric and polymeric aluminium cations, respectively, appear. The ratio of these cations to each other also depends on the time up to the flocculation. Accordingly, these cations especially the different polymeric aluminium species seem to be important for the efficiency of the basic aluminium chlorides as flocculants in water conditioning.     

Analytical laboratory comparison of major and minor constituents in an active crater lake

The crater lake water from Maly Semiachik volcano in Kamchatka was used for the international analytical laboratory comparison of major and minor elements, and hydrogen, sulfur, and oxygen isotope data. Eight institutions participated in this program, giving analytical results of 9 major and 20 minor elements mainly by using ICP-AES for cations and IC for anions. Among the major elements, Na, Mg and Si showed coefficients of variation (CV) of 10% or more, whereas B, Al, Fe, Mn had coefficients less than 7%. The CV% of the minor elements Co, Cu, P, Cr, Pb was much greater (>30%) while the V analyses agreed well (<10%). Ti, Sr, Zn, and F were intermediate (between 10 and 20 CV%). The errors observed for these constituents are inherent to the methods applied: large dilutions and spectrometric interferences. Even the major anions such as Cl (>2000 ppm) and SO₄ (>5000 ppm) gave considerable ranges (5.1 and 8.8 CV%, respectively) as did the obtained pH values (22 CV%). The measured δ¹⁸O of the water samples and δ³⁴S of sulfate are in excellent agreement but the δD values had CV% of 8. Technical recommendations are presented to improve the analytical results for these elements with significant deviations from the mean values.     

Dissolved major ions,Sr and 87Sr/86Sr of coastal lakes from Larsemann hills,East Antarctica: Solute sources and chemical weathering in a polar environment

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.     

Pressure dependence of diffusion in ionic solids

A continuum model of point defects in ionic solids is developed and applied to the estimation of the pressure dependence of diffusion (in alkali halides). Activation enthalpies are expressed using macroscopic physical constants (lattice energy, elastic constants, dielectric constants, etc.) by introducing empirical parameters related to the microscopic nature of defects. Systematic relations are found between these parameters and other physical properties (ionic radius, volume fraction of anions in crystals, etc.). The nature of parameters for anions is shown to be significantly different from that for cations, probably due to the difference in “softness” between anions and cations. Such relations make it possible to estimate activation energy and volume of diffusion from the lattice energy, ionic radius, elastic constants, dielectric constants and their pressure derivatives. The calculated activation volumes agree well with experimental data. The effect of phase transition is also examined by comparing NaCl and CsCl structures. It is suggested that by phase transition from a less dense (NaCl) structure to a denser one (CsCl), the anion diffusion constant may not decrease as much as expected from the associated change in other physical properties. The validity of the models of van Liempt and of Keyes is examined. It is shown that van Liempt's model works well except for the migration process (especially anions), and that Keyes' model does not work so well for all processes.     

Self-organized crystallization mechanism of non-equilibrium 2:1 type phyllosilicate systems

The crystallization mechanism of 2:1 type regular interstratified minerals is investigated in views of non-equilibrium thermodynamics. The structural chemistry of relative layers and their interstratified combinations is analyzed and six kinds of non-equilibrium chemical systems have been induced. The universal laws of chemical reactions which happened in the interface region of these non-equilibrium systems have been summarized. From these laws, two reaction systems crystallizing out Tosudite and Rectorite respectively have been recovered. The kinetic model of chemical reactions has been developed by means of the mass conservation law. The oscillatory solution showing regular interstratified features has also been obtained numerically. These results indicate that the difference in original chemical composition among systems can affect the chemical connotation of reactants, intermediate products and resultants, and the flow chart of chemical reaction, but cannot change their crystallization behavior of network-forming cations, bigger and smaller network-modifying cations during crystallization. Hence, their kinetic model reflecting the universal crystallization law of these cations is just the same. These systems will crystallize out regular interstratified minerals at suitable parameters, which always exist as domain with nanometer-sized in thickness and can be called the self-organized ordering structure.     

Linkage of liquid conductivity of glacier ice with its alkalinity over the north Qinghai-Xizang (Tibet) Plateau--Implication to the past dust recovery

Liquid conductivity (EC) measurement was conducted for the samples collected from several snow pits and ice cores over the Qinghai-Xizang (Tibet) Plateau, with their time range covering seasonal, decadal and centennial scales. Unlike the previous attention mostly focused on the acidity (H+) responding to the solid conductance (ECM) of glacial ice, we introduce the alkalinity (OH?) of snow and ice to show how it responds to EC. Strong linear relationship was established between EC and OH? for these snow pits and ice cores. Positive correlation is also established between EC and major cations (Ca2+, Mg2+, Na+ and K+). Since the cations are known as the proxies for the intensity of mineral dust influx onto glaciers of the northern Qinghai-Xizang Plateau, we believe that EC could be used as an indicator for the history of dust input in deep ice core study. In fact, records in Guliya ice core since the Little Ice Age (LIA) indicate that dust load in glacier may depend on the combination of temperature and humidity. "Cold-dry" combination favors the dust arising, and results in higher EC and OH- values, while "warm-wet" combination prevents dust form and EC and OH- values are lower. In the past century, with the atmospheric warming and precipitation increasing over the northern plateau, which means an atmospheric condition of dust decreasing, both EC and OH- displayed rapid decline.     

Acid-base status of soils in groundwater discharge zones — relation to surface water acidification

Critical load calculations have suggested that groundwater at depth of 2 m in Sweden is very sensitive to acid load. As environmental isotope studies have shown that most of the runoff in streams has passed through the soil, there is a risk in the near future of accelerated acidification of surface waters.

To assess the importance of the last soil horizon of contact before discharge, the upper 0–0.2m of soils in seven discharge zones were analysed for pools of base cations, acidity and base saturation. The sites were about 3–4 m² in size and selected from two catchments exposed to different levels of acid deposition.

The soils in the seven sites had high concentrations of exchangeable base cations and consequently high base saturation. The high correlation (r² = 0.74) between base saturation in the soils of the discharge zones and mean pH of the runoff waters suggested that the discharge zone is important for surface water acidification. The high pool of exchangeable base cations will buffer initially against the acid load. As the cation exchange capacity (meq dm⁻³) and base saturation were lower in the sites from the catchment receiving lower deposition, these streams may be more vulnerable to acidification in the near future. The high concentration of base cations in non-exchangeable fractions may also buffer against acidification as it is likely that some of these pools will become exchangeable with time.     

CONTROLS ON SURFACE WATER CHEMISTRY IN THE UPPER MERCED RIVER BASIN,YOSEMITE NATIONAL PARK,CALIFORNIA

Surface water draining granitic bedrock in Yosemite National Park exhibits considerable variability in chemical composition, despite the relative homogeneity of bedrock chemistry. Other geological factors, including the jointing and distribution of glacial till, appear to exert strong controls on water composition. Chemical data from three surface water surveys in the upper Merced River basin conducted in August 1981, June 1988 and August 1991 were analysed and compared with mapped geological, hydrological and topographic features to identify the solute sources and processes that control water chemistry within the basin during baseflow. Water at most of the sampling sites was dilute, with alkalinities ranging from 26 to 77 μequiv. l⁻¹. Alkalinity was much higher in two subcatchments, however, ranging from 51 to 302 μequiv. l⁻¹. Base cations and silica were also significantly higher in these two catchments than in the rest of the watershed. Concentrations of weathering products in surface water were correlated to the fraction of each subcatchment underlain by surficial material, which is mostly glacial till. Silicate mineral weathering is the dominant control on concentrations of alkalinity, silica and base cations, and ratios of these constituents in surface water reflect the composition of local bedrock. Chloride concentrations in surface water samples varied widely, ranging from <1 to 96 μequiv. l⁻¹. The annual volume-weighted mean chloride concentration in the Merced River at the Happy Isles gauge from 1968 to 1990 was 26 μequiv. l⁻¹, which was five times higher than in atmospheric deposition (4–5 μequiv. l⁻¹), suggesting that a source of chloride exists within the watershed. Saline groundwater springs, whose locations are probably controlled by vertical jointing in the bedrock, are the most likely source of the chloride. Sulphate concentrations varied much less than most other solutes, ranging from 3 to 14 μequiv. l⁻¹. Concentrations of sulphate in quarterly samples collected at the watershed outlet also showed relatively little variation, suggesting that sulphate may be regulated to some extent by a within-watershed process, such as sulphate adsorption.     

Effects of variable attribute weights on landform classification

This paper focuses on the attribute weight issue and advocates use of modi?able attribute weights in terrain‐based environmental analysis and classi?cation. A question was asked: ‘How much will the result of a terrain‐based environmental analysis be affected if the weights of used terrain attributes are changed?’ The literature on landform classi?cation and the fuzzy k‐means method was reviewed in particular to help clarify the background and importance of this weight assignment issue. As an example, the effects of modifying attribute weights were evaluated for fuzzy k‐means landform classi?cation in a case study area. A total of 102 classi?cations were compared with each other and with a soil map, and comparison methods were speci?cally designed to evaluate the differences between these classi?cations. The results show that fuzzy k‐means landform classi?cation is sensitive to weight adjustments of adopted terrain attributes. The sensitivity is particularly high when the attribute weights started to be tuned away from the standard (i.e. uniform) weight of one. Better matching between landform classi?cation and a soil map may be produced when attribute weights are tuned. In all, we advocate the widespread adoption of an exploratory attitude in assigning attribute weights for environmental analysis and classi?cation. Copyright © 2006 John Wiley & Sons, Ltd.     

Application of Superabsorbent Polymers for Improving the Ecological Chemistry of Degraded or Polluted Lands

About 3.5 billion ha of land, which amounts to almost 30% of the total solid land of the world, has been degraded by human activities. The ecological restoration of these lands is a major challenge for mankind since they are the only option left for increasing the amount of arable land and producing food for the ever growing worldwide population. One common feature of these degraded lands is the fact that their organic soil matter is degraded also. Rainfall therefore, changes from a blessing to a menace since it is not kept in the soil and therefore causes erosion. A solution for the restoration of these lands could be the application of superabsorbent polymers (SAPs) to these soils. These substances are like ‘artificial humus’ as they are hydrophilic and contain carboxylic groups. This enables them to bind cations and water. They have the following advantages for the restoration of degraded lands. They increase the plant available water in the soil which enables the plants to survive longer under water stress. SAP amendment to soils reduces the evapotranspiration rate of the plants. They induce a significantly higher growth rate in plants growing on SAP amended soil. They bind heavy metals and mitigate their action on plants. They mitigate the effects of salinity. The benefits of SAP amendment to soils substantially outweigh their costs.     

A Background Color Scheme for Piper Plots to Spatially Visualize Hydrochemical Patterns

The combination of ternary diagrams of cations and anions with a central diamond graph make the Piper plot very useful in visualizing groundwater chemistry datasets. One of the major drawbacks is that it is hard to link spatial attributes of the dataset to the plot. In this study, we propose a background color scheme of the Piper plot so that spatial representations of these data can be colored according to their location in the Piper plot. The color scheme is chosen to have maximum resolution while still being perceptually uniform. The linking between Piper plot and maps through this color scheme allows the interpretation of the trends and processes deduced from the Piper plot in terms of the location in the aquifer, the geology, and the groundwater flow dynamics. The colored Piper plot is applied to a groundwater quality dataset of the Condamine Alluvium in Queensland, Australia.     

Hydrochemical and water source variations across a floodplain mire,Insh Marshes,Scotland

Groundwater heads and chemical composition were measured at approximately two week intervals during the summer of 1993 along a 1 km transect across the Insh Marshes floodplain mire in Inverness-shire, Scotland. Groundwater heads were generally higher near the valley side slope, with lower pH values and greater dissolved organic carbon, A1 and C1 concentrations. In the centre of the transect, upward groundwater heads were identified and pH, conductivity and concentrations of base cations were much greater. Near the River Spey, pH and base cation concentrations decreased and A1 and C1 concentrations increased. Deep groundwater followed a similar spatial trend but was generally more base-rich than shallow groundwater. These variations reflect the influence of three major water sources with different chemical signatures. Runoff from the valley side slope increased dissolved organic carbon and A1 in the shallow groundwater, the upward flow of groundwater increased the pH and Ca concentration and inundation near the river decreased the base status and increased C1 and A1.     

河流阶地演化与走滑断裂滑动速率

断裂滑动速率是活动构造定量研究的最重要参数之一,不仅可以直接应用于活动构造的地震危险性预测和工程场地的地震安全性评价,还为地球动力学研究提供不可缺少的重要信息。原理上,断裂滑动速率可以用总位移量除以其累积时间而获得,但准确地确定断裂滑动速率并不是一件容易的事情,不同方法和研究者测定的同一条断裂的滑动速率可以相差3倍。文中通过对河流基座阶地演化及其对走滑断裂错动响应过程的分析发现,当一条山前河流切入河漫滩使其废弃形成阶地后,断裂的走滑位移使得河流两侧的阶地陡坎都遭到错动,其中一侧的下游阶地陡坎被错入河道而遭到河流的侵蚀,另一侧的下游阶地陡坎被错离河道,受到河流上游右侧地貌的保护而免遭侵蚀。因此,被错离河道一侧的阶地陡坎的位移在上阶地形成时就开始积累,阶地面的暴露年龄相当于位移累积的起始年代。另外,被错离河道一侧的阶地陡坎在下阶地停止侧蚀(可能同时开始接受沉积)时就开始累积位移,下阶地的初始沉积年代也代表阶地陡坎位移开始累积的时间。当然,如果能够获得被位移阶地陡坎的上下阶地年龄,就更能够把滑动速率限定在可靠的范围之内。在上述分析的基础上,提出3种利用河流阶地确定走滑断裂滑动速率的方法:第一是利用上下阶地年龄限定     

Complex patterns of catchment solute–discharge relationships for coastal plain rivers

Riverine solute versus discharge (C–Q) relationships provide information about the magnitude and dynamics of material fluxes from landscapes. We analysed long‐term patterns of C–Q relationships for 44 rivers in Florida across a suite of geogenic, nutrient, and organic solutes and investigated land cover, watershed size, and surficial geology as controls on these patterns. Solute concentrations generally exhibited far less variability than did discharge, with coherent solute‐specific behaviours repeated across watersheds. Geogenic solutes generally diluted with increasing discharge, whereas organic solutes generally enriched; patterns for nutrients were highly variable across watersheds, but on average exhibited chemostasis. Despite strong evidence of both geologic and land cover controls on solute flow‐weighted concentrations, these variables were poor predictors of C–Q slopes (β) or relative coefficients of variation (CV_C:CV_Q). CV_C:CV_Q generally increased with watershed size, and wetland area appeared to influence C–Q patterns for base cations and organic solutes. Perhaps most importantly, we observed significant slope breaks in C–Q association in approximately half of our observations, challenging the generality of using single power functions to describe catchment solute export patterns. For all solutes except phosphorus (P), C–Q slopes decreased above statistically identified breaks (slopes for P increased), with breaks consistently at or near median flow (i.e., 50% flow exceedance probability). This common pattern significantly impacts solute load estimates; failing to account for slope breaks overestimates nitrate and total organic carbon loads as much as 125% and underestimates P loads as much as 35%. In addition to challenging generic power‐law characterization of C–Q relationships for these coastal plain rivers, and exploring the load estimate consequences thereof, our study supports emerging insights about watershed hydrochemical behaviours across a wide array of solutes.     

The distribution of solute processes on an acid hillslope and the delivery of solutes to a stream: I. Exchangeable bases

This paper aims to identify the spatial distribution of exchangeable base cations in soils on an acid hillslope and to investigate possible cation release processes from slope soils to the stream. The basic assumption underlying this research is that the amount of exchangeable cations in soils reflects the nutrient stores and cation leaching processes across the slope where vegetation and parent materials are similar. The distribution of exchangeable Ca²⁺, Mg²⁺, K⁺ and Na⁺ has been investigated on a three-dimensional hillslope on the Quantock Hills, Somerset, UK. A two-way ANOVA shows that soil depth is predominant in explaining the total variance of exchangeable bases, despite the steep slope gradient and clear podzolic catena development. Major nutrient base cations, such as Ca²⁺, Mg²⁺ and K⁺, display homogeneous topsoil storage right across the slope. This spatial pattern may indicate that the spatial distribution of major nutrient cations is tightly controlled by the soil–vegetation system in nutrient-poor heathland environments. Na⁺ is an exception to this vegetation-controlled spatial distribution, because of its small involvement in the soil–vegetation and soil exchangeable systems. In subsurface soils, cations liberated from the soil–vegetation system are subject to redistribution over the slope according to the hydrological flowpaths operating on the slope, with some eventually released into the stream. The saturated wedge developed at the base of the slope plays a key role in the storage and release processes of base cations from slope soils to the stream. Ca²⁺, Mg²⁺ and Na⁺ carried by throughflow are stored in the saturated wedge and gradually released into the stream at times of high flow. K⁺, however, shows an apparently different spatial behaviour, being deficient in the saturated wedge. Copyright © 1999 John Wiley & Sons, Ltd.     

Comparison of Fiberglass and Other Polymeric Well Casings, Part III. Sorption and Leaching of Trace-Level Metals

This series of experiments was initiated to determine the overall suitability of three alternative polymeric well casing materials (fluorinated ethylene propylene [FEP], fiberglass-reinforced epoxy [FRE], and fiberglass-reinforced plastic [FRP]) for use in ground water monitoring wells and to compare these materials with polyvinyl chloride (PVC) and polytetrafluoroethylene (PTFE) well casings. This paper focuses on sorption and leaching of metals.
Generally, the fiberglass materials leached more metal contaminants than PVC, FEP, and PTFE. However, with one exception (Pb leaching from FRP), leached concentrations were below maximum allowable limits set by the U.S. Environmental Protection Agency (EPA) for drinking water. With respect to sorption, none of the polymers sorbed the anions tested, but all of them sorbed one or more of the cations tested. FEP and PTFE were much less sorptive than the other materials.     

Linkage of liquid conductivity of glacier ice with its alkalinity over the north Qinghai-Xizang (Tibet) Plateau

Liquid conductivity (EC) measurement was conducted for the samples collected from several snow pits and ice cores over the Qinghai-Xizang (Tibet) Plateau, with their time range covering seasonal, decadal and centennial scales. Unlike the previous attention mostly focused on the acidity (H⁺) responding to the solid conductance (ECM) of glacial ice, we introduce the alkalinity (OH⁻) of snow and ice to show how it responds to EC. Strong linear relationship was established between EC and OH⁻ for these snow pits and ice cores. Positive correlation is also established between EC and major cations (Ca²⁺, Mg²⁺, Na⁺ and K⁺). Since the cations are known as the proxies for the intensity of mineral dust influx onto glaciers of the northern Qinghai-Xizang Plateau, we believe that EC could be used as an indicator for the history of dust input in deep ice core study. In fact, records in Guliya ice core since the Little Ice Age (LIA) indicate that dust load in glacier may depend on the combination of temperature and humidity. “Cold-dry” combination favors the dust arising, and results in higher EC and OH⁻ values, while “warm-wet” combination prevents dust form and EC and OH⁻ values are lower. In the past century, with the atmospheric warming and precipitation increasing over the northern plateau, which means an atmospheric condition of dust decreasing, both EC and OH⁻ displayed rapid decline.     

Effect of Water Acidification on the Calcium and Magnesium Concentrations in Caddis Fly Larvae

Data on small lakes in the Finnish Laplandia are used to examine the dependence of Ca and Mg concentrations in caddis fly larvae (Polycentropodidae family) on the concentrations of these elements in water, pH, and the extent of water humification. The concentration of Ca is shown to be virtually independent of its concentration in water, and Mg concentrations are found to be inversely related. The coefficients of accumulation demonstrate a strong inverse dependence on the concentrations of these cations in water, as well as on water pH. The decrease in Ca and Mg concentration in the larvae caused by an increase in pH is shown to be slower than that in water, which is an indirect indication to the presence of mechanisms that maintain the macroelement concentrations in the living organisms at the level required for their normal functioning under the conditions of anthropogenic acidification of water bodies.     

Major ion chemistry of two cratonic rivers in the tropics: Weathering rates and their controlling factors

Continental weathering plays a dominant role in regulating the global carbon cycle, soil chemistry and nutrient supply to oceans. The CO₂-mediated silicate weathering acts as a major CO₂ sink, whereas sulphuric acid-mediated carbonate dissolution releases CO₂ to the atmosphere–ocean system. In this study, dissolved major ions and silica concentrations of two tropical (Damodar and Subarnarekha) river systems from India have been measured to constrain the type and rate of chemical weathering for these basins. The total dissolved solids (TDS) of these rivers, a measure of total solute supply from all possible sources, are about 2–3 times higher than that of the global average for rivers. Mass balance calculations involving inverse modelling estimate that 63 ± 11% of total cations are derived from rock weathering, of which 27 ± 7% of cations are supplied through silicate weathering. The sulphide-S concentrations are estimated by comparing the water chemistry of these two rivers with that of a nearby river (Brahmani) with similar lithology but no signatures of sulphide oxidation. The outflows of Damodar and Subarnarekha rivers receive 17% and 55% of SO₄ through sulphide oxidation, respectively. The sulphide oxidation fluxes from the ore mining areas, such as upper Damodar (0.52 × 10⁹ mol/yr) and lower Subarnarekha (0.66 × 10⁹ mol/yr) basins, are disproportionally (~9 times) higher compared to their fractional areal coverage to the global drainage area. The corresponding CO₂ release rate (2.84 × 10⁴ mol/km²/yr) for the Damodar basin is lower by five times than its CO₂ uptake rate (1.38 × 10⁵ mol/km²/yr). The outcomes of this study underscore the dominance of sulphide oxidation in controlling the dissolved chemical (cationic and sulphur) fluxes.