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1.
The chemistry of the rainwater indirectly reflects the composition of the ions in the atmosphere. The study of the rainwater gains its own importance as it forms the basis for the agricultural, domestic and drinking water. Twelve rainwater samples were collected along the southeastern coast of India during southwest monsoon. The samples were analyzed for the major anions (Cl?, SO4 2?, PO4 3? and HCO3 ?) and cations (Na+, K+, Ca2+ and Mg2+). The majority of the samples reflect acidic pH. The general dominance of the cations is in the order of Na+ > Ca2+ > K+ > Mg2+ and that of anions is HCO3 ? > Cl? > SO4 2? > PO4 3?. The water is classified as calcium bicarbonate to sodium bicarbonate type. The decrease of pH value also increases the pCO2. In order to study the impact of acidic and alkaline species on rainwater, correlation coefficients were determined for establishing the relationship between different ions. Good correlation was established between cations, and sulfate has no correlation with other ions and pH. Factor analysis reveals that land use pattern, marine source and methanogenesis from the tidal influenced mangroves play a major role in determining the rainwater chemistry of the region.  相似文献   

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3.
A comprehensive and systematic study to understand various geochemical processes as well as process drivers controlling the water quality and patterns of the hydrochemical composition of river water in Muthirapuzha River Basin, MRB (a major tributary of Periyar, the longest river in Kerala, India), was carried out during various seasons, such as monsoon, post-monsoon and pre-monsoon of 2007–2008, based on the data collected at 15 monitoring stations (i.e., 15 × 3 = 45 samples). Ca2+ and Mg2+ dominate the cations, while Cl? followed by HCO3 ? dominates the anions. In general, major ion chemistry of MRB is jointly controlled by weathering of silicate and carbonate rocks, which is confirmed by relatively larger Ca2+ + Mg2+/Na+ + K+ ratios as well as Ca2+/Na+ vs. Mg2+/Na+ and Ca2+/Na+ vs. HCO3 ?/Na+ scatter plots. The relationship between Cl? and Na+ implies stronger contributions of anthropogenic activities modifying the hydrochemical composition, irrespective of seasons. The water types emerged from this study are transitional waters or waters that changed their chemical character by mixing with waters of geochemically different ionic signatures. However, various ionic ratios, hydrochemical plots and graphical diagrams suggest seasonality over the hydrochemical composition, which is solely controlled by the rainfall pattern. Relatively higher pCO2 indicates the disequilibrium existing in natural waterbodies vis-à-vis the atmosphere, which is an outcome of both the contribution of groundwater to stream discharge and anthropogenic activities. Hence, continuous monitoring of hydrochemical composition of mountain rivers is essential in the context of climate change, which has serious implications on tropical mountain fluvial-hydro systems.  相似文献   

4.
South China is one of the regions severely suffering from acid rain in the world.However,few systematic studies of rural precipitation chemistry have been performed in comparison with the extensive studies on their urban counterparts of this region.In order to characterize the current acid rain status and identify its possible sources in the rural area of South China,we analyzed precipitation collected event by event from a rural forested watershed in southern Anhui Province between March 2007 and February 2010.The results showed that the concentrations of major ions within precipitation in the studied rural area were significantly lower than those reported for the urban areas of the same latitude in China.Nevertheless,the precipitation acidity(with an average pH value of 4.49) and the frequency of acid rain(95%) were considerably high.The relatively high ratio of(SO42+ NO 3)/(Ca2+ +NH4+) was the main cause of acid rain in this rural area,as SO 2 and NO x were the main precursors of acid rain,while Ca2+ and NH4+acted as the dominant neutralizers to the acidity.Source identification indicated that Ca2+ and Mg2+ mainly were derived from alkaline dust,SO42,NO 3 and NH4+originated mainly from anthropogenic sources such as industrial and agricultural activities,most Na +,Cl,K + and some of Mg2+ were derived from the sea.The results suggested that the major ions within precipitation in the rural area of South China were related to the meso-scale and long-range transport of particles and aerosols in the air.  相似文献   

5.
The physicochemical properties and major ion chemistry of the groundwater sources from alluvial aquifers along the stretch (60 km) of Jhelum River in Kashmir Himalaya were determined in order to identify hydro-geochemical processes and their suitability for drinking purposes. The data depicted that calcium and bicarbonates were dominating among the cations and anions. The results indicate the trend of cation dominance as Ca2+ > Na+ > Mg2+ > K+, whereas anion dominance was in the order of HCO3 ? > Cl? > SO4 2?. Ratio of calcium to magnesium indicated the dissolution of Ca2+ from CaCO3, which results in an increased levels of Ca2+ in the groundwater. Interpretation of Piper Trilinear plot understands the various geochemical processes affecting the groundwater quality and shows groundwater was dominated by Ca–HCO3 type. The pH was recorded in the slightly alkalinity range 7.2–7.8 and was showing positive correlation with HCO3 ?. The chloro-alkaline indices revealed 86% of the sources exchange by a type of base-exchange reactions, rest by cation–anion exchange. Gibbs diagram revealed groundwater sources fall in the category of rock dominance. The concentration of the nitrogen compounds was in the progression of NO3–N > NH4–N > NO2–N, and the PO4 ? fluctuated from 0.12 to 0.22 mg/L. Moreover, corrosivity ratio indicated that water from the majority of sources (71%) is safe to supply using pipes without any corrosive effects, while 29% of sources are corrosive in nature and need non-corrosive pipes for transporting and lifting of groundwater. The results revealed, groundwater samples were within permissible limits as prescribed by International and National standards, for drinking purposes. The State government and NGO’s can show their interest in utilizing such water resources to overcome the shortage of drinking water in a sustainable way for the daily consumption of the people living in the vicinity of Jhelum River.  相似文献   

6.
Major ions showed high concentrations, ionic strength and chemical activity in the surface waters of Govind Ballabh Pant Sagar reservoir. Various geochemical ratios showed the dominance of silicate over carbonate weathering and major ions such as Na+ + K+ account for about 52 % of the cation budget. The high Na+ and K+ showed sedimentation of rock/coal particles consisting of highly weathered silicate minerals contributed by the discharge of mine water, fly ash mixing during transportation, etc. Further, Ca2+ + Mg2+/Na+ + K+ ratio was <1 (0.92) indicating the occurrence of silicate weathering in the reservoir catchment. The comparative assessment showed that the proportion of Ca2+ + Mg2+/Na+ + K+ tends to be lower along the coal mining belts compared to non-coal mining regions in the world. The Ca2+/SO4 2? ratio <1 revealed not only H2CO3 but H2SO4 also acting as a source of protons for rock weathering. The cause underlying these differences can be related directly to geological substrate and anthropogenic activities.  相似文献   

7.
Groundwater survey has been carried out in the area of Gummanampadu sub-basin located in Guntur District, Andhra Pradesh, India for assessing the factors that are responsible for changing of groundwater chemistry and consequent deterioration of groundwater quality, where the groundwater is a prime source for drinking and irrigation due to non-availability of surface water in time. The area is underlain by the Archaean Gneissic Complex, over which the Proterozoic Cumbhum rocks occur. The results of the plotting of Ca2+ + Mg2+ versus HCO3 ? + CO3 2?, Ca2+ + Mg2+ versus total cations, Na+ + K+ versus total cations, Cl? + SO4 2? versus Na+ + K+, Na+ versus Cl?, Na+ versus HCO3 ? + CO3 2?, Na+ versus Ca2+ and Na+: Cl? versus EC indicate that the rock–water interaction under alkaline condition is the main mechanism in activating mineral dissociation and dissolution, causing the release of Ca2+, Mg2+, Na+, K+, HCO3 ?, CO3 2?, SO4 2? and F? ions into the groundwater. The ionic relations also suggest that the higher concentrations of Na+ and Cl? ions are the results of ion exchange and evaporation. The influences of anthropogenic sources are the other cause for increasing of Mg2+, Na+, Cl?, SO4 2? and NO3 ? ions. Further, the excess alkaline condition in water accelerates more effective dissolution of F?-bearing minerals. Moreover, the chemical data plotted in the Piper’s, Gibbs’s and Langelier–Ludwig’s diagrams, computed for the chloro-alkaline and saturation indices, and analyzed in the principal component analysis, support the above hypothesis. The groundwater quality is, thus, characterized by Na+ > Ca2+ > Mg2+ > K+: HCO3 ? + CO3 2? > Cl? > SO4 2? > NO3 ? > F? facies. On the other hand, majority of groundwater samples are not suitable for drinking with reference to the concentrations of TDS, TH, Mg2+ and F?, while those are not good for irrigation with respect to USSL’s and Wilcox’s diagrams, residual sodium carbonate, and magnesium hazard, but they are safe for irrigation with respect to permeability index. Thus, the study recommends suitable management measures to improve health conditions as well as to increase agricultural output.  相似文献   

8.
Size distribution of PM10 mass aerosols and its ionic characteristics were studied for 2 years from January 2006 to December 2007 at central Delhi by employing an 8-stage Andersen Cascade Impactor sampler. The mass of fine (PM2.5) and coarse (PM10?2.5) mode particles were integrated from particle mass determined in different stages. Average concentrations of mass PM10 and PM2.5 were observed to be 306 ± 182 and 136 ± 84 μg m?3, respectively, which are far in excess of annual averages stipulated by the Indian National Ambient Air Quality Standards (PM10: 60 μg m?3 and PM2.5: 40 μg m?3). The highest concentrations of PM10?2.5 (coarse) and PM2.5 (fine) were observed 505 ± 44 and 368 ± 61 μg m?3, respectively, during summer (June 2006) period, whereas the lower concentrations of PM10?2.5 (35 ± 9 μg m?3) and PM2.5 (29 ± 13 μg m?3) were observed during monsoon (September 2007). In summer, because of frequent dust storms, coarse particles are more dominant than fine particles during study period. However, during winter, the PM2.5 contribution became more pronounced as compared to summer probably due to enhanced emissions from anthropogenic activities, burning of biofuels/biomass and other human activities. A high ratio (0.58) of PM2.5/PM10 was observed during winter and low (0.24) during monsoon. A strong correlation between PM10 and PM2.5 (r 2 = 0.93) was observed, indicating that variation in PM10 mass is governed by the variation in PM2.5. Major cations (NH4 +, Na+, K+, Ca2+ and Mg2+) and anions (F?, Cl?, SO4 2? and NO3 ?) were analyzed along with pH. Average concentrations of SO4 2? and NO3 ? were observed to be 12.93 ± 0.98 and 10.33 ± 1.10 μg m?3, respectively. Significant correlation between SO4 2? and NO3 ? in PM1.0 was observed indicating the major sources of secondary aerosol which may be from thermal power plants located in the southeast and incomplete combustion by vehicular exhaust. A good correlation among secondary species (NH+, NO3 ? and SO4 2?) suggests that most of NH4 + is in the form of ammonium sulfate and ammonium nitrate in the atmosphere. During winter, the concentration of Ca2+ was also higher; it may be due to entrainment of roadside dust particles, traffic activities and low temperature. The molar ratio (1.39) between Cl? and Na+ was observed to be close to that of seawater (1.16). The presence of higher Cl? during winter is due to western disturbances and probably local emission of Cl? due to fabric bleaching activity in a number of export garment factories in the proximity of the sampling site.  相似文献   

9.
The assessment of hydrogeochemical processes that govern the water quality of inland freshwater aquifers in coastal environment, especially in Indian sub-continent, is occasionally attempted. To bridge the gap, a detail hydrochemical evaluation of groundwater occurring in coastal alluvium is attempted. Single set of high-density water sampling is done from a limited area to gain an in-depth knowledge of the processes that govern the water chemistry of the sandy aquifers. The water is of weak alkaline nature and less mineralized, EC being < 1,000 μS/cm in many samples. Major ion composition indicates that water is contaminated with excess concentration of nitrates. Ionic abundance is in the order of Cl? > Na+  > Ca2+ > HCO3 ? > SO4 2? > Mg2+  > NO3 ?. Na+ and Cl? are almost in similar proportions implying the influence of coastal climate on water quality. The water shows modest variation in their ionic assemblage among different sample points as evident from Schoeller scheme. Groundwater can be classified into three distinct facies viz. Cl?–Ca2+–Mg2+, Na+–Cl? and Ca2+–Mg2+–HCO3 ? types. The ionic assemblages, their indices, ratios and cross-plots substantiate that multiple processes were involved in the evolution of the water chemistry. Among them, silicate weathering, halite dissolution, ion exchange and base exchange played prominent role in the ion enrichment of groundwater. The aquatic chemistry is further influenced and modified by marine environment, evapotranspiration and anthropogenic inputs which is authenticated by good correlation (r 2 = 1) among the Na+–Cl?, EC–Mg2+, Na+ and Cl?. Gibbs plots established that evaporation is more responsible for contribution of minerals to the groundwater than aquifer material. Nitrate contamination can be attributed for poor sewerage disposal mechanism which is aggravated by fertilizer inputs, irrigation practices and agriculture activity. A contrasting correlation (r 2 ≥90 to <0.40) among select pairs of ions reassures dissimilar source of those ions, involvement of multiple processes and limited interaction of formation water with aquifer material.  相似文献   

10.
Groundwater of an aquifer located in the vicinity of a large coal washery near Zarand City, Iran consists of two hydrochemically differing facies, which have been informally designated as groundwater (A) and groundwater (B). Groundwater (A) is native, brackish in composition and is characterized by Na+ > Mg2+ > Ca2+ > K+ and SO4 2? > HCO3 ? > Cl? > NO3 ?. Spearman’s rank correlation coefficient matrices, factor analysis data, and values of chloro-alkaline indices, C ratio and Na+/Cl? molar ratio indicate that in the groundwater (A), the ionic load of Ca2+, Mg2+, Na+, K+, SO4 2? and HCO3 ? is derived essentially from weathering of both carbonates and aluminosilicates and direct cation and reverse cation–anion exchange reactions. Groundwater (B) is the polluted variant of the groundwater (A), brackish to saline in composition, and unlike the groundwater (A), consists of HCO3 ? as the dominant anion. In comparison with the groundwater (A), the groundwater (B) contains higher concentrations of all ions, and its average ionic load (av. = 59.74 me/L) is 1.43 times higher than that of the groundwater (A) (av. = 41.54 me/L). Additional concentrations of Ca2+, Mg2+, K+, SO4 2?, Cl? and HCO3 ? in the groundwater (B) are provided mainly by downward infiltrating water from the coal washery tailings pond and reverse cation–anion exchange reaction between tailings pond water and exchanger of the aquifer matrix during non-conservative mixing process of groundwater (A) and tailings pond water. Certain additional concentrations of Na+, K+ and NO3 ? in the groundwater (B) are provided by other anthropogenic sources. Quality wise, both groundwaters are marginally suitable for cultivation of salt-tolerant crops only.  相似文献   

11.
Balram Ambade 《Natural Hazards》2014,70(2):1535-1552
In the present work, chemical characterization and sources of fog water contaminants in the most polluted area of central India, Raipur, and its surroundings are described. The fog water (n = 22) was collected during 2010–2011 from six sites. The physical (i.e., pH, fog amount, electrical conductivity and TDS) and chemical (i.e., F?, Cl?, NO3 ?, SO4 2?, NH4 +, Na+, K+, Mg2+, Ca2+, Al, Mn, Fe, Cu, Zn, Pb and Hg) parameters of the fog water were investigated. The effect of meteorology, i.e., temperature, humidity and wind speed, on the precipitation of the fog water contaminants is discussed. The cluster and factor analysis are used to apportion the sources of the contaminants in the fog water.  相似文献   

12.
The work investigates the major solute chemistry of groundwater and fluoride enrichment(F~-) in the shallow phreatic aquifer of Odisha.The study also interprets the hydrogeochemical processes of solute acquisition and the genetic behavior of groundwater F~-contamination.A total of 1105 groundwater samples collected from across the state from different hydro-geomorphic settings have been analyzed for the major solutes and F~-content.Groundwater is alkaline in nature(range of pH: 6.6–8.7; ave.: 7.9) predominated by moderately hard to very hard types.Average cation and anion chemistry stand in the orders of Ca~(2+) Na~+ Mg~(2+) K~+and HCO_3~- Cl~- SO_4~(2-) CO_3~(2-)respectively.The average mineralization is low(319 mg/L).The primary water types are Ca-Mg-HCO_3 and Ca-Mg-Cl~-HCO_3, followed by Na-Cl, Ca-Mg-Cl, and Na-Ca-Mg-HCO_3~-Cl.Silicate-halite dissolution and reverse ion exchange are the significant processes of solute acquisition.Both the geogenic as well as the anthropogenic sources contribute to the groundwater fluoride contamination,etc.The ratio of Na~+/Ca~(2+) 1.0 comprises Na-HCO_3(Cl) water types with F~- 1.0 mg/L(range 1.0–3.5 mg/L)where the F~-bears geogenic source.Positive relations exist between F~-and pH, Na~+, TDS, and HCO_3~-.It also reflects a perfect Na-TDS correlation(0.85).The ratio of Na~+/Ca~(2+) 1.0 segregates the sample population(F~- range: 1.0–4.0 mg/L) with the F derived from anthropogenic sources.Such water types include Ca-Mg-HCO_3(Cl) varieties which are recently recharged meteoritic water types.The F~-levels exhibit poor and negative correlations with the solutes in groundwater.The Na-TDS relation remains poor(0.12).In contrast, the TDS levels show strong correlations with Ca~(2+)(0.91), Mg~(2+)(0.80) and even Cl~-(0.91).The majority of the monitoring points with the anthropogenic sources of groundwater F~-are clustered in the Hirakud Canal Command area in the western parts of the state, indicating the role of irrigation return flow in the F~-contamination.  相似文献   

13.
Twenty groundwater samples were collected from Enugu metropolis over two seasonal periods in order to characterize the groundwater and to determine its quality for domestic and irrigation purposes. The results show that groundwater of the area is strongly acidic to slightly alkaline in nature and varied from “soft water” to “moderately hard” water type. The major ionic trend is in the order Cl? > Na+ > HCO3 ? > K+ > Mg2+ > Ca2+ > SO4 2?and Mg2+ > Cl? > Na+ > K+ > Ca2+ > HCO 3 ?  > SO4 2? in abundance for dry and rainy seasons, respectively. The results also reveal that there is an increase in trend of the ionic concentrations during the dry season, which arises from weathering of the host rocks and anthropogenic activities. Two hydrochemical facies were identified, namely, Na+ –K+ –Cl? –SO4 2?and Ca2+ –Mg2+ –Cl? –SO4 2? , with Na+ –K+ –Cl? –SO4 2? as the dominant facies for the two seasons. Groundwater quality ranges from “very poor water” to “good water” and “water unsuitable for drinking purposes” to “good water” for the dry season and rainy season investigations, respectively. The groundwater is suitable for irrigation purposes for the two seasons.  相似文献   

14.
Agricultural activities act as dominant polluter of groundwater due to increased fertilizers and pesticides usage. Bist-Doab region, Punjab, India, is one such region facing deterioration of groundwater quality due to usage of fertilizers. This study aims in delineating and evaluating the groundwater quality in the region. Water samples are collected from canals, reservoir, and shallow and deep groundwater. Water types in canal and reservoir in Kandi region are Mg2+HCO3 ? and Mg2+Ca2+Na+HCO3 ?, respectively. While water types of shallow and deep groundwaters are found to be of two types: Na+Mg2+Ca2+HCO3 ? and Ca2+Mg2+Na+HCO3 ?. Presence of Mg2+ in groundwater at locations adjoining canals indicates recharge due to canal. The major ion (Na+, Mg2+, Ca2+, HCO3 ?) chemistry of the region is due to weathering of rocks that are rich in sodic minerals and kankar. Deep groundwater quality in the region meets BIS and WHO standards for drinking purpose, unlike shallow groundwater which is of poor quality at many locations. Both shallow and deep groundwater with high sodium concentration (>1.5 meq/l) affect cropping yield and permeability of soil matrix. High concentration of SO4 2? and NO3 2? (>1 meq/l) in shallow groundwater at few locations indicates influence of anthropogenic (fertilizer) activity. Factor analysis indicates that the major cations, bicarbonate and chloride are derived from weathering/dissolution of source rocks. Higher concentration of nitrate and presence of sulphate in shallow groundwater at few locations is due to usage of fertilizers and pesticides.  相似文献   

15.
Shallow groundwater (>30 mbgl) is an essential source of drinking water to rural communities in the Ndop plain, northwest Cameroon. As a contribution to water management, the effect of seasonal variation on the groundwater chemistry, hydrochemical controls, drinking quality and recharge were investigated during the peaks of the dry (January) and rainy (September) seasons. Field measurements of physical parameters were preceded by sampling 58 groundwater samples during both seasons for major ions and stable isotope analyses. The groundwater, which was barely acidic (mean pH of 6) and less mineralised (TDS < 272 mg/l), showed no significant seasonal variation in temperature, pH and TDS during the two seasons. The order of cation abundance (meq/l) was Na+ > Ca2+ > Mg2+ > K+ and Na+ > Mg2+ > Ca2+ > K+ in the dry and rainy seasons, respectively, but that of anions ( \( {\text{HCO}}_{3}^{ - } \)  >  \( {\text{NO}}_{3}^{ - } \)  > Cl? >  \( {\text{SO}}_{4}^{2 - } \)  > F?) was similar in both seasons. This suggests a negligible effect of seasonal variations on groundwater chemistry. The groundwater, which was CaMgHCO3 and NaHCO3, is chemically evolved rainfall (CaMgSO4Cl) in the area. Silicate mineral dissolution and cation-exchange were the main controls on groundwater chemistry while there was little anthropogenic influence. The major ions and TDS concentrations classified the water as suitable for human consumption as per WHO guidelines. The narrow cluster of δ18O and δD of same groundwater from both seasons between the δ18O and δD values of May–June precipitation along the Ndop Meteoric Water Line indicates meteoric origin, rapid recharge (after precipitation) and timing of recharge between May and June rainfall. Diffuse groundwater recharge mainly occurs at low altitudes (<1,400 m asl) within the plain. Besides major ions and TDS, the similar δ18O and δD of groundwater from both seasons indicate a consistent groundwater recharge and flow pattern throughout the year and resilience to present day short-term seasonal climatic variations. However, controlled groundwater abstraction is recommended given the increasing demand.  相似文献   

16.
The hydrogeochemical study of surface and subsurface water of Mahi River basin was undertaken to assess the major ion chemistry, solute acquisition processes and water quality in relation to domestic and irrigation uses. The analytical results show the mildly acidic to alkaline nature of water and dominance of Na+ and Ca2+ in cationic and HCO3 − and Cl− in anionic composition. In general, alkaline-earth elements (Ca2+ + Mg2+) exceed alkalis (Na+ + K+) and weak acids (HCO3 −) dominate over strong acids (SO4 2+ + Cl−) in majority of the surface and groundwater samples. Ca2+–Mg2+–HCO3 − is the dominant hydrochemical facies both in surface and groundwater of the area. The weathering of rock-forming minerals mainly controlled the solute acquisition process with secondary contribution from marine and anthropogenic sources. The higher concentration of sodium and dissolved silica, high equivalent ratios of (Na+ + K+/TZ+), (Na+ + K+/Cl−) and low ratio of (Ca2+ + Mg2+)/(Na+ + K+) suggest that the chemical composition of the water is largely controlled by silicate weathering with limited contribution from carbonate weathering and marine and anthropogenic sources. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the chemistry of river water favors kaolinite formation. Assessment of water samples for drinking purposes suggests that the majority of the water samples are suitable for drinking. At some sites concentrations of TDS, TH, F−, NO3 − and Fe are exceeding the desirable limit of drinking. However, these parameters are well within the maximum permissible limit except for some cases. To assess the suitability for irrigation, parameters like SAR, RSC and %Na were calculated. In general, both surface and groundwater is of good to suitable category for irrigation uses except at some sites where high values of salinity, %Na and RSC restrict its uses.  相似文献   

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19.
The groundwater abstracted at a well field near the Yamuna River in Central Delhi, India, has elevated ammonium (NH4 +) concentrations up to 35 mg/L and arsenic (As) concentrations up to 0.146 mg/L, constituting a problem with the provision of safe drinking and irrigation water. Infiltrating sewage-contaminated river water is the primary source of the NH4 + contamination in the aquifer, leading to reducing conditions which probably trigger the release of geogenic As. These conclusions are based on the evaluation of six 8–27-m deep drillings, and 13 surface-water and 69 groundwater samples collected during seven field campaigns (2012–2013). Results indicate that losing stream conditions prevail and the river water infiltrates into the shallow floodplain aquifer (up to 16 m thickness), which consists of a 1–2-m thick layer of calcareous nodules (locally known as kankar) overlain by medium sand. Because of its higher hydraulic conductivity (3.7 × 10?3 m/s, as opposed to 3.5 × 10?4 m/s in the sand), the kankar layer serves as the main pathway for the infiltrating water. However, the NH4 + plume front advances more rapidly in the sand layer because of its significantly lower cation exchange capacity. Elevated As concentrations were only observed within the NH4 + plume indicating a causal connection with the infiltrating reducing river water.  相似文献   

20.
Biogeochemical processes were investigated in alpine river—Kamni?ka Bistrica River (North Slovenia), which represents an ideal natural laboratory for studying anthropogenic impacts in catchments with high weathering capacity. The Kamni?ka Bistrica River water chemistry is dominated by HCO3 ?, Ca2+ and Mg2+, and Ca2+/Mg2+ molar ratios indicate that calcite weathering is the major source of solutes to the river system. The Kamni?ka Bistrica River and its tributaries are oversaturated with respect to calcite and dolomite. pCO2 concentrations were on average up to 25 times over atmospheric values. δ13CDIC values ranged from ?12.7 to ?2.7 ‰, controlled by biogeochemical processes in the catchment and within the stream; carbonate dissolution is the most important biogeochemical process affecting carbon isotopes in the upstream portions of the catchment, while carbonate dissolution and organic matter degradation control carbon isotope signatures downstream. Contributions of DIC from various biogeochemical processes were determined using steady state equations for different sampling seasons at the mouth of the Kamni?ka Bistrica River; results indicate that: (1) 1.9–2.2 % of DIC came from exchange with atmospheric CO2, (2) 0–27.5 % of DIC came from degradation of organic matter, (3) 25.4–41.5 % of DIC came from dissolution of carbonates and (4) 33–85 % of DIC came from tributaries. δ15N values of nitrate ranged from ?5.2 ‰ at the headwater spring to 9.8 ‰ in the lower reaches. Higher δ15N values in the lower reaches of the river suggest anthropogenic pollution from agricultural activity. Based on seasonal and longitudinal changes of chemical and isotopic indicators of carbon and nitrogen in Kamni?ka Bistrica River, it can be concluded that seasonal changes are observed (higher concentrations are detected at low discharge conditions) and it turns from pristine alpine river to anthropogenic influenced river in central flow.  相似文献   

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