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1.
Three wells in New Hampshire were sampled bimonthly over three years to evaluate the temporal variability of arsenic concentrations and groundwater age.All samples had measurable concentrations of arsenic throughout the entire sampling period and concentrations in individual wells had a mean variation of more than 7 μg/L.The time series data from this sampling effort showed that arsenic concentrations ranged from a median of 4 μg/L in a glacial aquifer well(SGW-65)to medians of 19μg/L and37 μg/L in wells(SGW-93 and KFW-87)screened in the bedrock aquifer,respectively.These high arsenic concentrations were associated with the consistently high pH(median≥8)and low dissolved oxygen(median0.1 mg/L)in the bedrock aquifer wells,which is typical of fractured crystalline bedrock aquifers in New Hampshire.Groundwater from the glacial aquifer often has high dissolved oxygen,but in this case was consistently low.The pH also is generally acidic in the glacial aquifer but in this case was slightly alkaline(median = 7.5).Also,sorption sites may be more abundant in glacial aquifer deposits than in fractured bedrock which may contribute to lower arsenic concentrations.Mean groundwater ages were less than 50 years old in all three wells and correlated with conservative tracer concentrations,such as chloride;however,mean age was not directly correlated with arsenic concentrations.Arsenic concentrations at KFW-87 did correlate with water levels,in addition,there was a seasonal pattern,which suggests that either the timing of or multiple sampling efforts may be important to define the full range of arsenic concentrations in domestic bedrock wells.Since geochemically reduced conditions and alkaline pHs are common to both bedrock and glacial aquifer wells in this study,groundwater age correlates less strongly with arsenic concentrations than geochemical conditions.There also is evidence of direct hydraulic connection between the glacial and bedrock aquifers,which can influence arsenic concentrations.Correlations between arsenic concentrations and the age of the old fraction of water in SGW-65 and the age of the young fraction of water in SGW-93 suggest that water in the two aquifers may be mixing or at least some of the deeper,older water captured by the glacial aquifer well may be from a similar source as the shallow young groundwater from the bedrock aquifer.The contrast in arsenic concentrations in the two aquifers may be because of increased adsorption capacity of glacio-fluvial sediments,which can limit contaminants more than fractured rock.In addition,this study illustrates that long residence times are not necessary to achieve more geochemically evolved conditions such as high pH and reduced conditions as is typically found with older water in other regions.  相似文献   

2.
《Applied Geochemistry》2000,15(3):311-325
Barium/Sr and Ca/Sr ratios have been used to model the relative importance of different sources of stream water. Major and trace element concentrations together with 87Sr/86Sr ratios were measured in precipitation, soil water, groundwater and stream water in a small (9.4 km2) catchment in northern Sweden. The study catchment is drained by a first order stream and mainly covered with podzolized Quaternary till of granitic composition. It is underlain by a 1.8 Ga granite. A model with mixing equations used in an iterative mode was developed in order to separate the stream water into 3 subsurface components: soil water, shallow groundwater, and deep groundwater. Contributions from precipitation are thus not included in the model. This source may be significant for the stream water generation, but it does not interfere with the calculations of the relative contributions from the subsurface components. The results show that the deep groundwater constitutes between 5 and 20% of the subsurface water discharge into the stream water. The highest values of the deep groundwater fraction occur during base flow. Soil water dominates during snowmelt seasons, whereas during base flow it is the least important fraction. Soil water accounts for 10–100% of the subsurface water discharge into the stream water. Shallow groundwater accounts for up to 80% of the subsurface water discharge with the lowest values at peak discharge during snowmelt seasons and the highest values during base flow. The validity of the model was tested by comparing the measured 87Sr/86Sr ratios in the stream water with the 87Sr/86Sr ratios predicted by the model. There was a systematic difference between the measured and modelled 87Sr/86Sr ratios which suggests that the fraction of soil water is overestimated by the model, especially during spring flood. As a consequence of this overestimation of soil water the amount of shallow groundwater is probably underestimated during this period. However, it is concluded that the differences between measured and predicted values are relatively small, and that element ratios are potentially effective tracers for different subsurface water flowpaths in catchments.  相似文献   

3.
The role of different minerals in base cation release and thus the increase of buffering capacity of groundwater against acid deposition is controversially discussed in the literature. The 87Sr/86Sr ratios and base cation concentration were investigated in whole rock leachates, mineral separates, precipitation, soil solution, groundwater and stream water samples in the Lehstenbach catchment (Germany) to identify the weathering sequence of the granite bedrock. Three different approaches were followed in parallel. It was assumed that the contribution of different minerals to base cation supply of the groundwater with increasing weathering intensity would be observed by investigating (1) unweathered rock leachates, deep groundwater and shallow groundwater, (2) groundwater samples from new groundwater wells, reflecting the initial weathering of the drilled bedrock, and groundwater from wells that were drilled in 1988, (3) stream water during baseflow, dominated by deep groundwater, and stream water during high flow, being predominantly shallow groundwater. Whereas the first approach yielded consistent patterns, there was some evidence that groundwater from the new wells initially reflected contamination by the filter gravel rather than cation release in an initial stage of weathering. Time series samples of stream water and groundwater solute concentrations and isotope ratios turned out to reflect varying fractions of soil water and precipitation water at baseflow and high flow conditions rather than varying contributions of different minerals that prevail at different stages of granite weathering.  相似文献   

4.
Research on large northern rivers suggests that as permafrost thaws, deeper groundwater flowpaths become active, resulting in greater baseflow, increased concentrations of weathering ions and reduced concentrations of dissolved organic carbon in the streamflow. In contrast, at the headwater-catchment scale, where understanding of groundwater/surface-water interactions is developed, inter-annual variability in climate and hydrology result in complex hydrological and chemical responses to change. This paper reports on a 4-year runoff investigation in an alpine discontinuous permafrost environment in Yukon, Canada, using stable isotopes, major dissolved ions and hydrometric data, to provide enhanced insight into the inter-annual-variability runoff-generation processes. Stable isotope results suggest that pre-event (old) water stored within the catchment dominates the snowmelt hydrograph, and dissolved ion results reveal that groundwater pathways occur predominantly in the near-surface during freshet. Dissolved organic carbon varies inter-annually, reflecting changing melt patterns, whereas weathering ions generated from deeper flowpaths become diluted. The total snow-water equivalent does not have a major influence on the fraction of snowmelt water reaching the stream or the runoff ratio. Results from multiple years highlight the considerable variability over short time scales, limiting our ability to detect climate-change influences on groundwater at the headwater scale.  相似文献   

5.
A numerical model of chemical weathering in soil horizons and underlying bedrock (WITCH) has been coupled to a numerical model of water and carbon cycles in forest ecosystems (ASPECTS) to simulate the concentration of major species within the soil horizons and the stream of the Strengbach granitic watershed, located in the Vosges Mountains (France). For the first time, simulations of solute concentrations in soil layers and in the catchment river have been performed on a seasonal basis. The model is able to reproduce the concentrations of most major species within the soil horizons, as well as catching the first-order seasonal fluctuations of aqueous calcium, magnesium and silica concentrations. However, the WITCH model underestimates concentrations of Mg2+ and silica at the spring of the catchment stream, and significantly underestimates Ca2+ concentration. The deficit in calculated calcium can be compensated for by dissolution of trace apatite disseminated in the bedrock. However, the resulting increased Ca2+ release yields important smectite precipitation in the deepest model layer (in contact with the bedrock) and subsequent removal of large amount of silica and magnesium from solution. In contrast, the model accurately accounts for the concentrations of major species (Ca, Mg and silica) measured in the catchment stream when precipitation of clay minerals is not allowed. The model underestimation of Mg2+ and H4SiO4 concentrations when precipitation of well crystallized smectites is allowed strongly suggests that precipitation of well crystallized clay minerals is overestimated and that more soluble poorly crystallized and amorphous materials may be forming. In agreement with observations on other watersheds draining granitic rocks, this study indicates that highly soluble trace calcic phases control the aqueous calcium budget in the Strengbach watershed.  相似文献   

6.
Potassium chloride (KCl) and potassium bromide (KBr) tracers were used to explore the role of geologic structure on groundwater recharge and flow at the Fractured Rock Research Site in Floyd County, Virginia, USA. Tracer migration was monitored through soil, saprolite, and fractured crystalline bedrock for a period of 3 months with chemical, physical, and geophysical techniques. The tracers were applied at specific locations on the ground surface to directly test flow pathways in a shallow saprolite and deep fractured-rock aquifer. Tracer monitoring was accomplished with differential electrical resistivity, chemical sampling, and physical monitoring of water levels and spring discharge. KCl, applied at a concentration of 10,000 mg/L, traveled 160 m downgradient through the thrust fault aquifer to a spring outlet in 24 days. KBr, applied at a concentration of 5,000 mg/L, traveled 90 m downgradient through the saprolite aquifer in 19 days. Tracer breakthrough curves indicate diffuse flow through the saprolite aquifer and fracture flow through the crystalline thrust fault aquifer. Monitoring saline tracer migration through soil, saprolite, and fractured rock provided data on groundwater recharge that would not have been available using other traditional hydrologic methods. Travel times and flowpaths observed during this study support preferential groundwater recharge controlled by geologic structure.  相似文献   

7.
天然成因的高氟地下水是世界范围内备受关注的环境问题和饮用水安全问题。前人对高氟地下水的形成过程已开展了大量研究,但是对于高原盆地复杂水文地质条件下不同类型含水层组(第四系松散层含水层、基岩裂隙或岩溶含水层以及新生代古近纪以来的碎屑岩含水层)高氟地下水的分布和形成过程尚不明确。本文以化隆—循化盆地为研究区,通过采集、测试研究区内的各类地下水样品,分析研究区内不同类型含水层中地下水的化学特征及同位素特征。结果表明,高氟地下水(1.007.73 mg/L)主要分布在沿黄河的河谷区域和巴燕低山丘陵区域的泉水和潜水中以及深部的承压水中,在垂向上高氟地下水无明显分布规律。接受黄河水入渗补给的河谷潜水中氟离子浓度较低,补给黄河的河谷潜水中氟离子浓度较高。贫钙富钠的弱碱性苏打型水有利于地下水中氟的富集。泉水和潜水中氟主要来源于萤石的溶解,而承压水中氟除了来源于萤石外,还来源于其他含氟矿物。对于潜水和第四系松散层泉水,蒸发浓缩作用促进了地下水中氟的富集。另外,阴离子竞争吸附作用、阳离子交换吸附作用是泉水(第四系松散层泉水和基岩裂隙泉水)和潜水中氟元素富集的主要原因,而承压水中氟离子浓度受竞争吸附作用影响较大,阳离子交换吸附作用影响较小。研究成果可为化隆—循化盆地低氟地下水的勘查和开发提供科学依据。  相似文献   

8.
Hydrogeochemical processes controlling surface water chemistry were examined in five small (<1.5 km 2) forested catchments that have contrasting bedrock lithologies of granite, and conglomerate, and are distributed in the southeast of Seto district, central Japan. Watersheds developed on these two bedrocks differ in their ability to neutralize atmospheric acid (pH ~4.5) deposition. The study was conducted to (1) characterize the hydrogeochemical processes controlling surface water chemistry, and (2) to elucidate acidification of spring and stream waters using data from three sampling campaigns conducted from August to October 2000. Stream and spring water solutes fall into two general groups according to concentration: alkaline, relatively high pH (5.2–7.7) and high cation concentrations (HCO 3 -, Cl -, base cations), and dilute, low pH (4.2–5.5) waters. Concentrations of trace metals (Al, Ba, Sr) showed a strong negative correlation with pH, suggesting the mobility of these metals in the dissolved load of catchments underlain by Tokai conglomerate. The strontium isotope ratio ( 87Sr/ 86Sr) of rock and soil, plant, precipitation, and surface water samples was used to identify different reservoirs within the ecosystem. Low Si concentrations in stream and spring waters from the conglomerate area, with a relatively high pool of SiO 2, >90 (wt%), suggest slow chemical weathering. The dissolved solute concentrations are generally of similar magnitude in stream waters within the catchments of similar bedrock lithology. The high inverse correlation ( r 2=0.72) between pH and SO 4 concentrations and the high positive correlation ( r 2 =0.90) between Ba and SO 4 concentrations in waters draining Tokai conglomerate suggest that barite (BaSO 4) is being dissolved in an acidic environment. The three catchments were identified as being sensitive to acidic deposition because the bedrock conglomerate provided little capacity to buffer acidic inputs. The soils from the granite area have a high cation-exchange capacity (CEC an average of 868 µmol/kg), and are nearly ten times greater than the soils from the conglomerate area. Because ion exchange, besides weathering, is the main source that counteracts soil acidification, the sensitivity to further acidification may increase.  相似文献   

9.
《Applied Geochemistry》1997,12(4):447-464
The controls on metal concentrations in a plume of acidic (pH 3.29–5.55) groundwater in the Moon Creek watershed in Idaho, U.S.A., were investigated with the use of property-property plots. A plot of Ca vs S demonstrated that a plume of contaminated groundwater was being diluted by infiltration of rain and creek water at shallow depths and by ambient groundwater near bedrock. The small amount of dissolved Fe (2.1 mg/l) was removed while dissolved Pb was added, reaching a maximum concentration of 0.37 mg/l. The other metals (Zn ≤ 16, Al ≤ 6.2, Cu ≤ 2.1 and Cd ≤ 0.077 mg/l) in the shallow groundwater were essentially conserved until they emerged as a seep along the creek bank. Upon mixing with the creek water, groundwater was diluted by factors between 11 and 50, and the pH of the mixture became neutral. Metals originating from the contaminated groundwater were removed in the creek in the following order: Fe > Al > Pb ≫ Cu > Mn > Zn = Cd.Pb and Cu continued to be removed from solution even as the creek passed adjacent to a tailings pile. In contrast, Zn concentrations in the creek increased adjacent to the tailings area, presumably as a result of the reemergence of the upgradient plume as the creek lost elevation.Below the tailings dam, contaminated creek water (400–800 μg Zn/l) was diluted by both smaller side streams and a creek of equal flow. The presence of 3 distinctive water masses required the use of two tracers (dissolved Si and S) to distinguish between mixing and geochemical reactions. The removal of metals was greater during low flow conditions. Pb was removed to the greatest extent, falling below detection limits (0.5 μ/l) at the first sampling location. Copper and Mn were removed to a lesser extent during low flow conditions and approached conservative behavior during high flow conditions. During a 5-km journey through two hydrological regimes, less than 10% of the dissolved Zn and Cd was lost.  相似文献   

10.
In the Gran Sasso fissured carbonate aquifer (central Italy), a long-term (2001–2007) spatio-temporal hydrochemical and 222Rn tracing survey was performed with the goal to investigate groundwater flow and water–rock interaction. Analyses of the physico-chemical parameters, and comparisons of multichemical and characteristic ratios in space and time, and subsequent statistical analyses, permitted a characterisation of the hydrogeology. At the regional scale, groundwater flows from recharge areas to the springs located at the aquifer boundaries, with a gradual increase of mineralisation and temperature along its flowpaths. However, the parameters of each group of springs may significantly deviate from the regional trend owing to fast flows and to the geological setting of the discharge spring areas, as corroborated by statistical data. Along regional flowpaths, the effects of seasonal recharge and lowering of the water table clearly cause changes in ion concentrations over time. This conceptual model was validated by an analysis of the 222Rn content in groundwater. 222Rn content, for which temporal variability depends on seasonal fluctuations of the water table, local lithology and the fracture network at the spring discharge areas, was considered as a tracer of the final stages of groundwater flowpaths.  相似文献   

11.
The pervious lateral bars (parafluvial zone) and beds (hyporheic zone), where stream water and groundwater exchange, are dynamic sites of hydrological and biological retention. The significance of these biogeochemical ‘hotspots’ to stream and groundwater metabolism is largely controlled by filtration capacity, defined as the extent to which subsurface flowpaths and matrix hydraulic conductivity modify water characteristics. Where hydraulic conductivity is high, gradients in biogeochemistry and microbial activity along subsurface flowpaths were hypothesized to be less marked than where hydraulic conductivity is low. This hypothesis was tested in two riffles and gravel bars in an Australian subtropical stream. At one site, gradients in chemical and microbial variables along flowpaths were associated with reduced hydraulic conductivity, longer water residence time and reduced filtration capacity compared with the second site where filtration capacity was greater and longitudinal biogeochemical trends were dampened. These results imply that factors affecting the sediment matrix in this subtropical stream can alter filtration capacity, interstitial microbial activity and biogeochemical gradients along subsurface flowpaths. This hydroecological approach also indicates potential for a simple field technique to estimate filtration capacity and predict the prevailing hyporheic gradients in microbial activity and biogeochemical processing efficiency, with significant implications for stream ecosystem function.  相似文献   

12.
Although phytoliths constitute part of the wetland suspended load, there are few studies focused on the quantification of them in the biogenic silica (BSi) pool. So, the aim of this paper is both to determine BSi content (diatoms and phytoliths) and its relationship with dissolved silica in surface waters, and the influence of soil and groundwater Si biogeochemistry in Los Padres wetland (Buenos Aires Province, Argentina). In the basin of the Los Padres wetland, dissolved silica (DSi) concentration is near 840 ± 232 μmol/L and 211.83 ± 275.92 μmol/L in groundwaters and surface waters, respectively. BSi represents an 5.6–22.1% of the total suspension material, and 8–34% of the total mineralogical components of the wetland bottom sediments. DSi and BSi vary seasonally, with highest BSi content (diatoms specifically) during the spring–summer in correlation to the lowest DSi concentration. DSi (660–917.5 μmol/L) and phytolith (3.35–5.84%) concentrations in the inflow stream are higher than in the wetland and its outflow stream (19.1–113 μmol/L; 0.45–3.2%, respectively), probably due to the high phytolith content in soils, the high silica concentration in the soil solution, and the groundwater inflow. Diatom content (5–16.8%) in the wetland and its outflow stream is higher than in the inflow stream (0.45–1.97%), controlling DSi in this system. The understanding of the groundwater–surface water interaction in an area is a significant element for determining the different components and the role that they play on the local biogeochemical cycle of Si.  相似文献   

13.
High and variable levels of salinity were investigated in an intermittent stream in a high-rainfall area (~800 mm/year) of the Mt. Lofty Ranges of South Australia. The groundwater system was found to have a local, upslope saline lens, referred to here as a groundwater salinity ‘hotspot’. Environmental tracer analyses (δ18O, δ2H, 87/86Sr, and major elements) of water from the intermittent stream, a nearby permanent stream, shallow and deep groundwater, and soil-water/runoff demonstrate seasonal groundwater input of very saline composition into the intermittent stream. This input results in large salinity increases of the stream water because the winter wet-season stream flow decreases during spring in this Mediterranean climate. Furthermore, strontium and water isotope analyses demonstrate: (1) the upslope-saline-groundwater zone (hotspot) mixes with the dominant groundwater system, (2) the intermittent-stream water is a mixture of soil-water/runoff and the upslope saline groundwater, and (3) the upslope-saline-groundwater zone results from the flushing of unsaturated-zone salts from the thick clayey regolith and soil which overlie the metamorphosed shale bedrock. The preferred theory on the origin of the upslope-saline-groundwater hotspot is land clearing of native deep-rooted woodland, followed by flushing of accumulated salts from the unsaturated zone due to increased recharge. This cause of elevated groundwater and surface-water salinity, if correct, could be widespread in Mt. Lofty Ranges areas, as well as other climatically and geologically similar areas with comparable hydrogeologic conditions.  相似文献   

14.
Atmospheric deposition of S in Sweden has decreased by some 80% over the last 15 a, resulting in a general reduction of SO4 concentrations in ground and surface water. This project, however, shows that artificial hydrological alteration in an acid wetland can reverse this trend and increase acidity and SO4 concentrations. The experiment involved the monitoring of two catchments in relatively virgin conditions. In one of the catchments, an experiment with intensive groundwater extraction from the bedrock was carried out. During the experiment, the runoff from the catchment decreased by 50%. Furthermore, the extraction of groundwater resulted in increased seasonal aeration of the centrally located wetland, leading to oxidation of reduced S bound to the soil layers of the wetland. The S changed to solute SO4, with a subsequent SO4 surge. Thus, the experiment resulted in an induced acidification of the wetland and runoff waters. The extraction of groundwater significantly increased the recharge of water from the overburden, glacial till and organic soils to groundwater in the bedrock, which in turn reduced the retention time in the bedrock aquifer. These changes resulted in the chemical signature of the groundwater in the bedrock becoming similar to those of the wetland. The findings revealed deterioration in the water quality in the bedrock due to increased concentrations of dissolved organic C and SO4, as well as a decrease in pH.  相似文献   

15.
There is a broad correlation between the εNd values for rivers (including both the water and the particulate material it carries) and the age of the source terrain. This paper presents Nd isotope distribution data for soil, soil water, groundwater, and stream water samples gathered in a small catchment in northern Sweden. The results show that the release of Nd and Sm from boreal forests into streams and, eventually, into the oceans is more complicated than previously realized. The weathering of till causes changes in both the Nd isotopic composition and Sm/Nd ratios. Both the Sm/Nd ratio and εNd were higher in strongly weathered soils horizons than in less weathered till, since minerals with high Sm/Nd ratios were, on average, more resistant to weathering than those with low Sm/Nd ratios. In contrast to the situation for the main minerals and the major elements, the weathering of rare earth elements (REE) was not restricted to the E-horizon: the measured REE concentrations continued to increase with depth in the C-horizon. In addition, REE released by weathering in the upper parts of the soil profile were partly secondarily retained at deeper levels. Therefore, the dissolved Nd released by weathering in the upper soil horizons was trapped and did not enter the groundwater directly. Rather, the Nd in the groundwater largely originated from weathering within the groundwater zone. However, this was not the only source of Nd in the stream water. The Nd isotope composition and Sm/Nd ratio were determined by the mixing between of Nd and Sm in the groundwater and REE-carrying organic material washed out of the soil profile. The groundwater close to the stream reaches the upper soil horizons during high discharge events such as snowmelts, and organic matter carrying Nd and Sm is washed out of the soils and thus released into the stream. Therefore, the Nd exported from catchment is derived from both the weathering within the groundwater zone, and the organic matter washed out from the soil. If longer timescales with more advanced weathering stages in the groundwater zone are considered, it cannot be ruled out that there will be a shift towards more radiogenic values in the exported Nd. Recorded shifts in the Nd isotopic composition in the ocean may thus not only reflect changed source regions, but also the weathering history of the same source region.  相似文献   

16.
The distribution and chemistry of the springs in the Tuscarora Creek watershed is controlled by both geologic structure and karst dissolution. The watershed is located in eastern West Virginia in the structurally complex Great Valley of the Appalachian Valley and Ridge province. The upper portion of the stream parallels strike along a mapped fault zone and is bordered by clastic rocks that comprise North Mountain. The lower reaches of the stream flow cross-strike through Cambro-Ordovician carbonates. The controlling chemical signature in the spring water is carbonate dissolution. Little evidence was seen for the recharge from adjacent clastic rocks although differences in the Ca/Mg molar ratio between springs indicated the presence of localized spring basins in headwater reaches. Na, Cl and Ca generally increased from upstream to downstream in the cross-strike reaches. Comparison of stream and cumulative spring discharge was consistent with significant groundwater base-flow contribution directly to the creek, particularly in the strike-parallel region. The largest spring in the watershed (>162 L/s) was sampled during and after a large storm event along with the adjacent creek. The creek displayed a typical dilution response with each flood pulse, whereas the spring had only a limited or delayed response. The overall chemical and thermal stability of the spring, relative to the creek, indicated the lack of significant direct hydraulic connection between the two. The conceptual model for the area includes localized flowpaths in the headwater region where the stream flow is parallel to strike and a thrust fault. In addition to the shallow localized flowpaths, a deeper, more regional flowpath likely exists for a large spring further downstream.  相似文献   

17.
Once or twice weekly, water sampling was undertaken for a two and a half year period in the Kalix River, northern Sweden. Soil water, groundwater, water in tributaries and mire water were also sampled at several occasions. Samples were filtered and analysed for major dissolved elements and TOC. Although only 5 of the bedrock in the Kalix River drainage basin is situated in the Caledonian mountains (mostly schist, with some outcrops of dolomite and limestone), the chemical composition of the river, at the river mouth, is clearly influenced by water from the mountain areas. High dissolved Ca/Mg ratios in June and July indicate a large influence of water from the mountain areas during summer. The dissolved Si/Mg ratio increases when water from the woodland (bedrock consisting of Precambrian granitoids) predominates during snowmelt in May, but the ratio is low during summer when water from the mountains is increased. However, the low Si concentrations in the mountain areas are probably not primarily the result of the different rocks but more a reflection of the less intense weathering of silicate minerals in the mountains. High Si/Mg ratios are closely related to high TOC. All the major dissolved elements, except TOC, are diluted by snowmelt in May. However, the dilution varies for different elements. Based on the interpretations of major element ratios the melt water discharge in May reflects two major compartments in the woodland; peatland areas and the upper section of the soil. During summer and autumn storm events in the woodland most of the storm water originated from peatland. High K/Mg ratios in the river in May are related to water discharge from the upper section of the till. Low S/Mg ratios in the river indicate an influence of mire water from the woodland both during melt water discharge in May and during increased water discharge in autumn. The Ca/Mg ratios in tributaries in the woodland are consistently lower during melt water discharge compared with values in August. The lower Ca/Mg ratio in May probably reflects water that has been in contact with the B-horizon in the till during spring flood. Data show that the TOC discharged during spring flood originates from two major compartments in the landscape, the upper soil profile and peatland. Storm discharge of TOC during the rest of the year originates mostly from peatland.  相似文献   

18.
《Applied Geochemistry》2003,18(5):675-691
The small karstic watershed of Lanmuchang, in a Hg–Tl mineralized area in SW Guizhou Province, China, exhibits an enrichment of toxic Tl in groundwater and related stream water. This affords an excellent demonstration of the natural processes of Tl dispersion, and the resultant impact on the local ecosystem. The distribution of Tl in the water system follows a decreasing concentration pattern from deep groundwater to stream water to shallow groundwater. Tl shows high levels (13–1100 μg/L) in deep groundwater within the Tl-mineralized area, decreasing with distance away from the mineralized area to background levels (0.005 μg/L). The distribution of Tl in the water system is constrained by Tl mineralization, water–rock interactions and hydrogeological conditions. Tl concentrations in waters generally correlate with concentrations of total dissolved solids, sulphate, Ca and pH values, suggesting the contribution of water-rock interactions to water geochemistry. Water–rock interactions are driven by weathering of Tl-bearing sulfides which decreases pH values in groundwater, and by dissolution of limestone enhanced by acid fluids. Tl in stream water in both the base-flow and flood-flow regimes shows higher concentrations than it does in shallow groundwater that serves as the stream's source (mainly springs, dug-well flows and karstic cave waters). Concentrations of Tl in stream water in the flood-flow regime are generally lower than in the base-flow regime due to dilution effects, but those in the waters of mid-stream are almost the same as in the base-flow regime, probably due to contribution from Tl-rich soil water seepage or from acid mine drainage (AMD). Unexpectedly, Tl concentrations in stream water in both regimes are remarkably higher (2–30 fold) downstream than up- and mid-stream. These pronounced increases of Tl concentration are likely caused by unidentified discharges of deep groundwater through fractured zones to the downstream trace. The groundwater-related Tl transfer processes affect the ecosystem through contamination of water supply and arable soil and ultimately the food chain with undoubted risks to human health. Therefore, the results of this study are important for environmental planning and regulations, and will also serve as baseline data for future research on Tl natural dispersion processes.  相似文献   

19.
The Waterloo Moraine is a stratigraphically complex system and is the major water supply to the cities of Kitchener and Waterloo in Ontario, Canada. Despite over 30?years of investigation, no attempt has been made to unify existing geochemical data into a single database. A composite view of the moraine geochemistry has been created using the available geochemical information, and a framework created for geochemical data synthesis of other similar flow systems. Regionally, fluid chemistry is highly heterogeneous, with large variations in both water type and total dissolved solids content. Locally, upper aquifer units are affected by nitrate and chloride from fertilizer and road salt. Typical upper-aquifer fluid chemistry is dominated by calcium, magnesium, and bicarbonate, a result of calcite and dolomite dissolution. Evidence also suggests that ion exchange and diffusion from tills and bedrock units accounts for some elevated sodium concentrations. Locally, hydraulic “windows??cross connect upper and lower aquifer units, which are typically separated by a clay till. Lower aquifer units are also affected by dedolomitization, mixing with bedrock water, and locally, upward diffusion of solutes from the bedrock aquifers. A map of areas where aquifer units are geochemically similar was constructed to highlight areas with potential hydraulic windows.  相似文献   

20.
In this case study, silica concentration, oxygen and strontium isotopes of water samples were used to study surface water–groundwater interaction at the Xin’an karst water system. The silica concentration in rain water is commonly less than 1 mg/l. In the areas around the south tributary of the Zhuozhang River, silica concentrations in the groundwater in Quaternary aquifers range between 4.04 and 7.66 mg/l while that of the surface water varies from 1.49 to 6.9 mg/l. Silica concentrations of most surface water samples increase with TDS, indicating the effect of groundwater recharge on river water chemistry. On the contour map of silica concentration of groundwater in Quaternary aquifers, samples located close to surface water often have lower silica concentrations as a result of surface water recharge. Both overland flow and surface water have impact on karst water according to our hydrogeochemical study of stable oxygen isotope, Sr isotope and strontium contents. Calculation results of three end member mixing model show that the contribution of karst water, surface water and overland flow water is 45, 28 and 27%, respectively.  相似文献   

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