首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 203 毫秒
1.
Hydrobiogeochemical processes controlling stream water chemistry were examined in four small (<5 km2) catchments having contrasting bedrock lithologies in the western Sierra Nevada foothills of California. The Mediterranean climate with its cool/wet and hot/dry cycle produces strong seasonal patterns in hydrological, biological and geochemical processes. Stream water solutes fall into three general groups according to seasonal fluctuation in concentration: strong, rainy season minimum–dry season maximum (Cl, SO42−, base cations); weak, rainy season minimum–dry season maximum (Si); and rainy season maximum–dry season minimum (NO3 and K+). Solute dynamics in soil solutions and stream water suggest that mixing of drainage waters from bedrock and soil sources regulate stream water solute concentrations. Patterns are further altered by the leaching of solutes accumulated in the soil over the summer period of desiccation and the temporal discoupling of nutrient cycles that occurs due to differences in the timing between vegetation growth (late spring) and leaching (early winter). Solute concentrations are remarkably similar between watersheds with varying bedrock types, with the exception of nitrate, sulfate and bicarbonate. Three watersheds have nitrogen-bearing metasedimentary bedrock that contributes to elevated nitrate concentrations in stream waters. Watersheds whose bedrock includes mineralized veins of sulfide and carbonate minerals similarly have greater sulfate and bicarbonate concentrations in stream water. Hydrobiogeochemical processes are highly dynamic at the seasonal and storm-event temporal scales and spatially complex at the watershed scale making management of stream water chemical composition, such as nitrate concentrations, very challenging.  相似文献   

2.
Streamwater discharge and chemistry of two small catchments on Catoctin Mountain in north-central Maryland have been monitored since 1982. Repetitive seasonal cycles in stream-water chemistry have been observed each year, along with seasonal cycles in the volume of stream discharge and in groundwater levels. The hypothesis that the observed streamwater chemical cycles are related to seasonal changes in the hydrological flow paths that contribute to streamflow is examined using a combination of data on groundwater levels, shallow and deep groundwater chemistry, streamwater discharge, streamwater chemistry, soil-water chemistry, and estimates of water residence times. The concentrations of constituents derived from rock weathering, particularly bicarbonate and silica, increase in streamwater during the summer when the water table is below the regolith-bedrock interface and stream discharge consists primarily of deep groundwater from the fractured-bedrock aquifer. Conversely, the concentrations in streamwater of atmospherically derived components, particularly sulfate, increase in winter when the water table is above the regolith-bedrock interface and stream discharge consists primarily of shallow groundwater from the regolith. Tritium and chlorofluorocarbon (CFC) measurements suggest that the groundwater in these systems is young, with a residence time of less than several years. The results of this study have implications for the design of large-scale water-quality monitoring programs.  相似文献   

3.
Abstract

The chemistry of streamwater, bulk precipitation, throughfall and soil waters has been studied for three years in two plantation forest and two moorland catchments in mid-Wales. Na and CI are the major ions in streamwater reflecting the maritime influence on atmospheric inputs. In all streams, baseflow is characterised by high pH waters enriched in Ca, Mg, Si and HCO3. Differences in baseflow chemistry between streams reflect the varying extent of calcite and base metal sulphide mineralization within the catchments. Except for K, mean stream solute concentrations are higher in the unmineralized and mineralized forest catchments compared with their respective grassland counterparts. In the forest streams, storm flow concentrations of H+ are approximately 1.5 times and Al four times higher than in the moorland streams. Annual catchment losses of Na, Cl, SO4, NO3, Al and Si are greatest in the forest streams. In both grassland and forest systems, variations in stream chemistry be explained by mixing waters from different parts of the catchment, although NO3 concentrations may additionally be controlled by N transformations occurring between soils and streams. Differences in stream chemistry and solute budgets between forest and moorland catchments are related to greater atmospheric scavenging by the trees and changes in catchment hydrology consequent on afforestation. Mineral veins within the catchment bedrock can significantly modify the stream chemical response to afforestation.  相似文献   

4.
Hydrology and solute concentrations of two intermittent Mediterranean streams draining two nested catchments were compared. The two catchments were mainly underlain by granitic rocks and different types of sericitic schists. Only the lowland catchment had an alluvial zone and a well‐developed riparian forest. The rainfall–runoff relationship and the correlation between daily flow concentrations showed that hydrological behaviour was similar at both sites during most of the year. However, reverse fluxes were detected during the wetting and drying up periods only in the stream with an alluvial zone. The intermittence in stream flow also had effects on absolute solute concentrations, temporal solute dynamics and streamwater stoichiometry. Streamwater chemistry was not affected by drainage area, except for cations produced mainly by bedrock dissolution (i.e. calcium and magnesium) that increased with increasing catchment size. Differences in the relationship among cations and anions were detected between the two streams, which could be attributed to biogeochemical processes occurring in the alluvial zone. The multivariate model used in this study showed that stoichiometry was more useful than absolute concentrations when analyzing the influence of different lithologies on streamwater chemistry. Such differences were amplified in autumn, likely due to a low hydrological connectivity between the two nested catchments. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

5.
Variations in the concentration of Cl in rainfall and stream runoff are presented for two catchments in the Hafren forest of mid-Wales, Great Britain. Despite the large fluctuations in rainfall concentrations, Cl in the streamwater remains relatively constant. Using the two-reservoir Birkenes model, an attempt was made to simulate observed Cl in streamwater. The original model was unable to reproduce the observations and several modifications are suggested to provide better simulations. The resulting model is not the only one capable of reproducing the observations; other hydrochemical models will most probably also achieve this although emphasis will in each case be placed on different aspects. In this paper, it is suggested that the stochastic properties of water movement and chemical processes can account for the streamwater chemistry responses observed. On the catchment scale these processes will lead to an apparently deterministic behaviour that may well be described by simple relationships.  相似文献   

6.
根据河套盆地周缘断裂带泉水的氢、氧同位素组成和水化学组分,讨论了该区地下水的化学类型、成因及其与地震活动的关系。于2014年9月下旬和2015年4月15日MS5.8阿左旗地震震后在河套盆地周缘的乌拉山断裂带、色尔腾断裂带、狼山断裂带以及桌子山断裂带采集了17个泉水和井水样品,测得水样的TDS分布在143.8~42 553.0mg/L范围内,δD和δ18O值分别在-83.6‰~66.56‰和-11.16‰~8.2‰的范围内,来源为大气降水。根据舒卡列夫分类法,震前水样可划分为13种水化学类型,震后西山咀、圐圙朴隆等5个点采样点泉水的水化学类型发生变化。其中,乌拉山断裂带的水样以HCO3-Ca型低矿化度地表水为主;色尔腾断裂带、狼山断裂带泉水受白垩系含水层影响,矿化度较高,富含HCO-3及SO2-4;桌子山一带受煤矿开采影响,水样以富SO2-4和Cl-的高矿化度水为特征。地震前后TDS、阴、阳离子以及γNa/γCl、γ(SO4+Cl)/γHCO3、γHCO3/γCl等毫克当量比值能够较好地反映地震。2015年4月15日阿左旗MS5.8地震后,呼鲁斯太、迪延阿贵庙及八一井的水化学组成变化较大,对地震响应较为敏感。呼鲁斯太地区泉水的TDS稍有降低,但HCO-3在阴离子中所占比例有所增加,表明震后该地区含水层的泉水与较低矿化度的含碳酸盐岩含水层水发生了混合;八一井的TDS值有所增加,γNa/γCl比值有所降低,表明深部高矿化度水的混入;迪延阿贵庙水样的TDS稍有下降,但NaCl的相对含量较震前有所升高,表明有低矿化度NaCl水的混入。本工作不仅确定了该区水文地球化学背景,而且对地震监测和预测具有一定参考价值。  相似文献   

7.
Concentration–discharge relationships have been widely used as clues to the hydrochemical processes that control runoff chemistry. Here we examine concentration–discharge relationships for solutes produced primarily by mineral weathering in 59 geochemically diverse US catchments. We show that these catchments exhibit nearly chemostatic behaviour; their stream concentrations of weathering products such as Ca, Mg, Na, and Si typically vary by factors of only 3 to 20 while discharge varies by several orders of magnitude. Similar patterns are observed at the inter‐annual time scale. This behaviour implies that solute concentrations in stream water are not determined by simple dilution of a fixed solute flux by a variable flux of water, and that rates of solute production and/or mobilization must be nearly proportional to water fluxes, both on storm and inter‐annual timescales. We compared these catchments' concentration–discharge relationships to the predictions of several simple hydrological and geochemical models. Most of these models can be forced to approximately fit the observed concentration–discharge relationships, but often only by assuming unrealistic or internally inconsistent parameter values. We propose a new model that also fits the data and may be more robust. We suggest possible tests of the new model for future studies. The relative stability of concentration under widely varying discharge may help make aquatic environments habitable. It also implies that fluxes of weathering solutes in streams, and thus fluxes of alkalinity to the oceans, are determined primarily by water fluxes. Thus, hydrology may be a major driver of the ocean‐alkalinity feedback regulating climate change. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

8.
Abstract

Knowledge of the hydrochemical dynamics of the trace metal manganese (Mn) in upland catchments is required for water quality management. Stream water Mn and other solutes and flow were monitored in two upland catchments in northern England with different soils: one dominated by peat (HS7), the other by mineral soils (HS4). Maximum Mn concentrations occurred at different times in the two catchments: in summer baseflow at HS4 and during late summer storm events at HS7. A two-component chemical mixing model was used to identify the hydrological processes controlling Mn concentrations in stream water. This approach was more successful for HS4 than HS7, probably because of different processes of Mn release in the two catchments and also difficulties in selecting conservative solutes. Factor analysis of the stream water chemistry data set for each catchment was more useful in identifying the controls on Mn release into runoff. The factors indicate that the main source of Mn at HS4 is the hydrological pathway supplying summer baseflow, whereas at HS7 Mn is released during the rewetting of dried peat soils. Manganese concentrations in stream water in upland catchments appear to depend on soil type and antecedent moisture conditions. This has implications for the design of sampling strategies in upland catchments and also for managing the quality of water supplies from such areas.  相似文献   

9.
李静  李营  陆丽娜  孙凤霞  谢超  崔月菊 《地震》2017,37(1):61-72
根据六盘山地区泉水的化学组成和氢、 氧同位素数据, 讨论了该区地下水的化学类型、 成因及其动态变化特征。 2012年11月和2014年7月在六盘山地区采集10处泉水样品, 氢氧同位素由液态水同位素分析仪测定, 离子组分浓度由离子色谱和化学滴定法测定。 水样的TDS范围为218~27508 mg/L, δ18O和δD值分别为-12.0‰~ -8.5‰, -88.5‰ ~-61.3‰。 δ18O和δD指示该区泉水来源于大气降水, 并受水循环条件及水岩反应程度的影响。 根据舒卡列夫分类法, 所采水样可划分为10种水化学类型, 受含水层岩性控制, 宁南地区的水化类型主要为SO4-Na型, 渭北西部地区的水化类型主要为HCO3-Ca·Mg型。 两次所采水样的离子浓度显示多数水样点的HCO-3具有夏高冬低的季节性变化特征, 千川村(QC)、 双井村(SJ)等因含水层赋存环境较封闭, 受降水干扰小; 硝口村(XKH)泉水的离子毫克当量比值变幅最大, 说明该泉点水岩反应程度变化较大, 易受断层带活动的影响。 研究结果确定了六盘山地区水文地球化学背景和水的来源, 为该区流体地球化学地震监测、 预测提供了背景资料。  相似文献   

10.
Streamwater samples were collected during 1987–1988 from two adjacent gauged watersheds, the subalpine-alpine East St. Louis and the Fool Creek Alpine, in the Fraser Experimental Forest, Colorado. The study objective was to compare the relationships between streamwater discharge and ion concentration in alpine and alpine-subalpine watersheds at a site receiving low inputs of atmospheric contaminants. Streamwater discharge accounts for much of the variation in ion concentration. Trajectories of time, discharge, and ion concentration suggest that patterns of nutrient flux are controlled primarily by the magnitude of streamwater discharge, and seasonal differences in the relative contributions of snowmelt and soil water. In the subalpine catchment, increased streamwater discharge accounted for most of the decline in concentration of ions, with high concentrations in soil water relative to precipitation. This relationship was not seen in the alpine catchment, probably because of the influence of large diurnal variation in the ratio of snowmelt to soil water. In both catchments, ions with comparatively high concentrations in precipitation and the snowpack relative to soil water showed less concentration decline with increased streamwater discharge. The recurring nature of the trajectories, especially in the subalpine catchment, suggests that the time, discharge, and ion concentration patterns may represent a general characteristic in moderate-sized, undisturbed Rocky Mountain catchments which do not receive high inputs of airborne contaminants.  相似文献   

11.
The quantitative evaluation of the effects of bedrock groundwater discharge on spatial variability of stream dissolved organic carbon (DOC), dissolved inorganic nitrogen (DIN) and dissolved inorganic phosphorous (DIP) concentrations has still been insufficient. We examined the relationships between stream DOC, DIN and DIP concentrations and bedrock groundwater contribution to stream water in forest headwater catchments in warm-humid climate zones. We sampled stream water and bedrock springs at multiple points in September and December 2013 in a 5 km2 forest headwater catchment in Japan and sampled groundwater in soil layer in small hillslopes. We assumed that stream water consisted of four end members, groundwater in soil layer and three types of bedrock groundwater, and calculated the contributions of each end member to stream water from mineral-derived solute concentrations. DOC, DIN and DIP concentrations in stream water were compared with the calculated bedrock groundwater contribution. The bedrock groundwater contribution had significant negative linear correlation with stream DOC concentration, no significant correlation with stream DIN concentration, and significant positive linear correlation with stream DIP concentration. These results highlighted the importance of bedrock groundwater discharge in establishing stream DOC and DIP concentrations. In addition, stream DOC and DIP concentrations were higher and lower, respectively, than those expected from end member mixing of groundwater in soil layer and bedrock springs. Spatial heterogeneity of DOC and DIP concentrations in groundwater and/or in-stream DOC production and DIP uptake were the probable reasons for these discrepancies. Our results indicate that the relationships between spatial variability of stream DOC, DIN and DIP concentrations and bedrock groundwater contribution are useful for comparing the processes that affect stream DOC, DIN and DIP concentrations among catchments beyond the spatial heterogeneity of hydrological and biogeochemical processes within a catchment.  相似文献   

12.
Nitrate concentrations in streamwater of agricultural catchments often exhibit interannual variations, which are supposed to result from land‐use changes, as well as seasonal variations mainly explained by the effect of hydrological and biogeochemical cycles. In catchments on impervious bedrock, seasonal variations of nitrate concentrations in streamwater are usually characterized by higher nitrate concentrations in winter than in summer. However, intermediate or inverse cycles with higher concentrations in summer are sometimes observed. An experimental study was carried out to assess the mechanisms that determine the seasonal cycles of streamwater nitrate concentrations in intensive agricultural catchments. Temporal and spatial patterns of groundwater concentrations were investigated in two adjacent catchments located in south‐western Brittany (France), characterized by different seasonal variations of streamwater nitrate concentrations. Wells were drilled across the hillslope at depths ranging from 1·5 to 20 m. Dynamics of the water table were monitored and the groundwater nitrate and chloride concentrations were measured weekly over 2 years. Results highlighted that groundwater was partitioned into downslope domains, where denitrification induced lower nitrate concentrations than into mid‐slope and upslope domains. For one catchment, high subsurface flow with high nitrate concentrations during high water periods and active denitrification during low water periods explained the higher streamwater nitrate concentrations in winter than in summer. For the other catchment, the high contribution of groundwater with high nitrate concentrations smoothed or inverted this trend. Increasing bromide/chloride ratio and nitrate concentrations with depth argued for an effect of past agricultural pressure on this catchment. The relative contribution of flows in time and correlatively the spatial origin of waters, function of the depth and the location on the hillslope, and their chemical characteristics control seasonal cycles of streamwater nitrate concentrations and can influence their interannual trends. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

13.
The water-table region (upper 50 cm of the saturated zone) of a 25 m deep phreatic sandstone aquifer, lying under fields irrigated with sewage effluents for up to 22 yrs, was monitored in 1971 and 1984. Average concentrations of NO3, Cl and SO2−4 of up to 225, 307 and 155 mg l−1, respectively, were detected in the upper 50 cm of the saturated region in two research wells in 1984. These concentrations, which are related to effluent and fertilizer input to groundwater, were two to four times higher than those found deep (37–55 m) below the water table in nearby (1000 m distant) production wells. Nitrate data and the estimated transit time through the unsaturated zone (2 m yr−1) support the model suggesting that the major source of nitrate pollution in the past should be related to the oxidation of soil organic matter. The SO2−4/Cl ratio is found to be a useful indicator for the arrival of SO2−4-fertilizers at the groundwater interface. The observations presented in this paper question the suitability of plans for using effluents as a water source for agriculture in regions which are the replenishment areas of phreatic aquifers.  相似文献   

14.
吕超甲  刘雷  周晓成  杜建国  易丽 《地震》2017,37(1):52-60
根据氢、 氧、 氦同位素与水化学组分资料, 讨论了甘肃东南地区温泉水的来源、 地球化学变化及其与2008年汶川MS8.0地震的关系。 测定结果表明: 样品的溶解性固体总量(TDS)范围为241.7~2 372.1 mg/L。 采集的7处温泉(通渭汤池河温泉、 清水地震台、 天水地震台、 武山地震台、 武山22号井、 成县地震台、 武都地震台)水样可归为四种化学类型: Na·Ca-SO4、 Ca·Mg-SO4、 Na-HCO3·SO4、 Ca·Mg-SO4·HCO3。 地下热水的化学类型与裂隙深度和围岩的岩性有关, 离子浓度和断裂深度基本成正相关。 通渭汤池河温泉和武都地震台的δ18O和δD值分别在-11.4‰ ~ -7.6‰和-85.7‰ ~ -57.1‰的范围内, 通渭汤池河温泉和武都地震台中3He/4He的值分别为0.4×10-7和12.7×10-7。 氢、 氧、 氦同位素组成特征表明温泉水源于大气降水, 在循环过程中经历了水岩反应, 且可能有地表水的混入。 2008年汶川MS8.0地震发生后, 研究区域内温泉水中K+、 Ca2+含量总体上升, SO2-4、 Cl-含量总体下降, Na+含量变化不明显; 热水循环深度受地震影响发生变化。 本文确定了甘肃东南地区温泉来源、 水化学类型成因及其与汶川MS8.0地震的关系。  相似文献   

15.
C. Soulsby 《Journal of Hydrology》1995,170(1-4):159-179
The hydrochemistry of stream water in an acidic afforested catchment in the Welsh uplands was monitored routinely between 1985 and 1990. Nineteen storm episodes were sampled intensively during this period. Although the general storm response of the stream can be characterised by increased concentrations of H+, Al and dissolved organic carbon (DOC), and a dilution of Ca and SiO2, the detailed hydrochemistry of individual acid episodes exhibited marked contrasts. The minimum pH reached during specific episodes ranged from 4.1 to 5.0, and peak dissolved Al concentrations varied from 9 to 44 μmol l−1. The reasons for such differences in the hydrochemical response can be identified for each individual episode by examining the complex interactions between (1) the quantity and quality of event precipitation, (2) antecedent patterns of weather and atmospheric deposition and (3) the hydrological processes which dominate the storm runoff response. The dynamic nature of catchment hydrology was found to exert a particularly strong influence on the hydrochemistry of specific acid episodes.  相似文献   

16.
In this paper, we examined the role of bedrock groundwater discharge and recharge on the water balance and runoff characteristics in forested headwater catchments. Using rigorous observations of catchment precipitation, discharge and streamwater chemistry, we quantified net bedrock flow rates and contributions to streamwater runoff and the water balance in three forested catchments (second‐order to third‐order catchments) underlain by uniform bedrock in Japan. We found that annual rainfall in 2010 was 3130 mm. In the same period, annual discharge in the three catchments varied from 1800 to 3900 mm/year. Annual net bedrock flow rates estimated by the chloride mass balance method at each catchment ranged from ?1600 to 700 mm/year. The net bedrock flow rates were substantially different in the second‐order and third‐order catchments. During baseflow, discharge from the three catchments was significantly different; conversely, peak flows during large storm events and direct runoff ratios were not significantly different. These results suggest that differences in baseflow discharge rates, which are affected by bedrock flow and intercatchment groundwater transfer, result in the differences in water balance among the catchments. This study also suggests that in these second‐order to third‐order catchments, the drainage area during baseflow varies because of differences between the bedrock drainage area and surface drainage area, but that the effective drainage area during storm flow approaches the surface drainage area. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

17.
Solute concentrations in streamflow typically vary systematically with stream discharge, and the resulting concentration–discharge relationships are important signatures of catchment biogeochemical processes. Solutes derived from mineral weathering often exhibit decreasing concentrations with increasing flows, suggesting dilution of a kinetically limited weathering flux by a variable flux of water. However, previous work showed that concentration–discharge relationships of weathering‐derived solutes in 59 headwater catchments were much weaker than this simple dilution model would predict. Instead, catchments behaved as chemostats, with rates of solute production and/or mobilization that were nearly proportional to water fluxes, on both event and interannual timescales. Here, we re‐examine these findings using data for a wider range of solutes from 2,186 catchments, ranging from ~10 to >1,000,000 km2 in drainage area and spanning a wide range of lithologic and climatic settings. Concentration–discharge relationships among this much larger set of larger catchments are broadly consistent with the previously described chemostatic behaviour, at least on event and interannual timescales for weathering‐derived solutes. Among these same catchments, however, site‐to‐site variations in mean concentrations of weathering‐derived solutes exhibit strong negative correlations with long‐term average precipitation and discharge, reflecting strong climatic control on long‐term leaching of the critical zone. We use multiple regression of site characteristics including discharge to identify potential controls on long‐term mean concentrations and find that lithologic and land cover controls are significant predictors for many analytes. The picture that emerges is one in which, on event and interannual timescales, weathering‐derived stream solute concentrations are chemostatically buffered by groundwater storage and fast chemical reactions, but each catchment's chemostatic “set point” reflects site‐to‐site differences in climatically driven evolution of the critical zone. In contrast to these weathering products, some nutrients and particulates are often near‐chemostatic across all timescales, and their long‐term mean concentrations correlate more strongly with land use than climatic characteristics.  相似文献   

18.
Hydrological events transport large proportions of annual or seasonal dissolved organic carbon (DOC) loads from catchments to streams. The timing, magnitude and intensity of these events are very sensitive to changes in temperature and precipitation patterns, particularly across the boreal region where snowpacks are declining and summer droughts are increasing. It is important to understand how landscape characteristics modulate event-scale DOC dynamics in order to scale up predictions from sites across regions, and to understand how climatic changes will influence DOC dynamics across the boreal forest. The goal of this study was to assess variability in DOC concentrations in boreal headwater streams across catchments with varying physiographic characteristics (e.g., size, proportion of wetland) during a range of hydrological events (e.g., spring snowmelt, summer/fall storm events). From 2016 to 2017, continuous discharge and sub-daily chemistry grab samples were collected from three adjacent study catchments located at the International Institute for Sustainable Development-Experimental Lakes Area in northwestern Ontario, Canada. Catchment differences were more apparent in summer and fall events and less apparent during early spring melt events. Hysteresis analysis suggested that DOC sources were proximal to the stream for all events at a catchment dominated by a large wetland near the outlet, but distal from the stream at the catchments that lacked significant wetland coverage during the summer and fall. Wetland coverage also influenced responses of DOC export to antecedent moisture; at the wetland-dominated catchment, there were consistent negative relationships between DOC concentrations and antecedent moisture, while at the catchments without large wetlands, the relationships were positive or not significant. These results emphasize the utility of sub-daily sampling for inferring catchment DOC transport processes, and the importance of considering catchment-specific factors when predicting event-scale DOC behaviour.  相似文献   

19.
Although temporal variation in headwater stream chemistry has long been used to document baseline conditions and response to environmental drivers, less attention is paid to fine scale spatial variations that could yield clues to processes controlling stream water sources. We documented spatial and temporal variation in water composition in a headwater catchment (41 ha) at the Hubbard Brook Experimental Forest, NH, USA. We sampled every 50 m along an ephemeral to perennial stream network as well as groundwater from seeps and 35 shallow wells across varying flow conditions. Groundwater influences on surface water in this region have not been considered to be important in past studies as relatively coarse soils were assumed to be well drained in steep catchments with flashy runoff response. However, seeps displayed perennial discharge, upslope accumulated areas (UAA) smaller than those for channel initiation sites and higher pH, Ca and Si concentrations than streams, suggesting relatively long groundwater residence time or long subsurface flow paths not bound by topographic divides. Coupled with a large range in groundwater chemistry seen in wells, these results suggest stream chemistry variation reflects the range of connectivity with, and quality of, groundwater controlled by hillslope hydropedological processes. The magnitude of variations of solute concentrations seen in the first order catchment was as broad as that seen at the fifth order Hubbard Brook Valley (3519 ha). Reduction in variation in solute concentrations with increasing UAA suggested a representative elementary area (REA) value of less than 3 ha in the first order catchment, compared with 100 ha for the fifth order basin. Thus, the REA is not necessarily an elementary catchment property. Rather, the partitioning of variation between highly variable upstream sources and relatively homogenous downstream characteristics may have different physical significance depending on the scale and complexity of the catchment under examination. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

20.
Large differences in chemistry between sampling points separated In short vertical intervals are often observed in contaminant plumes in both granular and fractured aquifers. However, most regional models assume that such differences will be reduced by dispersive mixing during transport. At a field site located in a discharge area on the Oak Ridge Reservation, Tennessee, ground water flows along discrete flowpaths, as evidenced by the presence of four distinct water types—Ca-HCO3, Ca-Na-HCO3, and Na-Ca-HCO3, and Na-Ca-HCO3-S04—in samples collected from shallow (< 3D in) multilevel wells. The preservation of distinct chemical signatures suggests that ground water must he contained in discrete flow zones during much of its transport time. The chemical composition of the water types can be explained primarily by strata-bound flow over varying flowpath lengths and secondarily by mixing of waters during cross-formational flow in a discharge zone. The hydrochemical facies identified by correlation of water types between the boreholes indicate the general orientation of ground water How paths. These inferred flowpaths are oblique to the orientation of the measured hydraulic gradient and are more closely aligned with bedding and the calculated flow direction. Results of this study indicate that discrete multilevel sampling for analysis of major ions, in addition to information gathered from tracer tests, borehole flow tests. and visual core observations, can provide valuable information on flow directions and preferential flowpaths for contaminant transport.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号