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1.
Water sources and flow paths contributing to stream chemistry were evaluated in four Japanese forested watersheds with steep topography (slopes ≥30°). Stream chemistry during periods without rainfall and during events with less than 100 mm of precipitation was similar to seepage water chemistry, but markedly different from that of soil water which had higher concentrations of NO3 and Ca2+ and lower concentrations of Na+ and HCO3. Also, stream Cl concentrations in a Cl‐treated watershed did not increase either during events with less than 100 mm of total rainfall or at baseflow conditions, even three years after the Cl treatment. These results suggest that groundwater within bedrock fissures of Paleozoic strata had a long residence time and was a major contributor to steam water under baseflow conditions and even during small precipitation events (≤100 mm). In contrast, for large precipitation events (≥100 mm), stream chemistry became more similar to soil water chemistry, especially within the steepest watershed. Also, for large precipitation events, stream Cl concentrations in the Cl‐treated watershed increased markedly. These results suggest that soil water was a major contributor to stream waters only during these large events. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

2.
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   

3.
4.
Wildfires are landscape scale disturbances that can significantly affect hydrologic processes such as runoff generation and sediment and nutrient transport to streams. In Fall 2016, multiple large drought-related wildfires burned forests across the southern Appalachian Mountains. Immediately after the fires, we identified and instrumented eight 28.4–344 ha watersheds (four burned and four unburned) to measure vegetation, soil, water quantity, and water quality responses over the following two years. Within burned watersheds, plots varied in burn severity with up to 100% tree mortality and soil O-horizon loss. Watershed scale high burn severity extent ranged from 5% to 65% of total watershed area. Water quantity and quality responses among burned watersheds were closely related to the high burn severity extent. Total water yield (Q) was up to 39% greater in burned watersheds than unburned reference watersheds. Total suspended solids (TSS) concentration during storm events were up to 168 times greater in samples collected from the most severely burned watershed than from a corresponding unburned reference watershed, suggesting that there was elevated risk of localized erosion and sedimentation of streams. NO3-N concentration, export, and concentration dependence on streamflow were greater in burned watersheds and increased with increasing high burn severity extent. Mean NO3-N concentration in the most severely burned watershed increased from 0.087 mg L−1 in the first year to 0.363 mg L−1 (+317%) in the second year. These results suggest that the 2016 wildfires degraded forest condition, increased Q, and had negative effects on water quality particularly during storm events.  相似文献   

5.
A hierarchical sampling programme (including continuous monitoring, twice-daily sampling and sampling at hourly intervals over selected 24 hour periods) was devised to support hydrochemical and hydrological research programmes on an alpine proglacial stream. The rationale for the research and for the sampling programme are explained and the hydrochemical time series generated over an ablation season are analysed to assess the degree to which they support the study aims. It appears that there is no satisfactory substitute for the chemical analysis of at least two water samples taken at approximately maximum and minimum discharge every day, if seasonal variations in meltwater chemistry are to be effectively characterized. Such time series data can be used to estimate Box-Jenkins transfer function-noise models between particular solutes (SO2−4, Ca2+, Mg2+, Na+ and possibly K+) and either discharge or electrical conductivity, which can then be used to fill any short gaps in the data. This approach is not satisfactory even for filling short gaps in the twice-daily determinations of pH, HCO3 and NO3. At the diurnal time-scale (based on hourly determinations over 24 hour periods) electrical conductivity seems to provide a good surrogate for most of the solutes studied. HCO3, SO2−4, Ca2+ and Mg2+ were found to be particularly strongly related to electrical conductivity and there was little if any significant serial autocorrelation in the residuals from all of the simple linear regression relationships that were estimated between individual species and conductivity. It is concluded that the hierarchical sampling design was suitable for the purposes of the study, and that the continuous monitoring of electrical conductivity provides excellent supporting information to the chemical analysis of water samples if it is used carefully as a means of short term calibration and interpolation of the solute record.  相似文献   

6.
Single collection stations for wet or bulk deposition are generally inadequate to describe atmospheric inputs to watersheds in complex terrain. Atmospheric deposition is delivered by wet, dry and cloud deposition processes, and these processes are controlled by a wide range of landscape features, including canopy type and structure, topographic exposure, elevation and slope orientation. As a result, there can be a very high degree of spatial variability within a watershed, and a single sampling point, especially at low elevation, is unlikely to be representative. Atmospheric inputs at the watershed scale can be calculated from the whole watershed mass balance if the outputs and within-watershed sources and sinks are known with sufficient accuracy. Alternatively, indices of atmospheric deposition such as Pb accumulation in the forest floor and SO2−4 flux in throughfall can be used to characterize patterns of total deposition, and these indices can be used to model deposition to the entire watershed based on known landscape features such as elevation and canopy type. © 1997 John Wiley & Sons, Ltd.  相似文献   

7.
Timber harvest temporarily increases water yield; however, relationships between hydrologic and nutrient chemistry changes have not been consistent. This study quantified the effects of forest harvesting and site preparation without fertilization and with modern best management practices on nutrient concentrations and yields in small headwater streams of the Southeastern Coastal Plain. We monitored two watershed pairs for 2 years prior to and 1 year following timber harvest and for 2 more years following site preparation and planting. Treatment watersheds were clearcut, and downstream portions of streamside management zones were thinned in Fall 2003. Site preparation (herbicide application and burning) and planting followed a year later. All operations followed 1999 Georgia forestry best management practices. Previously published research revealed a large increase in water yield following harvest. Nutrient concentrations varied significantly within and between monitoring periods, even in reference watersheds. Silvicultural activities had no discernible effect on phosphorus and ammonium concentrations; however, statistically significant increases in nitrate/nitrite (67–340 µg L−1) and total nitrogen concentrations (100–400 µg L−1) in treatment watersheds followed stand re‐establishment. Nutrient yields increased after timber harvest largely as a result of increased water yields, although increased nutrient yields were small relative to inter‐annual and inter‐watershed variability and variability. Annual water yield largely explained the variability in annual nitrogen and phosphorus export from reference and treatment streams (r2 values from 0.65 to 0.98). High NOx concentrations coming from an upstream agricultural area decreased 1600–1800 µg L−1 over several hundred metres in the treatment streams by dilution, uptake or denitrification. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

8.
Headwater streams drain the majority of most landscapes, yet less is known about their morphology and sediment transport processes than for lowland rivers. We have studied headwater channel form, discharge and erosive power in the humid, moderate‐relief Valley and Ridge and Blue Ridge provinces of the Appalachian Mountains. Field observations from nine headwater (<2 km2 drainage area), mixed bedrock–alluvial channels in a variety of boundary conditions demonstrate variation with respect to slope‐area channel initiation, basic morphology, slope distribution, hydraulic geometry, substrate grain size and role of woody debris. These channels display only some of the typical downstream trends expected of larger, lowland rivers. Variations are controlled mainly by differences in bedrock resistance, from the formation level down to short‐wavelength, outcrop‐scale variations. Hydrologic modeling on these ungauged channels estimates the recurrence of channel‐filling discharge and its ability to erode the channel bed. Two‐year recurrence discharge is generally larger and closer to bankfull height in the Valley and Ridge, due to low soil infiltration capacity. Discharge that fills the channel to its surveyed bankfull form is variable, generally exceeding two‐year flows at small drainage areas (<0·5 km2) and being exceeded by them at greater drainage areas. This suggests bankfull is not controlled by the same recurrence storm throughout a channel or physiographic region. Stream power and relative competence are also variable. These heterogeneities contrast relations observed in larger streams and illustrate the sensitivity of headwater channels to local knickpoints of resistant bedrock and armoring of channels by influx of coarse debris from hillslopes. The general lack of predictable trends or functional relationships among hydraulic variables and the close coupling of channel form and function with local boundary conditions indicate that headwater streams pose a significant challenge to landscape evolution modeling. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

9.
The southwestern Adirondack region of New York receives among the highest rates of atmospheric nitrogen (N) deposition in the USA. Atmospheric N deposition to sensitive ecosystems, like the Adirondacks, may increase the acidification of soils through losses of exchangeable nutrient cations, and the acidification of surface waters associated with enhanced mobility of nitrate (NO3?). However, watershed attributes, including surficial terrestrial characteristics, in‐lake processing, and geological settings, have been found to complicate the relationships between atmospheric N deposition and N drainage losses. We studied two lake‐watersheds in the southwestern Adirondacks, Grass Pond and Constable Pond, which are located in close proximity (~26 km) and receive similarly high N deposition, but have contrasting watershed attributes (e.g. wetland area, geological settings). Since the difference in the influence of N deposition was minimal, we were able to examine both within‐ and between‐watershed influences of land cover, the contribution of glacial till groundwater inputs, and in‐lake processes on surface water chemistry with particular emphasis on N solutes and dissolved organic carbon (DOC). Monthly samples at seven inlets and one outlet of each lake were collected from May to October in 1999 and 2000. The concentrations of NO3? were high at the Grass Pond inlets, especially at two inlets, and NO3? was the major N solute at the Grass Pond inlets. The concentrations of likely weathering products (i.e. dissolved Si, Ca2+, Mg2+, Na+) as well as acid neutralizing capacity and pH values, were also particularly high at those two Grass Pond inlets, suggesting a large contribution of groundwater inputs. Dissolved organic N (DON) was the major N solute at the Constable Pond inlets. The higher concentrations of DON and DOC at the Constable Pond inlets were attributed to a large wetland area in the watershed. The DOC/DON ratios were also higher at the Constable Pond inlets, possibly due to a larger proportion of coniferous forest area. Although DON and DOC were strongly related, the stronger relationship of the proportion of wetland area with DOC suggests that additional factors regulate DON. The aggregated representation of watershed physical features (i.e. elevation, watershed area, mean topographic index, hypsometric‐analysis index) was not clearly related to the lake N and DOC chemistry. Despite distinctive differences in inlet N chemistry, NO3? and DON concentrations at the outlets of the two lakes were similar. The lower DOC/DON ratios at the lake outlets and at the inlets having upstream ponds suggest the importance of N processing and organic N sources within the lakes. Although an inverse relationship between NO3? and DOC/DON has been suggested to be indicative of a N deposition gradient, the existence of this relationship for sites that receive similar atmospheric N deposition suggest that the relationship between NO3? and the DOC/DON ratio is derived from environmental and physical factors. Our results suggest that, despite similar wet N deposition at the two watershed sites, N solutes entering lakes were strongly affected by hydrology associated with groundwater contribution and the presence of wetlands, whereas N solutes leaving lakes were strongly influenced by in‐lake processing. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

10.
11.
The anion compositions (SO24, HCO3 and Cl) of runoff from the Haut Glacier d'Arolla, Switzerland and Austre Brøggerbreen, Svalbard are compared to assess whether or not variations in water chemistry with discharge are consistent with current understanding of the subglacial drainage structure of warm- and polythermal-based glaciers. These glacial catchments have very different bedrocks and the subglacial drainage structures are also believed to be different, yet the range of anion concentrations show considerable overlap for SO2−4 and HCO3. Concentrations of Cl are higher at Austre Brøggerbreen because of the maritime location of the glacier. Correcting SO2−4 for the snowpack component reveals that the variation in non-snowpack SO2−4 with discharge and with HCO3 is similar to that observed at the Haut Glacier d'Arolla. Hence, if we assume that the provenance of the non-snowpack SO2−4 is the same in both glacial drainage systems, a distributed drainage system also contributes to runoff at Austre Brøggerbreen. We have no independent means of testing the assumption at present. The lower concentrations of non-snowpack SO2−4 at Austre Brøggerbreen may suggest that a smaller proportion of runoff originates from a distributed drainage system than at the Haut Glacier d'Arolla.  相似文献   

12.
Snowmelt‐fed springs and small (0.5 km2) upland catchments in alpine areas of the western United States contribute significantly to the quantity and inorganic chemistry of water delivered to downstream basins but have not been studied extensively. Mineral weathering, transit time, and hydrologic mixing control the solute chemistry of waters that drain the upland zone of Niwot Ridge, Colorado Front Range, and adjacent areas in the granitic core of the Southern Rocky Mountains. Water in 37 springs sampled in this study flows in generally short steep paths (~0.3 km) through shallow regolith with mean transit times (MTT) of weeks to months, producing solutions dominated by Si, Ca2+, Na+, and HCO3?, locally SO42?. Rock type is a significant control on spring, surface, and shallow groundwater chemistry, and plagioclase (oligoclase) is the major source of dissolved Na+ and Si. Concentrations of Ca2+ exceed stoichiometric predictions of oligoclase weathering by ~3.5×; excess Ca2+ likely represents weathering of aeolian material, vein calcite, or trace minerals. Concentrations of base cations and Si increase slowly with estimated MTT of 0.2 years for Niwot Ridge spring waters, and several years for shallow groundwater sampled by wells. Chemical weathering of silicate minerals is slow with estimated rates of ~2.0 and 0.2 pmol·m?2·s?1 for oligoclase and microcline, respectively; the most mineralized spring waters are saturated only with respect to kaolinite and montmorillonite. More than 50% of the dissolved base cations + Si measured in Boulder Creek at Orodell (~25 km downstream) accumulate before water emerges from alpine springs on Niwot Ridge. Warming global temperatures are shifting more high‐elevation precipitation to rain, potentially changing run‐off patterns, transit time, and solute loads. Acquisition of solutes by alpine waters thus has implications far beyond small upland catchments.  相似文献   

13.
Investigating factors controlling the temporal patterns of nitrogen (N) and dissolved organic carbon (DOC) exports on the basis of a comparative study of different land uses is beneficial for managing water resources, especially in agricultural watersheds. We focused our research on an agricultural watershed (AW) and a forested watershed (FW) located in the Shibetsu watershed of eastern Hokkaido, Japan, to investigate the temporal patterns of N and DOC exports and factors controlling those patterns at different timescales (inter‐annual, seasonal, and hydrological event scales). Results showed that the annual patterns of N and DOC exports significantly varied over time and were probably controlled by climate. Higher discharge volumes in 2003, a wet year, showed higher N and DOC loadings in both watersheds. However, this process was also regulated by land use associated with N inputs. Higher concentrations and loadings were shown in the agricultural watershed. At the seasonal scale, N and DOC exports in the AW and the FW were more likely controlled by sources associated with land use. The Total N (TN) and Nitrate‐N (NO3?‐N) had higher concentrations during snowmelt season in the AW, which may be attributed to manure application in late autumn or early winter in the agricultural watershed. Concentrations of TN, NO3?‐N, dissolved organic nitrogen (DON), and DOC showed higher values during the summer rainy season in the FW, related to higher litter decomposition during summer and autumn and the fertilizer application in the agricultural area during summer. Higher DOC concentrations and loadings were observed during the rainy season in the AW, which is probably attributed to higher DOC production related to temperature and microbial activity during summer and autumn in grasslands. Correlations between discharge and concentrations differed during different periods or in different watersheds, suggesting that weather discharge can adequately represent the fact that N export depends on N concentrations, discharge level, and other factors. The differing correlations between N/DOC concentrations and the Si concentration indicated that the N/DOC exports might occur along different flow paths during different periods. During baseflow, the high NO3?‐N exports were probably derived from deep groundwater and might have percolated from uplands during hydrological events. During hydrological events, NO3?‐N exports may occur along near‐surface flow paths and in deep groundwater, whereas DOC exports could be related to near‐surface flow paths. At the event scale, the relationships between discharge and concentrations of N and DOC were regulated by antecedent soil moisture (shallow groundwater condition) in each watershed. These results indicated that factors controlling N and DOC exports varied at different timescales in the Shibetsu area and that better management of manure application during winter in agricultural lands is urgently needed to control water pollution in streams. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

14.
为揭示太湖流域降雨和湖水酸根阴离子长期变化特征及环境意义,通过历史数据收集和采样分析,对太湖流域降雨和湖水中的SO42-、NO3-变化特征和来源进行了研究.结果表明:自1990s以来太湖流域降雨中SO42-呈显著下降趋势,年平均下降率为0.28 mg/(L·a);NO3-浓度却呈显著上升趋势,年平均增长率为0.05 mg/(L·a),降雨中氮污染呈现加重的趋势.与之相反,湖水中SO42-呈显著上升趋势,年平均增长率为1.24 mg/(L·a);NO3-浓度却呈显著下降趋势,年平均下降率为0.02 mg/(L·a).30年以来,太湖水体SO42-/NO3-比值不断升高,远高于降水SO42-/NO3-比值.研究认为:流域SO2排放引起的酸沉降是湖水SO42-浓度增长的最重要原因,但氮氧化物排放并未引起湖水NO3-浓度升高,说明太湖流域对大气沉降的氮氧化物有滞留作用,而太湖水体是流域大气沉降硫酸盐的重要汇.综合治理太湖流域酸性物质排放对防止太湖水体酸化和治理富营养化都具有重要意义.  相似文献   

15.
淮北临涣矿采煤沉陷区不同水体水化学特征及其影响因素   总被引:3,自引:0,他引:3  
为研究淮北临涣矿采煤沉陷区不同水体的补给水源及溶质来源,在现场调查的基础上,系统采集丰水期、平水期、枯水期沉陷区积水、地表河水和浅层地下水样进行测试分析,采用Piper三线图、Gibbs图和因子分析方法,对不同水体水化学特征及其影响因素进行讨论.结果表明:地表水水体总溶解性固体(TDS)质量浓度表现为枯水期丰水期平水期,浅层地下水表现为枯水期平水期丰水期,地表水TDS质量浓度明显高于浅层地下水.地表水中主要阴阳离子为Na~+、Cl~-和SO_4~(2-),水化学类型主要为SO_4~(2-)-Cl~--Na~+型;浅层地下水离子以HCO_3~-、Ca~(2+)和Mg~(2+)为主,表现为HCO_3~--Ca~(2+)-Mg~(2+)型.结合Gibbs图和因子分析可知,地表水受蒸发作用、地表径流以及采煤活动等因素影响,浅层地下水在一定程度上体现出大气降水和地表水补给的特点,受岩石风化作用影响较为明显.  相似文献   

16.
There are still relatively few hydrochemical studies of glacial runoff and meltwater routing from the high latitudes, where non-temperate glacier ice is frequently encountered. Representative samples of glacier meltwater were obtained from Scott Turnerbreen, a ‘cold-based’ glacier at 78° N in the Norwegian high Arctic archipelago of Svalbard, during the 1993 melt season and analysed for major ion chemistry. Laboratory dissolution experiments were also conducted, using suspended sediment from the runoff. Significant concentrations of crustal weathering derived SO2−4 are present in the runoff, which is characterized by high ratios of SO2−4: (SO2−4+HCO3) and high p(CO2). Meltwater is not routed subglacially, but flows to the glacier terminus through subaerial, ice marginal channels, and partly flows through a proglacial icing, containing highly concentrated interstitial waters, immediately afront the terminus. The hydrochemistry of the runoff is controlled by: (1) seasonal variations in the input of solutes from snow- and icemelt; (2) proglacial solute acquisition from the icing; and (3) subaerial chemical weathering within saturated, ice-cored lateral moraine adjoining drainage channels at the glacier margins, sediment and concentrated pore water from which is entrained by flowing meltwater. Diurnal variations in solute concentration arise from the net effects of variable sediment pore water entrainment and dilution in the ice marginal streams. Explanation of the hydrochemistry of Scott Turnerbreen requires only one major subaerial flow path, the ice marginal channel system, in which seasonally varying inputs of concentrated snowmelt and dilute icemelt are modified by seepage or entrainment of concentrated pore waters from sediment in lateral moraine, and by concentrated interstitial waters from the proglacial icing, supplied by leaching, slow drainage at grain intersections or simple melting of the icing itself. The ice marginal channels are analogous neither to dilute supra/englacial nor to concentrated subglacial flow components. © 1998 John Wiley & Sons, Ltd.  相似文献   

17.
For the period from 1958 to 1996, streamflow characteristics of a highly urbanized watershed were compared with less‐urbanized and non‐urbanized watersheds within a 20 000 km2 region in the vicinity of Atlanta, Georgia: in the Piedmont and Blue Ridge physiographic provinces of the southeastern USA. Water levels in several wells completed in surficial and crystalline‐rock aquifers were also evaluated. Data were analysed for seven US Geological Survey (USGS) stream gauges, 17 National Weather Service rain gauges, and five USGS monitoring wells. Annual runoff coefficients (RCs; runoff as a fractional percentage of precipitation) for the urban stream (Peachtree Creek) were not significantly greater than for the less‐urbanized watersheds. The RCs for some streams were similar to others and the similar streams were grouped according to location. The RCs decreased from the higher elevation and higher relief watersheds to the lower elevation and lower relief watersheds: values were 0·54 for the two Blue Ridge streams, 0·37 for the four middle Piedmont streams (near Atlanta), and 0·28 for a southern Piedmont stream. For the 25 largest stormflows, the peak flows for Peachtree Creek were 30% to 100% greater than peak flows for the other streams. The storm recession period for the urban stream was 1–2 days less than that for the other streams and the recession was characterized by a 2‐day storm recession constant that was, on average, 40 to 100% greater, i.e. streamflow decreased more rapidly than for the other streams. Baseflow recession constants ranged from 35 to 40% lower for Peachtree Creek than for the other streams; this is attributed to lower evapotranspiration losses, which result in a smaller change in groundwater storage than in the less‐urbanized watersheds. Low flow of Peachtree Creek ranged from 25 to 35% less than the other streams, possibly the result of decreased infiltration caused by the more efficient routing of stormwater and the paving of groundwater recharge areas. The timing of daily or monthly groundwater‐level fluctuations was similar annually in each well, reflecting the seasonal recharge. Although water‐level monitoring only began in the 1980s for the two urban wells, water levels displayed a notable decline compared with non‐urban wells since then; this is attributed to decreased groundwater recharge in the urban watersheds due to increased imperviousness and related rapid storm runoff. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   

18.
Permafrost and fire are important regulators of hydrochemistry and landscape structure in the discontinuous permafrost region of interior Alaska. We examined the influence of permafrost and a prescribed burn on concentrations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON) and other solutes ( , Ca2+, K+, Mg2+, Na+) in streams of an experimentally burned watershed and two reference watersheds with varying extents of permafrost in the Caribou–Poker Creeks Research Watershed in interior Alaska. The low‐permafrost watershed has limited permafrost (3%), the high‐permafrost watershed has extensive permafrost (53%), and the burn watershed has intermediate permafrost coverage (18%). A three end‐member mixing model revealed fundamental hydrologic and chemical differences between watersheds due to the presence of permafrost. Stormflow in the low‐permafrost watershed was dominated by precipitation and overland flow, whereas the high‐permafrost watershed was dominated by flow through the active layer. In all watersheds, organic and groundwater flow paths controlled stream chemistry: DOC and DON increased with discharge (organic source) and base cations and (from weathering processes) decreased. Thawing of the active layer increased soil water storage in the high‐permafrost watershed from July to September, and attenuated the hydrologic response and solute flux to the stream. The FROSTFIRE prescribed burn, initiated on 8 July 1999, elevated nitrate concentrations for a short period after the first post‐fire storm on 25 July, but there was no increase after a second storm in September. During the July storm, nitrate export lagged behind the storm discharge peak, indicating a flushing of soluble nitrate that likely originated from burned soils. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

19.
Monitoring the effects of acidic deposition on aquatic ecosystems in the Northeastern US has generally required regular measurements of stream buffering chemistry (i.e. acid‐neutralizing capacity (ANC) and calcium Ca2+), which can be expensive and time consuming. The goal of this paper was to develop a simple method for predicting baseflow buffering chemistry based on the hydrogeomorphic properties of ten nested watersheds in the Neversink River basin (2·0–176·0 km2), an acid‐sensitive basin in the Catskill Mountains, New York State. The tributaries and main reach watersheds have strongly contrasting mean baseflow ANC values and Ca2+ concentrations, despite rather homogeneous vegetation, bedrock geology, and soils. A stepwise regression was applied to relate 13 hydrogeomorphic properties to the mean baseflow ANC values and Ca2+ concentrations. The regression analysis showed that watersheds with lower ANC values had a higher mean ratio of ‘quickflow’ runoff to precipitation during 20 non‐snowmelt runoff events (referred to as mean runoff ratio). The mean runoff ratio could explain at least 80% of the variability in mean baseflow ANC values and Ca2+ concentrations among the ten watersheds. Greater mean runoff ratios also correlated with steeper slopes and greater drainage densities, thus allowing the prediction of baseflow ANC values (r2 = 0·75) and Ca2+ concentrations (r2 = 0·77) with widely available spatial data alone. These results indicate that hydrogeomorphic properties can predict a watershed's sensitivity to acid deposition in regions where the spatial sources of stream buffering chemistry from the bedrock mineralogy and soils are fairly uniform. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

20.
Surface water draining granitic bedrock in Yosemite National Park exhibits considerable variability in chemical composition, despite the relative homogeneity of bedrock chemistry. Other geological factors, including the jointing and distribution of glacial till, appear to exert strong controls on water composition. Chemical data from three surface water surveys in the upper Merced River basin conducted in August 1981, June 1988 and August 1991 were analysed and compared with mapped geological, hydrological and topographic features to identify the solute sources and processes that control water chemistry within the basin during baseflow. Water at most of the sampling sites was dilute, with alkalinities ranging from 26 to 77 μequiv. l−1. Alkalinity was much higher in two subcatchments, however, ranging from 51 to 302 μequiv. l−1. Base cations and silica were also significantly higher in these two catchments than in the rest of the watershed. Concentrations of weathering products in surface water were correlated to the fraction of each subcatchment underlain by surficial material, which is mostly glacial till. Silicate mineral weathering is the dominant control on concentrations of alkalinity, silica and base cations, and ratios of these constituents in surface water reflect the composition of local bedrock. Chloride concentrations in surface water samples varied widely, ranging from <1 to 96 μequiv. l−1. The annual volume-weighted mean chloride concentration in the Merced River at the Happy Isles gauge from 1968 to 1990 was 26 μequiv. l−1, which was five times higher than in atmospheric deposition (4–5 μequiv. l−1), suggesting that a source of chloride exists within the watershed. Saline groundwater springs, whose locations are probably controlled by vertical jointing in the bedrock, are the most likely source of the chloride. Sulphate concentrations varied much less than most other solutes, ranging from 3 to 14 μequiv. l−1. Concentrations of sulphate in quarterly samples collected at the watershed outlet also showed relatively little variation, suggesting that sulphate may be regulated to some extent by a within-watershed process, such as sulphate adsorption.  相似文献   

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