Distribution, source and evolution of nitrate in a glacial till of southern Alberta, Canada

This paper addresses the distribution, origin and controls upon nitrate in a 30-km² area of the Interior Great Plains Region of southern Alberta, Canada. High concentrations of nitrate (> 100 mg l⁻¹ NO⁻₃-N) occurred in several isolated enclaves below the water table in brown weathered till. Nitrate concentrations of over 300 mg l⁻¹-N were encountered in groundwater samples collected from these enclaves. Low nitrate concentrations (< 1.1 mg l⁻¹ NO⁻₃-N) were also encountered in the weathered till upgradient and downgradient of the nitrate enclaves. Groundwater samples collected from the underlying grey nonweathered till and bedrock had NO⁻₃-N concentrations of < 1.1 mg l⁻¹.

Through the application of geochemical (NO⁻₃-N and NH⁺₄-N) studies, environmental isotope studies (tritium), microbial analyses (nitrifiers) and laboratory experiments, it was shown that the high nitrates found in the weathered till are the result of the oxidation of ammonium present within the tills. It is postulated that this oxidation occurred during the Holocene epoch when water tables were much lower than present-day levels (5–18 m, and 2 m below ground, respectively).

Through the use of Eh measurements, the enumeration of denitrifying bacteria and laboratory experiments, the potential for denitrification was shown to exist below the present-day water table in the weathered till as well as in the nonweathered till and bedrock. Isotopic data showed that less denitrification may be occurring within the nitrate enclaves than in adjacent downgradient areas.     

The seasonal variation of streamwater chemistry in three forested Mediterranean catchments

Streamwater chemistry is described for three streams draining undisturbed, evergreen broad-leaved forested catchments on phyllites in NE Spain: two streams with no or negligible flow in summer are located in the Prades massif, and one perennial stream is in the wetter Montseny mountains. Weekly data for a study period of 2–4 years are provided to (1) describe the seasonal variations in streamwater chemistry, (2) analyse the relationship between stream discharge and solute concentrations using a two-component mixing model and (3) search for patterns of temporal variation in stream solute concentrations after discounting the effects of discharge. At Prades, concentrations of all analysed ions, except NO⁻₃, showed marked seasonal variations in stream water, whereas at Montseny only ions related to mineral weathering (HCO⁻₃, Na⁺, Ca²⁺ and Mg²⁺) showed strong seasonality. Ion concentrations were more closely dependent on instantaneous discharge at Montseny than at Prades. The residuals of the relationship between solute concentrations and discharge retained a strong seasonality at Prades, but not at Montseny. These differences are related to the major hydrochemical processes that determine the streamwater chemistry at each site. The same processes are probably operative in the three catchments, but are of varying relative importance. At Montseny, the mixing of waters of different chemical composition seems to be the major process controlling streamwater chemistry, although the soilwater end-member composition predicted by the mixing model applied did not match the measured soilwater chemistry. In the drier Prades catchments, the two major hydrochemical processes determining the seasonal variation of streamwater chemistry are (1) the restart of flow after the summer drought, which flushes out the solutes accumulated during the dry period, and (2) the seasonal changes in groundwater chemistry that result from the interplay of water residence time, temperature and CO₂ partial pressure. In Mediterranean catchments with relatively high precipitation, such as Montseny, the seasonal variation in the streamwater chemistry is largely determined by the same processes as at humid-temperate sites, whereas in drier Mediterranean catchments, such as Prades, the major hydrochemical processes are clearly distinct.     

Comparison of methods for calculating annual solute exports from six forested appalachian watersheds

Six methods were compared for calculating annual stream exports of sulfate, nitrate, calcium, magnesium and aluminum from six small Appalachian watersheds. Approximately 250–400 stream samples and concurrent stream flow measurements were collected during baseflows and storm flows for the 1989 water year at five Pennsylvania watersheds and during the 1989–1992 water years at a West Virginia watershed. Continuous stream flow records were also collected at each watershed. Solute exports were calculated from the complete data set using six different scenarios ranging from instantaneous monthly measurements of stream chemistry and stream flow, to intensive monitoring of storm flow events and multiple regression equations. The results for five of the methods were compared with the regression method because statistically significant models were developed and the regression equations allowed for prediction of solute concentrations during unsampled storm flows. Results indicated that continuous stream flow measurement was critical to producing exports within 10% of regression estimates. For solutes whose concentrations were not correlated strongly with stream flow, weekly grab samples combined with continuous records of stream flow were sufficient to produce export estimates within 10% of the regression method. For solutes whose concentrations were correlated strongly with stream flow, more intensive sampling during storm flows or the use of multiple regression equations were the most appropriate methods, especially for watersheds where stream flows changed most quickly. Concentration–stream flow relationships, stream hydrological response, available resources and required level of accuracy of chemical budgets should be considered when choosing a method for calculating solute exports. © 1997 John Wiley & Sons, Ltd.     

The impact of land use on stream water quality in Slovakia

In the first part of this paper, the impact of forestry, agriculture and urban activities on the quality of surface water is analysed. Daily data from 15 forest and agricultural experimental catchments of the Institute of Hydrology, Slovak Academy of Sciences are used. It is shown, that the nitrate concentrations in surface water have decreased in Slovakia since 1989 as a result of decreased use of inorganic nitrogen fertilisers (lower intensity of agricultural production in Slovakia owing to recent economic changes). The annual nitrate specific load varies from 5.90 to 110 kg ha⁻¹ year⁻¹, the annual sulphate load varied from 29.16 to 509.60 kg ha⁻¹ year⁻¹ and the annual phosphate load varied from 0.0098 to 0.0224 kg ha⁻¹ year⁻¹ during 1990–1992.

In the second part, a two-step method of three-component hydrograph separation of rain-, soil- and groundwater is proposed. The method is used in the Manelo-Gribov microbasin (O.95 km²) in Eastern Slovakia. The annual contribution of surface runoff in total runoff volume was 57.5%, the contribution of interflow runoff was 21.1%, and the contribution of groundwater was 21.4%, during the period from 1 August to 31 July 1992. A deterministic regression model for predicting daily nitrate concentrations from values of stream daily discharge and flow component data was developed. A set of 1421 modelled NO₃⁻¹ data was compared with the set of measured data.     

Nutrient dynamics in Mediterranean temporary streams: A case study in Pardiela catchment (Degebe River, Portugal)

Most of the streams in the Mediterranean region are temporary, following predictable seasonal of flooding and drying, with a transition from lotic conditions to shallow lentic conditions. The goal of our study was to assess the nitrogen and phosphorus dynamics in channel-bed processes of temporary streams between floods. Results show that, during winter, temperatures ranged between 9.5 and 11.2 °C and oxygen concentration ranged from 8.0 to 9.5 mg L⁻¹, whereas, during summer, temperatures varied between 21.2 and 26.8 °C and oxygen between 1.2 and 5.3 mg L⁻¹, with oxygen depletion in the pools during the night. The nitrate concentrations were far more abundant during winter (February), while ammonium concentration increased after stream fragmentation into pools (especially in July when oxygen depletion conditions favoured ammonification). Results on sediment profiles showed that the most active sediment layers for NH₄-N are the top 2–3 cm, corresponding to the sediment depositional sites of the stream. Phosphate concentrations had larger variability, yet concentrations decreased from winter to spring and increased again in summer, when the shallow water pools were formed. Sediment profiles at the sediment depositional sites showed that PO₄-P was more dynamic in the first 6 cm.

In Mediterranean temporary streams, nutrient dynamics vary seasonally, as the system transits from lotic conditions to shallow lentic conditions, evidencing the regeneration of nutrients from organic and inorganic matter during the flow cessation period.     

Seasonal soil water storage changes beneath central Amazonian rainforest and pasture

Evaporation and infiltration were compared for tropical rainforest and pasture, near to Manaus, Brazil from October 1990 to February 1992 using measurements of soil water storage over a depth of 2 m. The soil is a clayey oxisol of low water available capacity. In both of the dry seasons studied, the maximum change in soil water storage in the forest was 154 mm and in the pasture it was 131 and 112 mm. Similar behaviour of the soil water reservoir below forest and pasture in the wet season implied that differences in evaporation and drainage were small. In the dry season, soil water storage behaviour in the upper metre of the soil was similar but there were marked differences in the second metre. The pasture took up little water from below 1.5 m but the forest appeared to utilise all of the available water in the 2 m profile in both seasons.

The water balance of the 2 m profile showed that the pasture evaporation rate was equal to that of the forest until storage had decreased 80 mm from the maximum. There was then a decline in pasture evaporation rate to 1.2 mm day⁻¹ as the storage decreased by a further 50 mm. In contrast, the forest uptake rate remained above 3.5 mm day⁻¹ until storage had decreased 140 mm from the maximum (within 15 mm of the extraction limit), before declining abruptly to less than 1.5 mm day⁻¹. There was strong evidence that the forest was able to abstract water from depths greater than 3.6 m.

Spatial variability of soil water storage was significantly greater beneath the pasture than beneath the forest, particularly following rainfall events in the dry season. This was largely the result of redistribution of rainfall as local surface runoff. There was no evidence of redistribution or runoff in the forest.     

High concentration of solutes at the upper part of the saturated zone (water table) of a deep aquifer under sewage-irrigated land

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 NO⁻₃, 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.     

Land management impacts on runoff sources in small Amazon watersheds

Forest clearing and conversion to cattle pasture in the lowland Amazon region has been linked to soil compaction and increased soil water storage, which combine to diminish soil infiltration, enhance quick lateral flows and increase the stream flow response to precipitation. Quantifying the importance of quick surficial flow in response to this land use change requires identification of water sources within catchments that contribute to stream flow. Using an end member mixing analysis approach, potential contributing sources of stream flow were evaluated during an entire rainy season in a forest and a pasture watershed drained by ephemeral‐to‐intermittent streams in the south‐western Amazon. Water yield was 17% of precipitation in the pasture and 0·8% of precipitation in the forest. During the early rainy season, throughfall, groundwater, and soil water contributed 79%, 18%, and 3%, respectively, to total forest stream flow. Over the entire rainy season, throughfall, groundwater, and shallow soil water provided 57%, 24%, and 19%, respectively, of stream flow. In the pasture watershed, overland flow dominated stream flow both in the early (67%) and late (57%) rainy season, with a mean contribution of 60% overland flow, 35% groundwater, and 5% soil water. The uncertainty associated with those estimates was studied using a Monte Carlo approach. In addition to large changes in total surface flow, marked differences were found in the proportions of total stream flow in the second half of the rainy season between the forest and pasture watershed. These results suggest that (1) there is great potential for alteration of the hydrological budgets of larger watersheds as the proportion of deforested land in the Amazon increases, and (2) as more rainfall is diverted into fast flowpaths to streams in established pastures, the potential to deliver water with higher solute concentrations generated by erosion or by bypassing sites of solute removal increases. Copyright © 2007 John Wiley & Sons, Ltd.     

Seasonal studies on cadmium concentration and toxicity, oxygen consumption, digestive gland glycogen, and lipid in dog whelks collected at Aberystwyth, Wales

The concentration of cadmium in Nucella was investigated at different times of the year at one site. There was no significant difference in tissue cadmium at the times of the year investigated but tissue zinc was more variable. Accumulation and toxicity of cadmium were studied using 50–600 μg Cd l⁻¹ for 21 days. There was no significant seasonal difference in the rate of cadmium uptake but mortality appeared to vary with the season. Nucella did not survive 21 days at 600 μg Cd l⁻¹, but at lower concentrations 50–100 μg Cd l⁻¹ all survived.

Although there was significant drop in oxygen consumption between 7 and 14 days it did not appear to be related to the cadmium exposure. Glycogen levels on the other hand showed a decrease after cadmium treatment, while lipid values remained unchanged. Results are discussed in relation to energy source, season, and adaptation to the environment.     

Linking hydrology and stream geochemistry in urban fringe watersheds

Urbanization represents a dramatic example of human interference with the hydrological cycle. Changes to ground cover affect both the hydrological and geochemical characteristics in a watershed. Ecosystem degradation also occurs in undisturbed watersheds at the “urban fringe” due to regional atmospheric deposition. These urban fringe catchments can also serve as an upstream source of various chemical constituents into downstream (urban) river systems. The current study focuses on the impacts of regional urbanization in the upper Arroyo Seco watershed located on the eastern edge of the Los Angeles basin, where estimates of dry deposition are considered some of the highest in North America. Collected hydrologic, geochemical and atmospheric data were assessed at seasonal time scales to evaluate current hydrochemical dynamics. Stream water chemical composition in the upper Arroyo Seco watershed exhibits significant seasonal variability, particularly for . Almost all study solutes show dilution behavior. However, hydrologically enhanced behavior was observed for with increased concentrations during the wet season. Seasonal stream concentration–discharge relationships were developed using a hyperbolic dilution model. The developed model was then used to predict concentrations for observational gaps in stream water chemical composition, allowing for seasonal and annual mass loadings to be estimated for the downstream urban stream. The hydrological signal in the resultant chemical loads is extremely strong, especially during the wet season. Both observations and model predictions indicate the watershed is a sink for atmospheric nitrate and a source for various cations.     

Seasonal connections between meteoric water and streamflow generation along a mountain headwater stream

In snowmelt-driven mountain watersheds, the hydrologic connectivity between meteoric waters and stream flow generation varies strongly with the season, reflecting variable connection to soil and groundwater storage within the watershed. This variable connectivity regulates how streamflow generation mechanisms transform the seasonal and elevational variation in oxygen and hydrogen isotopic composition (δ¹⁸O and δD) of meteoric precipitation. Thus, water isotopes in stream flow can signal immediate connectivity or more prolonged mixing, especially in high-relief mountainous catchments. We characterized δ¹⁸O and δD values in stream water along an elevational gradient in a mountain headwater catchment in southwestern Montana. Stream water isotopic compositions related most strongly to elevation between February and March, exhibiting higher δ¹⁸O and δD values with decreasing elevation. These elevational isotopic lapse rates likely reflect increased connection between stream flow and proximal snow-derived water sources heavily subject to elevational isotopic effects. These patterns disappeared during summer sampling, when consistently lower δ¹⁸O and δD values of stream water reflected contributions from snowmelt or colder rainfall, despite much higher δ¹⁸O and δD values expected in warmer seasonal rainfall. The consistently low isotopic values and absence of a trend with elevation during summer suggest lower connectivity between summer precipitation and stream flow generation as a consequence of drier soils and greater transpiration. As further evidence of intermittent seasonal connectivity between the stream and adjacent groundwaters, we observed a late-winter flush of nitrate into the stream at higher elevations, consistent with increased connection to accumulating mineralized nitrogen in riparian wetlands. This pattern was distinct from mid-summer patterns of nitrate loading at lower elevations that suggested heightened human recreational activity along the stream corridor. These observations provide insights linking stream flow generation and seasonal water storage in high elevation mountainous watersheds. Greater understanding of the connections between surface water, soil water and groundwater in these environments will help predict how the quality and quantity of mountain runoff will respond to changing climate and allow better informed water management decisions.     

Seasonal rainfall partitioning under runon and runoff conditions on sandy soil in Niger. On-farm measurements and water balance modelling

In sparsely cropped farming systems in semi-arid tropics, rainfall partitioning can be complex due to various interactions between vertical and horizontal water flows, both in the atmosphere and in the soil. Despite this, quantifying the seasonal rainfall partitioning is essential, in order to identify options for increased yields. Results are presented on water flow components, based on field measurements and water balance modelling, for three years (1994–96) in a farmer's field cultivated with pearl millet [Pennisetum glaucum (L.) Br.] in the Sahel (Niger). Water balance modelling was carried out for three common infiltration categories: runoff producing surfaces, surfaces receiving inflow of runon water from upstream zones, and a reference surface with zero runoff and runon. Runoff was calculated to 25%–30% of annual rainfall (which ranged from 488 to 596 mm), from crust observations, rainfall, soil wetness data, and infiltration estimates. Inflow of runon was estimated from field observations to 8%–18% of annual rainfall. The parameters in the functions for soil surface and canopy resistances were calibrated with field measurements of soil evaporation, stomatal conductance and leaf area. The model estimates of soil water contents, which were validated against neutron probe measurements, showed a reasonable agreement with observed data, with a root mean square error (RMSE) of approximately 0.02 m³ m⁻³ for 0–160 cm soil depth. Estimated productive water flow as plant transpiration was low, amounting to 4%–9% of the available water for the non-fertilised crop and 7%–24% for the fertilised crop. Soil evaporation accounted for 31%–50% of the available water, and showed a low variation for the observed range of leaf area (LAI <1 m² m⁻²). Deep percolation was high, amounting to 200–330 mm for the non-crusted surfaces, which exceeded soil evaporation losses, for 1994–95 with relatively high annual rainfall (517–596 mm). Even a year with lower rainfall (488 mm) and a distinct dry spell during flowering (1996), resulted in an estimated deep percolation of 160 mm for the non-fertilised crop. The crop did not benefit from the additional inflow of runon water, which was partitioned between soil water storage and deep percolation. The only exception to this was the fertilised crop in 1996, where runon somewhat compensated for the limited rainfall and the higher water demand as a result of a larger leaf area than the non-fertilised crop. The effects of rainfall erraticness, resulting in episodic droughts, explain why a crop that uses such a small proportion of the available water, in an environment with substantial deep percolation, still suffers from water scarcity. Application of small levels of phosphorus and nitrogen roughly doubled yields, from 380 to 620 kg ha⁻¹, and plant transpiration, from 33 to 78 mm. Evapotranspirational water use efficiency (WUE_ET) was low, 6500–8300 m³ ton⁻¹ grain for non-fertilised crop, which is an effect of the low on-farm yields and high non-productive water losses. The estimated seasonal rainfall partitioning indicates the possibility of quantifying vertical water flows in on-farm environments in the Sahel, despite the presence of surface overland flow.     

Organochlorine micropollutants in the Jiulong River Estuary and Western Xiamen Sea, China

Organochlorine contaminants including 12 polychlorinated biphenyl (PCB) congeners and 18 insecticides were determined in water, pore water and sediments of the Jiulong River Estuary and Western Xiamen Sea, China. The results showed that the levels of the total PCBs ranged from non-detectable to 1500 ng l⁻¹ in water, from 209 to 3870 ng l⁻¹ in pore water, and from 2.78 to 14.8 ng g⁻¹ dry weight in sediments. Total organochlorine insecticide concentrations were from below the limit of detection to 2480 ng l⁻¹ in water, from 267 to 33400 ng l⁻¹ in pore water, and from 4.22 to 46.3 ng g⁻¹ dry weight in sediments. Concentrations of PCBs and insecticides in pore water were significantly higher than those in surface water, due to the high affinity of these hydrophobic compounds for sediment phase. The PCB congeners with the highest concentrations were CB153, CB180 and CB194, which together accounted for 68–87% of total PCBs in water, pore water and sediment. Among the hexachlorocyclohexane (HCH) compounds, beta-HCH was found to be a major isomer. Analysis of 1,1,1-trichloro-2,2-bis-chlorophenyl-ethane (DDT) and its metabolites showed that 1,1-dichloro-2[o-chlorophenyl]-2[p-chlorophenyl]-ethylene (DDE) was dominant in the group. In comparison to a 1998 study in the Western Xiamen Sea, levels of organochlorines were enhanced due probably to recent inputs and changes in sediments.     

Glacier hydrochemistry, solute provenance, and chemical denudation at a surge-type glacier in Kuannersuit Kuussuat, Disko Island, West Greenland

In 1995–1998, Han 11 km terrestrial surge of Kuannersuit Glacier, an outlet glacier of the largest ice cap on Disko Island, West Greenland, affected the catchment dramatically. In order to estimate solute fluxes and provenances, bulk meltwaters were sampled at the main subglacial outlet during the initial part of the quiescent phase. The hydrochemistry is significantly influenced by a subglacial basaltic weathering regime with absence of carbonate minerals. The results show that marine and aerosol derived solutes have minimal contribution to the total ion content, whereas sequestration of atmospheric CO₂ associated with carbonation of Ca-rich feldspar and reactive volcanic glass is more dominant than previously reported from glacierized catchments. Application of a sampling strategy dividing water samples into four groups to determine the content of dissolved HCO₃⁻ and CO₃²⁻ shows that the cationic equivalent weathering rate range is 683–860 Σmeq⁺ m⁻² a⁻¹ and solute flux ranges between 76 and 98 t km⁻² a⁻¹. The crustal denudation rate is estimated to 26 t km⁻² a⁻¹, and the transient CO₂ drawdown amounts to 8500–13700 kg C km⁻² a⁻¹.     

Temporal trends of bulk precipitation and stream water chemistry (1977–1997) in a small forested area,Krusné hory,northern Bohemia,Czech Republic

The Krusné hory (Erzgebirge or Ore Mountains) has been heavily affected by high atmospheric pollutant deposition caused by fossil fuel combustion in an adjacent Tertiary coal basin. Long‐term routine sampling of bulk precipitation (1977–1996) and stream water (1977–1998) in a forested area on the south‐eastern slope of the mountains were used to evaluate trends and patterns in solute concentration and flux with respect to controlling processes. From 1977 to 1996, the annual volume‐weighted Ca²⁺ and SOconcentrations decreased in bulk precipitation. However, after 1989, when a pronounced and continuous decrease occurred in coal production, annual volume‐weighted concentrations decreased for most solutes, except H⁺. The concentration decreases were marked, with 1996 levels at or below 50% of those in 1989. The lack of a trend in H⁺ is attributed to similar decreases in both acid anions and neutralizing base cations. Stream water concentrations of most solutes, i.e. H⁺, Ca²⁺, Mg²⁺, SONOwere highest at the onset of sampling in 1977, decreased markedly from 1977 to 1983 and decreased more gradually from 1983 to 1998. The spruce forest die‐back and removal reduced dry deposition of these solutes by reducing the filtering action, which was provided by the forest canopy. A notable decrease in stream water Ca²⁺ concentrations occurred after 1995 and may be due to the depletion of Ca²⁺, which was provided by catchment liming in 1986, 1988 and 1989. Solute flux trends in bulk atmospheric deposition and stream water generally were not significant and the lack of trend is attributed to the large interannual variability in precipitation quantity and runoff, respectively. All solutes except Na⁺ varied seasonally. The average seasonal concentrations varied between the solutes, but for most solutes were highest in winter and spring and lowest in summer, correlating with the seasonal trend in runoff. For Ca²⁺, Mg²⁺ and SOthe concentration minimum occurs in September and the maximum occurs in February or March, correlating with the seasonal baseflow. These solutes are primarily controlled by the contribution of soil water and groundwater to stream flow. During snowmelt, the meltwater generally causes concentrations to decrease as soil water and groundwater are diluted. For NO₃ , average minimum concentrations occur in August at the end of the growing season concurrent with the lowest stream flow, and the maximum occurs in February and March with high stream flow during snowmelt. Seasonal stream water NOconcentration variations are large compared with the long‐term decrease. Copyright © 1999 John Wiley & Sons, Ltd.     

Residue levels of HCHs,DDTs and PCBs in shellfish from coastal areas of east Xiamen Island and Minjiang Estuary,China

Shellfish samples were collected from the coastal cultivating areas of east Xiamen Island and Minjing Estuary, China and analyzed for hexachlorocyclohexanes (HCHs), DDTs and polychlorinated biphenyls (PCBs) by GC. Concentration ranges of HCHs, DDTs and PCBs in the coastal area of east Xiamen Island were 0.18–345, 75.2–2143 and ND-23 ng g⁻¹ dry wt., respectively; those for Minjiang Estuary were ND-5.07, 21.5–2396 and ND-6.78 ng g⁻¹ dry wt., respectively. The results showed that the organochlorines were evidently accumulated in marine bivalve molluscs, particularly in oyster. The concentrations of organocholorine pollutants in shellfish samples varied with the sampling locations, the season of collection and organism species, but were generally higher than those in the sediments. The concentrations of DDTs in the shellfish were high as compared with HCHs and PCBs, so that DDTs can be considered as the typical organochlorines in the survey areas. The residue levels and compositions of HCHs, DDTs and PCBs are discussed.     

Effects of gravel and sand mulches on dew deposition in the semiarid region of China

Information regarding dew deposition on the stone-covered surface is scarce. The effects of gravel and sand mulches on dew condensation were studied during the late summer and fall of 1999 in the semiarid loess region of China. The results indicated that there were significant difference in daily dew amount between gravel mulch, sand mulch and dry loess soil (control). The average dew amount for gravel mulch was 0.071 mm d⁻¹ with extreme 0.022 and 0.20 mm d⁻¹. The average values for sand mulch and dry loess soil was 0.12 and 0.15 mm d⁻¹, respectively. The minimum dew amount was 0.048 mm d⁻¹ for sand mulch and 0.071 mm d⁻¹ for dry loess soil, and the maximum dew amount was approximate 0.25 mm d⁻¹ for both treatments. The results suggest that surface stone mulch can reduce dew deposition as compared to sand and dry loess soil.     

A comparison of solute fluxes and sources from glacial and non‐glacial catchments over contrasting melt seasons

Solute and runoff fluxes from two adjacent alpine streams (one glacial and one non‐glacial) were investigated to determine how the inorganic solute chemistry of runoff responded to seasonal and interannual changes in runoff sources and volume, and to differences in physical catchment properties. Intercatchment differences in solute composition were primarily controlled by differences in catchment geology and the presence of soils, whereas differences in total solute fluxes were largely dependent on specific discharge. The glacial stream catchment had higher chemical denudation rates due to the high rates of flushing (higher specific discharge). The non‐glacial Bow River had higher overall concentrations of solutes despite the greater prevalence of more resistant lithologies in this catchment. This is likely the result of both longer average water–rock contact times, and a greater supply of protons from organic soils and/or pyrite oxidation. Increases in snowpack depth/snowmelt runoff reduced the retention of nitrate in the Bow River catchment (i.e. increased nitrate export), probably by reducing net biological uptake, or by reducing the proportion of runoff that had contact with biologically active soil horizons that tend to remove nitrate. The two streams exhibited opposite solute flux responses to climate perturbations over three melt seasons (1998, 1999, and 2000). The 1998 El Niño event resulted in an unusually thin winter snowpack, and increased runoff and solute fluxes from the glacial catchment, but decreased fluxes from the Bow River catchment. Solute fluxes in the Bow River increased proportionally to discharge, indicating that increased snowmelt runoff in this catchment resulted in a proportional increase in weathering rates. In contrast, the proportional variation in solute flux in the glacial stream was only ∼70–80% of the variation in water flux. This suggests that increased ablation of glacier ice and the development of subglacial channels during the 1998 El Niño year apparently reduced the average water–rock contact time in the glacial catchment relative to seasons when the subglacial drainage system was primarily distributed in character. Copyright © 2005 John Wiley & Sons, Ltd.     

Water quality along a river continuum subject to point and diffuse sources

The water quality along the River Kennet, in the Thames basin of southern England, was examined in terms of the influence of point- and diffuse-nutrient inputs. The river is supplied mainly from a Cretaceous Chalk aquifer and hence the waters are of a calcium bicarbonate type. The nitrate largely comes from agricultural sources, with concentrations decreasing downstream due to plant uptake and probable denitrification. In contrast, soluble reactive phosphorus (SRP) is largely associated with sewage inputs and concentrations increase downstream in line with effluents from major towns such as Newbury and Reading. Adjacent to the river in the lower half of the catchment is the Kennet and Avon Canal and the two are in places hydrologically connected. The canal inputs may influence calcium carbonate (calcite) precipitation and increase suspended sediment and particulate phosphorus concentrations in the river. Monitoring upstream and downstream of Marlborough sewage treatment works (STW) showed that SRP concentrations in the effluent were highly variable due to variable efficiency of P stripping and still sufficiently concentrated to dominate downstream river SRP with potential impacts on stream ecology. Biological recovery in this river following P stripping at STWs is complex and controlling those spikes in SRP that are above a threshold of 100 μg l⁻¹ may be a critical requirement. More stringent effluent targets than are currently recommended may be needed (less than 800 μg RP l⁻¹) to achieve good ecological status in this river depending on SRP concentrations upstream.     

The physico-chemical conditions of Turkwel Gorge Reservoir, a new man made lake in Northern Kenya

Variations in some physical, chemical, and nutrient conditions were investigated at Turkwel Gorge Reservoir and its inflowing river, Suam between 1994 and 1995. Seasonal changes in inflow volume had the greatest impact on the reservoir and river conditions investigated. A wide fluctuation in inflow volume combined with a regulated outflow independent of season resulted in a draw down of over 10 m in each year. Flood inflows during the wet season resulted in the lowest values of Secchi depth (range, 0.09–2.16 m), electrical conductivity (EC, range = 140–200 mS cm⁻¹) and total alkalinity (TA, range = 75–111 mg l⁻¹) while the highest values were measured during the dry season. A functional relation between EC and TA (TA = 0.529 mg l⁻¹, EC: R² = 0.876) suggests a predominance of carbonates among the anions. Vertical profiles of temperature and dissolved oxygen (DO) revealed that the reservoir is monomictic with a wide variation in the depth of the daily mixed layer. High values of pH (range = 6.7–8.9) and DO (range = 4.9–9.2 mg l⁻¹) were associated with periods of peak phytoplankton photosynthesis while the lowest values followed reservoir mixing. Peak total nitrogen (TN, range = 119–526 μg l⁻¹) and total phosphorus (TP, range = 8.9–71.6 μg l⁻¹) levels during the wet season resulted from increased river loading. Values of dissolved reactive silica (DRS, range = 0.41–9.77 mg l⁻¹) showed a wet season decline which was related to diatom depletion during the wet season. Annual reservoir areal loading rates of 27.38, 10.90 and 408.5 mg m⁻² were computed for TN, TP and DRS respectively based on estimates of inflowing river loads in 1994.

At the inflowing river Suam, low levels of EC (range = 107–210 μS cm⁻¹) and TA (range = 62–125 mg l⁻¹) occurred during the wet season while the highest levels occurred shortly before the river dried up. The first flood water at the resumption of river inflow in March was characterized by very low levels of DO (range = 1.8–8.2 mg l⁻¹) and high levels of TN (range = 205–3354 μg l⁻¹) and TP (102–1259 μg l⁻¹). River pII (6.9–7.7) and DRs (range = 9.01–19.93 mg l⁻¹) varied irregularly throughout the year.