Capturing temporal variability for estimates of annual hydrochemical export from a first‐order agricultural catchment in southern Ontario,Canada

This 2‐year study (2000, 2001) reports annual nutrient (phosphorus, nitrate) export from a first‐order agricultural watershed in southern Ontario based on an intensive monitoring programme. The importance of storm and melt events in annual export estimates is demonstrated and the temporal variability in nutrient loading during events is related to processes occurring within the catchment. The feasibility of predicting event‐related nutrient export from hydrometric data is explored. The importance of sampling frequency throughout events is also shown. Export of total phosphorus (TP), soluble reactive phosphorus (SRP) and nitrate ( ) for 2000 and 2001 averaged 0·35 kg ha^?1 year^?1, 0·09 kg ha^?1 year^?1, and 35 kg ha^?1 year^?1 (as N) respectively. Approximately 75% of annual TP export, 80% of annual SRP export and 70% of annual export occurred during 28 events per year. A small number of large‐magnitude events (>34 mm) accounted for 18–42% of annual TP export, 0–61% of annual SRP export and 13–33% of annual NO export. Our results show that temporal variability in nutrient export is largely governed by discharge in this basin, and export can be predicted from discharge. SRP and TP export can also be predicted from discharge, but only for events that are not large in magnitude. The sampling interval throughout events is important in obtaining precise estimates of nutrient export, as infrequent sampling intervals may over‐ or under‐estimate nutrient export by ± 45% per event for P. This study improves our understanding of and P export patterns and our ability to predict or model them by relating temporal variability in event nutrient export to discharge and processes occurring within the basin, and also by exploring the significance of sampling interval in the context of the importance of individual events, season and temporal variability during events. Copyright © 2006 John Wiley & Sons, Ltd.     

Average sand particle trajectory examined by the Raindrop Detachment and Wind‐driven Transport (RD‐WDT) process

Recent studies of soil loss by the integrated action of raindrop impact and wind transport have demonstrated the significance of this mechanism. This paper presents data obtained during wind‐tunnel experiments examining the ‘Raindrop Detachment and Wind‐driven Transport’ (RD‐WDT) process to investigate average sand particle trajectory and the spatial extent at which the process operates. In the experimental design, at the same time as the horizontal wind velocities of 6·4, 10, and 12 m s^–1 passed through the tunnel, rainfall was simulated falling on very well sorted dune sand. The aspect and slope of the sand bed was varied to reproduce both windward (Ww) and leeward (Lw) slopes of 4º and 9º with respect to the prevailing wind direction. The average sand particle trajectories by the RD‐WDT process ( ) were estimated by a mass‐distribution function, which was integrated over a 7‐m uniform slope segment. The results showed that depended statistically upon the wind shear velocity (u*), and the effect of the slope gradient (θ) was insignificant on . This was different from that of the windless rain process ( ), ‘Raindrop Detachment and Splash‐driven Transport’ (RD‐ST), the spatial range of which relies strongly on θ. Additionally, was approximately 2·27 ± 2·2 times greater than the average path of a typical saltating sand particle of the rainless wind ( ), ‘Wind Erosion Saltation Transport’ (WE‐ST). Copyright © 2009 John Wiley & Sons, Ltd.     

Dynamics of Stream Water Quality during Snowmelt and Rainfall – Runoff Events in a Small Agricultural Catchment

Surface water quality can vary a lot with fluctuating discharge during a Rainfall – runoff event. This paper uses a set of hydrological and hydrochemical variables to explain concentration–discharge loops and hysteresis of ${\rm NO}_{3}^{- } $ , ${\rm NH}_{4}^{ + } $ and total suspended solids in a brook dewatering a small upland agricultural catchment in the Czech Republic. Our study is based on data collected by a continuous monitoring approach provided by an automatic ISCO sampler both from snow thawing and rainfall – runoff events. Methods of correlation, regression and principal component analysis (PCA) were employed to reveal possible relationships among the variables. For ${\rm NO}_{3}^{- } $ and ${\rm NH}_{4}^{ + } $ , we found several types of concentration–discharge loops due to the loop rotation direction and also the loop curvature shape, in mutual combinations, no matter which type of a hydrological event it was related to. PCA indicated that ${\rm NO}_{3}^{- } $ loops correlated mostly with the length of a rising hydrograph limb and with the slope of the initial phase of a falling hydrograph limb, 5‐day amount of precipitation and runoff coefficient. In case of ${\rm NH}_{4}^{ + } $ , the concentrations usually increased with elevated discharge, whereas PCA did not detect any closer linkages. For suspended solids, an unambiguous positive monotonic relationship was discovered. Although no definite pattern was found, this study showed the necessity of a continuous water quality monitoring system as an approach for capturing and understanding relationships between solute concentrations and runoff formation for tracing and modelling catchment pollution sources and describing transport processes.     

Groundwater quality in Mesogea basin in eastern Attica (Greece)

Studies on the hydrogeological conditions of the Mesogea basin in east Attica reveal that the aquifers developed on the post‐alpine formations at the inner part of the coastal brackish zone exhibit positive hydraulic head. These Neogene and Quaternary deposits present high salt concentrations. Selected points were sampled (total 85: 51 wells and 34 boreholes) in order to obtain hydrogeological and hydrochemical data for a better understanding of the structure, operation and dynamics of the aquifer of the area. Statistical methods, R‐mode factor analysis and scatter‐plot diagrams were used for the hydrochemical analysis and presentation of the data. The groundwater resources are relatively weak and there is significant quality degradation due to the geological structure of the greater area, as well as the bad management of the aquifer and anthropogenic activities. Groundwater is characterized by high salt concentrations. Electrical conductivity values range between 260 and 6970 µS cm^?1. High salt concentrations at the coastal aquifers are due to sea intrusion, whereas they are attributed to the dissolution of minerals of the geological environment in the inland area. The groundwaters of the study area can be classified into five water types: Ca–HCO₃, Mg–HCO₃, Na–HCO₃, Na–Cl and Mg–Cl. They are saturated in dolomite and calcite, whereas they are unsaturated in anhydrite. High ion concentrations, e.g. ] (0‐221 mg l^?1), ] (0·01‐1·88 mg l^?1), ] (0·01‐6·75 mg l^?1), as well as high heavy metals concentrations are attributed to anthropogenic impacts. Copyright © 2006 John Wiley & Sons, Ltd.     

The influence of fire and permafrost on sub‐arctic stream chemistry during storms

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.     

Mineral Content of Bottled and Desalinated Household Drinking Water in Kuwait

Three hundred and twenty‐two samples of desalinated household water were collected from 99 sampling locations that covered 95% of Kuwaiti's residential areas. Seventy‐one brands of bottled water were collected from Kuwaiti markets. The water quality parameters that were studied included pH, electrical conductivity (EC), total dissolved solids (TDS), F^?, Cl^?, Br^?, , , , , , , , and the major macronutrients Na⁺, K⁺, Ca²⁺, and Mg²⁺. The analysis yielded a large range of results for most of these parameters, with differences in some cases exceeding 10‐fold. With a few exceptions, the results were found to comply with US‐EPA and WHO standards. Only the water in two brands of bottled water was acidic (pH < 6.5). The TDS was found to be higher than the US‐EPA regulated value in 4 and 3% of the household samples and bottled water brands, respectively. The fluoride levels were generally higher in bottled water than in household water. However, the household water that was produced by the Doha desalination plant and some of the European brands of bottled water were the best samples studied in terms of their quantity of Ca²⁺, Mg²⁺, and Na⁺ compared with the DRI values for those substances. EC and TDS were positively correlated with , , Na⁺, K⁺, Ca²⁺, and Mg²⁺ for household water but only with Ca²⁺ and Mg²⁺ for bottled water.     

Factors controlling nitrogen release from two forested catchments with contrasting hydrochemical responses

Quantifying biogeochemical cycles of nitrogen (N) and the associated fluxes to surface waters remains challenging, given the need to deal with spatial and temporal variability and to characterize complex and heterogeneous landscapes. We focused our study on catchments S14 and S15 located in the Adirondack Mountains of New York, USA, which have similar topographic and hydrologic characteristics but contrasting stream nitrate ( ) concentrations. We characterized the mechanisms by which reaches the streams during hydrological events in these catchments, aiming to reconcile our field data with our conceptual model of factors that regulate nutrient exports from forested catchments. Combined hydrometric, chemical and isotopic (δ ) data showed that the relative contributions of both soil and ground water sources were similar between the two catchments. Temporal patterns of stream chemistry were markedly different between S14 and S15, however, because the water sources in the two catchments have different solute concentrations. During late summer/fall, the largest source of in S14 was till groundwater, whereas shallow soil was the largest source in S15. concentrations in surface water decreased in S14, whereas they increased in S15 because an increasing proportion of stream flow was derived from shallow soil sources. During snowmelt, the largest sources of were in the near‐surface soil in both catchments. Concentrations of increased as stream discharge increased and usually peaked before peak discharge, when shallow soil water sources made the largest contribution to stream discharge. The timing of peaks in stream concentrations was affected by antecedent moisture conditions. By elucidating the factors that affect sources and transport of N, including differences in the soil nutrient cycling and hydrological characteristics of S14 and S15, this study contributes to the overall conceptualization of release from temperate forested catchments. Copyright © 2007 John Wiley & Sons, Ltd.     

Hydraulic characteristics of a small Coastal Plain stream of the southeastern United States: effects of hydrology and season

Various physical and biological properties affect solute transport patterns in streams. We measured hydraulic characteristics of Payne Creek, a low‐gradient upper Coastal Plain stream, using tracer experiments and parameter estimation with OTIS‐P (one‐dimensional transport with inflow and storage with parameter optimization). The primary objective of this study was to estimate the effects of varying discharge, season, and litter accumulation on hydraulic parameters. Channel area A ranged from 0·081 to 0·371 m² and transient storage area A_s ranged from 0·027 to 0·111 m². Dispersion D ranged from 1·5 to 11·1 m² min⁻¹ and exchange coefficient α ranged from 0·009 to 0·038 min⁻¹. Channel area and dispersion were positively correlated to discharge Q, whereas storage area and exchange coefficient were not. Relative storage size A_s/A ranged from 0·17 to 0·59, and was higher during fall than other seasons under a similar Q. The fraction of median travel time due to transient storage ranged from 8·8 to 34·5% and was significantly correlated with Q through a negative power function. Both metrics indicated that transient storage was a significant component affecting solute transport in Payne Creek, especially during the fall. Comparison between the measured channel area A_c and A suggested that surface storage was dominant in Payne Creek. During fall, accumulation of leaf litter resulted in larger A and A_s and lower velocity and D than during other seasons with similar discharge. Seasonal changes in discharge and organic matter accumulation, and dynamic channel morphology affected the magnitude of transient storage and overall hydraulic characteristics of Payne Creek. Copyright © 2005 John Wiley & Sons, Ltd.     

Chemical dynamics of N-containing ionic species in a boreal forest snowcover during the spring melt period

A study of the changes in the ionic loads of NO, NH, SO and H⁺ in a boreal forest snowpack at Lake Laflamme, Québec was carried out using hydrological and chemical data from field lysimeters. The results showed that depletion of the N-containing species occurs periodically in the snowpack during meltwater discharge. Rain-on-snow events led to in-pack losses of NO and NH at a rate of 130 μeq m^?2 day^?1 and 101·3 μeq m^?2day^?1 respectively. On dry days, however, dry deposition and deposition of organic debris from the canopy resulted in increases of 183·3 μeq m^?2day^?1 for NO and 4·5 μeq m^?2day^?1 for NH in the pack. In contrast, SO₄^2? showed continual in-pack increases due to deposition of 5·0 μeq m^?2day^?1 for wet days and 92·6 μeq m^?2day^?1 for dry days. The depletion of NO and NH is due to microbiological uptake of these nutrients during periods when the free water content of the pack is high. Controlled melts in a laboratory snowmelt simulator containing snow and organic matter from the forest canopy at Lake Laflamme showed losses of NO and NH similar to those observed in the field. As the microbiological uptake proceeds at a rate comparable to that of ionic load increases in the pack by dry deposition, models of the chemical dynamics of snowmelt should take the former into account in any system where organic content of the snowpack is appreciable.     

Factors Affecting UV/H2O2 Oxidation of 17α‐Ethynyestradiol in Water

In this study, bench‐scale experiments were conducted to examine the UV/H₂O₂ oxidation of 17α‐ethynyestradiol (EE2) in water in a batch operation mode. The EE2 degradation exhibited pseudo‐first‐order kinetics, and the removal was ascribed to the production of hydroxyl radicals (^?OH) by the UV/H₂O₂ system. Typically, the EE2 oxidation rate increased with increasing UV intensity and H₂O₂ dose, and with deceasing initial EE2 levels and solution pH. At EE2₀ = 650 µg/L, UV intensity = 154 µW/cm², H₂O₂ = 5 mg/L, and neutral pH, the UV/H₂O₂ treatment was able to remove 90% of the EE2 content within 30 min. Four anions commonly present in water were found to inhibit EE2 degradation to varying degrees: > > Cl^? > . Our results demonstrate that the described UV/H₂O₂ process is an effective method to control EE2 pollution in water.     

Spatial–temporal variability and hydrologic connectivity of runoff generation areas in a North Alabama pasture—implications for phosphorus transport

This study delineated spatially and temporally variable runoff generation areas in the Sand Mountain region pasture of North Alabama under natural rainfall conditions, and demonstrated that hydrologic connectivity is important for generating hillslope response when infiltration‐excess (IE) runoff mechanism dominates. Data from six rainfall events (13·7–32·3 mm) on an intensively instrumented pasture hillslope (0·12 ha) were analysed. Analysis of data from surface runoff sensors, tipping bucket rain gauge and HS‐flume demonstrated spatial and temporal variability in runoff generation areas. Results showed that the maximum runoff generation area, which contributed to runoff at the outlet of the hillslope, varied between 67 and 100%. Furthermore, because IE was the main runoff generation mechanism on the hillslope, the data showed that as the rainfall intensity changed during a rainfall event, the runoff generation areas expanded or contracted. During rainfall events with high‐intensity short‐ to medium‐duration, 4–8% of total rainfall was converted to runoff at the outlet. Rainfall events with medium‐ to low‐intensity, medium‐duration were found less likely to generate runoff at the outlet. In situ soil hydraulic conductivity (k) was measured across the hillslope, which confirmed its effect on hydrologic connectivity of runoff generation areas. Combined surface runoff sensor and k‐interpolated data clearly showed that during a rainfall event, lower k areas generate runoff first, and then, depending on rainfall intensity, runoff at the outlet is generated by hydrologically connected areas. It was concluded that in IE‐runoff‐dominated areas, rainfall intensity and k can explain hydrologic response. The study demonstrated that only connected areas of low k values generate surface runoff during high‐intensity rainfall events. Identification of these areas would serve as an important foundation for controlling nonpoint source pollutant transport, especially phosphorus. The best management practices can be developed and implemented to reduce transport of phosphorus from these hydrologically connected areas. Copyright © 2009 John Wiley & Sons, Ltd.     

Spatial Variation of the Precipitation Chemistry in the Thrace Region of Turkey

Pollutants affect not only the environment in which they originate since they are also transported by air currents to other locations. For this reason, air pollution is a global problem for all countries and the air and water quality need to be monitored carefully. More information on precipitation chemistry is required to determine the source of pollution as well as its effects on the ecosystems. In this study, precipitation chemistry has been analyzed for the first time by using simple bulk collectors located at four different sites in Northwest Turkey for a period of two years. About 650 sequential rainwater samples were collected and analyzed for pH, electrical conductivity, anions such as , , Cl^?, and cations such as Na⁺, K⁺, Mg²⁺, Ca²⁺, and . The selected sites were under the effect of different environmental factors. Our results showed that the highest and concentrations were measured in the Northwest of the research area. Additionally, it has been found that Ca²⁺ ions are abundant within all rainwater samples.     

The Annual Characteristics of Rainwater HCHO in Guiyang City,Southwest of China

HCHO is ubiquitous and important chemical constitutes in the troposphere. The concentrations of the HCHO (aq) in the rainwater were measured in the Guiyang city, southeastern of China from May 2006 to April 2007 and 153 discrete samples were collected. Rainwater (N = 151) HCHO (aq) concentrations ranged from lower than method detection limit (MDL) to 40.2 µmol/L with a volume weighted mean value of 7.4 ± 8.8 µmol/L. The strong correlations between HCHO (aq) and HCOO^? (r = 0.69, n = 137), HCHO (aq) and nss‐ (r = 0.74, n = 137), HCHO (aq) and (r = 0.67, n = 137), HCHO (aq) and (r = 0.74, n = 133) suggest the significant influence of the anthropogenic input for the HCHO (aq) levels. The concentration levels of rainwater HCHO (aq) was inversely proportional to the amount of rainfall, indicating the below‐cloud process is the most important mechanism for rainwater HCHO (aq) scavenging processes. More than 70% of the HCHO (aq) wet deposition took place during the early stage of the rainfall. According to the air mass back‐trajectory analysis, the rainwater with industrial back‐trajectories coming from the north had the highest levels of HCHO (aq) while the rainwater with the green‐covered or marine back‐trajectories from the southeast had the lowest concentrations, and this indicate the HCHO (aq) originated from urban or industrial regions served as an important source of the rainwater. The annual HCHO (aq) wet deposition flux was calculated as 6.96 mmol/m² per year and the total deposition flux was estimated as 24.35 mmol/m² per year, 71.4% of which was dominated by dry deposition.     

When does bedload transport begin in steep boulder‐bed streams?

The paper presents the results of field measurements of critical conditions for bedload motion conducted in the Rio Cordon, a steep boulder‐bed stream in the Italian Alps, under conditions of high Reynolds numbers and low relative submergence poorly explored before. Two methods have been used to determine threshold of motion: the displacement of marked clasts and the flow competence approach, which uses the largest grain size diameter transported by each flood event. The high values of confirm the great relevance of non‐bedload effective shear stresses in step–pool streams given by the additional form drag associated with this morphology. Relative submergence effects on the dimensionless critical shear stress have been quantified by considering the relative submergence ratio R_h/D₈₄, and the major effect of relative size on the mobility of each particle in steep, widely graded bed mixtures has been evaluated. Finally, the dimensionless critical unit discharge has also been adopted in the regression equations as the critical hydraulic parameter, because it may represent an easier parameter to use than the critical shear stress for steep, rough mountain rivers. Copyright © 2006 John Wiley & Sons, Ltd.     

Geochemistry of meteoric diagenesis in carbonate islands of the northern Bahamas: 1. Evidence from field studies

Processes driving carbonate diagenesis in islands of the northern Bahamas are investigated using major ion, dissolved oxygen and dissolved organic carbon analyses of water samples from surface and ground waters, and measurements of soil gas P. Meteoric waters equilibrate with aragonite, but reactions are water controlled rather than mineral‐controlled and drive dissolution rather than concurrent precipitation of calcite. Surface runoff waters equilibrate with atmospheric P and rapidly recharge the vadose zone, limiting subaerial bedrock dissolution to only 6·6–15 mg l^?1 Ca. P of soil gas measured in the summer wet season ((7·4 ± 3·7) × 10^?3 atm) is elevated compared with that of the atmosphere, despite the thin skeletal organic nature of the soil and the discontinuous soil cover. Soil waters retained in surface pockets are equilibrated with respect to aragonite and have dissolved 51 ± 19 mg l^?1 Ca. This is substantially less than the 93 ± 18 mg l^?1 Ca in samples from pumping boreholes that sample meteoric waters from the freshwater lens. The high P of the freshwater lens ((16 ± 8·3) × 10^?3 atm for pumping boreholes) suggests that significant additional CO₂ may be derived by oxidation of soil‐ and surface‐derived organic carbon within the lens. The suboxic nature of the majority of the freshwater lens and the observed depletion in sulphate support this suggestion, and indicate that both aerobic and anaerobic oxidation may take place. Shallow lens samples from observation boreholes are calcite supersaturated and have a lower P than deeper lens waters, indicating that CO₂ degasses from the water table, driving precipitation of calcite cements. We suggest that the geochemical evolution of waters in the vadose zone and upper part of the freshwater lens may be determined by the presence of a body of ground air with P controlled by production in the freshwater lens and soil and by degassing to the atmosphere. Copyright © 2007 John Wiley & Sons, Ltd.     

Simulation of the size distribution and erosivity of raindrops and throughfall drops

This paper presents a model that simulates the size distribution and erosivity of raindrops and throughfall drops. It utilizes existing models of rainfall drop size distribution and fall velocity and combines them with newly collated evidence of throughfall drop size distributions. A sensitivity analysis reveals that the model is sensitive to parameters that are easily measured or estimated: rainfall intensity, the mean volume drop diameter of the intercepted throughfall, canopy cover, and canopy height. The results of the model may be used at two levels. Firstly, to calculate specifically the size and fall velocity of individual drops, parameters that are needed in studies examining the response of soil surfaces to forces applied by rainfall. Secondly, to produce erosivity indices, based on rainfall intensity but which take account of the effects of a vegetation canopy. The paper shows that while the kinetic energy of rainfall (E(0), J mm^?1 m^?2) may be calculated from an equation of the familiar form: the kinetic energy of throughfall under any canopy may be calculated by combining this equation with another that relates the energy of drops under a 100 per cent canopy cover (E(100)) and the canopy height: .     

Factors controlling groundwater chemistry in an agricultural area with complex topographic and land use patterns in mid‐western South Korea

Shallow and bedrock groundwater from granitic aquifers were investigated for the hydrogeochemistry of major and minor constituents in an agricultural area. Nitrate concentrations were observed up to 49 mg/l as NO₃‐N, with 22% of samples exceeding the drinking water standard, which could pose a significant threat because most residents rely on groundwater as their drinking water source. Principal component analysis revealed three principal components (PCs): (1) nitrate contamination, contributed by major cations, Cl^?, SO and NO , (2) reduction processes positively involving Fe, Mn and B, and negatively involving dissolved oxygen and NO and (3) natural mineralization, involving HCO and F^?. Cluster analysis, performed on the PC scores, resulted in seven sample groups, which were successfully identified by total depth, elevation and land use. The nitrate‐contaminated groups had mixed land uses, with locally concentrated residential areas. Uncontaminated groundwater groups were found in the natural environment, including high‐altitude spring water and bedrock groundwater with a higher degree of natural mineralization. Shallow groundwater groups in paddy fields in lowlands were affected by reducing environments, of which one group was characterized by high Fe, Mn and B, and negligible nitrate. Groundwater with intermediate nitrate and lower Cl^? and SO was found primarily in hilly terrains with orchards and vegetable gardens, indicating lower contaminant loadings than lowland areas. Higher concentrations of F^? and nitrate were observed in the nitrate‐contaminated water, which seemed unlikely to be explained by groundwater mixing. The strong acidity generated from nitrification may infiltrate deeper into the aquifer, induce accelerated weathering of bedrock and result in the coexistence of F^? and nitrate, which may be an evidence of intense nitrate loading, leading to soil acidification. Multivariate statistical analysis successfully delineated hydrochemical characteristics of groundwater attained by natural and anthropogenic processes in an agriculturally stressed area with complex topographic land use patterns. Copyright © 2009 John Wiley & Sons, Ltd.     

Spatial and temporal variations in summer precipitation in Japanese mountain areas

We examined spatial and temporal variations in precipitation measured during summer season between 1976 and 2007 for 28 stations located in mountain areas across Japan using the amount of precipitation (Pr), the mean depth of precipitation events (η), and the inverse of the mean interval times (λ). We obtained positive correlations between the period mean Pr (Pr ) and the period mean η ( ) and between Pr and the period mean λ ( ) for the 28 stations. Pr was more strongly related to than to , indicating the spatial variations in Pr that are primarily related to the variations in . In addition, Pr was more strongly related to η than to λ for most stations on the basis of data for 1976–2007, indicating that the year‐to‐year variations in Pr are primarily related to η. We also examined temporal trends in Pr, η and λ for 1976–2007 and found no systematic trends for 23 of the 28 stations, suggesting long‐term trends that are not common in mountain areas of Japan. The relationships between Pr and and between Pr and η presented in this study enable us to generate a temporal precipitation distribution pattern based on only Pr and Pr data, respectively. Furthermore, probabilistic stochastic hydrological models require precipitation characteristics as input; thus, this study contributes to the determination of hydrological cycles and their possible future changes in Japanese mountain areas and therefore to water resource management. Copyright © 2010 John Wiley & Sons, Ltd.     

Experimental Designs Applied to Desorption of Dichromate Ions after Separation and Preconcentration from Natural and Industrial Water by Modified Nano‐Alumina

Nano‐alumina modified by 9‐aminoacridine was used as a sorbent for separation and determination of dichromate ions from water. Statistical method, based on surface response design, has been used for the optimization of dichromate ions elution from 9‐aminoacridine nano‐alumina. The adsorbed dichromate ions were found to be eluted quantitatively with 0.8 mol L^?1 KCl in 1.6 mol L^?1 NaOH which optimized by response surface design. Under optimum conditions, the accuracy, precision (relative standard deviation, RSD%) and R‐square of the method were calculated as >98, <3, and >94%, respectively. Remarkable agreement between experimental and theoretical data was confirmed the predicted assumption. The method was applied to the simultaneous determination of dichromate in natural and industrial water samples. We also examined the retention of dichromate anions in the presence of Cl^?, , and anions at pH 3.     

Transformations of runoff chemistry in the Arctic tundra,Northwest Territories,Canada

The transformation of snowmelt water chemical composition during melt, elution and runoff in an Arctic tundra basin is investigated. The chemistry of the water flowing along pathways from the surface of melting snow to the 95·5 ha basin outlet is related to relevant hydrological processes. In so doing, this paper offers physically based explanations for the transformation of major ion concentrations and loads of runoff water associated with snowmelt and rainfall along hydrological pathways to the stream outlet. Late‐lying snowdrifts were found to influence the ion chemistry in adjacent reaches of the stream channel greatly. As the initial pulse of ion‐rich melt water drained from the snowdrift and was conveyed through hillslope flowpaths, the concentrations of most ions increased, and the duration of the peak ionic pulse lengthened. Over the first 3 m of overland flow, the concentrations of all ions except for NO increased by one to two orders of magnitude, with the largest increase for K⁺, Ca²⁺ and Mg²⁺. This was roughly equivalent to the concentration increase that resulted from percolation of relatively dilute water through 0·25 m of unsaturated soil. The Na⁺ and Cl^? were the dominant ions in snowmelt water, whereas Ca²⁺ and Mg²⁺ dominated the hillslope runoff. On slopes below a large melting snowdrift, ion concentrations of melt water flowing in the saturated layer of the soil were very similar to the relatively dilute concentrations found in surface runoff. However, once the snowdrift ablated, ion concentrations of subsurface flow increased above parent melt‐water concentrations. Three seasonally characteristic hydrochemical regimes were identified in a stream reach adjacent to late‐lying snowdrifts. In the first two stages, the water chemistry in the stream channel strongly resembled the hillslope drainage water. In the third stage, in‐stream geochemical processes, including the weathering/ion exchange of Ca²⁺ and Mg²⁺, were the main control of streamwater chemistry. Copyright © 2006 John Wiley & Sons, Ltd.