Response of surface water chemistry to reduced levels of acid precipitation: comparison of trends in two regions of New York,USA

In light of recent reductions in sulphur (S) and nitrogen (N) emissions mandated by Title IV of the Clean Air Act Amendments of 1990, temporal trends and trend coherence in precipitation (1984–2001 and 1992–2001) and surface water chemistry (1992–2001) were determined in two of the most acid‐sensitive regions of North America, i.e. the Catskill and Adirondack Mountains of New York. Precipitation chemistry data from six sites located near these regions showed decreasing sulphate (SO₄^2?), nitrate (NO₃^?), and base cation (C_B) concentrations and increasing pH during 1984–2001, but few significant trends during 1992–2001. Data from five Catskill streams and 12 Adirondack lakes showed decreasing trends in SO₄^2? concentrations at all sites, and decreasing trends in NO₃^?, C_B, and H⁺ concentrations and increasing trends in dissolved organic carbon at most sites. In contrast, acid‐neutralizing capacity (ANC) increased significantly at only about half the Adirondack lakes and in one of the Catskill streams. Flow correction prior to trend analysis did not change any trend directions and had little effect on SO₄^2? trends, but it caused several significant non‐flow‐corrected trends in NO₃^? and ANC to become non‐significant, suggesting that trend results for flow‐sensitive constituents are affected by flow‐related climate variation. SO₄^2? concentrations showed high temporal coherence in precipitation, surface waters, and in precipitation–surface water comparisons, reflecting a strong link between S emissions, precipitation SO₄^2? concentrations, and the processes that affect S cycling within these regions. NO₃^? and H⁺ concentrations and ANC generally showed weak coherence, especially in surface waters and in precipitation–surface water comparisons, indicating that variation in local‐scale processes driven by factors such as climate are affecting trends in acid–base chemistry in these two regions. Copyright © 2005 John Wiley & Sons, Ltd.     

Wildfire effects on extractable elements in ash from a Pinus pinaster forest in Portugal

The aim of this work is to study the effects of a wildfire on water‐extractable elements in ash from a Pinus pinaster forest located in Portugal. The pH, electrical conductivity (EC), calcium (Ca²⁺), magnesium (Mg²⁺), sodium (Na⁺), potassium (K⁺), sodium and potassium adsorption ratio (SPAR), aluminium (Al³⁺), manganese (Mn²⁺), iron (Fe²⁺), zinc (Zn²⁺), sulphur (S), silica (Si) and phosphorous (P) were analysed in ash sampled from a sloped area burned in a wildfire and from litter from a contiguous unburned area, with similar morphological conditions. The results showed that ash leachates had higher pH and EC, and were significantly richer in water‐extractable Ca²⁺, Mg²⁺, Na⁺, K⁺, SPAR, S and Si and significantly poorer in water‐extractable Al³⁺, Fe²⁺, Mn²⁺ and Zn²⁺ than litter solutions. No significant differences were observed in water‐extractable P. The fire changed the ash solute chemistry compared with the unburned litter and increased the sample variability of nutrient distribution with potential implications for plant recovery. Copyright © 2013 John Wiley & Sons, Ltd.     

Color-change processes of a plinian pumice and experimental constraints of color-change kinetics in air of an obsidian

Colors of plinian pumices were measured by spectrocolorimetry, and their quantitative color parameters in the L*a*b* color space were determined. A series of heating experiments of obsidian was conducted to simulate the color-change processes of rhyolitic glasses. In these experiments, following three stages of color-change processes were observed. Stage I showed a rapid b* (yellowishness) increase associated with fast dehydration controlled by water diffusivity (D _water). In stage II, a* (reddishness) increase was accompanied by Fe²⁺ decrease. Both a* increase and Fe²⁺ decrease can be simulated by a diffusion model. Obtained diffusivity D _oxidation were about two orders of magnitude smaller than D _water . The a*-value increase after the oxidation in stage III appeared to be quasi-linear with time, indicating the zeroth order reaction corresponding to the formation of hematite-like structures in rhyolitic glasses. The diffusion-limited a* increase model in stage II was applied to a natural plinian pumice fall unit to evaluate time periods of color-change processes through oxidation by air of fragmented rhyolitic materials.     

Gully morphological characteristics in the loess hilly‐gully region based on 3D laser scanning technique

Gully morphology characteristics can be used effectively to describe the status of gully development. The Chabagou watershed, located in the hilly‐gully region of the Loess Plateau in China, was selected to investigate gully morphological characteristics using a 3D laser scanning technique (LIDAR). Thirty‐one representative gullies located at different watershed locations and gully orders were chosen to quantitatively describe gully morphology and establish empirical equations for estimating gully volume based on gully length and gully surface area. Images and point cloud data for the 31 gullies were collected, and digital elevation models (DEMs) with 10‐cm resolution were generated. ArcGIS 10.1 was then used to extract fundamental gully morphological parameters covering gully length (L), gully width (W_T) and gully depth (D), and some derivative morphological parameters, including gully head curvature (C), gully width–depth ratio (w/d), gully bottom‐to‐top width ratio (W_B/W_T), gully surface area (A_g) and gully volume (V_g). The results indicated that gullies in the upper watershed and the second order were more developed based on their high values of gully head curvature. The potential for gully development increased from the second order to the fourth order. Within the same gully orders, gullies in the lower watershed were more active with more development potential. A method for differentiating between gully head and gully sidewalls based on the gully head curvature value was proposed with a mean relative error of 8.77%. U‐shaped cross‐sections were widely distributed in the upper watershed and upper positions of a gully, while V‐shaped cross‐sections were widely distributed in the lower watershed and lower positions of a gully. V–L and V–A_g empirical equations with acceptable accuracy were established and can be used to estimate gully erosion in the Loess hilly‐gully region. Copyright © 2017 John Wiley & Sons, Ltd.     

Inversion of gravity and magnetic anomalies over some bodies of simple geometric shape

The general expression for gravity and magnetic anomalies over thin sheets and sloping contacts may be expressed as a polynomial of the formFx ²+C₁Fx+C₂F+C₃x³+C₄x²+C₅x+C₆. The initial parameters of the source are obtained from the coefficientsC ₁, C₂,..., C₆ which may be solved by inverting a 6×6 matrix. The initial parameters are modified by successive iteration process using the difference formula until the root mean square error between the observed and calculated anomalies is a minimum. The regional background which may be in the form of a polynomial is estimated by the computer itself. This method is applied on a number of field anomalies and is found to yield reliable estimates of depth and other parameters of the source.     

Characterization and advanced oxidation treatment of dyeing effluent by Fenton’s reagent

Textile effluent from dyeing process has been a serious environmental threat for years. This study was intended to evaluate the performance of Fenton’s process for the removal of chemical oxygen demand (COD), colour and turbidity. Experiments were conducted by laboratory-scale reactors fed with cotton dyeing effluent. The Fenton process employs ferrous ions and hydrogen peroxide H₂O₂ under acidic pH conditions. The experimental variables studied include doses of iron salts and hydrogen peroxide, oxidation time, pH for oxidation and coagulation. The COD, color and turbidity removal reached a maximum of 97.2, 96.8 and 84.8% respectively at a reaction time of 20 min under optimum doses of H₂O₂ and Fe²⁺. Hydrogen peroxide dose ranging from 0.5 to 2.0 mL/500 mL and FeSO₄ · 7H₂O in the range of 0.5–4.0 gm/500 mL were selected to be examined at different reaction times between 10 and 30 min. Optimum dose of hydrogen peroxide and ferrous sulphate were 2.0 mL and 1.0 gm respectively for 500 mL of sample. In this study optimized pH 4.0 and 6.0 was found effective for oxidation and coagulation respectively.     

Degradation of an Azo Dye with Homogeneous and Heterogeneous Catalysts by Sonophotolysis

This study illustrates the degradation of an azo dye, Reactive Yellow 81 (RY81), by the combined irradiation of UV‐C and ultrasound in the presence of homogeneous (Fe²⁺) and heterogeneous (TiO₂, ZnO) catalysts. The efficiency of homogeneous and heterogeneous oxidation systems was evaluated in regard of the decolorization and mineralization of RY81. Decolorization followed pseudo‐first‐order kinetics with homogeneous and heterogeneous catalysts. Complete color removal was accomplished by homogeneous sonocatalytic and sonophotocatalytic oxidation processes with apparent rate constants of 0.96 × 10^?3 and 46.77 × 10^?3 s^?1, respectively, in the presence of Fe²⁺. However, partial color removal was obtained by heterogeneous sonocatalytic, photocatalytic, and sonophotocatalytic oxidation processes with apparent rate constants of 2.32 × 10^?3, 3.60 × 10^?3, and 3.67 × 10^?3 s^?1, respectively, in the presence of ZnO. TiO₂ had the worst catalytic effect of all of the oxidation processes. The addition of hydrogen peroxide increased the rate constants of the heterogeneous oxidation processes and decreased the rate constants of the homogeneous oxidation processes. RY81 mineralization was 62.8% for the US/UV/Fe²⁺ homogeneous oxidation process, which was the best oxidation process, whereas it was 43.5% for the US/UV/ZnO/H₂O₂ heterogeneous oxidation process within 2 h reaction time.     

A Study: Removal of Cu(II), Cd(II), and Pb(II) Ions from Real Industrial Water and Contaminated Water Using Activated Sludge Biomass

This study aims to remove of Cu²⁺, Cd²⁺, and Pb²⁺ ions from solution and to investigate the adsorption isotherms, adsorption kinetics, and ion‐exchange affinities of these metals using waste activated sludge (AS) biomass. The adsorptions of the metals on biomass were optimal at an acidic pH value of 6.0 based on its monolayer capacities. Maximum monolayer capacities of AS biomass (q_max) were calculated as 0.478, 0.358, and 0.280 mmol g^?1 for Cu²⁺, Cd²⁺, and Pb²⁺, respectively, and the adsorption equilibrium time was found as 60 min for each metal. The adsorbed amount of metal rose with increasing of initial metal ion concentration. The equilibrium adsorption capacity of AS for initial 0.25 mmol L^?1 metal concentration was determined as 0.200, 0.167, and 0.155 mmol g^?1 for Cu²⁺, Cd²⁺, and Pb²⁺ ions, respectively. These relevant values were determined as 0.420, 0.305, and 0.282 mmol g^?1 for Cu²⁺, Cd²⁺, and Pb²⁺ ions, respectively, when initial metal concentration was 0.50 mmol L^?1. In the multi‐metal sorption system, the adsorption capacity of AS biomass was observed in the order of Cu²⁺ > Cd²⁺ > Pb²⁺. In the presence of 100 mmol L^?1 H⁺ ion, the order of ion‐exchange affinity with H⁺ was found as Cu²⁺ > Cd²⁺ > Pb²⁺. The adsorption kinetics were also found to be well described by the pseudo‐second‐order and intraparticle diffusion models. Two different rate constants were obtained as k_i1 and k_i2 and k_i1 (first stage) was found to be higher than k_i2 (second stage).     

Model of vibrational level populations of Herzberg states of oxygen molecules at heights of the lower thermosphere and mesosphere

The paper presents a model of the kinetics of electronically excited O₂(c¹Σ_u⁻,v), O₂(A′³Δ_u,v), O₂(A³Σ_u⁺,v) molecules at heights of the lower thermosphere and mesosphere with allowance for electronic excitation transfer processes during molecular collisions. The model is used to calculate the relative O₂(A³Σ_u⁺,v) and O₂(A′³Δ_u,v) populations at heights of 80–110 km. The calculated populations are compared with the available literature results on experimental estimates, and good agreement is obtained. It is shown how the increase in the quenching rates of the considered states by oxygen atoms affects the calculation results.     

THE PROBLEM OF LONG-TERM STORAGE IN RESERVOIRS

Abstract

The geometry of a meandering stream depends strongly on the relative stream size (Q ^2/5 / g ^1/5)/D, on the valley slope, Sv, and on the charge, Q _s/Q, where Q and Q _s are the fluid and sediment discharges respectively, g is acceleration due to gravity and D is the mean sediment size. The geometry depends less strongly on the relative settling size of sediment, D/(v ^2/3 / g ^1/3), where v is the kinematic viscosity. For constant values of Q, S _v and D, the effect of increase of charge reduces the meander length, M _L, and the mean channel surface width, B, whereas meander width, M _B, bend radius, R _M, and mean channel depth, H, increase, For a constant value of (Q ^2/5 / g^1/5)/D the values of M _L, M _B, R _M and B increase with the increase of valley slope but the value of H tends to decrease.     

湖北道观河水库细鳞鲴的个体生殖力

研究了道观河水库细鳞鲴的个体生殖力。细鳞鲴样本由2~ -5~ 龄鱼组成,其个体绝对生殖力与体长、体重和年龄分别呈直线、对数函数和幂函数相关,体长相对生殖力与体长、体重和年龄分别呈双曲线、对数函数和幂函数相关,体重相对生殖力与它们相关不显著。多元逐步回归分析其绝对生殖力和体长相对生殖力均与体重和成熟系数密切相关,而体重相对生殖力仅与成熟系数相关。     

An anomalous subauroral red arc on 4 August, 1972: comparison of ISIS-2 satellite data with numerical calculations

This study compares the Isis II satellite measurements of the electron density and temperature, the integral airglow intensity and volume emission rate at 630 nm in the SAR arc region, observed at dusk on 4 August, 1972, in the Southern Hemisphere, during the main phase of the geomagnetic storm. The model results were obtained using the time dependent one-dimensional mathematical model of the Earth’s ionosphere and plasmasphere (the IZMIRAN model). The major enhancement to the IZMIRAN model developed in this study to explain the two component 630 nm emission observed is the analytical yield spectrum approach to calculate the fluxes of precipitating electrons and the additional production rates of N⁺₂, O⁺₂, O⁺(⁴S), O⁺(²D), O⁻(²P), and O⁺(²P) ions, and O(¹D) in the SAR arc regions in the Northern and Southern Hemispheres. In order to bring the measured and modelled electron temperatures into agreement, the additional heating electron rate of 1.05 eV cm⁻³ s⁻¹ was added in the energy balance equation of electrons at altitudes above 5000 km during the main phase of the geomagnetic storm. This additional heating electron rate determines the thermally excited 630 nm emission observed. The IZMIRAN model calculates a 630 nm integral intensity above 350 km of 4.1 kR and a total 630 nm integral intensity of 8.1 kR, values which are slightly lower compared to the observed 4.7 kR and 10.6 kR. We conclude that the 630 nm emission observed can be explained considering both the soft energy electron excited component and the thermally excited component. It is found that the inclusion of N₂(v > 0) and O₂(v > 0) in the calculations of the O⁺(⁴S) loss rate improves the agreement between the calculated N_e and the data on 4 August, 1972. The N₂(v > 0) and O₂(v > 0) effects are enough to explain the electron density depression in the SAR arc F-region and above F2 peak altitude. Our calculations show that the increase in the O⁺ + N₂ rate factor due to the vibrationally excited nitrogen produces the 5–19% reductions in the calculated quiet daytime peak density and the 16–24% decrease in NmF2 in the SAR arc region. The increase in the O⁺ + N₂ loss rate due to vibrationally excited O₂ produces the 7–26% decrease in the calculated quiet daytime peak density and the 12–26% decrease in NmF2 in the SAR arc region. We evaluated the role of the electron cooling rates by low-lying electronic excitation of O₂(a¹δ_g) and O₂(b¹σ_g⁺), and rotational excitation of O₂, and found that the effect of these cooling rates on T_e can be considered negligible during the quiet and geomagnetic storm period 3–4 August, 1972. The energy exchange between electron and ion gases, the cooling rate in collisions of O(³P) with thermal electrons with excitation of O(¹D), and the electron cooling rates by vibrational excitation of O₂ and N₂ are the largest cooling rates above 200 km in the SAR arc region on 4 August, 1972. The enhanced IZMIRAN model calculates also number densities of N₂(B³π_g⁺), N₂(C³π_u), and N₂(A³σ_u⁺) at several vibrational levels, O(¹S), and the volume emission rate and integral intensity at 557.7 nm in the region between 120 and 1000 km. We found from the model that the integral integral intensity at 557.7 nm is much less than the integral intensity at 630 nm.     

The Chemical Species Distribution of Aluminum in Composite Flocculants Prepared from Polyaluminum Chloride (PAC) and Polydimethyldiallylammonium Chloride (PDMDAAC)

In order to improve the coagulation/flocculation efficiency of polyaluminum chloride (PAC), a composite flocculant of PAC and polydimethyldiallylammonium chloride (PDMDAAC), or PAC‐PDMDAAC, was prepared. The chemical species distribution of aluminum in PAC and PAC‐PDMDAAC, which has a close relationship with their coagulation/flocculation performance, was investigated by Al‐Ferron complexation timed spectrophotometry and ²⁷Al‐NMR. The factors affecting the chemical species of aluminum in PAC‐PDMDAAC, such as the weight concentration of PDMDAAC (Wp), basicity (B) of PAC, and viscosity (η) of PDMDAAC, were studied. The flocculation efficiencies of PAC‐PDMDAAC, PAC and PDMDAAC were studied on a six‐spindle multiple stirrer unit. The results showed that the aluminum species distribution in PAC‐PDMDAAC depends on the Wp, B and η value. When the B value is 1.5 and η value is 1.22 dL/g, the composite flocculant with Wp = 15 % gives highest Al_b and Al₁₃ contents, and its flocculation efficiency is highest in the test flocculations.     

Degradation of Phenol in Aqueous Solution by Fenton,Sono‐Fenton and Sono‐photo‐Fenton Methods

The present work focuses on the performance of Fenton, sono‐Fenton, and sono‐photo‐Fenton processes for the oxidation of phenol present in aqueous solution. The effects of H₂O₂ concentration, Fe²⁺ concentration, pH, and initial phenol concentration on the oxidation of phenol were studied. The optimum Fe²⁺ and H₂O₂ concentrations for the Fenton process were 45 and 800 mg/L, respectively. For the sono‐Fenton process, the optimum Fe²⁺ and H₂O₂ concentrations were 30 and 800 mg/L, respectively. The optimal conditions for the sono‐photo‐Fenton process were found to be 20 mg/L of Fe²⁺ and 700 mg/L of H₂O₂. The optimum pH was found to be 3 for the processes investigated in the present study. The analysis of results showed that the sono‐photo‐Fenton method reduced the Fe²⁺ concentration by 30–50% and the H₂O₂ concentration by 12.5%. It was found that the sono‐photo‐Fenton technique showed better performance than the Fenton and sono‐Fenton processes for the oxidation of phenol. A lumped kinetic model was used to predict the chemical oxygen demand reduction and the model was found to fit the data.     

Monitoring of Impact of Ferti‐irrigation by Post‐methanated Distillery Effluent on Groundwater Quality

The impact assessment of molasses‐based distillery‐effluent irrigation on groundwater quality around village Gajraula in the district of Jyotiba Phule Nagar, Uttar Pradesh, India was studied by sampling groundwater on monthly intervals consecutively for summer, winter and monsoon seasons during 2006–2007 and water quality parameters, viz. pH, electrical conductivity (EC), chloride (Cl^?), sulphate (SO), nitrate (NO), chemical oxygen demand (COD), total solids (TS), total dissolved solids (TDS), sodium (Na⁺), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), zinc (Zn²⁺), iron (Fe³⁺), and total coliforms (TC) were monitored. Results depicted that the values of all parameters decreased with increasing depth of water table. Sulphate, nitrate and potassium contents were maximal in agricultural site during monsoon while EC, Cl^?, TS, TDS, Na⁺, Ca²⁺, Mg²⁺, Zn, and Fe were maximal in industrial sites during summer. Groundwater samples of residential site harboured maximum coliforms especially during monsoon, highlighting threat to groundwater. Significant positive correlation matrix between coliforms with nitrate, sulphate and potassium ions explained their survival on these nutrients. To overcome this, important measures emphasizing improvement in effluent treatment technology matching site‐specific characteristics are recommended for eco‐friendly ferti‐irrigation.     

Upper air mean dry-bulb and dew-point temperature profiles over Gauhati airport

Summary The best fit curves for upper air mean dry-bulb and dew-point temperatures over Gauhati airport (26°05N, 91°43E, 49 metres a.m.s.l.), for the month of April, have been calculated with the equation,x=A+By+Cy ²,y being the log value in mb of the isobaric level under consideration andx, the mean dry-bulb or dew-point temperature as the case may be, at the isobaric level under consideration. The values of constantsA, B andC for morning dry-bulb and dew-point curves come to be –29.54559, –93.65766 and +37.35048 and –118.84791, –31.15503 and +25.63585 respectively and values of these constants for evening curves come to be –35.86214, –94.15694 and +38.61870 and –127.55970, –29.97192 and +26.36538 respectively. These best fit curves help in finding out mean desired temperatures at any isobaric level in forecasting of thunderstorms and hailstorms, at a station, by dry-bulb and dew-point temperature anomaly technique propsed earlier by the authors.     

Preparation and evaluation of polyaluminum chloride sulfate (PACS) as a coagulant to remove natural organic matter from water

A series of polyaluminum chloride sulfate (PACS) coagulants, which have different SO₄^2–/Al³⁺ and OH/Al (γ) mole ratio, has been successfully developed using AlCl₃·6H₂O, Al₂(SO₄)₃·18H₂O and Na₂CO₃ as raw materials. The coagulation performance of PACS for removing natural organic matter (NOM) from surface water was evaluated, and the effect of SO₄^2–/Al³⁺ mole ratio and γ value in coagulants PACS on DOC and UV₂₅₄ removal was determined. Furthermore, the influence of pH and dosage of the selected PACS with a SO₄^2–/Al³⁺ ratio of 0.0664 and a γ value of 2.0, which achieved the best coagulation performance for the removal of DOC and UV₂₅₄ of all PACS coagulants, on the removal of DOC and UV₂₅₄ and residual aluminum concentration in treated water was investigated. The results were compared with the ones of polyaluminum chloride (PAC) with γ value of 2.0. The experimental data show that the performance of PACS as a coagulant was highly dependent on SO₄^2–/Al³⁺ mole ratio and γ value. Both for the selected PACS and for PAC, the best DOC and UV₂₅₄ removal results were obtained in the range of pH from 5.0 to 8.2 and at the coagulation dose of 5.0 mg/L as Al. Under the optimum coagulation conditions, the selected PACS gave higher DOC and UV₂₅₄ removal efficiencies, and lower residual aluminum concentrations in the treated water than PAC. The maximum removal of DOC and UV₂₅₄ for PACS was approximately 88.0% and 93.0%, respectively. At the optimum coagulant dose and pH 6.5, the concentration of residual aluminum in treated water by both selected PACS and PAC can comply with the regulated limits. The major mechanisms of NOM removal by PACS and PAC coagulation involve complexation‐charge‐neutralization‐precipitation.     

Hydrochemical characteristics and salinization processes of groundwater in the shallow aquifer of Eastern Laizhou Bay,China

Groundwater salinization has become a crucial environmental problem worldwide and is considered the most widespread form of groundwater contamination in the coastal zone. In this study, a hydrochemical investigation was conducted in the eastern coastal shallow aquifer of Laizhou Bay to identify the hydrochemical characteristics and the salinity of groundwater using ionic ratios, deficit or excess of each ions, saturation indices and factor analysis. The results indicate that groundwater in the study area showed wide ranges and high standard deviations for most of hydrochemical parameters and can be classified into two hydrochemical facies, Ca²⁺‐Mg²⁺‐Cl^‐ facies and Na⁺‐Cl^‐ facies. The ionic ratio, deficit or excess of each ions and SI were applied to evaluate hydrochemical processes. The results obtained indicate that the salinization processes in the coastal zones were inverse cation exchange, dissolution of calcite and dolomite, and intensive agricultural practices. Factor analysis shows that three factors were determined (Factor 1: TDS, EC, Cl^‐, Mg²⁺, Na⁺, K⁺, Ca²⁺ and SO₄^2‐; Factor 2: HCO₃^‐ and pH; Factor 3: NO₃^‐ and pH), representing the signature of seawater intrusion in the coastal zone, weathering of water–soil/rock interaction, and nitrate contamination, respectively. Copyright © 2011 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.     

Stable isotopic and geochemical identification of groundwater evolution and recharge sources in the arid Shule River Basin of Northwestern China

Stable isotopic (δD_VSMOW and δ¹⁸O_VSMOW) and geochemical signatures were employed to constrain the geochemical evolution and sources of groundwater recharge in the arid Shule River Basin, Northwestern China, where extensive groundwater extraction occurs for agricultural and domestic supply. Springs in the mountain front of the Qilian Mountains, the Yumen‐Tashi groundwater (YTG), and the Guazhou groundwater (GZG) were Ca‐HCO₃, Ca‐Mg‐HCO₃‐SO₄ and Na‐Mg‐SO₄‐Cl type waters, respectively. Total dissolved solids (TDS) and major ion (Mg²⁺, Na⁺, Ca²⁺, K⁺, SO₄^2?, Cl^? and NO₃^?) concentrations of groundwater gradually increase from the mountain front to the lower reaches of the Guazhou Basin. Geochemical evolution in groundwater was possibly due to a combination of mineral dissolution, mixing processes and evapotranspiration along groundwater flow paths. The isotopic and geochemical variations in melt water, springs, river water, YTG and GZG, together with the end‐member mixing analysis (EMMA) indicate that the springs in the mountain front mainly originate from precipitation, the infiltration of melt water and river in the upper reaches; the lateral groundwater from the mountain front and river water in the middle reaches are probably effective recharge sources for the YTG, while contribution of precipitation to YTG is extremely limited; the GZG is mainly recharged by lateral groundwater flow from the Yumen‐Tashi Basin and irrigation return flow. The general characteristics of groundwater in the Shule River Basin have been initially identified, and the results should facilitate integrated management of groundwater and surface water resources in the study area. Copyright © 2015 John Wiley & Sons, Ltd.