Photocatalytic Degradation of 17α‐Ethinylestradiol and Inactivation of Escherichia coli Using Ag‐Modified TiO2 Nanotube Arrays

Ag‐modified TiO₂ nanotube arrays (Ag/TiO₂ NAs) were prepared and employed as a photocatalyst for degradation of 17α‐ethinylestradiol (EE2) and inactivation of Escherichia coli. The as‐synthesized Ag/TiO₂ NAs were characterized by field‐emission scanning electron microscope (FESEM), X‐ray diffraction (XRD), and X‐ray photoelectron spectroscopy (XPS). It was found that metallic Ag nanoparticles were firmly deposited on the TiO₂ NAs with the pore diameter of 100 nm and the length of 550 nm. Photocatalytic degradation of EE2 and inactivation of E. coli were enhanced effectively in an analogical trend using Ag/TiO₂ NAs. In particular, Ag/TiO₂ NAs exhibited the antimicrobial activity even in the absence of light. The Ag acted as a disinfection agent as well as the dopant of the modified TiO₂ NAs photocatalysis by forming a Schottky barrier on the surface of TiO₂ NAs. Inorganic ions suppressed the rates of photocatalytic degradation of EE2, with HCO having a more pronounced effect than NO or SO. Humic acid (HA) was found to increase the rate of EE2 degradation.     

Geochemical characteristics and Sr‐Nd‐Hf isotope compositions of Late Triassic post‐collisional A‐type granites in Sarudik,SW Sumatra,Indonesia

Late Triassic A‐type granites are identified in this study in Sarudik, SW Sumatra. We present new data on zircon U–Pb geochronology, whole‐rock major and trace elements and Sr‐Nd‐Hf isotope geochemistry, aiming to study their petrogenesis and tectonic implications. LA‐ICP‐MS U–Pb dating of zircon separated from one biotite monzogranite sample yields a concordia age of 222.6 ±1.0 Ma, indicating a Late Triassic magmatic event. The studied granites are classified as weakly peralumious, high‐K calc‐alkaline granites. They exhibit high SiO₂, K₂O + Na₂O, FeO/(FeO + MgO) and Ga/Al ratios and low Al₂O₃, CaO, MgO, P₂O₅ and TiO₂ contents, with enrichment of Rb, Th and U and depletion of Ba, Sr, P and Eu, showing the features of A‐type granites. The granites have zircon ε_Hf(t) values from ?4.6 to ?0.4 and whole‐rock ε_Nd(t) values from ?5.51 to ?4.98, with Mesoproterozoic T_DM2 ages (1278–1544 Ma) for both Hf and Nd isotopes. Geochemical and isotopic data suggest that the source of these A‐type granites is the Mesoproterozoic continental crust, without significant incorporation of mantle‐derived component, and their formation is controlled by subsequent fractional crystallization. The Sarudik A‐type granites are further assigned to A2‐type formed in post‐collisional environment. Combined with previous knowledge on the western SE Asia tectonic evolution, we conclude that the formation of the Late Triassic A‐type granites is related to the post‐collisional extension induced by the crustal thickening, gravitational collapse, and asthenosphere upwelling following the collision between the Sibumasu and the East Malaya Block.     

Electro‐Catalytic Degradation of Phenol Organics with SnO2‐Sb2O3/Ti Electrodes

The effect of extraordinary degradation of phenol organics on the SnO₂‐Sb₂O₃/Ti electrode is investigated through experimental research and theoretical analysis. The phenol organics contained 4‐chloro‐phenol, 4‐bromo‐phenol, and 2‐iodo‐phenol. At a current density of 4 mA cm^–2 and an electrolysis time of 12 h, the degradation efficiency of the phenols was over 98% with a relatively short degradation time, whereas the degradation time of the PbO₂/Ti electrode surpassed 40 h while delivering 100% disposal efficiency. Therefore, the effectiveness of electrochemical (EC) oxidation by the SnO₂‐Sb₂O₃/Ti was superior to that of the PbO₂/Ti electrode. At the same time, the SnO₂‐Sb₂O₃/Ti had higher oxygen generation potential and lower electron consumption than the other electrodes. This was mainly due to the effect of the middle Sb₂O₃ layer, which due to its high porosity and good catalytic effect, contributed to a better catalysis than the SnO₂ part.     

Preparation of Nano‐Lepidocrocite and an Investigation of Its Ability to Remove a Metal Complex Dye

Lepidocrocite (γ‐FeOOH) nanoparticles were synthesized from iron(II) sulfate solution and characterized using X‐ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform‐IR (FT‐IR), nitrogen adsorption, and point of zero charge pH (pH_PZC) analyses. TEM, XRD, and FT‐IR analyses proved the synthesis of nano‐lepidocrocite. Surface area and pH_PZC of the synthesized lepidocrocite were 68.1 m² g^?1 and 4.8, respectively. Utilization of the synthesized lepidocrocite in the adsorption of Lanacron brown S‐GL (LBS‐GL) from aqueous solutions was investigated, and the effect of lepidocrocite dosage, pH, temperature, and contact time on this process were optimized and modeled using response surface methodology approach. The lepidocrocite dosage of 0.015 g, pH 3.5, temperature of 38°C, and contact time of 100 min were determined as optimum adsorption conditions. Isotherm and kinetics of the adsorption process were analyzed at the optimum conditions. The equilibrium data were fitted well to the Langmuir isotherm model. The maximum monolayer adsorption capacity was 528.21 mg g^?1. The adsorption process was described by the pseudo‐second‐order kinetic model. Furthermore, the effect of pH on the desorption of LBS‐GL was investigated. High LBS‐GL desorption efficiency was achieved at a high pH value.     

Geochemistry and petrology of garnet‐bearing S‐type Shir‐Kuh Granite,southwest Yazd,Central Iran

The Jurassic Shir‐Kuh granitoid batholith in Central Iran intrudes Lower Jurassic sandstones and shales. The batholith consists of three main facies: (i) a granodioritic facies to the north; (ii) a monzogranitic facies spread throughout the batholith; and (iii) a leucogranitic facies along the northwestern margin. The granodiorites are composed mainly of plagioclase, quartz, K‐feldspar, biotite, and some muscovite, garnet, cordierite, ilmenite, zircon, apatite, and monazite. This facies contains variable amounts of restite minerals which are mainly defined by calcic plagioclase cores and small aggregates of biotite. The monzogranites, with mineral assemblages similar to those in the granodiorites, range from relatively mafic (cordierite‐bearing) to felsic (muscovite‐rich) rocks. The leucogranites, exposed as small stock and dykes, consist mainly of quartz, K‐feldspar, and sodic plagioclase. The batholith is peraluminous, calc‐alkaline, and typical of S‐type, as indicated by Na₂O content (2.74%), molecular Al₂O₃/(CaO + Na₂O + K₂O) (A/CNK) ratio (1.17), K₂O/Na₂O ratio (1.39), and isotopic data ([⁸⁷Sr/⁸⁶Sr]_i = 0.715). The rocks are characterized by enrichment in large ion lithophile elements such as Rb, Th and K and depletion in high field strength elements such as Nb and Ti. Chondrite‐normalized rare earth element (REE) patterns are characterized by light rare earth element (LREE) enrichment, with values of (La/Yb)_N between 4.5 and 19.53, unfractionated heavy rare earth element (HREE) with values of (Gd/Yb)_N between 0.98 and 2.88, and a distinct negative Eu. The parental magma of the Shir‐Kuh Granite was derived from a plagioclase‐rich metasedimentary source (local anatexis of metagreywacke) in the crust, with heat input from mantle melt components. The separation of restite crystals from the primary melt followed by the fractional crystallization appears to have been an effective differentiation process in the batholith.     

Time‐lapse seismic modelling of CO2 fluid substitution in the Devonian Redwater Reef,Alberta, Canada

Common shot ray tracing and finite difference seismic modelling experiments were undertaken to evaluate variations in the seismic response of the Devonian Redwater reef in the Alberta Basin, Canada after replacement of native pore waters in the upper rim of the reef with CO₂. This part of the reef is being evaluated for a CO₂ storage project. The input geological model was based on well data and the interpretation of depth‐converted, reprocessed 2D seismic data in the area. Pre‐stack depth migration of the ray traced and finite difference synthetic data demonstrate similar seismic attributes for the Mannville, Nisku, Ireton, Cooking Lake, and Beaverhill Lake formations and clear terminations of the Upper Leduc and Middle Leduc events at the reef margin. Higher amplitudes at the base of Upper‐Leduc member are evident near the reef margin due to the higher porosity of the foreslope facies in the reef rim compared to the tidal flat lagoonal facies within the central region of the reef. Time‐lapse seismic analysis exhibits an amplitude difference of about 14% for Leduc reflections before and after CO₂ saturation and a travel‐time delay through the reservoir of 1.6 ms. Both the ray tracing and finite difference approaches yielded similar results but, for this particular model, the latter provided more precise imaging of the reef margin. From the numerical study we conclude that time‐lapse surface seismic surveys should be effective in monitoring the location of the CO₂ plume in the Upper Leduc Formation of the Redwater reef, although the differences in the results between the two modelling approaches are of similar order to the effects of the CO₂ fluid replacement itself.     

Oligocene crustal xenolith‐bearing alkaline basalt from Jandaq area (Central Iran): implications for magma genesis and crustal nature

The Oligocene alkaline basalts of Toveireh area (southwest of Jandaq, Central Iran) exhibit northwest–southeast to west–east exposure in northwest of the central‐east Iranian microcontinent (CEIM). These basalts are composed of olivine (Fo_70–90), clinopyroxene (diopside, augite), plagioclase (labradorite), spinel, and titanomagnetite as primary minerals and serpentine and zeolite as secondary ones. They are enriched in alkalis, TiO₂ and light rare earth elements (La/Yb = 9.64–12.68) and are characterized by enrichment in large ion lithophile elements (Cs, Rb, Ba) and high field strength elements (Nb, Ta). The geochemical features of the rocks suggest that the Toveireh alkaline basalts are derived from a moderate degree partial melting (10–20%) of a previously enriched garnet lherzolite of asthenospheric mantle. Subduction of the CEIM confining oceanic crust from the Triassic to Eocene is the reason of mantle enrichment. The studied basalts contain mafic‐ultramafic and aluminous granulitic xenoliths. The rock‐forming minerals of the mafic‐ultramafic xenoliths are Cr‐free/poor spinel, olivine, Al‐rich pyroxene, and feldspar. The aluminous granulitic xenoliths consist of an assemblage of hercynitic spinel + plagioclase (andesine–labradorite) ± corundum ± sillimanite. They show interstitial texture, which is consistent with granulite facies. They are enriched in high field strength elements (Ti, Nb and Ta), light rare earth elements (La/Yb = 37–193) and exhibit a positive Eu anomaly. These granulitic xenoliths may be Al‐saturated but Si‐undersaturated feldspar bearing restitic materials of the lower crust. The Oligocene Toveireh basaltic magma passed and entrained these xenoliths from the lower crust to the surface.     

Depth‐dependent hydraulic conductivity distribution patterns of a streambed

Characterization of streambed hydraulic conductivity from the channel surface to a great depth below the channel surface can provide needed information for the determination of stream‐aquifer hydrologic connectedness, and it is also important to river restoration. However, knowledge on the streambed hydraulic conductivity for sediments 1 m below the channel surface is scarce. This study describes a method that was used to determine the distribution patterns of streambed hydraulic conductivity for sediments from channel surface to a depth of 15 m below. The method includes Geoprobe's direct‐push techniques and Permeameter tests. Direct‐push techniques were used to generate the electrical conductivity (EC) logs and to collect sequences of continuous sediment cores from river channels, as well as from the alluvial aquifer connected to the river. Permeameter tests on these sediment cores give the profiles of vertical hydraulic conductivity (K_v) of the channel sediments and the aquifer materials. This method was applied to produce K_v profiles for a streambed and an alluvial aquifer in the Platte River Valley of Nebraska, USA. Comparison and statistical analysis of the K_v profiles from the river channel and from the proximate alluvial aquifer indicates a special pattern of K_v in the channel sediments. This depth‐dependent pattern of K_v distribution for the channel sediments is considered to be produced by hyporheic processes. This K_v‐distribution pattern implied that the effect of hyporheic processes on streambed hydraulic conductivity can reach the sediments about 9 m below the channel surface. Copyright © 2010 John Wiley & Sons, Ltd.     

Sulfur and Carbon Co‐doped TiO2 Composite Fabricated by Lignosulphonate and Its Suitability for Removal of Cadmium

Highly toxic divalent cadmium causes serious environmental issues. To quickly monitor and/or efficiently remove this potentially toxic metal ion as well as to explore its interfacial chemistry with metal oxides, a sulfur and carbon co‐doped titania (S/C‐TiO₂) composite is synthesized via a facile sol‐gel method with the assistance of sodium lignosulphonate (SLS). The prepared composite displays a well‐crystallized TiO₂ nanostructure comprising the anatase phase. Both S and C, which are derived from the SLS template, are found to enter the TiO₂ lattice. The S/C‐TiO₂ composite exhibits a porous structure with a wide pore size distribution. The newly synthesized composite shows adsorption capability for the potentially toxic metal Cd(II). The adsorption process requires <5 min to reach equilibrium. The measured equilibrium adsorption capacity is 19.42 mg g^?1, which is twice as high as that of bare TiO₂. The removal efficiency is as high as 97%. Moreover, the materials are suitable for contaminated solutions over a wide range of pH values and various initial cadmium concentrations. A mechanism for the enhanced adsorption behavior is also proposed.     

Degradation of Rhodamine B and Safranin‐T by MoO3:CeO2 Nanofibers and Air Using a Continuous Mode

One‐dimensional MoO₃ nanofibers doped with Ce (MoO₃ : CeO₂) are synthesized by a method combining a sol‐gel process and an electrospinning technique. The resulting MoO₃ : CeO₂ is characterized by X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT‐IR) spectroscopy, and scanning electron microscopy (SEM). The catalytic degradation of rhodamine B and safranin‐T with MoO₃ : CeO₂ nanofiber catalyst is investigated in a continuous flowing mode using air (O₂) as an oxidant. The results show that rhodamine B and safranin‐T are degraded effectively and the removal efficiencies are 98.3%, and 98.5%, respectively. In addition, the organic dyes are totally mineralized to simple inorganic species such as CO₃^–, Cl^– and NO₃^–.     

Development of Easy and Reproducible Immobilization Techniques Using TiO2 for Photocatalytic Degradation of Aquatic Pollutants

Two main routes of methods for the preparation of photocatalytic active titanium dioxide films on glass substrates were investigated: (1) the use of titanium dioxide powder and (2) the in situ generation of the catalyst via hydrolysis of titanium tetraisopropoxide (TTIP) or TiCl₄. The activities of the catalyst films were evaluated by measuring the degradation of dichloroacetic acid (DCA), clofibric acid, and terbuthylazine used as model organic compounds. The concentration decrease of DCA and the concentration increase of chloride ions as the decomposition product allowed to distinguish between photocatalytic degradation of DCA and adsorption onto the TiO₂ films. Furthermore, TiO₂ films of the commercially available materials P25 (Degussa) and Hombikat UV100 (Sachtleben Chemie) were used to investigate whether there was a difference in the degradation pathways of terbuthylazine as a model compound. For the experiments mini flow‐through reactors were constructed. The investigated immobilization techniques were easy to handle without need of any expensive equipment. All TiO₂ coatings showed good photocatalytic activities and mechanical stabilities with efficient long‐term stabilities. The best immobilization reproducibility was achieved by the spray coating technique and by the in situ method with the dipping sol‐gel process starting by TTIP. During the continuous use of the TiO₂ films no TiO₂ particles were found in the irradiated solutions.     

Mechanics of interrill erosion with wind‐driven rain

The vector physics of wind‐driven rain (WDR) differs from that of wind‐free rain, and the interrill soil detachment equations in the Water Erosion Prediction Project (WEPP) model were not originally developed to deal with this phenomenon. This article provides an evaluation of the performance of the interrill component of the WEPP model for WDR events. The interrill delivery rates were measured in the wind tunnel facility of the International Center for Eremology (ICE), Ghent University, Belgium with an experimental setup to study different raindrop impact velocity vectors. Synchronized wind and rain simulations with wind velocities of 6, 10 and 14 m s^–1 were applied to a test surface placed on windward and leeward slopes of 7, 15 and 20%. Since both rainfall intensity and raindrop impact velocity varied greatly depending on differences in the horizontal wind velocity under WDRs, the resultant kinetic energy flux (KE_r, in J m^–2 s^–1) was initially used in place of the WEPP model intensity term in order to incorporate the effect of wind on impact velocity and frequency of raindrops. However, our results showed only minor improvement in the model predictions. For all research data, the model Coefficients of Determination (r²) were 0·63 and 0·71, when using the WEPP and the KE_r approaches, respectively. Alternately, integrating the angle of rain incidence into the model by vectorally partitioning normal kinetic energy flux (KE_rn, in J m^–2 s^–1) from the KE_r greatly improved the model's ability to estimate the interrill sediment delivery rates (r² = 0·91). This finding suggested that along with the fall trajectory of wind‐driven raindrops with a given frequency, raindrop velocity and direction at the point of impact onto the soil surface provided sufficient physical information to improve WEPP sediment delivery rate predictions under WDR. Copyright © 2012 John Wiley & Sons, Ltd.     

Nested‐Scale Nutrient Flux in a Mixed‐Land‐Use Urbanizing Watershed

To improve quantitative understanding of mixed‐land‐use impacts on nutrient yields, a nested‐scale experimental watershed study design (n = 5) was applied in a 303(d), clean water act impaired urbanizing watershed of the lower Missouri River Basin, USA. From 2010 to 2013, water samples (n = 858 sample days per site) were analysed for total inorganic nitrogen (TIN‐N), nitrite (NO₂–N) nitrate (NO₃–N), ammonia (NH₃–N), and total phosphorus (TP‐P). Annual, seasonal, and monthly flow‐weighted concentrations (FWCs) and nutrient yields were estimated. Mean nutrient concentrations were highest where agricultural land use comprised 58% of the drainage area (NH₃ = 0.111 mg/l; NO₂ = 0.045 mg/l; NO₃ = 0.684 mg/l, TIN = 0.840 mg/l; TP = 0.127 mg/l). Average TP‐P increased by 15% with 20% increased urban land use area. Highly variable annual precipitation was observed during the study with highest nutrient yields during 2010 (record setting wet year) and lowest nutrient yields during 2012 (extreme drought year). Annual TIN‐N and TP‐P yields exceeded 10.3 and 2.04 kg ha^?1 yr^?1 from the agricultural dominated headwaters. Mean annual NH₃–N, NO₂–N, NO₃–N, TIN‐N, and TP‐P yields were 0.742, 0.400, 4.24, 5.38, and 0.979 kg ha^?1 yr^?1, respectively near the watershed outlet. Precipitation accounted for the majority of the explained variance in nutrient yields (R² values from 0.68 to 0.85). Nutrient yields were also dependent on annual precipitation of the preceding year (R² values from 0.87 to 0.91) thus enforcing the great complexity of variable mixed‐land‐use mediated source‐sink nutrient yield relationships. Study results better inform land managers and best management practices designed to mitigate nutrient pollution issues in mixed‐land‐use freshwater ecosystems. Copyright © 2015 John Wiley & Sons, Ltd.     

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.     

Solar Photocatalytic Decolorization and Detoxification of Industrial Batik Dye Wastewater Using P(3HB)‐TiO2 Nanocomposite Films

Solar photocatalytic decolorization and detoxification of batik dye wastewater using titanium dioxide (TiO₂) immobilized on poly‐3‐hydroxybutyrate (P(3HB)) film was studied. The effects of initial dye concentration, catalyst concentration, P(3HB) film thickness, and fabrication methods of the nanocomposite films were evaluated against methylene blue, a standard organic dye. It was observed that 0.4 g of P(3HB)‐40 wt% TiO₂ removed 96% of the color under solar irradiation. P(3HB) and TiO₂, mixed concurrently in chloroform followed by stirring for 24 h showed a more even distribution of the photocatalyst on the polymer surface and yielded almost 100% color removal. The photocatalytic films were able to completely decolorize real industrial batik dye wastewater in 3 h and induced a chemical oxygen demand (COD) reduction of 80%. Reusability of the 0.4 g P(3HB)‐40 wt% TiO₂ film in decolorizing the batik dye wastewater was also possible as it gave a high consistent value of decolorization percentage (>80%) even after the sixth repeated usage. Recovery step of the photocatalysts was also not required in this simple treatment system. The decolorized batik dye wastewater had less/no toxic effects on mosquito larvae, Aedes aegypti, and microalgae, Scenedesmus quadricauda indicating simultaneous detoxification process along with the decolorization process.     

Titanium solubility in coexisting garnet and clinopyroxene at very high pressure: the significance of exsolved rutile in garnet

Exsolution microstructures including ilmenite±garnet in clinopyroxene and rutile in garnet are common in clinopyroxenite and eclogite from the Sulu ultrahigh-pressure (UHP) terrane. In order to understand the phase relations and Ti solubility in both garnet and clinopyroxene in a natural TiO₂-bearing system, several experiments at 5-15 GPa, 1000-1400°C were carried out using the multianvil high-pressure apparatus. The Hujianlin ilmenite-rich garnet clinopyroxenite showing exsolution microstructure was selected as starting material, because it closely approaches a composition lying in the TiO₂-CaO-MgO-FeO-Al₂O₃-SiO₂ system. Except for minor melt in one experiment at 1400°C and 5 GPa, other run products contain majoritic garnet+clinopyroxene±ilmenite (or rutile) and exhibit neoblastic texture. With increasing pressure, Ti and Ca, Mg and Si contents of neoblastic garnet increase with decreasing Al. The principal coupled substitutions are Ca²⁺Ti⁴⁺→2Al³⁺ and Si⁴⁺Mg²⁺→2Al³⁺ responding to majorite component increase. Titanium solubility (0.8-4.5 wt% as TiO₂) in garnet and Grt_Ti/Cpx_Ti ratio have a pronounced positive correlation with pressure between 5 and 15 GPa. On the other hand, the coexisting clinopyroxene contains low Ti (0.17-0.53 wt% as TiO₂), and shows no significant pressure effect. Rutile exsolution in garnet is coupled to that of pyroxene exsolution; both are exsolved from majoritic garnet on decompression. Therefore, the amount of such exsolved lamellae is a potential indicator of high-pressure metamorphism in exhumed rocks, whereas the TiO₂ content of clinopyroxene coexisting with garnet is not sensitive to pressure change.     

Spatio‐temporal evaluation of the groundwater quality in Kafr Al‐Zayat District,Egypt

Eighteen groundwater well sites located in Kafr Al‐Zayat (Egypt) were sampled monthly from January 2009 to November 2011 for microbial content, Mn⁺², Fe⁺², total dissolved solids (TDS), total hardness, NO₃^?, and turbidity. The data were analyzed combining the integrated use of factor and cluster analyses as well as the geostatistical semi‐variogram modeling. The prime objectives were to assess the groundwater suitability for drinking, to document the factors governing the spatio‐tempral variability, and to recognize distinctive groundwater quality patterns to help enable effective sustainability and proactive management of the limited resource. The groundwater microbial, Mn⁺², Fe⁺², TDS, and total hardness contents violated the drinking water local standards while the turbidity and the nitrate content complied with them. Factor analysis indicated that the microbial content is the most influential factor raising the variability potential followed, in decreasing order, by Mn²⁺, Fe²⁺, TDS, NO₃^?, turbidity, and finally the total hardness. Turbidity resulting from urban and agricultural runoff was strongly associated with most of the quality parameters. Quality parameters fluctuate sporadically without concrete pattern in space and time while their variability scores peak in November every year. Three spatially distinctive quality patterns were recognized that were consistent with and affected by the cumulative effects of the local topography, depth to water table, thickness of the silty clay (cap layer), surface water, and groundwater flow direction and hence the recharge from contaminated surface canals and agricultural drains. Copyright © 2013 John Wiley & Sons, Ltd.     

Origin and palaeo‐environments of calcareous sediments in the Moshaweng dry valley,southeast Botswana

Quaternary sedimentation in the Moshaweng dry valley of southeastern Botswana is evaluated on the basis of geomorphological evolution and sedimentological analyses. Stratigraphic evidence reveals an upper surface (1095 m) containing abundant sil‐calcrete, an intermediate surface (1085 m) in which sil‐calcrete underlies nodular calcrete and lower (1075 m) surface in which sil‐calcrete and nodular calcrete are interbedded. This subdivision is reflected in the geochemical composition of the sediments which show an overall trend of decreasing SiO₂ content (and increasing CaCO₃ content) with depth from the highest to the lowest surface levels. The calcretes and sil‐calcretes represent modifications of pre‐existing detrital Kalahari Group sand and basal Kalahari pebbles which thinned over a Karoo bedrock high. Modification took place during wet periods when abundant Ca⁺⁺‐rich groundwater flowed along the structurally aligned valley system. With the onset of drier conditions, water table fluctuations led to the precipitation of nodular calcretes in the phreatic layer to a depth of about 20 m. A major geochemical change resulted in the preferential silicification of the nodular calcrete deposits. Conditions for silica mobilization may be related to drying‐induced salinity and in situ geochemical differentiation brought about by pebble dissociation towards the top of the sediment pile. As calcretization and valley formation progressed to lower levels, silica release took place on a diminishing scale. Thermoluminescence dating infers a mid‐Pleistocene age for sil‐calcrete formation suggesting that valley evolution and original calcrete precipitation are much older. Late stage dissolution of CaCO₃ from pre‐existing surface calcretes or sil‐calcretes led to the formation of pedogenic case‐hardened deposits during a time of reduced flow through the Moshaweng system possibly during the upper or late Pleistocene. Copyright © 2002 John Wiley & Sons, Ltd.     

Evolution of lithospheric mantle in the north of Nain‐Baft oceanic crust (Neo‐Tethyan ophiolite of Ashin,Central Iran)

This study is focused on a plagioclase‐bearing spinel lherzolite from Chah Loqeh area in the Neo‐Tethyan Ashin ophiolite. It is exposed along the west of left‐lateral strike‐slip Dorouneh Fault in the northwest of Central‐East Iranian Microcontinent. Mineral chemistry (Mg#^olivine < ~ 90, Cr#^{clinopyroxene} < ~ 0.2, Cr#^spinel < ~ 0.5, Al₂O₃^{orthopyroxene} > ~ 2.5 wt%, Al₂O₃^{clinopyroxene} > ~ 4.5 wt%, Al₂O₃^spinel > ~ 41.5 wt%, Na₂O^{clinopyroxene} > ~ 0.11 wt%, and TiO₂^{clinopyroxene} > ~ 0.04 wt%) confirms Ashin lherzolite was originally a mid‐oceanic ridge peridotite with low degrees of partial melting at spinel‐peridotite facies in a lithospheric mantle level. However, some Ashin lherzolites record mantle upwelling and tectonic exhumation at plagioclase‐peridotite facies during oceanic extension and diapiric motion of mantle along Nain‐Baft suture zone. This mantle upwelling is evidenced by some modifications in the modal composition (i.e. subsolidus recrystallization of plagioclase and olivine between pyroxene and spinel) and mineral chemistry (e.g. increase in TiO₂ and Na₂O of clinopyroxene, and TiO₂ and Cr# of spinel and decrease in Mg# of olivine), as a consequence of decompression during a progressive upwelling of mantle. Previous geochronological and geochemical data and increasing the depth of subsolidus plagioclase formation at plagioclase‐peridotite facies from Nain ophiolite (~ 16 km) to Ashin ophiolite (~ 35 km) suggest a south to north closure for the Nain‐Baft oceanic crust in the northwest of Central‐East Iranian Microcontinent.     

Sedimentation in arctic proglacial lakes: Mittivakkat Glacier,south‐east Greenland

Several sediment cores were collected from two proglacial lakes in the vicinity of Mittivakkat Glacier, south‐east Greenland, in order to determine sedimentation rates, estimate sediment yields and identify the dominant sources of the lacustrine sediment. The presence of varves in the ice‐dammed Icefall Lake enabled sedimentation rates to be estimated using a combination of X‐ray photography and down‐core variations in ¹³⁷Cs activity. Sedimentation rates for individual cores ranged between 0·52 and 1·06 g cm⁻² year⁻¹, and the average sedimentation rate was estimated to be 0·79 g cm⁻² year⁻¹. Despite considerable down‐core variability in annual sedimentation rates, there is no significant trend over the period 1970 to 1994. After correcting for autochthonous organic matter content and trap efficiency, the mean fine‐grained minerogenic sediment yield from the 3·8 km² basin contributing to the lake was estimated to be 327 t km⁻² year⁻¹. Cores were also collected from the topset beds of two small deltas in Icefall Lake. The deposition of coarse‐grained sediment on the delta surface was estimated to total in excess of 15 cm over the last c. 40 years. In the larger Lake Kuutuaq, which is located about 5 km from the glacier front and for which the glacier represents a smaller proportion of the contributing catchment, sedimentation rates determined for six cores collected from the centre of the lake, based on their ¹³⁷Cs depth profiles, were estimated to range between 0·05 and 0·11 g cm⁻² year⁻¹, and the average was 0·08 g cm⁻² year⁻¹. The longer‐term (c. 100–150 years) average sedimentation rate for one of the cores, estimated from its unsupported ²¹⁰Pb profile, was 0·10–0·13 g cm⁻² year⁻¹, suggesting that sedimentation rates in this lake have been essentially constant over the last c. 100–150 years. The average fine‐grained sediment yield from the 32·4 km² catchment contributing to the lake was estimated to be 13 t km⁻² year⁻¹. The ¹³⁷Cs depth profiles for cores collected from the topset beds of the delta of Lake Kuutuaq indicate that in excess of 27 cm of coarse‐grained sediment had accumulated on the delta surface over the last approximately 40 years. Caesium‐137 concentrations associated with the most recently deposited (uppermost) fine‐grained sediment in both Icefall Lake and Lake Kuutuaq were similar to those measured in fine‐grained sediment collected from steep slopes in the immediate proglacial zone, suggesting that this material, rather than contemporary glacial debris, is the most likely source of the sediment deposited in the lakes. This finding is confirmed by the ¹³⁷Cs concentrations associated with suspended sediment collected from the Mittivakkat stream, which are very similar to those for proglacial material. Copyright © 2000 John Wiley & Sons, Ltd.