Groundwater recharge in a sedimentary basin in semi-arid Mexico

Recharge mechanisms and the hydrochemical evolution of groundwater in a semi-arid, 6,840-km², intermountain basin in central Mexico were investigated using stable isotopes and major chemical constituents. Ionic ratio analysis helped to conceptualize and quantify in part the subsequent geochemical evolution in the aquifer system. Mass balance models (PHREEQC) were used to interpret and rectify the geochemical properties of the aquifer. The recharge conditions have not changed noticeably during the last several thousands of years. The recharge mechanisms are accompanied by leaching of meteoric salts on and near the ground surface during major rain events, which previously accumulated after minor rain events. Rapid and diffuse infiltration can be excluded. Indirect infiltration from wadis (arroyos) and depressions (playas) with little mixing in shallow groundwater contrasts with a high degree of mixing for water with deep circulation. The prevailing source of major cations (Ca²⁺, Mg²⁺, Na⁺, K⁺) is weathering of carbonates and albite, followed by exchange reactions on clays and hydroxides. Ca²⁺/Na⁺ exchange may interchange along the flow path with reverse (Na⁺/Ca²⁺) exchange, although the Ca²⁺/Na⁺ option is prevalent. Meteoric Ca and Mg inputs are relatively small; however, meteoric Na is insignificant. Irrigation return flow plays an important role in the western part of the study area, giving rise to elevated sulfate and chloride concentrations.

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Resumen Se han investigado los mecanismos de recarga y la evolución hidroquímica de las aguas subterráneas en una cuenca semiárida e intermontanosa de México central, de 6.840 km². Para ello, se han utilizado isótopos estables y los constituyentes químicos mayores. El análisis de las relaciones iónicas ha servido para conceptuar y cuantificar en parte su evolución geoquímica posterior dentro del sistema acuífero. Se ha recurrido a modelos de balance de masas (PHREEQC) para interpretar y rectificar las propiedades geoquímicas del acuífero. Las condiciones de recarga no han cambiado de forma apreciable durante los últimos miles de años. Los mecanismos de recarga se ven acompañados por el lixiviado de las sales meteóricas sobre y cerca de la superficie del terreno durante los episodios principales de lluvia, las cuales son acumuladas en episodios menores de lluvia. Se puede excluir la infiltración rápida y difusa. La infiltración indirecta desde arroyos ( wadis) y depresiones ( playas), que apenas se mezcla con las aguas subterráneas someras, contrasta con un elevado nivel de mezcla con el agua de circulación profunda. La fuente dominante de cationes mayores (calcio, magnesio, sodio, potasio) es la meteorización de los carbonatos y albita, mientras que las reacciones de intercambio en las arcillas e hidróxidos son menos importantes. El intercambio ión calcio-ión sodio puede ser reemplazado a lo largo de una línea de flujo por el intercambio opuesto (ión sodio-ión calcio), aunque la primera es prioritaria. Las aportaciones meteóricas de calcio y magnesio son relativamente pequeñas, mientras que la de sodio es insignificante. Los retornos de riego desempeñan un papel importante en la parte occidental del área de estudio, dando lugar a concentraciones elevadas de sulfato y cloruro.

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Résumé Les mécanismes de recharge et lévolution hydrochimique de leau souterraine dans un bassin de montagne de 6 840 km² en zone semi-aride, dans le centre du Mexique, ont été étudiés au moyen des isotopes stables et des composés chimiques majeurs. Lanalyse des rapports ioniques a aidé à conceptualiser et à quantifier en partie lévolution géochimique qui en résulte, dans le système aquifère. Des modèles de bilan de masse (PHREEQC) ont été utilisés pour interpréter et corriger les propriétés de laquifère. Les conditions de recharge nont pas changé notablement au cours des derniers millénaires. Les mécanismes de recharge sont accompagnés, durant les épisodes majeurs de précipitation, dun lessivage, à la surface du sol et à son voisinage, de sels météoriques accumulés auparavant pendant les petits épisodes de pluie. Linfiltration rapide et diffuse peut être exclue. Linfiltration indirecte à partir des oueds (arroyos) et des dépressions (playas) avec un faible mélange dans la nappe superficielle contraste avec le degré élevé de mélange de leau avec les circulations profondes. La source prépondérante des cations majeurs (Ca²⁺, Mg²⁺, Na⁺, K⁺) est laltération des carbonates et des feldspaths ; léchange de cations avec les argiles et les hydroxydes est moins important. Léchange de Ca²⁺ avec Na⁺ peut sinverser le long des axes découlements pour donner un échange de Na⁺ avec Ca²⁺, bien que le cas Ca²⁺/Na⁺ soit prépondérant. Les apports météoriques de Ca et de Mg sont relativement faibles, cependant que celui de Na météorique est insignifiant. Lécoulement par retour dirrigation joue un rôle important dans la partie occidentale de la région étudiée, produisant un accroissement des concentrations élevées en sulfate et en chlorure.

     

地下水中铀的反应运移模拟

地下水中铀的反应运移模拟对地下水保护和铀矿区的恢复都很重要, 因为铀是一种化学毒害性很高的放射性元素.在地下水及水与固体之间都应考虑对流、弥散、稀释、吸附等化学相互作用.介绍了德国德累斯顿市附近的Koenigstein矿区淋滤条件的可行性研究结果.由于反应运移模拟需占用大量的CPU时间, 所有的运行在一天内完成, 但用简单的混合法进行了稀释.对于这种研究, PHREEQC 2.2证明是一个功能很强的工具.与PHREEQC相对应的数据库WATEQ4F涉及到48种元素、400多种物质、300多种矿物.根据铀和镭的特性, 对其作了一定的修改, 以使它更具相容性和可靠性.      

Surface complexation modeling of Uranium(VI) sorption on quartz in the presence and absence of alkaline earth metals

Surface complexation models (SCMs) are widely utilized as a tool to study the mobility of radionuclide to the environment. In this study, two SCMs, electrostatic (ES) and non-electrostatic (NES) models are employed in order to simulate the sorption behavior of U(VI) on quartz in the absence of Mg, Ca, and Sr and ES model in the presence of alkaline earth metals. The surface reaction constants (log K) for ES and NES models were fitted to experimental data by coupling PEST with PHREEQC. The SCM prediction of U(VI) sorption on quartz in the absence of alkaline earth metals is in good agreement with the experimental data in the pH range 6.5–9. The estimated log K values are sensitive to both ES and NES model calculations. In U(VI)-Mg-quartz, U(VI)-Ca-quartz, and U(VI)-Sr-quartz systems, only the ES model shows the general trend of the experimental data. The estimated log K values are sensitive with respect to the surface reactions. Hence, the ES model is more suitable for model calculations of the U(VI)-Mg-quartz, U(VI)-Ca-quartz, and U(VI)-Sr-quartz systems.     

The cloud imaging and particle size experiment on the Aeronomy of Ice in the mesosphere mission: Instrument concept,design, calibration,and on-orbit performance

The Cloud Imaging and Particle Size Experiment (CIPS) is one of three instruments aboard the Aeronomy of Ice in the Mesosphere spacecraft. CIPS provides panoramic ultraviolet images of the atmosphere over a wide range of scattering angles in order to determine the presence of polar mesospheric clouds, measure their spatial morphology, and constrain the parameters of cloud particle size distribution. The AIM science objectives motivate the CIPS measurement approach and drive the instrument requirements and design, leading to a configuration of four wide-angle cameras arrayed in a ‘+’ arrangement that covers a 120° (along orbit track)×80° (across orbit track) field of view. CIPS began routine operations on May 24, 4 weeks after AIM was launched. It measures scattered radiances from PMCs near 83 km altitude to derive cloud morphology and particle size information by recording multiple exposures of individual clouds to derive PMC scattering phase functions and detect nadir horizontal spatial scales to approximately 3 km. This paper describes the instrument design, its prelaunch characterization and calibration, and flight operations. Flight observations and calibration activities confirm performance inferred during ground test, verifying that CIPS exceeds its measurement requirements and goals. These results are illustrated with example flight images that demonstrate the instrument measurement performance.     

Olivine intergranular plasticity at mantle pressures and temperatures

The ductile behavior of olivine-rich rocks is critical to constrain thermal convection in the Earth's upper mantle. Classical olivine flow laws for dislocation or diffusion creep fail to explain the fast post-seismic surface displacements observed by GPS, which requires a much weaker lithosphere than predicted by classical laws. Here we compare the plasticity of olivine aggregates deformed experimentally at mantle pressures and temperatures to that of single crystals and demonstrate that, depending on conditions of stress and temperature, strain accommodated through grain-to-grain interactions – here called intergranular strain – can be orders of magnitude larger than intracrystalline strain, which significantly weakens olivine strength. This result, extrapolated along mantle geotherms, suggests that intergranular plasticity could be dominant in most of the upper mantle. Consequently, the strength of olivine-rich aggregates in the upper mantle may be significantly lower than predicted by flow laws based on intracrystalline plasticity models.     

High-pressure yield strength of rocksalt structures using quartz Raman piezometry

The Raman frequencies of quartz are used to evaluate deviatoric stresses in rocksalt-structure media in diamond-anvil cell experiments to pressures up to 20 GPa. The piezospectroscopic effect in quartz is modeled by first-principles calculations. Non-hydrostatic stresses measured in halogen salts give yield strength estimates of 3 GPa in the B1 structure (NaCl), and 4.5 GPa for the B2 structure (KCl and KBr). Raman measurements in MgO show that the yield strength is reached at around 6 ± 1 GPa. Measurements on quartz alone indicate similar yield strength. The estimated yield strength in MgO is thus likely a lower bound, in consistency with former radial X-ray diffraction measurements that gave a yield strength of 8 ± 1 GPa, and lower-pressure large-volume press experiments indicating a yield strength of 6 GPa at 5 GPa. Former values of the yield strength below 2 GPa determined by pressure gradient measurements were underestimated due to unverified assumptions in boundary conditions. The yield strength increases with increasing coordination of ionic solids, likely contributing to increase viscosity at phase transitions near the upper–lower mantle boundary.     

Estimation of groundwater recharge using a GIS-based distributed water balance model in Dire Dawa, Ethiopia

Sustainable groundwater management requires knowledge of recharge. Recharge is also an important parameter in groundwater flow and transport models. Spatial variation in recharge due to distributed land-us.e, soil texture, topography, groundwater level, and hydrometeorological conditions should be accounted for in recharge estimation. However, conventional point-estimates of recharge are not easily extrapolated or regionalized. In this study, a spatially distributed water balance model WetSpass was used to simulate long-term average recharge using land-use, soil texture, topography, and hydrometeorological parameters in Dire Dawa, a semiarid region of Ethiopia. WetSpass is a physically based methodology for estimation of the long-term average spatial distribution of surface runoff, actual evapotranspiration, and groundwater recharge. The long-term temporal and spatial average annual rainfall of 626 mm was distributed as: surface runoff of 126 mm (20%), evapotranspiration of 468 mm (75%), and recharge of 28 mm (5%). This recharge corresponds to 817 l/s for the 920.12 km² study area, which is less than the often-assumed 1,000 l/s recharge for the Dire Dawa groundwater catchment.     

Application of Landsat 5 and Landsat 7 images data for water quality mapping in Mosul Dam Lake,Northern Iraq

Mosul Dam Lake is the main reservoir in Iraq, supporting the water demand of Mosul, Baghdad, and other cities. The aim of this study is to derive simple and accurate algorithms for the retrieval of water quality parameters for Mosul Dam Lake from Landsat 5 and Landsat 7 reflectance data. The water quality measurements were performed in situ during March and July 2011. These measurements included temperature, turbidity, Secchi disk, chlorophyll-a, nitrate, nitrite, phosphate, total inorganic carbon, dissolved organic carbon, total dissolved solids, and pH. In order to properly use the values of reflectance bands, images enhancement techniques have been used. The field measurements were compared with reflectance values of Landsat 5 and Landsat 7 bands using different band combination of empirical algorithms. Generally, the results of analysis showed significant correlation between these models and water quality parameters with R ²?>?0.7 and p?R ²?>?0.9 and p?R ²?>?0.9, and values of the root mean square error ranged from 0.9 to 0.001. ArcGIS 10 was used to simulate the distribution values of water quality parameters calculated from spectral values of TM5 and ETM+ bands. The results of spatial analysis demonstrate that it is possible to use the TM5 and ETM+ images to evaluate the water quality for Mosul Dam Lake.     

Effect of Microbial Siderophore DFOB on Pb, Zn, and Cd Sorption Onto Zeolite

Recent studies suggest that siderophores form stable complexes with divalent metals and affect their mobility. In this work, effects of trihydroxamate microbial siderophores and desferrioxamine-B (DFOB) on Pb(II), Zn(II), and Cd(II) sorption by two kinds of synthesized zeolites (13X and Na?CY) as a function of pH were investigated. Results showed that 13X zeolite has a higher sorption affinity for studied metals than Na?CY. DFOB strongly affected metal sorption on both zeolites. Under slightly acidic to neutral condition, DFOB increased the metal sorption on zeolites due to the sorption of positively charged heavy metal?CDFOB complexes. Whereas by increasing pH (>7), the mobilizing effect of DFOB was observed for Pb, Zn, and Cd. DFOB drastically decreased (80?%) Zn sorption in alkaline condition. As a result, siderophores can weaken the treatment efficiency of zeolites and increase the bioavailability of metals in soils. Surface complexation modeling revealed that the effects of DFOB on metal sorption by 13X and Na?CY zeolites can be explained by the differences in their surface charge. In general, the result shows the influence of DFOB on metal sorption by zeolites over the pH range 4?C9 and decreasing in the sequence Zn?>?Pb?>?Cd.     

Structural and mineralogical study of active and inactive hydrothermal fluid discharges in Panarea,Italy

The isle of Panarea (Aeolian Arc, Italy) is an active hydrothermal system, characterized by different types of fluid emissions, which cause various types of unique hydrothermal structures that are typical for hydrothermal fluid discharges. Such fluid discharge structures at shallow depths of less than 30 m have not been described in marine hydrothermal systems until now to the authors’ knowledge. The focus of the investigations was set on morphological, mineralogical, geochemical, and structural analyses. A broad variety of analytical methods was applied to gain as much information as possible. In addition to geological and sedimentological documentation and standard methods like making and analyzing thin and polished sections, optical microscopy or X-ray fluorescence analysis, the samples were investigated by X-ray computer tomography and scanning electron microscopy, including energy-dispersive X-ray spectroscopy. Because discharge features occur in various settings, a general classification of the features in the hydrothermal system was performed with special focus on their preservability in geological archives. In total, nine different facies types were distinguished based on genetic and/or morphological differences. All samples show laminated structures from µm to cm scale. The single laminae vary in shape and material witnessing various chemical compositions.