The mineralogy of the two uranium deposits (Victorino and San Marcos I) of Sierra San Marcos, located 30 km northwest of Chihuahua City, Mexico, was studied by optical microscopy, powder X-ray diffraction with Rietveld analysis, scanning electron microscopy with energy dispersive X-ray analysis, inductively coupled plasma spectrometry, and gamma spectrometry. At the San Marcos I deposit, uranophane Ca(UO2)2Si2O7·6(H2O) (the dominant mineral at both deposits) and metatyuyamunite Ca(UO2)(V2O8)·3(H2O) were observed. Uranophane, uraninite (UO2+x), masuyite Pb(UO2)3O3(OH)·3(H2O), and becquerelite Ca(UO2)6O4(OH)6 ·(8H2O) are present at the Victorino deposit. Field observations, coupled with analytical data, suggest the following sequence of mineralization: (1) deposition of uraninite, (2) alteration of uraninite to masuyite, (3) deposition of uranophane, (4) micro-fracturing, (5) calcite deposition in the micro-fractures, and (6) formation of becquerelite. The investigated deposits were formed by high-to low-temperature hydrothermal activity during post-orogenic evolution of Sierra San Marcos. The secondary mineralization occurred through a combination of hydrothermal and supergene alteration events. Becquerelite was formed in situ by reaction of uraninite with geothermal carbonated solutions, which led to almost complete dissolution of the precursor uraninite. The Victorino deposit represents the second known occurrence of becquerelite in Mexico, the other being the uranium deposits at Peña Blanca in Chihuahua State. 相似文献
Forest land affected by deforestation yields high soil and water losses.Suitable management practices need to be found that can reduce these losses and achieve ecological and hydrological sustainability of the deforested areas.Mulch has been found to be effective in reducing soil losses;straw mulch is easy to apply,contributes soil organic matter,and is efficient since the day of application.However,the complex effects of rice straw mulch with different application rates and lengths on surface runoff and soil loss have not been clarified in depth.The current paper evaluates the efficiency of rice straw mulch in reducing the hydrological response of a silty clay loam soil under high intensity and low frequency rainfall events(tap water with total depth of 49 mm and intensity of 98 mm/h)simulated in the laboratory.Surface runoff and soil loss at three lengths of the straw(10,30,and 200 mm)and three application rates(1,2,and 3 Mg/ha)were measured in 50 cm(width)×100 cm(length)×10 cm(depth)plots with disturbed soil samples(aggregate soil size<4 mm)collected in a deforested area.Bare soil was used as control experiment.Runoff volume and erosion were significantly(at p<0.05)lower in mulched soils compared to control plots.These reductions were ascribed to the water absorption capacity of the rice straw and the protection cover of the mulch layer.The minimum runoff was observed for a mulch layer of3 Mg/ha of straw with a length of 200 mm.The lowest soil losses were found with straw length of10 mm.The models developed predict runoff and erosion based on simple linear functions of mulch application rate and length,and can be used for a suitable hydrological management of soil.It is concluded that,thanks to rice straw mulch used as an organic soil conditioner,soil erosion and surface runoff are significantly(at p<0.05)reduced,and the mulch protection contributes to reduce the risk of soil degradation.Further research is,however,needed to analyze the upscaling of the hydrological effects of mulching from the plot to the hillslope scale. 相似文献
The calculation of volumes of fallout tephra layers is difficult because of the nonlinear dependence of thickness on area and because of the extrapolations required at the vent and in distal regions. Calculation using the trapezoidal rule, straight lines on log-log plots of area versus thickness, straight lines on plots of log thickness versus area1/2, and the crystal-concentration method are reviewed and the problems with each method discussed. The method using straight lines on plots of log thickness versus area1/2 is the most geologically reasonable because most deposits thin exponentially from source and therefore plot as straight lines using these coordinates. Errors and uncertainties in previous derivations for using this method are discussed and more general formulas presented. The method is also used to gain perspective on the missing distal volumes calculated by the crystal-concentration method compared to those calculated based only on isopach data. 相似文献
Fine extinction bands (FEBs) (also known as deformation lamellae) visible with polarized light microscopy in quartz consist of a range of nanostructures, inferring different formation processes. Previous transmission electron microscopy studies have shown that most FEB nanostructures in naturally deformed quartz are elongated subgrains formed by recovery of dislocation slip bands. Here we show that three types of FEB nanostructure occur in naturally deformed vein quartz from the low-grade metamorphic High-Ardenne slate belt (Belgium). Prismatic oriented FEBs are defined by bands of dislocation walls. Dauphiné twin boundaries present along the FEB boundaries probably formed after FEB formation. In an example of two sub-rhombohedral oriented FEBs, developed as two sets in one grain, the finer FEB set consists of elongated subgrains, similar to FEBs described in previous transmission electron microscopy studies. The second wider FEB set consists of bands with different dislocation density and fluid-inclusion content. The wider FEB set is interpreted as bands with different plastic strain associated with the primary growth banding of the vein quartz grain. The nanometre-scale fluid inclusions are interpreted to have formed from structurally bounded hydroxyl groups that moreover facilitated formation of the elongate subgrains. Larger fluid inclusions aligned along FEBs are explained by fluid-inclusion redistribution along dislocation cores. The prismatic FEB nanostructure and the relation between FEBs and growth bands have not been recognized before, although related structures have been reported in experimentally deformed quartz. 相似文献
Rare earth elements (REEs) are very important to technological development as well as to geochemical and environmental studies. In this work, hydrofluoric acid (HF) was replaced by condensed phosphoric acid (CPA) in the digestion of geological samples, and the quantification of REEs was performed by inductively coupled plasma‐optical emission spectrometry (ICP‐OES). Six international reference materials (RMs), named DC86318, CGL 111, CGL 124, CGL 126, OKA‐2 and COQ‐1 and three Brazilian ore samples, named Araxá, Catalão and Pitinga were analysed. Only zircon and xenotime, which are potential REE‐bearing minerals, were not completely dissolved. Nevertheless, no REE associated with zircon was detected. The investigated digestion method presented many advantages: It was relatively fast (3 h), avoided fluoride precipitation, it was less hazardous because handling diluted H3PO4 is safer than HF, NH4F or NH4HF2 aqueous solutions, it preserved the quartz fittings of the measurement equipment and the final solution contained lower levels of total dissolved solids than those produced by the fusion method. 相似文献
Passive treatment systems have become one of the most sustainable and feasible ways of remediating acid mine drainage (AMD). However, conventional treatments show early clogging of the porosity or/and coating of the reactive grains when high acidity and metal concentrations are treated. The performance of fine-grained reagents dispersed in a high porosity matrix of wood shavings was tested as an alternative to overcome these durability problems. The system consisted of two tanks of 3 m3 filled with limestone sand and wood shavings, and one tank of 1 m3 with caustic magnesia powder and wood shavings, separated by several oxidation cascades and decantation ponds. The system treated about 1.5 m3/day of AMD containing an average of 360 mg/L Fe, 120 mg/L Al, 390 mg/L Zn, 10 mg/L Cu, 300 μg/L As and 140 μg/L Pb, a mean pH of 3.08 and a net acidity of 2500 mg/L as CaCO3 equivalent. The water reached pH 5 and 6 in the first and second limestone tanks, respectively (suitable to remove trivalent metals); and pH 8–9 in the MgO tank (suitable to remove divalent metals). After 9 months of operation, the system achieved an average removal of 100% Al, Cu, As, Pb, more than 70% Fe, about 25% Zn and 80% acidity. Goethite, schwertmannite, hydrobasaluminite, amorphous Al(OH)3 and gypsum were the main precipitates in the two limestone tanks. Precipitation of divalent metals (Fe (II), Zn, and traces of Cd, Ni and Co) were complete inside the third tank of MgO, but preferential flow along the walls was responsible for its low treatment performance. Goethite, gypsum, Zn-schulenbergite and sauconite are the crystalline solid phases identified in the MgO tank. 相似文献
The mineral water of Vilajuïga village in Alt Empordà (NE Catalonia, Spain) owes its uniqueness to an emanation of geogenic CO2 that modifies groundwater hydrochemistry to produce a differentiated HCO3–Na- and CO2-rich groundwater among the usual Ca–HCO3 type found in this region. A hydrogeological conceptual model attributes its occurrence to the intersection of two faults: La Valleta and Garriguella-Roses. The former provides a thrust of metamorphic over igneous rocks, formed during the Paleozoic, over a layer of ampelitic shale that, from a hydrogeological perspective, acts as a confining layer. The Garriguella-Roses normal fault, which originated during the Neogene, permits the degassing of geogenic CO2 that is attributed to volcanic activity occurring in the Neogene. Groundwater mixing from the metamorphic and igneous rock units plus the local occurrence of CO2 creates a HCO3–Na water that still holds free-CO2 in solution. Interaction with the gas phase is restricted at the intersection of the two faults. Radiocarbon dating, after correcting for geogenic dead carbon, estimates an age of 8,000 years BP. The low tritium content (0.7 TU) indicates that Vilajuïga water is a mix of “older” groundwater recharged in the metamorphic rocks of the Albera range and “younger” groundwater from the igneous rocks of the Rodes range, over a recharge area of 45 km2 and a maximum elevation of 600 m. Given its origin as rare groundwater in the southern slope of the Eastern Pyrenees, purposeful monitoring is necessary to evaluate the groundwater vulnerability and anticipate impacts from nearby wells and climate-change effects.