Undrained cyclic behavior of bentonite–sand mixtures and factors affecting it

In this work, the cyclic behavior of bentonite–sand mixtures and factors affecting it were studied by means of a ring-shear apparatus and a scanning electron microscope. It was found that bentonite content had a significant influence on the liquefaction potential of the studied soils. A small amount of bentonite in the mixtures would cause the formation of “loose” microstructures, resulting in the occurrence of rapid liquefaction under cyclic loading, while a high bentonite content would cause the formation of clay matrixes, thus raising the soil resistance to liquefaction. In addition, the effect of pore water chemistry on the cyclic behavior of a high plasticity bentonite–sand mixture was carefully examined. It was also found that the presence of ions in pore water would change the clay microfabric, making it more open and thus more vulnerable to liquefaction. Finally, the effects of loading frequency on the cyclic behavior of mixtures with different amounts of bentonite were investigated. It was found that as the bentonite content increased, the influence became more pronounced.     

Geoelectric resistivity sounding of riverside alluvial aquifer in an agricultural area at Buyeo,Geum River watershed,Korea: an application to groundwater contamination study

Twenty profiles of vertical electric soundings (VES) were obtained in a riverside alluvium at the Buyeo area, South Korea, to examine the variations of subsurface geology and associated groundwater chemistry. The combination of the VES data with the borehole data provided useful information on subsurface hydrogeologic conditions. The vestige of an ancient river channel (e.g. oxbow lake) was identified on the resistivity profiles by the lateral continuation of a near-surface perched aquifer parallel to the river. Such a perched aquifer is typically developed in the area with a clay-rich silty surface alluvium which prohibits the infiltration of oxygen. Therefore, groundwater below the oxbow lake shows a very low nitrate concentration and Eh values under the strong anoxic condition. The distribution of water resistivity is correlated with that of measured total dissolved solids concentration in groundwater, while the earth resistivity of the aquifer shows a significant spatial variation. It is interpreted that the earth resistivity of the aquifer is mainly controlled by the soil type rather than by the water chemistry in the study area.     

The role of mineralogy,geochemistry and grain size in badland development in Pisticci (Basilicata,southern Italy)

Mineralogical, geochemical and grain‐size composition of soil and pore‐water chemistry parameters were characterized on both eroded (south‐facing) and non‐eroded (north‐facing) clayey‐silt slopes in the Basilicata region (southern Italy). Only a few grain‐size parameters and clay mineralogy discriminate eroded from non‐eroded substrates. Compared with the latter, the former have fractions of over 63 µm and 1–4 µm lower and fractions 4–63 µm higher. Grain‐size characters of crusts did not discriminate with respect to substrate. Bulk rock mineralogy was not distinctive, but the clay mineral assemblage shows that the eroded slope is enriched in kaolinite, mixed layers (illite–smectite) and chlorite, whereas illite decreases, although overlaps are common. Chemical data enable discrimination between eroded and non‐eroded slopes. pH, SAR (sodium adsorption ratio), TDS (total dissolved salts) and PS (percentage of sodium) are distinctive parameters for both eroded and non‐eroded slopes. TDS increases in depth in the non‐eroded slope, whereas the maximum TDS is just below the crust in the eroded one. On average, eroded substrates are higher in pH, SAR and PS than non‐eroded ones. The ESP (exchangeable sodium percentage) of the eroded slope has a higher value than the non‐eroded one. Crusts are less dispersive than eroded substrates, and non‐eroded substrates behave as crusts. This suggests that the portion of the slope most severely exposed to weathering tends to stabilize, due to strong decreases in SAR, PS and ESP. Several diagrams reported in the literature show similarly anomalous crust samples on eroded slopes, compared with other samples coming from greater depths on eroded slopes. In the present case study, the exchangeable form of Na characterizes crusts more than the soluble form. This study describes the erosional mechanism, which involves morphological and geographic exposure and climatic elements, as well as grain size, mineralogy, chemistry and exchangeable processes of soils. Copyright © 2006 John Wiley & Sons, Ltd.     

Paleolimnological investigation of recent acidity changes in Sawanoike Pond, Kyoto, Japan

Sawanoike Pond, an artificial reservoir constructed ca. 150 yrs. ago, lies in an area geologically sensitive to acidification and contains water that is presently weakly acidic (pH 5.5; alkalinity 15 eq 1^-1). Sediments from a core obtained from the northern part and a core from the central part of the pond were analyzed for organic matter, total organic carbon, total nitrogen, natural and artificial radionuclides, pollen, diatoms, metals and spheroidal carbonaceous particles. A peaty silt layer at the bottom of the central core was replaced by a silt layer initially rich in humic substances, but became more mineral-rich near the surface. Although most of the dominant diatoms throughout the cores were acidophilous taxa, some acidobiontic species increased moderately in abundance after the middle 1960's. Diatom-inferred pH values for the northern core are relatively low before about 1930, then increase, reaching a maximum level between the 1930's and the late 1940's. They then decrease to the surface and reach minimum level during the middle 1980's. Diatom-inferred pH declined by 0.4-0.5 units in the northern core and 0.2-0.3 units in the central core since ca. 1910, when vegetation around the shore changed to a community similar to that of recent years. An increase in labile Pb, Zn, Cd and spheroidal carbonaceous particles, indicative of atmospheric deposition of fossil fuel combustion by-products, preceded the decline in inferred pH. The inferred pH decline of the pond could be an acidification due to acidic precipitation caused by fossil fuel combustion.     

Numerical quantification of sources and phase partitioning of chemical species in cloud: application to wintertime anthropogenic air masses at the Puy de Dôme station

The Model of Multiphase Cloud Chemistry M2C2 has recently been extended to account for nucleation scavenging of aerosol particles in the cloud water chemical composition. This extended version has been applied to multiphase measurements available at the Puy de Dôme station for typical wintertime anthropogenic air masses. The simulated ion concentrations in cloud water are in reasonable agreement with the experimental data. The analysis of the sources of the chemical species in cloud water shows an important contribution from nucleation scavenging of particles which prevails for nitrate, sulphate and ammonium. Moreover, the simulation shows that iron, which comes only from the dissolution of aerosol particles in cloud water, has a significant contribution in the hydroxyl radical production. Finally, the simulated phase partitioning of chemical species in cloud are compared with measurements. Numerical results show an underestimation of interstitial particulate phase fraction with respect to the measurements, which could be due to an overestimation of activated mass by the model. However, the simulated number scavenging efficiency of particles agrees well with the measured value of 40% of total number of aerosol particles activated in cloud droplets. Concerning the origin of chemical species in cloud water, the model reproduces quite well the contribution of gas and aerosol scavenging estimated from measurements. In addition, the simulation provides the contribution of in-cloud chemical reactivity to cloud water concentrations.     

Spatial prediction model and its application to chemistry of atmospheric precipitation in Jordan

This study is concerned with the spatial variability of some wet atmospheric precipitation parameters such as; pH, conductivity (EC). The study also depicts the spatial variability of some ions (cations and anions) of atmospheric precipitation in Jordan such as, Ca²⁺, Mg²⁺, Na⁺ and K⁺, HCO₃⁻, Cl⁻, NO₃⁻ and SO₄²⁻. The basis of the work is to establish a relationship through the cumulative semivariogram technique between the distance ratios and the spatial dependence structure of the chemical composition of atmospheric precipitation. All semivariogram models are constructed in this study in order to understand the behavior of the spatial distribution. The spatial distributions of rainwater parameters show differences from station to station which is expressed in terms of angle, where the larger the angle the weaker the correlation. The semivariogram (SV) models are constructed to show the variation of the rainfall chemistry in Jordan. The SV models show weak correlation between mountain and leeside mountain stations, i.e. mountain and desert stations. On the other hand, good correlations are observed when transferring from south to north of the country. The larger is the found angle, the weaker is the correlation. For most of the SV model the correlation is found to be very weak between desert and mountainous locality. The Standard Regional Dependence Factor (SRDF) is used for prediction of the distribution of rain fall parameters. It shows the relative error between observed and predicted values of rainwater parameters. The overall regional relative error between the observed and estimated concentrations remains less than 15%.     

湖南金鸡岭花岗岩和伟晶岩中黑云母矿物化学及其对成岩成矿的启示

湖南晚侏罗世金鸡岭花岗岩体是南岭地区典型W—Sn成矿岩体之一,内部发育黑云母花岗质伟晶岩团块和文象花岗质条带状伟晶岩脉。金鸡岭花岗岩和黑云花岗伟晶岩中的黑云母具有相似的地球化学特征,均表现出高的FeO、TiO2、Al2O3含量和低的MgO、CaO、Na2O、MnO含量,以及富集成矿元素Nb、Ta、W、Sn,亏损Sr、Ce、Eu等微量元素特征,从花岗岩体到黑云花岗伟晶岩,岩浆的形成温度和氧逸度降低,云母中Al2O3、Li2O*含量升高,TiO2、MgO含量降低,黑云母由铁叶云母演变为黑鳞云母。结合前人资料,金鸡岭花岗岩与黑云花岗伟晶岩均源于元古宙地壳的深熔作用,伟晶岩为花岗岩浆在晚期分异演化的产物,形成于岩浆—热液转化阶段。伟晶岩阶段是稀有金属元素显著富集,乃至进一步成矿的重要阶段。     

A-type volcanics in Central Eastern Sinai, Egypt

Alkaline rhyolitic and minor trachytic volcanics were erupted 580–530 Ma ago. They occur with their A-type intrusive equivalents in Sinai, southern Negev and southwestern Jordan. At Taba-Nuweiba district, these volcanics outcrop in three areas, namely, Wadi El-Mahash, Wadi Khileifiya and Gebel El-Homra. Mineralogically, they comprise alkali feldspars, iron-rich biotite and arfvedsonite together with rare ferro-eckermannite. Geochemically, the older rhyolitic volcanics are highly evolved, enriched in HFSE including REE and depleted in Ca, Mg, Sr and Eu. The rhyolitic rocks of Wadi El-Mahash and Gebel El-Homra are enriched in K₂O content (5.3–10.1 wt.%) and depleted in Na₂O content (0.08–2.97 wt.%), while the rhyolites of Wadi Khileifiya have normal contents of alkalis. Their REE patterns are uniform, parallel to subparallel, fractionated [(La/Yb)_n = 5.4] and show prominent negative Eu-anomalies. They are classified as alkali rhyolites with minor comendites. The younger volcanics are classified as trachyandesite and quartz trachyte (56.6–62.9 wt.% SiO₂). Both older and younger volcanics represent two separate magmatic suites. The overall mineralogical and chemical characteristics of these volcanics are consistent with within plate tectonic setting. It is suggested that partial melting of crustal rocks yielded the source magma. Lithospheric extension and crustal rupture occurred prior to the eruption of these volcanics. The rather thin continental crust (35 km) as well as the continental upheaval and extensive erosion that preceded their emplacement favoured pressure release and increasing mantle contribution. The volatiles of the upper mantle were important agents for heat transfer, and sufficient for the anatexis of the crustal rocks. A petrogenetic hypothesis is proposed for the genesis of the recorded potassic and ultrapotassic rhyolitic rocks through the action of dissolved volatiles and their accumulation in the uppermost part of the magma chamber.