Determination of the distance of the fresh water–salt water interface extending into coastal confined aquifers

In a coastal zone an understanding of the distance of the fresh water–salt water interface and its extension inland is important for prevention of sea water intrusion. In this article estimating methods are described for calculating the distance of a fresh water–salt water interface in a coastal confined aquifer based on the submarine fresh groundwater discharge. This groundwater discharge is controlled not only by the aquifer properties and hydraulic head difference, but also by the position of the fresh water–salt water interface in the coastal zone. A homogeneous and isotropic coastal confined aquifer is considered and fresh groundwater flow in the confined aquifer is thought to be at a steady state. Two observation wells at different distances in a profile perpendicular to the coastline are required in calculation of the distance of the interface toe in the coastal zone. Four coastal confined aquifers with horizontal and sloping confining beds and with varying thickness are also considered. Reasonable results are obtained when examples are used to illustrate the application of the methods. The methods require hydraulic head data at the two wells and thickness of the confined aquifers, but the hydraulic conductivity and fresh groundwater flow rate of the confined aquifers are not needed.     

Geochemistry of the Rare Earth Elements in Natural Terrestrial Waters：A Review of What Is Currently Knows

The range of observed chemical compositions of natural terrestrial waters varies greatly especially when compared to the essentially constant global composition of the oceans.The concentrations of the REEs in natural terrestrial waters also exhibit more variation than what was reported in seawater,In terrestrial waters ,pH values span the range from acid up to alkaline,In addition,terrestrial waters can range from very dilute waters through to highly concentrated brines.The REE concentrations and their behavior in natural terrestrial waters reflect these compositional ranges,Chemical weathering of rocks represents the source of the REEs to natural terrestrial waters and ,consequently,the REE signature of rocks can impart their REE signature to associated waters,In addition,Because of the typical low solubilities of the REEs both surface and solution complexation can be important in fractionating REEs in aqueous solution.Both of these processes are important in all natural terrestrial waters,however,their relative importance varies as a function of the overall solution composition,In alkaline waters,for example,Solution complexation of the REEs with carbonate ions appears to control their aqueous distributions whereas in acid waters,the REE signature of the labile fraction of the REEs is readily leached from the rocks.In circumneutral pH waters,both processes appear to be important and their relative significance has not yet been determined.     

Introduction to the JES Special Issue on Multiple-Scale Geodynamics of Continental Interiors

A major mission of geosciences is to characterize the composition, structure and geodynamic history of the earth’s continental interiors. Because the evidence for such studies is spread over dif-ferent disciplines and in different spatial and temporal scales, advances in understanding the     

Complete Tertiary exhumation history of the Menderes massif, western Turkey: an alternative working hypothesis

The main exhumation of the Menderes massif, western Turkey, occurred along an originally N‐dipping Datça–Kale main breakaway fault that controlled depositions in the Kale and the Gökova basins during the Oligocene – Early Miocene interval. The isostatically controlled upward bending of the main breakaway fault brings the lower plate rocks to the surface. In the Early Miocene, E–W‐trending N‐ and S‐dipping graben‐bounding faults fragmented the exhumed, dome‐shaped massif. The development of half grabens by rolling master fault hinges has allowed further exhumation of the central Menderes massif. After the Pliocene, high‐angle normal faults cut all of the previous structures. This model suggests that the Menderes massif is a single large metamorphic core complex that has experienced a two‐stage exhumation process.     

Arching effect and displacement on theoretical estimation for lateral force acting on retaining wall

Natural Hazards - A new approach is proposed to evaluate the non-limit active earth pressure in c–φ soil based on the horizontal slices method and limit equilibrium method, which takes...     

An experimental study of Fe–Ni exchange between sulfide melt and olivine at upper mantle conditions: implications for mantle sulfide compositions and phase equilibria

The behavior of nickel in the Earth’s mantle is controlled by sulfide melt–olivine reaction. Prior to this study, experiments were carried out at low pressures with narrow range of Ni/Fe in sulfide melt. As the mantle becomes more reduced with depth, experiments at comparable conditions provide an assessment of the effect of pressure at low-oxygen fugacity conditions. In this study, we constrain the Fe–Ni composition of molten sulfide in the Earth’s upper mantle via sulfide melt–olivine reaction experiments at 2 GPa, 1200 and 1400 °C, with sulfide melt \(X_{{{\text{Ni}}}}^{{{\text{Sulfide}}}}=\frac{{{\text{Ni}}}}{{{\text{Ni}}+{\text{Fe}}}}\) (atomic ratio) ranging from 0 to 0.94. To verify the approach to equilibrium and to explore the effect of \({f_{{{\text{O}}_{\text{2}}}}}\) on Fe–Ni exchange between phases, four different suites of experiments were conducted, varying in their experimental geometry and initial composition. Effects of Ni secondary fluorescence on olivine analyses were corrected using the PENELOPE algorithm (Baró et al., Nucl Instrum Methods Phys Res B 100:31–46, 1995), “zero time” experiments, and measurements before and after dissolution of surrounding sulfides. Oxygen fugacities in the experiments, estimated from the measured O contents of sulfide melts and from the compositions of coexisting olivines, were 3.0?±?1.0 log units more reduced than the fayalite–magnetite-quartz (FMQ) buffer (suite 1, 2 and 3), and FMQ ??1 or more oxidized (suite 4). For the reduced (suites 1–3) experiments, Fe–Ni distribution coefficients \(K_{{\text{D}}}^{{}}=\frac{{(X_{{{\text{Ni}}}}^{{{\text{sulfide}}}}/X_{{{\text{Fe}}}}^{{{\text{sulfide}}}})}}{{(X_{{{\text{Ni}}}}^{{{\text{olivine}}}}/X_{{{\text{Fe}}}}^{{{\text{olivine}}}})}}\) are small, averaging 10.0?±?5.7, with little variation as a function of total Ni content. More oxidized experiments (suite 4) give larger values of K_D (21.1–25.2). Compared to previous determinations at 100 kPa, values of K_D from this study are chiefly lower, in large part owing to the more reduced conditions of the experiments. The observed difference does not seem attributable to differences in temperature and pressure between experimental studies. It may be related in part to the effects of metal/sulfur ratio in sulfide melt. Application of these results to the composition of molten sulfide in peridotite indicates that compositions are intermediate in composition (\(X_{{{\text{Ni}}}}^{{{\text{sulfide}}}}\)?~?0.4–0.6) in the shallow mantle at 50 km, becomes more Ni rich with depth as the O content of the melt diminishes, reaching a maximum (0.6–0.7) at depths near 80–120 km, and then becomes more Fe rich in the deeper mantle where conditions are more reduced, approaching (\(X_{{{\text{Ni}}}}^{{{\text{sulfide}}}}\)?~?0.28)?>?140 km depth. Because Ni-rich sulfide in the shallow upper mantle melts at lower temperature than more Fe-rich compositions, mantle sulfide is likely molten in much of the deep continental lithosphere, including regions of diamond formation.     

Fractional derivative modelling for rheological consolidation of multilayered soil under time-dependent loadings and continuous permeable boundary conditions

Acta Geotechnica - This paper investigates the one-dimensional rheological consolidation problem of multilayered soils subjected to different time-dependent loadings and continuous permeable...     

半空间埋置动点源荷载问题的传递矩阵法

引用了流体饱和两相多孔介质的动力控制方程分析半空间埋置动点源荷载问题的位移和变形。经过Laplace Hankel变换 ,控制方程化成常微分方程组。利用数学软件mathmatic对上述方程组求解 ,可以得到单层砂土的传递矩阵。分析过程中 ,假设在两层面上 ,位移与应力相互连续 ,可以借鉴有限元的思想进行耦合计算。这样就获得了在饱和砂土中施加竖向动荷载问题的Laplace Hankel变换解 ,其最终的解还需要通过Laplace Hankel逆变换得到     

Composition and assemblage characteristics of magnetic minerals in layer S<Subscript>5-1</Subscript> of Xifeng and Duanjiapo sections

Relatively strongly magnetic fine components (< 30μm, XS-4J and DS-4J) which are most environmentally sensitive were separated from layer S_5-1 in the Xifeng and Duanjiapo loess sections and analyzed by MPV-3 for their morphometric characteristics and reflectance, SEM-ESD for their element contents and XRD for their mineral phases, respectively. The results showed that minerals in both samples are dominated by detrial Fe-Ti oxides of aeolian origin. In sample XS-4J the reflectance and iron contents of magnetic minerals are usually high. In addition to magnetite (Fe₃O₄), maghemite (γFe₂O₃) and hematite (Fe₂O₃), some Fe-high oxide (72.25 wt%–86.67 wt%), ilmenite (FeTiO₃), and magnetite-ulvöspinel [Fe(FeCr)O₄, Fe (FeNi)O₄] were also detected. In sample DS-4J obvious negative linear correlations were found between Ti and Fe, and the contents of Mn, Si, Al and Ca are usually high and the minerals are dominated by magnetite (maghemite), goethite (FeOOH) and limonite (containing Si and OH). In addition, the signs of corrosion of magnetic minerals and newly crystallized magnetite (maghemite) were recognized. Differences in the composition and assemblage characteristics of magnetite minerals between XS and DS reflect significant differences in source rocks and preserving conditions.     

锶,硼和氟联合作用的亚急性毒理实验及环境意义

本文以自由饮水给药方式进行了锶、硼和氟联合作用的亚急性实验，以探讨锶、硼对氟的拮抗作用。实验结果，给予小鼠200×l0^-6 F 六个月后，可使其骨氟含量显著升高(P<0.01)，肾碱性磷酸酶活力(ALP)显著增高(P<0.01)，4、5个月后血清碱性磷酸酶(ALP)活力亦显著增高(P<0.O1)，同时给予80×l0^-1 B3+、100×l0^-6Sr2+ 时，可以显著降低骨氟含量，抑制血清、肾碱性磷酸酶的活力，表明锶与硼对氟存在拮抗作用。