Geochemistry of subsurface Late Quaternary ironstones in Rajshahi and Bogra Districts,Bangladesh: implications for genetic and depositional conditions

The present study deals with the geochemistry of Late Quaternary ironstones in the subsurface in Rajshahi and Bogra districts, Bangladesh with the lithological study of the boreholes sediments. Major lithofacies of the studied boreholes are clay, silty clay, sandy clay, fine to coarse grained sand, gravels and sands with(fragmentary) ironstones. The ironstones contain major oxides, Fe_2 O_3*(*total Fe)(avg. 66.6 wt%), SiO_2(avg. 15.3 wt%), Al_2 O_3(avg. 4.0 wt%), MnO(avg. 7.7 wt%), and CaO(avg. 3.4 wt%). These geochemical data imply that the higher percentage of Fe_2 O_3* along with Al_2 O_3 and MnO indicate the ironstone as goethite and siderite, which is also validated by XRD data. A comparatively higher percentage of SiO_2 indicates the presence of relative amounts of clastic quartz and manganese-rich silicate or clay in these rocks. These ironstones also have significant amounts of MnO(avg. 7.7 wt%) suggesting their depositional environments under oxygenated condition. Chemical data of these ironstones suggest that the source rock suffered deep chemical weathering and iron was mostly carried in association with the clay fraction and organic matter. Iron concretion was mostly formed by bacterial build up in swamps and marshes, and was subsequently embedded in clayey mud.Within the coastal environments, the water table fluctuates and goethite and siderite with mud and quartz became dry and compacted to form ironstone.     

Petrographic and geochemical characterization of weathered materials developed on BIF from the Mamelles iron ore deposit in the Nyong unit,South-West Cameroon

Iron ore deposits hosted by Precambrian banded iron formation(BIF) are the most important source of mineable iron.In Cameroon,they are located in the southern part of the country.This study reports the petrological and geochemical data of iron ores collected from a weathering profile in the Mamelles BIF deposit,SW Cameroon.The profile is composed of three levels which are from the bottom to the top:the saprock,the ferruginous horizon,and the loose horizon.Eight representative iron ore samples(rock fragments and loose clayey material)were collected along the profile and were subjected to petrographic and geochemical analyses.Their mineralogy consists of martite,goethite,quartz,and lesser amounts of hematite,magnetite,kaolinite,and halloysite.The presence of minerals such as kaolinite and goethite in the Mamelles iron ores suggests their supergene origin.Geochemically,the saprock is characterized by high iron content(70.25 wt% Fe_2 O_(3 t)),and low silica(26.38 wt% SiO_2) and alumina(1.14 wt% Al_2 O_3).The rock fragments collected from the ferruginous horizon display higher Fe_2 O_(3 t)(72-76.40 wt%),Al_2 O_3(2.80-5.43 wt%),and lower SiO_2(16.70-18.35 wt%) contents,suggesting the leaching of silica during the enrichment process.The loose clayey samples collected from both the ferruginous horizon and the upper loose horizon show lower iron and higher silica contents.When normalized to the underlying BIF saprock,both rock fragments and loose clayey ores display LREE enrichment,suggesting that they formed through supergene processes.Economically,most of the Mamelles iron ores are classified as medium-grade ores and a few display acceptable contents in contaminants.Overall,this petrological and geochemical study of the Mamelles iron ores revealed encouraging results.Given its strategic location near the deep seaport,the deposit should be investigated in more detail for its mining potential.     

Geochemical characterization of major elements in desert sediments and implications for the Chinese loess source

Mineral dust released from the desert is one of the important components of atmospheric aerosols. Arid and semi-arid deserts, sandy lands in northern China and their adjacent Gobi Desert lands in northern China and neighboring Mongolia(hereinafter referred to as Gobi) are potential sources of mineral dust in Asia. However, there is currently a lack of systematic studies on the characteristics of major elements in the potential mineral dust source area. This study investigates the major elements of 310 surficial sand samples in the stabilized and semi-stabilized dune fields from 12 deserts/sandy land and Gobi in northern China and southern Mongolian Gobi and compiles published data. We identify four regions with distinct geochemical characteristics:(1) Taklimakan, Kumtag and Qaidam deserts in western China;(2) Badain Jaran, Tengger, Hobq, and Mu Us deserts in the central and western regions of northern China;(3) Hulun Buir, Onqin Daga and Horqin sandy lands in northeast China; and(4) Gobi and Gurbantunggut deserts. The spatial distributions of the SiO_2 and CaO contents in Chinese deserts are highly variable. The average content of SiO_2 generally reflects an increasing trend from west to east, while the average content of CaO shows a decreasing trend from west to east. We demonstrate that the spatial variation of major elements is likely controlled by two key scenarios: the composition of source rocks and the mineral maturity caused by the supply of fresh materials. The SiO_2/(Al_2O_3+K_2O+Na_2O) ratio of desert sediments is relatively lower in western China and may be caused by high ferricmagnesia and high carbonate minerals; this ratio is relatively higher in the northeast sandy lands and may be linked to a lack of fresh material supply and the presence of high K-feldspar minerals in source rocks. The deserts can be further distinguished by ternary diagrams with SiO_2/10-CaO-Al_2O_3,(K_2O+Na_2O)-CaO-Fe_2O_3 and CaO-Na_2O-K_2O. The comparison of major elements between desert sediments and loess suggests that the western and/or central deserts in China may be the potential provenances of loess on the Loess Plateau.     

1600 K和20 GP温压条件下的顽火辉石电导率

在温度750～1600 K和压力10～20 GPa条件下,借助于Kawai-5000多面顶砧高温高压设备,就位测量了(Mg_0.9Fe_0.1) SiO₃ 顽火辉石的电导率.实验结果显示,顽火辉石的电导率在高温区以小极化子机制为主,在低温区以质子导电为主,因为实验后的样品中有一定的水含量.另外,X射线衍射实验表明压力（20 GPa）诱发了顽火辉石向林伍德石的相变,这是我们首次在顽火辉石的电导率实验中观测到林伍德石含水相变,而且含水林伍德石的电导率与已有的实验结果相当一致.     

加载、加热路径上橄榄石的相变及其对相变动力学参数计算的影响

本文研究了橄榄石原位相变实验中加载、加热路径上的相变及其对确定相变动力学参数的影响.利用文献［1］所给出的退火后先加温后加压,且相对低温条件下实验结果确定出的Ni₂SiO₄橄榄石相变动力学参数,计算了加载、加热路径上所发生的相变对确定成核率、长大率及相变体积分数的影响.结果表明,退火后先加压后加温,且相对高温条件下的实验数据受到加热路径上成核的影响.根据这样的实验数据得到的成核率会明显高于实际温压条件下的成核率.尤其是当多数实验都是高温实验时,根据这些成核率数据所确定的成核率参数会严重偏离其真值,从而严重影响对俯冲带颗粒粒度及俯冲带流变结构的计算.尽管目前有很多关于Mg₂SiO₄橄榄石长大率的实验数据,也有通过对挤碰物理图像的分析对(Mg_0.89Fe_0.11)₂SiO₄橄榄石成核率的估算,但只有文献［2］通过退火后先加压后加温的原位实验得到了Mg₂SiO₄橄榄石的相变成核率,且属于高温实验.根据本文的研究结果,我们认为亟需补充退火后先加温后加压或相对低温的实验数据以得到正确的地幔橄榄石成核率参数.     

Origin of High Electrical Conductivity in the Lower Continental Crust: A Review

Electromagnetic measurements have demonstrated that the lower continental crust has remarkable electrical anomalies of high conductivity and electrical anisotropy on a global scale (probably with some local exceptions), but their origin is a long-standing and controversial problem. Typical electrical properties of the lower continental crust include: (1) the electrical conductivity is usually 10⁻⁴ to 10⁻¹ S/m; (2) the overlying shallow crust and underlying upper mantle are in most cases less conductive; (3) the electrical conductivity is statistically much higher in Phanerozoic than in Precambrian areas; (4) horizontal anisotropy has been resolved in many areas; and (5) in some regions there appear to be correlations between high electrical conductivity and other physical properties such as seismic reflections. The explanation based on conduction by interconnected, highly conductive phases such as fluids, melts, or graphite films in grain boundary zones has various problems in accounting for geophysically resolved electrical conductivity and other chemical and physical properties of the lower crust. The lower continental crust is dominated by mafic granulites (in particular beneath stable regions), with nominally anhydrous clinopyroxene, orthopyroxene, and plagioclase as the main assemblages, and the prevailing temperatures are mostly 700–1,000°C as estimated from xenolith data, surface heat flow, and seismic imaging. Pyroxenes have significantly higher Fe content in the lower crust than in the upper mantle (peridotites), and plagioclase has higher Na content in the lower crust than in the shallow crust (granites). Minerals in the lower continental crust generally contain trace amounts of water as H-related point defects, from less than 100 to more than 1,000 ppm H₂O (by weight), with concentrations usually higher than those in the upper mantle. Observations of xenolith granulites captured by volcano-related eruptions indicate that the lower continental crust is characterized by alternating pyroxene-rich and plagioclase-rich layers. Experimental studies on typical lower crustal minerals have shown that their electrical conductivity can be significantly enhanced by the higher contents of Fe (for pyroxenes), Na (for plagioclase), and water (for all minerals) at thermodynamic conditions corresponding to the lower continental crust, e.g., to levels comparable to those measured by geophysical field surveys. Preferred orientation of hydrous plagioclase, e.g., due to ductile flow in the deep crust, and alternating mineral fabrics of pyroxene-rich and plagioclase-rich layers can lead to substantial anisotropy of electrical conductivity. Electrical conductivity properties in many regions of the lower continental crust, especially beneath stable areas, can mostly be accounted for by solid-state conduction due to the major constituents; other special, additional conduction mechanisms due to grain boundary phases are not strictly necessary.     

Adsorption of Complex Pollutants from Aqueous Solutions by Nanocomposite Materials

In view of water pollutants becoming more complex, both anionic and cationic pollutants need to be removed. The multi‐pollutants simultaneous removal is paid more and more attention. Hence, development composite materials for treatment complex wastewater are the aim of this study. In this research, iron–nickel nanoparticles deposited onto aluminum oxide (α‐Al₂O₃) and carbon nanotubes (CNTs) to form nanocomposite materials Fe–Ni/Al₂O₃ and Fe–Ni/CNTs, respectively, were used as adsorbents. The adsorption capacities of Fe–Ni/Al₂O₃ and Fe–Ni/CNTs for AO7, HSeO, and Pb²⁺ were observed to be 5.46, 8.28, 27.02, and 25.6 mg/g, 15.29 and 17.12 mg/g, separately. The composite materials with negative charges were superior in adsorption of anionic pollutants. Using orthogonal experimental design and analysis of variance to co‐treat dye AO7, HSeO and Pb²⁺ in aqueous solutions, seven testing factors were included: (1) adsorbent types, (2) amount of iron, (3) solution pHs, (4) AO7 concentrations, (5) Pb²⁺ concentrations, (6) HSeO concentrations and (7) reaction time. The experimental results showed that the removal of complex pollutants AO7, HSeO, and Pb²⁺ on Fe–Ni/CNTs could reach up to 90% in the optimal treatment conditions. When using Fe–Ni/CNTs as the adsorbent, the sorption isothermals were well fitted in the Freundlich isotherm, and R² could reach up to 0.98.     

Electrical conductivity of magmatic liquids: effects of temperature,oxygen fugacity and composition

The effects of temperature, f_O2 and composition on the electrical conductivity of silicate liquids have been experimentally determined from 1200 to 1550°C under a range of f_O2 conditions sufficient to change the oxidation state of Fe from predominantly Fe²⁺ to Fe³⁺. Oxidation of ferrous to ferric iron in the melt has no measurable effect on the conductivity of melts with relatively low ratios of divalent to univalent cations. Under strongly oxidizing conditions a minor decrease of conductivity is detected inth highΣM²/ΣM⁺ ratios. It is concluded that for purposes of estimating the conductivity of magmatic liquids, f_O2 may be ignored to a first approximation. Both univalent and divalent cation transport is involved in electrical conduction. Melts relying heavily on divalent cations for conduction, i.e. melts with relatively large ΣM²⁺/ΣM⁺ ratios, show strong departures from Arrheenius temperature dependence with the apparent activation energies decreasing steadily as the temperature increases. Conductivities dominated by the univalent cations, in melts with relatively small ΣM²⁺/ΣM⁺ ratios, show classical Arrhenius temperature dependence. These observations are discussed in terms of the general characteristics of the melt structure.Compositional variations within the magmatic range account for much less than an order of magnitude variation in electrical conductivity at a fixed temperature. This observation, combined with previous measurements of the conductivity of olivine (A. Duba, H.C. Heard and R. Schock, 1974) make it possible to state with reasonable confidence that melts occurring within the mantle will be more conductive by 3–4 orders of magnitude than their refractory residues. Potential applications to geothermometry are discussed.     

Petrographical and geochemical signatures of Jurassic rocks of Chari Formation,Western India:implications for provenance and tectonic setting

The sandstones of the Ridge and Athleta members of Chari Formation(Callovian-Oxfordian)exposed at Jara have been analyzed for their petrographical and geochemical studies. Texturally, these sandstones are medium to coarse grained, poorly to well sorted, sub-angular to sub-rounded, and show low to medium sphericity.These sandstones were derived from a mixed provenance including granites, granite-gneisses, low and high-grade metamorphic, and some basic rocks of Aravalli range and Nagarparkar massif. The petrofacies analysis reveals that these sandstones belong to the continental block and recycled orogen tectonic regime. The studied sandstones are modified by paleoclimate, distance of transport, and diagenesis. Mineralogically and geochemically, sandstones are classified as quartzarenite, subarkose, arkose, sublithic arenite, and wacke, respectively. The A-CN-K ternary plot and CIA, CIW, PIA, and ICV values suggest that the similar source rocks suffered moderate to high chemical weathering under a hot-humid climate in an acidic environment with higher PCO_2. Generally good to strong correlations between Al_2O3 and other oxides in these sediments indicate clay mineral control. The K_2O/Na_2O versus SiO_2 diagram indicates that the studied samples occupy passive margin fields but the SiO_2/Al_2O_3 versus K_2O/Na_2O plot suggests that the Athleta Sandstone and Ridge Sandstone fall within the passive margin field, while Ridge Shale falls within the active continental margin field.     

The Application of Combined Seismic and Electrical Measurements to the Determination of the Hydraulic Conductivity of a Lake Bed

The hydraulic properties of lake beds control the interactions between lakes and ground water systems, but these properties are normally difficult to measure directly. The authors'method combines seismic reflection and electrical measurements to map the relative hydraulic conductivity of lake bed sediments. A shipboard seismic profiling system provides sediment thickness, while a towed electrical array yields longitudinal conductance and electrical chargeability. The sediment's leakance (hydraulic conductivity/thickness) can be calculated from the longitudinal conductance data. Leakance may then be converted to relative hydraulic conductivity through the seismically derived sediment thicknesses. Simultaneously acquired electrical chargeability provides an independent measure of clay content. The seismic and electrical systems are computer automated and yield production rates of approximately five line-kilometers/hour or 300 electrical soundings/hour. The systems provide continuous hydraulic information along the ship track rather than the point information derived from coring.
The procedure and systems have been used to map the bed of Lake Michigan offshore from an area of heavy pumpage. This location has been chosen to test the method because lake water has intruded the aquifer in plumes largely controlled by lake bed hydraulics. Mapping these plumes onshore permits the inference of the spatial distribution of offshore hydraulic conductivities. Offshore seepage measurements and numerical, chemical transport modeling of this site have confirmed the reliability of the geophysically derived hydraulic conductivities and have also demonstrated the improvement in numerical results achieved through the availability of spatially determined hydraulic conductivities.     

DESIGN OF MODELS FOR ELECTROMAGNETIC SCALE MODELLING1

Electromagnetic scale modelling for most conductors encountered in prospecting requires models of conductivity in the range 10-1000 S/m. A polyester composite filled with aluminium fillers is used to design the required materials. The fillers are chosen with a high aspect ratio to achieve the desired conductivities without altering mechanical properties. The design process, consisting of a chemical reaction, is simple, repeatable and easy to realize in a geophysical laboratory. The conductivity of the designed material is estimated by an inductive method based upon the variation of the quality factor of a coil in which the samples are inserted. This method is much less influenced by the distribution and orientation of fillers in the resin matrix than a galvanic method. The conductivities obtained fill the major part of the interval 10-1000 S/m without requiring unreasonable mixing ratios. The homogeneity of the material was tested and the anisotropy was low at high conductivities. The electrical properties do not vary with time in free air or when immersed in salt water. We propose standard curves giving conductivities of composites filled with aluminium fibres and flakes. A large cylindrical model of fixed resin-to-filler ratio was made to show the capability of the technique to produce models of useful size. Its measured conductivity agrees well with the expected conductivity from the established standard curves. A scale modelling experiment with the horizontal loop technique was carried out over a horizontal thin sheet made of the material, and again the conductivity obtained from the results agrees reasonably well with the expected value. The noted difference between the inductively and galvanically measured conductivities of the proposed material presently restricts the use of the technique to EM scale experiments for which the host rock is considered very resistive.     

Experimental study on pumice and obsidian

Thermal experiment on the pumice at atmospheric pressure shows that welding begins at about 900° C and complete melting occurs at 1350° C. It is noticed that FeO content of pumice decreases first with increasing temperature, attaining minimum value at 1100° C, and then again increases with increasing temperature. Therefore, an equilibrium is expected in the presence of liquid phase as follows:

$$4FeO + O_2 = 2Fe_2 O_3 .$$     

Location and Characterization of Subsurface Anomalies Using a Soil Conductivity Probe

An electrical conductivity probe, designed for use with "direct push" technology, has been successfully used to locate buried drums, contaminant plumes, and to precisely locate and characterize a previously installed permeable reactive iron wall. The conductivity probe was designed to characterize various soil and sediment types as it was driven through the dry and saturated soil matrix; however, its ability to locate and characterize subsurface anomalies may also prove to be a valuable asset. The probe uses an electrical field that works like and mimics the results from an oilfield engineering tool called the Wenner array. This electrical field array penetrates into the soil matrix to measure the electrical conductivity of the soil matrix surrounding the probe to a radius of about two to four inches. This tool has allowed operating personnel to verify the location of manmade or natural subsurface anomalies with precision.     

甜水海钻孔TS95若干地球化学指标的非线性分析与意义

应用关联维分析和R／S分析对西昆伦甜水海孔TS95的4项指标（FeO,Fe2O3,Fe2O3/FeO和有机碳）进行分析,发现它们存在明显的混沌特征和Hurst现象,4项指标的混沌吸引子分别为：FeO－2．8;Fe2O3－3．2;Fe2O／FeO－2．9;有机碳2．5,饱和嵌入维数为5到6,表明控制该地区气候环境演化的动力系统是由有限维数确定的混沌系统,构筑该系统所需变量至少3到4个,最多5到6个,这种体上与深海氧同位素比较接近,与黄土剖面一些指标差异较大,4项指标折Hurst指数（FeO－0．85;Fe2O3－0．76;Fe2O3／FeO－0．65;有机碳－0．74）显示该地区气候环境演化存在明显的持续性成分,这与早期的研究一致,很可能与青藏高原的构造抬升有关,表明除了全球性气候环境波动背景外,局域性因素,如肝藏高原构造抬升和未海地区水系变迁,都会在各种气候环境演化的替代性指标上有所反映。4项指标Hurst指数的差异可能反映FeO容易迁移,受到了流域水系变化的影响,因而有机碳和Fe2O3可能是反映这种环境演化持续性分更好的指标。     

Tetrahedral occupancy of ferric iron in (Mg,Fe)O: Implications for point defects in the Earth's lower mantle

We investigated the concentration and site occupation of ferric iron (Fe³⁺) in (Mg,Fe)O to understand the influence of point defects on transport properties such as atomic diffusion, electrical conductivity and viscosity. We conducted Mössbauer spectroscopy of (Mg_0.8Fe_0.2)O single crystals synthesized at temperatures from 1673 to 2273 K and pressures from 5 to 15 GPa with Re–ReO₂ and Mo–MoO₂ oxygen fugacity buffers. The isomer shift of the Mössbauer spectra suggests that Fe³⁺ occupies mostly the tetrahedral site at reduced conditions and both the octahedral and tetrahedral sites at oxidized conditions. We formulate a thermodynamic model of point defect dissolution in (Mg,Fe)O which suggests that unassociated tetrahedral Fe³⁺ is more stable than unassociated octahedral Fe³⁺ at high-pressure and low oxygen fugacity due to the effect of configurational entropy. The pressure dependence of Fe³⁺ concentration indicates a change in the dominant site occupancy of Fe³⁺: (1) Fe³⁺ in the tetrahedral site, (2) Fe³⁺ in the octahedral site, and (3) defect clusters of Fe³⁺ and cation vacancy, in the order of increasing oxygen fugacity and decreasing pressure. This is in reasonable agreement with previously reported experiments on Fe³⁺ concentration, Mg–Fe interdiffusivity and electrical conductivity. We consider it plausible that (Mg,Fe)O accommodates Fe³⁺ in the tetrahedral site down to the lower mantle. Based on our results and available experimental data, we discuss the solubility competition between Fe³⁺ and protons (H⁺), and its implications for transport properties in the lower mantle.     

Pathways of carbon oxidation in continental margin sediments off central Chile

Rates and oxidative pathways of organic carbon mineralization were determined in sediments at six stations on the shelf and slope off Concepcion Bay at 36.5 degrees S. The depth distribution of C oxidation rates was determined to 10 cm from accumulation of dissolved inorganic C in 1-5-d incubations. Pathways of C oxidation were inferred from the depth distributions of the potential oxidants (O2, NO3-, and oxides of Mn and Fe) and from directly determined rates of SO4(2-) reduction. The study area is characterized by intense seasonal upwelling, and during sampling in late summer the bottom water over the shelf was rich in NO3- and depleted of O2. Sediments at the four shelf stations were covered by mats of filamentous bacteria of the genera Thioploca and Beggiatoa. Carbon oxidation rates at these sites were extremely high near the sediment surface (>3 micromol cm-3 d-1) and decreased exponentially with depth. The process was entirely coupled to SO4(2-) reduction. At the two slope stations where bottom-water O2 was > 100 microM, C oxidation rates were 10-fold lower and varied less with depth; C oxidation coupled to the reduction of O2, NO3-, and Mn oxides combined to yield an estimated 15% of the total C oxidation between 0 and 10 cm. Carbon oxidation through Fe reduction contributed a further 12-29% of the depth-integrated rate, while the remainder of C oxidation was through SO4(2-) reduction. The depth distribution of Fe reduction agreed well with the distribution of poorly crystalline Fe oxides, and as this pool decreased with depth, the importance of SO4(2-) reduction increased. The results point to a general importance of Fe reduction in C oxidation in continental margin sediments. At the shelf stations, Fe reduction was mainly coupled to oxidation of reduced S. These sediments were generally H2S-free despite high SO4(2-) reduction rates, and precipitation of Fe sulfides dominated H2S scavenging during the incubations. A large NO3- pool was associated with the Thioploca, and the shelf sediments were thus enriched in NO3- relative to the bottom water, with maximum concentrations of 3 micromol cm-3. The NO3- was consumed during our sediment incubations, but no effects on either C or S cycles could be discerned.     

Synthetic radargrams from electrical conductivity and magnetic permeability variations

The objective of this work is to assess the importance of electrical conductivity and magnetic permeability variations in ground penetrating radar (GPR) reflections commonly interpreted only in terms of permittivity variations. We use the matrix propagator approach to obtain the surface electric field associated with a horizontally layered model whose three electromagnetic properties vary from layer to layer. The solution is based on the plane wave boundary value problem using inverse Fourier transformation to accommodate particular GPR pulses. Our results indicate that while magnetic permeability is unimportant, reflections from electrical conductivity variations can be of the same order as those associated with electrical permittivity boundaries. In particular, we show that a realistic ground model composed of thin conductive layers can produce radargrams similar to those caused by a lossless permittivity contrast.     

Simulation of less‐mobile porosity dynamics in contrasting sediment water interface porous media

Considering heterogeneity in porous media pore size and connectivity is essential to predicting reactive solute transport across interfaces. However, exchange with less‐mobile porosity is rarely considered in surface water/groundwater recharge studies. Previous research indicates that a combination of pore‐fluid sampling and geoelectrical measurements can be used to quantify less‐mobile porosity exchange dynamics using the time‐varying relation between fluid and bulk electrical conductivity. For this study, we use macro‐scale (10 s of cm) advection–dispersion solute transport models linked with electrical conduction in COMSOL Multiphysics to explore less‐mobile porosity dynamics in two different types of observed sediment water interface porous media. Modeled sediment textures contrast from strongly layered streambed deposits to poorly sorted lakebed sands and cobbles. During simulated ionic tracer perturbations, a lag between fluid and bulk electrical conductivity, and the resultant hysteresis, is observed for all simulations indicating differential loading of pore spaces with tracer. Less‐mobile exchange parameters are determined graphically from these tracer time series data without the need for inverse numerical model simulation. In both sediment types, effective less‐mobile porosity exchange parameters are variable in response to changes in flow direction and fluid flux. These observed flow‐dependent effects directly impact local less‐mobile residence times and associated contact time for biogeochemical reaction. The simulations indicate that for the sediment textures explored here, less‐mobile porosity exchange is dominated by variable rates of advection through the domain, rather than diffusion of solute, for typical low‐to‐moderate rate (approximately 3–40 cm/day) hyporheic fluid fluxes. Overall, our model‐based results show that less‐mobile porosity may be expected in a range of natural hyporheic sediments and that changes in flowpath orientation and magnitude will impact less‐mobile exchange parameters. These temporal dynamics can be assessed with the geoelectrical experimental tracer method applied at laboratory and field scales.     

高温高压下上地幔岩石电导率实验研究

为了建立具有普遍适用性的上地幔电性结构,本文利用Kawai-1000t压机和Solartron IS-1260阻抗/增益-相位分析仪,在4.0~14.0 GPa、873~1673 K的条件下,采用交流阻抗谱法（频率范围10^-1~10⁶Hz）测量了不含水的地幔岩电导率.实验结果显示,岩石的电导率随温度升高而大幅度的增大;在较大的温度范围内岩石的导电机制发生了变化,中低温时为小极化子导电,此时激活焓为0.94 eV （±0.13） eV,激活体积为0.11（±0.92） cm³·mol^-1,高温时为和镁空穴相关的离子导电,此时激活焓为1.6~3.17 eV,激活体积为6.75（±7.43） cm³·mol^-1;本次测量的电导率比低压下岩石的电导率要高,比矿物的电导率也要高.用本次的实验结果回归计算得到Fennoscandian地区的上地幔的一维电导率剖面,发现200 km以上本次实验计算的结果和大地电磁测深的电导率剖面吻合的比较好,在200 km以下本次实验得到的要比野外测量的电导率稍稍高一点,可能是因为实验过程中没有完全避免水的影响.本次的实验结果比用有效均匀介质方法计算得到的pyrolite矿物模型的电导率要高出两个数量级,这样的结果显示只用一种矿物的电导率或是几种矿物理论计算的结果有一定的不合理性.     

Impedance spectroscopy analysis on electrical properties of serpentine at high pressure and high temperature

The electrical conductivity of serpentine is measured and the microscopic conductance mechanisms are investigated with impedance spectroscopy at 2.5–4.0 GPa and 220–780°C. The results show that the electrical conductivity is strongly dependent on the frequencies used, and that only arc I, which reflects grain interior conductance, occurs and dominates the whole conductance processes over 12-10⁵Hz at high pressure before dehydration. The arc II, which indicates the grain boundary process, begins to occur at the initial stage of dehydration. After dehydration, due to the presence of highly conductive networks of free water, the electrical conductivity is not dependent on frequencies any longer and the total electrical conductivity is dominated by process of ionic conductance of free water in interconnected networks. Dehydration of serpentine enhances pronouncedly the total electrical conductivity, through which highly conductive layers (HCL) may be formed in the earth’s interior.