Spatial correlation of deformation and mineral reaction in experimentally deformed plagioclase–olivine aggregates

Shear deformation of hot pressed plagioclase–olivine aggregates was studied in the presence and absence of mineral reaction. Experiments were performed at 900 °C, 1500 MPa, and a constant shear strain rate of 5×10⁻⁵ s⁻¹ in a solid medium apparatus. Whether the mineral reaction between plagioclase and olivine takes place or not is controlled by choosing the appropriate plagioclase composition; labradorite (An₆₀) does not react, anorthite (An₉₂) does. Labradorite–olivine aggregates deformed without reaction are very strong and show strain hardening throughout the experiment. Syndeformational reaction between olivine and anorthite causes a pronounced strain weakening. The reaction produces fine-grained opx–cpx–spinel aggregates, which accommodate a large fraction of the finite strain. Deformation and reaction are localised within a 0.5-mm-wide sample. Three representative samples were analysed for their fabric anisotropy R* and shape-preferred orientation α* (fabric angle with the shear plane) using the autocorrelation function (ACF). Fabric anisotropy can be calibrated to quantify strain variations across the sheared samples. In the deformed and reacted anorthite–olivine aggregate, there is a strong correlation between reaction progress and strain; regions of large shear strain correspond to regions of maximum reaction progress. Within the sample, the derived strain rate variations range up to almost one order of magnitude.     

石墨炉原子吸收光谱法测定土壤样品中镉

采用磷酸氢二铵作基体改进剂塞曼扣背景石墨炉原子吸收光谱法测定土壤样品中镉，方法检出限DL=0．012μg／g，精密度RSD在3．55％～7．33％，满足了土壤样品中镉测定的镉质量要求。     

Direct Current Plasma Emission Spectrometric Determination of Major, Minor and Trace Elements in Microwave Oven Acid Leachates of Powdered Whole Coal Samples

Major concentrations of Al₂O₃, Fe₂O₃, MgO, CaO, Na₂O and K₂O, minor levels of TiO₂, P₂O₅ and thirty petrologically, geochemically and environmentally significant trace elements have been determined in microwave oven acid leachates of whole powdered coal samples by direct current plasma‐atomic emission spectrometry (DCP‐AES). A single sample preparation procedure was suitable for all the determinations with no additional dilution step for major elements solution. Dried samples (0.5 g) were treated in low‐pressure PFA digestion vessels with HF/HCl/HNO₃/HClO₄ acids to quantitatively extract the analytes from the bulk material, while leaving the major part of organic matrix as a residue. The major constituents of geological samples, in particular the easily ionised elements (EIEs) such as alkali and alkaline earths, may complicate the instrumental determinations in DCP‐AES because of differential enhancements of elemental emission intensities and stray light interferences. Taking account of these factors, the coal matrix is considered to have very low major oxide totals as compared to many other common geo‐environmental and related materials (rocks, sediments, soil, ashes etc.). The sample size employed here, while yielding a relatively concentrated solution to cover a wide range of elemental determinations, provided a sample matrix that significantly diminished interferences for DCP measurements. The need for closely matching the unknowns and calibrators was eliminated except for overall acidity and an excess quantity of caesium for EIE buffering. Calibration of the spectrometer was accomplished by simple aqueous single element solutions as high concentration calibrators in addition to a reagent blank as a low concentration calibrator. Two point working curves were established to allow for the maximum concentrations of each element expected in the unknowns. The precision of determinations under routine conditions as well as the reproducibility of the leaching and precision of instrumental measurements have been evaluated. Relative standard deviations (RSD) were of 1–2% for those elements whose concentrations in solid samples were well above the limits of quantification. Method detection limits in the buffered solutions were also evaluated. To evaluate the accuracy of the microwave oven‐DCP method a suite of eight certified coal reference materials of differing rank, were analysed with good agreement with the certified and/or available published data. Results are presented for the uncertified major oxides in the AR series reference materials.     

反射地震走时层析成像中的大型稀疏矩阵压缩存储和求解

反射地震走时层析成像是一种精度较高的速度求取方法,最终可归结为线性方程组的求解.方程组具有很大的维数,常规解法需要很大的存储量和计算量.本文考虑到当投影函数取为走时残差,图象函数取为慢度残差时,灵敏度矩阵中的元素表示射线经过网格的长度的特殊物理意义,采用行索引的压缩存储方式,在射线追踪正演模拟过程中直接压缩存储灵敏度矩阵,在层析反演过程中利用压缩后的矩阵进行求解,大大降低了存储量和计算量.     

居民出行与轨迹行为交互模式挖掘与关联技术

出租车是居民出行的重要交通工具,其轨迹数据蕴含着丰富的居民出行信息.原始出租车轨迹数据因缺少语义信息无法直观反映居民出行规律.通过轨迹数据挖掘技术处理之后的出租车轨迹数据能够反映居民活动规律和行为模式,从而为城市规划决策提供参考依据.本文重点研究了基于语义的交互模式度量,通过出租车停留点推断其语义信息;然后根据语义信息...     

气候影响下膨胀土开裂的力学分析

采用线弹性断裂力学的方法,针对气候影响下的膨胀土开裂问题,提出了膨胀土开裂深度和裂缝间距的定量表达式,经比较与现场实测结果基本一致。并对开裂深度与泊松比、断裂韧度、基质吸力等土体特性参数的关系进行了详细的论述。     

Strain and competence contrast estimation from fold shape

A new method to estimate strain and competence contrast from natural fold shapes is developed and verified by analogue and numerical experiments. Strain is estimated relative to the nucleation amplitude, A_N, which is the fold amplitude when the amplification velocities caused by kinematic layer thickening and dynamic folding are identical. A_N is defined as the initial amplitude corresponding to zero strain because folding at amplitudes smaller than A_N is dominantly by kinematic layer thickening. For amplitudes larger than A_N, estimates of strain and competence contrast are contoured in thickness-to-wavelength (H/λ) and amplitude-to-wavelength (A/λ) space. These quantities can be measured for any observed fold shape. Contour maps are constructed using existing linear theories of folding, a new nonlinear theory of folding and numerical simulations, all for single-layer folding. The method represents a significant improvement to the arc length method. The strain estimation method is applied to folds in viscous (Newtonian), power-law (non-Newtonian) and viscoelastic layers. Also, strain partitioning in fold trains is investigated. Strain partitioning refers to the difference in strain accommodated by individual folds in the fold train and by the whole fold train. Fold trains within layers exhibiting viscous and viscoelastic rheology show different characteristic strain partitioning patterns. Strain partitioning patterns of natural fold trains can be used to assess the rheological behaviour during fold initiation.     

The effect of Ca-Tschermaks component on trace element partitioning between clinopyroxene and silicate melt

We have studied the influence of Ca-Tschermaks (Calcium Tschermaks or CaTs) content of clinopyroxene on the partitioning of trace elements between this phase and silicate melt at fixed temperature and pressure. Ion probe analyses of experiments carried out in the system Na₂O–CaO–MgO–Al₂O₃–SiO₂, at 0.1 MPa and 1218°C, produced crystal-melt partition coefficients (D) of 36 trace elements (Li, Cl, Sc, Ti, V, Cr, Fe, Co, Ge, Sr, Y, Zr, Nb, Mo, Ru, Rh, In, Sn, Sb, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta and W), for clinopyroxene compositions between 10 and 32 mol% CaTs. Partition coefficients for 2+ to 5+ cations show, for each charge, a near parabolic dependence of log D on ionic radius of the substituting cation, for partitioning into both the M1 and M2 sites of clinopyroxene. Fitting the results to the elastic strain model of Blundy and Wood [Blundy, J.D., Wood, B.J., 1994. Prediction of crystal-melt partition coefficients from elastic moduli. Nature 372, 452–454] we obtain results for the strain-free partition coefficients of theoretical cations (D₀), with site radius r₀, and for the site's Young's Modulus (E).

In agreement with earlier data our results show that increasing ^ivAl concentration in cpx is matched by increasing D, E_M1, E_M2 and D₀ for tri-, tetra- and pentavalent cations. The degree of fractionation between chemically similar elements (i.e. Ta/Nb, Zr/Hf) also increases. In contrast, D values for mono-, di- and hexavalent cations decrease with increasing ^ivAl in the cpx. The large suite of trace elements used has allowed us to study the effects of cation charge on D₀, r₀ and E. We have found that D₀ and r₀ decrease with increasing cation charge, e.g. r₀=0.66 Å for 4+ cations and 0.59 Å for 5+ cations substituting into M1. Values of E_M1 and E_M2 increase with cation charge as well as with increasing ^ivAl content. The increase in E_M2 is linear and close to the trend set by Hazen and Finger [Hazen, R.M., Finger, L.W., 1979. Bulk modulus-volume relationship for cation–anion polyhedra. J. Geophys. Res. 84 (10) 6723–6728] for oxides. E_M1 values are much higher and do not fit the trend predicted by the Hazen and Finger relationship.     

Experimental Petrology of the 1991-1995 Unzen Dacite, Japan. Part II: Cl/OH Partitioning between Hornblende and Melt and its Implications for the Origin of Oscillatory Zoning of Hornblende Phenocrysts

High-temperature–pressure experiments were carried outto determine the chlorine–hydroxyl exchange partitioncoefficient between hornblende and melt in the 1992 Unzen dacite.Cl in hornblende and melt was analyzed by electron microprobe,whereas OH in hornblende and melt was calculated assuming anionstoichiometry of hornblende and utilizing the dissociation reactionconstant for H₂O + O = 2(OH) in water-saturated melt, respectively.The partition coefficient strongly depends on the Mg/(Mg + Fe)ratio of hornblende, and is expressed as ln K₁ = (Cl/OH)_hb/(Cl/OH)_melt= 2·37 – 4·6[Mg/(Mg + Fe)]_hb at 2–3kbar and 800–850°C. The twofold variation in Cl contentin the oscillatory zoned cores of hornblende phenocrysts inthe 1991–1995 dacite cannot be explained by the dependenceof the Cl/OH partition coefficient on the Mg/(Mg + Fe)_hb ratio,and requires c. 80% variation of the Cl/OH ratio of the coexistingmelt. Available experimental data at 200 MPa on Cl/OH fractionationbetween fluid and melt suggest that c. 1·2–1·8wt % degassing of water from the magma can explain the required80% variation in the Cl/OH ratio of the melt. The negative correlationbetween Al content and Mg/(Mg + Fe) ratio in the oscillatoryzoned cores of the hornblende phenocrysts is consistent withrepeated influx and convective degassing of the fluid phasein the magma chamber. KEY WORDS: chlorine; element partitioning; hornblende; oscillatory zoning; Unzen volcano