Trace element partitioning between amphibole and hydrous silicate glasses at 0.6–2.6 GPa

Partitioning behavior between amphibole and silicate glass of thirty-three minor and trace elements(Sc,Ti, V, Cr, Co, Rb, Sr, P, Y, Zr, Nb, Cs, Ba, K, La, Ce, Pr,Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, Pb,Th, and U) have been determined experimentally. Products of crystallization of hydrous basalt melts from 0.6 GPa/860 °C up to 2.6 GPa/970 °C were obtained in a multianvil apparatus. Major and trace element compositions of amphibole and glass were determined with a combination of electron microprobe and laser ablation inductively coupled plasma mass spectrometry. The main mineral phase is calcic amphibole, and the coexisting glass compositions are tonalite, granodiorite, and granite. The compatibility of rare earth elements increase at 915 °C and then decrease at 970 °C, but the compatibility of most of these elements shows a continued, significant increase with increasing pressure. For high-field strength elements, large ion lithophile elements, actinide compatibility decrease with increasing temperature or pressure, but transition metals show a continued increase in compatibility within the temperature–pressure conditions. From mathematical and graphical fitting, we determined best-fit values for the ideal ionic radius(r_0, 1.01–1.04 ?), the strain-free partitioncoefficient(D_0, 1.18–1.58), and apparent Young's modulus(E, 142–370 GPa) for the M4 site in amphibole according to the lattice strain model. The D_0^M4 for rare earth elements rises at 915 °C and then drops at 970 °C at 0.6 GPa.However, the D_0^M4 values are positively proportional to the pressure for rare earth elements in the amphibole-glass pairs at 0.6–2.6 GPa and 970 °C. Furthermore, the derived best-fit values for r_0^M4 and E^M4 are almost constant and trend to increase with rising temperature and pressure,respectively. The partition coefficient is distinctly different for different melt compositions. The rare earth elements become more enriched in amphibole if the quenched glass is granodiorite or granite compared to the tonalitic glasses.     

细颗粒运移对土体力学特性的影响

在渗流条件下,松散土体中的细颗粒会逐渐被水流带走,从而改变土体的颗粒级配及微结构,进而影响土体的宏观力学参数如强度和弹性模量等。本文针对土体中细颗粒迁移对土体宏微观参数的影响,开展基于核磁共振仪器的微观孔喉结构观测实验及基于孔隙网络模型的计算。研究表明,沿土体深度方向细颗粒随孔隙渗流而下移,中部聚集程度最高,这样导致中部小孔隙明显大于上部和下部。在渗流过程中,孔隙水并不能充满整个区域,上、中、下部均存在没有被水波及的范围,中部未波及范围最大,渗流通道最少,相同流量下的孔隙水压更高,因此中部的强度和刚度变化也最大。     

声子在硅酸盐熔体缔合反应中的作用

本文采用量子统计方法，得到了声子熵的计算公式和初步结果，同时还提出在硅酸盐熔体两种阴离子结构团的缔合反应中，声学支声子所提供的声子熵起了重要作用。     

小导管注浆处理顶管涌水技术

结合实际顶管工程,从地质条件出发分析涌水原因和注浆处理涌水的作用机理,详细讨论了小导管处理涌水的施工工艺。注浆效果检查表明小导管注水泥-水玻璃双液浆处理裂隙和地下水发育的围岩涌水地质条件效果明显,加固措施可行,为顶管工程在施工中和后期运营提供安全保证。     

Water chemistry and control of weathering of Pichola Lake,Udaipur District,Rajasthan, India

The water chemistry of Pichola lake revealed that it is dominated by Na and HCO₃. The lake water chemistry strongly reflects the dominance of continental weathering aided by anthropogenic activity, such as tourist influx, developmental activities in the catchment area, and disposal of untreated municipal and domestic sewage into the lake basin. The supply of major ions is mainly through weathering of the silicate rock exposed in the drainage basin and the contribution from saline and alkaline soils/groundwater because of the semiarid conditions of the region. The increase in phosphate loading and consequent depletion of silica suggests biological consumption of the latter. The observed chemical data of Pichola lake was used to predict the mineral assemblages in the carbonate and aluminosilicate system. It demonstrates that calcite and dolomite are the possible minerals that are in equilibrium with the lake water system and that the lake water chemistry is in the range of stability of kaolinite.     

Geo-Neutrinos: A Systematic Approach to Uncertainties and Correlations

Geo-neutrinos emitted by heat-producing elements (U, Th and K) represent a unique probe of the Earth interior. The characterization of their fluxes is subject, however, to rather large and highly correlated uncertainties. The geochemical covariance of the U, Th and K abundances in various Earth reservoirs induces positive correlations among the associated geo-neutrino fluxes, and between these and the radiogenic heat. Mass-balance constraints in the Bulk Silicate Earth (BSE) tend instead to anti-correlate the radiogenic element abundances in complementary reservoirs. Experimental geo-neutrino observables may be further (anti)correlated by instrumental effects. In this context, we propose a systematic approach to covariance matrices, based on the fact that all the relevant geo-neutrino observables and constraints can be expressed as linear functions of the U, Th and K abundances in the Earth’s reservoirs (with relatively well-known coefficients). We briefly discuss here the construction of a tentative “geo-neutrino source model” (GNSM) for the U, Th, and K abundances in the main Earth reservoirs, based on selected geophysical and geochemical data and models (when available), on plausible hypotheses (when possible), and admittedly on arbitrary assumptions (when unavoidable). We use then the GNSM to make predictions about several experiments (“forward approach”), and to show how future data can constrain a posteriori the error matrix of the model itself (“backward approach”). The method may provide a useful statistical framework for evaluating the impact and the global consistency of prospective geo-neutrino measurements and Earth models.     

Viscosity of albite melt at high pressure and high temperature

 The viscosity of albite (NaAlSi₃O₈) melt was measured at high pressure by the in situ falling-sphere method using a high-resolution X-ray CCD camera and a large-volume multianvil apparatus installed at SPring-8. This system enabled us to conduct in situ viscosity measurements more accurately than that using the conventional technique at pressures of up to several gigapascals and viscosity in the order of 10⁰ Pa s. The viscosity of albite melt is 5.8 Pa s at 2.6 GPa and 2.2 Pa s at 5.3 GPa and 1973 K. Experiments at 1873 and 1973 K show that the decrease in viscosity continues to 5.3 GPa. The activation energy for viscosity is estimated to be 316(8) kJ mol⁻¹ at 3.3 GPa. Molecular dynamics simulations suggest that a gradual decrease in viscosity of albite melt at high pressure may be explained by structural changes such as an increase in the coordination number of aluminum in the melt. Received: 6 January 2001 / Accepted: 27 August 2001     

水对硅酸盐岩体系部分熔融行为的影响：第二临界端点的重要意义

水对硅酸盐岩体系的许多物理-化学行为有着非常重大的影响.具体对部分熔融过程来说,水可以显著地降低熔融温度、改变熔体性质、影响微量元素在固-液相之间的分配.近年来,科学家们就大量水对硅酸盐岩体系的部分熔融过程的影响进行了许多的高压实验,他们主要关注第二临界端点对熔融过程的重要作用:第二临界端点的出现极大地改变着部分熔融过程中的基本相关系.本文主要针对这些高压实验研究做一总结,并对未来研究方向做一初步探讨.     

Chemical textures on quartz grains: An experimental approach using salts

Two groups of fresh crushed Brazilian quartz grains (0.4–0.6 mm) were placed in 10 ml of various saturated salt solutions (sodium sulphate, sodium chloride, magnesium sulphate, sodium carbonate, and sodium carbonate and soil). One group was placed in an environmental cabinet programmed to simulate summer diurnal temperature and relative humidity values recorded in Wheeler Valley, a dry valley in southern Victoria Land, Antarctica. The other group was allowed to remain at normal laboratory conditions. Quartz grains from both groups were removed at pre-selected intervals for examination using the scanning electron microscope. After 50 hours chemical surface textures were formed on the quartz grains in all but the sodium sulphate solution. At the 140 hour interval all the salt solutions used were producing chemical surface textures on the quartz grains. This paper demonstrates that chemical surface textures can be produced on quartz grain surfaces by saturated salt solutions in a short period of time and may prove to be representative of chemical surface textures produced in a saturated saline environment.     

The role of supergene sulphuric acid during weathering in small river catchments in low mountain ranges of Central Europe: Implications for calculating the atmospheric CO2 budget

The geochemistry of dissolved and suspended loads in river catchments of two low mountain ranges in Central Europe allows comparison of pertinent chemical weathering rates. Distinct differences in lithology, i.e. granites prevailing in the Black Forest compared to Palaeozoic sediments in the Rhenish Massif, provide the possibility to examine the influence of lithology on weathering. Here we determine the origin of river water using the stable isotope ratio δ¹⁸O_H2O and we quantify the geogenic proportions of sulphate from stable isotope ratios δ³⁴S_SO4 and δ¹⁸O_SO4. Particularly in catchments with abundant pyrite, determination of the geogenic amount of sulphate is important, since oxidation of pyrite leads to acidity, which increases weathering. Our results show that spatially averaged silicate weathering rates are higher for the river catchments Acher and Gutach in the Black Forest (10–12 t/km²/yr) compared to the river catchments of the Möhne dam and the Aabach dam in the Rhenish Massif (2–6 t/km²/yr). Correspondingly, the CO₂ consumption by silicate weathering in the Black Forest (334–395 × 10³ mol/km²/yr) is more than twice as high as in the Rhenish Massif (28–151 × 10³ mol/km²/yr). These higher rates for watersheds of the Black Forest are likely due to steeper slopes leading to higher mechanical erosion with respective higher amounts of fresh unweathered rock particulates and due to the fact that the sediments in the Rhenish Massif have already passed through at least one erosion cycle. Carbonate weathering rates vary between 12 and 38 t/km²/yr in the catchments of the Rhenish Massif. The contribution of sulphuric acid to the silicate weathering is higher in the catchments of the Rhenish Massif (9–16%) than in the catchments of the Black Forest (5–7%) due to abundant pyrite in the sediments of the Rhenish Massif. Three times higher long-term erosion rates derived from cosmogenic nuclides compared to short-term erosion rates derived from river loads in Central Europe point to three times higher CO₂ consumption during the past 10³ to 10⁴ years.