Weathered and fresh samples of metamorphic rocks from Sri Lanka were collected from various localities and analysed for major elements by XRF method (RIGAKU, KG-X System, Japan). The content of water was determined by the ignition method.
The XRF results, obtained from these samples form the basis of a new index of chemical weathering, particularly for Sri Lanka, which is named the Silica-Titania Index, and is calculated as follows: Silica-Titania Index = {(SiO2/TiO2)/[(SiO2/TiO2) × (Al2O3/TiO 2) × (SiO2/Al2O3)]} × 100(molecular proportions).
The index can be used to determine the degree of weathering in chemically weathered silicate rocks of other countries in tropical regions. A triangular diagram plots the position of this index. The point load strengths of fresh rocksand weathered rocks with different degrees of weathering were correlated with the values of this new chemical index. The relative variation in strengths of fresh rocks and weathered rocks clearly indicates its suitability and usefulness for engineering geologists. 相似文献
Bulk transfer coefficients were evaluated from eddy correlation flux measurements on a fixed pier during onshore winds. The mean values are CD = 1.69 × 10-3, CH = 2.58 × 10-3 and CE = 1.51 × 10-3. The drag coefficient, CD, gradually increases with wind speed but CH and CE are independent of wind speed. According to theory and empirical formulas based on experimental results over flat grassland, the transfer coefficients should gradually increase with increasing instability. This is confirmed experimentally in the stable region in our case. However, the drag coefficient appears to decrease with increasing instability, which is against the theoretical result. A stability dependence is not clearly observed for CH or CE. 相似文献
The orthorhombic MgSiO3 perovskite has been synthesized with the aid of a double-stage split-sphere-type high-pressure apparatus at about 280 kbar and 1000°C. The unit cell dimensions are: a = 4.7754(3)Å, b = 4.9292(4)Å and c = 6.8969(5)Å with the probable space group Pbnm. Calculated density is 4.108 g cm?3. Crystal structure determination has been carried out by means of both the geometrical simulation (DLS) technique and the ordinary powder X-ray analysis. The results indicate that the MgSiO3 perovskite is closer to the ideal perovskite than ScAlO3 perovskite. 相似文献
An analysis of the textures of pallasites has been made using data concerning the kinetic and rheological properties of silicates and metals. Pallasites containing rounded olivines (e.g., the Springwater and Brehnam pallasites) have been heated to above the solidus temperature of the metallic iron phases, ~ 1270 K. The rounded olivines of grain size 0.5–1.0 cm observed in the Springwater pallasites were formed between 1270 and 1370 K. On the other hand, those of grain size 0.5–1.0 mm as found in the Brehnam pallasites may have been heated to above 1370 K; however, the duration of heating at such high temperatures must have been less than 5 × 103 y. Pallasites containing angular olivines with microscopically rounded corners (e.g., the Eagle Station, Dora pallasites) have suffered shock events fracturing the olivine grains, which may correspond to collisions during the accretional stage of the parent body, and experienced successive annealing during cooling from a temperature between 1150 and 1270 K. 相似文献
From measurements in the atmospheric surface layer over a paddy field, the Kolmogorov constants for CO2 and longitudinal wind velocity were obtained. In this study, the nondimensional dissipation rate nc = (1–16v)-1/2 for CO2 variance and = (1–16v)-1/4 – v for turbulent energy were used, assuming the equality of the local production term and the local dissipation term, and neglecting the divergence flux term in the budget equation. The value of the constant for CO2 was consistent with recent determinations for temperature and humidity. The constant for longitudinal wind velocity showed good agreement with other recent observations. 相似文献
Pressure effects on the lattice parameters of β- and γ-Mg2SiO4 have been measured at room temperature and at pressures up to 100 kbar using a multi-anvil high-pressure X-ray diffraction apparatus. The volume changes (ΔV/V0) at 90 kbar are 5.4 · 10?2 and 4.2 · 10?2 for β- and γ-Mg2SiO4, respectively. Isothermal bulk moduli at zero pressure have been calculated from least-square fits of the data to straight lines. They turn out to be 1.66 ± 0.4 and 2.13 ± 0.1 Mbar for β- and γ-Mg2SiO4, respectively. The α → γ transition obeys Wang's linear Vφ?ρ relation but the α → β transition does not. 相似文献
High-pressure phase relations in ZnSiO3 and Zn2SiO4 were investigated at about 1000°C and in the pressure range of 100–500 kbar, using a double-staged split-sphere type of high-pressure apparatus.Clinopyroxene-type ZnSiO3 transforms directly into a polymorph with the ilmenite structure at 120 kbar. The hexagonal unit cell dimensions of the ZnSiO3 ilmenite are determined to be under ambient conditions.The following reactions are also recognized at about 1000°C: and: The stabilities of silicate ilmenites, especially the absence of ilmenite of transition metal silicate composition, is discussed. It is pointed out that data on phase relations in zinc silicates may be informative for the consideration on those in magnesium silicates under very high pressures. It is suggested that the silicate ilmenite may be a major constituent in the lower mantle. 相似文献
Melting relations of primitive peridotite were studied up to 25 GPa. The change of the liquidus phase from olivine to majorite occurs at 16 GPa. We confirmed the density crossover of the FeO-rich peridotite melt and the equilibrium olivine (Fo90) at 7 GPa. Sinking of equilibrium olivine (Fo95) in the primitive peridotite melt was observed up to 10 GPa. The compression curves of FeO-rich peridotitic and komatiite melts reported in this and earlier work suggest that the density crossover in the Earth's mantle will be located at 11–12 GPa at 2000°C, consistent with an previous estimation by C.B. Agee and D. Walker.
The density crossover can play a key role in the Moon and the terrestrial planets, such as the Earth, Venus and Mars. Majorite and some fraction of melt could have separated from the ascending diapir and sunk downwards at the depths below the density crossover. This process could have produced a garnet-rich transition zone in the Earth's mantle. The density crossover may exist in the FeO-rich lunar mantle at around the center of the Moon. The density crossover which exists at the depth of 600 km in the Martian mantle plays a key role in producing a fractionated mantle, which is the source the parent magmas of the SNC meteorites. 相似文献
Partitioning of copper, zinc, iron and manganese into oxide, sulfide, organic and silicate fractions has been determined with a selective chemical leaching technique on sediment samples from a core collected in Osaka Bay. The samples have been dated by the210Pb method. Most of the copper and zinc in the polluted surface sediment layer are contained in both oxide and sulfide fractions. This suggests that the transformation of oxides and hydroxides to sulfides under anoxic conditions within the sediment is significant for the fixation of copper and zinc discharged through human activities into the sediment. Manganese is apparently enriched in oxide and hydroxide fractions of the surface layer due to the post-depositional migration of manganese within the sediment. The copper, zinc and manganese contents of the 30 % H2O2 soluble fraction (mostly organic fraction) decrease with depth in the sediment core, and correlate significantly with the organic carbon content. The heavy metal (Cu, Zn, Fe and Mn) contents of the silicate fraction, without exchangeable sites, are almost constant with depth. 相似文献
The ‘International Intercomparison Exercise of fCO2 Systems’ was carried out in 1996 during the R/V Meteor Cruise 36/1 from Bermuda/UK to Gran Canaria/Spain. Nine groups from six countries (Australia, Denmark, France, Germany, Japan, USA) participated in this exercise, bringing together 15 participants with seven underway fugacity of carbon dioxide (fCO2) systems, one discrete fCO2 system, and two underway pH systems, as well as systems for discrete measurement of total alkalinity and total dissolved inorganic carbon. Here, we compare surface seawater fCO2 measured synchronously by all participating instruments. A common infrastructure (seawater and calibration gas supply), different quality checks (performance of calibration procedures for CO2, temperature measurements) and a common procedure for calculation of final fCO2 were provided to reduce the largest possible amount of controllable sources of error. The results show that under such conditions underway measurements of the fCO2 in surface seawater and overlying air can be made to a high degree of agreement (±1 μatm) with a variety of possible equilibrator and system designs. Also, discrete fCO2 measurements can be made in good agreement (±3 μatm) with underway fCO2 data sets. However, even well-designed systems, which are operated without any obvious sign of malfunction, can show significant differences of the order of 10 μatm. Based on our results, no “best choice” for the type of the equilibrator nor specifics on its dimensions and flow rates of seawater and air can be made in regard to the achievable accuracy of the fCO2 system. Measurements of equilibrator temperature do not seem to be made with the required accuracy resulting in significant errors in fCO2 results. Calculation of fCO2 from high-quality total dissolved inorganic carbon (CT) and total alkalinity (AT) measurements does not yield results comparable in accuracy and precision to fCO2 measurements. 相似文献