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141.
-The hydrodynamic coefficients C_d and C_m are not only dependent on the size of slender cylin-der,its location in water,KC number and Re number,but also vary with environmental conditions,i.e.,in regular waves or in irregular waves,in pure waves or in wave-current coexisting field.In this paper,thenormalization of hydrodynamic coefficients for various environmental conditions is discussed.When aproper definition of KC number and proper characteristic values of irregular waves are used,a unified re-lationship between C_d,C_m and KC number for regular waves,irregular waves,pure waves and wave-cur-rent coexisting field can be obtained.  相似文献   
142.
The distribution of diamonds within individual kimberlite pipes is poorly documented in the public domain due to the proprietary nature of the data. The study of the diamond distribution within two pipes, Fox and Koala, from the EKATI Diamond Mine, NWT, Canada, in conjunction with detailed facies models has shown several distinct relationships of deposit type and grade distribution. In both pipes, the lithological facies represent grade units which can be distinguished from each other in terms of relative size and abundance of diamonds. A positive relationship between olivine grain size and abundance with diamond size and abundance is observed, indicating that sorting of fragmental kimberlites influences diamond distribution. Though surface geological processes do not control the diamond potential of the erupting magma, they can be responsible for concentrating diamonds into economically significant proportions. A good understanding of the eruption, transport and depositional processes responsible for the individual lithological units and the diamond distribution within them is important for successful resource estimation. This may lead to recognition of areas suitable for selective mining, making a marginal deposit economic.  相似文献   
143.
The crystal structure of ilinskite, NaCu5O2(SeO3)2Cl3, a rare copper selenite chloride from volcanic fumaroles of the Great fissure Tolbachik eruption (Kamchatka peninsula, Russia), has been solved by direct methods and refined to R 1?=?0.044 on the basis of 2720 unique observed reflections. The mineral is orthorhombic, Pnma, a?=?17.769(7), b?=?6.448(3), c?=?10.522(4) Å, V?=?1205.6(8) Å3, Z?=?4. The The CuOmCln coordination polyhedra share edges to form tetramers that have 'additional' O1 and O2 atoms as centers. The O1Cu4 and O2Cu4 tetrahedra share common Cu atoms to form [O2Cu5]6+ sheets. The SeO3 groups and Cl atoms are adjacent to the [O2Cu5]6+ sheets to form complex layers parallel to (100). The Na+ cations are located in between the layers. A review of mixed-ligand CuOmCln coordination polyhedra in minerals and inorganic compounds is given. There are in total 26 stereochemically different mixed-ligand Cu-O-Cl coordinations.  相似文献   
144.
Earthquake records from a 1984 temporary seismograph array set up in La Molina, Lima, Peru, are re-analysed. The array comprised eight three-component geophones; seven soil based and one rock based. Values of horizontal-to-vertical spectral ratio (HVSR) for two small earthquakes peaked at around 1.3 Hz. In one distant earthquake, four of the seven soil-based stations showed a peak at 1.25 Hz in soil-to-rock spectral ratio (SSR), the same dominant frequency observed during an aftershock of a damaging earthquake. Because this frequency is not compatible with the shear wave velocity profile attributed to La Molina, and because the spectral peak is confined to a small ground area, it is concluded that the peak is caused by a localised deposit of soft soil. Because the area associated with the spectral peak includes the area of great damage in 1974, it is concluded that coherent monochromatic behaviour is responsible for the damage.  相似文献   
145.
We have determined the production yields for radionuclides in Al2O3, SiO2, S, Ar, K2SO4, CaCO3, Fe, Ni and Cu targets, which were irradiated with slow negative muons at the Paul Scherrer Institute in Villigen (Switzerland). The fluences of the stopped negative muons were determined by measuring the muonic X-rays. The concentrations of the long-lived and short-lived radionuclides were measured with accelerator mass spectrometry (AMS) and γ-spectroscopy, respectively. Special emphasis was put on the radionuclides 10Be, 14C and 26Al produced in quartz targets, 26Al in Al2O3 and S targets, 36Cl in K2SO4 and CaCO3 targets, and 53Mn in Fe2O3 targets. These targets were selected because they are also the naturally occurring target minerals for cosmic ray interactions in typical rocks. We also present results of calculations for depth-dependent production rates of radionuclides produced after cosmic ray μ capture, as well as cosmic ray-induced production rates of geologically relevant radionuclides produced by the nucleonic component, by μ capture, by fast muons and by neutron capture.  相似文献   
146.
A parametric study of the instantaneous radiative impact of contrails is presented using three different radiative transfer models for a series of model atmospheres and cloud parameters. Contrails are treated as geometrically and optically thin plane parallel homogeneous cirrus layers in a static atmosphere. The ice water content is varied as a function of ambient temperature. The model atmospheres include tropical, mid-latitude, and subarctic summer and winter atmospheres. Optically thin contrails cause a positive net forcing at top of the atmosphere. At the surface the radiative forcing is negative during daytime. The forcing increases with the optical depth and the amount of contrail cover. At the top of the atmosphere, a mean contrail cover of 0.1% with average optical depth of 0.2 to 0.5 causes about 0.01 to 0.03 Wm−2 daily mean instantaneous radiative forcing. Contrails cool the surface during the day and heat the surface during the night, and hence reduce the daily temperature amplitude. The net effect depends strongly on the daily variation of contrail cloud cover. The indirect radiative forcing due to particle changes in natural cirrus clouds may be of the same magnitude as the direct one due to additional cover.  相似文献   
147.
Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log mAu–mNaCl–T frame fixed linear dependence between log mAu and T at any studied iso‐pleth (mNaCl) in the form of log mAu = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log mAu) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied fO2/fS2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower fO2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H2O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H2O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 mHCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log mPt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)2 and Mn2(OH)3Cl). These phases are metastable and transfer to Mn3O4 with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn3O4, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn2O3–MnO2 buffer. So at 400C, dissolved Au (log mAu) increases from –4. 40 in water to –1. 00 in 0. 1 mHCl, and ones of Pt (log mPt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.  相似文献   
148.
Assuming a radially stratified Newtonian mantle in a steady-state approximation, we demonstrate that the permeability of a viscosity interface at 660-km depth strongly depends on the wavelength of buoyancy forces driving the flow. The flow induced by long-wavelength loads penetrates through the boundary freely even if the viscosity increases by two orders. In contrast, the boundary is practically impermeable for short-wavelength loads located in the upper mantle. Thus, a stepwise increase of viscosity is a significant obstacle for small descending features in the upper mantle, but huge upper mantle downwellings, or upwellings formed in the-lower mantle can overcome it easily. This indicates that certain care is necessary in interpreting the seismic structure of the mantle by means of flow models. The global tomographic image includes only the first few degrees of the harmonic series and, consequently, its interpretation in terms of a present-day flow field results in a predominantly whole-mantle circulation even for extreme viscosity contrasts.  相似文献   
149.
—?The potential for large excavation-induced seismic events may be recognised, even if the timing of an event may be inherently unpredictable. In this case, modelling the wave propagation from a potential event could allow the dynamic motions around an excavation to be projected, and for areas of danger to be anticipated. However, the above and other potential applications require accurate models of wave interaction with the openings, as well as with the fractured rock which surrounds such excavations. This paper considers real recorded waveforms and how well these waveforms are modelled by explicit mechanical models of the source, the medium and the excavation. Models of experiments at three different scales of the problem are presented: small and large amplitude waveforms recorded around a deep-level mining tunnel in a synthetic rockburst experiment; waveforms from laboratory experiments of waves through plates of steel representing fractures; waveforms from active pulses in an acoustic emission experiment in a small volume of fractured rock at the surface of an underground excavation. The results show that elastic wave propagation around an excavation was a first approximation for small amplitude waves, but was less successful for modelling large amplitude waves and more fractured rock. Fractures in the models were represented explicitly with displacement discontinuities. Waveforms through known fracture geometries were particularly well-reproduced, and indicate the importance of fracture stiffness, the in situ stress state, and stress-dependence of the fractures in such models. Overall, the models are sufficiently successful at representing recorded behaviour, to be encouraging for the goal of representing accurate wave motions around excavations.  相似文献   
150.
A high-resolution spectrum clearly shows the presence of A 6Σ+X 6Σ+(0,0;0,1;1,0;2,0;2,1) and (2,2) bands system of CrH molecular lines in the spectral range 10,000 cm−1 to 14,050 cm−1. At least 3928 lines of the six bands, accounting for 57% of the lines registered in the laboratory can be identified with certainty in the sunspot spectrum. Most of the lines are found blended with TiO, CaH, MgH and other atomic species. These molecular lines are typically much more temperature sensitive than atomic lines, which make them ideal, complementary tool for studying cool stellar atmospheres as well as the internal structure of sunspots. Equivalent width for an adequate number of well identified molecular lines of these bands using the Gaussian-profile approximation method versus rotational quantum number J has been used to determine the effective rotational temperature of the CrH molecule. The range of effective rotational temperature value obtained from these bands is 1766 K to 2442 K. This range agrees well with the effective rotational temperatures derived for other molecules in sunspot umbrae.  相似文献   
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