A revised procedure for discharge measurement by means of the salt dilution method     

Dag Hongve 《水文研究》1987,1(3):267-270

Discharge measurement by means of injection of a NaCl-solution and integration of the electrical conductivity as a function of time is a traditional and well-documented method for use in turbulent streams. The ease of the chemical measurements permits results to be calculated in the field. This work has shown that dry fine-grained salt may substitute the salt solution. Correction factors for water temperature and background conductivity are derived from experiments. A simple procedure for calculation of the discharge is described.  相似文献   

京包线201国道特大桥梁GPS控制测量方案设计与应用     

孙清娟  王辉 《北京测绘》2012,(3):87-88

GPS由于具有作业精度、作业效率高等特点,正逐步取代导线测量而成为线路工程平面控制的一种重要方法。文章探讨了GPS建立线路平面控制测量的方案并以具体的工程案例验证了方案的可行性。  相似文献   

Determination of Molybdenum, Antimony and Tungsten at sub μg g⁻¹ Levels in Geological Materials by ID-FI-ICP-MS     

Akio Makishima  Eizo Nakamura 《Geostandards and Geoanalytical Research》1999,23(2):137-148

We have developed a rapid and accurate method for the determination of Mo, Sb and W in geological samples using isotope dilution inductively coupled plasma-mass spectrometry with a flow injection system (ID-FI-ICP-MS). The chemical procedure requires HF digestion of the sample with a Mo-Sb-W mixed spike, subsequent evaporation and dissolution of Mo, Sb and W from Mg and Ca fluorides with HF. Recovery yields of Mo, Sb and W in the extraction were > 94% for samples of peridotite, basalt and andesite composition, with the exception of W in samples of peridotite composition for which recovery was 81%. No matrix effects were observed in the determination of the isotope ratios of Mo, Sb and W in solutions prepared from peridotite, basalt and andesite samples down to a dilution factor of 100. Detection limits of Mo, Sb and W in silicate materials were at the several ng g⁻¹ level. Analysis of the silicate reference materials PCC-1, DTS-1, BCR-1, BHVO-1, AGV-1 from the US Geological Survey and JP-1, JB-1, -2, -3, JA-1, -2, and -3 from the Geological Survey of Japan as well as the Smithsonian reference Allende powder yielded reliable Mo, Sb and W concentrations. The repeatability in the analysis of basalts and andesites was < 9%. This technique requires only 0.2 ml sample solution, and is therefore suitable for analyzing small and/or precious samples such as meteorites, mantle peridotites and their mineral separates.  相似文献   

Field calibration of a formula for entrance mixing of river inflows to lakes: Lake Taupo,North Island,New Zealand     

Robert H. Spigel  Clive Howard‐Williams  Max Gibbs  Scott Stephens  Barry Waugh 《新西兰海洋与淡水研究杂志》2013,47(4):785-802

Field measurements were used to validate predictions for the initial dilution of negatively buoyant, cold‐water inflows to Lake Taupo, as part of a study to quantify mixing processes associated with the two largest inflows to the lake. The predictions were made using a formulation originally derived for positively buoyant, warm‐water inflows to cooling ponds. The formulation predicts the total dilution of an inflow during its inertia‐dominated phase between its entrance to the lake and the point where buoyancy forces are great enough to cause the inflow to plunge and form a submerged density current. In one of the measured inflows, the inflowing jet was free to entrain from both sides; in the other, entrainment was restricted on one side by attachment of the inflowing jet to the shoreline of a bay just upstream of the plunge point. In the former example, the unmodified coefficients from the cooling pond formulation provided an excellent prediction of initial dilution. In the latter example, entrainment was reduced and different coefficients were derived. In both examples the inflows remained attached to the lake bed throughout their course until their liftoff at depths of 45–55 m to form interflows. The difference between coefficients for the two inflows indicates that the coefficient values should be considered site‐specific. The formulation is not valid for inflows that separate from the bottom of the inflow channel before plunging. The entrance mixing formulation was incorporated in a more general model of lake stratification, DYRESM, which already includes a well‐documented routine for routing underflows down submerged channels on the bed of a lake. Application of the model to the inflows measured in Lake Taupo gave good results for two model outputs that were not involved in the calibration of the entrance mixing formulation, but that are affected by the result of the initial dilution calculation—the temperatures in the river plume after it has plunged, and the insertion depth.  相似文献   

由视谱直接反演真谱参数的实用方法   总被引：2，自引：0，他引：2  

张桂青  罗延钟 《地球科学》1991,16(2):229-239

  相似文献   

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李国重  李建文  归庆明 《大地测量与地球动力学》2010,30(2):67-70

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Determination of Ge, As, Se and Te in Silicate Samples Using Isotope Dilution-Internal Standardisation Octopole Reaction Cell ICP-QMS by Normal Sample Nebulisation     

Akio Makishima  Eizo Nakamura 《Geostandards and Geoanalytical Research》2009,33(3):369-384

A method for the determination of Ge, As, Se and Te in silicate samples using isotope dilution-internal standardisation (ID-IS) octopole reaction cell (ORC) ICP-QMS by normal sample nebulisation was developed. The method does not involve either hydride generation or ion exchange. Germanium, Se and Te were determined by isotope dilution (ID), and As was determined by ID-IS. A silicate sample with an added Ge-Se-Te spike was digested with an HF-HNO₃-HBr mixture, dried, re-dissolved with HF and the supernatant liquid was directly aspirated into an ORC-ICP-QMS instrument with He or H₂ gas. No matrix effects were observed down to a dilution factor (DF) of ∼ 70 for Ge, Se and Te and DF of ∼ 1000 for As, which resulted in 3s detection limits in silicates of 2, 1, 0.1 and 4 ng g⁻¹, respectively. Advantages of the method are the simple sample introduction as well as a capability of determining S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by ID-IS-ICP-QMS/SFMS from the same solution. Furthermore, the total sample solution consumption was only 0.253 ml with DF = 2000. Therefore, only a 0.13 mg test portion was required. To demonstrate the applicability of this technique, Ge, As, Se and Te in eight silicate reference materials were determined, as well as S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta in four carbonaceous chondrites.  相似文献   

Point dilution tests to calculate groundwater velocity: an example in a porous aquifer in northeast Italy     

L. Piccinini  M. Pola 《水文科学杂志》2013,58(8):1512-1523

ABSTRACT

The point dilution test is a single-well technique for estimating horizontal flow velocity in the aquifer surrounding a well. The test is conducted by introducing a tracer into a well section and monitoring its decreasing concentration over time. When using a salt tracer, the method is easy and inexpensive. Traditionally, the horizontal Darcy velocity is calculated as a function of the rate of dilution and is based on the simple assumption that the decreasing tracer concentration is proportional both to the apparent velocity into the test section and to the Darcy velocity in the aquifer. In this article, an alternative approach to analyse the results of point dilution tests is proposed and verified using data acquired at a test site in the middle Venetian plain, northeast Italy. In this approach, the one-dimensional equilibrium advection–dispersion equation is inverted using the CXTFIT model to estimate the apparent velocity inside the test section. Analysis of the field data obtained by the two approaches shows good agreement between the methods and suggests that it is possible to use the equilibrium advection–dispersion equation to estimate apparent velocity over a wide range of velocities.