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We present data for the concentrations of eleven rare earth elements (La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er, Yb, Lu) in eleven international geochemical reference materials obtained by isotope dilution multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). We have analysed both rock powders and synthetic silicate glasses, and the latter provide precise data to support the use of these as reference materials for in situ trace element determination techniques. Our data also provide precise measurements of the abundance of mono-isotopic Pr in both glasses and powders, which allows more accurate constraints on the anomalous redox-related behaviour of Ce during geochemical processes. All materials were analysed in replicate providing data that typically reproduce to better than one percent. Sm/Nd ratios in all these materials also reproduce to better than 0.2% and are accurate to < 0.2% and can thus be used as calibrants for Sm-Nd geochronology. Our analyses agree well with existing data on these reference materials. In particular, for NIST SRM 610, USGS BHVO-2, AGV-1 and AGV-2, our measured REE abundances are typically within < 2% (and mostly 1%) of REE concentrations previously determined by isotope dilution analysis and thermal ionisation mass spectrometry, consistent with the higher degree of precision and accuracy obtained from isotope dilution techniques. Close agreement of results between basaltic glass reference materials USGS BHVO-2G and BCR-2G and the BHVO-2 and BCR-2 powders from which they were created suggests that little fractionation, concentration or dilution of REE contents occurred during glass manufacture.  相似文献   
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A new computer programme was written in programming language TURBOC, which enables us to apply a procedure involving seventeen statistical tests (a total of sixty five single or multiple outlier versions of these tests) for outlier detection in univariate sample at a high confidence level of 99% (significance level α= 0.01). The outlying observations should be evaluated first for technical reasons and then rejected manually from the data base until no more outliers are detected and the final statistical parameters are computed from the remaining data. This programme has been used successfully to process two reference material data bases: WS-E from England and Soil-5 from Peru. The final mean values for WS-E are more reliable (characterized by smaller standard deviations and narrower confidence limits) than those obtained earlier using a different statistical approach. The application of a large number of statistical tests to Soil-5 also resulted in smaller standard deviation values for most elements than the method involving a limited number of such tests. For WS-E, some laboratories seem to have produced multiple data that were detected as statistical outliers. A close analysis of the distribution of outliers as a function of laboratory, country and analytical method leads to a technical justification for these outlying observations, probably in terms of inadequate QA/QC practices. Use of geochemical criteria indicates that the new mean values in WS-E might be closer to the "true" concentrations. This procedure of outlier detection and elimination is therefore recommended in the study of the existing RM.  相似文献   
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