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Fitzsimons, I. C. W., Harte, B., Clark, R. M. (2000) SIMS stable isotope measurement: counting statistics and analytical precision. Mineralogical Magazine, 64 (1) 59-83 doi:10.1180/002646100549139

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Reference TypeJournal (article/letter/editorial)
TitleSIMS stable isotope measurement: counting statistics and analytical precision
JournalMineralogical Magazine
AuthorsFitzsimons, I. C. W.Author
Harte, B.Author
Clark, R. M.Author
Year2000 (February)Volume64
Issue1
PublisherMineralogical Society
DOIdoi:10.1180/002646100549139Search in ResearchGate
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Mindat Ref. ID243144Long-form Identifiermindat:1:5:243144:8
GUID0
Full ReferenceFitzsimons, I. C. W., Harte, B., Clark, R. M. (2000) SIMS stable isotope measurement: counting statistics and analytical precision. Mineralogical Magazine, 64 (1) 59-83 doi:10.1180/002646100549139
Plain TextFitzsimons, I. C. W., Harte, B., Clark, R. M. (2000) SIMS stable isotope measurement: counting statistics and analytical precision. Mineralogical Magazine, 64 (1) 59-83 doi:10.1180/002646100549139
Abstract/NotesAbstractAnalytical precision is vital in the interpretation of stable isotope data collected by secondary ion mass spectrometry (SIMS) given the small analysis volumes and the small magnitude of natural isotopic variations. The observed precision of a set of measurements is represented by the standard deviation(precision of an individual measurement) or the standard error of the mean (precision of the mean value). The SIMS data show both systematic variations with time and random Poisson variability, but the former largely cancel out when data for two different isotopes are expressed as a ratio. The precision of a SIMS isotope ratio routinely matches that predicted by Poisson counting statistics and can approach that of conventional bulk analysis techniques for counting times of several hours. All sample analyse must be calibrated for instrumental mass fractionation using SIMS analyses of a standard material. There is often a gradual drift in the mass fractionation with time, but this can be modelled by least-squares regression of the standard isotope ratios. Drift in the sample analyses is eliminated by using the relevant point on this regression line to calibrate each sample. The final precision of a corrected isotope ratio must take into account the scatter in both the sample and the standard data.


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