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Scientific Investigations Report 2008–5089

U.S. GEOLOGICAL SURVEY
Scientific Investigations Report 2008–5089

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Guidelines for Interpreting Results of Radiochemical Analyses

Concentrations of radionuclides are reported with an estimated sample standard deviation, s, which is obtained by propagating sources of analytical uncertainty in measurements. The following guidelines for interpreting analytical results are based on an extension of a method proposed by Currie (1984).

In the analysis for a particular radionuclide, laboratory measurements are made on a target sample and a prepared blank. Instrument signals for the sample and the blank vary randomly. Therefore, distinguishing between two key aspects of the problem of detection is essential: (1) the instrument signal for the sample must be larger than the signal observed for the blank before a decision can be made that the radionuclide was detected, and (2) an estimation must be made of the minimum radionuclide concentration that will yield a sufficiently large observed signal before a correct decision can be made for detection or nondetection of the radionuclide. The first aspect of the problem is a qualitative decision based on an observed signal and a definite criterion for detection. The second aspect of the problem is an estimation of the detection capabilities of a given measurement process.

In the laboratory, instrument signals must exceed a critical level of 1.6s, where s is the sample standard deviation, before the qualitative decision can be made as to whether the radionuclide was detected. At 1.6s, there is about a 95-percent probability that the correct conclusion—not detected—will be made. Given a large number of samples, as many as 5 percent of the samples with measured concentrations greater than or equal to 1.6s, concluded as detected, might not contain the radionuclide. These measurements are referred to as false positives and are errors of the first kind in hypothesis testing.

Once the critical level of 1.6s has been defined, the minimum detectable concentration may be determined. Concentrations that equal 3s represent a measurement at the minimum detectable concentration. For actual concentrations equal to or greater than 3s, there is a 95-percent or higher probability that the radionuclide was detected in a sample. In a large number of samples, the conclusion—not detected—will be made in 5 percent of the samples that contain actual concentrations at the minimum detectable concentration of 3s. These measurements are referred to as false negatives and are errors of the second kind in hypothesis testing.

Actual radionuclide concentrations between 1.6s and 3s have larger errors of the second kind. That is, there is a larger-than-5-percent probability of false negative results for samples with actual concentrations between 1.6s and 3s. Although the radionuclide might have been detected, such detection may not be considered reliable; at 1.6s, the probability of a false negative is about 50 percent.

The critical level and minimum detectable concentrations are based on counting statistics alone and do not include systematic or random errors inherent in laboratory procedures. The values 1.6s and 3s vary slightly with background or blank counts, with the number of gross counts for individual analyses, and for different radionuclides.

In this report, radionuclide concentrations less than 3s are considered less than a “reporting level.” The critical level, minimum detectable concentration, and reporting level aid the reader to interpret analytical results and do not represent absolute concentrations of radioactivity, which may or may not have been detected. Analytical uncertainties in this report are reported as 1s for consistency with conventions used in previous reports.

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