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Radioanalytical data interpretation when the ratio reading/median is lognormally distributed.

机译:比率读数/中位数呈对数正态分布时的放射分析数据解释。

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The purpose of this paper is to assist those who might be confronted by non-normal and non-homoscedastic error distributions representable by continuous probability density functions. Methods are presented to demonstrate how mathematical algorithms can be developed to obtain a "best fit" calibration line and how uncertainty ranges in interpretations of unknowns can be obtained from the calibration. The data used to demonstrate these methods were obtained from Brookhaven National Laboratory fission track analysis data for plutonium in urine. Examination of the variability in the fission track analysis data, during the period of time that the demonstration data were collected, revealed that the deviations from the mean were neither normal nor lognormal, but the ratios of tracks divided by the median at each plutonium level were lognormally distributed. Consequently, the differences between the logarithms of observed tracks and the median were normally distributed. The new "best fit" line was obtained by minimizing a reduced chi-square statistic made up of the squared differences in logarithms, divided by the variance in logarithms and degrees of freedom. Thus, to detect a worker urine sample to be above the 58-person "control" population 95 percentile [about 3.2 microBq (85 aCi)] at the 95% probability level (0.05 Type H error) would now require an average of about 11 microBq (300 aCi) per sample, compared to 5 microBq per sample (132 aCi per sample) in a previous paper. This paper presents the algorithms used to obtain the new calibration line and the uncertainty distributions of interpretations at various analyte levels. The importance of maintaining process control over the statistical interpretation of bioassay data as well as for the radiochemical procedures for achieving the lowest feasible level of detection is demonstrated.
机译:本文的目的是为那些可能会遇到由连续概率密度函数表示的非正态和非随机误差分布的人提供帮助。提出了一些方法来证明如何开发数学算法以获得“最佳拟合”校准线,以及如何从校准中获得不确定性解释的不确定性范围。用于证明这些方法的数据来自布鲁克海文国家实验室的尿中p裂变径迹分析数据。在收集示范数据的过程中,对裂变径迹分析数据的变化进行了检查,结果表明,与平均值的偏差既不是正常值也不是对数正态值,但是在每个p水平上,径迹比除以中位数即为对数正态分布。因此,观测轨迹的对数与中位数之间的差异呈正态分布。通过最小化由对数的平方差除以对数和自由度的方差组成的减少的卡方统计量来获得新的“最佳拟合”线。因此,要在95%的概率水平(0.05型H误差)下检测到工人尿液样本高于58个“对照”人群的95个百分位数[约3.2 microBq(85 aCi)],现在平均需要约11 microBq(300 aCi)每个样品,而之前的论文中每个样品5 microBq(132 aCi)。本文介绍了用于获取新校准线的算法以及各种分析物水平下解释的不确定性分布。证明了对生物测定数据的统计解释以及放射化学程序保持过程控制以实现最低可行检测水平的重要性。

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