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电子探针X射线微分析法定量测定耳石膜中元素的标准:校准曲线和电子束灵敏度

Standards for quantification of elements in the otolithic membrane by electron probe X-ray microanalysis: calibration curves and electron beam sensitivity.

作者信息

López-Escámez J A, Crespo P V, Cañizares F J, Campos A

机构信息

Department of Histology and Cell Biology, Faculty of Medicine, University of Granada, Spain.

出版信息

J Microsc. 1993 Sep;171(Pt 3):215-22. doi: 10.1111/j.1365-2818.1993.tb03378.x.

DOI:10.1111/j.1365-2818.1993.tb03378.x
PMID:8246271
Abstract

An absolute quantitative standardization technique has been developed to measure Ca and K weight fractions (WF) in the otolithic membrane of the saccule and utricle by scanning electron microscopy and electron probe X-ray analysis using the peak-to-background (P/B) ratio method. Microcrystalline salt standards were used to calibrate Ca and K K alpha P/B or Y = (P/B).Z2/A (Z = atomic number; A = atomic weight) against WF at 10, 15, 20 and 25 kV accelerating voltage. The effect of voltage on the calibration, plotting the coefficient of correlation (r) as a function of voltage, was not dependent on the voltage in the range 10-25 kV for Ca standards. K standards were also independent when P/B was corrected for Z2/A. Background counts in the otoconia (Bo) were obtained at 5, 25, 50, 100, 200 and 500 s and used to test the electron beam sensitivity of saccular and utricular otoconia. Bo was not dependent on the spectra acquisition time, with the exception of Bo under K alpha K peak in the saccule at 10 kV. Ca and K WF were determined at 10, 15, 20 and 25 kV in the saccule and utricle, showing similar values regardless of the voltage used. This method of calibration offers several advantages, such as stability, homogeneity, known composition of the standards, high reproducibility at different voltages even without Z2/A correction and the similarity between the otoconia and crystal standards. We recommend the application of this method for other elements and biomineral systems.

摘要

已开发出一种绝对定量标准化技术,通过扫描电子显微镜和电子探针X射线分析,使用峰背比(P/B)法测量球囊和椭圆囊耳石膜中钙和钾的重量分数(WF)。使用微晶盐标准品在10、15、20和25 kV加速电压下,针对WF校准钙和钾的Kα P/B或Y = (P/B).Z2/A(Z = 原子序数;A = 原子量)。绘制相关系数(r)作为电压函数的校准电压效应,对于钙标准品而言,在10 - 25 kV范围内不依赖于电压。当P/B针对Z2/A进行校正时,钾标准品也具有独立性。在5、25、50、100、200和500秒时获取耳石中的背景计数(Bo),并用于测试球囊和椭圆囊耳石的电子束灵敏度。Bo不依赖于光谱采集时间,但在10 kV时球囊Kα K峰下的Bo除外。在10、15、20和25 kV下测定球囊和椭圆囊中钙和钾的WF,无论使用何种电压,显示的值相似。这种校准方法具有几个优点,例如稳定性、均匀性、标准品成分已知、即使不进行Z2/A校正,在不同电压下也具有高重现性以及耳石与晶体标准品之间的相似性。我们建议将此方法应用于其他元素和生物矿物系统。

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