《Table 1 Statics of standard materials duringα-cellulose calibration》

《Table 1 Statics of standard materials duringα-cellulose calibration》   提示:宽带有限、当前游客访问压缩模式
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《Application and verification of simultaneous determination of cellulose δ~(13)C and δ~(18)O in Picea shrenkiana tree rings from northwestern China using the high-temperature pyrolysis method》


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Note:All of the stable isotopes are from the IAEA(International Atomic Energy Agency)products except for the values with a superscript letter.All of the work to calibrate the reference materials was conducted by at least two laboratories.a,the value was

We calibrated the stable isotope measurements using two methods:the multi-standard calibration and the two-point calibration(Evans et al.,2016).The runtime drift correction,amplitude correction,and bias correction in mean and deviation were conducted in the two-point calibration(Evans et al.,2016).In the multi-standard calibration,we compared the stable isotope values with the mean values from four standards with known values.Here,we used the Sigma-Aldrichα-cellulose standard and three IAEA(International Atomic Energy Agency)standards(IAEA-CH3 standard,benzoic acid IAEA 601,and IAEA-C3 standard)for the calibration(Table1).In the two-point calibration,we used two standard cellulose materials(Sigma-Aldrichα-cellulose and IAEA-CH3;Table 1),and performed the correction based on the mean difference between the measured values and the mean of these two known standard values.