Spectral analysis software improves confidence in plant and soil water stable isotope analyses performed by isotope ratio infrared spectroscopy (IRIS)

被引:83
作者
West, A. G. [1 ]
Goldsmith, G. R. [2 ]
Matimati, I. [1 ]
Dawson, T. E. [2 ,3 ]
机构
[1] Univ Cape Town, Dept Bot, ZA-7701 Rondebosch, South Africa
[2] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Ctr Stable Isotope Biogeochem, Berkeley, CA 94720 USA
基金
美国安德鲁·梅隆基金会;
关键词
RING-DOWN SPECTROSCOPY; MASS-SPECTROMETRY; HYDROGEN; DISCREPANCIES; DELTA-O-18; SAMPLES;
D O I
10.1002/rcm.5126
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Previous studies have demonstrated the potential for large errors to occur when analyzing waters containing organic contaminants using isotope ratio infrared spectroscopy (IRIS). In an attempt to address this problem, IRIS manufacturers now provide post-processing spectral analysis software capable of identifying samples with the types of spectral interference that compromises their stable isotope analysis. Here we report two independent tests of this post-processing spectral analysis software on two IRIS systems, OA-ICOS (Los Gatos Research Inc.) and WS-CRDS (Picarro Inc.). Following a similar methodology to a previous study, we cryogenically extracted plant leaf water and soil water and measured the delta(2)H and delta(18)O values of identical samples by isotope ratio mass spectrometry (IRMS) and IRIS. As an additional test, we analyzed plant stem waters and tap waters by IRMS and IRIS in an independent laboratory. For all tests we assumed that the IRMS value represented the "true" value against which we could compare the stable isotope results from the IRIS methods. Samples showing significant deviations from the IRMS value (>2 sigma) were considered to be contaminated and representative of spectral interference in the IRIS measurement. Over the two studies, 83% of plant species were considered contaminated on OA-ICOS and 58% on WS-CRDS. Post-analysis, spectra were analyzed using the manufacturer's spectral analysis software, in order to see if the software correctly identified contaminated samples. In our tests the software performed well, identifying all the samples with major errors. However, some false negatives indicate that user evaluation and testing of the software are necessary. Repeat sampling of plants showed considerable variation in the discrepancies between IRIS and IRMS. As such, we recommend that spectral analysis of IRIS data must be incorporated into standard post-processing routines. Furthermore, we suggest that the results from spectral analysis be included when reporting stable isotope data from IRIS. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:2268 / 2274
页数:7
相关论文
共 14 条
[1]
New methods for fully automated isotope ratio determination from hydrogen at the natural abundance level [J].
Brand, WA ;
Avak, H ;
Seedorf, R ;
Hofmann, D ;
Conradi, T .
ISOTOPES IN ENVIRONMENTAL AND HEALTH STUDIES, 1996, 32 (2-3) :263-273
[2]
Comments on "Discrepancies between isotope ratio infrared spectroscopy and isotope ratio mass spectrometry for the stable isotope analysis of plant and soil waters" [J].
Brand, Willi A. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2010, 24 (17) :2687-2688
[3]
Cavity ring-down spectroscopy versus high-temperature conversion isotope ratio mass spectrometry; a case study on δ2H and δ18O of pure water samples and alcohol/water mixtures [J].
Brand, Willi A. ;
Geilmann, Heike ;
Crosson, Eric R. ;
Rella, Chris W. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2009, 23 (12) :1879-1884
[4]
Comprehensive inter-laboratory calibration of reference materials for δ18O versus VSMOW using various on-line high-temperature conversion techniques [J].
Brand, Willi A. ;
Coplen, Tyler B. ;
Aerts-Bijma, Anita T. ;
Boehlke, J. K. ;
Gehre, Matthias ;
Geilmann, Heike ;
Groening, Manfred ;
Jansen, Henk G. ;
Meijer, Harro A. J. ;
Mroczkowski, Stanley J. ;
Qi, Haiping ;
Soergel, Karin ;
Stuart-Williams, Hilary ;
Weise, Stephan M. ;
Werner, Roland A. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2009, 23 (07) :999-1019
[5]
REDUCTION OF WATER WITH ZINC FOR HYDROGEN ISOTOPE ANALYSIS [J].
COLEMAN, ML ;
SHEPHERD, TJ ;
DURHAM, JJ ;
ROUSE, JE ;
MOORE, GR .
ANALYTICAL CHEMISTRY, 1982, 54 (06) :993-995
[6]
*GAT RES INC, 2010, LWIA SPECTR CONT ID
[7]
Sample preparation device for quantitative hydrogen isotope analysis using chromium metal [J].
Gehre, M ;
Hoefling, R ;
Kowski, P ;
Strauch, G .
ANALYTICAL CHEMISTRY, 1996, 68 (24) :4414-4417
[8]
Demonstration of high-precision continuous measurements of water vapor isotopologues in laboratory and remote field deployments using wavelength-scanned cavity ring-down spectroscopy (WS-CRDS) technology [J].
Gupta, Priya ;
Noone, David ;
Galewsky, Joseph ;
Sweeney, Colm ;
Vaughn, Bruce H. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2009, 23 (16) :2534-2542
[9]
High-precision laser spectroscopy D/H and 18O/16O measurements of microliter natural water samples [J].
Lis, G. ;
Wassenaar, L. I. ;
Hendry, M. J. .
ANALYTICAL CHEMISTRY, 2008, 80 (01) :287-293
[10]
*PIC INC, 2010, WHIT PAP CHEMC SOLV