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硝酸盐中的氧同位素:用于¹⁸O:¹⁷O:¹⁶O测量的新型参考物质以及硝酸盐 - 水同位素平衡观测

Oxygen isotopes in nitrate: new reference materials for 18O:17O:16O measurements and observations on nitrate-water equilibration.

作者信息

Böhlke J K, Mroczkowski S J, Coplen T B

机构信息

US Geological Survey, 431 National Center, Reston, VA 20192, USA.

出版信息

Rapid Commun Mass Spectrom. 2003;17(16):1835-46. doi: 10.1002/rcm.1123.

Abstract

Despite a rapidly growing literature on analytical methods and field applications of O isotope-ratio measurements of NO(3)(-) in environmental studies, there is evidence that the reported data may not be comparable because reference materials with widely varying delta(18)O values have not been readily available. To address this problem, we prepared large quantities of two nitrate salts with contrasting O isotopic compositions for distribution as reference materials for O isotope-ratio measurements: USGS34 (KNO(3)) with low delta(18)O and USGS35 (NaNO(3)) with high delta(18)O and 'mass-independent' delta(17)O. The procedure used to produce USGS34 involved equilibration of HNO(3) with (18)O-depleted meteoric water. Nitric acid equilibration is proposed as a simple method for producing laboratory NO(3)(-) reference materials with a range of delta(18)O values and normal (mass-dependent) (18)O:(17)O:(16)O variation. Preliminary data indicate that the equilibrium O isotope-fractionation factor (alpha) between [NO(3)(-)] and H(2)O decreases with increasing temperature from 1.0215 at 22 degrees C to 1.0131 at 100 degrees C. USGS35 was purified from the nitrate ore deposits of the Atacama Desert in Chile and has a high (17)O:(18)O ratio owing to its atmospheric origin. These new reference materials, combined with previously distributed NO(3) (-) isotopic reference materials IAEA-N3 (=IAEA-NO-3) and USGS32, can be used to calibrate local laboratory reference materials for determining offset values, scale factors, and mass-independent effects on N and O isotope-ratio measurements in a wide variety of environmental NO(3)(-) samples. Preliminary analyses yield the following results (normalized with respect to VSMOW and SLAP, with reproducibilities of +/-0.2-0.3 per thousand, 1sigma): IAEA-N3 has delta(18)O = +25.6 per thousand and delta(17)O = +13.2 per thousand; USGS32 has delta(18)O = +25.7 per thousand; USGS34 has delta(18)O = -27.9 per thousand and delta(17)O = -14.8 per thousand; and USGS35 has delta(18)O = +57.5 per thousand and delta(17)O = +51.5 per thousand.

摘要

尽管关于环境研究中硝酸根(NO₃⁻)氧同位素比值测量的分析方法和现场应用的文献迅速增加,但有证据表明,所报告的数据可能无法进行比较,因为具有广泛不同δ¹⁸O值的参考物质不易获得。为了解决这个问题,我们制备了大量两种氧同位素组成不同的硝酸盐作为氧同位素比值测量的参考物质进行分发:低δ¹⁸O的USGS34(KNO₃)和高δ¹⁸O及“质量无关”δ¹⁷O的USGS35(NaNO₃)。制备USGS34所采用的方法涉及硝酸(HNO₃)与贫¹⁸O的大气降水的平衡。硝酸平衡被提议作为一种简单方法,用于制备具有一系列δ¹⁸O值以及正常(质量依赖)¹⁸O:¹⁷O:¹⁶O变化的实验室硝酸根(NO₃⁻)参考物质。初步数据表明,[NO₃⁻]与H₂O之间的平衡氧同位素分馏因子(α)随温度升高而降低,从22℃时的1.0215降至100℃时的1.0131。USGS35是从智利阿塔卡马沙漠的硝酸盐矿床中提纯得到的,由于其大气来源,具有较高的¹⁷O:¹⁸O比值。这些新的参考物质,与先前分发的硝酸根(NO₃⁻)同位素参考物质IAEA - N3(=IAEA - NO - 3)和USGS32相结合,可用于校准当地实验室参考物质,以确定各种环境硝酸根(NO₃⁻)样品中氮和氧同位素比值测量的偏移值、比例因子以及质量无关效应。初步分析得出以下结果(相对于VSMOW和SLAP进行归一化,重复性为±0.2 - 0.3‰,1σ):IAEA - N3的δ¹⁸O = +25.6‰,δ¹⁷O = +13.2‰;USGS32的δ¹⁸O = +25.7‰;USGS34的δ¹⁸O = -27.9‰,δ¹⁷O = -14.8‰;USGS35的δ¹⁸O = +57.5‰,δ¹⁷O = +51.5‰。

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