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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Joel Savarino</dc:contributor>
  <dc:contributor>J.K. Böhlke</dc:contributor>
  <dc:contributor>Mark Thiemens</dc:contributor>
  <dc:creator>Greg Michalski</dc:creator>
  <dc:date>2002</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;A thermal decomposition method was developed and tested for the simultaneous determination of δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O and δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο in nitrate. The thermal decomposition of AgNO&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt; allows for the rapid and accurate determination of &lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O/&lt;/span&gt;&lt;sup&gt;16&lt;/sup&gt;&lt;span&gt;O and &lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;O/&lt;/span&gt;&lt;sup&gt;16&lt;/sup&gt;&lt;span&gt;O isotopic ratios with a precision of ±1.5‰ for δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O and ±0.11‰ for Δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο (Δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο = δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο − 0.52 × δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O). The international nitrate isotope reference material IAEA-NO3 yielded a δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O value of +23.6‰ and Δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο of −0.2‰, consistent with normal terrestrial mass-dependent isotopic ratios. In contrast, a large sample of NaNO&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt; from the Atacama Desert, Chile, was found to have Δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο = 21.56 ± 0.11‰ and δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O = 54.9 ± 1.5‰, demonstrating a substantial mass-independent isotopic composition consistent with the proposed atmospheric origin of the desert nitrate. It is suggested that this sample (designated USGS-35) can be used to generate other gases (CO&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;, CO, N&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;O, O&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;) with the same Δ&lt;/span&gt;&lt;sup&gt;17&lt;/sup&gt;&lt;span&gt;Ο to serve as measurement references for a variety of applications involving mass-independent isotopic compositions in environmental studies.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1021/ac0256282</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>American Chemical Society</dc:publisher>
  <dc:title>Determination of the total oxygen isotopic composition of nitrate and the calibration of a Δ17Ο nitrate reference material</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>