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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>A. Albertino</dc:contributor>
  <dc:contributor>P.E. Sauer</dc:contributor>
  <dc:contributor>H. Qi</dc:contributor>
  <dc:contributor>R. Molinie</dc:contributor>
  <dc:contributor>F. Mesnard</dc:contributor>
  <dc:creator>A. Schimmelmann</dc:creator>
  <dc:date>2009</dc:date>
  <dc:description>Accurate determinations of stable isotope ratios require a calibration using at least two reference materials with different isotopic compositions to anchor the isotopic scale and compensate for differences in machine slope. Ideally, the S values of these reference materials should bracket the isotopic range of samples with unknown S values. While the practice of analyzing two isotopically distinct reference materials is common for water (VSMOW-SLAP) and carbonates (NBS 19 and L-SVEC), the lack of widely available organic reference materials with distinct isotopic composition has hindered the practice when analyzing organic materials by elemental analysis/isotope ratio mass spectrometry (EA-IRMS). At present only L-glutamic acids USGS40 and USGS41 satisfy these requirements for ??&lt;sup&gt;13&lt;/sup&gt;C and ??&lt;sup&gt;13&lt;/sup&gt;N, with the limitation that L-glutamic acid is not suitable for analysis by gas chromatography (GC). We describe the development and quality testing of (i) four nicotine laboratory reference materials for on-line (i.e. continuous flow) hydrogen reductive gas chromatography-isotope ratio mass-spectrometry (GC-IRMS), (ii) five nicotines for oxidative C, N gas chromatography-combustion-isotope ratio mass-spectrometry (GC-C-IRMS, or GC-IRMS), and (iii) also three acetanilide and three urea reference materials for on-line oxidative EA-IRMS for C and N. Isotopic off-line calibration against international stable isotope measurement standards at Indiana University adhered to the 'principle of identical treatment'. The new reference materials cover the following isotopic ranges: ??&lt;sup&gt;2&lt;/sup&gt;H&lt;sub&gt;nicotine&lt;/sub&gt; -162 to -45%o, ??&lt;sup&gt;13&lt;/sup&gt;C&lt;sub&gt;nicotine&lt;/sub&gt; -30.05 to +7.72%, ?? &lt;sup&gt;15&lt;/sup&gt;N&lt;sub&gt;nicotine&lt;/sub&gt; -6.03 to +33.62%; ??&lt;sup&gt;15&lt;/sup&gt;N &lt;sub&gt;acetanilide&lt;/sub&gt; +1-18 to +40.57%; ??&lt;sup&gt;13&lt;/sup&gt;C&lt;sub&gt;urea&lt;/sub&gt; -34.13 to +11.71%, ??&lt;sup&gt;15&lt;/sup&gt;N&lt;sub&gt;urea&lt;/sub&gt; +0.26 to +40.61% (recommended ?? values refer to calibration with NBS 19, L-SVEC, IAEA-N-1, and IAEA-N-2). Nicotines fill a gap as the first organic nitrogen stable isotope reference materials for GC-IRMS that are available with different ??&lt;sup&gt;13&lt;/sup&gt;N values. Comparative ??&lt;sup&gt;13&lt;/sup&gt;C and ??&lt;sup&gt;15&lt;/sup&gt;N on-line EA-IRMS data from 14 volunteering laboratories document the usefulness and reliability of acetanilides and ureas as EA-IRMS reference materials.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1002/rcm.4277</dc:identifier>
  <dc:language>en</dc:language>
  <dc:title>Nicotine, acetanilide and urea multi-level&lt;sup&gt;2&lt;/sup&gt;H-,&lt;sup&gt;13&lt;/sup&gt;C- and&lt;sup&gt;15&lt;/sup&gt;N-abundance reference materials for continuous-flow isotope ratio mass spectrometry</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>