<?xml version='1.0' encoding='utf-8'?>
<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>John T.G. Hamilton</dc:contributor>
  <dc:contributor>David B. Harper</dc:contributor>
  <dc:contributor>Laurence G. Miller</dc:contributor>
  <dc:contributor>Clare Lamb</dc:contributor>
  <dc:contributor>James T. Kennedy</dc:contributor>
  <dc:contributor>Angela Downey</dc:contributor>
  <dc:contributor>Sean McCauley</dc:contributor>
  <dc:contributor>Allen H. Goldstein</dc:contributor>
  <dc:creator>Robert M. Kalin</dc:creator>
  <dc:date>2001</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;Gas chromatography/mass spectrometry/isotope ratio mass spectrometry (GC/MS/IRMS) methods for &amp;delta;&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C measurement of the halomethanes CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;Cl, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;Br, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;I and methanethiol (CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;SH) during studies of their biological production, biological degradation, and abiotic reactions are presented. Optimisation of gas chromatographic parameters allowed the identification and quantification of CO&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;, O&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;Cl, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;Br, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;I and CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;SH from a single sample, and also the concurrent measurement of &amp;delta;&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C for each of the halomethanes and methanethiol. Precision of &amp;delta;&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C measurements for halomethane standards decreased (&amp;plusmn;0.3, &amp;plusmn;0.5 and &amp;plusmn;1.3&amp;permil;) with increasing mass (CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;Cl, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;Br, CH&lt;/span&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;span&gt;I, respectively). Given that carbon isotope effects during biological production, biological degradation and some chemical (abiotic) reactions can be as much as 100&amp;permil;, stable isotope analysis offers a precise method to study the global sources and sinks of these halogenated compounds that are of considerable importance to our understanding of stratospheric ozone destruction.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1002/rcm.219</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Wiley</dc:publisher>
  <dc:title>Continuous flow stable isotope methods for study of  δ&lt;sup&gt;13&lt;/sup&gt;C fractionation during halomethane production and degradation</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>