<?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>Y. Kolodny</dc:contributor>
  <dc:creator>David Z. Piper</dc:creator>
  <dc:date>1987</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;The stable isotopes of carbon and sulfur in a major marine sedimentary phosphate deposit from the northwestern United States (the Phosphoria Formation of Permian age) characterize the chemical properties of the depositional environment. The δ&lt;/span&gt;&lt;sup&gt;34&lt;/sup&gt;&lt;span&gt;S and δ&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C analyses suggest deposition under conditions of variable redox from a solution the acidity of which was controlled by reaction with carbonate rocks and exchange with seawater. The δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O concentration of apetite indicates phosphatization in a shallow sea, during three glacial and intervening interglacial stages. These data tend to corroborate the interpretation of field studies by others, that the apatite formed on a continental shelf in an area of intense oceanic upwelling during several episodes of sea level change.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1016/0198-0149(87)90044-6</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>The stable isotopic composition of a phosphorite deposit: δ13C, δ34S, and δ18O</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>