<?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>Richard L. Reynolds</dc:contributor>
  <dc:contributor>Robert O. Rye</dc:contributor>
  <dc:creator>Martin B. Goldhaber</dc:creator>
  <dc:date>1978</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;Petrologic and sulfur isotopic studies have been carried out on drill core samples from a roll-type uranium deposit in the mid-Tertiary Catahoula Tuff, Webb County, south Texas. Epigenetic iron disulfide minerals formed in two distinct stages. The first stage involved sulfidization of the host rock by sulfide (H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;&amp;nbsp;S, HS-)-bearing solutions that emanated from a fault about 1.5 km downdip from and subparallel to the orebody. Pyrite was the dominant iron disulfide mineral formed from this fault sulfide. The isotopic composition (delta&amp;nbsp;&lt;/span&gt;&lt;sup&gt;34&lt;/sup&gt;&lt;span&gt;&amp;nbsp;S) of first-stage iron disulfide is quite heavy (&amp;gt;0 per mil), in part because the fault-derived H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;&amp;nbsp;S was isotopically heavy. The development of the second-stage sulfides was related to processes that formed the uranium roll. Iron disulfide minerals produced during this second stage commonly occur as rims around the first-stage sulfides. The rims are exclusively marcasite in and adjacent to ore, but the pyrite content in these rims increases with increasing distance from ore. The sulfur of the second-stage sulfides in the vicinity of the roll front is isotopically light (--25 to --40 per mil). The virtual absence of organic carbon in the host sand precludes a bacterial origin for the ore-stage iron disulfide minerals and, therefore, eliminates bacterial metabolism as the mechanism for isotopic fractionation. Instead, the sulfur source for ore-stage sulfides was preore (first stage) sulfides, remobilized via partial oxidation to soluble metastable sulfur oxyanions.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.2113/gsecongeo.73.8.1690</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Society of Economic Geologists</dc:publisher>
  <dc:title>Origin of a South Texas roll-type deposit; II, Sulfide petrology and sulfur isotope studies</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>