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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. H. Hofstra</dc:contributor>
  <dc:creator>P. Emsbo</dc:creator>
  <dc:date>2003</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;The final event in a complicated hydrothermal history&amp;nbsp;&lt;/span&gt;at&lt;span&gt;&amp;nbsp;the&amp;nbsp;&lt;/span&gt;Meikle&lt;span&gt;&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;&amp;nbsp;&lt;/span&gt;deposit&lt;span&gt;&amp;nbsp;was&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;&amp;nbsp;deficient but caused extensive&amp;nbsp;&lt;/span&gt;postore&lt;span&gt;&amp;nbsp;&lt;/span&gt;dissolution&lt;span&gt;&amp;nbsp;of carbonate,&amp;nbsp;&lt;/span&gt;collapse&lt;span&gt;&amp;nbsp;brecciation, and precipitation of&amp;nbsp;&lt;/span&gt;calcite&lt;span&gt;&amp;nbsp;and&amp;nbsp;&lt;/span&gt;barite&lt;span&gt;&amp;nbsp;crystals in the resulting cavities. Although previously interpreted to be part of the&amp;nbsp;&lt;/span&gt;Carlin&lt;span&gt;-type hydrothermal system, crosscutting relationships and U-Th-Pb geochronology constrain this hydrothermal event to late Pliocene time (ca. 2 Ma), nearly 36 Ma after ore formation. Mineralogic, fluid inclusion, and stable isotope data indicate that&amp;nbsp;&lt;/span&gt;postore&lt;span&gt;&amp;nbsp;hydrothermal fluids were reduced, H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S-rich, unevolved meteoric waters ((δ&amp;nbsp;&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O = -17‰) of low temperature (ca. 65°C). The δ&amp;nbsp;&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O values of&amp;nbsp;&lt;/span&gt;barite&lt;span&gt;&amp;nbsp;and&amp;nbsp;&lt;/span&gt;calcite&lt;span&gt;&amp;nbsp;indicate that these minerals were in isotopic equilibrium, requiring that&amp;nbsp;&lt;/span&gt;barite&lt;span&gt;&amp;nbsp;SO&amp;nbsp;&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;was derived from the oxidation of reduced sulfur; however, preexisting sulfides in&amp;nbsp;&lt;/span&gt;breccia&lt;span&gt;&amp;nbsp;cavities were not oxidized. The δ&amp;nbsp;&lt;/span&gt;&lt;sup&gt;34&lt;/sup&gt;&lt;span&gt;S (15‰) values of&amp;nbsp;&lt;/span&gt;barite&lt;span&gt;&amp;nbsp;are higher than those of local bulk sulfide and supergene alunite indicating that SO&amp;nbsp;&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;was not derived from supergene oxidation of local sulfide minerals. The 15 per mil δ&amp;nbsp;&lt;/span&gt;&lt;sup&gt;34&lt;/sup&gt;&lt;span&gt;S value suggests that the H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S in the fluids may have been leached from sulfur-rich organic matter in the local carbonaceous sedimentary rocks. A reduced H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S-rich fluid is also supported by the bright cathodoluminescence of&amp;nbsp;&lt;/span&gt;calcite&lt;span&gt;&amp;nbsp;which indicates that it is Mn rich and Fe poor.&amp;nbsp;&lt;/span&gt;Calcite&lt;span&gt;&amp;nbsp;has a narrow range of δ&amp;nbsp;&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C values (0.3-1.8‰) that are indistinguishable from those of the host Bootstrap limestone, indicating that CO&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;&amp;nbsp;in the fluid was from&amp;nbsp;&lt;/span&gt;dissolution&lt;span&gt;&amp;nbsp;of the local limestone. These data suggest that&amp;nbsp;&lt;/span&gt;dissolution&lt;span&gt;&amp;nbsp;and brecciation of the Bootstrap limestone occurred where H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S-rich fluids encountered more oxidizing fluids and formed sulfuric acid (H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;SO&amp;nbsp;&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;). Intense fracturing in the mine area by previous structural and hydrothermal events probably provided conduits for the descent of oxidized surface water which mixed with the underlying H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S-rich waters to form the dissolving acid. The surface-derived fluid apparently contained sufficient oxygen to produce H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;SO&amp;nbsp;&lt;/span&gt;&lt;sub&gt;4&lt;/sub&gt;&lt;span&gt;&amp;nbsp;from H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S but not enough to alter pyrite to Fe oxide. Although H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S is an important&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;-transporting ligand, the temperature was too low to transport a significant amount of&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;. The presence of analogous&amp;nbsp;&lt;/span&gt;calcite&lt;span&gt;- and&amp;nbsp;&lt;/span&gt;barite&lt;span&gt;-lined cavities in other&amp;nbsp;&lt;/span&gt;Carlin&lt;span&gt;-type deposits suggests that the generation (and oxidation) of H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S-rich meteoric waters was a common phenomenon in north-central&amp;nbsp;&lt;/span&gt;Nevada&lt;span&gt;. Previous sulfur isotope studies have also shown that the Paleozoic sedimentary rocks were the principal source of H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S in Devonian sedimentary exhalative-type, Jurassic intrusion-related, Eocene&amp;nbsp;&lt;/span&gt;Carlin&lt;span&gt;-type, and Miocene low-sulfidation&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;&amp;nbsp;deposits in the region. The similar sulfur source in all of these systems suggests that basin brines, magmatic fluids, and meteoric waters all evolved to be H&amp;nbsp;&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;S-rich ore fluids by circulation through Paleozoic sedimentary rocks. Thus, although not directly related to&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;&amp;nbsp;mineralization, the recent hydrologic history of the&amp;nbsp;&lt;/span&gt;deposit&lt;span&gt;&amp;nbsp;provides important clues to earlier ore-forming processes that were responsible for&amp;nbsp;&lt;/span&gt;gold&lt;span&gt;&amp;nbsp;mineralization.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.2113/gsecongeo.98.6.1243</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Society of Economic Geologists</dc:publisher>
  <dc:title>Origin and significance of postore dissolution collapse breccias cemented with calcite and barite at the Meikle gold deposit, Northern Carlin trend, Nevada</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>