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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>J. Li</dc:contributor>
  <dc:contributor>Ao Zhang</dc:contributor>
  <dc:contributor>Jihua Hao</dc:contributor>
  <dc:contributor>Shaunna M. Morrison</dc:contributor>
  <dc:contributor>Daniel Hummer</dc:contributor>
  <dc:contributor>Nathan Yee</dc:contributor>
  <dc:creator>Elisha Kelly Moore</dc:creator>
  <dc:date>2024</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;Uranium (U) is an important global energy resource and a redox sensitive trace element that reflects changing environmental conditions and geochemical cycling. The redox evolution of U mineral chemistry can be interrogated to understand the formation and distribution of U deposits and the redox processes involved in U geochemistry throughout Earth history. In this study, geochemical modeling using thermodynamic data, and mineral chemistry network analysis are used to investigate U geochemistry and deposition through time. The number of U&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;mineral localities surpasses the number of U&lt;/span&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;mineral localities in the Paleoproterozoic. Moreover, the number of sedimentary U&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;mineral localities increases earlier in the Phanerozoic than the number of U&lt;/span&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;sedimentary mineral localities, likely due to the necessity of sufficient sedimentary organic matter to reduce U&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;–U&lt;/span&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;span&gt;. Indeed, modeling calculations indicate that increased oxidative weathering due to surface oxygenation limited U&lt;/span&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;uraninite (UO&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;) formation from weathered granite and basalt. Louvain network community detection shows that U&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;forms minerals with many more shared elements and redox states than U&lt;/span&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;span&gt;. The range of weighted Mineral Element Electronegativity Coefficient of Variation (wMEE&lt;/span&gt;&lt;sub&gt;CV&lt;/sub&gt;&lt;span&gt;) values of U&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;minerals increases through time, particularly during the Phanerozoic. Conversely, the range of wMEE&lt;/span&gt;&lt;sub&gt;CV&lt;/sub&gt;&lt;span&gt;&amp;nbsp;values of U&lt;/span&gt;&lt;sup&gt;4+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;minerals is consistent through time due to the relative abundance of uraninite, coffinite, and brannerite. The late oxidation and formation of U&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;minerals compared to S&lt;/span&gt;&lt;sup&gt;6+&lt;/sup&gt;&lt;span&gt;&amp;nbsp;minerals illustrates the importance of the development of land plants, organic matter deposition, and redox-controlled U deposition from ground water in continental sediments during this time-period.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1029/2023GC011267</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>American Geophysical Union</dc:publisher>
  <dc:title>Uranium redox and deposition transitions embedded in deep-time geochemical models and mineral chemistry networks</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>