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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>Peter B. Larson</dc:contributor>
  <dc:contributor>Michael A. Cosca</dc:contributor>
  <dc:creator>Allen K. Andersen</dc:creator>
  <dc:date>2019</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;The&amp;nbsp;carbonatite&amp;nbsp;dike swarm&amp;nbsp;and vein stockwork at the center of the&amp;nbsp;Paleogene&amp;nbsp;Bear Lodge alkaline complex (BLAC), Wyoming, USA, is host to diverse&amp;nbsp;REE&amp;nbsp;mineral assemblages that are largely a result of subsolidus modification and REE redistribution. Pseudomorphic replacement of primary burbankite by an assemblage of ancylite, strontianite, and&amp;nbsp;barite&amp;nbsp;is the result of interaction with late-stage&amp;nbsp;hydrothermal fluids&amp;nbsp;that added Sr, Ba, S, F, and REE, analogous to the replacement processes described for some carbonatite complexes of Russia's Kola Peninsula. Carbon and oxygen&amp;nbsp;stable isotope&amp;nbsp;ratios indicate that the primary carbonatite&amp;nbsp;mineralogy&amp;nbsp;experienced degassing/pneumatolysis and alteration by fluids of variable temperature, CO&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;/H&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;O ratios, and/or&amp;nbsp;meteoric water&amp;nbsp;content. Isotopic differences of matrix&amp;nbsp;calcite&amp;nbsp;between Group 1 carbonatites (avg. δ&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C = −7.3‰; δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O = 9.1‰) and Group 2 carbonatites (avg. δ&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C = −9.9‰; δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O = 10.2‰) are consistent with loss of CO&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;&amp;nbsp;during&amp;nbsp;degassing. The open-system alteration of burbankite caused a pronounced positive δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O-shift in bulk ancylite&amp;nbsp;pseudomorphs&amp;nbsp;(δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O: 14.3–25.7‰) relative to matrix calcite (δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O: 8.7–11.2‰).&amp;nbsp;Oxygen isotope&amp;nbsp;compositions of&amp;nbsp;biotite&amp;nbsp;(δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O: 4.5–5.9‰) and K-feldspar (δ&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O: 7.3–7.9‰) in unoxidized carbonatite are typical of primary magmatic&amp;nbsp;silicates&amp;nbsp;and suggest that fluids responsible for the burbankite-to-ancylite conversion remained predominantly magmatic (carbohydrothermal). Concomitant increases toward the surface in&amp;nbsp;&lt;/span&gt;&lt;sup&gt;13&lt;/sup&gt;&lt;span&gt;C and&amp;nbsp;&lt;/span&gt;&lt;sup&gt;18&lt;/sup&gt;&lt;span&gt;O,&amp;nbsp;oxidation, matrix carbonate dissolution, and the replacement of REE carbonates (ancylite, carbocernaite, and burbankite) by Ca-REE fluorocarbonates (bastnäsite, parisite, synchysite) suggest interaction with late-stage, low temperature (&amp;lt;250 °C) fluids characterized by lower CO&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;/H&lt;/span&gt;&lt;sub&gt;2&lt;/sub&gt;&lt;span&gt;O ratios, and an increasing meteoric water component. The first&amp;nbsp;&lt;/span&gt;&lt;sup&gt;40&lt;/sup&gt;&lt;span&gt;Ar/&lt;/span&gt;&lt;sup&gt;39&lt;/sup&gt;&lt;span&gt;Ar ages from carbonatite-hosted biotite and K-feldspar at the BLAC are between 51.45 ± 0.08 and 51.89 ± 0.14 Ma. Although carbonatite is commonly observed as the final intrusive phase in alkaline igneous complexes, relative-age relationships and previously published&amp;nbsp;geochronology&amp;nbsp;for Bear Lodge rocks indicate that alkaline silicate&amp;nbsp;magmatism&amp;nbsp;both preceded and followed carbonatite&amp;nbsp;emplacement.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1016/j.lithos.2018.11.030</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>C–O stable isotope geochemistry and 40Ar/39Ar geochronology of the Bear Lodge carbonatite stockwork, Wyoming, USA</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>