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dc.contributor.authorArnold, Leavitt Clark, 1940-
dc.creatorArnold, Leavitt Clark, 1940-en
dc.date.accessioned2015-05-01T09:44:40Zen
dc.date.available2015-05-01T09:44:40Zen
dc.date.issued1964en
dc.identifier.urihttp://hdl.handle.net/10150/551760en
dc.description.abstractThis is a study of the supergene mineralogy of the San Xavier West mine located in the Pima mining district, Pima County, Arizona. The number and composition of secondary species collected are found to be closely related to the relative amounts of the various primary minerals and to the manner in which they were emplaced in the host rock. Supergene mineral species were selected that appeared to be in equilibrium with their environment, and certain assumptions are made concerning the stability fields of these minerals. The equilibrium conditions in most cases can be narrowed and often closely defined by combining the stability fields of several secondary minerals. On this basis, two acid environments and one alkaline environment are found to exist and are separable on the basis of mineralogy. The fields of chalcanthite and melanterite define a highly acid environment while those of goslarite and malachite define an environment of lower acidity. The association of calcite, rosasite, hemimorphite, and malachite indicate an alkaline environment. The acidity of the environments is principally determined by the amount of pyrite present, and pH may be lower than 3 if pyrite is abundant and reactive carbonate material lacking. Also, knowledge of stability relations allowed the history of enrichment and subsequent oxidation to be followed in a case where a transitional species has been removed from reaction by inclusions with gypsum.
dc.language.isoen_USen
dc.publisherThe University of Arizona.en
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en
dc.subjectMineralogy -- Arizona -- Pima County.en
dc.titleSupergene mineralogy and processes in the San Xavier mine area, Pima County, Arizonaen
dc.typetexten
dc.typeThesis-Reproduction (electronic)en
dc.identifier.oclc28562394en
thesis.degree.grantorUniversity of Arizonaen
thesis.degree.levelmastersen
thesis.degree.disciplineGraduate Collegeen
thesis.degree.nameM.S.en
dc.description.noteThis item was digitized from a paper original and/or a microfilm copy. If you need higher-resolution images for any content in this item, please contact us at repository@u.library.arizona.edu.en
dc.identifier.bibrecord.b28577681en
dc.identifier.callnumberE9791 1964 99en
refterms.dateFOA2018-06-18T17:55:05Z
html.description.abstractThis is a study of the supergene mineralogy of the San Xavier West mine located in the Pima mining district, Pima County, Arizona. The number and composition of secondary species collected are found to be closely related to the relative amounts of the various primary minerals and to the manner in which they were emplaced in the host rock. Supergene mineral species were selected that appeared to be in equilibrium with their environment, and certain assumptions are made concerning the stability fields of these minerals. The equilibrium conditions in most cases can be narrowed and often closely defined by combining the stability fields of several secondary minerals. On this basis, two acid environments and one alkaline environment are found to exist and are separable on the basis of mineralogy. The fields of chalcanthite and melanterite define a highly acid environment while those of goslarite and malachite define an environment of lower acidity. The association of calcite, rosasite, hemimorphite, and malachite indicate an alkaline environment. The acidity of the environments is principally determined by the amount of pyrite present, and pH may be lower than 3 if pyrite is abundant and reactive carbonate material lacking. Also, knowledge of stability relations allowed the history of enrichment and subsequent oxidation to be followed in a case where a transitional species has been removed from reaction by inclusions with gypsum.


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