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Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration
Raman spectroscopy of fine-grained hydrothermal alteration minerals, and phyllosilicates in particular, presents certain challenges. However, given the increasingly widespread recognition of field portable visible–near infrared–shortwave infrared (Vis-NIR-SWIR) spectroscopy as a valuable tool in the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649817/ https://www.ncbi.nlm.nih.gov/pubmed/34608818 http://dx.doi.org/10.1177/00037028211047869 |
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author | Arbiol, Carlos Layne, Graham D. |
author_facet | Arbiol, Carlos Layne, Graham D. |
author_sort | Arbiol, Carlos |
collection | PubMed |
description | Raman spectroscopy of fine-grained hydrothermal alteration minerals, and phyllosilicates in particular, presents certain challenges. However, given the increasingly widespread recognition of field portable visible–near infrared–shortwave infrared (Vis-NIR-SWIR) spectroscopy as a valuable tool in the mineral exploration industry, Raman microspectroscopy has promise as an approach for developing detailed complementary information on hydrothermal alteration phases in ore-forming systems. Here we present exemplar high-quality Raman and Vis-NIR-SWIR spectra of four key hydrothermal alteration minerals (pyrophyllite, white mica, chlorite, and alunite) that are common in precious metal epithermal systems, from deposits on the island of Newfoundland, Canada. The results reported here demonstrate that Raman microspectroscopy can accurately characterize pyrophyllite, white mica, chlorite, and alunite and provide details on their compositional variation at the microscale. In particular, spectral differences in the 1000–1150 cm(−1) white mica Raman band allows the distinction between low-Tschermak phases (muscovite, paragonite) and phases with higher degrees of Tschermak substitution (phengitic white mica composition). The peak position of the main chlorite Raman band shifts between 683 cm(−1) for Mg-rich chlorite and 665 cm(−1) for Fe-rich chlorite and can be therefore used for semiquantitative estimation of the Fe(2+) content in chlorite. Furthermore, while Vis-NIR-SWIR macrospectroscopy allows the rapid identification of the overall composition of the most abundant hydrothermal alteration mineral in a given sample, Raman microspectroscopy provides an in-depth spectral and chemical characterization of individual mineral grains, preserving the spatial and paragenetic context of each mineral and allowing for the distinction of chemical variation between (and within) different mineral grains. This is particularly useful in the case of alunite, white mica, and chlorite, minerals with extensive solid solution, where microscale characterization can provide information on the alteration zonation useful for mineral exploration and provide insight into mineral deposit genesis. |
format | Online Article Text |
id | pubmed-8649817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-86498172021-12-08 Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration Arbiol, Carlos Layne, Graham D. Appl Spectrosc Submitted Papers Raman spectroscopy of fine-grained hydrothermal alteration minerals, and phyllosilicates in particular, presents certain challenges. However, given the increasingly widespread recognition of field portable visible–near infrared–shortwave infrared (Vis-NIR-SWIR) spectroscopy as a valuable tool in the mineral exploration industry, Raman microspectroscopy has promise as an approach for developing detailed complementary information on hydrothermal alteration phases in ore-forming systems. Here we present exemplar high-quality Raman and Vis-NIR-SWIR spectra of four key hydrothermal alteration minerals (pyrophyllite, white mica, chlorite, and alunite) that are common in precious metal epithermal systems, from deposits on the island of Newfoundland, Canada. The results reported here demonstrate that Raman microspectroscopy can accurately characterize pyrophyllite, white mica, chlorite, and alunite and provide details on their compositional variation at the microscale. In particular, spectral differences in the 1000–1150 cm(−1) white mica Raman band allows the distinction between low-Tschermak phases (muscovite, paragonite) and phases with higher degrees of Tschermak substitution (phengitic white mica composition). The peak position of the main chlorite Raman band shifts between 683 cm(−1) for Mg-rich chlorite and 665 cm(−1) for Fe-rich chlorite and can be therefore used for semiquantitative estimation of the Fe(2+) content in chlorite. Furthermore, while Vis-NIR-SWIR macrospectroscopy allows the rapid identification of the overall composition of the most abundant hydrothermal alteration mineral in a given sample, Raman microspectroscopy provides an in-depth spectral and chemical characterization of individual mineral grains, preserving the spatial and paragenetic context of each mineral and allowing for the distinction of chemical variation between (and within) different mineral grains. This is particularly useful in the case of alunite, white mica, and chlorite, minerals with extensive solid solution, where microscale characterization can provide information on the alteration zonation useful for mineral exploration and provide insight into mineral deposit genesis. SAGE Publications 2021-10-05 2021-12 /pmc/articles/PMC8649817/ /pubmed/34608818 http://dx.doi.org/10.1177/00037028211047869 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Submitted Papers Arbiol, Carlos Layne, Graham D. Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration |
title | Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration |
title_full | Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration |
title_fullStr | Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration |
title_full_unstemmed | Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration |
title_short | Raman Spectroscopy Coupled with Reflectance Spectroscopy as a Tool for the Characterization of Key Hydrothermal Alteration Minerals in Epithermal Au–Ag Systems: Utility and Implications for Mineral Exploration |
title_sort | raman spectroscopy coupled with reflectance spectroscopy as a tool for the characterization of key hydrothermal alteration minerals in epithermal au–ag systems: utility and implications for mineral exploration |
topic | Submitted Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649817/ https://www.ncbi.nlm.nih.gov/pubmed/34608818 http://dx.doi.org/10.1177/00037028211047869 |
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