Diagenesis of 1900-year-old siliceous sinter (opal-A to quartz) at Opal Mound, Roosevelt Hot Springs, Utah, USA

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dc.contributor.author Lynne, Bridget en
dc.contributor.author Campbell, Kathleen en
dc.contributor.author Moore, JN en
dc.contributor.author Browne, Patrick en
dc.coverage.spatial Jackson Hole en
dc.date.accessioned 2014-11-02T22:37:33Z en
dc.date.issued 2005-08-15 en
dc.identifier.citation Sedimentary Geology, 2005, 179 (3-4), pp. 249 - 278 en
dc.identifier.issn 0037-0738 en
dc.identifier.uri http://hdl.handle.net/2292/23394 en
dc.description.abstract White, vitreous, siliceous sinter dated by C-14 at similar to 1900 years BP is located along the crest of the Opal Mound deposit at Roosevelt Hot Springs, Utah, U.S.A. Deposition at vents resulted from the Opal Mound fault opening conduits to the surface, allowing thermal fluids to discharge. Fault movement subsequently fractured the sinter and initiated a second period of fluid discharge. Colorful silica was deposited in this later period and formed the distal slope sinter, dated at similar to 1600 years BP. The sinter preserves both end-members in the mineralogical maturation of silica, from initial opal-A to mature quartz, and also records incremental intermediate steps, as revealed by X-ray powder diffractrometry and by scanning electron, optical and Raman laser microscopy. Textural and mineralogical changes from one silica phase to another transpired gradually and gradationally. During diagenesis, incremental morphological changes alternated three times through nano- to micro-particle size transitions. The three corresponding mineralogical steps comprise: (1) opal-A to opal-CT, (2) opal-CT to opal-C, and (3) opal-C to quartz. Mineralogical changes preceded all morphological changes. Each step was initiated when silica nanostructures reached a critical diameter of 200 nm. The initial starting point of fresh (modem), polymeric, siliceous sinter deposition worldwide is nano-spherical particles of colloidal opal-A. Opaline sinter at Opal Mound is slightly more mature, reflectmg the beginning of the aging process, and comprises botryoidal clusters of silica microspheres (< 8 mu m diameter). The conversion from these agglomerated microspheres to opal-CT bladed lepispheres at Opal Mound is marked by the reorganization of the microspheres into randomly oriented rows (similar to 800 nm in length) of aligned nanospheres, up to 200 nm diameter. Each row merges into joined beads, which sharpen into classic opal-CT morphology of bladed lepispheres (similar to 4 mu m diameter). During this first diagenetic step, the X-ray powder diffraction trace undergoes an early shift in peak position, from similar to 4.0 to 4.09 angstrom, lining itself up in the position of the next more advanced mineralogical state, prior to emergence of the classic opal-CT blades. In the second step, the bladed lepispheres subsequently change into rectangular nano-rods (similar to 50 x 100 nm long segments) during early opal-C development. During the third step of early quartz formation, the opal-C nano-rods recrystallize into groups of blocky nanostructures, each up to 200 x 300 nm. Quartz crystals grow at the expense of and pseudomorph opal-C, shown by remnant bands of blocky nanostructures at the base of the quartz crystals. Two generations of quartz crystals occur at Opal Mound: (1) diagenetic, which developed as opal-C nanostructures recrystallize to quartz; and (2) hydrothermal, formed by the injection ofWhite, vitreous, siliceous sinter dated by C-14 at similar to 1900 years BP is located along the crest of the Opal Mound deposit at Roosevelt Hot Springs, Utah, U.S.A. Deposition at vents resulted from the Opal Mound fault opening conduits to the surface, allowing thermal fluids to discharge. Fault movement subsequently fractured the sinter and initiated a second period of fluid discharge. Colorful silica was deposited in this later period and formed the distal slope sinter, dated at similar to 1600 years BP.The sinter preserves both end-members in the mineralogical maturation of silica, from initial opal-A to mature quartz, and also records incremental intermediate steps, as revealed by Xray powder diffractrometry and by scanning electron, optical and Raman laser microscopy. Textural and mineralogical changes from one silica phase to another transpired gradually and gradationally. During diagenesis, incremental morphological changes alternated three times through nano- to micro-particle size transitions. The three corresponding mineralogical steps comprise: (1) opal-A to opal-CT, (2) opal-CT to opal-C, and (3) opal-C to quartz. Mineralogical changes preceded all morphological changes. Each step was initiated when silica nanostructures reached a critical diameter of 200 nm. The initial starting point of fresh (modem), polymeric, siliceous sinter deposition worldwide is nano-spherical particles of colloidal opal-A. Opaline sinter at Opal Mound is slightly more mature, reflectmg the beginning of the aging process, and comprises botryoidal clusters of silica microspheres (< 8 mu m diameter). The conversion from these agglomerated microspheres to opal-CT bladed lepispheres at Opal Mound is marked by the reorganization of the microspheres into randomly oriented rows (similar to 800 nm in length) of aligned nanospheres, up to 200 nm diameter. Each row merges into joined beads, which sharpen into classic opal-CT morphology of bladed lepispheres (similar to 4 pm diameter). During this first diagenetic step, the X-ray powder diffraction trace undergoes an early shift in peak position, from similar to 4.0 to 4.09 A, lining itself up in the position of the next more advanced mineralogical state, prior to emergence of the classic opal-CT blades. In the second step, the bladed lepispheres subsequently change into rectangular nano-rods (similar to 50 x 100 nm long segments) during early opal-C development. During the third step of early quartz formation, the opal-C nano-rods recrystallize into groups of blocky nanostructures, each up to 200 x 300 nm. Quartz crystals grow at the expense of and pseudomorph opal-C, shown by remnant bands of blocky nanostructures at the base of the quartz crystals. Two generations of quartz crystals occur at Opal Mound: (1) diagenetic, which developed as opal-C nanostructures recrystallize to quartz; and (2) hydrothermal, formed by the injection of silica-infused thermal fluids into fractures and veins within the sinter deposit. Several silica phases commonly co-exist within individual samples. Moganite, a metastable silica phase, occurs with opal-CT, opal-C and diagenetic quartz, but is most abundant with opal-CT. Hence, the complete diagenetic continuum from opal-A to quartz is preserved within this sinter deposit. It formed in the short time span of <= 1900 years. (c) 2005 Elsevier B.V. All rights reserved. en
dc.language EN en
dc.publisher Elsevier Science en
dc.relation.ispartofseries Sedimentary Geology en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy http://www.sherpa.ac.uk/romeo/issn/0037-0738/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject siliceous sinter en
dc.subject diagenesis en
dc.subject Opal-A en
dc.subject Opal-CT en
dc.subject opal-C en
dc.subject moganite en
dc.subject quartz en
dc.subject silica phase en
dc.subject morphology en
dc.subject TAUPO VOLCANIC ZONE en
dc.subject YELLOWSTONE-NATIONAL-PARK en
dc.subject NEW-ZEALAND en
dc.subject NORTH-ISLAND en
dc.subject HYDROTHERMAL SYSTEM en
dc.subject LOW-TEMPERATURE en
dc.subject THERMAL AREA en
dc.subject MINERALS en
dc.subject RAMAN en
dc.subject MICROCRYSTALLINE en
dc.title Diagenesis of 1900-year-old siliceous sinter (opal-A to quartz) at Opal Mound, Roosevelt Hot Springs, Utah, USA en
dc.type Journal Article en
dc.identifier.doi 10.1016/j.sedgeo.2005.05.012 en
pubs.issue 3-4 en
pubs.begin-page 249 en
pubs.volume 179 en
dc.rights.holder Copyright: Elsevier Science en
pubs.end-page 278 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 47772 en
pubs.org-id Engineering en
pubs.org-id Engineering Science en
pubs.org-id Science en
pubs.org-id School of Environment en
pubs.record-created-at-source-date 2010-09-01 en


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