Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe

Detalhes bibliográficos
Autor(a) principal: Monteiro, H. S. [UNESP]
Data de Publicação: 2020
Outros Autores: Vasconcelos, P. M., Farley, K. A., Avila, J. N., Miller, H. B. D., Holden, P., Ireland, T. R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
DOI: 10.1016/j.chemgeo.2019.119436
Texto Completo: http://dx.doi.org/10.1016/j.chemgeo.2019.119436
http://hdl.handle.net/11449/196579
Resumo: We present protocols for high-spatial resolution measurement of oxygen isotope ratios of goethite (alpha-FeOOH) with the Sensitive High Mass Resolution Ion Microprobe - Stable Isotopes (SHRIMP-SI) and propose a natural sample as a potential goethite reference material (RM) for ion microprobe analysis. We assess the effects of goethite chemical composition, crystallographic orientation, and texture on the accuracy and repeatability of SHRIMP-SI delta O-18 (delta O-18(SIMS)) results. Synthetic goethites evaluated as potential delta O-18(SIMS) RM are powdery, porous, and finely crystalline; they do not yield repeatable results. A dense colloform goethite from the Capao topaz mine, Minas Gerais, Brazil, fulfills major prerequisites: it is stoichiometrically relatively pure, yields repeatable oxygen isotope results, and occurs in abundance to produce a RM for long-term use. We use an average laser fluorination delta O-18(LF-VSMOW) value of 17.3 0.3%o (1SD) obtained for five aliquots of this RM to normalize all delta O-18(SIMS) measurements. Multiple delta O-18(SIMS) analyses of a large fragment of the Capao L4 (CL4) RM analyzed in three different runs yield an overall repeatability of -17.3 +/- 0.5 parts per thousand (25D, n = 294) for all three runs combined. Natural variability and crystal orientation effects are the main reasons for the excess spread of the 8180sims results compared to the spot internal precision (ca. 0.2 parts per thousand). All delta O-18(SIMS) analyses (n = 1027) in various aliquots of CL4, randomly oriented and analyzed in 26 sessions during eight distinct runs, yield an overall repeatability of 17.3 +/- 0.7%0 (2SD), confirming that CL4 is a suitable SIMS RM. After ascertaining its suitability as a RM, we used CL4 to standardize analyses of other natural goethite samples with the SHRIMP-SI and compared delta O-18(SIMS) and laser fluorination results to test the relationship between natural properties (e.g., porosity, minor elements substituting for Fe), preparation procedures (e.g., polish and relief), instrument conditions, and the overall precision and accuracy of the SIMS analyses. Samples containing minor elements substituting for Fe (e.g., Al, Mn, Cu, Zn, etc.) or as contaminants (e.g., Si, P) require significant matrix corrections. Because we could not find homogenous natural goethite samples showing a large range in metal concentrations, we extrapolate our calibration curves beyond the composition of our calibration goethite samples. delta O-18(SIMS) results corrected for instrument mass fractionation (using CL4) and compositionally dependent matrix effects (using several calibration goethites of known elemental composition) are less precise but statistically indistinguishable from their laser fluorination results. However, porous samples are unsuitable for SHRIMP-SI delta O-18 analysis. Dense colloform samples yield repeatable results for individual growth bands, showing that the high spatial resolution, moderate precision, and speed of analysis of the SHRIMP-SI can resolve variations in oxygen isotope composition acquired during sample growth. (U-Th)/He geochronology of equivalent aliquots from the same goethite samples reveal that the combination of the two methods permits the extraction of temporal variation in the isotopic compositions of meteoric solutions in the geological past.
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spelling Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobeGoethiteSHRIMP-SI(U Th)/HeOxygen isotopesIon microprobeMatrix effectWe present protocols for high-spatial resolution measurement of oxygen isotope ratios of goethite (alpha-FeOOH) with the Sensitive High Mass Resolution Ion Microprobe - Stable Isotopes (SHRIMP-SI) and propose a natural sample as a potential goethite reference material (RM) for ion microprobe analysis. We assess the effects of goethite chemical composition, crystallographic orientation, and texture on the accuracy and repeatability of SHRIMP-SI delta O-18 (delta O-18(SIMS)) results. Synthetic goethites evaluated as potential delta O-18(SIMS) RM are powdery, porous, and finely crystalline; they do not yield repeatable results. A dense colloform goethite from the Capao topaz mine, Minas Gerais, Brazil, fulfills major prerequisites: it is stoichiometrically relatively pure, yields repeatable oxygen isotope results, and occurs in abundance to produce a RM for long-term use. We use an average laser fluorination delta O-18(LF-VSMOW) value of 17.3 0.3%o (1SD) obtained for five aliquots of this RM to normalize all delta O-18(SIMS) measurements. Multiple delta O-18(SIMS) analyses of a large fragment of the Capao L4 (CL4) RM analyzed in three different runs yield an overall repeatability of -17.3 +/- 0.5 parts per thousand (25D, n = 294) for all three runs combined. Natural variability and crystal orientation effects are the main reasons for the excess spread of the 8180sims results compared to the spot internal precision (ca. 0.2 parts per thousand). All delta O-18(SIMS) analyses (n = 1027) in various aliquots of CL4, randomly oriented and analyzed in 26 sessions during eight distinct runs, yield an overall repeatability of 17.3 +/- 0.7%0 (2SD), confirming that CL4 is a suitable SIMS RM. After ascertaining its suitability as a RM, we used CL4 to standardize analyses of other natural goethite samples with the SHRIMP-SI and compared delta O-18(SIMS) and laser fluorination results to test the relationship between natural properties (e.g., porosity, minor elements substituting for Fe), preparation procedures (e.g., polish and relief), instrument conditions, and the overall precision and accuracy of the SIMS analyses. Samples containing minor elements substituting for Fe (e.g., Al, Mn, Cu, Zn, etc.) or as contaminants (e.g., Si, P) require significant matrix corrections. Because we could not find homogenous natural goethite samples showing a large range in metal concentrations, we extrapolate our calibration curves beyond the composition of our calibration goethite samples. delta O-18(SIMS) results corrected for instrument mass fractionation (using CL4) and compositionally dependent matrix effects (using several calibration goethites of known elemental composition) are less precise but statistically indistinguishable from their laser fluorination results. However, porous samples are unsuitable for SHRIMP-SI delta O-18 analysis. Dense colloform samples yield repeatable results for individual growth bands, showing that the high spatial resolution, moderate precision, and speed of analysis of the SHRIMP-SI can resolve variations in oxygen isotope composition acquired during sample growth. (U-Th)/He geochronology of equivalent aliquots from the same goethite samples reveal that the combination of the two methods permits the extraction of temporal variation in the isotopic compositions of meteoric solutions in the geological past.Australian Research Council (ARC)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univ Estadual Paulista, Dept Planejamento Terr & Geoprocessamento, BR-13506900 Rio Claro, SP, BrazilUniv Queensland, Sch Earth & Environm Sci, Brisbane, Qld 4072, AustraliaAustralian Natl Univ, Res Sch Earth Sci, Canberra, ACT 2601, AustraliaCALTECH, Div Geol & Planetary Sci, Pasadena, CA 91125 USAUniv Estadual Paulista, Dept Planejamento Terr & Geoprocessamento, BR-13506900 Rio Claro, SP, BrazilAustralian Research Council (ARC): DP160104988Australian Research Council (ARC): LP1401008005Australian Research Council (ARC): LE0560868Elsevier B.V.Universidade Estadual Paulista (Unesp)Univ QueenslandAustralian Natl UnivCALTECHMonteiro, H. S. [UNESP]Vasconcelos, P. M.Farley, K. A.Avila, J. N.Miller, H. B. D.Holden, P.Ireland, T. R.2020-12-10T19:49:26Z2020-12-10T19:49:26Z2020-02-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article24http://dx.doi.org/10.1016/j.chemgeo.2019.119436Chemical Geology. Amsterdam: Elsevier, v. 533, 24 p., 2020.0009-2541http://hdl.handle.net/11449/19657910.1016/j.chemgeo.2019.119436WOS:000513871400025Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengChemical Geologyinfo:eu-repo/semantics/openAccess2021-10-23T08:18:26Zoai:repositorio.unesp.br:11449/196579Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:09:55.833307Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
title Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
spellingShingle Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
Monteiro, H. S. [UNESP]
Goethite
SHRIMP-SI
(U Th)/He
Oxygen isotopes
Ion microprobe
Matrix effect
Monteiro, H. S. [UNESP]
Goethite
SHRIMP-SI
(U Th)/He
Oxygen isotopes
Ion microprobe
Matrix effect
title_short Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
title_full Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
title_fullStr Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
title_full_unstemmed Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
title_sort Protocols for in situ measurement of oxygen isotopes in goethite by ion microprobe
author Monteiro, H. S. [UNESP]
author_facet Monteiro, H. S. [UNESP]
Monteiro, H. S. [UNESP]
Vasconcelos, P. M.
Farley, K. A.
Avila, J. N.
Miller, H. B. D.
Holden, P.
Ireland, T. R.
Vasconcelos, P. M.
Farley, K. A.
Avila, J. N.
Miller, H. B. D.
Holden, P.
Ireland, T. R.
author_role author
author2 Vasconcelos, P. M.
Farley, K. A.
Avila, J. N.
Miller, H. B. D.
Holden, P.
Ireland, T. R.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Univ Queensland
Australian Natl Univ
CALTECH
dc.contributor.author.fl_str_mv Monteiro, H. S. [UNESP]
Vasconcelos, P. M.
Farley, K. A.
Avila, J. N.
Miller, H. B. D.
Holden, P.
Ireland, T. R.
dc.subject.por.fl_str_mv Goethite
SHRIMP-SI
(U Th)/He
Oxygen isotopes
Ion microprobe
Matrix effect
topic Goethite
SHRIMP-SI
(U Th)/He
Oxygen isotopes
Ion microprobe
Matrix effect
description We present protocols for high-spatial resolution measurement of oxygen isotope ratios of goethite (alpha-FeOOH) with the Sensitive High Mass Resolution Ion Microprobe - Stable Isotopes (SHRIMP-SI) and propose a natural sample as a potential goethite reference material (RM) for ion microprobe analysis. We assess the effects of goethite chemical composition, crystallographic orientation, and texture on the accuracy and repeatability of SHRIMP-SI delta O-18 (delta O-18(SIMS)) results. Synthetic goethites evaluated as potential delta O-18(SIMS) RM are powdery, porous, and finely crystalline; they do not yield repeatable results. A dense colloform goethite from the Capao topaz mine, Minas Gerais, Brazil, fulfills major prerequisites: it is stoichiometrically relatively pure, yields repeatable oxygen isotope results, and occurs in abundance to produce a RM for long-term use. We use an average laser fluorination delta O-18(LF-VSMOW) value of 17.3 0.3%o (1SD) obtained for five aliquots of this RM to normalize all delta O-18(SIMS) measurements. Multiple delta O-18(SIMS) analyses of a large fragment of the Capao L4 (CL4) RM analyzed in three different runs yield an overall repeatability of -17.3 +/- 0.5 parts per thousand (25D, n = 294) for all three runs combined. Natural variability and crystal orientation effects are the main reasons for the excess spread of the 8180sims results compared to the spot internal precision (ca. 0.2 parts per thousand). All delta O-18(SIMS) analyses (n = 1027) in various aliquots of CL4, randomly oriented and analyzed in 26 sessions during eight distinct runs, yield an overall repeatability of 17.3 +/- 0.7%0 (2SD), confirming that CL4 is a suitable SIMS RM. After ascertaining its suitability as a RM, we used CL4 to standardize analyses of other natural goethite samples with the SHRIMP-SI and compared delta O-18(SIMS) and laser fluorination results to test the relationship between natural properties (e.g., porosity, minor elements substituting for Fe), preparation procedures (e.g., polish and relief), instrument conditions, and the overall precision and accuracy of the SIMS analyses. Samples containing minor elements substituting for Fe (e.g., Al, Mn, Cu, Zn, etc.) or as contaminants (e.g., Si, P) require significant matrix corrections. Because we could not find homogenous natural goethite samples showing a large range in metal concentrations, we extrapolate our calibration curves beyond the composition of our calibration goethite samples. delta O-18(SIMS) results corrected for instrument mass fractionation (using CL4) and compositionally dependent matrix effects (using several calibration goethites of known elemental composition) are less precise but statistically indistinguishable from their laser fluorination results. However, porous samples are unsuitable for SHRIMP-SI delta O-18 analysis. Dense colloform samples yield repeatable results for individual growth bands, showing that the high spatial resolution, moderate precision, and speed of analysis of the SHRIMP-SI can resolve variations in oxygen isotope composition acquired during sample growth. (U-Th)/He geochronology of equivalent aliquots from the same goethite samples reveal that the combination of the two methods permits the extraction of temporal variation in the isotopic compositions of meteoric solutions in the geological past.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-10T19:49:26Z
2020-12-10T19:49:26Z
2020-02-05
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.chemgeo.2019.119436
Chemical Geology. Amsterdam: Elsevier, v. 533, 24 p., 2020.
0009-2541
http://hdl.handle.net/11449/196579
10.1016/j.chemgeo.2019.119436
WOS:000513871400025
url http://dx.doi.org/10.1016/j.chemgeo.2019.119436
http://hdl.handle.net/11449/196579
identifier_str_mv Chemical Geology. Amsterdam: Elsevier, v. 533, 24 p., 2020.
0009-2541
10.1016/j.chemgeo.2019.119436
WOS:000513871400025
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Chemical Geology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 24
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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dc.identifier.doi.none.fl_str_mv 10.1016/j.chemgeo.2019.119436