Barite, Anhydrite and Gypsum Reference Materials for In Situ Oxygen and Sulfur Isotope Ratio Measurements

Author:

Li Bin12ORCID,Wiedenbeck Michael1,Couffignal Frédéric1,Álvarez‐Valero Antonio M.3,Bao Hui‐Ming4,Fan Chang‐Fu5,Han Juan6,Jin Gui‐Shan6,Peng Yong‐Bo4,Syczewski Marcin Daniel1,Tait Kimberly T.78,Wilke Franziska D.H.1,Wortmann Ulrich G.8

Affiliation:

1. GFZ German Research Centre for Geosciences Telegrafenberg, 14473 Potsdam Germany

2. Key Laboratory of Metallogenic Prediction of Nonferrous Metals and Geological Environment Monitoring (Ministry of Education), School of Geosciences and Info‐Physics Central South University Changsha 410083 P.R. China

3. Departamento de Geología Universidad de Salamanca 37008 Salamanca Spain

4. International Center for Isotope Effects Research and School of Earth Sciences and Engineering Nanjing University Nanjing 210093 P.R. China

5. MLR Key Laboratory of Metallogeny and Mineral Assessment, Institute of Mineral Resources Chinese Academy of Geological Sciences Beijing 100037 China

6. Beijing Research Institute of Uranium Geology Beijing 100029 China

7. Department of Natural History Royal Ontario Museum Toronto ON M5S 2C6 Canada

8. Department of Earth Sciences University of Toronto 22 Ursula Franklin St., Toronto Ontario M5S 3B1 Canada

Abstract

Secondary ion mass spectrometry was used to test the δ18O and δ34S nanogram‐scale homogeneity of a suite of candidate sulfate minerals, ultimately selecting three barite, two anhydrite, and two gypsum samples from the Royal Ontario Museum that have repeatabilities for their SIMS measurements of better than ±0.39‰ and ±0.37‰ (1s) for oxygen and sulfur isotope ratios, respectively. Metrological splits of each of the seven materials were sent to multiple gas source isotope ratio mass spectrometry laboratories in order to establish their absolute 18O/16O and 34S/32S ratios. The inter‐laboratory results of GS‐IRMS analyses yielded reasonably narrow ranges in δ18OVSMOW, whereas larger variations in δ34SVCDT values were found between the results from the gas source laboratories. All samples have good reproducibility within laboratories of GS‐IRMS 103δ18O values of between ±0.24‰ and ±0.44‰ (1s). The reproducibility within laboratories of GS‐IRMS 103δ34S values range from ±0.07‰ to ±0.99‰ (1s). Here we also discuss some of the current analytical limitations affecting these isotope‐mineral systems. A total of 256 metrological splits have been prepared from each of these seven materials; these aliquots will be made available to the global geochemical community.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Geochemistry and Petrology,Geology,Geochemistry and Petrology,Geology

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