nerc.ac.uk

Improving the routine analysis of siderite for δ 13 C and δ 18 O in environmental change research

Lacey, J.H.; Sloane, H.J.; Leng, M.J. ORCID: https://orcid.org/0000-0003-1115-5166; Crowley, S.F.. 2023 Improving the routine analysis of siderite for δ 13 C and δ 18 O in environmental change research. Rapid Communications in Mass Spectrometry, 37 (6), e9456. 10.1002/rcm.9456

Before downloading, please read NORA policies.
[thumbnail of Open Access Paper]
Preview
Text (Open Access Paper)
Rapid Comm Mass Spectrometry - 2022 - Lacey - Improving the routine analysis of siderite for 13C and 18O in environmental.pdf - Published Version
Available under License Creative Commons Attribution 4.0.

Download (2MB) | Preview

Abstract/Summary

Rationale The carbon (δ13C) and oxygen (δ18O) isotope composition of siderite (FeCO3) is used widely to understand and quantify geochemical processes in order to reconstruct past climate and environmental change. However, few laboratories follow precisely the same protocol for the preparation and analysis of siderite-bearing materials, which combined with the absence of international reference materials and mineral-specific acid fractionation factors, leads potentially to significant differences in isotope data generated by individual laboratories. Here we examine procedures for the isotope analysis of siderite and discuss factors potentially contributing to inconsistencies in sample measurement data. Methods Isotope analysis of siderite is first assessed using similar versions of the classical off-line, sealed vessel acid digestion method by comparing data sets obtained from intercomparison materials measured at two participating laboratories. We then compare data from the classical method against those generated using an automated preparation technique using data produced from an independent set of test materials. Results Measurement of siderite δ13C is generally both repeatable and reproducible, but measurement of δ18O may be subject to large (~1 ‰), method-dependent bias for siderite reacted at differing temperatures (70 °C and 100 °C) under classical and automated CO2 preparation conditions. The potential for poor oxygen isotope measurement reproducibility is amplified by local differences in sample preparation protocols and procedures used to calibrate measurement data to international reference scales. Conclusions We offer suggestions for improving the repeatability and reproducibility of δ13C and δ18O analysis on siderite. The challenge of producing consistent isotope data from siderite can only be resolved by ensuring the availability of siderite reference materials to facilitate identical treatment as a basis for minimising method-dependent contributions to data inconsistency between laboratories.

Item Type: Publication - Article
Digital Object Identifier (DOI): 10.1002/rcm.9456
ISSN: 0951-4198
Date made live: 10 Jan 2023 12:51 +0 (UTC)
URI: https://nora.nerc.ac.uk/id/eprint/533850

Actions (login required)

View Item View Item

Document Downloads

Downloads for past 30 days

Downloads per month over past year

More statistics for this item...