1. Matrix Corrected SIMS In Situ Oxygen Isotope Analyses of Marine Shell Aragonite for High Resolution Seawater Temperature Reconstructions.
- Author
-
Medd, Oliver M., Otter, Laura M., Williams, Ian S., Stern, Richard A., Förster, Michael W., Eggins, Stephen M., Rodriguez‐Sanz, Laura, Abram, Nerilie J., He, Miaohong, Ellwood, Michael J., Hargreaves, Jessica A., Fallon, Stewart J., and Knowles, Brett M.
- Subjects
SECONDARY ion mass spectrometry ,OCEAN temperature ,OXYGEN isotopes ,STABLE isotope analysis ,SEAWATER composition - Abstract
Marine shells incorporate oxygen isotope signatures during growth, creating valuable records of seawater temperature and marine oxygen isotopic compositions. Secondary ion mass spectrometry (SIMS) measures these compositions in situ at finer length‐scales than traditional stable isotope analyses. However, determining oxygen isotope ratios in aragonite, the most common shell mineral, is hampered by a lack of ideal reference materials, limiting the accuracy of SIMS‐based seawater temperature reconstructions. Here, we tested the capability of SIMS to produce seawater temperature reconstructions despite the matrix calibration challenges associated with aragonite. We cultured Anadara trapezia bivalves at four controlled seawater temperatures (13–28°C) and used strontium labeling to mark the start of the temperature‐controlled shell increment, allowing for more spatially precise SIMS analysis. An improved matrix calibration was developed to ensure more accurate bio‐aragonite analyses that addressed matrix differences between the pure abiotic reference materials and the bio‐aragonite samples with intricate mineral‐organic architectures and distinct minor and trace element compositions. We regressed SIMS‐IRMS biases of abiotic and biogenic aragonites that account for their systematic differences in major, minor, and trace elements, allowing for more accurate SIMS analyses of the temperature‐controlled shell increment. The thorough matrix calibration allowed us to provide a SIMS‐based seawater‐corrected oxygen isotope thermometer of T(°C) = 23.05 ± 0.36 − 4.48 · (δ18Oaragonite [‰ VPDB] − δ18Oseawater [‰ VSMOW] ± 0.25) and 103lnαaragonite‐seawater = (17.78 ± 0.88) · 103/T (K) − (29.44 ± 2.40) that agrees with existing aragonitic IRMS‐based thermometer relationships and improves the applicability of SIMS‐based paleo‐environmental reconstructions of marine bio‐aragonites. Plain Language Summary: In this study, we grew marine bivalves under tightly constrained aquaculture conditions at four different seawater temperatures and marked the start of the growth period in the shell structure using strontium labeling. The newly grown shell material between the strontium‐labeled increment and the shell edge was analyzed for its oxygen isotopic composition. The compositions were measured in situ using a high resolution ion microprobe and a newly developed analytical post‐processing strategy specifically designed for biomineral samples with mineral‐organic architectures. The strategy involved two reference materials and the major, minor, and trace element content in the shell and the reference materials. The new approach resulted in an accurate and robust model for determining past seawater temperatures from fossil or historic shells based on their oxygen isotope composition at over an order of magnitude finer length scales than traditional oxygen isotope analyses. Key Points: Bivalve mollusks were cultured at different temperatures under tightly constrained seawater composition and environmental conditionsSIMS δ18O accuracy was improved with a new paired proxy‐like matrix bias correction using major, minor, and trace element abundancesThe first high‐resolution SIMS‐based stable oxygen isotope calibration for determining modern and ancient seawater temperatures is derived [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF