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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]

Radiocarbon dates on charred plant remains are often used to define the chronology of archives such as lake cores and fluvial sequences. However, charcoal is often older than its depositional context because old-wood can be burnt and a range of transport and storage stages exist between the woodland and stream or lake bed ("inherited age"). In 1978, Blong and Gillespie dated four size fractions of charcoal found floating or saltating in the Macdonald River, Australia. They found larger fragments gave younger age estimates, raising the possibility that taphonomic modifications could help identify the youngest fragments. In 1978 each date required 1000s charcoal fragments. This study returns to a sample from the Macdonald River to date individual charcoal fragments and finds the inherited age may be more than 1700 years (mode 250 years) older than the collection date. Taphonomic factors, e.g., size, shape or fungal infestation cannot identify the youngest fragments. Only two fragments on short-lived materials correctly estimated the date of collection. In SE Australia, this study suggests that wood charcoal will overestimate the age of deposition, taphonomic modifications cannot be used to identify which are youngest, and multiple short-lived materials are required to accurately estimate the deposition age. [ABSTRACT FROM AUTHOR]

Foraminifera are widely used in paleoclimatic and paleoceanographic studies, providing information about past ocean conditions. However, in order to use these tracers, it is essential to obtain an accurate chronology. Radiocarbon has proven to be a powerful tool in developing robust chronologies. Sample sizes of a few milligrams of carbonate material are needed for precise radiocarbon determination using accelerator mass spectrometry (AMS). In the specific case of paleoceanographic and paleoenvironmental studies, Foraminifera microfossils are the most important indicator of oceanic conditions. However, for establishing the chronology of deposition, sample availability is often limited. In AMS facilities using solid ion sources, such as the Radiocarbon Laboratory of the Universidade Federal Fluminense (LAC-UFF), in Brazil, CO2 samples need to be converted to graphite after physical and chemical pre-treatment to remove contamination. Reducing the sample sizes increases the relative contribution of contamination and can favor increased background levels. In this work, we tested different amounts of 14C-free carbonate samples as a means to evaluate the pattern of contamination. For the sealed tube Zn/TiH2 graphitization method, we tested prebaking the graphitization tubes and compared storage procedures. As a result, the background for regular-sized samples was decreased, and accurate measurement of carbonate samples containing ca. 0.5 mg C could be performed. Prebaked graphitization tubes can safely be stored in desiccator cabinets for up to 4 weeks. Foraminifera samples with mass as low as 1 mg (ca. 0.1 mg C) can now be measured at the LAC-UFF AMS facility, provided that C contamination can be estimated and corrected. The developments presented in this work allowed for the study of species-specific Foraminifera and other small-sized carbonate samples. [ABSTRACT FROM AUTHOR]