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ABSTRACT Late Holocene relative sea-level reconstructions are commonly generated using proxies preserved in salt-marsh and mangrove sediment. These depositional environments provide abundant material for radiocarbon dating in the form of identifiable macrofossils (salt marshes) and bulk organic sediment (mangroves). We explore if single-step graphitization of these samples in preparation for radiocarbon dating can increase the number and temporal resolution of relative sea-level reconstructions without a corresponding increase in cost. Dating of salt-marsh macrofossils from the northeastern United States and bulk mangrove sediment from the Federated States of Micronesia indicates that single-step graphitization generates radiocarbon ages that are indistinguishable from replicates prepared using traditional graphitization, but with a modest increase in error (mean/maximum of 6.25/15 additional 14 C yr for salt-marsh macrofossils). Low 12 C currents measured on bulk mangrove sediment following single-step graphitization likely render them unreliable despite their apparent accuracy. Simulated chronologies for six salt-marsh cores indicate that having twice as many radiocarbon dates (since single-step graphitization costs ∼50% of traditional graphitization) results in narrower confidence intervals for sample age estimated by age-depth models when the additional error from the single-step method is less than ∼50 14 C yr (∼30 14 C yr if the chronology also utilizes historical age markers). Since these thresholds are greater than our empirical estimates of the additional error, we conclude that adopting single-step graphitization for radiocarbon measurements on plant macrofossils is likely to increase precision of age-depth models by more than 20/10% (without/with historical age markers). This improvement can be implemented without additional cost. 

ABSTRACT This note describes improvements of UV oxidation method that is used to measure carbon isotopes of dissolved organic carbon (DOC) at the National Ocean Sciences Accelerator Mass Spectrometry Facility (NOSAMS). The procedural blank is reduced to 2.6 ± 0.6 μg C, with Fm of 0.42 ± 0.10 and δ 13 C of –28.43 ± 1.19‰. The throughput is improved from one sample per day to two samples per day. 

ABSTRACT This study describes a procedural blank assessment of the ultraviolet photochemical oxidation (UV oxidation) method that is used to measure carbon isotopes of dissolved organic carbon (DOC) at the National Ocean Sciences Accelerator Mass Spectrometry Facility (NOSAMS). A retrospective compilation of Fm and δ 13 C results for secondary standards (OX-II, glycine) between 2009 and 2018 indicated that a revised blank correction was required to bring results in line with accepted values. The application of a best-fit mass-balance correction yielded a procedural blank of 22.0 ± 6.0 µg C with Fm of 0.30 ± 0.20 and δ 13 C of –32.0 ± 3.0‰ for this period, which was notably higher and more variable than previously reported. Changes to the procedure, specifically elimination of higher organic carbon reagents and improved sample and reactor handling, reduced the blank to 11.0 ± 2.75 µg C, with Fm of 0.14 ± 0.10 and δ 13 C of –31.0 ± 5.5‰. A thorough determination of the entire sample processing blank is required to ensure accurate isotopic compositions of seawater DOC using the UV oxidation method. Additional efforts are needed to further reduce the procedural blank so that smaller DOC samples can be analyzed, and to increase sample throughput.