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 δ13C 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 δ13C 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 δ13C 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.

The Ongamira Valley (Córdoba, Argentina) shows a persistent occupational history of its territory. Even one of the first Argentinian radiocarbon (14C) dates was calculated in this valley; for 70 years, the chronology was based on relative dates (stratigraphy and its cultural content). For this reason, since 2010 a 14C dating program has been developed focusing on the chronology of eight of the 60 sites identified so far for the valley. This work reports the outcomes of this program with 27 new dates. These data have been related to characteristics of the material culture, use of space and mobility of hunter-gatherer societies. The results have allowed us to bring new insights into a continuous occupation of the valley since the Middle Holocene according to the human peopling models proposed. It has also been possible to provide greater chronological precision to various activities related to feeding practices, use of space associated with rock-shelters, palaeoenvironmental changes and incorporation of new technologies into daily practices.

Fungal hyphae associated with tree roots extending into the surrounding substrate are suspected to have to contaminated buried plant material with recent carbon in two examples and to have resulted in erroneously young radiocarbon ages. This problem might be overcome by choosing sampling sites far from trees or by analyzing the lignin component of samples, although the latter is presently difficult.

Shells from Neolithic shell midden sites have been routinely dated in Korea, but they have not been calibrated based on the correction values (ΔR) for the marine reservoir effect (MRE). A lack of proper calibration has left dates on shells incomparable to those on terrestrial samples, and thus unusable in building the chronological sequence of shell middens. Here, we report the two new ΔR values of a pre-bomb (pre-1950) blue mussel from the south coast. We applied the two new and the two previously reported ΔR values to the three dates on marine shells from the Bibongri shell midden in southeastern Korea. Our ΔR adjusted calibration and the comparison to dates on charcoal and bone remains clarify an ambiguity in the stratigraphy and the Early Neolithic chronology at Bibongri. Our contribution is to provide the ΔR values that can be further applied to other Neolithic shell middens along the south coast.

We developed a passive sampler for time-integrated collection and radiocarbon (14C) analysis of soil respiration, a major flux in the global C cycle. It consists of a permanent access well that controls the CO2 uptake rate and an exchangeable molecular sieve CO2 trap. We tested how access well dimensions and environmental conditions affect collected CO2, and optimized cleaning procedures to minimize 14CO2 memory. We also deployed two generations of the sampler in Arctic tundra for up to two years, collecting CO2 over periods of 3 days–2 months, while monitoring soil temperature, volumetric water content, and CO2 concentration. The sampler collects CO2 at a rate proportional to the length of a silicone tubing inlet (7–26 µg CO2-C day-1·m Si-1). With constant sampler dimensions in the field, CO2 recovery is best explained by soil temperature. We retrieved 0.1–5.3 mg C from the 1st and 0.6–13 mg C from the 2nd generation samplers, equivalent to uptake rates of 2–215 (n=17) and 10–247 µg CO2-C day-1 (n=20), respectively. The method blank is 8 ± 6 µg C (mean ± sd, n=8), with a radiocarbon content (fraction modern) ranging from 0.5875–0.6013 (n=2). The sampler enables more continuous investigations of soil C emission sources and is suitable for Arctic environments.

Quantifying the local marine reservoir age (ΔR) and its change over time is critical for precise radiocarbon calibration of marine samples and for the study of the ocean carbon cycle. ΔR values are scarce for the African coast facing the Indian Ocean, and the few values available were obtained from pre-bomb shells collected during the 19th century. Here, the ΔR value for calibrated year 1110 ± 25 (1σ) CE was reconstructed from radiocarbon dating and Bayesian analysis of marine and terrestrial materials coexisting in a tsunami deposit discovered in Pangani Bay (Tanzania, western Indian Ocean coast). The reconstructed ΔR of –8 ± 40 (1σ, n = 3) is similar to pre-bomb regional estimates and provides new information to investigate regional ΔR change over time. The Bayesian analysis of the dated samples revises the age of the tsunami event found in Pangani Bay to 1064–1157 cal CE (95.4% confidence level) or 1110 ± 25 (1σ) cal CE, about one century younger compared to the previous estimate. Our results indicate that the new ΔR value and the proposed calibration approach can be used to refine existing chronologies in the region, with implications for paleo-environmental reconstructions and archaeological studies of Early Swahili societies.

We developed a simple and cost-effective method for extracting carbon from dissolved inorganic carbon (DIC) in water samples without a carrier gas. This method only slightly modifies the existing vacuum line for CO2 purification in radiocarbon research laboratories by connecting several reservoirs and traps. The procedure consists of repeated cycles of CO2 extraction from water into the headspace of the reaction container, expansion of the extracted gas into the vacuum line, and cryogenic trapping of CO2. High CO2 yield (∼98%) was obtained from a variety of water samples with a wide range of DIC concentrations (0.4–100 mmol·L−1, in the case of 1.2 mgC). The δ13C fractionation depended on the CO2 yield, while the 14C concentration was constant within the error range, regardless of the CO2 yield. The average δ13C discrepancy between the results of this method and direct analyses made using the GC-IRMS was 0.02 ± 0.06‰. The standard deviations (1σ) in fraction of modern carbon (F14C) ranged from 0.0002 to 0.0004 for waters below 0.01 of F14C, and below 0.8% of F14C values for waters above 0.1. We conclude that this method is useful for effectively extracting CO2 from DIC in water and yields accurate 14C data.

Radiocarbon (14C) analysis of carbon dioxide (CO2) can be extremely useful in carbon cycle studies because it provides unique information that can infer the age and source of this greenhouse gas. Cartridges containing the CO2-adsorbing zeolite molecular sieve are small and highly portable, which makes them more suitable for field campaigns in remote locations compared to some other CO2 collection methods. However, sampling with molecular sieve cartridges usually requires additional equipment, such as an infrared gas analyser, which can reduce portability and pose limitations due to power demands. In addition, 14C analysis of CO2 is increasingly being used in field experiments which require high numbers of replicate CO2 collections, placing extra pressure on an expensive and cumbersome collection apparatus. We therefore designed and built a molecular sieve CO2 sampling kit that utilizes a small, low power CO2 sensor. We demonstrate the reliability of the new kit for the collection of CO2 samples for 14C analysis in a series of laboratory and field tests. This inexpensive sampling kit is small, light-weight, highly portable, and has low power demands, making it particularly useful for field campaigns in remote and inaccessible locations.