We present atmospheric radiocarbon concentrations in CO2 integrated samples taken between January 2019 and December 2021 in the Mexico City Metropolitan Area (MCMA) and explain the variations in terms of changes in emission sources associated with the COVID-19 lockdown restrictions imposed from March 2020. Δ14C values for samples collected during 2019 range between –44.15‰ and –13.17‰, with lower values during months with higher fossil fuels consumption and air stagnation, whereas higher values were found for periods with high number of fires around MCMA or wet months with higher contribution of heterotrophic respiration. For samples collected during 2020, Δ14C values range between –17.7‰ and 2.25‰, with an increasing trend immediately after the initial lockdown and higher values obtained for samples collected during lockdown phases 2 and 3 and the period of extremely high epidemic risk. This agrees with the 38% and 52% decrease in gasoline and diesel sales. Once essential activities gradually opened from July 2020, Δ14C follow a decreasing trend as vehicle traffic started to increase again. Δ14C values for samples collected during 2021 range from –32.89‰ to –10.27‰, with the higher value obtained during a period of extremely high epidemic risk with a 30% reduction in gasoline and diesel consumption. Despite the complexity of emission sources in MCMA, from Δ14C variations it was possible to identify changes in fossil CO2 emissions resulting from the significant reduction in vehicle traffic due to the COVID-19 lockdown and the restrictions imposed to control transmission of the disease.

Microbial processing of soil organic matter is a significant driver of C cycling, yet we lack an understanding of what shapes the turnover of this large terrestrial pool. In part, this is due to limited options for accurately identifying the source of C assimilated by microbial communities. Laboratory incubations are the most common method for this; however, they can introduce artifacts due to sample disruption and processing and can take months to produce sufficient CO2 for analysis. We present a biomass extraction method which allows for the direct 14C analysis of microbial biomolecules and compare the results to laboratory incubations. In the upper 50 cm soil depths, the Δ14C from incubations was indistinguishable from that of extracted microbial biomass. Below 50 cm, the Δ14C of the biomass was more depleted than that of the incubations, either due to the stimulation of labile C decomposition in the incubations, the inclusion of biomolecules from non-living cells in the biomass extractions, or differences in C used for assimilation versus respiration. Our results suggest that measurement of Δ14C of microbial biomass extracts can be a useful alternative to soil incubations.

Dissolved inorganic carbon (DIC) in ocean water is a major sink of fossil fuel derived CO2. Carbon isotopes in DIC serve as tracers for oceanic water masses, biogeochemical processes, and air-sea gas exchange. We present a timeseries of surface DIC δ13C and Δ14C values from 2011 to 2022 from Newport Beach, California. This is a continuation of previous timeseries (Hinger et al. 2010; Santos et al. 2011) that together provide an 18-year record. These data show that DIC Δ14C values have declined by 42‰ and that DIC δ13C values have declined by 0.4‰ since 2004. By 2020, DIC Δ14C values were within analytical error of nearby clean atmospheric CO2 Δ14C values. These long-term trends are likely the result of significant fossil fuel derived CO2 in surface DIC from air-sea gas exchange. Seasonally, Δ14C values varied by 3.4‰ between 2011 and 2022, where seasonal δ13C values varied by 0.7‰. The seasonal variation in Δ14C values is likely driven by variations in upwelling, surface eddies, and mixed layer depth. The variation in δ13C values appears to be driven by isotopic fractionation from marine primary producers. The DIC δ13C and Δ14C values record the influence of the drought that began in 2012, and a major upwelling event in 2016.

Massive ground ice found in the Barrow Permafrost Tunnel at 3–7 m depths from the surface has been interpreted as an ice wedge and used to reconstruct early Holocene environmental changes. To better understand the development of this ground ice, we conducted radiocarbon dating for 34 samples of plant remains from the massive ground ice and underlying sediment layer. A significantly large gap in the measured radiocarbon ages (more than 24 ka) between massive ice and the underlying sediment layer throughout the tunnel profile suggested at least two possibilities. One is that the lower and older sediment layer had thrust upwards at the boundary between intruding ice wedge and adjacent sediment, and the growing ice had pushed the sediment sideways. Another is that erosional events had removed surface materials at about 12–36 ka BP (14–41 cal ka BP) before the overlaying sediment layer with massive ground ice developed. The overall distribution of radiocarbon ages from the massive ice supported the ice-wedge hypothesis as a formation mechanism, although our results showed several age inversions and large fluctuations. Dating of densely spaced samples revealed two ground-ice regions with similar ages around 11–11.5 and 10–10.5 ka BP divided by a relatively narrow region of transitional ages along the tunnel long-axis. This distribution may be explained by a possible misalignment between the sampling direction and the ice-wedge growth line or by intermittent ice growth with repeated cracking at more random locations than the classic ice-wedge growth model suggested.

Polycyclic aromatic hydrocarbons (PAHs) are major air pollutants that are ubiquitously produced by the combustion of organic materials, and it is extremely important to identify their pollution sources. In this study, molecular fingerprinting and compound class-specific radiocarbon dating (CCSRA) were performed on PAHs from canal sediments and air samples collected in Kolkata, India’s third largest city (population approximately 16 million), where PAHs pollution has been a serious problem. Average PAH (Σ12-parent PAHs) concentrations in air samples were 65.1 ng m–3 in summer and 70.9 ng m–3 in winter and in canal sediments were 32.7 µg g–1, which are classified as “very high-level” pollution. Molecular fingerprinting using methyl-PAH/PAH (MPAHs/PAHs) ratios and isomer pair ratios with molecular weights of 178, 202, 228, and 276 suggested that wood and coal combustion were the dominant sources of PAHs in the sediment, and that atmospheric PAHs were influenced by oil combustion in addition to them. The fraction of contemporary carbon (ƒC) of sedimentary PAHs (0.056–0.100), together with the extremely low MPAHs/PAHs ratio results, lead to the conclusion that the major source of the high concentration of PAHs in the canals is from coal combustion. On the other hand, the ƒC of atmospheric PAHs (0.272–0.369) was close to the share of biomass fuels in India’s domestic fuel consumption in 2011 (about 35%). Furthermore, the observed ƒC-discrepancy between atmospheric and sedimentary PAHs in the same urban environment was interpreted to give an insight into the loading pathway of PAHs to canal sediments in Kolkata.

Seven accelerator mass spectrometry radiocarbon (AMS 14C) dates (7260±106∼7607±95 BP averaged 7444±103 BP) on a giant oyster shell, collected from an ancient shore of the Taipei Basin, are similar to the LSC (liquid scintillation counting) 14C age (7260±46 BP) of a grass sample inside the shell. The calibrated 14C ages of the C. gigas by Marine20 are 7490±240∼7805±230 cal BP (average 7660±96 cal BP), generally agreed with the calibrated LSC 14C ages of the grass and the oyster shell. Combined with other 14C ages of shoreline samples in the Taipei Basin, it is evident that sea level rose from 8600 to 7600 cal BP and reached a stand higher than modern sea level. During this marine transgression, the sedimentation rate along the shoreline was very high because 14C dating was not able to detect age differences for 4–5 m thick sediment sequences. Sixty-nine analyses of δ18O and δ13C from the oldest part of the shell exhibit clear seasonal cycles, with a 4-year period of growth in the 5.5-cm section. According to the δ18O values, the ancient oyster grew in a warmer-than-present shoreline environment, suggesting that the current absence of the giant oyster in Taiwan is not due to warming conditions.

The long-standing assumption that aboveground plant litter inputs have a substantial influence on soil organic carbon storage (SOC) and dynamics has been challenged by a new paradigm for SOC formation and persistence. We tested the importance of plant litter chemistry on SOC storage, distribution, composition, and age by comparing two highly contrasting ecosystems: an old-growth coast redwood (Sequoia sempervirens) forest, with highly aromatic litter, and an adjacent coastal prairie, with more easily decomposed litter. We hypothesized that if plant litter chemistry was the primary driver, redwood would store more and older SOC that was less microbially processed than prairie. Total soil carbon stocks to 110 cm depth were higher in prairie (35 kg C m−2) than redwood (28 kg C m−2). Radiocarbon values indicated shorter SOC residence times in redwood than prairie throughout the profile. Higher amounts of pyrogenic carbon and a higher degree of microbial processing of SOC appear to be instrumental for soil carbon storage and persistence in prairie, while differences in fine-root carbon inputs likely contribute to younger SOC in redwood. We conclude that at these sites fire residues, root inputs, and soil properties influence soil carbon dynamics to a greater degree than the properties of aboveground litter.

The comparisons among 126 14C dates of Carex samples including separated leaf and root parts with acid (A)-treatment and acid-base-acid (ABA)-treatment, and 48 published 14C dates of bulk peat plants on a 92-cm core from Jinchuan Mire in NE China, indicate old carbon influence (OCI) on the 14C dates. The OCI varies with plant species, pretreatment and peat depth. In vascular peat plants such as Carex, humin fractions (remains after ABA treatment) and humic acids are representative of the original plant precursor, while fulvic acids are regarded as the secondary mobile product which should be removed for 14C dating. ABA- treatment removes both fulvic acids and humic acids, whereas A-treatment gets rid of only fulvic acids. Carex roots uptake more dissolved CO2 in peat water. Carex leaves may use more CO2 (involving degassing CO2) above the peat surface. By removing humic acids throughout ABA treatment, the OCI may vary differently over depth (time). ABA treatment cannot eliminate the fixed OCI in humin fractions of vascular peat plants, instead, this treatment may enhance OCI by removing humic acid which may represent the true age of the plants. In addition, Bacon model results on this core could not show rapid changes in accumulation rate.

In order to better characterise carbonaceous components in atmospheric aerosols and to assess the contributions of fossil carbon (FC) and non-fossil carbon (NFC) sources and their seasonality in the Eastern Mediterranean, we collected fine (PM1.3) aerosols at a remote marine background site, the Finokalia Research Station, Crete, Greece, over a period of one-year. PM1.3 samples were analysed for elemental carbon (EC), organic carbon (OC), water-soluble OC (WSOC), and stable carbon isotope ratio (δ13CTC) and radiocarbon content (14CTC) (pMC) of total carbon (TC). All the parameters, i.e., PM1.3, δ13CTC and 14CTC showed a clear temporal pattern with higher values in summer and lower values in autumn. The 14CTC ranged from 54.7 to 99.1 pMC with an average of 74.5 pMC during the entire year. The FC content in TC (FCTC) was found to be slightly lower in winter and almost stable in other seasons, whereas the NFC contents (NFCTC) showed a clear seasonality with the highest level in summer followed by spring and the lowest level in winter. Based on these results together with the seasonal distributions of organic tracers, we found that biomass burning (BB) and soil dust are two major sources of the fine aerosols in winter. Although biogenic emissions of VOCs followed by subsequent secondary oxidation processes are significant in summer followed by spring and autumn, pollen is a significant contributor to TC in spring. This study showed that emissions from fossil fuel combustion are significant (25.5%) but minor compared to NFC sources in the eastern Mediterranean.

The results of radiocarbon variation studies observed in annual tree rings from the NW Pacific (USA Northwest) (Stuiver and Braziunas 1993) and Europe (England, Brehm et al. 2021; Slovakia, Povinec 1977, 1987) are reviewed with the aim of better understanding the 11-year radiocarbon cycle and possible impacts of solar proton events on 14C levels in the atmosphere and biosphere. The average Δ14C amplitude in tree rings for the period of 1798–1944 was 1.3 ± 0.3‰, the average periodicity was 11 ± 1 years, and the average time shift between the sunspot numbers and Δ14C records was 3 ± 1 years. A new solar activity minimum (Gleissberg minimum, 1878–1933) has been identified in the Δ14C data sets from the NW Pacific and England, showing Δ14C excess of 7‰, comparable to the Dalton minimum (1797–1823). No significant changes in Δ14C levels were identified that could be associated with solar proton events during 1800–1950.

Over the course of one year (2021), we monitored the carbon isotope composition of atmospheric CO2 at three locations in Croatia: the Adriatic port city of Rijeka (Cfa climate) and at two rural sites: Gornje Jelenje (Cfb climate) in the vicinity of a main road and clean-air site Parg (Dfb climate). Carbon isotope composition at all sites shows seasonal variation, ranging from –41.3 to 25.2‰ for Δ14C and from –13.1 to –11.3‰ for δ13C. Rijeka systematically has the lowest and Parg the highest Δ14C, and δ13C at the sites are not statistically different one from another. The Δ14C of leaves of deciduous trees reflect the trend of atmospheric Δ14C. Based on the assumption that the investigated area is under the influence of two main sources of CO2: fossil and natural (sea exchange, biosphere, and undisturbed – clean air atmospheric component) the approximate share of fossil CO2 in total atmospheric CO2 has been estimated for Rijeka (2.1 ± 1.3%) and Gornje Jelenje (1.0 ± 0.9%). Comparison of our results with the data from European CO2 sampling stations indicates strong influence of CO2 from sea and biosphere. Backward trajectories indicate a possibility of Δ14CCO2 contribution from distant EU nuclear power plants, but movement of air masses should be considered in more detail to confirm this.

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.

The National Environmental Isotope Facility (NEIF) Radiocarbon Laboratory at the Scottish Universities Environmental Research Centre (SUERC) performs radiocarbon measurement of a wide range of sample matrices for applications in environmental research. Radiocarbon is applied to palaeoenvironmental, palaeoceanographic, and palaeoclimatic investigations, as well as work to understand the source, fate, turnover, and age of carbon in the modern carbon cycle. The NEIF Radiocarbon Laboratory supports users in the development and deployment of novel sampling techniques and laboratory approaches. Here, we give an overview of methods and procedures used by the laboratory to support the field collection, laboratory processing, and measurement of samples. This includes in-house development of novel and/or specialized methods and approaches, such as field collection of CO2 and CH4, hydropyrolysis, and ramped oxidation. The sample types covered include organic remains (e.g., plant material, peat, wood, charcoal, proteins), carbonates (e.g., speleothems, foraminifera, mollusc shell, travertine), waters (dissolved organic and inorganic carbon), gases (CO2 and CH4), soils and sediments (including sub-fractions).

Radiocarbon (14C) methodology was used to investigate the presence of biocarbon in different bio-based disposable packaging products. Packaging waste contributes to a municipal solid waste, which is increasing environmental concerns and resulting in the enhancement of EU regulations that aim to reduce packaging waste. The 14C amount in samples reflects how much of the biocarbon has been used. In this study, the concentration of 14C was determined in commonly used types of disposable packaging, such as cups, plates, straws, cutlery, and baking paper. Samples were made of materials such as paper, wheat bran, sugarcane, and wood. The mean concentration of the 14C isotope, measured by the accelerator mass spectrometry (AMS) technique, is greater than 100 pMC in all tested samples, indicating that the samples are modern. The relatively high 14C concentration values in the waterproof layer of the sample indicate that bioplastic, rather than plastic, was used in its production. The highest 14C isotope concentration values were measured for samples that used the oldest biomass (wood and paper), and the lowest for products from current crops (sugarcane and wheat bran), which is consistent with the trend of changes in 14C concentration in the biosphere. The study also addresses the problem of heterogeneity and representativeness of subsamples.

In 2001, five French public organizations (CNRS, CEA, IRD, IRSN, and the Ministère de la Culture) signed an agreement to purchase a new accelerator mass spectrometer to provide radiocarbon dating services at the national level. The Laboratoire de Mesure du Carbone 14 (LMC14) was set up in Saclay (France) around ARTEMIS, an AMS system based on a 3MV Pelletron from NEC and installed in early 2003. In 2015, the LMC14 joined the Laboratoire des Sciences du Climat et de l’Environnement, making it possible to develop research projects in addition to the service activity and since 2021, the LMC14 has been a member of the IAEA Collaborating Centre “Atoms for Heritage” at the Université Paris-Saclay. Since 2003, 70,000 samples have been measured. Two-thirds of the samples have been prepared on site and one-third in two associated laboratories in Paris and Lyon. Over the past years, the LMC14 has participated in several international inter-comparisons and has continuously improved its capabilities by developing new protocols for preparation and measurement. In this paper, the radiocarbon dating services of the last 20 years for research institutions, museums and environmental monitoring are reviewed and recent results from environmental and archaeological research programs are highlighted.

Radiocarbon observations (Δ14C) in dissolved inorganic carbon (DIC) of seawater provide useful information about ocean carbon cycling and ocean circulation. To deliver high-quality observations, the Laboratory of Ion Beam Physics (LIP) at ETH-Zurich developed a new simplified method allowing the rapid analysis of radiocarbon in DIC of small seawater samples, which is continually assessed by following internal quality controls. However, a comparison with externally produced 14C measurements to better establish an equivalency between methods was still missing. Here, we make the first intercomparison with the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) facility based on 14 duplicate seawater samples collected in 2020. We also compare with prior deep-water observations from the 1970s to 1990s. The results show a very good agreement in both comparisons. The mean Δ14C of 12 duplicate samples measured by LIP and NOSAMS were statistically identical within one sigma uncertainty while two other duplicate samples agreed within two sigma. Based on this small number of duplicate samples, LIP values appear to be slightly lower than the NOSAMS values, but more measurements will be needed for confirmation. We also comment on storage and preservation techniques used in this study, including the freezing of samples collected in foil bags.

Skin-based samples (leather, skin, and parchment) in archaeological, historic and museum settings are among the most challenging materials to radiocarbon (14C) date in terms of removing exogenous carbon sources—comparable to bone collagen in many respects but with much less empirical study to guide pretreatment approaches. In the case of leather, the 14C content of materials used in manufacturing the leather can vary greatly. The presence of leather manufacturing chemicals before pretreatment and their absence afterward is difficult to demonstrate, and the accuracy of dates depends upon isolating the original animal proteins and removing exogenous carbon. Parchments differ in production technique from leather but include similar unknowns. It is not clear that lessons learned in the treatment of one are always salient for treating the other. We measured the 14C content of variously pretreated leather, parchment, skin samples, and extracts, producing apparent ages that varied by hundreds or occasionally thousands of years depending upon sample pretreatment. Fourier Transform Infrared Spectroscopy (FTIR) and C:N ratios provided insight into the chemical composition of carbon reservoirs contributing to age differences. The results of these analyses demonstrated that XAD column chromatography resulted in the most accurate 14C dates for leather and samples of unknown tannage, and FTIR allowed for the detection of contamination that might have otherwise been overlooked.

As there exists a growing demand for chronological research and tracer applications using radiocarbon (14C) analyses of samples smaller than 100 μg C, a compact micro-specific hydrogen graphitization method has been developed at the Xi’an Accelerator Mass Spectrometry (AMS) Center. This article describes the performance of the system and the mass of carbon background produced during ultra-small sample preparation. Furthermore, we discuss the results of contamination corrections and perform 14C analyses on small samples with known age or reference values. The results reveal that our 14C analysis of ultra-small samples of 10–100 μg C can obtain accurate and reliable results, and the micro-scale 14C-AMS analysis technique meets our research objectives for dating and tracer applications.

Radiocarbon (14C) measurements undertaken by the NERC Radiocarbon Laboratory using accelerator mass spectrometry (AMS) are now freely available on a new online database. The data presented covers measurement of the wide range of sample types that are processed for research projects in the fields of Earth and environmental science, supported by the United Kingdom’s Natural Environment Research Council. Sample types within the database include organic remains, soils, sediments, carbonates, dissolved organic and inorganic carbon, and carbon dioxide. Currently, the database contains 14C data for over 2400 individual samples that were measured and reported between 2005 and 2013, but it is envisaged that this will expand considerably as more data are made available. Contextual information such as sampling location and associated publications are provided where available, and searches can be performed on sample location, sample type, project number, and publication code. This new database compliments an existing, publicly available database of measurements performed using radiometric methods by the laboratory which has recently been expanded to present over 2000 measurements. It is hoped that this archive will prove useful to workers in the community who would benefit from greater availability of measurements for particular locations or sample types, and for the purposes of performing meta-analyses, and/or synthesis of larger datasets.