Lead carbonates were used as cosmetic and pigment since Antiquity. The pigment, known as lead white, was generally composed of cerussite and hydrocerussite. Unlike most ancient pigments, lead white was obtained by a synthetic route involving metallic lead, vinegar and organic matter. Fermentation of organic matter produces heat and CO2 emission, leading to the formation of carbonates. As lead white is formed by trapping CO2, radiocarbon (14C) dating can thus be considered. We have developed a protocol to prepare lead white. We selected modern pigments for the experiment implementation and ancient cosmetic and paintings for dating. After characterization of the samples by XRD, thermal decomposition of cerussite at various temperatures was explored in order to select the appropriate conditions for painting samples. CO2 extraction yield, SEM and XPS were used to characterize the process. Thermal decomposition at 400°C was successfully applied to mixtures of lead white with other paint components (oil as binder, calcite as filler/extender) and to historical samples. We obtained radiocarbon measurements in agreement with the expected dates, demonstrating that thermal decomposition at 400°C is efficient for a selective decomposition of lead white and that paintings can be directly 14C-dated by dating lead white pigment.

Although radiocarbon (14C) dating is commonly used for archeological music instruments, little research has been conducted on modern instruments (16th–19th centuries). New technology, based on the Mini Carbon Dating System (MICADAS), enables some of the recurring challenges (e.g. sampling size) to be circumvented and paves the way for a new field of investigation. We here address the Indian instrumentarium, about which very little is known. We investigate the making and the restoration phases of two vina, a kinnari vina (E.1444), and a rudra vina or bin (E.997.24.1). By comparing 14C measurements made on several samplings of elements of the instruments with museological information, we were able to specify a unique calibrated interval of ages [1666 AD–1690 AD] for the kinnari vina, with a restoration phase [1678 AD–1766 AD] for the upper nut. The bin is likely attributed to the [1650 AD–1683 AD] interval.

Surface radiocarbon (Δ14C) in the North Pacific has been monitored using a commercial volunteer observation ship since the early 2000s. Here we report the temporal and spatial variations in Δ14C in the summer surface water when the surface ocean is vertically stratified over a 13-yr period, 2004–2016. The long-term Δ14C decreasing trend after the late 1970s in the subtropical region has continued to the present and the rate of decrease of the Kuroshio and Kuroshio Extension, North Pacific and California current areas is calculated to be –3.3, –5.2 and –3.3 ‰/yr, respectively. After 2012 the Δ14C of the Kuroshio and Kuroshio Extension area, however, has remained at an approximately constant value of around 50‰. The result may indicate that subtropical surface Δ14C in the western North Pacific has reached an equilibrium with atmospheric Δ14CO2. The Δ14C in the subarctic region is markedly lower than values in the subtropical region and it seems that the decreasing tendency of surface Δ14C has changed to an increasing tendency after 2010. The results may indicate that bomb-produced 14C, which has accumulated below the mixed layer in the past few decades, has been entrained into the surface layer by deep convection.

Radiocarbon (14C) conclusively demonstrates that the very important Yarkon-Tanininm aquifer, named after the two springs where the drainage presumably occurs, is in actuality two distinct aquifers—Upper and Lower. The springs have higher 14C activities than the exploitation wells that surround them (all drilled into the Upper aquifer). The springs are situated at faults that allow the Lower aquifer water to rise due to its higher pieziometric head and drain along with the Upper aquifer. The Lower aquifer water flows rapidly along a path that includes a karstic system. The Upper aquifer flows more slowly, primarily through a system of cracks in the carbonate aquifer. The Upper aquifer groundwater in the Beer-Sheba extension flows northwards at approximately ~4–7 m/yr.

The stratigraphic succession of the Mar Piccolo basin (Gulf of Taranto, Southern Italy) is well known in the scientific literature dealing with the last interglacial since its morphological evolution is influenced by sea level changes during Late Pleistocene-Holocene. The local Holocene sea level history is well known thanks to data deriving from peat and ash layers identified in different sediment cores obtained underwater and in coastal areas. Peat sediments are frequently interlayed with muddy-sand beds rich in Cerastoderma glaucum (Poiret, 1789). In the literature of the Mediterranean basin, AMS 14C dating on C. glaucum is widely used also in paleo-environmental reconstruction because this bivalve is considered an useful marker of sea level, though in lagoonal systems, large age offsets have been reported in different areas. Due to the availability of precise chronological and geochronological markers, in order to validate the use of C. glaucum in paleo sea level reconstruction, AMS 14C dating campaign was carried out on this bivalve deriving from several cores drilled in the Mar Piccolo basin and its nearby areas. Nineteen AMS 14C dating analyses carried out on C. glaucum sampled from different sediment cores up to a maximum of 30 m from the seafloor are presented. These results show an inconsistency of the ages in relation to a sea-level rise reconstruction model. The interpretation of the data was performed after the estimation of the local age offset calculated by analyzing six live samples, collected in 2017 in Mar Piccolo and in Croatia, and two samples dated to 1968–1969. The results show that for both the classes of samples (2017 and 1960s) an age offset ranging from 600 to 800 yr can be estimated.

Replicate radiocarbon (14C) measurements of organic and inorganic control samples, with known Fraction Modern values in the range Fm = 0–1.5 and mass range 6 μg–2 mg carbon, are used to determine both the mass and radiocarbon content of the blank carbon introduced during sample processing and measurement in our laboratory. These data are used to model, separately for organic and inorganic samples, the blank contribution and subsequently “blank correct” measured unknowns in the mass range 25–100 μg. Data, formulas, and an assessment of the precision and accuracy of the blank correction are presented.

Over the past 30 years, the format of the radiocarbon (14C) intercomparison studies has changed, however, the selection of sample types used in these studies has remained constant—namely, natural and routinely dated materials that could subsequently be used as in-house reference materials. One such material is peat which has been used 12 times, starting with the ICS in 1988. Peat from Iceland (TIRI), Ellanmore (TIRI), Letham Moss (ICS, VIRI, and SIRI), and St Bees, UK (FIRI and VIRI) have been used, as well as a near-background peat from Siberia. In the main, these peat samples have been provided as the humic acid fraction, with the main advantage being that the humic acid is extracted in solution and then precipitated (the solution phase providing the homogenisation) which is a key requirement for a reference material. In this paper, we will revisit the peat results and explore their findings. In addition, for the last 8 years, the Letham Moss sample has been used in the SUERC 14C laboratory as an in-house standard or reference material. This has resulted in several thousand measurements. Such a rich data set is explored to illustrate the benefits arising from the intercomparison program.

To determine the 237Np concentration originating from global fallout in the environment, samples were collected from Guangxi, south of China, and measured by accelerator mass spectrometry (AMS) at CIRCE. Serials standard samples and environment samples were prepared and measured using 242Pu as a tracer. The result indicates that the detection limit of 237Np as low as 10–15 g can be obtained. The concentration of 237Np in the environmental samples is less than 49.09 pg/kg (i.e. 1.280 mBq/kg), and the most probable value of 237Np is approximately 20 pg/kg (i.e. 0.53 mBq/kg).

We have investigated the possibility of direct accelerator mass spectrometry radiocarbon (AMS 14C) measurement of carbonate samples at ANSTO using the STAR 2 MV tandem accelerator. Each carbonate sample was powdered, mixed with metal powder and pressed into an aluminum cathode for direct carbonate measurement by AMS 14C. Of the three high-purity metal powders (Fe, Nb, and Ag) used in our investigation, Nb was found to be the best metal, which delivered higher carbon beam currents and lower background. Beam currents for targets containing the optimal carbonate mass of 1.5–2.0 mg were ∼8% of those obtained from graphite targets of standard size (>0.5 mg C). Typical measured blank for Carrara marble (IAEA-C1) of ∼40 ka was obtained. Background-corrected 14C values of carbonate targets agreed well with their associated values obtained from high-precision analysis of graphite targets within 2σ uncertainties. Typical precision of this rapid AMS analysis was ∼1% for samples <8 ka. Despite lower precision for carbonate target ages (compared to standard graphite target ages), these ages are useful for palaeobiological applications where a large number of dates are required, such as time-averaging studies.

High Voltage Engineering Europa (HVE) has designed a vacuum-insulated tandem accelerator dedicated to radiocarbon (14C) analysis. A unique feature of the design is a magnetic charge state selector that is incorporated in the high voltage terminal, which reduces the primary source of background that originates from the injection of 13CH− to negligible levels. As a result, background levels in the low 10−16 regimes are anticipated, thus supporting the most stringent 14C dating applications. Another feature of the system is the incorporation of several slit feedback loops for stabilization of the position of the ion beam throughout the system, which avoids drift and ensures stable, long-term operation. Finally, this article presents measurements and quantitative analysis of background contributions from 13CH−.

This work summarizes the methodical capabilities, improvements, and new developments in the radiocarbon laboratory of the accelerator mass spectrometry (AMS) facility at the University of Cologne, Germany, which was established in 2010. During the past years, the laboratory has specialized in the analysis of small and gaseous samples. We thus, recently installed a second ion source dedicated for radiocarbon (14C) analysis of CO2 samples at our 6 MV Tandetron AMS from High Voltage Engineering Europe B.V. that is coupled with the gas injection system from Ionplus and an EuroVector EA 3000 elemental analyzer. This work summarizes all pretreatment methods and analytical facilities established in our laboratory during the last years including 14C analysis of individual organic compounds and of CO2 trapped on molecular sieves. We also report different blank values including our long-term blank since 2011, which is for normal-sized, solid samples (650–1000 µg C) 0.0012 ± 0.0004 F14C (54,305 ± 2581 yr BP, n = 484). The precision obtained for modern samples measured as graphite is 0.5% and for gaseous samples injected with the GIS ≤2%.

Methane contributes substantially to global warming as the second most important anthropogenic greenhouse gas. Radiocarbon (14C) measurements of atmospheric methane can be used as a source apportionment tool, as they allow distinction between thermogenic and biogenic methane sources. However, these measurements remain scarce due to labor-intensive methods required. A new setup for the preparation of atmospheric methane samples for radiocarbon analysis is presented. The system combines a methane preconcentration line with a preparative gas chromatography technique to isolate pure methane samples for a compound-specific radiocarbon analysis. In order to minimize sample preparation time, we designed a simplified preconcentration line for the extraction of methane from 50 L atmospheric air, which corresponds to 50 µg C as required for a reliable 14C analysis of methane-derived CO2 gas measurement with accelerator mass spectrometry (AMS). The system guarantees a quantitative extraction of methane from atmospheric air samples for 14C analysis, with a good repeatability and a low processing blank. The setup was originally designed for the measurement of samples with low methane concentrations, but it can also be adapted to apportion sources from environmental compartments with high methane levels such as freshwaters or wetlands.

Methane is the second most important anthropogenically produced greenhouse gas, and radiocarbon (14C) analysis is extremely valuable in identifying its age and source in the environment. At the NERC Radiocarbon Facility (East Kilbride, UK) we have developed expertise in analysis of methane 14C concentration and methodological approaches to field sampling over the past 20 years. This has opened a wide range of applications, which have mainly focused on (1) the age and source of methane emitted by peatlands and organic soils (e.g. to quantify the release of ancient carbon), (2) the source of aquatic emissions of methane, and (3) the age of methane generated by amenity and illegal landfill. Many of these scientifically important applications involve challenging sampling and measurement considerations, which our development program has continually aimed to overcome. Here, we describe our current methods, and recent improvements to aid field collection of samples in remote locations. We present the results of tests which (1) show the effectiveness of our methods to remove contaminants, especially CO2, (2) quantify the 14C background contribution, and (3) demonstrate the reliability of metal gas storage canisters for sample storage.

In coastal and island archaeology, carbonate mollusk shells are often among the most abundant materials available for radiocarbon (14C) dating. The marsh periwinkle (Littorina irrorata) is one of these such species, ubiquitously found along the Atlantic and Gulf coasts of the United States in both modern and archaeological contexts. This paper presents a novel approach to dating estuarine mollusks where rather than attempting to characterize the size and variability of reservoir effects to “correct” shell carbonate dates, we describe a compound-specific approach that isolates conchiolin, the organic matter bound with the shell matrix of the L. irrorata. Conchiolin typically constitutes <5% of shell weight. In L. irrorata, it is derived from the snail’s terrestrial diet and is thus not strongly influenced by marine, hardwater, or other carbon reservoir effects. We compare the carbon isotopes (δ13C and Δ14C) of L. irrorata shell carbonate, conchiolin, and bulk soft tissue from six modern, live-collected specimens from Apalachicola Bay, Florida, with samples that represent possible sources of carbon within their environment including surface sediments, marsh plant tissues, and dissolved inorganic carbon (DIC) in water. Ultimately, this paper demonstrates that samples obtained from wet chemical oxidation of L. irrorata conchiolin produces accurate 14C dates.

In southwestern Florida, USA, terraformed landscapes built almost entirely of oyster shells (Crassostrea virginica) reflect a unique pre-Columbian tradition of shell-built architecture. The ability to reliably date oyster shells is essential to identifying spatial, temporal, and functional relationships among shellworks sites, yet to date there has been no systematic attempt to quantify or correct for carbon reservoir effects in this region. Here we present 14 radiocarbon (14C) ages for 5 known-age, pre-bomb oyster shells collected between AD 1932–1948, as well as 6 14C ages for archaeological oyster/charcoal pairs from the Turner River Mound Complex, Everglades National Park. We report our current best estimate of ΔR = 92 ± 74 yr for Greater Southwest Florida, and ΔR = –15 ± 42 yr for the Turner River archaeological site. Future research should focus on paired archaeological specimens to obtain spatially and temporally relevant estimates of ΔR.

The second home-made single stage accelerator mass spectrometer (SSAMS) system dedicated to radiocarbon (14C) measurements was built after the first SSAMS system was moved to Guangxi Normal University. With some improvements to the second SSAMS system, the performance has been improved. With the conditions of total ion energy of 200KeV, ions charge states of 1+ and helium as stripper gas, 14C measurements with precision of 0.5% and a background level of 0.5 pMC were achieved. Details of the system and the experimental performance are given here.

Radiocarbon (14C) ages were determined for 10 iron samples from the war booty offering site in the Nydam peat bog (SE Denmark), and compared to archaeologically inferred periods of deposition. Additional 14C measurements were carried out for modern iron standards made with charcoal of known isotopic composition to evaluate possible effects of handling. Modern iron standards give depleted 14C concentrations, compared to the initial charcoal 14C composition, and may indicate carbon fractionation effects during carbon dissolution in the iron lattice. Further studies are needed to verify if this is a common effect during iron production. 14C dating of two swords and one ax head are in comparatively good agreement with expected deposition times and indicate only small old-wood effects. In contrast, 14C dating of iron rivets from the Nydam (B) oak boat proved difficult due to corrosion with siderite (FeCO3) and conservation with wax. A step-combustion procedure was applied, using a low (∼570–600°C) temperature prior to the high (∼970–1000°C) combustion temperature for carbon extraction, aiming to remove siderite and wax before collecting the original carbon dissolved in the iron lattice. Nevertheless, measured 14C ages of the iron rivets differ by about 200–300 years from the dendro-date of the Nydam (B) oak boat they belong to, indicating persisting aging effects (e.g. old-wood, contamination with fossil carbon added during iron making and/or handling prior 14C dating). Also, a possible recycling of older iron cannot be excluded.

We report on an initial long-term study of dissolved inorganic and organic carbon (DIC) from Sabino Creek, located in Sabino Canyon, Pima County, Arizona. The purpose of this study was to monitor changes in dissolved radiocarbon (14C) with time and to understand the processes contributing to these variations. Our results span the period 2009–2016 and show a mixing trend between dissolved inorganic and organic carbon modern end-members with an older component. This study provides preliminary information for more detailed research on recycling of organic components in this stream system.

The Bristol Radiocarbon Accelerator Mass Spectrometry (BRAMS) Facility was established at the University of Bristol after the commissioning of our dedicated sample preparation laboratories and the installation and acceptance of the BrisMICADAS AMS in 2016. Routine measurements commenced in mid-2016, once validation was completed for each sample type. Herein, we give an overview of the standard pretreatment methods currently employed in the Facility and the results of radiocarbon (14C) determinations on a wide range of standards, blank materials, and intercomparison samples which have been measured during our extensive pretreatment method validation program and during our routine 14C analyses.

Bone is one of the most complex sample materials used for radiocarbon (14C) dating. The installation of the EnvironMICADAS AMS at HEKAL (department of ICER) in 2011 required the adoption of new sample preparation techniques for small bone samples. Since then, hundreds of procedural background and known-age bones have been processed using our modified Longin method (MLM) and dated along with unknown samples. Their results are used in this study to assess the reproducibility of our current bone preparation method and the real uncertainty of the final age result. In addition, using the background samples, which are included in each bone measurement batch, blank correction of the unknown samples could also be performed. The mean F14C value of our bone blanks is generally better than 0.005 (∼42,500 BP) alongside 0.0013 SD. Good reproducibility was confirmed by the results of the laboratory known-age bone as well, where the standard deviation of the mean is better than 0.0025. In addition, the results of the three bone samples used in an ultrafiltration (UF) test study did not show notable differences from the ones obtained by our current protocol in 1σ uncertainty range but more experiments will be performed in the near future.