The paper describes a study undertaken to examine the dispersion pattern of gaseous emissions, as indicated by 14C uptake in natural materials, around the nuclear reprocessing plant at Sellafield, Cumbria, UK. The extent and directional dispersion of the released 14C is established and its variability over an extended period assessed. Results of measurements taken during three sampling seasons (1981, 1982, 1983) of the 14C activity in hawthorn berries collected over a wide area are presented and the dispersion pattern contours constructed from them are examined. Only limited agreement of the results with the theoretical relationship 1/r is found and both meteorology and topography are seen to be important in determining the shape of the observed patterns.

Facilities for radiocarbon dating were established at the University of Frankfurt/Main in the Institute of Anthropology. The Radiocarbon Laboratory provides assistance to the Amino-Acid-Dating Laboratory. This list reports on 14C dates measured up to September 1983.

The laboratory is installed in the basement of a three-story building and is equipped with a 2L copper proportional counter filled to 1013 mbar with purified CO2. The counter is protected against cosmic and surrounding radiation by a 3.5 ton lead shield and a copper multiwire anticoincidence ring-counter flushed with purified 90Ar/10CH4. Electronics are of the commercial NIM type. Charcoal and wood samples are treated by standard acid-alkali-acid methods. Bone samples are treated according to the collagen methods described by Berger, Horney, and Libby (1964), Longin (1971), Protsch (1972; 1975), and Protsch and Berger (1973).

The dates listed were obtained using a stainless steel counter with an active volume of 1.3 L and a background of 16.3 cpm at an absolute filling pressure of 152 cm Hg. The present proportional counter in use is made of O.F.H.C. copper, and has an active volume of 1.25 L and a background of 5.2 cpm, at an absolute counter filling pressure of 152 cm Hg. CO2 is used as the counting gas and the counter is filled to a pressure of between 76 cm and 228 cm of Hg (depending on the sample size) at a temperature of 23 ± 0.3°C. The counter is shielded, starting from the top, by 5 cm of lead and 26 cm of iron, and is surrounded by an array of 22 Geiger tubes, and then finally by 2.5 cm of mercury. The thickness of the sides and base is greater than 10 cm of iron. As yet no neutron shielding is used and this probably accounts for the large fluctuations of background with barometric pressure (0.32 cpm per 1 cm Hg change in the pressure).

Mesopotamia is often regarded the “cradle of civilization.” The development of water management practices in the region is thought to have played a key role in the emergence of these early civilizations. We present the first direct dating of a palaeo-canal system at the ancient city of Girsu, Mesopotamia (modern Iraq) (occupied between 4800 and 1600 BC). We describe the use of archaeological and radiocarbon (14C) dating techniques to establish the age of this canal system. Our results show considerable differences between shell 14C dates on the one hand and charcoal 14C dates and archaeological evidence on the other. This likely reflects the impact of freshwater reservoir effects from the Tigris and Euphrates Rivers. Although the FRE from rivers is widely acknowledged, its impact on 14C dates in Mesopotamia is rarely discussed and poorly understood. Our results provide a first indication of its variability and magnitude. With the publication of our results we aim to highlight the problem and re-initiate collaborative research efforts in improving 14C dating in this important region.

To achieve high-precision and reproducible results from radiocarbon (14C) dating of carbonate samples in paleoclimate research, a new CO2 extraction line was designed, constructed, and characterized at the Heidelberg Radiocarbon Lab of the Institute of Environmental Physics, Heidelberg. The setup includes a circular glass-tube design, which is operated at vacuum pressure levels of the order of 10–5 mbar. The efficiency of the extraction process was assessed, showing significantly favorable conditions for solid piece samples (99.58 ± 4.69)% over powdered samples (88.28 ± 10.03)%. Process blank values are below 0.2 pMC apparent 14C activity. Repeated measurements of IAEA C2 standards with an average value of (41.09 ± 0.23) pMC attest high accuracy and reproducibility of the instrument. Six consecutive samples of 6 to 12 mg carbonate mass can be processed in one run of roughly 2.5 hours. Thus, the new setup contributes to time-efficient and reproducible radiocarbon dating results for paleoclimate research at the Institute of Environmental Physics. In a first application, Dead Carbon Fraction (DCF) values of a Holocene alpine stalagmite from Schratten Cave are presented, revealing extraordinarily high offsets between atmospheric and stalagmite 14C with DCF values between (49.4 ± 0.4)% and (61.6 ± 0.4)%.

We present new marine reservoir ΔR correction terms for the central and northern Kuril Islands. We estimate ΔR from a series of archaeological charcoal-shell pairs from two archaeological sites using standard calibration procedures and Monte Carlo simulation. The combined ΔR estimate for all paired samples for the Kuril samples is 508±127 yr. In the context of available North Pacific Rim ΔR estimates, the new Kuril data support the interpretation of a well-mixed, 14C-depleted North Pacific Subarctic Gyre. For the broader subarctic North Pacific region, a ΔR estimate in the range of 440±127 yr is a reasonable correction for any coastal marine shell date, and may be applied to fish and marine mammal dates for taxa known to reside within these waters throughout their life-histories. This generalization fails as one moves south from Hokkaido along the East Asian coast. There, well-equilibrated subtropical water minimize the ΔR offset.

The article presents results of measurements of radiocarbon (14C) concentration in sub-annual dendrochronologically dated tree rings of English oak (Quercus robur L.) from Grabie village near Kraków (southern Poland). Samples of early wood (EW) and late wood (LW) spanning the years 664–658 BCE. α-cellulose was extracted from each sample and their radiocarbon content was measured at the ATOMKI laboratory in Debrecen, Hungary. The EW and LW data confirm a prolonged increase in Δ14C values around 665–663 as was observed by Park et al. (2017), Rakowski et al. (2019), or Sakurai et al. (2020). In addition, we found that this event may consist of two relatively small events, as was proposed by Sakurai et al. (2020). Based on obtained in this and previous study data we estimate that the occurrence of the two events were between 665 and 664 BCE (Rakowski et al. 2019), and in late spring of 663 BCE (May–June, before beginning of LW formation).

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.

An example of how man's contaminants are introduced, deposited, and retained in sediments giving a chronological record of events has been developed for Lake Washington, Seattle. Significant amounts of both inorganic and organic compounds in the environment originate from fossil fuel sources, such as power plants and motor vehicles. Many organic compounds are introduced also from contemporary biogenic materials. Through the combined carbon isotope analysis technique (CCIA), we can distinguish between fossil and contemporary carbon sources classes (using 14C), as well as sources within each class (using 13C). To establish the chronology of the organic carbon pollutant input to the lake sediment, the ages of the layers were determined using 210pb dating techniques. Sediment profiles of trace metals and a fallout radionuclide plutonium were also obtained and compared with the carbon isotope profiles. The results show that the total organic carbon (TOC) concentration correspond to 93% modern carbon before 1905. This 14C concentration in TOC decreased to ∼60% modern in the 1930's and now is between 95 and 80% modern. The lipid fraction is ca 30% modern and the total aromatic hydrocarbon fraction reached a minimum of 5% modern in 1954. The large decrease in 14C of TOC around 1930 is believed to be due to coal dust or fly ash. The trace metal concentration also increased substantially at this time. The pattern observed in the sediment thus reflects the change in the local energy consumption pattern from a predominately coal to an oil-based economy. From the plutonium profile we infer that mixing occurs for 3 or 4 years before the sediment layers are compacted.

The Healy’s Lucky Strike site in central Alaska has an exceptional Holocene loess-paleosol sequence that has afforded us the ability to look at variation in 14C dating of soil organic matter (SOM) fractions in a high-latitude loess setting. Our work has focused on comparing the radiocarbon ages of charcoal and wood to base-soluble humic acids (HA) and base-insoluble soil residue (SR) fractions from bulk soil samples. Charcoal/wood ages were younger than HA ages reflecting the later stages of vegetation development at the surface of the soils prior to being covered by loess accumulation; the HA ages generally reflect the overall timing of soil formation and mean residence time of SOM. Soil residue ages are older than charcoal/wood and HA ages. SOM ages at this location become increasingly older than charcoal/wood ages with depth, reaching 750 to 8070 yr in difference and associated with weakly developed soils at the lowest depths. We suggest the drastic SOM age differences at this site result from the differential incorporation of small particles of coal throughout the sedimentary matrices introduced older contaminants to SR fractions.

Here, we reply to the attempt by Bonsall et al. (2015) to re-assess our results from the sulfur isotopic study of bone collagen from Mesolithic and Neolithic sites along the Danube in the Iron Gates Gorges area (Nehlich et al. 2010). Although we are highly interested to see our data re-assessed, we found certain misinterpretations, mistaken assumptions, and factual errors regarding our results. Therefore, we want to respond and re-assess our previous data, too. We establish for a few individuals a quantitative dietary reconstruction to demonstrate the reliability of our earlier interpretations.

This study evaluates the radiocarbon dating of ceramic samples from Tupiguarani sites in Brazil, a settlement type dating up to 3000 cal BP. In this work, residues from ceramic samples from four archaeological sites in Rio de Janeiro (Morro Grande, Serrano, Barba Couto, and Bananeiras) were analyzed. In order to identify the most suitable sample preparation protocols, the humic fraction was isolated from the bulk material at the Oxford Radiocarbon Accelerator Unit (ORAU), whereas the acid-base-acid (ABA) residue fraction method was applied at the Radiocarbon Laboratory of the Fluminense Federal University (LAC-UFF). The dating results were compared to the current knowledge about the occupational periods of the sites. For the Morro Grande site, the results of humic and ABA residue fractions show a difference of more than 1500 yr. For the Serrano site, the 14C ages obtained from the two pretreatments are identical, and as with the Barba Couto and Bananeiras sites, indicate an occupation during the Brazilian colonial period of the 16th century AD and are compatible with the archaeological data.

This paper presents the results of cross-dating of mammoth remains from northwestern Chukotka, northeastern Siberia. Our results suggest that several dates obtained by the radiocarbon laboratory at the Institute of Geology and Mineralogy, Siberian Branch of the Russian Academy of Sciences, Novosibirsk (laboratory code SOAN) appear to be too recent. Cross-dating in different laboratories revealed significant differences in the ages obtained compared to SOAN. This highlights the need to critically assess 14C dates, and where necessary, confirm results in independent laboratories.

Submicron-sized airborne particulate matter (PM) is not collected well on regular quartz or glass fiber filter papers. We used a micro-orifice uniform deposit impactor (MOUDI) to fractionate PM into 6 size fractions and deposit it on specially designed high-purity thin aluminum disks. The MOUDI separated PM into fractions 56–100, 100–180, 180–320, 320–560, 560–1000, and 1000–1800 nm. Since the MOUDI has a low flow rate (30 L/min), it takes several days to collect sufficient carbon on 47-mm foil disks. The small carbon mass (20–200 μg C) and large aluminum substrate (∼25 mg Al) present several challenges to production of graphite targets for accelerator mass spectrometry (AMS) analysis. The Al foil consumes large amounts of oxygen as it is heated and tends to melt into quartz combustion tubes, causing gas leaks. We describe sample processing techniques to reliably produce graphitic targets for 14C AMS analysis of PM deposited on Al impact foils.

Reliable series of high-precision radiocarbon dates in a stratified archaeological context are of great importance for interdisciplinary chronological and historical studies. The Early Bronze Age in the Near East is characterized by the beginning of the great civilizations in Egypt and Mesopotamia, as well as by urbanization in the Levant. We present stratified high-precision dates of short-lived material of Tell es-Sultan (Jericho), covering Late Proto-Urban/EB I, EB II and EB III layers from Trench III. Our calibrated dates, refined by Bayesian sequence analysis involving Gibbs sampling, are ca. 150–300 yr older than conventional archaeological age assessments. The corpus of 14C dates measured in the first decades after the discovery of 14C dating should not be taken too seriously. The 14C dates of Jericho measured by the British Museum 14C laboratory in 1971 appear to be erroneous.

Radiocarbon (14C) dating is routinely used, yet occasionally, issues still arise surrounding laboratory offsets, and unexpected and unexplained variability. Quality assurance and quality control have long been recognized as important in addressing the two issues of comparability (or bias, accuracy) and uncertainty or variability (or precision) of measurements both within and between laboratories (Long and Kalin 1990). The 14C community and the wider user communities have supported interlaboratory comparisons as one of several strands to ensure the quality of measurements (Scott et al. 2018). The nature of the intercomparisons has evolved as the laboratory characteristics have changed s. The next intercomparison is currently being planned to take place in 2019–2020. The focus of our work in designing intercomparisons is to (1) assist laboratories by contributing to their QA/QC processes, (2) supplement and enhance our suite of reference materials that are available to laboratories, (3) provide consensus 14C values with associated (small) uncertainties for performance checking, and (4) provide estimates of laboratory offsets and error multipliers which can inform subsequent modeling and laboratory improvements.

Most of the 14C measurements reported here were made between October 1986 and June 1987. Equipment, measurement, and treatment of samples are as reported previously (R, 1968, v 10, p 36–37; 1976, v 18, p 290; 1986, v 28, no. 3, p 1111).

The renewal of east Atlantic deep water and its large-scale circulation and mixing have been studied in observed distributions of temperature, silicate, ΣCO2, and 14C. 14C variations in northeast Atlantic deep water below 3500m depth are small. Δ14C values range from − 100‰ to −125‰. 14C bottom water concentrations decrease from Δ14C =−117‰ in the Sierra Leone Basin to Δ14C = − 123‰ in the Iberian Basin and are consistent with a mean northward bottom water flow. The characteristic of the water that flows from the west Atlantic through the Romanche Trench into the east Atlantic was determined by inspection of θ/Δ14C and θ/SiO2 diagrams. A mean potential temperature of θ = 1.50 ± .05°C was found for the inflowing water. A multi-box model including circulation, mixing, and chemical source terms in the deep water has been formulated. Linear programing and least-squares techniques have been used to obtain the transport and source parameters of the model from the observed tracer fields. Model calculations reveal an inflow through the Romanche Trench from the west Atlantic, which predominates over any other inflow, of (5 ± 2) Sv (potential temperature 1.50°C), a convective turnover of (150 ± 50) years and a vertical apparent diffusivity of (4 ± 1) cm2/s. Chemical source terms are in the expected ranges.

Accelerator mass spectrometry (AMS) radiocarbon measurements of organic samples require combustion to obtain CO2 for graphitization. Furthermore, determination of δ13C values is required in order to correct the 14C age due to carbon isotope fractionation effects. δ13C analysis is commonly carried out by stable isotope mass spectrometry because most applications demand high-precision δ13C values in addition to the requirements of 14C dating. A simplifying step is therefore to combine the combustion for stable isotope analysis with cryogenic trapping of CO2 for AMS graphite targets. Presented here is a simple CO2 trapping device based on a modified Gilson 220XL sampling (manifold) robot coupled to the inlet manifold system of a GV Instruments IsoPrime stable isotope mass spectrometer. The system is capable of batch combustion and analysis of up to 40 samples and is under full computer control by the mass spectrometer software. All trapping parameters such as flush time prior to trapping and total trap time are adjustable through the standard software user interface. A low 14C activity of background materials and high precision and accuracy of stable isotope analysis of carbon and nitrogen are demonstrated.

Here, we present the results of carbon isotope and elemental analysis of one-year-old Pinus Sylvestris L. needles collected in 2021 from 10 sampling sites in a highly populated and industrialized area of Poland. The needles were exposed to air pollution for one year. The chemical analysis of the samples was performed using different methods: radiocarbon analysis by accelerator mass spectrometry, stable isotope analysis using isotope ratio mass spectrometry, and elemental analysis by inductively coupled plasma-atomic emission spectroscopy. Variations in the carbon isotopes and elemental composition of pine needles were due to a mixture of carbon dioxide originating from different sources such as households, vehicle traffic, and industrial factories.