In 2021, the National Research Institute of Cultural Heritage (NRICH) installed a new accelerator mass spectrometer (AMS) to date Korean national heritage. Before conducting radiocarbon dating, the facility was set up and its performance was assessed. AMS system parameters have been optimized. Measurement of standard and blank samples was verified. Intercomparison analyses were also performed using heritage samples. The F14C value of NIST 4990C was 1.3406 and the background level was 0.0024. Both IAEA-C7 and C8 were confirmed to match the reference value within the 1-σ range. The NIST 4990C measurement results confirmed high precision and accuracy, with 1-σ values below 2‰. In the intercomparison, the error for each sample was 2‰. Thus, based on this study, NRICH plans to launch a dating service specializing in cultural heritage.

This brief review describes the discovery of cosmic rays by Victor Hess from the Vienna Radium Institute and the later contribution of Marietta Blau through her observation of “disintegration stars” in photographic emulsion plates exposed to cosmic-ray bombardment. Marietta Blau, a nearly forgotten cosmic-ray pioneer from the Vienna Radium Institute, developed the nuclear emulsion technique for studying nuclear reactions, eventually discovering the disintegration of nuclei through high-energy cosmic rays. Blau survived the Holocaust by escaping to Mexico City from 1939 to 1944. Starting in 1948 at Columbia University, later as a staff member of Brookhaven National Laboratory and then University of Miami, she performed fundamental and original research with nuclear emulsions exposed to 3-GeV protons at the Brookhaven Cosmotron and to 6-GeV protons at the Berkeley Bevatron. Blau returned to Vienna in 1960, where at the Radium Institute a classical β-decay counting facility for radiocarbon dating had been installed, which was finally superseded by the Vienna Environmental Research Accelerator (VERA), a modern versatile accelerator mass spectrometry facility.

This work presents the integration of an elemental analyzer (EA) and an isotope ratio mass spectrometer (IRMS) into the 6 MV AMS system at the Institute for Nuclear Physics, University of Cologne. The AMS measurement of δ13C values for IAEA-C6 reference material resulted in –11.39(226)‰, compared to –10.28(32)‰ obtained by IRMS. The EA-IRMS system was also tested with IAEA-C3, IAEA-C5, and IAEA-C7 reference materials, yielding –24.79(9), –25.18(15), and –14.76(18)‰ respectively. Compared to the IAEA information values given as –24.91(49), –25.49(72) and –14.48(21)‰ respectively. To investigate an observed sample mass dependency, environmental samples from Spitzbergen were examined, showing δ13C values of –25.17(55), –25.80(31), and –26.17‰ in Cologne, while Hamburg recorded –24.8(1), –25.5(1), and –26.2(13)‰. In summary, this new setup could enable online analysis and quasi-simultaneous measurements of 14C, δ13C, and δ15N for ultra-small samples, utilizing precise δ13C values from IRMS for fractionation correction of the 14C/14C isotopic ratio.

A new vacuum line to extract CO2 from carbonate and dissolved inorganic carbon (DIC) in water was established at Guangxi Normal University. The vacuum line consisted of two main components: a CO2 bubble circulation region and a CO2 purification collection region, both of which were made of quartz glass and metal pipelines. To validate its reliability, a series of carbonate samples were prepared using this system. The total recovery rate of CO2 extraction and graphitization exceeded 80%. Furthermore, the carbon content in calcium carbonate exhibited a linear relationship with the CO2 pressure within the system, demonstrating its stability and reliability. The system was also employed to prepare and analyze various samples, including calcium carbonate blanks, foraminiferal, shell, groundwater, and subsurface oil-water samples. The accelerator mass spectrometry (AMS) results indicated that the average beam current for 12C- in the samples exceeded 40 μA. Additionally, the contamination introduced during the liquid sample preparation process was approximately (1.77 ± 0.57) × 10−14. Overall, the graphitized preparation system for carbonate and DIC in water exhibited high efficiency and recovery, meeting the requirements for samples dating back to approximately 30,000 years.

The absorption and distribution of radiocarbon-labeled urea at the ultratrace level were investigated with a 14C-AMS biotracer method. The radiopharmaceutical concentrations in the plasma, heart, liver, spleen, lung, kidney, stomach, brain, bladder, muscle, testis, and fat of rats after oral administration of 14C urea at ultratrace doses were determined by AMS, and the concentration-time curves in plasma and tissues and pharmacokinetic distribution data were obtained. This study provides an analytical method for the pharmacokinetic parameters and tissue distribution of exogenous urea in rats at ultratrace doses and explores the feasibility of evaluation and long-term tracking of ultratrace doses of drugs with AMS.

A newly developed compact AMS, LEA (Low Energy Accelerator), is tested and compared with a state-of-the-art AMS system MICADAS (Mini Carbon Dating System), which has a precision performance of better than 1‰ for modern 14C. The main difference between these two systems is the acceleration voltage, which has been reduced from 200 kV with the MICADAS system to 50 kV with the LEA system. In order to execute the final performance tests, exactly same samples (2 sets consisting of 7 standards, 4 blanks, 26 wood samples) are measured on both systems successively. The results show that the LEA system is fully operational, and the performance is entirely comparable with that of the MICADAS system.

Since 2018, the radiocarbon laboratory of Lanzhou University has been equipped with a compact accelerator mass spectrometer—a 200-KV mini carbon dating system (MICADAS), together with an auto graphitization equipment (AGE III). The laboratory has for a long time prepared graphite targets for 14C dating of plant fossils, charcoal, bones, and bulk organic matter. Herein, we give an overview of the operating status and performance of the dating facility. The long-term measurements of the standard and blank samples indicated that the results for MICADAS in Lanzhou University were accurate and stable and of high sensitivity. Fifteen sets of organic materials collected from archaeological sites in northwest China were selected for an inter-comparison study involving the participation of four specialist laboratories. The 14C dating results for the homogenized archaeological samples from several of the laboratories showed a high degree of consensus. The long-term performance and inter-comparison data for MICADAS confirmed that the radiocarbon laboratory of Lanzhou University could provide stable and accurate 14C dating results. In this context, the 14C dating results for a number of key archaeological/environmental samples were validated.

A new system for preparing 14C samples was established for a compact accelerator mass spectrometer (GXNU-AMS) at Guangxi Normal University. This sample preparation system consists of three units: a vacuum maintenance unit, a CO2 purification unit, and a CO2 reduction unit, all of which were made of quartz glass. A series of radiocarbon (14C) preparation experiments were conducted to verify the reliability of the system. The recovery rate of graphite obtained was more than 80%. The carbon content in the commercial toner and wood sample was linearly fitted to the CO2 pressure in the measurement unit of the system. The results showed a good linear relationship, indicating that the reliability of the sample preparation system. AMS measurements were conducted on a batch of standard, wood, and dead graphite samples prepared using this system. The results showed that the beam current of 12C- for each sample was more than 40 μA, the carbon contamination introduced during the sample preparation process was ∼ 2 × 10–15, and that the new sample preparation system is compact, low-contamination, and efficient and meets the GXNU-AMS requirements for 14C samples.

The present paper is an announcement of first absolute age dating directly on fossilized bones and teeth of the Pleistocene mammalian fauna from the Manjra valley, District Latur, Maharashtra, India. The fossilized samples were measured using the AMS facility at Inter-University Accelerator Centre, New Delhi, India. The results gave the time frame of 21,423 BP to 24,335 BP that correspond close to and the threshold of LGM and sheds important light on the palaeoecology of the area that supported diverse megafaunal species in the Upper Manjra valley. These calendar dates not only have wider significance in terms of first ever approximate chronological frame for the Pleistocene fauna in Peninsular India but also offer methodological innovations especially when the adequate bioapatite is absent in the fossilized bones and teeth from the fossil record.

This study is on the absolute age dating of a multicultural site of Erenda, East Medinipur district, in coastal West Bengal, India. Charcoal samples were collected and measured using the accelerator mass spectrometry (AMS) facility at the Inter-University Accelerator Centre, New Delhi, India. These samples were collected from secured stratigraphic context of two excavated trenches. A careful collection of samples from two trenches provided us with the first calendar dates, 950 BCE and 1979 BCE, of protohistoric sites in coastal West Bengal. These calibrated calendar dates not only have wider significance in terms of archaeology but also methodological implications to understand the relevance of application of AMS from the dynamic coastal landscape in the humid tropics during the late Holocene period.

A setup for ion-laser interaction was coupled to the state-of-the-art AMS facility VERA five years ago and its potential and applicability as a new means of isobar suppression in accelerator mass spectrometry (AMS) has since been explored. Laser photodetachment and molecular dissociation processes of anions provide unprecedented isobar suppression factors of >1010 for several established AMS isotopes like 36Cl or 26Al and give access to new AMS isotopes like 90Sr, 135Cs or 182Hf at a 3-MV-tandem facility. Furthermore, Ion-Laser InterAction Mass Spectrometry has been proven to meet AMS requirements regarding reliability and robustness with a typical reproducibility of results of 3%. The benefits of the technique are in principle available to any AMS machine, irrespective of attainable ion beam energy. Since isobar suppression via this technique is so efficient, there often is no need for any additional element separation in the detection setup and selected nuclides may even become accessible without accelerator at all.

An international consortium of radiocarbon (14C) laboratories was established to date the origin of the St. George’s Rotunda in Nitrianska Blatnica (Slovakia), because its age was not well established in previous investigations. Altogether, 20 samples of wood, charcoal, mortar and plaster were analyzed. The 14C results obtained from the different laboratories as well as between the different sample types were in good agreement, resulting in a 14C calibrated age of 783–880 AD (94.2% probability) for the Rotunda. Although the 14C results have very good precision, the specific plateau-shape of the calibration curve in this period caused the wide range of the calibrated age. The probability distribution from OxCal calibration shows, however, that about 86% of the probability distribution lies in the period before 863 AD, implying that the Rotunda could have been constructed before the arrival of Constantine (St. Cyril) and St. Methodius to Great Moravia. The Rotunda thus probably represents the oldest standing purpose-built Christian church in the eastern part of Central Europe.

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).

Decommissioning of nuclear reactors requires determination of all remnant long-lived isotopes that were produced during their long functioning time of the respective facilities. Radiocarbon (14C) is such an isotope (T1/2 = 5730 yr), widely produced by neutron reactions in a thermal column of a nuclear reactor. Accelerator mass spectrometry (AMS) uses 14C for precise dating of up to 50,000 years old archaeological artifacts. This study presents a premier AMS measurement of high concentrated 14C samples that are strictly forbidden in laboratories dedicated to perform 14C dating. The determined 14C activities range from the natural level (isotopic ratio 14C/12C = 1.2 × 10–12) up to values of 10,000 times higher. 14C bulk and depth profile concentrations were measured in the thermal column disks of a decommissioned nuclear reactor. Results have shown that the 14C concentration in the thermal column, close the reactor core is about 75 kBq/g and decreases to 0.7 Bq/g and the end of the column. Such AMS measurements are applicable for decommissioning and waste management of nuclear reactors.

Temporal variations of the radionuclide 10Be are broadly synchronous across the globe and thus provide a powerful tool to synchronize ice core chronologies from different locations. We compared the 10Be record of the Akademii Nauk (AN) ice core (Russian Arctic) for the time period CE 1590–1950 to the 10Be records of two well-dated Greenland ice cores (Dye3 and NGRIP). A high correlation (r = 0.59) was found between the AN and Dye3 records whereas the correlation with NGRIP was distinctly lower (r = 0.45). Sources of deviations may include local fluctuations in the deposition of 10Be due to changes in the precipitation patterns, and artefacts due to the core-sampling strategy. In general, the existing age model was validated, confirming the AN ice core to be a unique and well-dated source of palaeoclimate parameters for the Russian Arctic. We further used numerical simulations to test the influence of the core-sampling strategy on the results and derived an optimized sampling strategy for the deeper parts of the ice core.

For many of archaeology’s rarest and most enigmatic bone artifacts (e.g. human remains, bone ornaments, worked bone), the destruction of the 500 mg material necessary for direct accelerator mass spectrometry (AMS) dating on graphite targets would cause irreparable damage; therefore many have not been directly dated. The recently improved gas ion source of the MICADAS (MIni CArbon DAting System) offers a solution to this problem by measuring gaseous samples of 5–100 µg carbon at a level of precision not previously achieved with an AMS gas ion source. We present the results of the first comparison between “routine” graphite dates of ca. 1000 µg C (2–3 mg bone collagen) and dates from aliquots of gaseous samples of <100 µg C (<0.2 mg bone collagen), undertaken with the highest possible precision in mind. The experiment demonstrates the performance of the AixMICADAS in achieving reliable radiocarbon measurements from <0.2 mg collagen samples back to 40,000 14C BP. The technique has great implications for resolving chronological questions for key archaeological artifacts.

Accelerator mass spectrometry (AMS) measurements of the radiocarbon content in very old samples are often challenging and carry large relative uncertainties due to possible contaminations acquired during the preparation and storage steps. In case of such old samples, the natural surrounding levels of 14C from gases in the atmosphere, which may well be the source of contamination among others, are 2–3 orders of magnitude higher than the samples themselves. Hence, serious efforts are taken during the preparation steps to have the samples pristine until measurements are performed. As samples often have to be temporarily stored until AMS measurements can be performed, storage conditions also become extremely crucial. Here we describe an assessment of this process of contamination in background AMS samples. Samples, both as pressed graphite (on AMS targets) and graphite powder, were stored in various storage conditions (CO2-spiked air) to investigate the extent of contamination. The experiments clearly show that the pressed targets are more vulnerable to contamination than the unpressed graphite. Experiments conducted with enriched CO2-spiked laboratory air also reveal that the contaminating carbon is not only limited to the target surface but also penetrates into the matrix. A combination of measurements on understanding the chemical nature of the graphitization product, combined with long-available knowledge on “adventitious carbon” from the surface science community, brought us to the conclusion that contamination is to a certain extent inevitable. However, it can be minimized, and should be dealt with by sputter-cleaning the samples individually before the actual measurement.

Accelerator mass spectrometry (AMS) is the most sensitive method for measuring 129I in environmental samples available today, with a detection limit of about 10–15 for 129I/127I. A drawback of the technique is the time-consuming chemical separation required to prepare AMS targets from raw samples. This step significantly limits applications requiring rapid analyses and large numbers of samples, for example, in monitoring studies associated with nuclear accidents. This work introduces a direct method for 129I measurements by AMS that does not require chemical separation. In this approach, stable iodine (127I) is added to a matrix of niobium (Nb) powder and mixed with dried raw sample. This mixture is pressed directly into a sputter target for AMS analysis. Two types of environmental samples have been tested in this work, seaweed and sediment. No anomalous behavior was noted in the Cs+ sputtering behavior of the targets prepared from these materials. The 129I/127I ratios and 129I concentrations measured by this rapid method were found to be in agreement with reported values that used a conventional AMS method for the same material. Based on our findings, we expect that such rapid measurements can be applied to a wide variety of materials, in addition to seaweed and sediment, as long as the sputtering-induced adverse effects do not prevent the stable operation of the ion source. The method is especially useful for screening large numbers of samples before more precise analyses are made.

Growth rates and the ability to date an organism can greatly contribute to understanding its population biology and community dynamics. 1n 1954, V. N. Andreev proposed a method to date regularly branched members of Cladonia, a fruticose lichen, using total thallus length and number of internodes. No research, however, has demonstrated the reliability of this technique or compared its estimates to those derived by other means. In this study, we demonstrate the utility of 14C/C ratios to determine lichen age and growth rate in Cladonia stygia (Fr.) Ruoss collected from north-western Alaska, USA. The average growth rate using 14C/C ratios was 6·5 mm yr−1, which was not significantly different from growth rates derived by Andreev's internode method (average = 6·2 mm yr−1); thus, suggesting the reliability of Andreev's simple field method for dating lichens.

Accelerator mass spectrometry (AMS) is an ultrasensitive analytical technique for measuring rare nuclides such as 14C, 26Al and 41Ca. The low detection limit and wide dynamic range of AMS allow long-term and highly sensitive tracer studies in nutrition that cannot be performed with other methods. The present paper is intended to provide a description of AMS to the interested nutritionist and present proven applications. AMS is compared to liquid scintillation counting and stable isotope MS. A description of common AMS methodology is presented that consists of determining the dose, preparing the sample, diluting the sample (if necessary), and measuring the sample. Applications include Ca metabolism, Al uptake from the environment, dietary intake of carcinogens, fat meta-bolism and folate metabolism. Throughout this discussion the experimental advantages (small doses that pose no health risk, extremely long experimental lifetime, small sample sizes and high sensitivity) made possible by the unique analytical capabilities of AMS are emphasized. The future of AMS is discussed. As the number of AMS centres, instruments, and studies increases, the number of nutritional applications that employ AMS will continue to grow. The coupling of AMS with other analytical techniques (e.g. high performance liquid chromatography) will be developed as access to AMS improves.