For determining age scintillation variant was used. Measurement of a large quantity of benzol [benzene] permitted reaching a limit of 62,000 yr without isotope enrichment. Precautions against contamination of the samples with contemporary carbon and tritium were taken in laboratory handling. Dating began only after it had been established that contamination had not taken place during chemical treatment. Benzol which displayed no radioactivity was synthesized from anthracite. Special measures were taken to remove humic acids from the sample by boiling the powdered sample for three days with three fresh lots of 2% solution of NaOH (Arslanov et al., 1966a, p. 134).

In 2008–2009, during construction of the ring road around the town of Sztabin in NE Poland, archaeological rescue excavations were carried out at site no. 12 in Horodnianka. The excavations revealed the remains of a defensive settlement from the Bronze Age, with a total surface of 3 ha. Concentric wooden palisades reinforcing the settlement were situated on sandy, elevated embankments of the Biebrza River. Altogether, 189 samples of archaeological wood, mainly oak (Quercus sp.), were collected. Dendrochronological analysis demonstrated that the trees were cut down within a relatively short period of only 22 yr. On the basis of 22 contemporaneous dendrochronological sequences, the average curve HOR_AA1 (89 yr long) was constructed. However, attempts at dating the average curve against the chronologies from adjacent areas were unsuccessful. Therefore, determination of the time interval represented by the palisade oaks was attempted with the wiggle-matching method. Radiocarbon dating using liquid scintillation counting (LSC) was conducted for 6 suitable samples selected from the average curve. The 14C results, after calibration, suggest the dates of cutting the oaks outlining the Horodnianka chronology most probably fall in the time interval 870–795 cal BC. This means that Horodnianka could be the furthest northeastern defensive fortification of the Lusatian culture.

This date list mainly reports on samples processed from 1982 to 1991. Each sample is converted to methanol. Radiocarbon is measured in a Teflon™ vial containing a mixture of 40 g of methanol and 50 cc of xylene, 1% Butyl PBD and 0.1% PBBO using low-background scintillation counters Aloka LSC-800, LB-I and LB-III. The background of LB-III is ca. 8 cpm and counting efficiency is ca. 70%. The recent 14C standard used is 95% of NBS oxalic acid; 5568 yr is used as the half-life of 14C.

Construction of a new science complex in Osong, Cheongwon-gun, Korea, has allowed the investigation of 14 different Paleolithic localities, excavated during 2005–2007. Here, we investigated localities 1 and 12 of the Mansuri Paleolithic site to obtain chronological information using radiocarbon dating. The soil deposition rates varied from 0.09 to 0.15 mm/yr over the period ranging from 33 to 31 kyr BP for locality 1. Locality 12 samples were more recent, <10 ka, and have similar accumulation rates, averaging 0.11 mm/yr. The soil ages of locality 12 were found to be younger than 10 kyr BP. Results for both soil and organic materials at this locality gave much younger ages at shallower depths than the ages expected by the Korean Paleolithic cultural history for this region. Therefore, these more recent deposits may not be associated with the cultural layers and are interpreted to have been hydrologically modified following emplacement. 14C dates of the soil and organic materials at locality 12 confirm that there is evidence for multiple human occupations throughout the last 9 kyr BP.

The C14 Laboratory at Kiel University was established in 1963. It continues measurements, which were made at the Institut für Kernphysik, Kiel, on age determination with Chlorine 36, which is produced by cosmic ray neutrons (Bagge and Willkomm, 1963, 1966). The first C14-counting apparatus was completed in 1964 and dating work started at the end of 1964 after extensive general tests of counter working conditions (Erlenkeuser, 1965). The data reported here have been obtained during the first half of 1965. During this period the dating measurements were interrupted on numerous occasions by measurements of background and the oxalic standard in order to check long-time variations of the apparatus.

A radiocarbon (14C) dating technique with accelerator mass spectrometry (AMS) was applied to estimate the year of death and the year of birth of unidentified human remains. Because many of the samples have been preserved in formaldehyde, it was necessary to evaluate the influence of formaldehyde on carbon ages. Samples intentionally preserved in formaldehyde during the known period were measured, and their Δ14C values were compared with results obtained from fresh samples. The influence of formaldehyde on soft tissue was 14 times larger than that on cortical bone. Unfortunately, an effective method for removing the influence of formaldehyde has not yet been found. 14C ages could be obtained only from the samples not preserved in formaldehyde. The years of birth were determined by the ages of the dentin samples, while the years of death were determined by the ages of the bone and soft tissue samples. Multiple sampling from a body provides an advantage in determination of one of two possible ages of a sample obtained using the bomb peak. Victims of the Korean War were ascertained by the year of death. The year of death and the age at death of unidentified bodies were also determined for forensic investigation.

This list includes mainly the results of datings done from 1967 to 1969. Methods are essentially the same as those described in Radiocarbon, 1966, v. 8, p. 46–53, 1967, v. 9, p. 38–42, and 1969, v. 11, p. 15–21. Samples synthesized to benzene and counted by liquid scintillation spectrometry. Age calculations are based on 95% of the activity of the NBS oxalic acid standard and computed from the Libby half-life of 5570 yr and reference A.D. 1950. The error listed is the one-sigma statistical counting error. Most samples were counted for 2000 to 3000 min. HCL and NaOH pretreatments were applied to samples as required.

We present case studies on three objects of high importance for cultural heritage in southern Poland, dated in years 2018–2022 at the Gliwice 14C and Mass Spectrometry Laboratory with radiocarbon (14C) and dendrochronology methods. The first was a richly ornamented wooden cane, discovered during excavations on the market in Bytom city. The cane can be associated with medieval court proceedings. The archaeological context indicates the 13th century AD, and the 14C result corresponds perfectly with this time, confirming that it is the oldest object of this type in Poland. The second was a 4-m-tall oak column from St. Leonard Church in Lipnica Murowana, a UNESCO heritage site. The local story said it was previously devoted to Światowid, a pagan deity. Our analysis excluded the pre-Christian age, as the tree was felled no earlier than the late 15th century, which is in agreement with historical records. The third was a wooden Saint Lawrence Church in Bobrowniki. The presbytery was covered with up to five layers of polychromic paintings, some of high artistic value. We dated three samples from the original wooden board, and by wiggle-matching, the calibrated age interval was narrowed to 1731–1754 cal AD.

This list reports certain measurements made from 1965 to 1967. These samples are devoted to a special study of organic matter in soils. The work in large part is the subject of a thesis defended in Paris by S. M. Nakhla, 1968.

The results of a short program of landscape, buildings and materials analysis undertaken at Achanduin Castle, Lismore, Scotland (NM 8043 3927) are presented from the pilot phase of the Scottish Medieval Castles & Chapels C14 Project (SMCCCP). The study presents the first independent chronological evidence relating to the construction of this important medieval building, by radiocarbon analysis of a limited assemblage of Mortar-Entrapped Relict Limekiln Fuel (MERLF) fragments. Informed by a wider investigation of structural phasing and sample taphonomy, these measurements are constrained within a series of different Bayesian models, to generate a range of comparative estimates for the building’s constructional chronology. The precision with which the construction of this building can now be dated, from other evidence associated with the site, makes the Achanduin Castle study a useful point of reference for wider materials research.

Radiocarbon (14C) is one of the key radionuclides for the performance and safety assessment of a radioactive waste disposal, due to its high activity concentration in waste materials from the nuclear cycle and to its mobility. The measurement of the 14C content in spent ion exchange resins from nuclear reactors is important for the safety assessment of the disposal concept and for the choice of the appropriate treatment/disposal method. Ion exchange resins are commonly used in nuclear reactors as filters for the purification of process liquids or wastes streams and they retain molecules containing radioactive isotopes, among which is 14C. Their efficiency, both as filters and as waste containers, is strictly connected with the morphology. The preservation of spherical shape upon aging is one of the key parameters for their quality assessment and for the evaluation of the potential release of 14C during storage conditions. In this study, the change in IERs morphology during storage periods has been investigated in order to verify correlation with 14C release. Both brand new and aged specimens have been studied in order to assess the quality of the resins after 10 yr of storage and to contribute to the understanding of 14C release mechanisms.

A Bayesian multiple-frequency model has been developed for spectral analysis of data with unknown correlated noise. A description of the model is given and the method is applied to decadal atmospheric INTCAL98 Δ14C data. The noise of the INTCAL98 data is found to be red, and there seems to be no support for continuous harmonic frequencies in the data.

The present research is focused on the dating of the Oglakhty burial ground, the key site of stage I of the Tashtyk culture. Despite the numerous well-preserved burials of that type investigated at the Oglakhty complexes, their chronological position has remained unclear. From the early 20th century until the present, 2 different time periods had been identified for the Tashtyk burials: (1) from the 1st century BC until the 1st century AD and (2) from the 1st until the 2nd century AD. New data obtained in the 1990s suggested a different age for Tashtyk burials, namely the 3rd–4th centuries AD. This considerable shift in chronology needed to be checked with independent data. The chronological position of one of the Oglakhty burials, tomb 4, has been investigated with the use of wiggle-matching, applied to wooden logs used in the construction of tomb 4. The resulting dates for this burial strongly suggest its age as being limited to the 3rd–4th centuries AD, which is corroborated by the archaeological dates of the imported artifacts found in the grave and which is in agreement with the chronological position of the Oglakhty site, as proposed by previous investigations.

Regional offsets from Northern Hemisphere radiocarbon (14C) calibration curves are widely recognized for monsoon Asia and often hinder accurate 14C dating. In this paper, we explore the possible linkage between summer monsoon intensity and 14C offsets using tree-ring δ18O and 14C data from Thailand. We developed a 297-yr floating tree-ring δ18O chronology comprising seven teak log-coffin samples from the Ban Rai rock shelter site, northwestern Thailand. The outermost ring of our chronology was estimated to date from 358–383 CE, within a 95.4% (2σ) probability range, based on a total of 10 14C measurements that were wiggle-matched against a mixed calibration curve evenly weighted from the IntCal20 and SHCal20 curves. Backward trajectory analysis showed that an intensified (weakened) summer monsoon detected in a modern tree-ring δ18O chronology was most likely to be induced by increased (decreased) air mass transport from the tropical Indian Ocean, which is an area of intense upwelling where the 14C concentration is lower than the atmospheric 14C level. However, partly because of the limited sample size and dating uncertainty, the direct linkage between the tree-ring δ18O series and 14C records obtained from our teak log-coffin samples could not be statistically verified.

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.

During a rainfall event in early September 2006, the transport behavior of particulate organic carbon (POC) in a small river (Teshio River, northern Japan) with alluvial plain and forest characteristics was investigated chiefly with carbon isotopes. The radiocarbon (Δ14C value) of POC varied widely from –56%‰ at the beginning of the rain event to –10%‰ at peak rainfall. The Δ14C values have a positive correlation with C/N ratios and a negative correlation with Δ13C values except for the data from when both turbidity and water level were at their maximums due to rainfall. These results indicate that the sources of organic matter in the river come from the surface layer of soil as the water level rises during a rainfall event.

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.

Radiocarbon (14C) is the one of the most important radionuclides released from the nuclear facilities to the environment. Currently, inorganic 14C is checked during regular environmental monitoring as part of the groundwater monitoring program of the Paks Nuclear Power Plant. Several studies have shown that organic 14C can be also an important and sensitive tool for detection of possible leakage of nuclear technological systems. For this reason, a wet oxidation method was developed for the accelerator mass spectrometry (AMS) 14C measurement technique to determine the 14C activity concentration of the total dissolved carbon content of water samples, coming from environmental monitoring wells. The overall efficiency of the oxidation was around 94 ± 5% for different types of tested organic compounds. The typical 14C background (1–2 pMC) is obtained by preparation of blank samples, which allows a detection level of around 5·10–5 Bq L–1. The activity of the organic fraction can be calculated using the formula presented in the study. The method was applied for water samples deriving from environmental monitoring wells of a pressurized-water reactor (PWR) type of NPP. The results of our investigations over the 14 different water samples around the Paks NPP show that DO14C contribution to the total 14C activity concentration was between 5–25%.