This article presents the results of radiocarbon dating and a chronology of the Preobrazhenka 6 site of the Odino culture (Baraba forest steppe, western Siberia). Currently available 14C data for the necropolis do not allow accurate determination of the presence or absence of reservoir effects, and as such, further research is needed. Accelerator mass spectrometry (AMS) 14C dating of paired samples of terrestrial faunal and fish remains from a Neolithic pit suggest the absence of a reservoir effect in fish bone collagen. Middle Bronze Age burials have therefore been estimated to date to the 23rd–20th centuries cal BC. Pits with fish remains are dated earlier than burials, to the 63rd–61st centuries cal BC. Stable isotope measurements of human bone collagen (high δ15N and low δ13C values) indicate diets based on C3 plants and fish. Apparently, the role of animal protein in the diet was not significant. Dental paleopathology analysis has confirmed the important role of wild plants in human diet. Neolithic fish bones are elevated in δ13C [–13.5‰, average mean (n = 4)]. They are significantly different from the associated values of fish from the Late Bronze Age settlement of Chicha 1 [–22.5‰, average mean (n = 10)], which is also located in the Baraba forest steppe. The difference in δ13C values in fish bones may be determined by the origin of the samples, being derived either from lakes or rivers.

Tracing human history in west central Africa suffers from a scarcity of historical data and archaeological remains. In order to provide new insight into this problem, we reviewed 733 radiocarbon dates of archaeological sites from the end of the Late Stone Age, Neolithic Stage, and Early and Late Iron Age in Cameroon, Gabon, Central African Republic, Equatorial Guinea, Republic of Congo, and the western Democratic Republic of Congo. This review provides a spatiotemporal framework of human settlement in the forest biome. Beyond the well-known initial spread of Iron Age populations through central African forests from 2500 cal BP, it depicts the geographical patterns and links with the cultural evolution of the successive phases of human expansion from 5000 to 3000 cal BP and then from 3000 to 1600 cal BP, of the hinterland depopulation from 1350 to 860 cal BP, and of recolonization up to 500 cal BP.

Regional levels of radiocarbon have been monitored in order to investigate the impact of fossil fuel combustion on the activity of atmospheric 14CO2 in central Europe. Data from atmospheric 14CO2 monitoring stations in the Czech Republic, Slovakia, and Hungary for the period 2000–2008 are presented and discussed. The Prague and Bratislava monitoring stations showed a distinct local Suess effect when compared to the Jungfraujoch clean-air monitoring station. However, during the summer period, statistically insignificant differences were observed between the low-altitude stations and the high-mountain Jungfraujoch station. 14C data from the Hungarian monitoring locality at Dunaföldvár and the Czech monitoring station at Košetice, which are not strongly affected by local fossil CO2 sources, indicate similar grouping and amplitudes, typical for a regional Suess effect.

A high-resolution age model was developed for Kettle Lake, North Dakota, USA, from a series of 53 accelerator mass spectrometry (AMS) radiocarbon ages calibrated with Bayesian statistical methods, which provide a monotonically increasing series of calibrated ages with depth. Evident in the sediment are several slumps, debris flows, or landslides, which are confirmed by 14C dating. Removal of these facies produces a continuous sedimentary sequence for the past 13,000 yr with exception of one ≃260-yr hiatus associated with a 1.5-m-thick slump deposit. All ages except one are on terrestrial macrofossils and charcoal. A test age on aquatic organic detritus shows a hardwater effect of 600 yr at ≃2000 cal BP. Two ages from the same level on herbaceous charcoal and Chenopodium seeds are statistically the same, which further demonstrates the suitability of charcoal from grassland environments for AMS 14C age control. However, 2 specimens of wood charcoal are too old relative to bracketing ages and glacial geologic history. These ages confirm the sedimentary interpretation of redeposition and provide a caution about the longevity of wood charcoal in the environment and its suitability for age control in lacustrine sediments.

Tree-ring series were collected for radiocarbon analyses from the vicinity of Paks nuclear power plant (NPP) and a background area (Dunaföldvár) for a 10-yr period (2000–2009). Samples of holocellulose were prepared from the wood and converted to graphite for accelerator mass spectrometry (AMS) 14C measurement using the MICADAS at ETH Zürich. The 14C concentration data from these tree rings was compared to the background tree rings for each year. The global decreasing trend of atmospheric 14C activity concentration was observed in the annual tree rings both in the background area and in the area of the NPP. As an average of the past 10 yr, the excess 14C emitted by the pressurized-water reactor (PWR) NPP to the atmosphere shows only a slight systematic excess (∼6′) 14C in the annual rings. The highest 14C excess was 13′ (in 2006); however, years with the same 14C level as the background were quite frequent in the tree-ring series.

In the “sublimation technique,” carbon dioxide entrapped in ice is recovered by sublimation, converted to graphite and ratio of 14C/13C in the CO2 determined by AMS measurements. We describe here several experiments performed to check the validity of such measurements and to study the effect of cosmogenically produced in-situ14C on the measurements.

The University of Arizona Radiocarbon Laboratory purchased a state-of-the-art LKB Quantulus LSC and placed it into a new underground counting chamber. We have investigated the performance of the Quantulus in this setting comparing different vial types, checking background sources and experimenting with sample size.

Southern Poland is home to numerous large mining and energy industry facilities, which consume relatively great amounts of fossil fuels. Temporal and spatial distribution of CO2 emissions to the atmosphere were estimated on the basis of 13C and 14C isotope measurements in atmospheric CO2 and in α-cellulose from pine tree rings. The Suess effect was evaluated in the atmospheric CO2 from the High Tatra Mountains (Kasprowy Wierch) and the urban area (Kraków), as well as in tree rings from Niepołomice Forest near Kraków. Two different models were used to estimate the emission component recorded in tree ring δ13C on the background of climatic changes.

The mortar samples of the Castle of Cannero (Lake Maggiore, Italy) have been characterized and radiocarbon (14C) dated. The presence of LDH phases was identified. The hydraulic reaction was evaluated by a multi-analytical approach. Careful extraction, preparation and purification of the binder fraction have been performed. Contaminations due to LDH phases have been removed allowing reliable absolute dating of the structures.

Non-hydraulic lime-based mortars represent only part of the binding materials found in archaeological and historical structures, and a new challenge is the application of 14C dating techniques on mortars that feature hydraulic reactions. This research work aims at 14C dating a series of Mg-rich hydraulic mortars from the Castle of Cannero (Lake Maggiore, Italy), from which both charcoals and mortar samples were collected. A multi-analytical approach employing X-ray powder diffraction (XRPD), optical microscopy (OM), and scanning electron microscopy/energy-dispersive microanalysis (SEM-EDS) was adopted in order to carefully characterize the samples. A wet gravimetric separation for the extraction of the fine fraction mainly composed by the mortar binder was carried out and the binder fraction was characterized by XRPD in order to investigate the presence of contaminants. The binding fractions are characterized by the widespread occurrence of hydrotalcite-type minerals, considered contaminants in 14C dating of mortars because of their capability to exchange carbonate anions even after the hardening process. A further purification treatment by thermal decomposition was performed before 14C dating by AMS. The obtained dates were consistent with archaeological expectations, confirming the potential of the developed purification methodology for hydraulic mortars dating.

The people of the Paracas and Nasca cultures, the creators of the famous geoglyphs, lived in the desert of the southern coast of Peru between about 800 BC and AD 650. The archaeological chronology of these cultures has been based almost exclusively on a sequence of ceramic styles. The absolute dating of some of the style phases was supported by a few radiocarbon dates (Rowe 1967). Here, we present an absolute chronology of the Paracas and Nasca cultures based on 14C dating of more than 100 organic samples from settlement and tomb relics, as well as on material derived from geoglyph sites in the Nasca/Palpa region (south Peru). The main focus has been on Nasca period settlement centers near Palpa, Los Molinos and La Muña, the Paracas period site of Jauranga, and the Initial period site of Pernil Alto. Most of the 14C samples were dated at the accelerator mass spectrometry (AMS) facility of the ETH Zurich (Switzerland). The targets were produced in the newly built graphitization line at the Heidelberg 14C laboratory (Germany). Clay (adobe) bricks, which are quite a common building material in Peru, were successfully tested to be used for AMS 14C dating of adobe architecture in Peruvian archaeology.

One of the greatest challenges of contemporary archaeology is to synthesize the large amount of radiocarbon and archaeological data into a useful dialogue. For the late Epipaleolithic and the Early Neolithic of the Near East, many 14C ages have been published without precise stratigraphic documentation. Consequently, for archaeological age models we often must use some more elementary approaches, such as probabilistic summation of calibrated ages. The stratigraphy of Körtik Tepe allows us for the first time to study an extended series of 14C ages of the earliest Holocene. In particular, we are able to analyze the data according to stratigraphic position within a well-documented profile. However, because of a plateau in the 14C age calibration curve at the transition from the Younger Dryas to the Early Holocene, dates of this period can be interpreted only if an extended sequence of dates is available. Due to problems remaining in the calibration procedure, the best way to achieve an interpretation is to compare the results of different 14C calibration software. In the present paper, we use the results of the calibration programs OxCal and CalPal. This approach has important implications for future age modeling, in particular for the question of how to date the transition from the Epipaleolithic to the PPNA precisely and accurately.

We report a practical system to mass-produce accelerator mass spectrometry (AMS) targets with 10–100 μg carbon samples. Carbon dioxide is reduced quantitatively to graphite on iron fibers via manganese metal, and the Fe-C fibers are melted into a bead suitable for AMS. Pretreatment, reduction and melting processes occur in sealed quartz tubes, allowing parallel processing for otherwise time-intensive procedures.

Chemical and isotopic (13C, 14C) blanks, target yields and isotopic fractionation were investigated with respect to levels of sample size, amounts of Fe and Mn, pretreatment and reduction time, and hydrogen pressure. With 7-day pretreatments, carbon blanks exhibited a lognormal mass distribution of 1.44 μg (central mean) with a dispersion of 0.50 μg (standard deviation). Reductions of 10 μg carbon onto targets were complete in 3–6 h with all targets, after correction for the blank, reflecting the 13C signature of the starting material. The 100 μg carbon samples required at least 15 h for reduction; shorter durations resulted in isotopic fractionation as a function of chemical yield. The trend in the 13C data suggested the presence of kinetic isotope effects during the reduction. The observed CO2-graphite 13C fractionation factor was 3–4% smaller than the equilibrium value in the simple Rayleigh model. The presence of hydrogen promoted methane formation in yields up to 25%.

Fe-C beaded targets were made from NIST Standard Reference Materials and compared with graphitic standards. Although the 12C ion currents from the beads were one to two orders of magnitude lower than currents from the graphite, measurements of the beaded standards were reproducible and internally consistent. Measurement reproducibility was limited mainly by Poisson counting statistics and blank variability, translating to 14C uncertainties of 5–1% for 10–100 μg carbon samples, respectively. A bias of 5–7% (relative) was observed between the beaded and graphitic targets, possibly due to variations in sputtering fractionation dependent on sample size, chemical form and beam geometry.

We report carbon isotope abundances of dissolved inorganic carbon (DIC) in surface seawater collected from a time-series site off the Newport Beach Pier in Orange County, California. These data represent the first time series of Δ14C data for a coastal southern California site. From a suite of samples collected daily from 16 October to 11 November 2004, Δ14C values averaged 32.1 ± 4.4‰. Freshwater input from the Santa Ana River to our site caused Δ14C and δ13C values to decrease. Since this initial set of measurements, a time-series site has been maintained from November 2004 to the present. Surface seawater has been collected bimonthly and analyzed for Δ14C, δ13C, salinity, and ΣCO2 concentrations. Water samples from the Santa Ana River were collected during the wet season. California sea mussels and barnacle shells, ranging from 4 to 6 months old, were also collected and analyzed. Results from May 2005 to January 2008 show no long-term changes in δ13C DIC values. Δ14C DIC values over the 2005–2006 period averaged 33.7‰; high Δ14C values were observed sporadically (every 6–7 months), suggesting the presence of open water eddies at our site. Finally, in 2007, a stronger upwelling signal was apparent as indicated by correlations between Δ14C, salinity, and the Bakun index, suggesting that the Δ14C record is an indicator of upwelling in the Southern California Bight.

Data on radiocarbon (14C), 137Cs, 210Pb, and 241Am levels in an ombrotrophic peat sequence from a montane site on the east coast of Ireland are compared with data from a similar sequence at an Atlantic peatland site on the west coast. The 14C profiles from the west and east coasts show a broadly similar pattern. Levels increase from 100 pMC or less in the deepest horizons examined, to peak values at the west and east coast sites of 117 ± 0.6 pMC and 132 ± 0.7 pMC, respectively (corresponding to maximal fallout from nuclear weapons testing around 1964), thereafter diminishing to levels of 110–113 pMC near the surface. Significantly, peak levels at the east coast site are considerably higher than corresponding levels at the west coast site, though both are lower than reported peak values for continental regions. The possibility of significant 14C enrichment at the east coast site due to past discharges from nuclear installations in the UK seems unlikely. The 210Pbex inventory at the east coast site (6500 Bq m−2) is significantly higher than at the west coast (5300 Bq m−2) and is consistent with the difference in rainfall at the two sites. Finally, 137Cs and 241Am inventories at the east coast site also exceed those at the west coast site by similar proportions (east:west ratio of approximately 1:1.2).

The process of calibrating radiocarbon determinations onto the calendar scale requires the setting of a specific statistical model for the calibration curve. This model specification will bear fundamental importance for the resulting inference regarding the parameter of interest—namely, in general, the calendar age associated to the sample that has been 14C-dated.

Traditionally, the 14C calibration curve has been modelled simply as the piece-wise linear curve joining the (internationally agreed) high-precision calibration data points; or, less frequently, by proposing spline functions in order to obtain a smoother curve.

We present a model for the 14C calibration curve which, based on specific characteristics of the dating method, yields a piece-wise linear curve, but one which rather than interpolating the data points, smooths them. We show that with this specific model if a piece-wise linear curve is desired, an underlying random walk model is implied as covariance structure (and vice versa). Furthermore, by making use of all the information provided by the calibration data in a comprehensive way, we achieve an improvement over current models by getting more realistic variance values for the calibration curve.

The suppression of interferences from atomic and molecular isobars is a key requirement for the extension of accelerator mass spectrometry (AMS) to the analysis of new cosmogenic isotopes and for increasing the range of applications for small AMS systems. In earlier work, it was shown that unwanted isobars can be eliminated by anion-gas reactions (Litherland et al. 2007). Recently, a prototype system in which such reactions could be applied to ions from an AMS ion source, the Isobar Separator for Anions (ISA), was described (Eliades et al. 2009). This system decelerates the beam of rare anions from keV to eV energies, guides them through a single radiofrequency quadrupole (RFQ) gas cell, and re-accelerates them for further analysis in a 2.5MV AMS system. Tests of this system with Cl and S anions and NO2 gas showed a suppression of S with respect to Cl of over 6 orders of magnitude, with a transmission of ∼30% for the Cl beam. In this work, results of the analysis of a range of standard reference materials are reported; these show the linearity of the system for measuring the 36Cl/35Cl ratio over a span of 2 orders of magnitude. Further tests, using the AMS system as a diagnostic tool, have provided clues about the loss of Cl at higher cell pressure and the nature of the residual low level of S transmission. These lead to the assessment of various gases for cooling the Cl– beam. Suppression measurements for 41K in the analysis of 41Ca, using NO2 as a reaction gas, are also discussed. These preliminary measurements have provided data for the development of a more advanced system with separate cooling and reaction cells.

Systematic investigations and experience from several application projects on small carbon samples over a number of years have resulted in measuring the radiocarbon content of 10 μg C samples with an overall precision of typically 1%. A substantial reduction of the carbon contamination during graphitization was achieved, resulting in 31±30 ng modern and <100 ng 14C-free carbon. Thus, graphitization is no longer the limiting factor because earlier sample preparation steps usually introduce much larger contamination. The method has been extended to a variety of materials and applied to various projects. Realistic conditions for procedure development can only be achieved in the context of applications on true samples; methods developed are the lyophilization of samples in solution, combustion, ultraviolet oxidation, or carbonate hydrolysis with phosphoric acid, which allows to prepare samples for a wide range of applications. Insights gained from systematic investigations and from real applications are presented.

The reinstallment, operation, and the 14C measurements reported here were made since 1976 in the LATYR, the Radiocarbon Dating Laboratory of the Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata. Sample preparation is preceded by careful visual separation and hand removal of gross impurities. This is followed in all cases (charcoal, wood) with successive washings of the sample with boiling 2% HCl and 1% NaOH solution for removal of carbonates and humic acids. Thereafter, it is washed with distilled water and acidified to pH = 3. Individual variations in the pretreatment are not described in the date list, but they are usually reported directly to the collector together with the data obtained.

We investigated a simple, reliable radiocarbon measurement procedure for water samples using the direct absorption method for sample preparation, followed by low-level liquid scintillation spectrometry. This process has involved quantitative evaluation of the conversion steps in order to estimate the appropriate working parameters. The 14C activity of dissolved inorganic carbon (DIC) for several types of water (ranging from seawater to groundwater) has been measured, paying attention to the preparation requirements of each type of water. The main advantage of this method is the simplified sample preparation, allowing measurement of a great number of samples in less time. This method was designed for routine analysis of water samples, and it is proposed particularly for use in 14C monitoring programs of CANDU-type reactors.

The measurements presented in this date list were made in the Radiocarbon Dating Laboratory at Teledyne Isotopes during 1969–70. Samples were analyzed by techniques described in R., 1968, v. 10, p. 246. Methods and references to sample pretreatment are provided in R., 1970, v. 12, p. 87. Errors associated with the age determinations are calculated by combining standard deviations from oxalic acid standard, background, and actual sample data. Samples which approach modern or background are reported with at least 2σ limits. Counting time for calculation of errors of background and standard is the same as that used for the sample. The error associated with the De Vries effect and the uncertainty of the half-life are not included.