The Laboratory for the Analysis of Radiocarbon with AMS (LARA) was established at the University of Bern in 2013. Since then, the quality of sample preparation and radiocarbon measurement procedures have been validated for different materials such as plant remains, macrofossils, bulk sediment, charcoals, and wood. This article presents the optimization of sample pretreatment of bones based on protocols described in the literature. The extraction of collagen was performed with an acid-base-acid treatment, gelatinization, coarse filtration, lyophilization, and graphitization. Dating results were validated as satisfactory for the Holocene by investigation of 36 individual samples previously dated by other 14C laboratories including VIRI/SIRI materials and from well-known archaeological contexts. An additional blank contribution for bone treatment was determined by comparison with the preparation of other sample materials. The cases of two outliers from the Holocene were studied in detail.

Archaeological surveys conducted in the Negev and Sinai during the 20th century were commonly interpreted as representing short settlement periods interrupted by long gaps. The time factor was usually based on archaeological estimates rather than comprehensive physical dating. For example, the perceived age and time duration of “hole-mouth” pottery sherds and tabular flint scrapers became a source of circular reasoning to “date” sites and their “duration.” Thus, desert sites became to be perceived as temporary, seasonal, short-lived, while the cultures of desert populations were somehow undervalued. However, radiocarbon dating of desert sites from the Late Neolithic to the Early Bronze Age IV presents a very different scenario. The deserts of the Southern Levant exhibit a full sequence of settlement, a longer life span of individual sites, and a higher level of activity and creativity of the desert people. This paper describes the controversy and presents the 14C data that form the basis for the revised view.

We present new updates to the calendar and radiocarbon (14C) chronologies for the Cariaco Basin, Venezuela. Calendar ages were generated by tuning abrupt climate shifts in Cariaco Basin sediments to those in speleothems from Hulu Cave. After the original Cariaco-Hulu calendar age model was published, Hulu Cave δ18O records have been augmented with increased temporal resolution and a greater number of U/Th dates. These updated Hulu Cave records provide increased accuracy as well as precision in the final Cariaco calendar age model. The depth scale for the Ocean Drilling Program Site 1002D sediment core, the primary source of samples for 14C dating, has been corrected to account for missing sediment from a core break, eliminating age-depth anomalies that afflicted the earlier calendar age models. Individual 14C dates for the Cariaco Basin remain unchanged from previous papers, although detailed comparisons of the Cariaco calibration dataset to those from Hulu Cave and Lake Suigetsu suggest that the Cariaco marine reservoir age may have shifted systematically during the past. We describe these recent changes to the Cariaco datasets and provide the data in a comprehensive format that will facilitate use by the community.

This study establishes the chronological framework of the sedimentary sequence deposited Dead Sea, ICDP 5017-1, Radiocarbon chronology during the past 50 ka at the deepest part of the Dead Sea (the ICDP 5017-1 site), which was recovered by the Dead Sea Deep Drilling Project (DSDDP) under the auspices of the International Continental Scientific Drilling Program (ICDP). The age-depth model is constructed using 38 14C dates of terrestrial plant remains in a composite 150-m-long profile, generated by anchoring 32 marker layers identified in five cores. The sedimentary records at the ICDP 5017-1 site fills gaps in those obtained from the exposed sections at the high margins of the lake, particularly in times of lake-level retreat, and allows for a high-resolution comparison between the lake’s margins and deepest floor.

The accelerator mass spectrometry (AMS) center at Horia Hulubei National Institute for R&D in Physics and Nuclear Engineering, Bucharest, is based on the latest-generation 1 MV Tandetron® accelerator, produced by High Voltage Engineering Europa (HVEE), The Netherlands. The AMS center became fully functional at the start of 2013, and at the end of 2015 the laboratory established the RoAMS international code and it was added to the list of AMS laboratories maintained by Radiocarbon journal. An important aspect in the establishment of a new AMS laboratory is the declaration and documentation of the adopted protocols and to demonstrate the reliability and reproducibility of the measurements in comparison to internationally recognized reference materials. In this paper, we present the dating results on the Sixth International Radiocarbon Intercomparison (SIRI) samples that were pretreated, graphitized, and measured in our laboratory. The newly developed sample preparation laboratory can handle sample materials as (1) organic materials, (2) wood, (3) bones, and (4) carbonates. The results of our measurements are in very good agreement with the SIRI consensus values and confirm the reliability of our sample preparation laboratory and also the good performance of the HVEE AMS system. The blank levels for the SIRI materials are 0.277±0.045/0.333±0.046 percent modern carbon (pMC) for wood samples, 0.441±0.038 pMC for bone collagen, and 0.239±0.030 pMC for carbonate materials, considering an average mass of 1 mg sample graphite.

Most of the determinations reported here were obtained with the 2 L counter described in our first date list (GSC I). All age calculations are based on a C14 half-life of 5568 ± 30 yr and 0.95 of the activity of the NBS oxalic-acid standard, and the ages are quoted in years before 1950. The age errors include: counting errors of sample, background, and standard, the error in the half-life of C14, and an error term to account for the average variation of ±1.5% in the C14 concentration during the past 1100 yr. ‘Greater than’ ages are based on the 4 σ criterion (GSC II).

Most of the C14 measurements reported here were made between October 1971 and October 1972. Equipment, measurement, and treatment of samples are the same as reported previously (R., 1968, v. 10, p. 36-37; 1970, v. 12, p. 534).

Wood from regular timbering of a shallow seated mine in Tuscany gave 14C ages of 5730 ± 100 years BP, much too old to be attributed to one of the known civilizations of Italy. This mine is located in a region of declining volcanic activity, noticeable especially through numerous emanations (natural or incidentally induced by drillings). It was suspected that the analyzed wood had grown in an environment where the normal atmosphere had been diluted by volcanic emanations. To check this hypothesis, living plants (trees, bushes and reeds) and volcanic emanations have been sampled and their 14C content measured. All present day plants are depleted in 14C, giving a fictitious age different from 0 (1805, 1820, 2540, 4350 years BP). Of the gaseous emanations sampled, two have a high pressure and show virtually no 14C (>41,000 years BP). Two others have a pressure close to atmospheric, and small amounts of 14C were introduced by atmospheric contamination (22,570 and 30,580 years BP).

Conclusion: plants grown in the vicinity of volcanic emanations have 14C activities that are too low because of a natural 14C dilution and yield anomalously high ages. The δ13C values obtained for two of these plants (—27.4‰ and —23.7‰) are close to the average for plants in general (—25‰), whereas the CO2 of mofettes is heavier than atmospheric CO2.

Regular 14C sampling of discharged air began in 1988 at Paks Nuclear Power Plant (NPP), Hungary, and in 1991 at NPPs in Krsko, Slovenia and Bohunice, Slovakia. Monitoring of 14C discharges is carried out at all NPPs with similar differential samplers continuously collecting 14C in the form of 14CO2 and 14CnHm. The main results of airborne discharge monitoring are as follows: 14C activity concentration varied roughly within a factor of two around their mean values, 125 Bq m-3 and 90 Bq m-3 for Paks and for Krsko NPP, respectively. The pattern of discharge for Bohunice NPP is slightly different from that at the other two stations. At Bohunice, there has been a continuous increase in the discharge rate at power unit V1, starting with 70 Bq m-3 in 1991 and reaching a value of 190 Bq m-3 in 1995. The values for power unit V2 are 50 Bq m-3 and 82 Bq m-3. The average normalized yearly discharge rates are 0.887 (TBqGWe-1yr-1) for Paks, 0.815 (V1) and 0.500 (V2) for Bohunice, and 0.219 for Krsko. Most of the discharged 14C is in hydrocarbon form, 95% for Paks and Bohunice V2, but the CO2 fraction may reach 25% or 43% at Bohunice V1 and Krsko, respectively. At Bohunice V1, not only the discharge rate increased but the 14CO2 ratio to the total changed from 30% to 13%. The local radiological impact is estimated to be 1.5 μSv a-1 for Paks, 1.7 μSv a-1 for Bohunice, and 0.12 μSv a-1 for Krsko. The 14C excess in the environment has been measured at Paks NPP since 1989. Based on the monitoring data, the long-term average 14C excess from the Paks NPP was D14C=50% for hydrocarbons. Tree-ring analysis has shown a slight excess around Krsko NPP: D14C is equal to 199.9% for a tree at 1 km from the NPP compared with a “reference” one for which D14C was equal to 111.6% (in 1994).

We selected SN1006, the brightest and closest to Earth of all supernovas historically observed, for a study of 14C production by e−,e+-bremsstrahlung cascades initiated by hard γ rays (>10 MeV) from that event. During the cascade, bremsstrahlung energies eventually fall within a giant (n,γ), (n,2γ) cross-section, peaking at 23 MeV and approaching effectively zero below 10 MeV and above 40 MeV. The neutrons are absorbed primarily in the reaction 14N(n,p)14C. Cellulose from single-year tree rings from ad 1003 to ad 1020 was measured to determine ∆14C. Three years after the first visual observation of SN1006, ∆14C rose and remained above pre-ad 1009 values until ad 1018. Comparison of the 7 years before ad 1009 with the 9 years following show an average increase of 6.1 ± 1.6 (s.d.)‰ (significant at the 99.6% confidence level). Such a pulse of 14C requires a total production of neutrons of 17.1 × 107n cm−2e, implying an input of 11.3 × 104 ergs cm−2e γ-ray energy. This requires the total supernova γ-ray energy (>10 MeV) to have been 1 × 1050 ergs.

In practice, obtaining radiocarbon (14C) composition of organic matter (OM) in sediments requires first removing inorganic carbon (IC) by acid-treatment. Two common treatments are acid rinsing and fumigation. Resulting 14C content obtained by different methods can differ, but underlying causes of these differences remain elusive. To assess the influence of different acid-treatments on 14C content of sedimentary OM, we examine the variability in 14C content for a range of marine and river sediments. By comparing results for unacidified and acidified sediments [HCl rinsing (RinseHCl) and HCl fumigation (FumeHCl)], we demonstrate that the two acid-treatments can affect 14C content differentially. Our findings suggest that, for low-carbonate samples, RinseHCl affects the Fm values due to loss of young labile organic carbon (OC). FumeHCl makes the Fm values for labile OC decrease, leaving the residual OC older. High-carbonate samples can lose relatively old organic components during RinseHCl, causing the Fm values of remaining OC to increase. FumeHCl can remove thermally labile, usually young, OC and reduce the Fm values. We suggest three factors should be taken into account when using acid to remove carbonate from sediments: IC abundance, proportions of labile and refractory OC, and environmental matrix.

The source of endogenic organic and inorganic carbon in lacustrine sediments is the dissolved inorganic carbon (DIC) in the lake water. The relation between the radiocarbon levels of DIC in Lake Kinneret and of CO2 in the atmosphere has been investigated. The ratio of the former to the latter was found to be 0.814 ± 0.013. This ratio is used for calibrating the age of the sediment according to the natural fluctuations in the atmospheric levels of 14C that occurred during the past 10,000 years.

Measurements have continued with the 6 L counter which has proved reliable at pressures as high as 2.6 atm and as low as 0.3 atm. It has now been enclosed in a double ring of 27 geiger tubes which has reduced the background count to 10 cpm at 2 atm. So far, we have had no success with the 1.5 L Oeschger-type proportional counter. Failure to obtain steady readings is probably due to continued outgassing from the teflon insulation. All insulating parts have now been remanufactured from the same source of teflon as was used in the 6 L counter, and the Oeschger counter is being reassembled.

Results are still given without correction for δC13. Errors quoted refer only to the standard deviation calculated from a statistical analysis of count rates and the Libby half-life of 5570 ± 30 yr.

Saline groundwaters from the Israeli coastal aquifer were analyzed for their radiocarbon and tritium content to assess the rate of seawater penetration. The low 14C values (28–88 pMC versus 100–117 pMC in seawater) imply an apparent non-recent seawater source, or water-rock interactions along the penetration route. The latter process is supported by measurable tritium values at some locations, which imply a relatively rapid rate of seawater intrusion. In other locations, low tritium values (<2 T.U.) indicate that recent seawater (<50 yr) did not penetrate inland. The low δ13C values in saline groundwater (average of −5.3‰ versus 0‰ in seawater) indicate that the dissolved carbon pool is comprised of a significant fraction of organic carbon. A linear negative correlation between δ13C and 14C implies that this organic source is old (low 14C values).

The Ice-Free Corridor has been hypothesized as the main migration route into the Americas since the 1930s. Radiocarbon dates have been used by archaeology, geology, and palynology to date the corridor. A total of 564 14C dates ranging between 20,000 and 8000 BP from the corridor area were gleaned from the published literature. After assessing these dates for suitability, 255 were plotted over four time periods. The results indicate that the corridor was not feasible as an early human migration route until after 11,000 B P, or after the appearance of Clovis south of the continental glaciers.

We report AMS 14C measurements on subannual samples of coral from the Galapagos Islands that span the period, 1970–1973. Both the major 1972 El Niño/Southern Oscillation event and intra-annual changes in regional upwelling of 14C-depleted waters associated with alternation of surface-ocean current patterns are evident in the record. Our data show that the corals preserve a detailed record of past intra-annual variations of the 14C content of surface ocean water.

This article presents a modified method for extraction of dissolved inorganic carbon (DIC) from seawater for radiocarbon measurement by accelerator mass spectrometry (AMS). Standard tests indicate that the extraction efficiencies of DIC are >96%, and the respective precisions of Δ14C-DIC and δ13C-DIC analyses are 6‰ and 0.1‰ or better. Using the method, we report Δ14C-DIC profiles collected from the shelf and slope in the East China Sea (ECS) of the northwest Pacific Ocean. Both the DIC concentration and Δ14C-DIC in the shelf and slope regions seem primarily affected by the Kuroshio Current. It is estimated that 54–65% of the bottom water in the shelf region could be from the intrusion of Kuroshio intermediate water, which carries a high concentration and low Δ14C values of DIC, and which influenced the DIC and its 14C signature on the shelf. Compared with the Δ14C-DIC profiles at other sites in the northwest Pacific reported previously, it appears that the Δ14C-DIC distributions are mainly controlled by the major oceanic currents in the region, and large variations in Δ14C-DIC occurred mostly in the upper 800 m of the water column. The similarity of Δ14C-DIC at depth suggests that the deep-water circulation patterns have been relatively stable in the northwest Pacific Ocean in the last 20 yr.

The NOSAMS facility at Woods Hole Oceanographic Institution has started to develop and apply techniques for measuring very small samples on a standard Tandetron accelerator mass spectrometry (AMS) system with high-current hemispherical Cs sputter ion sources. Over the past year, results on samples ranging from 7 to 160 μg C showed both the feasibility of such analyses and the present limitations on reducing the size of solid carbon samples. One of the main factors affecting the AMS results is the dependence of a number of the beam optics parameters on the extracted ion beam current. The extracted currents range from 0.5 to 10 μA of 12C− for the sample sizes given above. We here discuss the setup of the AMS system and methods for reliable small-sample measurements and give the AMS-related limits to sample size and the measurement uncertainties.

When did the trade in lucrative spices from South Asia to the West commence? Recent organic residue analyses performed on small early Iron Age (11th–late 10th century BCE) Phoenician clay flasks provide the first concrete archaeological evidence that such sustainable trade took place much earlier than hitherto suspected. The analysis shows that several of the flasks contained cinnamon, which in this period could only have originated in South/Southeast Asia. Here, we first summarize the rationale and results of that study. Subsequently, we provide an updated review of all sources of data relevant to the question at hand—archaeological, analytical, and textual. Finally, we offer suggestions for future research on the Asian spice trade with the West.

In archaeological dating, the greatest confidence is usually placed upon radiocarbon results of material that can be directly related to a defined archaeological event. Human bone should fulfill this requirement, but bone dates obtained from Pacific sites are often perceived as problematic due to the incorporation of 14C from a range of different reservoirs into the collagen via diet. In this paper, we present new human bone gelatin results for 2 burials from the SAC archaeological site on Watom Island, Papua New Guinea, and investigate the success of calibrating these determinations using dietary corrections obtained from δ34S, δ15N, and δ13C isotopes.