Tephra from the Cape Riva (Y-2) eruption of Santorini has been found across the eastern Mediterranean. It presents an important link between marine and terrestrial records. A Poisson process (P Sequence) age-depth prior, with model averaging, is used to model individual previously published radiocarbon sequences, cross-linked with an exponential phase model parameter to obtain a robust age. Multiple sequences and 14C determinations from 3 eastern Mediterranean data sets (Seymour et al. 2004; Margari et al. 2009; Müller et al. 2011; Roeser et al. 2012) are used in the model. The modeled age of the Y-2 tephra produced within this study is 22,329–21,088 cal BP at 95.4% probability.

The Kawagodaira Volcano is located on the northwest slope of Amagi Volcano on the Izu Peninsula of central Japan. The fine pumice that erupted from Kawagodaira Volcano is widely distributed in the central and western parts of the Japanese mainland. Here, we report an accurate eruption age determined by radiocarbon wiggle-matching of a Japanese cedar timber excavated from the pyroclastic deposit at the pumice flow terminal of Kawagodaira Volcano. The 14C wiggle-match estimate for the Kawagodaira Volcano eruption is 1210–1187 cal BC (95.4% confidence level).

A series of annual tree-ring measurements has been performed in order to reconstruct the radiocarbon concentration variation in the Korean atmosphere from AD 1650 to 1850. The absolute ages of the samples were determined using dendrochronology. Alpha-cellulose extraction was applied to prepare the tree-ring samples for precise 14C measurement. The 14C concentrations of the tree rings were then plotted with the dendrochronological ages and showed that during the period AD 1650–1850, the discrepancy in 14C concentration in the Korean atmosphere from IntCal data is small enough to use IntCal data without any further correction. This is nearly one third of the average offset of the 400 yr from AD 1250 to 1650. One of the probable causes for the regional offset around Korea is the contribution of 14C-depleted CO2 released from the northern Pacific Ocean, where old deep water upwells to the surface. It is likely that the release rate of 14C-depleted CO2 decreased due to the temperature change during the Little Ice Age.

To investigate the radiocarbon concentration of atmospheric CO2 over the past few millennia in Japan, we measured the 14C age of annual rings from 3 Japanese trees with calendar dates ranging from ∼2000 yr old to present, and we compared the tree-ring 14C age with the corresponding 14C age from IntCal09. In some instances, the 14C ages of the annual rings of Japanese trees are not consistent with the IntCal09 data sets. Often, the 14C ages of tree rings are older than those from IntCal09, but younger than those from the SHCal04 data sets. The average shifts in the Nagoya 14C age from IntCal09 data sets and 1σ errors were determined to be +26 ± 36, +24 ± 30, +16 ± 22, +5 ± 21, and +14 ± 22 14C yr for the intervals AD 72– 382, 589–1072, 1413–1615, 1617–1739, and 1790–1860, respectively. The Japanese Archipelago is situated near the boundary of the Intertropical Convergence Zone in summer, and the 14C concentration of atmospheric CO2 over Japan can be influenced by air masses of the Southern Hemisphere with lower 14C concentrations during periods of higher solar activity and heightened East Asian summer monsoons. Our results suggest that the Japanese Archipelago is located in a critical zone where it is difficult to calibrate the 14C age of tree-ring samples using existing calibration data sets. It should be noted that calibration of the 14C dates of Japanese samples with IntCal09 may induce additional systematic shifts of calibrated ages toward older ages by about 30 yr compared with the sample optimum calendar ages.

Caves and rockshelters are critical loci for the analysis and understanding of human trajectories in the past. Use and re-uses of the same context, however, might have had serious impacts on depositional aspects. This is particularly true for the archaeological history of desert environments, such as the central Sahara, where most of the deposits are made of loose sand, rich in organic matter. Besides traditional stratigraphic reconstructions and a detailed study of the material culture, radiocarbon measurements from different contexts analyzing several types of material (bone, dried and charred coprolite, uncharred and charred plant remains, etc.) can highlight intrinsic critical aspects of 14C determinations. These measurements must be carefully evaluated to provide a correct chronological assessment of the life history of the site. We present the statistics derived from the set of about 50 14C measurements from the site of Takarkori, southwest Libya, where early Holocene foragers and then groups of cattle herders inhabited the area from ∼10,200 to 4600 cal yr BP. We have used the BCal Bayesian 14C calibration program designed for statistical presentation of the calibrated data and the estimation of their probability for different phases. Results indicate that the Takarkori rockshelter was occupied during 4 phases of the following cultures: Late Acacus from 10,170 to 8180 cal yr BP; Early Pastoral, 8180–6890 cal yr BP; Middle Pastoral, 7160–5610 cal yr BP; and Late Pastoral, 5700–4650 cal yr BP.

Radiocarbon is one of the most significant radionuclides affecting the safety margins of near-surface repositories for the disposal of low- and intermediate-level, short-lived radioactive waste, arising from the operation and decommissioning of nuclear power plants (NPPs). One of the goals of the present study was to characterize radioactive waste from Ignalina NPP (Lithuania) (storage tanks TW18B01 and TW11B03) from the spent ion-exchange resins/perlite stream to determine the 14C-specific activity of inorganic and organic carbon compounds. The approach applied is based on classical radiochemical separation methods, including acid-stripping techniques and wet oxidation with subsequent catalytic combustion. The suitability of the method for 14C-specific activity determination in ion-exchange resin samples with a minimum detectable activity of 0.5 Bq/g by liquid scintillation counting (LSC) was demonstrated. The extraction efficiency of inorganic and organic carbon compounds based on model samples with known 14C activity was estimated. The fraction of 14C associated with organic compounds ranged from 42% to 63% for storage tank TW18B01 and from 30% to 63% for storage tank TW11B03. The specific activity of inorganic 14C was estimated as 12.6 Bq/g with a relative standard deviation (RSD) of 29% for storage tank TW18B01, and 177.5 Bq/g with a RSD of 35% for storage tank TW11B03. Based on volume and density data, the total 14C activity for radioactive waste stored in tanks TW18B01 and TW11B03 was estimated as 3.59E + 10 Bq (±32%) and 4.15E + 11 Bq (±28%), respectively.

From October 2010 to November 2011, the urban atmospheric CO2 concentration in Guangzhou ranged from 550 to 460 ppm, with mean monthly concentration fluctuating between 530 and 470 ppm. A lower concentration was observed in summer and autumn, while a higher concentration occurred in spring and winter. The urban atmospheric CO2 δ13C value varied between −9.00 and −13.10%, with mean monthly value fluctuating between −9.60 and −11.80%. There was no significant relationship between the CO2 concentration and δ13C value, reflecting the influence from the fossil-fuel-derived CO2 on the urban atmospheric CO2. The urban atmospheric CO2 Δ14C value fluctuated dramatically from 29.1 ± 2.5% to −85.2 ± 3. 1%, with a mean annual value of −16.4 ± 3.0%. A similar seasonal variation of Δ14C value with the concentrations was observed: the higher Δ14C values mainly appeared in summer and autumn (July to September), with a mean value of about −5.2 ± 2.9%, while lower Δ14C values occurred in spring and winter (December to April), about −27.1 ± 3.2% average. Based on the atmospheric Δ14C values, the calculated fossil-fuel-derived CO2 concentrations range between 1 and 58 ppm, with the mean annual concentration around 24 ppm. Similarly, a lower fossil-fuel-derived CO2 concentration appeared in summer and autumn (July to September) with a mean value of ∼17 ppm, while the higher fossil-fuel-derived CO2 concentration occurred in spring and winter (December to April) with an average value of ∼29 ppm. A comparison of the CO2 concentrations before and after the Guangzhou Asian Games (in November 2010) and the Spring Festival of 2011 confirmed that human activities can greatly decrease the fossil-fuel-derived CO2 emissions to the urban atmosphere in Guangzhou.

The need to address radiological impacts from radiocarbon released to the biosphere has been recognized for some time. In 2011, the Swedish Radiation Safety Authority (SSM) commissioned a study to develop a 14C model of the soil-plant-atmosphere system that would provide them with an independently developed assessment capability. This paper summarizes that study, which comprised a review of contemporary models, the development of a new conceptual model, SSPAM14C, and the application of SSPAM14C to a set of experimental data relating to the atmospheric exposure of cabbages.

Radiocarbon is present in solid radioactive wastes arising from the nuclear power industry, in reactor operating wastes, and in graphite and activated metals that will arise from reactor decommissioning. Its half-life of 5730 yr, among other factors, means that 14C may be released to the biosphere from radioactive waste repositories. These releases may occur as 14C-bearing gases, especially methane, or as aqueous species, and enter the biosphere from below via natural processes or via groundwater pumped from wells. Assessment of radiation doses to humans due to such releases must take account of the major role of carbon in biological processes, requiring specific 14C assessment models to be developed. Therefore, an intercomparison of 5 14C assessment models was organized by the international collaborative forum, BIOPROTA. The intercomparison identified significantly different results for the activity concentrations in the soil, atmosphere, and plant compartments, based upon the different modeling approaches. The major source of uncertainty was related to the identification of conditions under which mixing occurs and isotopic equilibrium is established. Furthermore, while the assumed release area plays a role in determining the calculated atmospheric 14C concentrations, the openness of the plant canopy and the wind profile in and above the canopy are the key drivers. The intercomparison has aided understanding of the processes involved and helped to identify areas where further research is required to address some of the uncertainties.

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.

Dendrochronological studies are limited in tropical regions because not many tree species form annual growth rings. This work reports an evaluation of the dendrochronological potential of tropical ash (Fraxinus uhdei) and its use as a bioindicator of fossil CO2 concentration in urban areas by means of radiocarbon analysis on growth rings. We analyzed a cross-section of a tree that grew during the period 1932–2007 in San Luis Potosí, one of the most industrialized cities in Mexico. The Δ14C values obtained follow the same variation pattern as the calibration curve of the Northern Hemisphere (NH) zone 2 (Hua and Barbetti 2004), with the peak centered in 1964, but they are lower by up to 124′. The high correlation coefficient (r = 0.990, p < 0.001) between the variation patterns indicates that this species does form annual growth rings, and the lower values can be attributed to the 14C dilution caused by fossil CO2 emissions. The magnitude of the Suess effect varied between −6.9% and −0.5%, equivalent to fossil CO2 concentrations ranging between 21.9 and 1.5 ppmv. The Suess effect and fossil CO2 values have significant variations with no apparent monotone increasing trend, suggesting that the CO2 emissions during the studied period have diverse sources. It is concluded that F. uhdei has potential for dendrochronological studies in tropical areas because its growth rings are formed annually and, furthermore, it can be used as a bioindicator of atmospheric 14C variations and fossil CO2 concentration in urban areas.

Δ14C values of leaves of deciduous trees provide a means to map the regional-scale fossil fuel ratio in the atmosphere. We collected a batch of ginkgo (Ginkgo biloba Linnaeus, a deciduous tree) leaf samples from across Korea in the month of July in both 2010 and 2011 to obtain the regional distribution of Δ14C. The Δ14C values of the samples were measured using accelerator mass spectrometry (AMS) at the Korea Institute of Geoscience and Mineral Resources (KIGAM). The average of the Δ14C values from clean air sites in Korea in 2011 measured slightly lower than the average of Δ14C values in 2010. Distribution maps of Δ14C of 2011 and 2010 in Korea were made based on a series of Δ14C values of ginkgo leaf samples from Korea using the Geostatistical and Spatial analyst tools in ESRI's ArcMap software. The distribution maps of Δ14C showed that Δ14C values in the western part of Korea are lower than those in the eastern part of Korea. This is because the western part of Korea is densely populated and contains many industrial complexes, and also because westerly winds from China, containing CO2 from fossil fuel use, blow into Korea. We compared the distribution maps of 2010 and 2011 and tried to find traces of the Fukushima power plant accident in Japan.

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.

Radiocarbon-based accelerator mass spectrometry (AMS) facilities at Uppsala University include a measurement center for archaeological applications and a separate entity dedicated to life science research. This paper addresses the latter, with the intention of giving a brief description of the biomedical activities at our laboratory, as well as presenting new data. The ultra-small sample preparation method, which can be used down to a few μg C samples, is outlined and complemented with new results. Furthermore, it is shown that the average secondary ion current performance for small samples can be improved by increasing the distance between the cathode surface and the pressed graphite surface. Finally, data is presented for a new application: Amyloidoses are a group of diseases where the conformational changes in specific proteins' structure lead to the formation of extracellular deposits that spread and increase in mass and eventually may lead to total organ failure and death. The formation timeframe is unknown and yet it is an important clue for the elucidation of the mechanism. We present results on bomb-peak dating of 4 different types of purified amyloid proteins from human postmortem heart and spleen samples. The data indicates that the average measured age of the carbon originating from the systemic amyloid types studied here correspond to a few years before the death of the subject. This suggests that a major part of the fibril formation takes place during the last few years before death, rather than as an accumulation of amyloid deposits over decades.

The radiocarbon concentration of different atherosclerotic plaque fragments obtained from 20 patients in Portugal, operated in 2000–2001, has been measured in order to define the year of plaque formation. A difference of 1.8–15 yr was observed, with the mean and median both 9 yr, between the bomb-pulse date estimated with the CALIBomb software and the operation date. Stable isotope (δ13C and δ15N) analysis was also performed and provides insight to the diet of the subjects. The wide range of measured stable isotope values could indicate that the subjects' diet varied, including an abundance of marine foodstuffs. It could also mean a different isotope fractionation process for the different plaque fragments (cap, core, interface to media) and a possible difference in tissues in which the various fragments are formed. Analysis of δ13C and δ15N values of each patient separately revealed subjects considered more influenced by marine foodstuffs consumption.

The question of whether the rise in CO2 levels observed during the industrial era has influenced the rates of tree biomass growth represents one of the main unsolved questions in the field of climate change science. In this framework, the African tropical forest represents one of the most important carbon (C) sinks, but detailed knowledge of its response to elevated CO2 is still lacking, especially regarding tree growth rate estimations. A major limitation to determining growth rates in the African tropical region is that many trees lack seasonality in cambial activity determining annual growth rings. In this study, several species of trees characterizing the African tropical forest have been investigated to estimate their biomass growth rate by means of a procedure based on 14C and growth models. A total of 71 subsamples were analyzed for a Entandrophragma cylindricum (sapele) tree, and 38 and 25 wood subsamples for Erythrophleum suaveolens (tali) and Triplochiton scleroxylon (ayous) trees, respectively, using radiocarbon measurements at the Centre for Isotopic Research on Cultural and Environmental Heritage (CIRCE). All measured modern samples were in agreement with the Southern Hemisphere (SH) 14C bomb-spike curve. Observed preliminary results indicate a decrease in the growth rate of the sapele tree (∼350 yr old) in the industrial period compared to the pre-industrial era. Growth rates for trees of the other 2 species were higher than sapele, with ayous being the fastest-growing species.

Knowledge of the groundwater age is indispensable for understanding groundwater flow in crystalline rocks. The present study is the first to discuss the radiocarbon ages of groundwater in Abukuma granite, Fukushima Prefecture, northeast Japan. The vertical profiles of 14C dates and δ13C are obtained from 3 boreholes (depths of 140, 230, and 306 m). Chemical and carbon isotopic compositions suggest that dead-carbon contamination of groundwater occurred during groundwater storage in the fractures. 14C concentration was corrected by using isotopic mass balance in which dead-carbon contamination of the groundwater was considered. The 14C dates ranged from modern to ≃16 ka. The relationship between tritium and 14C data in 1 borehole suggests the simultaneous inflow of shallow groundwater to deeper levels occur for the depths between 60 and 100 m. The vertical profiles of 14C dates indicate a relatively constant age of 10–16 ka for groundwater deeper than 100 m, which may have been influenced by rapid sea-level changes after the glacial period.

We present the results of a comprehensive study aimed at tracing the evolution of carbon isotopic composition of the TDIC (total dissolved inorganic carbon) reservoir from the unsaturated zone down to the discharge area, in a sandy aquifer near Kraków, southern Poland. A multilevel well penetrating the unsaturated zone in the study area was equipped with horizontally mounted lysimeters with ceramic suction cups to collect samples of pore water and metal probes to collect soil air. Strong seasonal fluctuations were observed of soil pCO2 extending down to the water table, coupled with distinct, well-defined depth profiles of δ13CTDIC reaching approximately −10′ at 8 m depth and almost constant radiocarbon content in the TDIC pool, comparable to 14CO2 levels in the local atmosphere. Simple models (closed/open system) do not account for the observed depth variations of carbon isotopic composition of the TDIC pool. This suggests that the TDIC reservoir of pore waters is evolving under conditions gradually changing from an open towards a closed system. In order to explain 13C and 14C content of dissolved carbonates in groundwater in the recharge area of the studied aquifer, additional sources of carbon in the system are considered, such as organic matter decomposition accompanied by reduction of dissolved nitrates and sulfates. The piston-flow l4C ages of groundwater in the confined part of the studied system were calculated using 2 approaches: 1) the correction model proposed by Fontes and Garnier (1979) was used to calculate groundwater ages, utilizing the chemical and carbon isotopic data available for the sampled wells; and 2) inverse geochemical modeling was performed for selected pairs of wells using NETHPATH code. The calculated 14C ages of groundwater range from approximately 0.6 to 37.5 ka BP. Although both methods appeared to be in a broad agreement, NETHPATH calculations revealed that isotopic exchange processes between TDIC pool and solid carbonates present in relatively small amounts in the aquifer matrix play an important role in controlling the 13C and 14C signatures of the dissolved carbonate species in groundwater and should be taken into account when 14C ages are calculated.

As a main source of freshwater and particles, the Rhône River plays a major role in the biogeochemical cycle of organic carbon (OC) in the Mediterranean Sea. To better understand the origin of organic matter and the processes leading to its export to the coastal sea near the Rhône River, we measured radiocarbon (Δ14C) and stable carbon isotopes (δ13C) in the sediments of the delta, after density fractionation. In April 2007, 3 sites located along an offshore transect (A, C, and E) were sampled for surface sediments, and bulk sediment was separated into 4 fractions of different densities (<1.6, 1.6–2, 2–2.5, and >2.5 g cm−3). In order to better understand the evolution of the OC along the transect, we investigated the OC sources and their evolution for each density fraction. Bulk OC shows a large increase in δ13C from −27.2′ nearshore to −24.5′ at offshore stations while Δ14C decreased from 59′ to −320′. The distribution of δ13C with density displayed a convex pattern at all stations. Except for fraction >2.5 g cm−3, δ13C increases by 2.5′ between stations A and E, indicating a loss of terrestrial signature. The distribution of Δ14C versus density had a concave pattern at all stations: at a single station, it showed a large heterogeneity with a difference of 500–600′ between the <1.6 and 2–2.5 g cm−3 fractions. A decrease in Δ14C of −400′ among the different density fractions was observed along the offshore transect. The density fraction >2.5 g cm−3 had less variability, with an average δ13C of −24.6 ± 0.4′ and Δ14C of −370 ± 115′. Several processes may explain this distribution: retention in the prodelta of large particles; mineralization of all fractions during the transport and deposition in the delta and shelf sediments; and dilution of terrestrial particles in continental shelf pool.

A study of CO2 in soil gas was conducted in a bare plot in the unsaturated zone (USZ) of Yatir Forest, northern Negev, Israel. In 2006, 6 tubes for sampling of soil gas were inserted into the USZ to depths of 30, 60, 90, 120, 200, and 240 cm. Profiles of soil gas in the USZ were collected from the tubes 5 times between October 2007 and September 2008. Measurements of the collected profiles of soil gas were of CO2 (ppm), δ13C (′), and Δ14C (′). At all times, the concentration of CO2 in the soil gas was higher than in the air at the surface (CO2 ≃ 400 ppm; δ13C ≃ −9′). The main source of the CO2 in soil gas is from biotic activity released through roots of trees and of seasonal plants close to the surface. In the winter, the CO2 concentrations were lowest (6000 ppm) and the δ13C was −20′. In the spring and through the summer, the CO2 concentration increased. It was estimated that the major source of CO2 is at ≃240 cm depth (δ13C ≃ −22′; CO2 ≃ 9000 ppm) or below. Above this level, the concentrations decrease and the δ13C (′) become more positive. The 14C values in the measured profile are all less than atmospheric and biotic 14C. It was deduced that biotic CO2 dissolves in porewater to form carbonic acid, which then dissolves secondary carbonate (δ13C ≃ −8′; 14C ≃ −900′) from the sediments of the USZ. With the 14C data, the subsequent release of CO2 into the soil gas was then estimated. The 14C data, supported by the 13C and CO2 data, also indicate a biotic source at the root zone, at about 90 cm depth.