Two new 14C reference materials have been developed for international use, filling a gap in the present C1–C6 series available from the IAEA. By mixing a modern and a synthetic substance, 150 kg of C7 (ca. 50 pMC activity) and C8 (ca. 15 pMC activity), respectively, were obtained.

The need for increased quality assurance for radiocarbon measurements performed by the monitoring laboratories at nuclear stations has spurred the introduction of a number of interlaboratory comparisons. We organized two such intercomparisons: the first set, circulated in 1994, consisted of two milk samples, one containing current global levels of 14C, the other containing an added spike of 14C-methylated casein. The second set, circulated in 1995, consisted of two samples of natural vegetation growing on the site of the Chalk River Laboratories (CRL), containing two different levels of 14C, both well above global background. The response to our invitation to participate in these studies was very encouraging; six laboratories took part in the first intercomparison, eleven in the second. The list included both monitoring laboratories and those whose main function is 14C dating. Understandably, some of the latter preferred not to analyze the higher-activity samples. The results in 3 of the 4 data sets were consistent with a statistical distribution based on the reported errors. This report provides details of two intercomparisons, including the preparation of the samples, which may now be considered potential secondary reference materials, the range of analytical techniques in use at the participating laboratories, and a statistical analysis of the results returned to us.

We illustrate here the combined use of geographic information system (GIS) technology and a radiocarbon database for analysis of the environmental components and ancient sites in Western Siberia during the period 10–45 ka bp. In total, 230 14C dates from 75 Late Pleistocene outcrops and Paleolithic sites were used to generate paleolandscape maps and to establish the features of the spatiotemporal distribution of Paleolithic sites.

Interlaboratory comparisons have been widely used in analytical chemistry and radiochemistry as an important part of ongoing quality assurance programs. The 14C community has been no exception in this respect, and in just under 20 years, there have been a number of significant and very extensive interlaboratory trials organized by individual laboratories and the International Atomic Energy Agency (IAEA) to the benefit of the 14C community (both labs and users) (Otlet et al. 1980; ISG 1982; Scott et al. 1990; Rozanski et al. 1992; Scott et al. 1992; Gulliksen and Scott 1995). The comparisons have varied widely in terms of sample type and preparation, but all have had as their primary goal the investigation of the comparability of results produced under possibly quite different laboratory protocols. As techniques have been developed and new labs formed, the reference materials created as a result of the intercomparisons have presented an opportunity for checking procedures and results. Users have been reassured by the existence of regular comparisons as one sign of the concern that laboratories have to ensure highest quality results, but also confused about how to make use of the results from past exercises in the interpretation of sets of dates from many laboratories. The laboratories have also learned valuable lessons from participation in such studies. These have included identification of systematic offsets and additional sources of variation and in studies which have used realistic samples requiring pretreatment, chemical synthesis and counting, it has been possible to identify the stage at which such problems have arisen and to quantify the relative contributions to the overall variation. In this paper, we will briefly review the comparisons so far, draw some conclusions from their findings, and make proposals for the future organization of intercomparisons.

The Earth is within the Contemporaneous Solar Maximum (CSM), analogous to the Medieval Solar Maximum (MSM). If this analogy is valid, solar activity will continue to increase well into the 21st century. We have completed 75 single-ring and 10 double-ring measurements from ad 1065 to ad 1150 to obtain information about solar activity during this postulated analog to solar activity during the MSM. δ14C decreases steadily during the period ad 1065 to ad 1150 but with cyclical oscillations around the decreasing trend. These oscillations can be successfully modeled by four cycles. These four frequencies are 1/52 yr-1, 1/22 yr-1, 1/11 yr-1, and 1/5.5 yr, i.e., the 4th harmonic of the Suess cycle, the Hale and Schwabe cycles and the 2nd harmonic of the Schwabe cycle.

We present results of 14C dating of several tree-ring series from the Late Glacial and Early Holocene, analyzed at the Heidelberg University radiocarbon laboratory. Although these are floating series, they contribute high-resolution information about the variability of atmospheric 14C during those periods.

Using the model of Stacker and Wright (1996), we investigate the effect of a succession of ocean ventilation changes on the atmospheric concentration of radiocarbon, δ14Catm, the surface reservoir ages, the top-to-bottom age differences, and the calendar-14C age relationships in different regions of the ocean. The model includes a representation of the cycling of 14C through the atmosphere, the ocean and the land biosphere. Ocean ventilation changes are triggered by increasing rates of freshwater discharge into the North Atlantic, which are determined according to a simple feedback mechanism between the melting rates and the climatic state of the North Atlantic region. The results demonstrate that ventilation changes can cause δ14Catm fluctuations of 25%, surface reservoir age fluctuations of 100 yr in the Pacific (200 yr in the Atlantic) and top-to-bottom age variations of 500 yr in the Pacific (1000 yr in the Atlantic). We also show that 14C age estimates based on marine organisms that live in the near-surface region of the ocean and take up the signal of surface 14C can result in apparent age reversals if the assumption of a constant reservoir age is made.

A living spruce tree was collected near the explosion center of the Tunguska event that occurred in 1908. We measured annual ring width and studied anatomical features to reconstruct the possible vegetational changes caused by the biological aftereffects of the Tunguska explosion. δ14C of annual rings from 1908 to 1910 was measured with a Tandetron accelerator mass spectrometer. The annual ring width decreased rapidly in 1908–1912, drastically increased in 1913, and decreased gradually thereafter. Traumatic resin ducts were observed in the transition zone between early- and latewood of the annual ring formed in 1908. We thus reconstruct these vegetational changes in the Tunguska forest: the Tunguska explosion damaged forest trees severely for ca. 3 yr, releasing rich nutrients from burned plants into the soil, and subsequently the vegetation was stimulated to recover by decreased socio-biological competition and better lighting conditions. δ14C values range from −28.2 to −1.5% for Tunguska spruce, and from −29.7 to 12.6% for Hinoki cypress. These fluctuations are within the ranges presented in Stuiver and Becker (1993), suggesting no evidence of anomalies of cometary origin in carbon isotopic composition. We found no significant difference between δ14C of Tunguska spruce and of Hinoki cypress.

Samples of >40 pine trees were collected from around the Chernobyl NPP for radiocarbon measurement, to determine the spatial distribution of excessive 14C in tree rings from 1986 consequent upon accidental radiocarbon release. Tree samples were collected during 1995–1996 from sites situated at distances >2.5 km from the NPP and covering a variety of directions in relation to the NPP. To evaluate δ14C for 1986 annual rings, we compared 14C levels for separate 1985–1987 annual rings, taking into account the trend of operational releases. Early and late wood samples for 1986 annual tree rings were measured separately to increase the sensitivity and precision of measurements. The maximum value observed for excessive accidental radiocarbon levels (δ14C) was found to be 124 pMC (281.6 Bq kg-1 C). We present δ14C values for examined sites; their spatial distribution shows a high irregularity of atmospheric 14C depending on direction from the NPP. Using obtained data, we reconstruct the temporal behavior of 14C release during the Chernobyl accident with the aid of atmospheric transport modeling. The total amount of 14C released from 26 April to 5 May 1986 has been estimated as 44 TBq.

We present an overview of recent multidisciplinary, multi-institutional efforts to identify and date major sources of combustion aerosol in the current and paleoatmospheres. The work was stimulated, in part, by an atmospheric particle “sample of opportunity” collected at Summit, Greenland in August 1994, that bore the 14C imprint of biomass burning. During the summer field seasons of 1995 and 1996, we collected air filter, surface snow and snowpit samples to investigate chemical and isotopic evidence of combustion particles that had been transported from distant fires. Among the chemical tracers employed for source identification are organic acids, potassium and ammonium ions, and elemental and organic components of carbonaceous particles. Ion chromatography, performed by members of the Climate Change Research Center (University of New Hampshire), has been especially valuable in indicating periods at Summit that were likely to have been affected by the long range transport of biomass burning aerosol. Univariate and multivariate patterns of the ion concentrations in the snow and ice pinpointed surface and snowpit samples for the direct analysis of particulate (soot) carbon and carbon isotopes. The research at NIST is focusing on graphitic and polycyclic aromatic carbon, which serve as almost certain indicators of fire, and measurements of carbon isotopes, especially 14C, to distinguish fossil and biomass combustion sources.

Complementing the chemical and isotopic record, are direct “visual” (satellite imagery) records and less direct backtrajectory records, to indicate geographic source regions and transport paths. In this paper we illustrate the unique way in which the synthesis of the chemical, isotopic, satellite and trajectory data enhances our ability to develop the recent history of the formation and transport of soot deposited in the polar snow and ice.

Radiocarbon from the Chernobyl accident was released mainly in two forms: fine dispersed reactor graphite, and carbon dioxide from burning graphite. The CO2 was partly assimilated by annual and perennial vegetation. Reactor graphite dispersed over a wide territory was taken up biochemically by micromicetes, transforming non-organic carbon of the reactor graphite into organic matter. Organic matter of micromicetes is the main nutrition product for soil organisms such as bacteria, worms, larvae of insects, small beetles, etc. The following relatively independent trophic chains are considered: 1. carbon dioxide → leaves, grass → insects; 2. graphite → micromicetes, protozoa, insects. The 14C content in beetles of different species sampled in the 30-km hot zone of the Chernobyl accident site in 1986–1988 agrees well with the contamination levels of insect habitats as well as with their biology.

A two-decade-long record of environmental isotopes (2H, 3H, 14C, 18O) in Croatia is presented and the data are statistically analyzed. The atmospheric 14C activity for the period before the actual measurements started is reconstructed by measuring tree rings from the clean-air sites, and the past tritium activity in precipitation is estimated by the correlation of our data with the Vienna station record. The long-term 3H record helped to determine a locally contaminated sampling site, and new clean sites are put into operation. The 14C data were fitted by an analytical function and the prediction of future levels is given assuming that the rate of the 14C releases remains constant. From the long-term stable isotope data record, the local meteoric water line and the temperature gradient of δ18O in precipitation are determined.

Time series of δ14C, δ13C, and concentration of atmospheric CO2 covering the last 12 years are available at the Kraków sampling site (southern Poland) representing an urban area exposed to anthropogenic pollution of both local and regional origin. The samples represent continuous monitoring in biweekly intervals. Observations covering the time period 1983–1994 show a linear decrease of the 13C/12C ratio (δ13C = −9.6% in Jan. 1983) with a slope of −0.02% a−1. The decreasing tendency in the case of 14C (δ14C = 221% in January 1983) is weaker with a broad minimum in 1991 (δ14C = 124%) and subsequent gradual increase by ca. 10%, coinciding with a substantial reduction of coal consumption in Poland (26% reduction in 1991–1994 for heat and electricity production), partly compensated in agglomerations by increased gas consumption. The 12-year record of the CO2 concentration in Kraków points to a constant value fluctuating at a high level (average: 373 ppmv) reaching a maximum yearly average of 376 ppmv. These carbon isotope signatures were used for the separation of fossils from biogenic and “background” components, reflecting the strength of relevant sources. The monthly mean of the fossil component varies from ca. 10 ppmv in June to 27.5 ppmv in March while the yearly mean decreased ca. 16 ppmv since 1991.

We report on a review of 14C production and release from the nuclear industry in the United Kingdom (UK). Using earlier predictions (Bush, White and Smith 1984) it is estimated that a total of 1764 TBq of 14C would have been produced in UK graphite-moderated reactors up to the end of 1995, and 135 TBq of this total would have been released. Release rates, based on reported discharges, of 5.1 and 0.93 TBq GW(e)a-1 have been derived for Magnox reactors and Advanced Gas Cooled Reactors (AGRs), respectively. Using these new figures, cumulative discharges of 14C up to 1995 from reactors have been estimated at 531 TBq. The combination of these reactor discharges and the reported discharges from Sellafield (388 TBq) and Amersham (52 TBq) suggest a total cumulative release of 971 TBq of 14C up to the end of 1995.

14C is one of the radionuclides that are produced to different degrees by neutron-induced reactions in all types of nuclear reactors. Part of the 14C created is continuously released into the surrounding environment during normal operation as airborne effluents in various chemical forms (such as CO2, CO and hydrocarbons) through the ventilation system of the plant. Because of the biological importance of carbon and the long half-life of 14C, it is of interest to measure the releases and their incorporation into living material. We report here on the 14C activity concentrations in annual tree rings and the air around two Swedish nuclear power plants, as well as the background 14C activity levels from two reference sites in southern Sweden from 1973–1996. We used both accelerator mass spectrometry (AMS) and decay counting in the investigation.

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).

Radiocarbon is an important constituent of the low level, liquid, radioactive effluent discharged from the Sellafield nuclear fuel reprocessing plant in northwest England, but despite the fact that it gives the highest collective dose commitment of all the nuclides in the waste, its behavior in the Irish Sea is poorly defined. There is therefore a clear requirement for an improved understanding of 14C behavior in the Irish Sea, to assist with dose evaluation modeling and definition of the mixing and accumulation characteristics of the sediment in this area. In this context, results are presented here for a temporal study of 14C activities in four geochemical fractions of seawater and in a sediment core from the vicinity of the Sellafield effluent outfall. Clear 14C enrichments in the dissolved inorganic carbon (DIC) and particulate organic carbon (POC) components of seawater were observed, with temporal trends in activity that were related to variations in the Sellafield discharge. Smaller, but nevertheless detectable, enrichments were also observed for particulate inorganic carbon (PIC) and dissolved organic carbon (DOC) in the seawater. The distribution of 137Cs and 241Am revealed that the sediment core could be classified into three zones in which the intensity of mixing decreased discontinuously with depth. Bulk carbonate 14C analyses of the core demonstrated the presence of glacial or pre-glacial carbonate in the system, but failed to show any evidence of contaminant 14C input or provide information on sediment accumulation processes. In contrast, analysis of bulk organic matter from the sediment provided clear evidence of the recent perturbation of a well mixed system by input of younger material, consistent with the recent input of contaminant 14C from Sellafield and possibly weapons testing fallout.

Statistical analysis is becoming much more widely used in conjunction with radiocarbon dating. In this paper I discuss the impact of Bayesian analysis (using computer programs such as OxCal) on archaeological research. In addition to simple analysis, the method has implications for the planning of dating projects and the assessment of the reliability of dates in their context.

A new formalism for describing chronological models is introduced here: the Chronological Query Language (CQL), an extension of the model definitions found in the program OxCal.

New methods of Bayesian analysis can be used to overcome some of the inherent biases in the uncertainty estimates of scientific dating methods. Most of these methods, including 14C, uranium series and thermoluminescence (TL), tend to favor some calendar dates over others. 14C calibration overcomes the problem where this is possible, but a Bayesian approach can be used more generally.

The conventional 14C time scale between 11,500 and 22,000 sidereal years has been calibrated by TIMS U/Th dates for corals. Only a few studies have been made for the time beyond this range. Obtaining samples suitable for numerical dating or estimating the reservoir correction of the 14C dates has been difficult, but we do not have these problems with TIMS U/Th dating of interstadial and interglacial lignite, because reservoir corrections are unnecessary.

Varved sediments of the tropical Cariaco Basin provide a new 14C calibration data set for the period of deglaciation (10,000 to 14,500 years before present: 10–14.5 cal ka bp). Independent evaluations of the Cariaco Basin calendar and 14C chronologies were based on the agreement of varve ages with the GISP2 ice core layer chronology for similar high-resolution paleoclimate records, in addition to 14C age agreement with terrestrial 14C dates, even during large climatic changes. These assessments indicate that the Cariaco Basin 14C reservoir age remained stable throughout the Younger Dryas and late Allerød climatic events and that the varve and 14C chronologies provide an accurate alternative to existing calibrations based on coral U/Th dates. The Cariaco Basin calibration generally agrees with coral-derived calibrations but is more continuous and resolves century-scale details of 14C change not seen in the coral records. 14C plateaus can be identified at 9.6, 11.4, and 11.7 14C ka bp, in addition to a large, sloping “plateau” during the Younger Dryas (∼10 to 11 14C ka bp). Accounting for features such as these is crucial to determining the relative timing and rates of change during abrupt global climate changes of the last deglaciation.