We present a simple method for manually separating pollen concentrates for radiocarbon accelerator mass spectrometry (AMS) dating using a mouth pipetting system. The required equipment is readily available from scientific equipment supply houses at minimal cost. Pollen samples from lake sediments required about 4 h of hand picking, whereas samples from marine sediments required about 8 h labor. Pollen dates from marine sediments were much older than expected. We are attempting to resolve whether this is due to contamination of the pollen or the presence of significant quantities of old reworked pollen. Pollen dates from lake sediments associated with Mazama Ash were consistent with other published ages; however, replicate dates on pollen samples from above the ash were consistently older than the surrounding sediment. Our results suggest that caution must be used when interpreting pollen dates if the potential for sediment reworking is present.

A suite of 6 bone gelatin accelerator mass spectrometry (AMS) radiocarbon dates for Rattus exulans Peale and associated beta decay 14C dates for Austrovenus stutchburyi shell are presented for 4 middens at Pauatahanui, Wellington, New Zealand. Mean calibrated age ranges of Rattus exulans (520–435 BP and 350–330 BP at 95% confidence level) and shell (465–375 BP at 95% confidence level) from the 4 midden sites overlap. The agreement between Rattus exulans bone gelatin dates and associated shell provides an inter-sample comparison of 14C dating using both gas counting (beta decay) and AMS dating techniques. We examine the adequacy of the standard gelatinization treatment for bone samples, which has been employed consistently at the laboratory since 1995.

A 23-yr record of the measuring accuracy of the Copenhagen radiocarbon dating laboratory has retrospectively been provided through a true blind test. A total of 92 samples of oak from old tree trunks were dated in the period 1971 to 1993 and their dendrochronological age determined independently. The 14C activity of the dendrochronological samples measured in the Copenhagen radiocarbon laboratory was compared to the activity of the tree rings of the same age measured by Stuiver and Pearson (1993) for calibration purposes. The average difference was found to be 54 ± 72 14C yr. The results further indicate that the actual standard deviation is only 7% higher than that quoted by the laboratory. The investigation has shown a long-term stability of laboratory accuracy with no systematic laboratory variations either with respect to sample age or to the time of measurement from 1971 to 1993.

We present results that validate a new wet oxidation, stepped-combustion procedure for dating “old” charcoal samples. An acid–base–wet oxidation (ABOX) pretreatment procedure has been developed that is used in place of the conventional acid-base-acid (ABA) pretreatment. Combustions and graphitizations are performed in a vacuum line that is insulated from the atmosphere by a second backing vacuum to eliminate the risk of atmospheric leakage into the line at any stage of the procedure. Combustions are performed at 3 temperatures (330 °, 630 ° and 850 °) with a graphite target produced from the CO2 evolved during each combustion step. In this way, the removal of any contamination can be monitored, and a high degree of confidence can be placed on the final age. The pretreatment, combustion, graphitization, and measurement blank for the procedure, based on the analysis of a “radiocarbon-dead” graphite, is 0.5 ± 0.5 μg C (1σ, n=14), equivalent to 0.04 ± 0.02 pMC or an “age” of approximately 60 ka for a 1 mg graphite target. Analyses of a “radiocarbon-dead” natural charcoal after ABOX pretreatment and stepped combustion suggest that the total blank (including contamination not removed by pretreatment) may be higher than for graphite, ranging up to 0.10 ± 0.02 pMC. Additional experiments confirm good agreement with accepted values for the international low-14C “New Kauri” standard (0.16–0.25 pMC). They also confirm excellent reproducibility, with 3 separate dates on different aliquots of a charcoal sample from Ngarrabullgan Cave (Queensland, Australia) ranging from 35.2 to 35.5 ka 14C BP. It is also demonstrated that the ABOX pretreatment, in conjunction with the new vacuum line described here, is able to remove contamination not removed by the conventional ABA pretreatment, suggesting that the technique can be used to produce reliable 14C dates on charcoal up to at least 50 ka.

We tested the feasibility of dating freshwater and terrestrial molluscs from the semiarid and arid zone in China, since these types of shell material deposit only aragonite to form their shell structure, and shell integrity can be easily observed using X-ray diffraction. We also tested the possibility of estimating microenvironmental changes from shell δ13C values, but variations within shell populations preclude the use of these values as a reliable indicator. Reservoir ages were calculated for living shells of the same species as fossil shells by using their measured 14C ages, which were recalculated using an average value of atmospheric 14C activity for the years spanning their time of collection as the modern standard. The results indicate that freshwater and terrestrial shells are potentially useful as dating material, provided extreme care is taken in their collection and other datable material (in this case wood and pollen) is within the profile to act as a comparison.

The radiocarbon activity of carbon collected by vacuum distillation from a single partially saturated tuff began to decline after approximately 60% of the water and carbon had been extracted. Disproportionate changes in 14C activity and δ13C during distillation rule out simple isotopic fractionation as a causative explanation. Additional phenomena such as matrix diffusion and ion exclusion in micropores may play a role in altering the isotopic value of extracted carbon, but neither can fully account for the observed changes. The most plausible explanation is that distillation recovers carbon from an adsorbed phase that is depleted in 14C relative to DIC in the bulk pore water.

Three modes of reporting 14C activities are in use, in part analogous to the internationally accepted (IAEA) conventions for stable isotopes: (1) absolute activity, the specific activity of 14C or the activity per gram of carbon; (2) activity ratio, the ratio between the absolute activities of a sample and the standard; and (3) relative activity, the difference between the absolute activities of a sample and standard material, relative to the absolute standard activity. The basic definitions originate from decisions made by the radiocarbon community at its past conferences. Stuiver and Polach (1977) reviewed and sought to specify the definitions and conventions. Several colleagues, however, have experienced inadequacies and pitfalls in the definitions and use of symbols. Furthermore, the latter have to be slightly amended because of the use of modern measuring techniques.

This paper is intended to provide a consistent set of reporting symbols and definitions, illustrated by some practical examples.

A promising species for tropical dendrochronology is Pinus lagunae, a pine tree found in Baja California Sur (Mexico) around lat 23.5°N. In 1995, we sampled a total of 27 wood cores from 13 Pinus lagunae trees in Sierra La Victoria (23°36'N, 109°56'W), just north of Sierra La Laguna, at an elevation of 1500–1600 m. Selected trees were locally dominant, but their ring-width patterns could not be crossdated. To test the hypothesis that visible growth layers in Pinus lagunae are formed annually, we measured radiocarbon amounts in individual rings by means of accelerator mass spectrometry (AMS). Twenty-three 14C measurements were used to trace the location of the 1963–64 “bomb spike” in 3 wood increment cores. By comparing the location of that δ14C extreme with the number of visible radial wood increments, it was possible to conclude that 2 cores had a number of locally absent rings, while the 3rd one included a few years with more than one growth layer. Therefore, ring-width patterns of sampled Pinus lagunae were not consistent from one tree to another, most likely because of climatic regime in combination with microsite features. While the possibility of generating Pinus lagunae tree-ring chronologies cannot entirely be ruled out, the development of dendrochronological proxy records of climate from coniferous species in tropical North America should focus on species and sites that experience a more pronounced seasonality.

Accelerator mass spectrometric (AMS) radiocarbon analyses of live-collected, prebomb samples of shell carbonates of the land snails Rabdotus dealbatus and R. alternatus from Texas were carried out to quantify the characteristic age anomalies of land snails from limestone areas. Age anomalies are similar for the two species; they average +700 yr and vary by ±180 yr (1σ) among samples. Serial analysis of 1 shell reveals a significant ontogenetic trend in 14C age anomalies, with older apparent ages (up to 1200 yr) in the apical part of the shell and younger and uniform ages in the last whorl. No trend in age anomalies was found across a broad range of rainfall conditions (from 300 to 1000 mm mean annual rainfall).

We have studied 6 reference sections of bog and lake sediments in the Leningrad and Novgorod provinces to develop a geochronological scale for vegetational and paleoclimatic changes in northwestern Russia during the Late Glacial and Holocene. Every 10-cm layer along the peat and gyttja sections (4–8.5 m thick) was investigated palynologically and the great majority of them were radiocarbon dated. Using the data obtained, standard palynological diagrams were plotted and vegetation history reconstructed. The palynozones indicated on the diagrams were related to the climatic periods and subperiods (phases) of the Blytt-Sernander scheme. On the basis of 230 14C dates obtained, we derived the geochronology of climatic periods and phases, as well as the chronology for the appearance and areal distribution of forest-forming tree species. The uppermost peat layers were dated by using the “bomb effect”. We compared the stages of Holocene vegetation and paleoclimatic changes discovered for the Leningrad and Novgorod provinces with the those obtained for Karelia, which we had studied earlier using the same methodology.

Bone samples from the Greenland Viking colony provide us with a unique opportunity to test and use 14C dating of remains of humans who depended upon food of mixed marine and terrestrial origin. We investigated the skeletons of 27 Greenland Norse people excavated from churchyard burials from the late 10th to the middle 15th century. The stable carbon isotopic composition (δ13C) of the bone collagen reveals that the diet of the Greenland Norse changed dramatically from predominantly terrestrial food at the time of Eric the Red around AD 1000 to predominantly marine food toward the end of the settlement period around AD 1450. We find that it is possible to 14C-date these bones of mixed marine and terrestrial origin precisely when proper correction for the marine reservoir effect (the 14C age difference between terrestrial and marine organisms) is taken into account. From the dietary information obtained via the δ13C values of the bones We have calculated individual reservoir age corrections for the measured 14C ages of each skeleton. The reservoir age corrections were calibrated by comparing the 14C dates of 3 highly marine skeletons with the 14C dates of their terrestrial grave clothes. The calibrated ages of all 27 skeletons from different parts of the Norse settlement obtained by this method are found to be consistent with available historical and archaeological chronology. The evidence for a change in subsistence from terrestrial to marine food is an important clue to the old puzzle of the disappearance of the Greenland Norse, obtained here for the first time by measurements on the remains of the people themselves instead of by more indirect methods like kitchen-midden analysis.

Twenty-two radiocarbon activity measurements were made by accelerator mass spectrometry (AMS) on 2 Holocene stalagmites from Belgium (Han-stm1b) and from southwest France (Vil-stm1b). Sixteen thermal ionization mass spectrometric (TIMS) U/Th measurements were performed parallel to AMS analyses. The past dead carbon proportion (dcp) due to limestone dissolution and old soil organic matter (SOM) degradation is calculated with U/Th ages, measured calcite 14C activity and atmospheric 14C activity from the dendrochronological calibration curves. Results show that the dcp is different for the 2 stalagmites: between 10,800 and 4780 yr from present dcp=17.5% (σ=2.4; n=10) for Han-stm1b and dcp=9.4% (σ=1.6; n=6) between 3070 and 520 yr for Vil-stm1b. Despite a broad stability of the dcp during the time ranges covered by each sample, a slight dcp increase of about 5.0% is observed in the Han-stm1b sample between 8500 and 5200 yr. This change is synchronous with a calcite δ13C increase, which could be due to variation in limestone dissolution processes possibly linked with a vegetation change. The dcp and δ13C of the 2 studied samples are compared with 5 other modern stalagmites from Europe. Results show that several factors intervene, among them: the vegetation type, and the soil saturation leading to variable dissolution process systems (open/closed). The good correlation (R2=0.98) between the U/Th ages and the calibrated 14C ages corrected with a constant dcp validates the 14C method. However, the dcp error leads to large 14C age errors (i.e. 250–500 yr for the period studied), which is an obstacle for both a high-resolution chronology and the improvement of the 14C calibration curves, at least for the Holocene.

Measurements on same-age tree-ring samples from proximal Ural Mountain trees by the Ioffe Institute research group and at the University of Arizona demonstrate a variance corresponding to a standard deviation of ±5.1% for Ioffe compared to ±2.1% for Tucson. There is also a calibration difference of 4.3 ±1.2 ‰. Comparison of the same years measured in Seattle on wood from the Pacific Northwest shows an offset of 2.2 ± 0.5 ‰. This is not a calibration error, but rather is expected from the well-documented evidence for divergence and upwelling of 14C-depleted CO2 along the west coast of North America.

We present an analysis of radiocarbon dates on Dead Sea Scrolls that have a bearing on the question of the Scroll documents’ relation to Christian origins. We assess details of dating reports, discuss paleographical evidence, and consider the content of the documents. When collated, these findings may be seen as compatible with a view that personalities mentioned in the Scrolls were contemporary with the founders of Christianity.

Accelerator mass spectrometry (AMS) radiocarbon measurements were made on 120 samples collected between Antarctica and South Africa along 30°E during the WOCE-France CIVA1 campaign in February 1993. Our principal objective was to complement the Southern Ocean's sparse existing data set in order to improve the 14C benchmark used for validating ocean carbon-cycle models, which disagree considerably in this region. Measured 14C is consistent with the θ-S characteristics of CIVA1. Antarctic Intermediate Water (AAIW) forming north of the Polar Front (PF) is rich in 14C, whereas surface waters south of the PF are depleted in 14C. A distinct old 14C signal was found for the contribution of the Pacific Deep Water (PDW) to the return flow of Circumpolar Deep Waters (CDW). Comparison to previous measurements shows a 14C decrease in surface waters, consistent with northward displacement of surface waters, replacement by old deep waters upwelled at the Antarctic Divergence, and atmospheric decline in 14C. Conversely, an increase was found in deeper layers, in the AAIW. Large uncertainties, associated with previous methods for separating natural and bomb 14C when in the Southern Ocean south of 45°S, motivated us to develop a new approach that relies on a simple mixing model and on chlorofluorocarbon (CFC) measurements also taken during CIVA1. This approach leads to inventories for CIVA1 that are equal to or higher than those calculated with previous methods. Differences between old and new methods are especially high south of approximately 55°S, where bomb 14C inventories are relatively modest.