AMS radiocarbon results from the World Ocean Circulation Experiment in the Pacific Ocean show dramatic changes in the inventory and distribution of bomb-produced 14C since the time of the GEOSECS survey (8/73–6/74). Near-surface Δ14C values for the eastern portion of both the northern and southern subtropical gyres decreased by 25–50‰, with the change being greater in the north. Equatorial near-surface values have increased by ca. 25‰. Changes in the 250–750-m depth range are dramatically different between the northern and southern basins. The intermediate and mode waters of the southern basin have increased by as much as 75‰ since GEOSECS. Waters of similar density in the northern hemisphere are not exposed to the Southern Ocean circulation regime and are significantly less ventilated, showing maximum changes of ca. 50‰.

In the best case, radiocarbon measurements allow artificial objects to be dated with a precision of 10 calendar years when conventional wiggle-matching onto the IntCal09 calibration curve is applied. More precise dating can only be achieved by using annually resolved 14C calibration data, particularly in timespans when there are rapid changes in atmospheric 14C concentration. The recently observed jump in atmospheric 14C concentration of 1.5% between AD 774 and 775, though expected to be rare, is a good example for such a rapid change. We demonstrate by example that is possible to precisely 14C date the cutting year of a timber in the historically important and well-preserved Holy Cross chapel of the convent St. John the Baptist in Val Müstair, Switzerland.

Chemical and structural similarities between poorly preserved charcoal and its contaminants, as well as low radiocarbon concentrations in old samples, complicate 14C age determinations. Here, we characterize 4 fossil charcoal samples from the late Middle Paleolithic and early Upper Paleolithic strata of Kebara Cave, Israel, with respect to the structural and chemical changes that occur when they are subjected to the acid-base-acid (ABA) treatment. Differential thermal analysis and TEM show that acid treatment disrupts the structure, whereas alkali treatment results in the reformation of molecular aggregates. The major changes are ascribed to the formation of salt bridges at high pH and the disruption of the graphite-like crystallites at low pH. Weight losses during the treatments are consistently greater for older samples, implying that they are less well preserved. Based on the changes observed in vitro due to pH fluctuations, various methods for removing contamination, as well as a mechanism for preferential preservation of charcoal in nature, are proposed.

We report on a statistical analysis of a large set of radiocarbon dates for reconstruction of paleoclimate. Probability density functions were constructed by summing the probability distributions of individual 14C dates. Our analysis was based on 2 assumptions: 1) The amount of organic matter in sediments depends on paleogeographical conditions; 2) The number of 14C-dated samples is proportional to the amount of organic matter deposited in sediments in the examined time intervals. We quantified how many dates are required to give statistically reliable results. As an example, 785 peat dates from Poland were selected. The dates encompassed the Holocene and Late Glacial period. All dates came from the Gliwice Radiocarbon Laboratory. Results were compared with other paleoenvironmental records. Detailed analysis of the frequency distributions showed that preferential sampling plays an important part in the shape determination. The general rule to take samples from locations where visible changes of sedimentation are apparent (e.g. from the top and the bottom of the peat layer) results in narrow peaks in the probability density function near the limits of the Holocene subdivision.

A previous radiocarbon dating and stable isotope study of directly associated ungulate and human bone samples from Late Mesolithic burials at Schela Cladovei in Romania established that there is a freshwater reservoir effect of approximately 500 yr in the Iron Gates reach of the Danube River valley in southeast Europe. Using the δ15N values as an indicator of the percentage of freshwater protein in the human diet, the 14C data for 24 skeletons from the site of Lepenski Vir were corrected for this reservoir effect. The results of the paired 14C and stable isotope measurements provide evidence of substantial dietary change over the period from about 9000 BP to about 300 BP. The data from the Early Mesolithic to the Chalcolithic are consistent with a 2-component dietary system, where the linear plot of isotopic values reflects mixing between the 2 end-members to differing degrees. Typically, the individuals of Mesolithic age have much heavier δ15N signals and slightly heavier δ13C, while individuals of Early Neolithic and Chalcolithic age have lighter δ15N and δ13C values. Contrary to our earlier suggestion, there is no evidence of a substantial population that had a transitional diet midway between those that were characteristic of the Mesolithic and Neolithic. However, several individuals with “Final Mesolithic” 14C ages show δ15N and δ13C values that are similar to the Neolithic dietary pattern. Provisionally, these are interpreted either as incomers who originated in early farming communities outside the Iron Gates region or as indigenous individuals representing the earliest Neolithic of the Iron Gates. The results from Roman and Medieval age burials show a deviation from the linear function, suggesting the presence of a new major dietary component containing isotopically heavier carbon. This is interpreted as a consequence of the introduction of millet into the human food chain.

A semi-automated continuous-flow system used to process archaeological bone to purified gelatin or amino acids for 14C dating is described. Powdered bone is retained in flow cells specifically designed to permit the sequential leaching of the bone with acid, alkali and water. Crude collagen obtained by this process is gelatinized, and than either purified directly using a macroporous cation exchange resin (BioRad AGMP-50), or hydrolyzed and the amino acids desalted on BioRad 50W-X8 resin. When compared with previous methods used by the laboratory, the new method allows more samples to be treated to a higher degree of purification. Examples of dates obtained on “standard” bones are presented, and confirm that no contamination is introduced from the components used in the new process.

This paper presents radiocarbon results from a single Diploastrea heliopora coral from Vanuatu that lived during the Younger Dryas climatic episode, between ca. 11,700 and 12,400 calendar yr bp. The specimen has been independently dated with multiple 230Th measurements to permit calibration of the 14C time scale. Growth bands in the coral were used to identify individual years of growth. 14C measurements were made on each year. These values were averaged to achieve decadal resolution for the 14C calibration. The relative uncertainty of the decadal 14C data was below 1% (2σ). The data are in good agreement with the existing dendrochronology and allow for high-resolution calibration for most years. Variations in the fine structure of the 14C time series preserved in this specimen demonstrate sporadic rapid increases in the Δ14C content of the surface ocean and atmosphere. Certain sharp rises in Δ14C are coincident with gaps in coral growth evidenced by several hiatuses. These may be related to rapid climatic changes that occurred during the Younger Dryas. This is the first coral calibration with decadal resolution and the only such data set to extend beyond the dendrochronology-based 14C calibration.

We have compared accelerator mass spectrometry (AMS) radiocarbon results on wood samples at or near the limit of 14C dating, pretreated with a standard acid-base-acid (ABA) protocol, with those obtained from cellulose prepared from the same samples by several modifications of the Jayme-Wise cellulose extraction method (Green 1963). These tests were carried out to determine the most efficient way to ensure low backgrounds in 14C measurements of well-preserved ancient wood samples.

A simple method for preparing pollen concentrates for 14C AMS dating is applied to organic and inorganic deposits from a peat bog in south Westland, New Zealand, from which preliminary AMS dating indicated age inversions and severe younger carbon contamination problems. The AMS ages of the pollen concentrates provided consistently older age estimates for each sample than ages derived from their respective organic residue or combined pollen and organic residue fractions. It is likely that the younger age estimates of the organic residue fractions result from the incorporation of younger plant material into the sample and possible contamination from younger humic acids percolating through the site.

14C analysis of monospecific samples of planktonic and benthic foraminifera were performed in deep-sea sediment cores from the Atlantic and Pacific Oceans by Accelerator Mass Spectrometry (AMS). These measurements demonstrate that the Younger Dryas cold event, first described in the north Atlantic, is also present at the same time in the north Pacific Ocean. The comparison of the 14C ages of planktonic and benthic foraminifera from the same sediment level in two Pacific cores shows that the ventilation time of the Pacific Ocean was greater than today during the last ice age, but significantly less than today during the deglaciation.

The issue of comparability of measurements (and thus bias, accuracy, and precision of measurement) from diverse laboratories is one which has been the focus of some attention both within the radiocarbon community and the wider user communities. As a result, the 14C community has undertaken a widescale, far-reaching, and evolving program of intercomparisons, to the benefit of laboratories and users alike. The benefit to the users is, however, indirect, since the 14C intercomparisons have not been used to generate “league tables” of performance, but rather to allow individual laboratories to check procedures and modify them as required.

The historical progression of 14C laboratory intercomparisons from the Third (TIRI, completed in 1995, Gulliksen and Scott 1995) and Fourth (FIRI, completed in 2000, Scott 2003; Boaretto et al. 2000; Bryant et al. 2002) suggests that a Fifth (VIRI) should also be expected. We describe the plans for VIRI.

We present a status report of the accelerator mass spectrometry (AMS) facility at the University of California, Irvine, USA. Recent spectrometer upgrades and repairs are discussed. Modifications to preparation laboratory procedures designed to improve sample throughput efficiency while maintaining precision of 2–3‰ for 1-mg samples (Santos et al. 2007c) are presented.

The new facility Artemis was installed in 2003 in Saclay, France. This 3MV NEC Pelletron is dedicated to high-precision radiocarbon measurements for French 14C laboratories. We will present information on Artemis along with our sample preparation methods. Results from measurements on some intercalibration samples will be given along with the values of measured blanks. Finally, we report on some problems we have encountered when measuring sputter cathodes with high CH− outputs.

The effects of nonconservative sources (inputs) and sinks (outputs) of carbon are indicated by the behavior of Δ14C and δ13C of the total dissolved inorganic carbon (ΣCO2) in San Francisco Bay and Chesapeake Bay. Isotopic distributions and model calculations indicate that in North San Francisco Bay the net CO2 flux to the atmosphere and carbon utilization in the water column are balanced by benthic production. Municipal waste appears to be a dominant source in South San Francisco Bav. In Chesapeake Bay, atmospheric exchange has increased the Δ14C and δ13C in the surface water. Decomposition of organic matter in the water column is indicated to be the dominant source of excess ΣCO2 in the deep water.

This paper presents 31 new ΔR results of known-age, pre-AD 1950 shells from the South Pacific subtropical gyre region, spanning from the Tuamotu Archipelago in the east to New Caledonia in the west. This doubles the number of available ΔR values for the Oceania region. These values indicate that the regional offset (ΔR) from the modeled radiocarbon marine age has remained relatively constant over the last 100 yr prior to 1950. Variation from the norm can be attributed to various influences including localized upwelling around islands, the presence of a hardwater effect, direct ingestion of old carbon by the live shellfish, or enhanced exchange with atmospheric CO2 as a consequence of photosynthetic activity or increased aeration.

This paper includes a brief history of the calibration of the radiocarbon time scale from the first recognition of the necessity of calibration in 1962 to INTCAL98. Thirty-six years of effort by dendrochronologists and the 14C community have pushed the tree-ring calibration back to 11,854 yr BP. All of this part of the calibration has been done by high-precision beta counting. Uranium-thorium (U-Th) dating of coral samples coupled with accelerator mass spectrometry (AMS) measurement of 14C has extended a fairly detailed calibration back beyond the Bølling warm episode to 15,000 BP. Earlier than 15,000 BP, piecewise linear approximation extends INTCAL98 calibration to 24,200 BP.

Blending 1-, 2-, 3-, 10-, and 20-yr tree-ring samples containing regional and data offsets into a decadal time scale does not make an ideal error and bias free δ14C record. Nevertheless, spectral analysis reveals some statistically significant fundamental frequencies as well as interesting “beat” frequencies and the second harmonic of the around 208-yr cycle that is considered to be solar in origin. Although, some very prominent peaks such as the 88-yr (Gleissberg) are clearly solar in origin, some of the lower frequencies such as of the 512-yr period may have an origin in thermohaline circulation. Thus, INTCAL98 provides useful data for geophysical and solar physics research. Lastly, single year δ14C analysis would be useful for revealing invaluable information for solar physics, astrophysics and geophysics not accessible by decadal data. We provide several examples.

It is well known that, during the widely used AAA pretreatment (de Vries and Barendsen 1954), alkali treatment is responsible for the incorporation of modern carbon due to the precipitation of atmospheric CO2 as carbonate. Until now, the last step of the experiment, consisting in acid treatment (most of the time with hydrochloric acid) was considered to be sufficient to eliminate all of lab contamination. But wood, peat and sediment present a complex molecular structure. During radiocarbon chemical treatments, functional groups still present in the molecules are likely to form ionic bonds with “modern” carbonates. These new chemical bonds resist a “classical” acid treatment and are responsible for rejuvenation. This short paper presents preliminary results for two common 14C cases: rejuvenation of a 0.4 pMC wood and of an Oxygen Isotope Stage 3 (OIS3) paleosol. For both cases, contamination due to incorporation of modern carbon during chemical treatment is evaluated and an alternative protocol is proposed.

The availability of absolutely (dendrochronologically) dated German oak has allowed the Belfast laboratory to extend its published high-precision 14C measurements of Irish oak (Pearson et al. 1986) by 2680 yr. The samples were selected at contiguous 20-yr intervals, following a precedent adopted and considered satisfactory in previous publications. All samples were measured for at least 200,000 counts within the 14C channel. The statistical counting error, together with the error on standards, backgrounds and applied corrections, give a realistic precision quoted on each sample of ± 2.5‰ (± 20 yr). This error is considered high-precision for sample ages of 7000–8000 BP.

We present studies of 9 modern (up to 400-yr-old) peat sections from Slovenia, Switzerland, Austria, Italy, and Finland. Precise radiocarbon dating of modern samples is possible due to the large bomb peak of atmospheric 14C concentration in 1963 and the following rapid decline in the 14C level. All the analyzed 14C profiles appeared concordant with the shape of the bomb peak of atmospheric 14C concentration, integrated over some time interval with a length specific to the peat section. In the peat layers covered by the bomb peak, calendar ages of individual peat samples could be determined almost immediately, with an accuracy of 2–3 yr. In the pre-bomb sections, the calendar ages of individual dated samples are determined in the form of multi-modal probability distributions of about 300 yr wide (about AD 1650–1950). However, simultaneous use of the post-bomb and pre-bomb 14C dates, and lithological information, enabled the rejection of most modes of probability distributions in the pre-bomb section. In effect, precise age-depth models of the post-bomb sections have been extended back in time, into the “wiggly” part of the 14C calibration curve.

Our study has demonstrated that where annual resolution is concerned, tissues of Sphagnum are the only representative material for 14C dating, although even samples of pure Sphagnum collected from a very thin slice of the peat section contain tissues grown in different years, so they integrate the atmospheric 14C signal over a period of time. This time period (0.5–8 yr, depending on the site) seems to correlate with the peat accumulation rate, but it also depends on how the sampled peat sections were handled. When constructing age-depth models, for some peat sections we used the strategy of multi-stage 14C dating. This led to a drastic reduction in the uncertainty of the age-depth models, by dating only a few additional samples in the profile.

Our study is the first in which peat sections from the late pre-bomb time (AD 1900–1960) have been precisely dated at a high temporal resolution. In this time interval, 14C ages of all the samples dated were younger than those derived from the atmospheric calibration curve, apparently due to the effect of integration. Evidently, the determination of calendar ages based on 14C dating of single peat samples from that interval may be affected by a serious error if the possibility of integration is ignored.

Patterns of 14C enrichment in the superficial plant debris and mineral soil horizons of an established woodland have been monitored at regular intervals during the past 15 years. These data are compared with a model evaluation of carbon turnover based on the recorded changes in atmospheric 14C concentration since AD 1900.

Leaf litter and decomposing plant debris are characterized by steady-state turnover values of ca 2 and ca 8 years, respectively. A two-component system of ‘fast’ (≤20 yr) and ‘slow’ (ca 350 yr) cycling carbon is indicated for the surface (0–5cm) soil humus; below 10cm, the “fast’ component is rare (<5%).

Selective microbal humification of leaf litter, branch, and root debris is proposed to explain a delay of several years in the peak transfer of ‘bomb’ 14C to the soil carbon pool.