Five radiocarbon analyses were performed on 5 different sources within Soreq Cave, which was used as a model for the Judea Group Aquifer of Israel (pMCq0). The transit time of rainwater through the roof of the cave to sources within it had been determined with tritium. From this information, the year of deposition of rain on the roof of the cave, which later appeared in one of the sources, was estimated and the atmospheric 14C concentration at that time was ascertained (pMCa0). The parameter Q = pMCq0 / pMCa0 was found to be Q = 0.60 ± 0.04. This makes it possible to calculate the age of water in any well in the Judea Group Aquifer of Israel by measuring its 14C concentration (pMCqt) by use of the decay equation and applying Q.

The radiocarbon concentration of dissolved inorganic carbon in groundwater is most logically and completely represented as the product of 5 time-variable factors; these are mutually independent, and all must be considered and evaluated to determine a groundwater residence time. In the case of one factor, the 14C/(12C+13C) ratio of atmospheric CO2, its time variability can be side-stepped by assuming it to be constant at the pre-bomb 1950 value, and assigning an apparent half-life in the radioactive decay term. Apparent half-lives are calculated here for 5 separate periods extending back to 24,000 BP, working from the INTCAL98 atmospheric calibration. This approach can be extended further back in time when the necessary atmospheric calibrations are updated with greater certainty. The procedure is applied to the recently-explored Wairau Deep Aquifer, underlying central areas of the coastal Wairau Plain, Marlborough. The evolution of dissolved inorganic carbon concentration for this river-recharged groundwater is apparent from distinct trends in 13C, and is confirmed by hydrochemical modelling. Extension to the 14C concentrations yields minimum/maximum limits for groundwater residence times to 3 wells. In all 3 cases, the maximum is uncertain due to present uncertainty of the apparent half-life applicable before 24,000 BP. Residence times for the 2 wells closest to the recharge area are at least 17,400 yr, while that for a well further down the aquifer is at least 38,500 yr. Recharge, therefore, occurred during the Otiran glaciation, while the present-day near-surface fluvioglacial deposits of the Wairau Plain were accumulating. Drawdown-recovery records over 3 yr indicate a permeable connection to compensating recharge, enabling limited exploitation for vineyard irrigation.

Radiocarbon, 18O, and chemical concentrations have been used to identify groundwater recharged during the last ice age near Nelson, New Zealand. Moutere Gravel underlies most of the Moutere Depression, a 30-km-wide system of valleys filled with Plio-Pleistocene gravel. The depression extends northwards into Tasman Bay, which was above sea level when the North and South Islands of New Zealand were connected during the last glaciation. The aquifers are tapped by bores up to 500 m deep. Shallow bores (50–100 m) tap “pre-industrial” Holocene water (termed the “modern” component) with 14C concentrations of 90 ± 10 percent modern carbon (pMC) and δ18O values of −6.8 ± 0.4, as expected for present-day precipitation. Deeper bores discharge water with lower 14C concentrations and more negative 18O values resulting from input of much older water from depth. The deep end-member of the mixing trend is identified as paleowater (termed the “glacial” component) with 14C concentration close to 0 pMC and more negative 18O values (-7.6). Mixing of the modern and glacial components gives rise to the variations observed in the 14C, 18O, and chemical concentrations of the waters. Identification of the deep groundwater as glacial water suggests that there may be a large body of such water onshore and offshore at deep levels. More generally, the influence of changing sea levels in the recent past (geologically speaking) on the disposition of groundwaters in coastal areas of New Zealand may have been far greater than we have previously realized.

A new calibration curve for the conversion of radiocarbon ages to calibrated (cal) ages has been constructed and internationally ratified to replace IntCal98, which extended from 0–24 cal kyr BP (Before Present, 0 cal BP = AD 1950). The new calibration data set for terrestrial samples extends from 0–26 cal kyr BP, but with much higher resolution beyond 11.4 cal kyr BP than IntCal98. Dendrochronologically-dated tree-ring samples cover the period from 0–12.4 cal kyr BP. Beyond the end of the tree rings, data from marine records (corals and foraminifera) are converted to the atmospheric equivalent with a site-specific marine reservoir correction to provide terrestrial calibration from 12.4–26.0 cal kyr B P. A substantial enhancement relative to IntCal98 is the introduction of a coherent statistical approach based on a random walk model, which takes into account the uncertainty in both the calendar age and the 14C age to calculate the underlying calibration curve (Buck and Blackwell, this issue). The tree-ring data sets, sources of uncertainty, and regional offsets are discussed here. The marine data sets and calibration curve for marine samples from the surface mixed layer (Marine04) are discussed in brief, but details are presented in Hughen et al. (this issue a). We do not make a recommendation for calibration beyond 26 cal kyr BP at this time; however, potential calibration data sets are compared in another paper (van der Plicht et al., this issue).

In Quebrada de los Burros in coastal southern Peru (Tacna department), human settlements containing shells and charcoal deposits have been excavated since 1995. The sea surface 14C reservoir ages, estimated by calculating the difference of 14C age between marine shells and terrestrial organic materials, exhibit high values during the lower and middle Holocene and decrease abruptly after 4000 cal BP. The increase of reservoir age at around 7000–8000 cal BP suggests an enhancement of Peruvian coastal upwelling intensity and changes in ocean circulation at intermediate depth.

The National Electrostatics Corporation has built and tested a prototype low energy, open-air, single stage carbon accelerator mass spectrometry (AMS) system (patent pending). The configuration tested has a standard 40-sample, multi-cathode SNICS source on a 300-kV deck. The beam is mass analyzed before acceleration to a gas stripper located at ground. The 14C+ ions are separated from 13C+ and 12C+ arising from the molecular breakup by a 90° analyzing magnet immediately after the gas stripper which acts as a molecular dissociator. The 14C+ beam passes through an electrostatic spherical analyzer before entering the particle detector. The observed 14C/12C precision is better than 5% with a sensitivity of better than 0.05 dpm/gmC. A first single stage AMS system has been ordered. The configuration of this system will be discussed.

A total of 294 beachrock samples were collected from 116 sites on 15 islands in the Nansei Islands chain, southwestern Japan, and were radiocarbon dated. The beachrocks began to form at about 6900 BP and some are still under development in the islands. Values of isotope fractionations of different materials making up the beachrocks ranged between +9.4‰ and −5.7‰. Isotope fractionations outside the range of 0 ± 2‰ suggest that these beachrocks were strongly influenced by underground water and running freshwater when they were cemented. The sea level during the late Holocene has remained the same for at least the past 5000 yr, except for several uplifted coasts.

New radiocarbon calibration curves, IntCal04 and Marine04, have been constructed and internationally ratified to replace the terrestrial and marine components of IntCal98. The new calibration data sets extend an additional 2000 yr, from 0–26 cal kyr BP (Before Present, 0 cal BP = AD 1950), and provide much higher resolution, greater precision, and more detailed structure than IntCal98. For the Marine04 curve, dendrochronologically-dated tree-ring samples, converted with a box diffusion model to marine mixed-layer ages, cover the period from 0–10.5 cal kyr BP. Beyond 10.5 cal kyr BP, high-resolution marine data become available from foraminifera in varved sediments and U/Th-dated corals. The marine records are corrected with site-specific 14C reservoir age information to provide a single global marine mixed-layer calibration from 10.5–26.0 cal kyr BP. A substantial enhancement relative to IntCal98 is the introduction of a random walk model, which takes into account the uncertainty in both the calendar age and the 14C age to calculate the underlying calibration curve (Buck and Blackwell, this issue). The marine data sets and calibration curve for marine samples from the surface mixed layer (Marine04) are discussed here. The tree-ring data sets, sources of uncertainty, and regional offsets are presented in detail in a companion paper by Reimer et al. (this issue).

Recent measurements on dendrochronologically-dated wood from the Southern Hemisphere have shown that there are differences between the structural form of the radiocarbon calibration curves from each hemisphere. Thus, it is desirable, when possible, to use calibration data obtained from secure dendrochronologically-dated wood from the corresponding hemisphere. In this paper, we outline the recent work and point the reader to the internationally recommended data set that should be used for future calibration of Southern Hemisphere 14C dates.

Paired radiocarbon and 230Th/U dating was performed on 13 surface corals from submerged reefs in the Marquesas and from raised terraces in Vanuatu. The absolute ages of the corals analyzed ranged from 3000 to 15,000 cal yr. Estimates of the difference between the absolute and 14C ages of these corals are in agreement with previous determinations up until 11,500 cal yr. The resulting mean sea surface reservoir age R is determined at 390 ± 60 yr for the Marquesas region (9°S), which is slightly higher than the R value at 280 ± 50 yr for the Tahiti Islands (18°S). Multiple 14C analyses of 2 corals from the Marquesas present scattered 14C ages at ~12,000 and ~15,100 cal yr. This could be attributed to rapid changes of the 14C content of surface waters around the Marquesas Islands or to a subtle submarine diagenesis.

High precision for radiocarbon cannot be reached without profound insight into the various sources of uncertainty which only can be obtained from systematic investigations. In this paper, we present a whole series of investigations where in some cases 16O:17O:18O served as a substitute for 12C:13C:14C. This circumvents the disadvantages of event counting, providing more precise results in a much shorter time. As expected, not a single effect but a combination of many effects of similar importance were found to be limiting the precision.

We will discuss the influence of machine tuning and stability, isotope fractionation, beam current, space charge effects, sputter target geometry, and cratering. Refined measurement and data evaluation procedures allow one to overcome several of these limitations. Systematic measurements on FIRI-D wood show that a measurement precision of ±20 14C yr (1 σ) can be achieved for single-sputter targets.

Precision and accuracy in accelerator mass spectrometry (AMS) dating relies on the systematic reduction of errors at all stages of the dating process, from sampling to AMS measurement. With new AMS systems providing much better precision and accuracy for the final stage of the process, we need to review the process as a whole to test the accuracy of reported results. A new High Voltage Engineering Europa (HVEE) AMS system was accepted at Oxford in September 2002. Since then, the system has been in routine use for AMS dating and here we report on our experiences during the first year. The AMS system itself is known to be capable of making measurements on single targets to a precision of better than 0.2% for the 14C/13C ratio and better than 0.1% for the 13C/12C ratio. In routine operation, we measure known-age wood to a precision of just above 0.3%, including uncertainties in background and pretreatment. At these levels, the scatter in results is no higher than reported errors, suggesting that uncertainties of ±25 to ±30 14C yr can be reliably reported on single target measurements. This provides a test of all parts of the process for a particular material in a particular state of preservation. More generally, sample pretreatment should remove as much contamination as feasible from the sample while adding as little laboratory contamination as possible. For more complex materials, such as bone, there is clearly more work needed to prove good reproducibility and insignificant offsets in all circumstances. Strategies for testing accuracy and precision on unknown material are discussed here, as well as the possibilities of one day reaching precisions equivalent to errors of <±20 14C yr.

We report on the development and implementation of a model-based statistical method for the estimation of radiocarbon calibration curves using diverse data. The method takes account of uncertainty on both the 14C and calendar scales, coherently integrating data, the calendar age estimates of which arise from different dating methods. It also allows for correlation between observations, if they have particular sources of uncertainty in common. We adopt an approach based on a random walk model, tailoring it to take account of possible calendar age offsets between different data sources by adding a random effect component. The latter allows us to use the same modeling framework for constructing the new calibration curve IntCal04, the comparison curve NotCal04, the Southern Hemisphere curve SHCal04, and the marine calibration curve Marine04.