Late Holocene relative sea-level reconstructions are commonly generated using proxies preserved in salt-marsh and mangrove sediment. These depositional environments provide abundant material for radiocarbon dating in the form of identifiable macrofossils (salt marshes) and bulk organic sediment (mangroves). We explore if single-step graphitization of these samples in preparation for radiocarbon dating can increase the number and temporal resolution of relative sea-level reconstructions without a corresponding increase in cost. Dating of salt-marsh macrofossils from the northeastern United States and bulk mangrove sediment from the Federated States of Micronesia indicates that single-step graphitization generates radiocarbon ages that are indistinguishable from replicates prepared using traditional graphitization, but with a modest increase in error (mean/maximum of 6.25/15 additional 14C yr for salt-marsh macrofossils). Low 12C currents measured on bulk mangrove sediment following single-step graphitization likely render them unreliable despite their apparent accuracy. Simulated chronologies for six salt-marsh cores indicate that having twice as many radiocarbon dates (since single-step graphitization costs ∼50% of traditional graphitization) results in narrower confidence intervals for sample age estimated by age-depth models when the additional error from the single-step method is less than ∼50 14C yr (∼30 14C yr if the chronology also utilizes historical age markers). Since these thresholds are greater than our empirical estimates of the additional error, we conclude that adopting single-step graphitization for radiocarbon measurements on plant macrofossils is likely to increase precision of age-depth models by more than 20/10% (without/with historical age markers). This improvement can be implemented without additional cost.

Jacob’s Well, located in modern city of Nablus and ancient Shechem (Tall Balata) in the northern West Bank of Palestine, attracts modern day tourists and pilgrims. It is found in the eastern suburbs of the city. Since 333 AD, pilgrims have been writing accounts of the well, and it has been venerated by both Christian and Jewish communities throughout its history. It is believed to be the well referred to in the New Testament, where Jesus conversed with a Samaritan woman, the orthodox saint, Photini. It now forms the central feature in the crypt of the St Photini Greek Orthodox church in the walled grounds of a monastery. In order to gain more information on the chronology of the site, we analyzed human skeletal remains found at the site in 1997. These consist of three skulls and a femur. One of the skulls was found in a sarcophagus alongside the church and the two other skulls and a femur were found in a burial ground alongside the monastery, north of the church, over which a room has now been built. Radiocarbon analysis reveals that the remains date to four historical periods or events: the early Christian period, before structural additions to the well by Constantine the Great in the fourth century; the Samaritan Revolts (AD 529 and 556), the Sassanid Invasion (AD 614–628), and Abbasid rule (AD 750–1258). Dating of one skull suggests it may have been that of Germanus, a fourth century bishop of Nablus, and that there may have been a very early structure, shrine, or burial chamber at the site before the fourth century. We provide contextual information based on historical and contemporary literature.

The Gaspereau Lake Reservoir Site Complex in Nova Scotia, Canada, yielded a large ceramic assemblage that permitted the first fine-grained analysis of ceramic change in the region at the Middle–Late Woodland Transition from ca. 1550 BP to ca. 1150 BP. The aim of this study was to refine the standard regional chronology first proposed by researchers J B Petersen and D Sanger. To do this, ceramics were directly dated using accelerator mass spectrometry (AMS), and the assemblage was categorized and analyzed to identify clusters of attributes. Ten AMS dates were acquired on carbonized food residue on the interiors of pottery and yielded the largest continuous ceramic sequence in the Maritime Provinces of Canada. This sequence was used to infer a change in manufacturing practices between the Middle (2150–1300 BP) and Late (1300–500 BP) Woodland periods and to propose five new subperiods between 1650 BP and 950 BP. Increasing incidence of coil breaks and temper percentage from the Middle to the Late Woodland were found to be chronologically sensitive. The analysis showed that, at Gaspereau Lake, a gradual shift from finely decorated and manufactured pottery to expediently made pottery suggests that pottery was made in larger numbers to support large-scale gatherings.

Precise manometric pressure, volume, and temperature (P-V-T) measurements of carbon in samples, standards, and blanks are critical for radiocarbon studies. While P and T uncertainties depend on instrument choice and environmental stability, V uncertainties depend on their method of measurement and are often overlooked. We used numerical simulations and error propagation to find optimum procedures for measuring “cold-finger” volumes equipped with capacitance diaphragm gauges (CDGs) by two common application of Boyle’s Law: cryogenic transfers and serial gas expansions with a reference flask of known volume. Minimum relative uncertainties of cold-finger volumes are comparable for these two methods (∼0.002), but the serial gas expansion method is preferred due to its convenience. Serial gas expansions can be performed to high precision by using dry air, an initial pressure ∼76% full-scale (e.g., 760 Torr), and a reference flask with an optimal volume based on preliminary estimates of cold-finger volumes and an empirical power function. The volumes of cold-fingers ≥ 12 cm3 can be determined with minimum achievable relative uncertainties of 0.0021 to 0.0023. This limit translates to minimum achievable relative uncertainties of 0.0026 to 0.0027 for P-V-T measurements of moles of gas simulated here.

A simple way to upgrade the Peking University 500kV NEC radiocarbon facility (CAMS) for 10Be measurements is presented. In a first phase, a silicon nitride foil as passive boron degrader was mounted in front of the electrostatic deflector near the focal plane of 10Be. The Si detector at the end of the beam line was replaced with a high-resolution ΔE-Eres gas ionization chamber. In addition, a Faraday cup for the measurement of 9Be1+ was installed. Tests with this arrangement showed promising results: a 10Be/9Be background level of 3.4 × 10–14 and an overall transmission for 10Be of 2.2% were obtained. Measurements of standards showed very good stability and reproducibility. In the next step, it is planned to add a second magnet to reduce the background and to partly compensate losses due to energy and angular straggling in the degrader foil by the energy and angular refocusing effect of a magnetic sector field. With this final arrangement, a performance with 10Be/9Be background levels at 10−15 and 10Be overall transmission of 6–7% can be expected. The design proposed in this paper has the advantage that the modifications can be realized in a rather inexpensive way and that the measurement performance for 14C will not be affected.

The earliest years of photography were full of experimentation and innovation; many photographers from this era carefully documented their experimental procedures. Consequently, it is possible to reproduce historically accurate photographs and negatives today. One of the oldest forms of photographic technology is the waxed paper negative, popular during the mid-19th century. It consists of a photosensitive sheet of writing paper coated with a layer of wax to render it transparent. Modern waxed paper negatives made using 19th century paper can potentially pass for historically significant 19th century negatives. This poses problems to museums and others interested in studying or collecting authentic 19th century photographic images. We have developed methods for separating the organic components of waxed paper negatives and measuring their radiocarbon content as a means of distinguishing between modern and historic waxed paper negatives. By detecting the presence or lack of bomb carbon in a given negative, this process can act as a tool for authentication. We have mainly focused on the extraction and 14C measurement of the wax component, reasoning that modern photographers might have easy access to 19th century paper, but would less likely use 19th century beeswax.

A workshop on atmospheric radiocarbon measurements was held in conjunction with the 21st International Radiocarbon conference in July 2012. The main topics were intercomparison of measurements of 14C in atmospheric CO2, the potential for use of gas standards for atmospheric 14C measurements, reporting of uncertainties, and expansion of intercomparison activities to other atmospheric trace gases. This report documents the discussions and conclusions of this workshop.

It is known that 12C beam transmission through the accelerator decreases at high beam currents. This effect depends on machine design and varies across different types of AMS instruments. For beam currents of about 100 μA, the effect is small on the 500 kV tandem CAMS unit, whereas beam saturation is observed for similar high beam currents on the 250 kV SSAMS unit. While this effect is very evident for high 12C beam currents, we have also observed that even the 13C beam is found to suffer modest transmission loss with beam current. As a result, the 13C/12C ratio does not remain constant with beam current. By correcting for the effects of 12C beam saturation and decreased 13C transmission, we have obtained online δ13C values that are more accurate and precise at moderately high beam currents for SSAMS.

This note describes point and interval estimation of a settlement time from a collection of radiocarbon dates. An application concerning the settlement time of New Zealand is presented.

Microbial mats (kopara in Polynesian) that develop in shallow brackish to hypersaline ponds on the rims of atolls were investigated for their accumulation process and rate. Two sequences of ∼30-cm-deep kopara, composed of 7 and 5 layers distinguished by their colors and sedimentological facies were collected in 1996 from the Tetiaroa atoll, French Polynesia. The combination of radiocarbon activity measurements on both organic and carbonate constituents, reservoir effect estimation, and comparison with the Southern Hemisphere atmospheric bomb-peak 14C record allowed us to establish a fine chronology of the layer successions documenting the mode of formation, erosion, and restoration of these microbial mat deposits.

This list begins a program of publishing our large backlog of unpublished dates. The dates listed here are not a specific block of dates but simply those ready for publication. In many cases we have received comments from submitters, to whom we are grateful. Where no comment is included, none was received.

The following list of dates is compiled from samples prepared since publication of our last date list (R, 1974, v 16, p 131–141). The counting equipment and operating procedures are the same. Ages are quoted with a 1σ counting error which includes statistical variation of the sample count as well as for background and standard, using ad 1950 as the reference year and 95% NBS oxalic acid for 14C dating as the standard. The half-life value used is 5570 years.

The results described herein are measurements performed in 1961. Sample preparation and conversion into acetylene have been described (Wendt, Schneekloth and Budde, 1962). In calculating errors we did not follow the procedure used in our Date List I, where only the standard deviations of counting rates were used. The errors attached to the dates listed below include systematic errors due to sample preparation and small changes in the counting characteristics of sample, background, and standard counting gas.

The automatic β-counting system plays a significant role in obtaining high-level reproducibility and reliability in conventional radiocarbon dating. I review here the results achieved by using the “Fully Automatic Radiocarbon Dating System” developed by Omoto (1982). Since setting up the system in 1981, I was able not only to save operator time in β counting, but also to obtain accurate dates with only minimal uncertainties. Another positive result was the introduction of the automatic voltage correction program, which produced excellent results for counting sample materials over a long period.

The extraction of dissolved carbonate species for age dating from a 100L water sample by the direct-precipitation method (DPM) and by the gas-evolution method (GEM) has been investigated. Stable carbon-isotope fractionation between initial and final carbon dioxide evolved was ca 11‰ by GEM and 1‰ by DPM. GEM will produce isotopically lighter carbon dioxide compared with DPM if carbonate recovery is low. Extraction efficiency of > 95% can be achieved by GEM in 3 hours using nitrogen gas at a sweeping rate of 2000cc per minute. DPM requires precipitates to settle overnight to assure > 95% recovery. GEM is little affected by a high concentration of sulfate ions, whereas DPM is greatly affected by sulfate resulting in less yield.

The management of counting files, the calculation of radiocarbon age, and the creation and maintenance of databases for storage and retrieval of laboratory data are time-consuming and exacting tasks. These routine functions are essential to the successful operation of all 14C dating laboratories. However, since the number of 14C dating laboratories worldwide is rather limited, it is unlikely that a commercial software company will produce a program for use in 14C age calculation and associated data management. We have therefore developed Windows based software to meet some of these needs.

The results presented in this list are mostly from our earlier years of operation, the most recent of which were measured in 1984. It is the second of a series of special lists being prepared hopefully to clear the backlog of unpublished dates of this laboratory. All samples are of archaeological origin from the United Kingdom; most have originated from “rescue” type excavations and all were sponsored by the Ancient Monuments Laboratory of the Historic Buildings and Monuments Commission.