The South Arabian chronology has been problematic for a long time and this is also a true vexata quaestio for the ancient history of South Arabia. Three different chronologies have been suggested for the first literate phase of South Arabian cultures, which may date to the 11th century BC, the late 8th century BC, or the 5th century BC (see de Maigret 1996:157–63; de Maigret and Robin 1989: 276–8; Pirenne 1988; Robin 1997; Figure 1). At the site of Yalâ, potsherds with incised South Arabian inscriptions have been recovered in a stratum dating at least to the 8th century BC, if not earlier, and offer evidence of the existence of South Arabian culture at that time (de Maigret and Robin 1989:288–9).

A radiocarbon facility has been installed at the University of California, Riverside (UCR) to support interdisciplinary studies including archaeologic, archaeometric, geophysical, and geologic research. The laboratory was built between 1970 and 1973. Initially, a sample pretreatment and combustion system designed for a proportional CO2 counting system was installed. It was designed after concepts developed at the University of California Los Angeles (UCLA) and New Zealand (Institute of Nuclear Sciences) Laboratories, and began processing samples in November 1972.

The application of traditional gas or liquid scintillation counting (LSC) is necessary for assessing radionuclide activity in countries without operating accelerator mass spectrometry (AMS) facilities. A simple and relatively inexpensive system of mini gas counters for measurement of radiocarbon in archaeological and environmental samples has been set up recently in the Kraków laboratory (Department of Environmental Physics, University of Mining and Metallurgy). The system is composed of a gas purification and counter filling line, three identical 15-mL copper/quartz counters, active and passive shielding, and an electronic unit with data acquisition. One counter measures 22 mg of carbon as CO2 with efficiency >95% at a background reduced to 0.044 cpm by a NaJ(Tl) guard counter and lead shield. The detection limit (1 σ) for a two-week measurement of 48 mL of CO2 is 0.52 pMC. The corresponding counting error of a 100 pMC environmental sample is 1.3 pMC for 22 mgC (one counter) and 0.75 pMC for 66 mgC (three counters filled with the same sample).

Radiometric and AMS radiocarbon dating of a 6-m sediment core from Loch Ness, Scotland, indicates that it represents perhaps the very end of the Late Pleistocene, and the first ca. 7500 yr of the Holocene. Counts of laminations observed in the Holocene section of the core suggest that they are present in sufficient number to constitute annual laminations (varves), an hypothesis consistent with the pollen record, which contains a sequence of zones representative of the Early, Middle and part of the Late Holocene regional vegetation history. On the basis of BSEM and X-ray studies of sediments, and modern seston trap data, the laminations are believed to be produced by winter floods, which introduce increased silt loading into the Loch. Sediment for the rest of the year is mostly composed of clay-sized material. This hypothesis is being further tested, however, by continuing sedimentological and microfossil studies.

Time-depth relations for the core based on calibrated 14C dates and lamination counts, respectively, illustrate the close correspondence between the two sets of data. The latter are therefore now being used to develop a varve chronology for the Holocene for Loch Ness. This will then in turn be used for further chronological studies, and for investigations of palaeoclimatic variations over the eastern North Atlantic, to which the signal of lamination thickness in the sediments is thought to be particularly sensitive. They may also eventually be used for calibration studies, employing 14C dating of specific carbon compounds, or groups of compounds extracted from the sediment using modern organic geochemical methods.

The Chair, Renee Kra, opened the Workshop with the announcement that the IRDB will be officially located at the Geosciences Department, University of Arizona, Tucson, and will begin operating on January 2, 1989.

The chemical form of 14C released from irradiated stainless steel is a key parameter in the safety assessment of the subsurface disposal system in Japan. In this study, to identify the chemical form of the released carbon, unirradiated stainless-steel powders, which were found to be water-atomized powders with a silicon oxide film, were immersed in NaOH and HCl solutions under low-oxygen conditions for approximately 25 days. The results showed that the main chemical forms of the carbon were colloidal carbon in the NaOH solution and colloidal carbon and formic and acetic acids in the HCl solution. Almost no hydrocarbons were detected in both solution systems. Concerning the source of the colloidal carbon and carboxylic acids, the hypothesis that carbon in the oxide layer is released is considered to be reasonable. The very small amounts of hydrocarbons generated prevented us from discussing the source of the hydrocarbons. To validate the hypothesis and obtain further information on the hydrocarbons, additional experiments are necessary. In particular, for long-term safety assessment, it is important to determine whether the colloidal carbon, carboxylic acids and hydrocarbons are continuously released during the corrosion process. Therefore, information on the temporal evolution of the carbon should be obtained.

The understanding of the 14C behavior in waste packages could lead, in the Spanish context, to a revision of the management strategies for radioactive waste and a revaluation of the near surface repository devoted to the disposal of waste containing this radionuclide in high concentrations. To achieve this objective, and in the context of the EU project Carbon-14 Source Term (CAST), the authors of the work presented in this paper have performed leaching experiments with irradiated graphite considering two different scenarios. One, in which the leaching solution simulates some of the expected conditions in a repository where a granite/bentonite mixture has been used as backfill material, and the other, using deionized water as a high efficiency chemical removal agent and for comparison purposes. The analytical approach to measure the release rate and speciation of 14C from irradiated graphite samples in the aqueous and gaseous phase is also described. The main results obtained shows that, after 359 days of leaching, no 14C activity was detected above the detection limits, and only leaching rates regarding beta-gamma emitters were observed: 2×10–6 cm/day for 137Cs and 1×10–5 cm/day for 60Co in granite/bentonite water media and 4×10–6 cm/day for 137Cs in pure water.

Museum collections are extremely valuable sources of material for ongoing research, although the conservation history of some objects is not always recorded, which can be problematic for chemical analyses. While most contamination is removed using the acid-base-acid treatment, this may not be the case for cross-linked contamination. The XAD resin protocol was implemented at the radiocarbon (14C) laboratory in the Muséum national d’Histoire naturelle, and the setup was tested using known age bone samples and a consolidated Palaeolithic bone. Known age samples were consolidated with shellac or Paraloid, aged for a month, treated with or without the XAD resin and 14C dated. Bone blank results showed that XAD resin was able to remove shellac, which was not the case for the ABA-only method. Results from VIRI I were more variable and VIRI F was possibly too young to show the effects of the consolidants. Two 14C dates on the Palaeolithic bone after XAD treatment are statistically the same, while a sample without XAD treatment was significantly older, suggesting that the contaminant was not fully removed by the ABA-only treatment. This study demonstrates the potential of the XAD treatment to clean heritage bone samples stored in museums prior to geochemical analyses.

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.

This article discusses radiocarbon dating results of documents preserved at the Central Library of the University of Tehran (hereafter, CLUT) as part of the project “Irankoran.” The paper adds new evidence to an ongoing campaign of dating Qurʾāns and Oriental manuscripts by the Corpus Coranicum Project. The dated manuscripts include one kūfī fragment of the Qurʾān on parchment (no. 10950) and a selection of Islamic and Persian manuscripts, all from the second millennium: the Arabic dictionary Muǧmal al-Luġah (Meškāt no. 203), the medical encyclopedia Ḏaḫīrah-ye Kh w ārazmšāhī (no. 5156), the epic Panǧ Ganǧ of Neẓāmī (no. 5179), the book of wisdom Ādāb al-Falāsifah (no. 2165) attributed to Ḥunayn b. Isḥāq (d. 873 CE), and one of the oldest extant manuscripts of the Avesta Wīdēwdād (no. 11263). Although the authenticity of their colophons is disputed, radiocarbon dating supports the dates of the colophons; even in cases where they were suspected of being tampered with, they most likely present the accurate original dates of the corresponding manuscripts. Only in the case of Ādāb al-Falāsifah (no. 2165), radiocarbon dating of the parchment has identified the manuscript as non-authentic. Inconsistent carbon dating results of two samples taken from Ḏaḫīrah-ye Khwārazmšāhī (no. 5156) and Panǧ Ganǧ (no. 5179) provide evidence of later replaced/added leaves.

At the Ninth International Radiocarbon Conference a paper was presented concerning possible short-term 14C variations in 4000-year-old red deer antlers (Cervus elaphus) found in Neolithic flint mines in Norfolk, England (Burleigh and Hewson, 1980). It was argued, on archaeologic grounds, that the true age of the samples varied by a few years at most. Their radiocarbon ages, however, varied by a considerably greater amount than could be explained by the errors in the measurements. Duplication of the measurements confirmed this unexpected variation.

Farmer and Baxter (1972) claimed a significant correlation of atmospheric 14C levels in the northern hemisphere with sunspot number based on radiocarbon assay of single tree rings for the period 1829 to 1865. In contrast, Stuiver (1978) stated that a series of single-year Douglas Fir measurements did not show a statistically significant periodicity.

This paper reports measurements made on a series of single-year dendrochronologic samples of approximately the same age as the red deer antlers, which have been carried out at the British Museum Research Laboratory. The results show that the variation in 14C between rings is not statistically significant; some other explanation must be sought for the anomalous antler measurements.

This list includes results of measurements made during 1974-1978. When requested, MASCA corrected dates (Ralph et al, 1973) are reported.

The sources and fate of radiocarbon (14C) in the Dead Sea hypersaline solution are evaluated with 14C measurements in organic debris and primary aragonite collected from exposures of the Holocene Ze’elim Formation. The reservoir age (RA) is defined as the difference between the radiocarbon age of the aragonite at time of its precipitation (representing lakeʼs dissolved inorganic carbon [DIC]) and the age of contemporaneous organic debris (representing atmospheric radiocarbon). Evaluation of the data for the past 6000 yr from Dead Sea sediments reveal that the lakeʼs RA decreased from 2890 yr at 6 cal kyr BP to 2300 yr at present. The RA lies at ~2400 yr during the past 3000 yr, when the lake was characterized by continuous deposition of primary aragonite, which implies a continuous supply of freshwater-bicarbonate into the lake. This process reflects the overall stability of the hydrological-climate conditions in the lakeʼs watershed during the late Holocene where bicarbonate originated from dissolution of the surface cover in the watershed that was transported to the Dead Sea by the freshwater runoff. An excellent correlation (R2=0.98) exists between aragonite ages and contemporaneous organic debris, allowing the estimation of ages of various primary deposits where organic debris are not available.

The samples in this list were measured by the methane proportional counter method reported by Burke and Meinschein (1955). Shell samples were mechanically cleaned and washed with water. Where necessary, cold, very dilute HCI was used to remove the powdery exterior. Sedimentary wood and mud or clay samples were treated with hot concentrated HCI and washed with water before burning. Four other types of materials recovered from sediments were dated: (1) the total organic carbon, (2) benzene-soluble organic material, (3) foraminiferal tests, and (4) “dispersed carbonate”. The foraminiferal samples were recovered from the sediment by washing on a 120-mesh screen. These were then converted to carbon dioxide by acid treatment. “Dispersed carbonate” was recovered in the form of CO2, by acid (HCI) treatment of the sediment wash which had been depleted of Foraminifera. The total organic carbon samples were recovered by combustion to CO2 after all carbonates had been removed by acid treatment. Organic extractables were also converted to CO2 by combustion.

Each material needs to be characterized by estimating its activity, which creates a reference value for each material. This value then can be considered as the “known” activity of the material and future analyses can be compared to this to quantify the accuracy of the measurement. In this way, the materials remain useful for laboratory quality assurance.

Distributions of Δ14CTOC studied in bottom sediments collected during 2011–2016 in the Curonian Lagoon and in the open Baltic Sea indicated wide variations of Δ14CTOC values. Laboratory experiments on differential carbon utilization by Pseudomonas putida isolated from bottom sediments were carried out for better understanding of impacts of different sources on Δ14CTOC variations. Preferential glucose uptake (up to 80%) as a carbon source and a rather low (2–10%) inorganic carbon incorporation was found in media with diesel fuel. Pseudomonas putida a specific biomarker analyzed in biomass cultivated on the media with different carbon sources has been used to characterize microbial communities responsible for degradation of organic substances in bottom sediments. Large 14C depletions observed in sediments collected in the Gotland Deep of the Baltic Sea may indicate leakage from dumped chemical weapons.

Measurements have continued with the same proportional counter system, pretreatment procedure, methane preparation and measurement, and calculation, as described previously (R, 1970, v 12, p 298-318). Uncertainties quoted are single standard deviations originating from standard, sample, background counting rates and half-life. No 13C/12C ratios were measured.