We have developed a technique using a single apparatus to recover the inorganic and organic carbon from a small (few milligrams) aliquot of dried marine material for radiocarbon analysis. The main advantages of using a single apparatus are: 1) less sample is required, 2) decreased handling reduces contamination, and 3) less time and materials are used. Blank values of ∼5 μg and 19–44 μg are obtained for the inorganic and organic carbon extractions, respectively. δ14C results from sinking particulate organic and inorganic carbon are presented for samples collected in deep-sea sediment traps deployed for 10–30 day periods at 650 and 100 m above bottom (mab) in the northeast Pacific Ocean.

The Committee on Missing Persons in Cyprus (CMP) is a bicommunal committee with the mandate to locate and identify the skeletal remains of 2002 persons who were reported missing during the inter-communal fighting of 1963–64, as well as the events of July and August 1974. During the periods of conflict, several archaeological sites and old cemeteries were used as primary burial sites, among several other types of burials, as they were easily accessed by the persons involved in the interment and little effort was needed to conceal the bodies. The relatively large post-mortem interval and the generally poor post-mortem preservation of the skeletal remains poses an additional challenge in the forensic examination process and the identification of the remains, particularly in the absence of a context or other associated artifacts/evidence. Between 2016 and 2020, the CMP has been collaborating with CEDAD to clarify the relevancy of several cases by using radiocarbon dating. The CMP submitted 139 cases to CEDAD out of which 112 were determined as not linked to the 1963–64 and 1974 events and then not relevant for the CMP project. For the remaining samples radiocarbon dating was used to determine death age.

We present the results of a multifaceted study of an antiphonary—liturgical song book—presumably made in Venice in 1607, now in the Ringve, National Music Museum of Norway in Trondheim1. The book is hand-sewn on raised cords, bound in full leather on cardboard covers, originally with metal clamps. The paper block consists of pages printed in black and red that include both song texts and music scores. The red ink is based on vermillion and red lead while the black ink is carbon based. The treads and cords were made of flax. The leather used was made from goat skin. Radiocarbon results confirmed the printing date. The antiphonary shows several signs of repair including the possibility of re-binding. Animal-based glue was used for the repairs as well as for the sizing of both original and repair paper. Two potential periods were identified for reparations, 1670–1710 AD and 1782–1830 AD. This case study was conducted prior to the opening of a new permanent exhibition, Soundtracks, at the Ringve Museum where the book is displayed.

The 14C age of charcoal and wood from Lebanon and central Europe is compared partly with the dendrochronologically determined age of the samples and partly with the archaeologically expected value. While the dendrologic values approximately confirm the correction curve of Ralph, Michael, and Han (1973), charcoal of burned layers seemes to be generally 2 to 3 centuries older than expected from contemporary archaeologically retrieved materials.

When used with 14C records, an accurate reconstruction of the 13C/12C changes of atmospheric CO2 may be a key constraint to determining the historic activity of the biosphere as CO2 source or sink. We recently detailed the derivation of an atmospheric δ13C record for 1930–1979 from Arizona juniper tree rings (Leavitt and Long, 1983). Each tree was close to a weather station, allowing us to account for the effects of climate on the tree-ring δ13C records. The resulting atmospheric δ13C trend shows an overall decrease of ca 1.3‰, but instead of decreasing exponentially over the whole 50-year period, the best-fit curve decreases exponentially to ca 1960 and then flattens out. The drop from 1956 to 1978 was ca 0.55‰, still very similar to the measured atmospheric drop over that period of 0.65 ± 0.13‰ (Keeling, Mook, and Tans, 1979).

Corrections are made to Stuart Fiedel’s (2022) recent errors and misrepresentations related to the late Pleistocene sites of Monte Verde and Huaca Prieta and to South American Fishtail projectile points.

Natural C14 measurements have been performed at the Dept. of Physics, National Taiwan University since 1965, using a cylindrical proportional counter of 1000 ml (Hsu et al., 1965). The proportional counter is operated with CO2 as the filling gas at a pressure of 1216 mm Hg at room temperature of 20°C. Working voltage is 4.7 Kv, with a plateau length of more than 700 v and a plateau slope of ca. 1% per 100 v. Background is reduced to 5.1 counts/min and the counting rate of the NBS oxalic acid standard is 9.4 counts/min at the normal counting pressure of 1216 mm Hg.

By constraining organic carbon (OC) turnover times and ages, radiocarbon (14C) analysis has become a crucial tool to study the global carbon cycle. However, commonly used “bulk” measurements yield average turnover times, masking age variability within complex OC mixtures. One method to unravel intra-sample age distributions is ramped oxidation, in which OC is oxidized with the aid of oxygen at increasing temperatures. The resulting CO2 is collected over prescribed temperature ranges (thermal fractions) and analyzed for 14C content by accelerator mass spectrometry (AMS). However, all ramped oxidation instruments developed to date are operated in an “offline” configuration and require several manual preparation steps, hindering sample throughput and reproducibility. Here we describe a compact, online ramped oxidation (ORO) setup, where CO2 fractions are directly collected and transferred for 14C content measurement using an AMS equipped with a gas ion source. Our setup comprises two modules: (i) an ORO unit containing two sequential furnaces, the first of which holds the sample and is ramped from room temperature to ∼900°C, the second of which is maintained at 900°C and holds catalysts (copper oxide and silver) to ensure complete oxidation of evolved products to CO2; and (ii) a dual-trap interface (DTI) collection unit containing two parallel molecular sieve traps, which alternately collect CO2 from a given fraction and handle its direct injection into the AMS. Initial results for well-characterized samples indicate that 14C content uncertainties and blank background values are like those obtained during routine gas measurements at ETH, demonstrating the utility of the ORO-DTI setup.

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.

Eight atmospheric carbon dioxide samples (as calcium carbonate—CaCO3—precipitates) from Lindesnes site (58ºN, 7ºE), belonging to 1963 and 1980 (four samples from each year) and stored at the National Laboratory for Age Determination (NTNU), have been reevaluated through radiocarbon (14C) analysis. Previous 14C results indicated the presence of a contaminant, which was not removed through different chemical cleansing procedures (e.g., hydrochloric acid—HCl and/or hydrogen peroxide—H2O2). Here, we present a follow up investigation using 14C step-combustion and Fourier-transform infrared spectroscopy (FTIR) analysis. Results from 14C data indicate unsuccessful removal of the contaminant, while further FTIR analysis displayed the presence of moisture. This finding alludes to the possibility that the contaminant is of ambient air-CO2 deeply embedded in CaCO3 powders (within clogged CaCO3 pores and/or bonded to the lattice). Samples were found exposed to air-CO2 and humidity. These conditions may have lasted for years, possibly even decades, leading to the 14C offsets detected here.

Although paleomagnetic secular variations (PSV) often corroborate radiocarbon (14C)-based lacustrine sediment chronologies, this is not the case at the high-altitude site Khar Nuur in the Mongolian Altai Mountains. Our results show that the inclination pattern resembles those from a regional reference record from Shireet Naiman Nuur and global geomagnetic field models very well, but with a constant offset of 730 ± 90 yr. Possible reservoir effects from terrestrial pre-aging and hardwater effects can be excluded as the cause of the ∼730-yr offset because the different dated compounds correspond very well to each other, and modern reservoir effects are negligible. Instead, the constant ∼730-yr offset in the PSV pattern is likely the result of a constant lock-in depth of 26 ± 2 cm below the sediment-water interface at Khar Nuur. This assumption is supported by comparison of paleoclimatological proxies from Shireet Naiman Nuur, where similarities are obvious for the 14C-based chronology of Khar Nuur without a ∼730-yr adjustment. Therefore, the previously published 14C-based chronology of Khar Nuur provides a reliable age control. Accepting the lock-in depth of 26 ± 2 cm, the good consistency in inclination between Khar Nuur and global geomagnetic field models highlights the reliability of the latter even in a paleomagnetically understudied area.

About ten radiocarbon laboratories operate in Japan and have dated more than 25,000 samples since 1960. Geomorphic development and human activities since the last glaciation have been documented with radiocarbon determinations. In order to apply these dates more effectively, the author finds it necessary to create and maintain a radiocarbon database system, which he has been doing since 1985, using a personal computer system linked to a telephone line. A researcher may access, search and retrieve data from the Radiocarbon Database System of Japan.

This list reports measurements made on archaeologic samples by our laboratory from September 1980 to May 1982. Results of measurements made during that period which lack review by submitters will be reported in a subsequent date list. Dates were obtained by liquid scintillation counting of benzene using the laboratory procedure outlined previously (R, 1982, v 24, p 344–351). All dates are expressed in 14C years relative to ad 1950 based on the Libby half-life for 14C of 5568 yr. The laboratory standard continues to be ANU sucrose. Data analysis is now performed with the aid of an RT-11 microcomputer interfaced with our Packard model 3255 LS counter. Dates have been corrected for isotopic fractionation only when the δ13C value is given. No corrections have been made for natural 14C variations. The following descriptions of samples are based on information provided by the submitters.

C14 measurements of archaeologic and geochemical samples using sample synthesized benzene in a Beckman LS-100 liquid scintillation spectrometer are reported. Rather high background counting rates of ca. 8 to 9 cpm and counting efficiency of ca. 45 to 48% for 4 cc counting vial of potassium free glass are observed. The counting vial (total volume of 10 cc) is supported by an aluminum bar for geometry control. Background and standard counting rates measured during the past 17 months are listed in Tables 1 and 2, respectively. Slight seasonal variations were observed.

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.