For many of archaeology’s rarest and most enigmatic bone artifacts (e.g. human remains, bone ornaments, worked bone), the destruction of the 500 mg material necessary for direct accelerator mass spectrometry (AMS) dating on graphite targets would cause irreparable damage; therefore many have not been directly dated. The recently improved gas ion source of the MICADAS (MIni CArbon DAting System) offers a solution to this problem by measuring gaseous samples of 5–100 µg carbon at a level of precision not previously achieved with an AMS gas ion source. We present the results of the first comparison between “routine” graphite dates of ca. 1000 µg C (2–3 mg bone collagen) and dates from aliquots of gaseous samples of <100 µg C (<0.2 mg bone collagen), undertaken with the highest possible precision in mind. The experiment demonstrates the performance of the AixMICADAS in achieving reliable radiocarbon measurements from <0.2 mg collagen samples back to 40,000 14C BP. The technique has great implications for resolving chronological questions for key archaeological artifacts.

Samples of >40 pine trees were collected from around the Chernobyl NPP for radiocarbon measurement, to determine the spatial distribution of excessive 14C in tree rings from 1986 consequent upon accidental radiocarbon release. Tree samples were collected during 1995–1996 from sites situated at distances >2.5 km from the NPP and covering a variety of directions in relation to the NPP. To evaluate δ14C for 1986 annual rings, we compared 14C levels for separate 1985–1987 annual rings, taking into account the trend of operational releases. Early and late wood samples for 1986 annual tree rings were measured separately to increase the sensitivity and precision of measurements. The maximum value observed for excessive accidental radiocarbon levels (δ14C) was found to be 124 pMC (281.6 Bq kg-1 C). We present δ14C values for examined sites; their spatial distribution shows a high irregularity of atmospheric 14C depending on direction from the NPP. Using obtained data, we reconstruct the temporal behavior of 14C release during the Chernobyl accident with the aid of atmospheric transport modeling. The total amount of 14C released from 26 April to 5 May 1986 has been estimated as 44 TBq.

The shell carbonate of pre- and post-bomb samples of 2 species of terrestrial gastropods (Theba pisana and Cernuella virgata) sampled along the coast of Apulia, southern Italy, were dated using accelerator mass spectrometry and carbon stable isotopes were analyzed. The analyses show, for both species, significant anomalies in the radiocarbon age due to the possible presence of a 14C-depleted source of carbon in the formation of the shell aragonite. The magnitude of the age anomaly was quantified in the studied area to ∼1000 14C yr.

Aquatic macrophytes from a lacustrine environment are highly prone to a reservoir effect, resulting in an overestimation of age. This is often caused by the incorporation of dissolved carbon (CO2 and HCO3–) through photosynthesis from lake waters that have a different 14C activity than the atmosphere. The atmosphere-water disparity is often produced by a mixing of carbon between the water body and its terrestrial surroundings, a process highly prone to temporal variations. Thus, only a comprehensive understanding of the 14C budget over time enables a reliable chronology of lacustrine records. We studied lacustrine sediments from Lake Heihai on the northern Tibetan Plateau with a recent reservoir effect of 6465 ± 75 14C yr as estimated from accelerator mass spectrometry (AMS) dating of three living aquatic plants. Age inversions in a well-laminated composite core from the lake suggest that the reservoir effect markedly changed over the depositional period. In the lower part of the core, an excellent correlation was observed between the allochthonous input of dolomite and the inverse 14C ages, indicating the incorporation of dissolved 14C-dead carbon from a limestone catchment in the plant material. For the upper part of the core, sediment recycling of Holocene high-stand deposits may have further contributed to the reservoir effect. These findings give rise to a reliable process- and provenance-based chronology within a confidence interval supported by 137Cs measurements and magnetostratigraphic investigations. Our results highlight the need to identify the interactions of lakes with their surroundings to estimate reservoir-corrected ages in lacustrine settings.

14C and 13C enrichment values are reported for a series of surface soil profiles which represent the progressive transition from mor to mull humus induced by birch (Betula pendula) colonization.

Variations in Δ and δ13C, which range between 85 to 154‰ modern and −28.1 to −25.3‰ (PDB), respectively, reflect changes in the rate and mode of organic decomposition. The most marked alterations in soil character occur over the first few decades following the introduction of birch, with clear isotopic evidence for the deeper penetration and accelerated mineralization of organic material.

To obtain a better understanding of the relationship between calcrete genesis and the results of different absolute dating methods, thermoluminescence (TL), radiocarbon (14C) and uranium/thorium (U/Th) were applied to coeval sample; take from a very young calcrete profile in Namibia. The methodically different ages reflect the characteristics of the applied dating methods, the genetics of calcrete and different events of calcrete genesis. The conventional 14C ages and the TL dates cover the last 50 ka, while the corresponding U/Th dates of coeval samples are many times larger, Uranium-series dates are not related to the deposition of the host material or to its cementation if the ages are smaller than ca. 120 ka. The TL clock is set to zero during eolian transport and the corresponding radiometric ages of the quartz and feldspar grains date the time of their deposition. The 14C ages of the cement correspond, on the other hand, to a time shortly after the onset of the cementation and long before its termination. In the case of very old calcrete, the mixture of young and old cement results in ambiguous ages if they cannot be confirmed by an independent technique.

This paper outlines the radiocarbon program applied to the excavation and skeletal assemblage from the cemetery of the medieval Priory and Hospital of St. Mary Spital in London. Problems encountered in dating medieval cemeteries are outlined. The problems were addressed through the application of Bayesian modeling to validate and refine conventional approaches to constructing phases of archaeological activity. It should be noted that this project was solely funded by the developer of the land; such projects rarely undertake even modest programs of 14C dating. We aim to show how the investment of a proportionally small sum, compared to the overall project costs, may reap significant benefits.

The accompanying date list includes age determinations completed during the period December 1, 1961 to November 1, 1962. All measurements were made with the 2 L counter described in our first date list (GSC I). Sample preparation, counting procedures, and calculation of dates were as described in GSC I except as outlined below:

1. a. Base and acid treatments were carried out with 1N HCl and 2% NaOH instead of 2N HCl and 4% NaOH, because the less-concentrated solutions were still strong enough to accomplish the desired purification.

2. b. The Mg(C104)2 drying columns were removed from the purification train in order to test their effect, if any, on the purity of the gas. Since there was no detectable change in the purity of the gas these columns were left out of the purification line.

3. c. Ages were calculated using 0.950 of the activity of the N.B.S. oxalic-acid standard as the reference activity and a.d. 1950 as the zero reference year, in line with the recommendations of the editors of Radiocarbon.

Shahack-Gross and Finkelstein (2015) further developed their theory, based on microarchaeology, that there was no agriculture in the Negev Highlands during the Iron Age. We critically evaluate their article in this rejoinder and propose that their conclusion is an example of overinterpretation from a small amount of indirect data. Based on phytoliths in two courtyards and a few rooms, i.e. structures not related to farming, they construed the absence of agriculture during the Iron Age in an area of 2000 km2. We present new radiocarbon, macroarchaeological, and microarchaeological data of Horvat Haluqim, showing that agriculture in the Negev Highlands based on runoff/floodwater capture and related terrace wall construction did not begin with the Roman–Byzantine period. Terrace agriculture in the Negev is older and includes also the Iron Age.

Mollusk shells provide brief (<5 yr per shell) records of past marine conditions, including marine radiocarbon reservoir age (R) and upwelling. We report 21 14C ages and R calculations on small (∼2 mg) samples from 2 Mesodesma donacium (surf clam) shells. These shells were excavated from a semi-subterranean house floor stratum 14C dated to 7625 ± 35 BP at site QJ-280, Quebrada Jaguay, southern Peru. The ranges in marine 14C ages (and thus R) from the 2 shells are 530 and 170 14C yr; R from individual aragonite samples spans 130 ± 60 to 730 ± 170 14C yr. This intrashell 14C variability suggests that 14C dating of small (time-slice much less than 1 yr) marine samples from a variable-R (i.e. variable-upwelling) environment may introduce centuries of chronometric uncertainty.

The aim of this paper is to evaluate the compatibility between the Holocene relative sea-level (RSL) curves proposed for the Brazilian littoral and mangrove dynamics along a fluvial valley in the state of southern Bahia. This was done integrating geomorphological, sedimentological, palynological, and stable isotopic data from two cores collected at the mouth of the Jucuruçu River and at a site 23 km inland, near the city of Prado, northeastern Brazil. Core PR07, sampled from a fluvial plain at about 4.5±1 m above the RSL, reveals mangrove pollen (5–20%) and estuarine/terrestrial organic matter (δ13C=~–25‰, C/N=7.3–67) between 4.5 m (~7400 cal yr BP) and 1.75 m depth (~5350 cal yr BP). Core PR11, sampled from a mangrove tidal flat, also revealed mangrove pollen taxa (5-28%) since 660 cal yr BP. Core PR07 indicated absence of mangrove pollen and increase of sedimentary organic matter sourced from terrestrial C3 plants (δ13C=~–27‰, C/N=22–159) during the last 5350 cal yr BP. Probably, the changes in vegetation and sedimentary organic matter identified in core PR07 were caused by the combined effects of the RSL fluctuations, with a highstand at about 5350 cal yr BP of 2.7±1.35 m, and changes in fluvial discharge.

Lynch's Crater in northeastern Australia provides a long, continuous record of environmental change within the Late Quaternary. Here, we present newly determined radiocarbon ages, using acid-base-acid stepped combustion (ABA-SC) and acid-base-wet oxidation stepped combustion (ABOX-SC) pretreatment strategies. The new results largely confirm the original untreated radiocarbon results for the uppermost 9 m of sediments, (ca. 35 ka BP). Below this depth, results from both pretreatment methods are in stratigraphic agreement and extend the dating of the record from 38 ka BP to about 48 ka BP, although an apparent increased sedimentation rate below 12 m is questionable. The scarcity of “charcoal” in several of the samples raises questions regarding the application of ABOX-SC to lake or swamp sediments, with evidence for contributions from younger, chemically resistant bacterial carbon along with fine “charcoal” in some samples. However, the extent to which this phenomenon is significant to the final age estimate appears to be sample specific, and is probably dependent upon the length of the wet oxidation step in the pretreatment.

In order to evaluate the variability in surface water masses in the Western Pacific Warm Pool, we report high-precision radiocarbon measurements in annual and seasonal bands from Pontes lutea corals collected from the Palau Archipelago (7°N, 134°E). Annual coral bands from 1945 to 2008 and seasonal samples from 1953 to 1957 were analyzed to capture the initial early input of bomb 14C from surface thermonuclear weapons testing in the Marshall Islands. Results show a pre-bomb average δ14C value of-54.9% between 1945 and early 1953. Beginning early in 1954, there is a rapid increase to a maximum of-23.1% at the start of 1955. Values continued to rise after 1957 to a post-bomb peak of 141% by 1976. The large initial rise in δ14C cannot be accounted for by air-sea CO2 exchange. Results therefore suggest that the primary cause of this increase is the lateral advection of fallout-contaminated water from the Marshall Islands to Palau via the North Equatorial Current and then to the North Equatorial Countercurrent.

I have developed a method of dating early medieval Irish buildings using charcoal encased in mortar. Due to the inclement weather over centuries, timbers do not preserve well in these structures, leaving little suitable material for 14C dating. Initially, several buildings of known age were analyzed to verify the mortar charcoal technique. Then, a series of buildings for which no definite architectural-historical dates existed, e.g., churches, houses, oratories and round towers, was successfully tested. I discuss here the results of this dating approach, and provide architectural historians with a firmer understanding of the origin and antiquity of early Irish buildings.

Selected stable carbon isotope measurements published in Radiocarbon over a 12-year period have been abstracted, plotted, and summarized, to give more reliable estimates of the mean value and range of δ13C for five classes of natural material (human bone collagen, non-human animal bone collagen, plant materials, wood, and charcoal), and to provide a firmer base line for stable carbon isotope dietary and environmental studies.

The following is a list of C14 dates obtained since the preparation of the manuscript for publication of Michigan Radiocarbon Dates VI in December 1960. The method of measurement and treatment of data are the same as described in the introduction to Michigan lists III and IV. Since the time of publication of list VI, a full description of the counting technique and equipment has been published (Crane, 1961a, b).

Precision of AMS single-target measurements is usually based on counting statistics and variance during the data acquisition cycle. Additional longer-term variability may be studied by looking at the variability of the standards from cycle to cycle.

The radiocarbon (14C) calibration curve so far contains annually resolved data only for a short period of time. With accelerator mass spectrometry (AMS) matching the precision of decay counting, it is now possible to efficiently produce large datasets of annual resolution for calibration purposes using small amounts of wood. The radiocarbon intercomparison on single-year tree-ring samples presented here is the first to investigate specifically possible offsets between AMS laboratories at high precision. The results show that AMS laboratories are capable of measuring samples of Holocene age with an accuracy and precision that is comparable or even goes beyond what is possible with decay counting, even though they require a thousand times less wood. It also shows that not all AMS laboratories always produce results that are consistent with their stated uncertainties. The long-term benefits of studies of this kind are more accurate radiocarbon measurements with, in the future, better quantified uncertainties.

During 1962 the La Jolla Radiocarbon Laboratory continued to follow essentially the same technique as in previous years. Three counters were used:

1. 1. The “Bern Counter,” an Oeschger-Houtermans instrument manufactured at the Physical Institute of the University of Bern; described in La Jolla I (p. 197).

2. 2. The “Brussels Counter,” another Oeschger-Houtermans instrument, manufactured in Brussels by Manufacture Belge de Campes et de Matériel Électronique, S. A.; characterized in La Jolla II (p. 204).

3. 3. The “400-cc La Jolla Counter,” recently constructed at the University of California, San Diego to facilitate the age determination of samples containing less than 1 g of carbon. Because the first model, now in use, was constructed of brass—not the optimal material—the background count is relatively high (ca. 5.0 counts/min). Advantages lie in its high stability. For samples that yield 0.5 L or more of acetylene, this counter can be used quite satisfactorily. Check runs, using the same sample in this counter and in the Bern and Brussels counters, agree closely.

An international review of liquid scintillation low-level counting procedures and instrumentation made it possible to assess in detail those elements which lead to high-precision liquid scintillation radiocarbon dating with a Figure of Merit of 32,000. Current research is documented and future possibilities are alluded to.