We model the exchange of carbon between the different reservoirs (atmosphere, ocean mixed layer, deep ocean and biosphere). The influence of the biosphere is investigated using two extreme assumptions: 1) no net biospheric effect and 2) biospheric uptake of CO2 proportional to the atmospheric content of CO2 and time-dependent deforestation. Observations of atmospheric CO2 at Mauna Loa and the South Pole may be fit by both these assumptions.

Food production is one of the most significant achievements in Andean history. The domestication of plants and animals presented an enormous challenge, relating to changing technologies, settlement patterns, and social organization. This paper aims to assess Atacama Desert population dynamics and their relationship to the domestication of plants and animals through chronological modeling using kernel density estimation on radiocarbon (14C) dates, assuming that a higher 14C probability density is related to more intense human occupation. The analysis is based on a 14C dataset comprising 1003 14C dates (between 11,000 and 150 BP) from 243 archaeological sites in the Arica and Tarapacá regions of northern Chile, collected from published data. We observed two population-dynamics inflection points for these regions. First, starting at ca. 3000 BP, constant population growth occurred, which was related to horticulture in the Arica region and to agriculture in the Tarapacá region. Second, between ca. 1000 and 400 BP, a general population rise occurred due to the consolidation of intensive agriculture in the lowlands and precordillera altitudinal belts in both regions and the integration of the coast and the altiplano into macro-regional population dynamics.

Results of the International Collaborative Study show an unexpectedly large scatter of individual dates as well as systematic biases. Very high values of linear correlation coefficients are observed for all results of Stage 2 and for benzene samples of Stage 1. We observed moderate correlations for carbonate samples and the lowest for natural samples of wood and peat of Stage 3. The correlation is practically negligible among results obtained in different stages. The probable reasons for such effects are seen in medium-term changes in the calibration of the counting systems.

The following radiocarbon dates are a partial list of samples measured since Sept 1977. The chemical and counting procedures are the same as indicated previously (R, 1978, v 20, p 134-138).

It has long been assumed that radiocarbon (Δ14C) content of dissolved inorganic carbon (DIC) is equal to that of particulate organic carbon (POC) in surface seawater; however, little research has been conducted to explicitly test this assumption. Here, we report Δ14C measurements of surface POC samples and compare them with contemporaneous DIC Δ14C measurements from the northeast Pacific Ocean (Hwang et al. 2004; Druffel et al. 2010). Samples were collected from surface waters at Station M off California between 1995 and 2004. The POC Δ14C values decreased 3.2% per year from 1995 to 2004, similar to the decline observed in the DIC Δ14C values during the same period. Overall, our results show no statistical difference between POC and DIC Δ14C—consistent with the assumption that DIC and POC Δ14C values can generally be considered equivalent. However, significant variability was observed for POC Δ14C values during several fall/summer events, where POC Δ14C signatures were lower than DIC Δ14C values. An evaluation of 2 sample pretreatments also suggests that non-homogenized POC samples deviated less from average POC Δ14C values and more closely matched the DIC Δ14C average for the time series. The presence of seasonal POC/DIC Δ14C disagreements, combined with sample processing effects, suggest that infrequent contributions of allochthonous, older carbon may have originated from deeper in the water column, especially during periods when upwelling in this area was prominent.

Skin-based samples (leather, skin, and parchment) in archaeological, historic and museum settings are among the most challenging materials to radiocarbon (14C) date in terms of removing exogenous carbon sources—comparable to bone collagen in many respects but with much less empirical study to guide pretreatment approaches. In the case of leather, the 14C content of materials used in manufacturing the leather can vary greatly. The presence of leather manufacturing chemicals before pretreatment and their absence afterward is difficult to demonstrate, and the accuracy of dates depends upon isolating the original animal proteins and removing exogenous carbon. Parchments differ in production technique from leather but include similar unknowns. It is not clear that lessons learned in the treatment of one are always salient for treating the other. We measured the 14C content of variously pretreated leather, parchment, skin samples, and extracts, producing apparent ages that varied by hundreds or occasionally thousands of years depending upon sample pretreatment. Fourier Transform Infrared Spectroscopy (FTIR) and C:N ratios provided insight into the chemical composition of carbon reservoirs contributing to age differences. The results of these analyses demonstrated that XAD column chromatography resulted in the most accurate 14C dates for leather and samples of unknown tannage, and FTIR allowed for the detection of contamination that might have otherwise been overlooked.

To test the hypothesis that cellulose in linen can be carboxylated at high temperatures in the presence of CO2, water and silver, we heated two aliquots of cellulose extracted from old wood in glass ampoules, adding Ag powder to one to test its potential action as a catalyst for the carboxylation reaction. AMS measurement of the heated aliquots showed no statistically significant difference in 14C content from the “uncarboxylated” cellulose. We conclude that carboxylation is not a systematic source of error in the dating of cellulose-containing materials such as the linen in the Shroud of Turin.

A fully automatic continuous-flow gas injection interface was built to couple an elemental analyzer with a MICADAS accelerator mass spectrometer (AMS) as a low-cost option that does not require an absorber trap for CO2 injection. The complication of the variable ion current during gas injection can be overcome by understanding and controlling the mass flow-dependent ionization yield. The time-varying CO2 concentrations and carbon mass flows are estimated with a mathematical model in order to investigate their relationship with the abundant isotope (12C–) signal. This model is based on a complete CO2 diffusion equation and instantaneous mass flow. It shows a good agreement between model calculations and the measurements. A reversible suppression of the formation of ions occurs, if the carbon mass flow exceeds 2.0–2.3 µg C/min. This result repeats for different injection capillaries and for different carrier volumetric flow rates.

Given below are the dates of archaeologic and Quaternary samples measured by the proportional counting of methane gas. Details of the techniques used were published earlier (Agrawal et al., 1965).

Radiocarbon (14C) dating is often carried out upon multi-specimen samples sourced from bioturbated sediment archives, such as deep-sea sediment. These samples are inherently heterogeneous in age, but existing 14C calibration techniques were originally developed for age homogeneous material, such as archaeological artifacts or individual tree rings. A lack of information about age heterogeneity leads to a systematic underestimation of a sample’s true age range, as well as the possible generation of significant age-depth artifacts during periods of the Earth’s history coinciding with highly dynamic atmospheric Δ14C. Here, a new calibration protocol is described that allows for the application of sedimentological priors describing sediment accumulation rate, bioturbation depth and temporally dynamic species abundance. This Bayesian approach produces a credible calibrated age distribution associated with a particular laboratory 14C determination and its associated sedimentological priors, resulting in an improved calibration, especially in the case of low sediment accumulation rates typical of deep-sea sediment. A time-optimized computer script (biocal) for the new calibration protocol is also presented, thus allowing for rapid and automated application of the new calibration protocol. This new calibration protocol could be applied within existing age-depth modeling software packages to produce more accurate geochronologies for bioturbated sediment archives.

Triliths are megalithic monuments scattered across the coastal plains of southern and southeastern Arabia. They consist of aligned standing stones with a parallel row of large hearths and form a space, the meaning of which is undoubtedly significant but nonetheless still unknown. This paper presents a new radiocarbon (14C) dataset acquired during the two field seasons 2018–2019 of the TSMO (Trilith Stone Monuments of Oman) project which investigated the spatial and temporal patterns of the triliths. The excavation and sampling of trilith hearths across Oman yielded a dataset of 30 new 14C dates, extending the use of trilith monuments to as early as the Iron Age III period (600–300 BC). The earlier dates are linked to two-phase trilith sites in south-central Oman. The three 14C pairs collected from the two-phase trilith sites indicated gaps between the trilith construction phases from 35 to 475 years (2 σ). The preliminary spatio-temporal analysis shows the geographical expansion of populations using trilith monuments during the 5th to 1st century BC and a later pull back in the 1st and 2nd century AD. The new 14C dataset for trilith sites will help towards a better understanding of Iron Age communities in southeastern Arabia.

The release and the speciation of carbon species from irradiated JRQ carbon steel samples, representative of the reactor pressure vessel of Belgian nuclear power plants, were studied in a saturated portlandite aqueous solution, relevant for the Belgian Supercontainer design, as perceived for the geological disposal of high-level nuclear waste. To achieve this, we performed simple immersion and potentiostatic corrosion tests. In addition, the corrosion rate (which determines the 14C release) was estimated by measuring the release of 60Co. Gas chromatography showed that during the static corrosion test, the carbonaceous species methane, carbon dioxide, ethene, and ethane were produced. Under the hypothesis that all the carbon released from the JRQ steel was transformed into carbon-base gaseous compounds, this corresponds to a corrosion rate of approximately 100 nm/yr, which is in good agreement with literature data.

There are two units with RBMK-1500 type reactors at the Ignalina Nuclear Power Plant (Ignalina NPP) in Lithuania where graphite was used as a neutron moderator and reflector. These reactors are now being decommissioned, and Lithuania has to find a solution for safe irradiated graphite disposal. It cannot be disposed of in a near surface repository due to large amounts of 14C (radiocarbon, carbon-14); thus, a deep geological repository (DGR) is analyzed as an option. This study had the aim to evaluate 14C migration from the RBMK-1500 irradiated graphite disposed of in a potential DGR in crystalline rocks taking into account the outcomes of the research performed under the collaborative European project CAST (CArbon-14 Source Term) and to identify the potential to reduce the conservatism in the assumptions that was introduced in the lack of data and led in the overestimated 14C migration. The information gathered during the CAST project was used to model 14C transport in the near field by the water pathway and to perform uncertainty analysis. The study demonstrated that more realistic assumptions could reduce the estimated 14C flux from the near field by approximately one order of magnitude in comparison with the previous estimations based on very conservative assumptions.

This list reports a portion of the analysis completed on archaeologic and paleo-environmental samples measured in the UCR laboratory between August 1974 and August 1976. Results of measurements made during that period on sample suites which are not as yet completed or lack review by submitters will be reported in a subsequent date list.

The study of human remains can provide valuable information about aspects of past populations. Here we present an updated database consisting of 590 radiocarbon (14C) dates for human remains from Holocene South Africa before European contact. We calibrated or recalibrated all the previously published dates using the most recent calibration curve for the southern hemisphere. Each date is roughly georeferenced and plotted according to their Stone Age or Iron Age contexts, revealing the broad distribution pattern of dated Holocene human remains across South Africa—perhaps reflecting aspects of past population distribution and densities, but also underscoring historical collection practices, archaeological research focus, and preservation conditions. We use Kernel Density Estimation models to show peaks and troughs of dated remains through time, with Later Stone Age peaks at ∼5.5 ka cal BP, ∼2 ka cal BP and ∼0.5 ka cal BP, and Iron Age peaks ∼1.1 ka cal BP and ∼0.5 ka cal BP, some of which show broad correspondence to climatic data. Our data, based on dated remains only, do not provide a full reflection of past populations, and our large-scale, coarse-grained analysis cannot yet assess the reasons for the peaks in dated human remains in detail. Yet, the study provides a new resource, and a data-driven overview that highlights aspects to be explored with further contextual analyses against the available archaeological records, population histories and climatic indicators through time and across space.

Edward Smith Deevey, Jr died on November 29, 1988, following a heart attack. He was Graduate Research Curator of Paleoecology at the Florida Museum of Natural History, University of Florida, Gainesville. As a reflection of his expertise in many academic disciplines, Ed held Graduate Research Professorships in four University of Florida departments: zoology, botany, geology and Latin American studies.

The 14C dates given below are continued from our previous list (R, 1972, v 14, p 223–238), and results obtained mainly during 1971–2 are described. A 2.7L stainless steel counter and a 3.3L copper counter are used as previously, yielding background counting rates of 6.9 and 6.0 cpm, respectively, when filled with dead CO2 at ca 1.8 atm. Dates have been calculated on the basis of the 14C half-life of 5568 yr and 95% of NBS oxalic acid is modern standard. No correction has been made for any of the samples in this list.

This list contains the results of 14C determinations obtained at the laboratory in 1984. Our laboratory measures 14C activity in the form of methane with a proportional counter built by Heidelberg University and an electronic unit built by Berthold, Benelux Analytical Instruments. The sample counting time is 4000 minutes with printouts at 100 minute intervals. Sample error is reported as one standard deviation. δ13C for mortar is measured by the University of Lyon Laboratory, δ13C was not measured or estimated for other samples.

It has been shown that contamination from humic acids, chitin, fungal products, etc., contributing young carbon, and from bitumen and carbonate, contributing old carbon, may not be completely removed from wood and char samples by the usual hydrochloric acid and sodium hydroxide pretreatments of the samples. A procedure is offered for the isolation of a pure chemical substance from such samples, cellulose from wood and uncombined carbon from char, that must represent the original material. Cellulose is prepared by boiling the resin-free sample in 1.25% H2SO4 and 1.25% NaOH, adding Schweitzer's reagent, filtering, and precipitating from the filtrate by acidification. Uncombined carbon is separated from char samples as the flocculant precipitate remaining after boiling in 70% HNO3, followed by settling overnight from a large volume of 6M HNO3. A simple procedure for the chemical examination of char samples is also offered for the estimation of the amounts of bitumen, carbonate, combined, and uncombined carbon in char.