Radiocarbon dating by accelerator mass spectrometry (AMS) of the shell bar section of Qaidam Basin, NE Tibetan Plateau, shows that this section was formed between ~39.7 and ~17.5 14C kyr BP and represented the highest paleolake development period since the Late Pleistocene. It was difficult to obtain reliable dates due to the low organic carbon content, which was formed mainly by authochtonous algae-bacteria (Zhang et al. 2007a). In order to improve the dating, 14C ages of both the alkali residual and acid-soluble components of the organic carbon were measured to check the consistency of the dating results. Total organic carbon (TOC) content and stable carbon isotopes (δ13Corg) might also be used as critical references for checking the reliability of dates. For example, in our study of the shell bar section from Qaidam Basin, we found that when the TOC content was higher than 0.15% and/or δ13Corg was lower than −23, the AMS dates were reliable. AMS dating of fossil shells demonstrated that they could provide valuable age information. The ages given by fossil shells are comparable to those of bulk carbonate from a similar sampling site, and are about 15~18 kyr older than the ages given by organic matter. Due to the U/Th dating requirements and open nature of the system, we concluded that U/Th dating results are unreliable and that this technique is unsuitable for dating halite deposits from Qaidam Basin.

The performance of the CO2-accepting SO-110 ion source at Oxford Radiocarbon Accelerator Unit has been investigated in detail. The purpose was to clarify the possibilities of accelerator mass spectrometry (AMS) radiocarbon measurements with real-time separation, e.g. GC AMS or HPLC AMS. The construction of a gas test injector based on the continuous-flow technique made it possible to characterize the response of the ion source to continuous and pulsed input of CO2 gas. The source exhibited remarkably good linearity over a wide range of CO2-pulse sizes and fast rise time, but the peak shape varied and memory effects were significant. Appropriate tuning of the gas source proved to be critical.

A variety of physical and chemical techniques are used to fractionate soil organic matter, but detailed comparisons of the different approaches and tests of how separation methods influence the properties of isolated organic matter pools are lacking. In this case study based on A horizon samples of 2 California coniferous forests soils, we 1) evaluate the effects of root removal and ultrasonic dispersion on the properties of the <2 g cm-3 light fraction and 2) compare the properties of fractions obtained by sequential density separations of ultrasonically treated soil with those obtained by density followed by acid/base hydrolysis (Trumbore et al. 1996).

A root-removal effort based on hand-picking visible roots reduced the radiocarbon content and increased the estimated turnover time of the light fraction by roughly 12%. Root-removal protocols that vary between investigators thus can potentially confound variability in carbon cycling for this fraction caused by environmental factors, such as climate. Ultrasonic dispersion did not have a clear effect on the light fraction C and N content or isotopic signature, but led to a decrease in the % C and C/N of the recovered heavy fractions, and losses of 12–19% of the total soil C to the sodium metatungstate density solution.

Sequentially isolated density fractions clearly differed in mineralogy and organic matter chemistry, but natural-abundance 14C analyses indicated that distinct mineral phases did not correspond to unique C-turnover pools. Density fractions containing kaolinite group minerals alone and in combination with hydroxy-interlayered vermiculite were found to harbor both fast and slow cycling carbon. In contrast, severe chemical treatment isolated a carbon pool with the lowest overall 14C content and longest inferred mean turnover time. Overall, our results show that care must be taken when relying on physical (density) separation to isolate soil fractions with different dynamics, as the details of treatment will influence the results.

We investigated sample dilution as a technique for accelerator mass spectrometry (AMS) radiocarbon analysis of very small samples (down to 30 μg). By diluting such samples up to a total weight of 200 μg, we can still perform reliable AMS measurements and improve the success rate significantly for targets that are difficult to measure. A disadvantage of this dilution technique is a loss of measurement precision. In addition, calculations of the 14C/12C isotope ratios and the uncertainties therein are not straightforward because of peculiarities in isotope fractionation processes in the AMS system. Therefore, to make sample dilution a routine method in our laboratory, we did extensive theoretical and experimental research to find the optimum conditions for all relevant parameters. Here, we report on the first detailed study dealing with all aspects of sample dilution. Our results can be applied in general. As an illustrative test case, we analyze 14C data for CO2 extracted from an ice core, from which samples of 35 μg C or less are available.

Accelerator mass spectrometry (AMS) radiocarbon dating of ostracod and gastropod shells from the southwestern Black Sea cores combined with tephrochronology provides the basis for studying reservoir age changes in the late-glacial Black Sea. The comparison of our data with records from the northwestern Black Sea shows that an apparent reservoir age of ∼1450 14C yr found in the glacial is characteristic of a homogenized water column. This apparent reservoir age is most likely due to the hardwater effect. Though data indicate that a reservoir age of ∼1450 14C yr may have persisted until the Bølling-Allerød warm period, a comparison with the GISP2 ice-core record suggests a gradual reduction of the reservoir age to ∼1000 14C yr, which might have been caused by dilution effects of inflowing meltwater. During the Bølling-Allerød warm period, soil development and increased vegetation cover in the catchment area of the Black Sea could have hampered erosion of carbonate bedrock, and hence diminished contamination by “old” carbon brought to the Black Sea basin by rivers. A further reduction of the reservoir age most probably occurred contemporary to the precipitation of inorganic carbonates triggered by increased phytoplankton activity, and was confined to the upper water column. Intensified deep water formation subsequently enhanced the mixing/convection and renewal of intermediate water. During the Younger Dryas, the age of the upper water column was close to 0 yr, while the intermediate water was ∼900 14C yr older. The first inflow of saline Mediterranean water, at ∼8300 14C yr BP, shifted the surface water age towards the recent value of ∼400 14C yr.

We present the first marine reservoir age and δR determination for the island of St. Helena using marine mollusk radiocarbon dates obtained from an historical context of known age. This represents the first marine reservoir age and δR determination in the southern Atlantic Ocean within thousands of kilometers of the island. The depletion of 14C in the shells indicates a rather larger reservoir age for that portion of the surface Atlantic than models indicate. The implication is that upwelling old water along the Namibian coast is transported for a considerable distance, although it is likely to be variable on a decadal timescale. An artilleryman's button, together with other artifacts found in a midden, demonstrate association of the mollusk shells with a narrow historic period of AD 1815-1835.

In the Angkor monuments of Cambodia, pieces of wood remain (as head frames of doorways, crossbeams, ceiling boards, etc.) in the following 8 monuments: Bakong, Lolei, Baksei Chamkrong, North Khleang, Angkor Wat, Banteay Kdei, Bayon, and Gates of Angkor Thorn. Accelerator mass spectrometry (AMS) radiocarbon dating carried out on 15 wood samples collected from the above 8 monuments revealed that most of the wood samples are original, except for the head frame of a doorway in Baksei Chamkrong, the ceiling boards in the northwest tower, and a crossbeam with pivot hole in the southwest tower of the Inner Gallery of Angkor Wat. The 14C age for the head frame of a doorway in the inner wall under the central tower of North Khleang supports the hypothesis that the inner walls are additions from a later period.

In 2001–2002, a settlement of the Baden culture was excavated in the vicinity of Balatonoszöd. During the rescue excavation along the M7 highway, in an area of 100,000 m2, 2800 pits dug into the subsoil, 320 hearths, and cultural layers rich in material were discovered. The material of the Baden culture represents phases IB–IC (Boleraz), IIA (Transitional), IIB–III (Early Classical) according to Němejcová-Pavúková's (1981, 1998) typological system. We took 20 samples from the large number of human and animal skeletons for radiocarbon dating, of which 16 measurements were successful. These results provide absolute dates for a Baden culture settlement with the longest occupation and the largest excavated surface in Hungary. This provides an opportunity to review the chronological position of the Baden culture, with special emphasis on its beginning and end.

In order to estimate the modern reservoir age of the seawater (R) and the corresponding local offset from the global marine radiocarbon calibration curve (δR) for coastal sites of Senegal and Mauritania, we analyzed pre-bomb mollusk shells collected between AD 1837 and 1945. In total, 27 shell samples were measured, including 19 from Senegal and 8 from Mauritania. The results for Senegal for the weighted mean of R is 511 ± 50 BP and δR is 176 ± 15 BP; for Mauritania, R is 421 ± 15 BP and δR is 71 ± 13 BP. While these values indicate a significant difference from the global mean value of R for Senegal, the R value for coastal Mauritania is close to the average ocean value R of ~400 yr (Stuiver and Braziunas 1993).

Accelerator mass spectrometry (AMS) radiocarbon dates were obtained for 18 mollusk shells collected alive along the Buenos Aires province coast, Argentina, over the period AD 1914–1935. Reservoir ages were estimated for all samples on the basis of the tree-ring calibration curve for the Southern Hemisphere (SHCal04, McCormac et al. 2004) and the marine δR values calculated as the difference between the conventional 14C age and the age deduced from the marine, mixed-layer model calculation (Marine04, Hughen et al. 2004). For most coastal locations, a great δR scatter was observed, ranging from 191 to 2482 yr, which is explained by the input of varying content of dissolved carbonate by rivers and groundwater (“hardwater effect”) and indicates a serious limitation for shell-based 14C chronologies. Within the interior of Bahía Blanca estuary, δR values ranged from −40 to 50 ± 46 as a consequence of the local geological particularities of the environment. This suggests that, with some restrictions, the marine calibration curve with standard parameters (δR = 0) could be used at this location.

Chemical and structural similarities between poorly preserved charcoal and its contaminants, as well as low radiocarbon concentrations in old samples, complicate 14C age determinations. Here, we characterize 4 fossil charcoal samples from the late Middle Paleolithic and early Upper Paleolithic strata of Kebara Cave, Israel, with respect to the structural and chemical changes that occur when they are subjected to the acid-base-acid (ABA) treatment. Differential thermal analysis and TEM show that acid treatment disrupts the structure, whereas alkali treatment results in the reformation of molecular aggregates. The major changes are ascribed to the formation of salt bridges at high pH and the disruption of the graphite-like crystallites at low pH. Weight losses during the treatments are consistently greater for older samples, implying that they are less well preserved. Based on the changes observed in vitro due to pH fluctuations, various methods for removing contamination, as well as a mechanism for preferential preservation of charcoal in nature, are proposed.

We have developed sample pretreatments for silk for radiocarbon dating. Characteristics of silk under different types of pretreatment were investigated, as well as the behavior of dye and possible contaminants. We found that dye could be removed completely, together with all other foreign materials bigger than 1.2 μm, using a glass microfiber filter after decomposition with 6N HCl. The decomposed proteins were concentrated using Centriprep® ultrafiltration concentrators with 3 different molecular weight cut-offs. By taking a molecular weight fraction—which selects for secondary structures of silk protein—14C dating of silk samples can be made more reliable. This study confirms that uniformly fractured polypeptide chains of silk provide an appropriate fraction for 14C age dating to select silk protein against dye particles and undecomposed foreign contaminants.

We measured radiocarbon ages of 22 decadal replications and 1 bulk group from 5 tree-ring specimens using acid-base-acid pretreatment and accelerator mass spectrometry (AMS). The study has the goal of refining the precision and resolution of a segment of the conventional Bronze Age chronology in the Eurasian steppe attributed to the multicultural community known as Andronovo. The archaeological timbers were gathered from 3 cemeteries at the Lisakovsky cluster of sites in Kazakhstan, where there is a prominent Andronovo occurrence that appears to show evidence of overlapping Alakul and Fedorovo cultures in the southern margin of the Eurasian steppe. The new set of Andronovo calendar dates derived from 14C wiggles and a composite floating tree-ring chronology places the cultural overlap from 1780 to 1660 cal BC. Results indicate older ages of artifacts from the Lisakovsky site than were previously determined by the typological chronology, shifting them from the Late Bronze Age to also include the transition between the Middle and Late Bronze Age. The chronological order of the Lisakovsky cemeteries provides strong evidence of contemporaneity of the Alakul and Fedorovo cultures in the Tobol River Valley for a portion of the 120-yr period of occupation. We discuss an application of the dated Alakul-Fedorovo overlap to the relationship and origin of different groups of the Andronovo community in the Ural region. Our results demonstrate the substantial power that tree rings from Bronze Age timbers provide for developing a precise and highly resolved calendar chronology of prehistoric human occupation in the Eurasian steppe during the 2nd millennium BC.

The pretreatment of samples for radiocarbon measurements, transforming a variety of materials into graphite solid targets, represents a critical point in the accelerator mass spectrometry (AMS) procedure. We describe the new, state-of-the-art CIRCE AMS preparation laboratory, particularly the setup and optimization of an alternative method, the zinc reduction method, for graphite target production, compared to the more common hydrogen reduction method. Measured 14C values on standard and blank samples reduced via zinc reaction revealed mean background levels, accuracy, and sensitivity comparable to those obtained by our conventional hydrogen reaction lines. Zinc line reduction at the CIRCE laboratory represents an effective and powerful alternative to the conventional hydrogen reduction, ensuring higher sample throughput with lower costs at a comparable performance level.

This paper includes determinations of archaeological samples coming from different sites and performed at the ENEA Radiocarbon Laboratory.

This study presents the results of archaeological samples submitted for dating at the recently constructed University of Tennessee Center for Archaeometry and Geochronology (UTCAG) radiocarbon dating laboratory (Knoxville, Tennessee, USA). The samples selected for this initial study were obtained from excavations at the McCrosky Island site (40SV43) in Sevier County, Tennessee, USA. Three of the samples dated were split between the UTCAG laboratory and another laboratory to assess the UTCAG laboratory protocols. In an effort to further validate the laboratory methods employed, several other samples were submitted without prior knowledge of contextual data. The dates obtained for these samples were then compared to their association with recovered artifacts and/or archaeological context.

This is Radiocarbon's annual list of active radiocarbon laboratories and personnel known to us. Conventional beta-counting facilities are listed in Part I, and accelerator mass spectrometry (AMS) facilities are listed in Part II. Laboratory code designations, used to identify published dates, are given to the left of the listing. (See p 501 for a complete list of past and present lab codes.)