A new compact accelerator mass spectrometry (AMS) system dedicated to the measurement of radiocarbon has been commissioned at the Accium BioSciences headquarters in Seattle. The entire facility (including ancillary laboratories for the preparation of graphite targets) has been designed to handle samples with a wide range of 14C concentrations. In this paper, we discuss the technical details of the new facility and present performance test results demonstrating state-of-the-art capabilities. In particular, modern samples can be readily measured with 0.3% precision and accuracy, machine background levels are consistently in the low 10-16 (14C/12C), and chemical background is approximately equivalent to a fraction of modern of 0.004. In addition, when 100-times-modern samples were processed, no increase in background was observed, either during sample processing or during AMS measurement. This corresponds to a dynamic range for 14C analysis of 6 orders of magnitude.

Since the development of accelerator mass spectrometry (AMS) for radiocarbon dating in the late 1970s, its ability to date small samples of bone has been of huge importance in archaeology and Quaternary paleoecology. The conventional approach to sample preparation has been to extract and gelatinize protein, which is then combusted and graphitized for analysis. However, this “bulk protein” can contain a heterogeneous mixture of non-collagenous molecules, including humic acids and other soil components that may be of a different age than the bone and therefore affect the accuracy of its 14C date. Sample pretreatment methods have been an important area of development in recent years but still show inadequacies for the dating of severely contaminated bone. The idea of isolating and dating individual compounds such as single amino acids, to improve dating accuracy, has been discussed in the literature since the 1960s. Hydroxyproline, for example, makes up over 10% of bone collagen but is extremely rare in most other animal proteins, increasing the chances of its presence being endogenous to the individual being dated. Its successful isolation has therefore been considered a potential “gold standard” for dating archaeological bone; however, extracting and suitably purifying single amino acids from bone has proved a challenging task.

A multicounter radiocarbon dating system was developed applying the experiences of the previous one-channel low-level counting facility. The counter system consists of nine electrolytic copper proportional counters of identical diameters with sensitive volumes of 0.35–0.7dm3 and filled with either methane at high pressure (6 bar) or CO2 at 1 bar. The inner counters are surrounded by an anticoincidence shield consisting of five multiwire proportional flat counters filled with propane. The pulses of the detectors are handled by integrated amplifiers, discriminators and anticoincidence units interfaced to a microprocessor-controlled data evaluation unit. Software is written in BASIC using ASSEMBLER sub-routines. The overall precision of the system for modern carbon samples using high-pressure methane-filled counters (B ≍ 0.7 cpm, S ≍ 14 cpm) is better than 4 after a counting period of seven days.

14C measurements were made on present-day plant material with short integration times (tree leaves and sprouts) in the Eifel area, western Germany, where ancient volcanism produces gaseous emanations of considerable yield. Plants growing near sources emanating 14C-free CO2 show a significant depletion in the period of their growth. The same effect is found in the 14C content of recent samples from the Thera (Santorini) Archipelago/Greece. This mixing of “dead” CO2 may lead to pseudo ages in archaeologic or geologic samples of up to 1600 years in samples from the vicinity of CO2 emanating sources.

The Keck Carbon Cycle accelerator mass spectrometry facility at the University of California, Irvine, operates a National Electronics Corporation 40-sample MC-SNICS ion source. We describe modifications that have increased beam current output, improved reliability, and made the source easier to service.

High precision for radiocarbon cannot be reached without profound insight into the various sources of uncertainty which only can be obtained from systematic investigations. In this paper, we present a whole series of investigations where in some cases 16O:17O:18O served as a substitute for 12C:13C:14C. This circumvents the disadvantages of event counting, providing more precise results in a much shorter time. As expected, not a single effect but a combination of many effects of similar importance were found to be limiting the precision.

We will discuss the influence of machine tuning and stability, isotope fractionation, beam current, space charge effects, sputter target geometry, and cratering. Refined measurement and data evaluation procedures allow one to overcome several of these limitations. Systematic measurements on FIRI-D wood show that a measurement precision of ±20 14C yr (1 σ) can be achieved for single-sputter targets.

Radiocarbon measurements on a 109-year-old (1868-1977) core of Montastrea annularis coral from Glover Reef, Belize, in the Gulf of Honduras, reveal uptake of fossil fuel CO2 and bomb 14C by surface ocean waters. The history of Δ14C values revealed by this Belize growth agree remarkably well with results for coral growth from the Florida Straits. It is concluded that these corals are reliable recorders of 14C concentrations of dissolved inorganic carbon (DIOC) in surface waters representative of the Gulf Stream.

In 1969, at the Nobel Symposium on “Radiocarbon Variations and Absolute Chronology” in Uppsala, a curve was presented that illustrated the functional dependence of measured conventional radiocarbon dates on true historical ages of wood samples (Suess, 1971). The curve was derived from the results of La Jolla measurements of radiocarbon in bristlecone pine wood dendrochronologically dated by and obtained from Professor C W Ferguson of the University of Arizona (Ferguson, 1968). The curve was intended to be adequate for deriving calibrated radiocarbon dates and also for allowing fairly reliable estimates of the accuracy of the absolute dates obtained in this manner. The basis for the validity of this calibration is the well known fact that, for all practical purposes, wood samples that had grown at the same time show the same radiocarbon content. However, the reverse is not always true: Wood samples showing the same radiocarbon content do not necessarily have the same age because of the windings and steps of the curve (Stuiver and Suess, 1966).

A method has been developed at the Arizona AMS facility for production of graphite directly from CO2 by catalytic reduction of CO/H2 mixtures. The method is a modification of procedures discussed by Vogel et al (1984). Currents of 12C− from these targets vary considerably, but have a median value which is 70% of that achieved from spectroscopic graphite. Precisions of ±60 to 100 yr are routinely achieved for 14C ages of 5000-yr-old samples containing one milligram of carbon. The yield of 14C from “blank” targets is 0.6 ± 0.1% of that from modern material.

We show that high-precision radiocarbon (Δ14C) measurements from annual bands of a Hawaiian surface coral decreased by 7‰ from AD 1893 to 1952. This decrease is coincident with the Suess Effect, which is mostly due to the dilution of natural levels of 14C by 14C-free fossil fuel CO2. This decrease is equal to that expected in surface waters of the subtropical gyres, and indicates that the surface waters of the North Pacific were in steady state with respect to long term mixing of CO2 during the past century. Correlation between Δ14C and North Pacific gyre sea surface temperatures indicates that vertical mixing local to Hawaii and the North Pacific gyre as a whole is the likely physical mechanism to result in variable Δ14C. Prior to 1920, this correlation starts to break down; this may be related to the non-correlation between biennial Δ14C values in corals from the southwest Pacific and El Niño events observed during this period as well.

We describe the operation of a commercial system as modified for preparation of CO2 for the CO2 source. AMS samples are automatically combusted in a CHN analyzer, and stable isotope measurements are made on line. We describe the performance of this equipment, with reference to yield, sample contamination, memory effect, accuracy of isotope measurement, convenience and cost. We discuss the current status of dating using the CO2 source. This is the only source in operation at Oxford, and has been in routine dating since September 1989. We assess the practicalities of operation, including the latest measurements on background, memory, sample-size requirements and operating schedules. We also describe modifications to the sputter beam optics and to the gas handling systems.

Charcoal is the result of natural and anthropogenic burning events, when biomass is exposed to elevated temperatures under conditions of restricted oxygen. This process produces a range of materials, collectively known as pyrogenic carbon, the most inert fraction of which is known as black carbon (BC). BC degrades extremely slowly and is resistant to diagenetic alteration involving the addition of exogenous carbon, making it a useful target substance for radiocarbon dating particularly of more ancient samples, where contamination issues are critical. We present results of tests using a new method for the quantification and isolation of BC, known as hydropyrolysis (hypy). Results show controlled reductive removal of non-BC organic components in charcoal samples, including lignocellulosic and humic material. The process is reproducible and rapid, making hypy a promising new approach not only for isolation of purified BC for 14C measurement but also in quantification of different labile and resistant sample C fractions.

Radiocarbon dating provides the principal chronometric data for the Middle and Upper Palaeolithic, Epipalaeolithic, and Chalcolithic periods in the southern Levant. It is a secondary source of dating evidence for the Early Bronze age, when archaeological correlations with Syria and especially Egypt become available. For the Middle and Late Bronze age, Iron age, Persian, Hellenistic, Roman, and Byzantine periods, 14C dating has only limited value because the technique is less precise than the normally available archaeologic and historic materials.

This list includes age measurements carried out from November 1969 to December 1970. All archaeologic and geologic samples come from Italian territory. Laboratory equipment, largely unchanged, has been described (Alessio et al., 1970).

Holocene tree-ring chronologies have been established for south-central Europe covering the past 11,000 years. The Hohenheim absolute oak chronology extends to 4089 bc. The C-calibrated mid-Holocene floating oak master covers a 3181-year period from ca 4045 to 7225 bc. The earliest well-replicated floating oak master (estimated calendar age 7215 to 7825 bc) extends the European oak dendrochronology back to Boreal times.

Further extension of the Holocene dendrochronology has been achieved by subfossil oak and pine trees from the Rhine, Main, and Danube Rivers. A 774-year floating series of Preboreal pine has been established. 14C ages range (from younger to older end) from 9200 to 9800 BP. Within this series a major atmospheric 14C variation is indicated, resulting in nearly constant 14C ages (9600 BP) over a period of 370 tree-rings.

The European oak and pine tree-ring chronologies cover without major gaps the entire Holocene epoch. Based on the length of the dendro-records, an approximate solar year age of 11,280 years is calculated for the Holocene/Pleistocene boundary.

The Preboreal pine forests along the rivers were replaced by mixed oak forests between 9200 and 8800 BP. By linking the earliest oak masters and the Preboreal pine series, the European dendrochronology can be extended up to the end of Late Glacial times.

This list contains dates related to the chronology ofthe last glaciation in Europe. Since several of theolder results which already have appeared in printneed correction or re-interpretation it wasconsidered necessary to incorporate as many of themas possible into this list. Notably the datespublished by de Vries (1958) are included here andreconsidered in the light of our presentunderstanding of the climatic succession. It isnoteworthy that, although the interpretation mayhave changed slightly, most of those measurementsare still as valid today as they were eight yearsago.

The different categories of samples and their treatments at the radiocarbon (14C) laboratory in Jena, Germany, are described. The Jena 14C laboratory is dedicated to studying the global carbon cycle through the analysis of soil, plant, gas, charcoal, and wood samples. The respective preparation procedures for different samples types are presented, including wet-chemistry pretreatments for soil decalcification, charcoal purification using an acid–base–oxidation procedure (ABOx), and α-cellulose extraction from wood and leaves. In particular, investigations of the background corrections for each sample type are emphasized. Furthermore, an investigation of the contamination resulting from the storage of graphite is presented. Four storage conditions are investigated for storage times up to 30 months.

To obtain a precise radiocarbon Holocene chronology in coastal areas, it is necessary to estimate the modern 14C reservoir age R(t) and its possible variations with time in relation to paleoenvironmental changes. The modern reservoir 14C age was estimated by comparing AMS 14C ages of 2 recent mollusk shells found in sediment cores sampled in the Palavasian lagoonal system (south of France) with ages derived from 210Pb and 137Cs data and historical accounts of identifiable storm events. The calculated modern R(t) value of 943 ± 25 14C yr is about 600 yr higher than the global mean sea surface reservoir age. This high value, probably due to the relative isolation of the lagoon from marine inputs, is in good agreement with other R(t) estimates in Mediterranean lagoonal systems (Zoppi et al. 2001; Sabatier et al. 2008). 14C ages were also obtained on a series of Holocene mollusk shells sampled at different depths of the ∼8-m-long core PB06. Careful examination of the 14C ages versus depth relationships suggests that R(t) in the past was lower and similar to the value presently measured in the Gulf of Lion (618 ± 30 14C yr, Siani et al. 2000). The change in R(t) from 618 to 943 yr is thought to result from final closure of the coastal lagoon by the sandy barrier, due to the along-shore sediment transfer.

The basic chronology of Inca imperial expansion in Andean South America derives from historical accounts from the Spanish Colonial era, but several issues with this traditional chronology have arisen in recent decades. Advances in radiocarbon dating and calibration now give us some ability to refine or rebuild the chronology, and guidelines for obtaining the most useful dates are discussed. Dates recently obtained from the site of Chamical in the southern highlands of Ecuador are evaluated according to those guidelines, and they suggest Inca expansion to the north began 1 to 2 decades earlier than allowed in the traditional chronology. The chronology of Inca expansion presented in the Spanish chronicles is called into question by these and other dates, and by a reconsideration of the nature of sources of Inca history utilized by Spanish writers. Evidence suggests a primary Inca form of recording provincial conquests resulted in lists that were ordered geographically. However, those records were interpreted by colonial writers as being chronologically ordered, which led to written histories of Inca expansion that are not consistent with the actual historical sequence of events. As a result, the preferred approach to building a chronology of Inca expansion should be based on 14C dates, with historical sources used to supplement rather than structure the timeline.

One of the largest sources of uncertainty in radiocarbon dating stems from the sample pretreatment procedures used to minimize contamination. A major source of carbon contamination in charcoal from archaeological sites is humic substances carried by groundwater. Here we present a method, independent of 14C dating itself, to evaluate the effectiveness of the cleaning procedure of charcoal. Raman spectra of mixtures of humic substances (HS) and laboratory prepared charcoal indicate that Raman spectroscopy can be used as a semi-quantitative measure of the amount of humic substances associated with archaeological charcoal. Raman spectral analysis of archaeological charcoal samples subjected to different cleaning regimes supports this contention. Such measurements can provide quality control for charcoal preparation procedures and may assist in the interpretation of carbon-dating results.