The Oxford Radiocarbon Accelerator Unit (ORAU) has used an ultrafiltration protocol to further purify gelatin from archaeological bone since 2000. In this paper, the methodology is described, and it is shown that, in many instances, ultrafiltration successfully removes low molecular weight contaminants that less rigorous methods may not. These contaminants can sometimes be of a different radiocarbon age and, unless removed, may produce erroneous determinations, particularly when one is dating bones greater than 2 to 3 half-lives of 14C and the contaminants are of modern age. Results of the redating of bone of Late Middle and Early Upper Paleolithic age from the British Isles and Europe suggest that we may need to look again at the traditional chronology for these periods.

Within the framework of radioecological studies, 90Sr was determined in wheat grains, soil, and deposition samples. The radiochemical purification of 90Y consisted of liquid-liquid extraction by tributyl phosphate (TBP), followed by hydroxide and oxalate precipitations and, if necessary, the removal of thorium by anion exchange chromatography. The procedure proved to be very robust and reliable, having yttrium yields of 92.7 ± 4.6% for 1-kg wheat samples, 90.9 ± 4.2% for 50-g soil samples, and 90.6 ± 3.2% for wet and dry deposition samples. 90Y was determined by Cerenkov counting and proportional counting. By optimizing the Cerenkov counting window, a figure of merit (FOM) of 4750 could be reached using a Quantulus™ 1220 system. Minimum detectable activities were in the range of 10 mBq.

The isotopic composition of ancient wood has the potential to provide information about past environments. We analyzed the δ13C, δ18O, and δ2H of cellulose of conifer trees from several cross-sections at each of 9 sites around the Great Lakes region ranging from ∼4000 to 14,000 cal BP. Isotopic values of Picea, Pinus, and Thuja species seem interchangeable for δ18O and δ2H comparisons, but Thuja appears distinctly different from the other 2 in its δ13C composition. Isotopic results suggest that the 2 sites of near-Younger Dryas age experienced the coldest conditions, although the Gribben Basin site near the Laurentide ice sheet was relatively dry, whereas the Liverpool site 500 km south was moister. The spatial isotopic variability of 3 of the 4 sites of Two Creeks age shows evidence of an elevation effect, perhaps related to sites farther inland from the Lake Michigan shoreline experiencing warmer daytime growing season temperatures. Thus, despite floristic similarity across sites (wood samples at 7 of the sites being Picea), the isotopes appear to reflect environmental differences that might not be readily evident from a purely floristic interpretation of macrofossil or pollen identification.

Conventional and accelerator mass spectrometry (AMS) radiocarbon, TL, OSL, and IRSL dating results on samples from the cores D100 and I70 from Ejina Basin, one of the most important inland basins in arid-hyperarid NW China, show that it is difficult to determine the ages of sediments at different depths. AMS ages of core D100 samples demonstrate that the sediments at depths from 10 to 90 m were formed between 14 to 30 kyr BP. The inverted ages from both the D100 and I70 cores imply that there was a strong reworking of the sediments during and after deposition processes. The inverted ages also indicate drastic fluctuations of groundwater bearing soluble organic matters, which might be related to neotectonic activities and climate changes during the period. Consequently, it is impossible to establish an accurate and reliable chronology for the cores based only on these dates. All AMS ages, if they are reliable and acceptable, indicate a high deposition rate (5∼8 mm/yr), and since all TL, OSL, and IRSL ages are much older than those given by AMS, it makes these methods questionable for determining the ages of lacustrine-fluvial-alluvial deposits.

A chronological synthesis of prehistoric campsites in alpine and subalpine zones (∼2–3 km asl) at Haleakalā, Maui Island, USA, is based on relative stratigraphy from 24 test excavations, associated artifacts of known or probable time periods, and 12 radiocarbon dates. The results indicate intensive use of the unfavorable high-altitude environment in the range of AD 1400–1600, with very limited use slightly earlier. Numerous campsites were used repeatedly near the Haleakalā crater rim and scattered on the lower western mountain slope. Prior to this time, activity in this inhospitable setting was infrequent and occurred on a small scale.

In the journal Radiocarbon, Hall et al. (2005:383) claim that 35-CS-9, located in Bandon Ocean Wayside State Park on the southern Oregon coast, is one of the few Oregon coast sites “that includes sediments and artifacts dating to the early Holocene and possibly to the late Pleistocene.” Their claim for an early Holocene or late Pleistocene human occupation rests on a single radiocarbon date of 11,000 ± 140 BP (12,710–12,680 cal BP) taken from charcoal found at least 20 cm below the nearest artifact. Although Hall et al. compile various kinds of geoarchaeological evidence to support this claim, their case is not convincing. While we applaud aspects of their analyses, the inferences they have drawn are not substantiated by the evidence they present. We agree that 35-CS-9 is a significant site but believe claims for the antiquity of its human use have been exaggerated.

Radiocarbon dates on samples aimed to date the settlement of Iceland are given together with comments by the laboratory, since many of the results and descriptions given by Sveinbjörnsdóttir et al. (2004) in Radiocarbon, together with new results, are in error. The intention of this paper is to present correct dates and further relevant information regarding samples used earlier and to discuss possible complications inherent in the method of Sveinbjörnsdóttir et al. (2004). Examples are given of how critical the collection, treatment, and interpretation of samples may be. An age difference between birch charcoal and grains for a site is expected due to various reasons. If the difference amounts up to ∼100 yr, as reported by Sveinbjörnsdóttir et al. (2004), it must only to a small degree be due to biological age. Reference to an excavation report, details regarding stratigraphy, and discussions of the risk for displacement and contamination are missing in their paper. A final evaluation of the time for settlement should not be done until more research is completed and other possible or earlier suggested or even dated sites are discussed. A summary is given of the research on the island and volcanic effects on the 14C activity of the atmospheric CO2, especially over Iceland.

The accelerator mass spectrometry facility at Seoul National University (SNU-AMS) began functioning in December 1998 and was first reported at the Vienna AMS conference in October 1999 and at the 17th International Radiocarbon Conference in Israel in June 2000. At the Vienna conference, we reported our accelerator system (Kim et al. 2000) and details of the basic sample preparation system (Lee et al. 2000), such as the combustion line to produce CO2; the catalytic reduction line for the graphitization of CO2; and the pretreatment procedures for wood, charcoal, and peat samples. The recent progress of the AMS facility (Kim et al. 2001) and the extension of the sample pretreatment system to iron and bone samples were reported at the 17th International Radiocarbon Conference (Cheoun et al. 2001). In the meantime, extensive testing of accuracy and reproducibility has been carried out, and ∼1000 unknown archaeological and geological samples have been measured every year. In this report, the archaeological, geological, and environmental data carried out in 1999 are presented in terms of yr BP.

The accelerator mass spectrometry facility at Seoul National University (SNU-AMS) began functioning in December 1998 and was first reported at the Vienna AMS conference in October 1999 and at the 17th Radiocarbon Conference in Israel in June 2000. At the Vienna conference, we reported our accelerator system (Kim et al. 2000) and the basic sample preparation system (Lee et al. 2000), including the combustion line to produce CO2; the catalytic reduction line for the graphitization of CO2; and also pretreatment procedures for wood, charcoal, and peat samples. Recent progress of the AMS facility (Kim et al. 2001) and extension of the sample pretreatment system to iron and bone samples were reported at the 17th Radiocarbon Conference (Cheoun et al. 2001). In the meantime, extensive testing of accuracy and reproducibility has been carried out, and ∼1000 unknown archaeological and geological samples have been measured every year. A report of data carried out in 1999 is presented by Kim et al. (this issue). In this report, the archaeological, geological, and environmental data carried out in 2000 are presented in terms of yr BP.

A 3MV multi-element accelerator mass spectrometer (AMS) has been installed in Xi'an, China, and preliminary tests have been completed. The results of both background and precision tests for 4 nuclides are 3.1 × 10–16, 0.2% (14C); 1.8 × 10–14, 1.4% (10Be); 2.3 × 10–15, 1.14% (26Al); and 2.0 × 10–14, 1.75% (129I). The unique features of this facility are the newly developed ion source accepting solid and CO2 samples; the specially designed low-energy injector, including a “beam blanking unit” and “Q-snout”; the acceleration tube structure with the combined magnetic and electrostatic suppression; and the function of the slit stabilization in the post-acceleration system. These features are discussed in terms of the end-user's point of view.