A Tandem Van de Graaff accelerator has been modified for use in the direct measurement of natural abundances of 10Be and 14C. A description of the system is given and some 10Be results on oceanographic samples are discussed.

We performed pollen analysis and accelerator mass spectrometry (AMS) radiocarbon dating on cored sediments (KS0412-3) from Kashibaru Marsh, located in the western part of the Sefuri Mountains in northern Kyushu, southwestern Japan, to investigate environmental change around the marsh. Sediment accumulation began in this marsh around cal AD 1200 and continued with an estimated average sedimentation rate of about 4 mm/yr. Human rice cultivation at this location began around cal AD 1300 and was abandoned due to the deposition of a thick sand layer at around cal AD 1400. Since this event, the area has been maintained as a “natural” marsh.

The accelerator mass spectrometry (AMS) facility at Seoul National University (SNU-AMS) was accepted in December 1998 and results reported first at the Vienna AMS conference in October 1999 and at the 17th Radiocarbon Conference in Israel, June 2000. At the Vienna conference, we reported our accelerator system and sample preparation systems (Kim et al. 2000). Recent developments of the AMS facility have been regularly reported at AMS conferences (Kim et al. 2001, 2004, 2007). Meanwhile, about 1000 unknown archaeological, geological, and environmental samples have been measured every year. In this report, the archaeological and geological data carried out in 2001 are presented in terms of years BP (before present, AD 1950), following the SNU-AMS date lists I and II published in Radiocarbon (Kim et al. 2006a,b).

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.

An attempt is presented to establish an absolute chronology of early Slavonic habitation in the region of the mouth of the Odra River up to the Baltic and to find associations with a series of stave boats and dugouts of different levels of technology and navigation. The methodology of the research project is presented and some conclusions of a general nature are drawn from the results already obtained.

During the last seven years, there has been a concerted effort in eastern Australia to obtain 14C ages from detrital shell samples of prograded sand barriers composed of beach ridges and chenier deposits (Cook and Polach, 1973; Cook and Mayo, 1977; Thom, Polach, and Bowman, 1978; Thom et al, 1981). These ages were used to establish the age sequence of deposition and rates of progradation. This date list is the result of work in two areas of the Gulf of Carpentaria, Queensland, Australia, where 57 shell samples were collected for 14C dating. For details of this research, see Rhodes et al (1980).

Organic and carbonate carbon in sediments deposited in the Cariaco Basin and on the Mississippi River Delta and the total dissolved inorganic carbon in four water column profiles comprise the samples in this list. Except as noted below the samples were processed using the benzene synthesis and other procedures described by Mathews, et al (1972).

Within the United States, the State of California ranks first in recorded earthquake frequencies. Annually, thousands of shocks are registered on seismometers and many hundreds are actually noticed directly by Californians. In modern times, about one quake per year, destructive to property, has occurred, yet the very large and disastrous events approaching magnitude 8 and higher on the Richter scale are spaced a few decades apart: 1857 in Southern California centered on Tejon Pass, 1872 in the Owens Valley, and 1906 in San Francisco. Unfortunately, the historical record for earthquakes is short in California when compared with accounts for Europe or China, both of which list quakes over a time period of some 2000 to 3000 years. In California, the first historically noted event dates to barely 200 years ago, when in 1769, members of an expedition of the Spanish explorer Gaspar de Portola were knocked to the ground along the Santa Ana River during a large earthquake.

Samples processed since the last list was published (R, 1978, v 20, no. 3, p 192–199) are reported here. The dates were obtained by liquid scintillation counting of benzene, using laboratory procedures outlined in previous articles (R, 1976, v 18, no. 2, p 151–160; R, 1977, v 19, no. 3, p 383–388).

Measurements have continued with the same proportional counter system, pretreatment procedure, methane preparation and measurement, and calculation, as described previously (R, 1970, v 12, p 298-318). Uncertainties quoted are single standard deviations originating from standard, sample, background counting rates and half-life. No 13C/12C ratios were measured.

The following radiocarbon measurements are a partial list of geologic samples dated since September 1975. The technique used is described in R, v 18, p 210-220. Dates are calculated using a 14C half-life of 5568 yr and errors are reported as one standard deviation. This includes only the counting errors on the sample, background and modern standard.

The Russian Far East is characterized by widespread peat bogs with a sufficiently thick peat accumulation. A series of radiocarbon dates from the studied peat bogs (in Lower Amur) were obtained. Analysis of these dates shows that the total peat formation in this territory began in the Late Pleistocene–Holocene (11830 ± 820, TIG-157; 9975 ± 120, SOAN-4025). The rates of peat accumulation and the humidity index were counted. In addition, the botanical composition and degree of peat decomposition were defined. These data allow to study in more detail climate fluctuation and the 14C chronology of Holocene events in the region studied.

We are observing a dramatic increase of CO2 in the atmosphere, unprecedented in the last several million years. Carbon isotopic ratios have been very useful in helping to untangle the respective roles of anthropogenic emissions and sources/sinks of CO2 in the oceans or terrestrial biosphere. However, this untangling has not been as simple as was often hoped. The isotope ratio signatures produced by emissions and removals that are present in atmospheric CO2 are always vigorously being erased by isotopic exchange with the oceans and terrestrial ecosystems, without there necessarily being any effect on total CO2. Especially in the last decades this pure isotopic exchange effect has led to gross errors that have clouded the public debate on climate change, obscuring mankind’s role. This paper traces my own struggle with the scientific and public sides of this issue, which I ran into from the start of my career in Groningen and throughout my years at NOAA. It is still relevant today.

The SUERC Radiocarbon Laboratory reports approximately 3000 unknown samples per year with an additional 1200 samples processed for quality assurance purposes. In addition to the primary OxII standard (SRM-4990C) required for AMS batch normalization, secondary “known-age” standards have been used over many years to evaluate individual batch quality. These have included wood (as prepared alpha-cellulose), barley mash, humic acid, a background mammoth bone, known-age bones, and a whisky sample. In this paper, we present some of the results gathered over routine laboratory operation (for more than 10 years) and examine the results illustrating how they are being used to monitor and quality assure performance. Since many of these samples have also been used in the Glasgow intercomparisons, we will also reflect on the results, as well as the actual and potential uses of such samples.

An ancient pottery workshop belonging to the Han Dynasty was excavated in Caoxie village, Hepu County. Caoxie village is an important archaeological site in Hepu County, Beihai City, in south China's Guangxi Zhuang Autonomous Region. It is believed that Hepu County was the oldest departure point on the ancient maritime trading route during the Han Dynasty (206 BC to AD 220) due to the ideal natural geographical conditions and the existence of a large number of Han tombs. Radiocarbon measurements on wood and charcoal samples from the Caoxie village site were performed at the Peking University AMS facility (PKU-AMS), Beijing, and the Centre for Isotopic Research for Cultural and Environmental Heritage (CIRCE) at Naples Second University, Italy. Calibrated ages were obtained with code CALIB 5 (Stuiver and Reimer 1993). The results of these measurements are presented and the related chronology is discussed.

The following radiocarbon dates are a partial list of samples measured for a variety of projects and materials since January 1980. Chemical and counting procedures remain the same as indicated in R v 20, p 274-282.

Detonation of the first fission bomb at White Sands, New Mexico, on July 16, 1945, produced a tremendous neutron flux capable of creating tritium and radiocarbon byproducts. We sampled a 115-year-old pinyon (Pinus edulis) 10km east of the Trinity test site to determine 14C evidence of this event. The most likely mechanism for this enrichment in the 1945 tree ring would be fixation of 14CO2 produced at the blast site and carried with the fallout cloud over the pinyon site. Analysis of cellulose of the 1944 and 1945 rings shows δ13C values of −19.9 and −19.5, respectively, and 14C activity (fraction of modern uncorrected for δ13C) as 0.991 ± .005 and 0.991 ± .006, respectively. It is likely that the duration and/or concentration of the 14CO2 exposure was not sufficient to increase 14C activity expected for that year.