In this study, we test the possibility of using databases of radiocarbon ages to estimate boundaries of climatic chronozones. The Alaska region was chosen and compared with chronozones of 2 European countries: Poland and the Netherlands. The study included setting up a database of 14C ages published for climatic records from Alaska. Some 974 14C determinations on organic samples were selected and used to establish chronozones for the Late Glacial and the Holocene for the Alaska region. The selected data were calibrated and a summed probability density function (PDF) was calculated. The shape analysis of the constructed frequency distribution of 14C dates on calendar timescales together with the assumption about preferential sampling seems to be a useful tool for establishing calendar ages for boundaries of climatic periods, i.e. chronozones.

Isotope hydrology investigations were carried out with the aim to study isotope variability in mineral and thermal waters (MTW) of Slovakia. The aquifers of MTW were formed by Triassic limestones and dolomites, which are found in the mountains as well as in the pre-Tertiary substratum of depressions and lowlands. The MTW were of artesian and/or open structures. At present, there are only boreholes available, as natural outflows have already been captured by them. Large spatial isotope variability (14C between 2 and 33.6 pMC, δ18O between −11.8‰ and −9.8‰, and δ13C between −12.7‰ and +3.4‰ for bicarbonates and −21‰ and –4.9‰ for free CO2) and heterogeneity of MTW was observed, indicating different origins of MTW. Corrected radiocarbon apparent ages of MTW indicate that they mostly infiltrated during the Würm and Holocene periods.

Dispersion and deposition of terrestrial organic matter by flooding on the inner shelf were studied using C/N ratios, δ13C, and Δ14C values of sedimentary organic matter. Surface sediment samples (top 2 cm) were collected from coastal areas near the Saru River in southwestern Hokkaido, northern Japan, 1 yr after a flood event in 2006. Riverine suspended solids were also collected at a fixed station downstream during 2006–2008. Sandy sediments were located at the front of the river mouth and the western part of the sampling area, with the δ13C of organic matter ranging from −23.8‰ to −22.0‰, Δ14C of –655‰ to –388‰, and an organic carbon/total nitrogen (C/N) ratio of 5.9–7.7. On the other hand, silt and clay sediments were distributed in a restricted area 11–16 km from the river mouth, with lighter δ13C (–26.7‰ to −24.1‰) and higher Δ14C (–240‰ to –77‰) of organic matter and C/N ratio (7.8–13.3). From end-member analysis, the apparently younger and less degraded organic matter in the silt and clay sediments consists mainly of terrestrial organic matter released by flood events. They remain in the depression, although most flood deposits were moved to deep-sea environments.

Carbon isotopes (14C and 13C) of dissolved organic carbon (DOC) in a Japanese oligotrophic lake (Lake Towada) were measured to study the origin and cycling of dissolved organic matter (DOM) in Lake Towada. Lake water samples were collected at 3 depths (0, 30, and 80 or 85 m) during 4 months (April, June, August, and October) in 2006. 14C measurements of DOC were performed by accelerator mass spectrometry (AMS) at the National Institute for Environmental Studies (NIES-TERRA) in Japan. Δ14C and δ13C values of DOC in Lake Towada showed light carbon isotopic values ranging from –750 to −514‰ and –29.0 to –27.8‰, respectively. These values are similar to those of humic substances reported. The very low carbon isotopic values of DOC in Lake Towada suggest a very small contribution of DOC derived from fresh phytoplankton to the lake DOC. There is an extremely high linear relationship between the Δ14C and δ13C of DOC in Lake Towada when all data points are plotted (r2 =0.818, p < 0.01), suggesting that the DOC in Lake Towada has 2 specific sources contributing heavy and light carbon isotopes. Although the freshly produced DOC of phytoplankton origin can be decomposed easily, the variation in the autochthonous DOC should influence the carbon isotopic values of DOC in Lake Towada.

We present a novel application for radiocarbon dating by aging 4 scales from a single large adult lungfish (Neoceratodus forsteri) from the Burnett River, in Queensland, Australia. The relict fish species lack a solid crystalline otolith, which precludes the use of the otolith annuli as a reliable age indicator. Previous attempts to age lungfish using a number of techniques have had only limited success. We report on ages obtained from the dense lamellar bone of the scale, which were isolated from the organic layers that thicken and subsequently obscure the 14C signal. Using the characteristics of the bomb curve, 2 parameter von Bertanalffy growth functions were fit, providing an estimate of absolute age to be ∼65–70 yr. The information gleaned from this study will aid in assessing the population structure, and therefore management, of this vulnerable species.

Huge landslides triggered by strong earthquakes or torrential rains can result in unstable natural dams that pose serious risks to humans. In this study, we attempt to document the age of an ancient earthquake that produced a landslide-dammed lake. A buried forest found in the Toyama River area of the southern Nagano Prefecture, central Japan, provides evidence of this event. The dammed lake formation has been previously estimated to have occurred in AD 714. However, the age of the dam and the way it was formed have never been directly determined. To determine the position and timing of the landslide dam, we analyzed the radiocarbon content of branches and wood fragments from a brecciated deposit. We show that the 14C dating method is suitable for clarifying the timing of burial for a variety of trees, although the method does not produce a narrow age for the event. In addition to the dating, we determined the landslide dam's position and reconstructed the formation of the lake.

Lake Mývatn is an interior highland lake in northern Iceland that forms a unique ecosystem of international scientific importance and is surrounded by a landscape rich in archaeological and paleoenvironmental sites. A significant freshwater reservoir effect (FRE) has been identified in carbon from the lake at some Viking (about AD 870–1000) archaeological sites in the wider region (Mývatnssveit). Previous accelerator mass spectrometry (AMS) measurements indicated this FRE was about 1500–1900 14C yr. Here, we present the results of a study using stable isotope and 14C measurements to quantify the Mývatn FRE for both the Viking and modern periods. This work has identified a temporally variable FRE that is greatly in excess of previous assessments. New, paired samples of contemporaneous bone from terrestrial herbivores and omnivores (including humans) from Viking sites demonstrate at least some omnivore diets incorporated sufficient freshwater resources to result in a herbivore-omnivore age offset of up to 400 14C yr. Modern samples of benthic detritus, aquatic plants, zooplankton, invertebrates, and freshwater fish indicate an FRE in excess of 5000 14C yr in some species. Likely geothermal mechanisms for this large FRE are discussed, along with implications for both chronological reconstruction and integrated investigation of stable and radioactive isotopes.

Chemical preservatives (e.g. mercuric chloride) are routinely added to freshwater samples to prevent biological activity compromising the isotopic signature of dissolved organic matter (DOM) with time. However, alternative preservation methods are needed due to regulations restricting the use of preservatives with potentially adverse environmental and health impacts, rendering such additions unviable. This study investigates whether a non-chemical storage method is sufficient to maintain the radiocarbon and stable carbon and nitrogen signatures of freshwater DOM from a low order river system draining a peaty catchment. Some 50 L of stream water were collected in 1 plastic carbuoy and, within 24 hr, 1-L aliquots were transferred to acid-washed plastic bottles. Five aliquots were analyzed immediately to determine the baseline values for 14C (pMC), δ13C (VPDB‰), δ15N (AIR‰), %C (mg L–1), and %N (mg L–1). Of the remaining subsamples, 20 were frozen and a further 20 refrigerated at <4 °C. After 7, 30, 90, and 180 days, 5 frozen and 5 refrigerated aliquots were analyzed in the same manner as the baseline aliquots. Analysis of the results shows that there is no statistically significant interaction between the variables storage method or length of storage for any of the determinants. Storage method has a statistically significant effect on 14C (pMC) and [C] (mg L–1). Length of storage has a statistically significant effect on δ13C (VPDB‰), [C] (mg L–1), and [N] (mg L–1) values. Neither storage method nor length of storage appear to have a statistically significant effect on 815N (AIR‰) values.

This work presents an attempt to date brines and determine flow rates of hypersaline groundwater in the extremely dynamic system of the Dead Sea (DS), whose level has dropped in the last 30 yr by ∼20 m. The processes that affect the carbon species and isotopes of the groundwater in the DS area were quantified in order to estimate their flow rate based on radiocarbon and tritium methods. In contrast to the conservative behavior of most ions in the groundwater, the carbon system parameters indicate additional processes. The dissolved inorganic carbon (DIC) content of most saline groundwater is close to that of the DS, but its stable isotopic composition (δ13CDIC) is much lower. The chemical composition and carbon isotope mass balance suggest that the low δ13CDIC of the saline groundwater is a result of anaerobic organic matter oxidation by bacterial sulfate reduction (BSR) and methane oxidation. The radiocarbon content (14CDIC) of the saline groundwater ranged from 86 pMC (greater than the ∼82 pMC value of the DS in the 2000s) to as low as 14 pMC. The similarity between the 14CDIC value and Na/Cl ratio of the groundwater at the DS shore and that of the 1980s DS brine indicates that the DS penetrated to the aquifer at that time. The low 14CDIC values in some of the saline groundwater suggest the existence of ancient brine in the subaquifer.

An automatic water sampling unit was developed to monitor the radioactive emission (radiocarbon and other corrosion and fission products) from nuclear facilities into the groundwater. Automatic sampling is based on the principal of ion exchange using built-in resin columns in the submerging samplers. In this way, even the short-term emissions can be detected. According to our experiments, the 14C activity concentrations and the δ13C values of the samples made by the ion exchange method are systematically underestimated compared to the real values. The carbonate adsorption feature of the sampling unit was studied under laboratory and field conditions. For this purpose, a test method was developed. The observed sampling efficiencies and additionally some carbon contamination for the sampling method itself have to be taken into consideration when we estimate the amount of 14C contamination introduced into the groundwater from a nuclear facility. Therefore, a correction factor should be made for the 14C anion exchange sampling. With the help of this correction, the results converge to the expected value.

We report radiocarbon measurements of dissolved inorganic carbon (DIC) in surface water samples collected daily during 12 cruises to Station M in the northeast Pacific off central California. Individual surface Δ14C values ranged from 22‰ to 70‰ over 10 yr. Variability of average cruise values is highest during winter likely due to increased mixing. A general decrease of Δ14C values was observed at a rate of about 3‰ per year between 1994 and 2004, about half of that in atmospheric CO2 during this period (Levin and Kromer 2004). The Δ14C results ranged from 2–18‰ during individual cruises and were often significantly larger than the total uncertainty for individual measurements (±3.9‰). This indicates that a single Δ14C result from a surface site is not sufficient to capture the true variability of Δ14C in the surface ocean.

New ΔR values are presented for 10 known-age shells from the Kimberley region of northwest Australia. Previous estimates of ΔR for the Kimberley region are based on only 6 individual shell specimens with dates of live collection known only to within 50 yr (Bowman 1985a). Here, we describe the results of our recent attempts to constrain ΔR variability for this region by dating a suite of known-age pre-AD 1950 shell samples from the Australian Museum and Museum Victoria. A regional ΔR of 58 ± 17 14C yr for open waters between Broome and Cape Leveque is recommended based on 7 of these specimens. The criteria used to select shells for dating and inclusion in the regional mean are discussed.

The marine radiocarbon reservoir effect (MRE) occurs as a spatially and temporally dependent variable owing to localized changes in oceanic water composition. This study investigates ΔR values (deviations from the global average MRE whose ΔR = 0) during the period 500–1350 BP for the east coast of Scotland, where a complex estuarine system exists that drains into the semi-enclosed North Sea basin. Due to the availability of suitable archaeological samples, the data set has a distinct Medieval focus that spans the area from Aberdeen in the north to East Lothian in the south. Many of the ΔR values are not significantly different from 0 (the global average), but there are occasional excursions to negative values (max –172 ± 20) indicating the presence of younger water. These values show greater variability compared to other published data for this general region, suggesting that considerable care must be taken when dating marine derived samples from archaeological sites on the east coast of Scotland.

We report and compare radiocarbon observations made on 2 meridional oceanographic sections along 150°W in the South Pacific in 1991 and 2005. The distributions reflect the progressive penetration of nuclear weapons-produced 14C into the oceanic thermocline. The changes over the 14 yr between occupations are demonstrably large relative to any possible drift in our analytical standardization. The computed difference field based on the gridded data in the upper 1600 m of the section exhibits a significant decrease over time (approaching 40 to 50‰ in Δ14C) in the upper 200–300 m, consistent with the decadal post-bomb decline in atmospheric 14C levels. A strong positive anomaly (increase with time), centered on the low salinity core of the Antarctic Intermediate Water (AAIW), approaches 50–60‰ in Δ14C, a clear signature of the downstream evolution of the 14C transient in this water mass. We use this observation to estimate the transit time of AAIW from its “source region” in the southeast South Pacific and to compute the effective reservoir age of this water mass. The 2 sections show small but significant changes in the abyssal 14C distributions. Between 1991 and 2005, Δ14C has increased by 9‰ below 2000 m north of 55°S. This change is accompanied overall by a modest increase in salinity and dissolved oxygen, as well as a slight decrease in dissolved silica. Such changes are indicative of greater ventilation. Calculation of “phosphate star” also indicates that this may be due to a shift from the Southern Ocean toward North Atlantic Deep Water as the ventilation source of the abyssal South Pacific.

Radiocarbon was measured in the surface seawater dissolved inorganic carbon (DIC) of the Bay of Bengal during November 2006. A meridional transect of the Δ14C in DIC was obtained from measurements in closely spaced samples collected roughly along 88°E. The Δ14C of these samples ranged from 44‰ to 57.7‰ (mean 51.8 ± 1.1‰, n = 12), and 38‰ at one station in the northern Bay of Bengal. The overall pattern of 14C distribution in DIC of surface Bay of Bengal during 2006 was roughly similar to that during the WOCE expedition of 1995. These results indicate a Δ14C decline rate of ∼4‰ per decade since WOCE in the surface Bay of Bengal, which is much smaller compared to a decline rate of ∼25‰ per decade observed in the 2 decades between the GEOSECS and WOCE expeditions, due to the smaller atmosphere-ocean Δ14C gradient.

In this study, molluscan shells housed at the University Museum, the University of Tokyo, provided a new set of region-specific correction values (ΔR) for the western Pacific, in particular for the central part of the main islands in the Japanese Archipelago and the southwest islands of Japan. The values of 40 total samples were calculated from 11 regions. North of the main islands and in the Ryukyu Islands, the mean ΔR values showed comparatively small values, 5–40 14C yr; in the central part of the main islands, these values were 60–90 14C yr.

Mollusk shells provide brief (<5 yr per shell) records of past marine conditions, including marine radiocarbon reservoir age (R) and upwelling. We report 21 14C ages and R calculations on small (∼2 mg) samples from 2 Mesodesma donacium (surf clam) shells. These shells were excavated from a semi-subterranean house floor stratum 14C dated to 7625 ± 35 BP at site QJ-280, Quebrada Jaguay, southern Peru. The ranges in marine 14C ages (and thus R) from the 2 shells are 530 and 170 14C yr; R from individual aragonite samples spans 130 ± 60 to 730 ± 170 14C yr. This intrashell 14C variability suggests that 14C dating of small (time-slice much less than 1 yr) marine samples from a variable-R (i.e. variable-upwelling) environment may introduce centuries of chronometric uncertainty.

We report compound-specific radiocarbon analyses of organic matter in ocean sediments from the northeast Pacific Ocean. Chemical extractions and a preparative capillary gas chromatograph (PCGC) were used to isolate phospholipid fatty acids (PLFA) and n-alkanes from 3 cores collected off the coast of California, USA. Mass of samples for accelerator mass spectrometry (AMS) 14C analysis ranged from 13–100 μg C. PLFA extracted from anaerobic sediments in the Santa Barbara Basin (595 m depth) had modern Δ14C values (–20 to +54‰), indicating bacterial utilization of surface-produced, post-bomb organic matter. Lower Δ14C values were obtained for n-alkanes and PLFA from coast (92 m depth) and continental slope (1866 m) sediments, which reflect sources of old organic matter and bioturbation. We present a brief analysis of the blank carbon introduced to samples during chemical processing and PCGC isolation.

We present a time-saving modification to the ultraviolet (UV) oxidation method for analyzing dissolved organic carbon (DOC) concentration, Δ14C, and δ13C measurements in seawater and standard materials. A low background (∼0.2 ± 0.2 μM) was reported for pre-irradiated Milli-Q (MQ) water that was used to dilute samples for DOC 14C analysis (Beaupré et al. 2007). We use MQ water without pre-irradiation (background ∼0.9 ± 0.2 μM) to dilute the sample. This method is suitable for small-volume, high-concentration samples (mass of sample DOC overwhelms mass of MQ water DOC). An acceptable precision of Δ14C measurements (5–9‰) is maintained. This revised method reduces the preparation time for diluted DOC Δ14C samples from 2 days to 1 day.

A sample preparation workshop was convened at the 20th International Radiocarbon conference, with about 30–40 attendees. The term “sample preparation” was not further specified to allow participants to address the laboratory issues most important to them. Given the short time available, the focus quickly narrowed to details of graphite preparation for accelerator mass spectrometry (AMS), with particular interest in procedures for small samples, and hence we have changed the title to reflect the focus. Here, we summarize the workshop discussion, adding additional background information and references to publications. Several aspects of graphite preparation are included: catalyst types and ratio of catalyst to carbon; optimal reaction temperatures for various sample sizes; methods for water removal; types of pressure transducers; preconditioning of catalyst; and problems with blank values in very small samples. The pros and cons of sample dilution were also discussed.