Seasonal deuterium excess in a Tien Shan ice core: Influence of moisture transport and recycling in Central Asia

Stable water isotope (δ18O, δD) data from a high elevation (5100 masl) ice core recovered from the Tien Shan Mountains, Kyrgyzstan, display a seasonal cycle in deuterium excess (d = δD − 8*δ18O) related to changes in the regional hydrologic cycle during 1994–2000. While there is a strong correlation (r2 = 0.98) between δ18O and δD in the ice core samples, the regression slope (6.9) and mean d value (23.0) are significantly different than the global meteoric water line values. The resulting time-series ice core d profile contains distinct winter maxima and summer minima, with a yearly d amplitude of ∼15–20‰. Local-scale processes that may affect d values preserved in the ice core are not consistent with the observed seasonal variability. Data from Central Asian monitoring sites in the Global Network of Isotopes in Precipitation (GNIP) have similar seasonal d changes. We suggest that regional-scale hydrological conditions, including seasonal changes in moisture source, transport, and recycling in the Caspian/Aral Sea region, are responsible for the observed spatial and temporal d variability

Radiochemical analysis of concrete samples from accelerator waste

For the decommissioning and disposal of shielding concrete from accelerator facilities, the Swiss Authorities require information on the radionuclide inventory. Besides the easy-to-measure γ-emitters 152Eu, 60Co, 44Sc, 133Ba, 154Eu, 134Cs, 144Ce, 22Na, also long-lived radionuclides emitting α- or β-radiation like 129I, 10Be, 36Cl, 239/240Pu and 238U have to be studied in order to obtain an overview to which extent they are produced and whether they represent a safety issue. In this study, we present the chemical separation and determination of selected radionuclides in shielding concrete from two different positions in the accelerator facilities at the Paul Scherrer Institute (PSI), the BX2 station, which was shut down in 1998, and the environment of the target M station, where the samples were taken in 1985 during reconstruction. The results of the measurements show that in no case the radionuclide content represents a safety risk. The components can be decommissioned corresponding to the Swiss safety regulation

14C contamination testing in natural abundance laboratories: a new preparation method using wet chemical oxidation and some experiences

Substances enriched with radiocarbon can easily contaminate samples and laboratories used for natural abundance measurements. We have developed a new method using wet chemical oxidation for swabbing laboratories and equipment to test for 14C contamination. Here, we report the findings of 18 months’ work and more than 800 tests covering studies at multiple locations. Evidence of past and current use of enriched 14C was found at all but one location and a program of testing and communication was used to mitigate its effects. Remediation was attempted with mixed success and depended on the complexity and level of the contamination. We describe four cases from different situations

Seasonal Deuterium Excess in a Tien Shan Ice Core: Influence of Moisture Transport and Recycling in Central Asia

Stable water isotope (delta(18)O, deltaD) data from a high elevation (5100 masl) ice core recovered from the Tien Shan Mountains, Kyrgyzstan, display a seasonal cycle in deuterium excess (d = deltaD - 8* delta(18)O) related to changes in the regional hydrologic cycle during 1994 - 2000. While there is a strong correlation (r(2) = 0.98) between delta(18)O and dD in the ice core samples, the regression slope (6.9) and mean d value (23.0) are significantly different than the global meteoric water line values. The resulting time-series ice core d profile contains distinct winter maxima and summer minima, with a yearly d amplitude of similar to 15 - 20parts per thousand. Local-scale processes that may affect d values preserved in the ice core are not consistent with the observed seasonal variability. Data from Central Asian monitoring sites in the Global Network of Isotopes in Precipitation (GNIP) have similar seasonal d changes. We suggest that regional-scale hydrological conditions, including seasonal changes in moisture source, transport, and recycling in the Caspian/ Aral Sea region, are responsible for the observed spatial and temporal d variability

Radionuclides in surface waters around the damaged Fukushima Daiichi NPP one month after the accident : Evidence of significant tritium release into the environment

Following the Fukushima nuclear accident (2011), radionuclides mostly of volatile elements (e.g., 131I, 134,137Cs, 132Te) have been investigated frequently for their presence in the atmosphere, pedosphere, biosphere, and the Pacific Ocean. Smaller releases of radionuclides with intermediate volatility, (e.g., 90Sr), have been reported for soil. However, few reports have been published which targeted the contamination of surface (fresh) waters in Japan soon after the accident. In the present study, 10 surface water samples (collected on April 10, 2011) have been screened for their radionuclide content (3H, 90Sr, 129I, 134Cs, and 137Cs), revealing partly unusually high contamination levels. Especially high tritium levels (184 ± 2 Bq·L−1; the highest levels ever reported in scientific literature after Fukushima) were found in a puddle water sample from close to the Fukushima Daiichi nuclear power plant. The ratios between paddy/puddle water from one location only a few meters apart vary around 1% for 134Cs, 12% for 129I (131I), and around 40% for both 3H and 90Sr. This illustrates the adsorption of radiocesium on natural minerals and radioiodine on organic substances (in the rice paddy), whereas the concentration differences of 3H and 90Sr between the two waters are mainly dilution driven.Peer reviewe

Plutonium release from Fukushima Daiichi fosters the need for more detailed investigations

The contamination of Japan after the Fukushima accident has been investigated mainly for volatile fission products, but only sparsely for actinides such as plutonium. Only small releases of actinides were estimated in Fukushima. Plutonium is still omnipresent in the environment from previous atmospheric nuclear weapons tests. We investigated soil and plants sampled at different hot spots in Japan, searching for reactor-borne plutonium using its isotopic ratio Pu-240/Pu-239. By using accelerator mass spectrometry, we clearly demonstrated the release of Pu from the Fukushima Daiichi power plant: While most samples contained only the radionuclide signature of fallout plutonium, there is at least one vegetation sample whose isotope ratio (0.381 +/- 0.046) evidences that the Pu originates from a nuclear reactor (Pu239+240 activity concentration 0.49 Bq/kg). Plutonium content and isotope ratios differ considerably even for very close sampling locations, e.g. the soil and the plants growing on it. This strong localization indicates a particulate Pu release, which is of high radiological risk if incorporated.CDC NIOSH Mountain and Plains Education and Research Center/T42OH009229-07NRC/NRC-HQ-12-G-38-0044CDC NIOSH Mountain and Plains Education and Research Center/T42OH009229-07NRC/NRC-HQ-12-G-38-004

The Ticino-Toce glacier system (Swiss-Italian Alps) in the framework of the Alpine Last Glacial Maximum

We present a new glacier chronology from one of the major end moraine systems of the Southern Alps. Timing and extent of the Last Glacial Maximum (LGM) advance of the Ticino-Toce glacier were reconstructed in detail based on landform relationships and surface exposure dating. 10Be and 36Cl ages from 41 erratic boulders constrain the last maximum of the Ticino-Toce glacier to have lasted from 25.0 ± 0.9 ka to 19.9 ± 0.7 ka. Over this period of ca. 5000 years the Ticino-Toce glacier underwent only minor oscillations, during which the glacier front remained close to its LGM maximum position. Underpinned by our detailed geomorphological reconstruction, the ages further demonstrate that the Verbano piedmont lobe was significantly larger (about 200 km2) than shown on recent maps. A short-lived glacier readvance around 19.7 ± 1.1 ka terminated internal to the LGM maximum margins. Collapse of the Verbano lobe must have set in soon after and final withdrawal from the foreland occurred no later than 19 ka. The new Ticino-Toce chronology matches temporal constraints of major glacier systems emerging from adjacent Alpine accumulation areas. This points to in-phase glacier advances across the Western Alps, apart from the southwestern massifs for which a slightly earlier reaching of the Late Pleistocene maximum position of the Lyon lobe was shown recently. A two- potentially three-fold LGM advance structure with intervening retreat intervals, as reported for two major amphitheatres (Garda, Tagliamento) to the east is distinctly not supported by our data for the Ticino-Toce glacier. This contrast in glacier behaviour between the central and eastern Southern Alps is ascribed to shifting precipitation patterns after ca. 23–22 ka, away from southern to predominantly northwestern air flow and a greater independence of southerly moisture transport for the central Southern Alps

Online 13C and 14C gas measurements by EA-IRMS–AMS at ETH Zürich

Studies using carbon isotopes to understand the global carbon cycle are critical to identify and quantify sources, sinks, and processes and how humans may impact them. 13C and 14C are routinely measured individually; however, there is a need to develop instrumentation that can perform concurrent online analyses that can generate rich data sets conveniently and efficiently. To satisfy these requirements, we coupled an elemental analyzer to a stable isotope mass spectrometer and an accelerator mass spectrometer system fitted with a gas ion source. We first tested the system with standard materials and then reanalyzed a sediment core from the Bay of Bengal that had been analyzed for 14C by conventional methods. The system was able to produce %C, 13C, and 14C data that were accurate and precise, and suitable for the purposes of our biogeochemistry group. The system was compact and convenient and is appropriate for use in a range of fields of research

COMBINED C-14 ANALYSIS OF CANVAS AND ORGANIC BINDER FOR DATING A PAINTING

The use of accelerator mass spectrometry (AMS) for age determinations of paintings is growing due to decreasing sample size requirements. However, as only the support material is usually dated, the validity of the results may be questioned. This work describes a novel sampling and preparation technique for dating the natural organic binder using radiocarbon (C-14) AMS. In the particular case of oil paintings, the natural oil used has a high probability of being representative of the time of creation, hereby circumventing the problem of the originality of the support material. A multi-technique approach was developed for a detailed characterization of all paint components to identify the binder type as well as pigments and additives present in the sample. The technique was showcased on a painting of the 20th century. The results by C-14 AMS dating show that both the canvas and binding medium predate the signed date by 4-5 yr. This could be the time span for keeping painting material in the atelier. The method developed provides, especially given the low amounts of material needed for analysis, a superior precision and accuracy in dating and has potential to become a standard method for oil painting dating