2 research outputs found

    Temporal Variation of Iodine Isotopes in the North Sea

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    Monitoring temporal variability of <sup>129</sup>I in the North Sea, a relatively large reservoir of radioactive discharges from the nuclear fuel reprocessing facilities, is vital for the environmental situation in the region. New information on concentration levels and distribution of <sup>129</sup>I and <sup>127</sup>I and their species forms (iodide and iodate) are gained here through sampling of surface water in 2010. The results show generally large spatial and temporal (compared to data from 2005) fluctuations of total <sup>129</sup>I and <sup>127</sup>I, and iodide and iodate. In samples south of 53°N, the level of <sup>127</sup>I<sup>–</sup> in 2010 was generally comparable or higher than in 2005. The results also show total <sup>129</sup>I concentrations comparable in the south, but 2–8 times lower in the north, to the analyses made in 2005. Different from total <sup>129</sup>I, the <sup>129</sup>I<sup>–</sup>/<sup>129</sup>IO<sub>3</sub><sup>–</sup> values in the northern part were 2 times higher in 2010 than values observed in 2005. These variations in total <sup>129</sup>I and <sup>127</sup>I and their species are related to coastal water offshore propagation and surface currents that are linked to long-term and seasonal climatic changes over the North Atlantic and North Sea. Inventory estimation shows that >90% of <sup>129</sup>I resides in the Southern and German Bights, which also suggests negligible contribution from the Sellafield facility discharges when compared with that from the La Hague. Variability in discharge rate from La Hague may also affect the distribution patterns of <sup>129</sup>I in the North Sea on the monthly scale

    Iodine-129 in Snow and Seawater in the Antarctic: Level and Source

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    Anthropogenic <sup>129</sup>I has been released to the environment in different ways and chemical species by human nuclear activities since the 1940s. These sources provide ideal tools to trace the dispersion of volatile pollutants in the atmosphere. Snow and seawater samples collected in Bellingshausen, Amundsen, and Ross Seas in Antarctica in 2011 were analyzed for <sup>129</sup>I and <sup>127</sup>I, including organic forms; it was observed that <sup>129</sup>I/<sup>127</sup>I atomic ratios in the Antarctic surface seawater ((6.1–13) × 10<sup>–12</sup>) are about 2 orders of magnitude lower than those in the Antarctic snow ((6.8–9.5) × 10<sup>–10</sup>), but 4–6 times higher than the prenuclear level (1.5 × 10<sup>–12</sup>), indicating a predominantly anthropogenic source of <sup>129</sup>I in the Antarctic environment. The <sup>129</sup>I level in snow in Antarctica is 2–4 orders of magnitude lower than that in the Northern Hemisphere, but is not significantly higher than that observed in other sites in the Southern Hemisphere. This feature indicates that <sup>129</sup>I in Antarctic snow mainly originates from atmospheric nuclear weapons testing from 1945 to 1980; resuspension and re-emission of the fallout <sup>129</sup>I in the Southern Hemisphere maintains the <sup>129</sup>I level in the Antarctic atmosphere. <sup>129</sup>I directly released to the atmosphere and re-emitted marine discharged <sup>129</sup>I from reprocessing plants in Europe might not significantly disperse to Antarctica
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