Institut de Radioprotection et de Sûreté Nucléaire, Laboratoire de Radioécologie de Cherbourg-Octeville, IRSN/PSE-ENV/SRTE/LRC, Rue max Pol Fouchet, BP 10, 50130 Octeville, France; Institut Français de Recherche pour l'Exploitation de la Mer, Laboratoire Océan Côtier, IFREMER/PDG-ODE/LOPS/OC, Centre Bretagne - ZI de la Pointe du Diable, 29280 Plouzané, France.
Institut de Radioprotection et de Sûreté Nucléaire, Laboratoire de Radioécologie de Cherbourg-Octeville, IRSN/PSE-ENV/SRTE/LRC, Rue max Pol Fouchet, BP 10, 50130 Octeville, France.
Sci Total Environ. 2019 Mar 15;656:1289-1303. doi: 10.1016/j.scitotenv.2018.11.448. Epub 2018 Nov 30.
Tritium concentrations in oceans were compiled from the literature, online databases and original measurements in order to determine the global distribution of tritium concentrations according to latitude and depth in all oceans. The total inventory of tritium decay corrected in 2016 has been estimated using evaluation of the natural and artificial contributions in 23 spatial subdivisions of the total ocean. It is determined equal to 26.8 ± 14 kg including 3.8 kg of cosmogenic tritium. That is in agreement with the total atmospheric input of tritium from nuclear bomb tests and the natural inventory at steady-state estimated from natural production rates in the literature (27.8-29.3 kg in the Earth). We confirm the global increase in tritium according to latitude observed in the Northern hemisphere since 1967 with a maximum in the Arctic Ocean. The minimum tritium concentrations observed in the Southern Ocean were close to steady-state with known natural tritium deposition. We focused on the temporal evolution of surface (0 to 500 m) tritium concentrations in a selected area of the North Atlantic Ocean (30°N-60°N) where we found the 2016 concentration to be 0.60 ± 0.10 TU (1σ). Results showed that in that area, between 1988 and 2013, tritium concentrations: i) decreased faster than the sole radioactive decay, due to a mixing with lower and lateral less concentrated waters, and ii) decreased towards an apparent steady state concentration. The half-time mixing rate of surface waters and the steady state concentration were respectively calculated to be 23 ± 5 years (1σ) and 0.38 ± 0.07 TU (1σ). This apparent steady-state concentration in the North Atlantic Ocean implies a mean tritium deposition of 1870 ± 345 Bq·m (1σ), five folds higher than the known inputs (natural, nuclear tests fallout and industrial releases, ~367 Bq·m) in this area.
为了根据纬度和深度确定所有海洋中氚浓度的全球分布,我们从文献、在线数据库和原始测量中汇编了海洋中的氚浓度数据。使用对 23 个海洋总区划中天然和人为贡献的评估,估算了 2016 年经修正的氚衰变质点的总存量。估计值为 26.8±14kg,其中包括 3.8kg 的宇宙成因氚。这与从核爆炸试验中输入大气的氚的总量以及从文献中的天然生成率估算的稳定态天然库存(地球中的 27.8-29.3kg)相符。我们确认了自 1967 年以来北半球观测到的与纬度相关的全球氚增加,在北冰洋达到最大值。在南大洋观测到的氚浓度最低接近稳定态,与已知的天然氚沉积量相符。我们专注于北大西洋(30°N-60°N)选定区域的表层(0 至 500m)氚浓度的时间演变,发现 2016 年的浓度为 0.60±0.10TU(1σ)。结果表明,在该区域,1988 年至 2013 年间,氚浓度:i)由于与较低和侧向浓度较低的水混合,衰减速度快于放射性衰变,ii)朝着明显的稳定状态浓度衰减。表层水的混合半衰期和稳定状态浓度分别计算为 23±5 年(1σ)和 0.38±0.07TU(1σ)。北大西洋海洋中的这种明显的稳定态浓度意味着该地区的氚平均沉积量为 1870±345Bq·m(1σ),是该地区已知输入(天然、核试验沉降物和工业排放,~367Bq·m)的五倍。