Published January 2015 | Version v1
Journal article

Tritium and 14C background levels in pristine aquatic systems and their potential sources of variability

  • 1. Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PRP-ENV, SESURE/LERCM, BP 3, 13115 Saint-Paul-lès-Durance (France)
  • 2. Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PRP-ENV, STEME/LMRE, Le Bois des Rames, 91400 Orsay (France)
  • 3. CEREGE, Aix-marseille Université-CNR-IRD-Collège de France, Europôle Méditerranéen de l'Arbois, BP80, 13545 Aix-en-Provence (France)
  • 4. ANDRA, 1 Rue Jean Monnet, 92298 Châtenay Malabry (France)

Description

Tritium and 14C are currently the two main radionuclides discharged by nuclear industry. Tritium integrates into and closely follows the water cycle and, as shown recently the carbon cycle, as does 14C (Eyrolle-Boyer et al., 2014a, b). As a result, these two elements persist in both terrestrial and aquatic environments according to the recycling rates of organic matter. Although on average the organically bound tritium (OBT) activity of sediments in pristine rivers does not significantly differ today (2007–2012) from the mean tritiated water (HTO) content on record for rainwater (2.4 ± 0.6 Bq/L and 1.6 ± 0.4 Bq/L, respectively), regional differences are expected depending on the biomass inventories affected by atmospheric global fallout from nuclear testing and the recycling rate of organic matter within watersheds. The results obtained between 2007 and 2012 for 14C show that the levels varied between 94.5 ± 1.5 and 234 ± 2.7 Bq/kg of C for the sediments in French rivers and across a slightly higher range of 199 ± 1.3 to 238 ± 3.1 Bq/kg of C for fish. This variation is most probably due to preferential uptake of some organic carbon compounds by fish restraining 14C dilution with refractory organic carbon and/or with old carbonates both depleted in 14C. Overall, most of these ranges of values are below the mean baseline value for the terrestrial environment (232.0 ± 1.8 Bq/kg of C in 2012, Roussel-Debet, 2014a) in relation to dilution by the carbonates and/or fossil organic carbon present in aquatic systems. This emphasises yet again the value of establishing regional baseline value ranges for these two radionuclides in order to account for palaeoclimatic and lithological variations. Besides, our results obtained from sedimentary archive investigation have confirmed the delayed contamination of aquatic sediments by tritium from the past nuclear tests atmospheric fallout, as recently demonstrated from data chronicles (Eyrolle-Boyer et al., 2014a,b). Thus Sedimentary archives can be successfully used to reconstruct past 14C and OBT levels. Additionally, sediment repositories potentially represent significant storages of OBT that may account for in case of further remobilisation. We finally show that floods can significantly affect the OBT and 14C levels within suspended particles or sediments depending on the origin of particles reinforcing the need to acquire baseline value range at a regional scale. - Highlights: • Currently OBT activity of sediments in pristine rivers does not significantly differ from the mean HTO content of rain waters (2.4 ± 0.6 Bq/L and 1.6 ± 0.4 Bq/L, respectively). • Nevertheless regional discrepancies from these mean values are expected depending on the biomass inventories affected by atmospheric global fallout from nuclear testings and the recycling rate of organic matter within watersheds. • 14C levels in pristine rivers vary between 94.5 ± 1.5 and 234 ± 2.7 Bq/kg of C for the sediments and across a slightly higher range of 199 ± 1.3 to 238 ± 3.1 Bq/kg of C for fishes. • These 14C ranges of values overall are below the mean baseline value for the terrestrial environment (232.0 ± 1.8 Bq/kg of C in 2012) in relation with dilution by carbonates and/or fossil organic carbon present in aquatic systems. • OBT and 14C levels downstream of liquid discharges from nuclear facilities are largely affected by inputs from pristine tributaries, floods origin and chronologies

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jenvrad.2014.09.015

Additional details

Identifiers

DOI
10.1016/j.jenvrad.2014.09.015;
PII
S0265-931X(14)00281-1;

Publishing Information

Journal Title
Journal of Environmental Radioactivity
Journal Volume
139
Journal Page Range
p. 24-32
ISSN
0265-931X
CODEN
JERAEE

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.