A new compilation of the atmospheric 85krypton inventories from 1945 to 2000 and its evaluation in a global transport model
- 1. Max-Planck-Institut fuer Meteorologie, Bundesstrasse 55, D-20146 Hamburg (Germany)
- 2. IANUS, Darmstadt University of Technology, Hochschulstr. 4a, D-64289 Darmstadt (Germany)
- 3. Bundesamt fuer Strahlenschutz (BfS), P.O. Box 10 01 49, D-38201 Salzgitter (Germany)
Description
This paper gives the yearly 85Kr emissions of all known reprocessing facilities, which are the main sources of 85Kr in the atmosphere since 1945, for the years 1945 until 2000. According to this inventory 10,600 PBq (Peta = 1015) of 85Kr have been globally emitted from the year 1945 until the end of 2000. The global atmospheric inventory at the end of the year 2000 amounts to 4800 PBq. These emissions have been incorporated into the ECHAM4 atmospheric general circulation model as point sources. Monthly mean model results are compared with measurements made at different locations and times. The influence of each source on the measured concentrations at various locations is studied. The calculated concentrations are found to give reasonably good agreement with the observations, indicating that the emission inventory is realistic. Although, at all northern hemispheric observation sites the model tends to slightly overestimate the concentrations. A possible reason for this overestimation can be found in model features (coarse resolution in time and space). The most prominent discrepancy that is consistently repeated at all northern hemispheric stations occurs in the early 1990s. This could most likely be related to an overestimate of sources. Possibly, the Russian emissions declined earlier than assumed in the current database. Another discrepancy between observations and simulations indicating an incompleteness of the release data is found at some southern hemispheric sites. The variability of their observations could only be explained by regional sources. However, several spikes occur after 1992 when no reprocessing facility is known to be in operation in the southern hemisphere. Production of isotopes for radiopharmaceuticals like technetium-99m from highly enriched uranium is the most likely explanation
Additional details
Identifiers
- DOI
- 10.1016/j.jenvrad.2004.09.005;
- PII
- S0265-931X(04)00288-7;
Publishing Information
- Journal Title
- Journal of Environmental Radioactivity
- Journal Volume
- 80
- Journal Issue
- 2
- Journal Page Range
- p. 183-215
- ISSN
- 0265-931X
- CODEN
- JERAEE
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36046795
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- EMISSION; ENVIRONMENTAL IMPACTS; GENERAL CIRCULATION MODELS; HIGHLY ENRICHED URANIUM; INVENTORIES; KRYPTON 85; NUCLEAR FUELS; POINT SOURCES; RADIOECOLOGICAL CONCENTRATION; RADIOPHARMACEUTICALS; REPROCESSING; SOUTHERN HEMISPHERE; TECHNETIUM 99
- Descriptors DEC
- ACTINIDES; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; DRUGS; EARTH PLANET; ECOLOGICAL CONCENTRATION; ELEMENTS; ENERGY SOURCES; ENRICHED URANIUM; EVEN-ODD NUCLEI; FUELS; HOURS LIVING RADIOISOTOPES; INTERMEDIATE MASS NUCLEI; INTERNAL CONVERSION RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPE ENRICHED MATERIALS; ISOTOPES; KRYPTON ISOTOPES; LABELLED COMPOUNDS; MATERIALS; MATHEMATICAL MODELS; METALS; MICROSECONDS LIVING RADIOISOTOPES; NUCLEI; ODD-EVEN NUCLEI; PLANETS; RADIATION SOURCES; RADIOACTIVE MATERIALS; RADIOISOTOPES; REACTOR MATERIALS; SEPARATION PROCESSES; TECHNETIUM ISOTOPES; URANIUM; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.