Page 172 - Soil and water contamination, 2nd edition
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Radionuclides                                                         159
                   Iodine-131
                   Iodine-131 is only short-lived (half-life 8.04 d) and is therefore highly radioactive, but only
                   significantly so in the first weeks after a release of radionuclides  into the environment. Iodide
                   (I ) is the primary species of I in soil except under exceptional arid and alkaline conditions.
                     -
                   Iodide sorbs poorly to most soil materials, but can be taken up by some clays, organic
                                                                                   131
                   matter, and metal sulphides (Zhang et al., 2002). The main exposure pathway of  I is from
                                                 131
                   cow’s milk. Cows that have ingested  I deposited on the leaves of grass transfer it rapidly
                   to their milk. Radioiodine is easily accumulated in the thyroid gland, especially in humans
                                                                                         131
                   who suffer iodine shortage, and so may induce thyroid cancer. The biological half-life  of  I
                   is approximately 100 days in the thyroid, 14 days in bone, and 7 days in the kidney and
                   reproductive organs.
                   Caesium-137
                                                                   +
                   Caesium is chemically similar to potassium  and occurs as Cs  cation in soil and water. It is
                   very soluble but also readily adsorbed by clay minerals . Directly after atmospheric deposition
                                                                        137
                   of radiocaesium, it is very mobile in runoff water, but the bulk of   Cs is adsorbed by soil
                   materials in the topsoil. Fixation of caesium by illitic clay minerals causes the mobility and
                   bioavailability  to decrease by a factor of ten during the first five years after initial deposition.
                   After this period, the decrease of bioavailability follows radioactive decay  (half-life 30.17 y)
                   (Smith et al., 2000). The gamma radiation  emitted by decay product   137m Ba (see Table 8.6)
                   is of most concern from a health perspective. Caesium-137 uptake by crops is the main
                   pathway of Cs transfer into the animal and human food chains. Since Cs competes with
                   potassium,   137 Cs uptake is greater in soils with low potassium content. Like potassium, Cs
                   tends to be absorbed in neural and muscle tissues. The average biological half-life  of   137 Cs
                   is about 45 days. Furthermore, radiation  from soil contaminated by   137 Cs contributes
                   significantly to external radiation exposure.


                   Strontium-90
                       137
                            90
                   Like  Cs,  Sr has a relative long radioactive half-life (28.64 y) and is readily absorbed by
                                      2+
                   plants in the form of Sr . It is chemically similar to calcium  and therefore accumulates in
                   bone and bone marrow. Since Sr is not specifically adsorbed by clay minerals , it is more
                   mobile than  Cs in soil and water.
                             137
                   Plutonium
                   Plutonium and other transuranic elements do not exist naturally, with the exception of the
                   small amounts of Pu generated by natural fission. Natural fission is very rare and is only
                   found in a few locations: for example, the Oklo natural reactor in Gabon. In general,
                   plutonium exhibits a complex and diverse geochemistry. It may change its oxidation state
                   due to slight changes in redox potential and often two or more of its oxidation states co-exist
                   (Runde, 2002). At the low concentrations in which they occur under natural conditions in
                   soil and water, the major process that determines their environmental behaviour is sorption
                   onto particulates and clay mineral surfaces. Surface contamination, rather than uptake by
                   plant roots, is the main pathway of Pu accumulation in plants and crops (Zhang  et al.,
                   2002). Although there is some controversy about whether Pu is one of the most dangerous
                   substances known, there is no doubt that it is very toxic. Therefore, the toxicity  of Pu as a
                   heavy metal accumulating in the bone and liver is likely to be greater than its radiotoxicity,
                   which is relatively low due to the relatively long physical half-lives. Nevertheless, most Pu
                     isotopes are alpha emitters and may induce lung cancer when inhaled: for example, due to
                   airborne resuspension  of contaminated soil particles by wind erosion  .











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