The effect of salinity on the concentrations of radium and thorium in sediments
Abstract
The effect of salinity on the sorption behaviour of radium and thorium has
been studied with the aim of assessing the suitability of the 226Ra/232Th
activity ratio (AR) as a tracer in saline waters. Radium has been reported
in the literature as being highly mobile in saline water, and easily
desorbed from sediments, whereas thorium is believed to remain tightly
bound. Results of analyses of bed sediments from an inland river system
with a record of past regimes of high dissolved salt concentrations were
consistent with this behaviour. Radium-226 activity in the bed sediments
was shown to be deficient with respect to its parent, 23°Th, indicating a
loss of radium from the sediments.
A more detailed field study examined the extent of radium loss as a
function of salinity in an estuary. Desorption of ²²⁶Ra from freshwater
suspended sediment increased to a maximum value (58% ±7 of the total
sediment concentration) as the salinity of the estuary rose. Maximum
radium desorption was reached in the 6-10 ppt salinity range. Net
desorption then remained unchanged despite further rises in salinity.
Laboratory experiments indicated that the kinetics of radium desorption is
rapid, with maximum desorption from river sediments reached within 1 h of
contact with saline water. The net radium loss from freshwater sediment
occurs as a result of the competition effects from other dissolved cations
for ion-exchange sites on the sediment. Cation exchange is probably the
dominant mechanism of radium release, although alpha recoil appears to be
at least partly responsible for the higher losses of ²²⁴Ra and ²²³Ra by
increasing their accessibility for ion-exchange reactions.
The effects of solid/liquid ratio and particle size of the sediment on
radium sorption in saline water were also investigated. The results
indicate that, when exposed to saline water, the greatest radium loss from
freshwater sediments will occur from clay sized particles when they are
present in the water column at low concentrations. Proportionally less
radium is desorbed from coarse-grained bed sediments. There was no evidence of any net loss of thorium from sediment as salinity
is increased. In fact, laboratory experiments indicate that the transfer
of dissolved or colloidal thorium onto sediment particles is enhanced in
saline water. From the differing sorption behaviour of radium and thorium
it is concluded that the ²²⁶R a / ²³²Th AR is not a suitable sediment tracer
in saline water. However, the 23° T h / ²³²Th AR can provide a stable tracer
of sediment movement in estuaries and is the preferred sediment tracer in
saline rivers. In some circumstances the ²²⁸R a/²²⁶Ra AR may also be
useful. The dissolved concentrations of all radium isotopes show strongly
non-conservative increases in the Bega estuary. The shorter-1 ived
isotopes, ²²⁴Ra, ²²³Ra and ²²⁸Ra are particularly highly enriched. The
most likely source of these isotopes is the pore water of bottom sediments.
This work has shown that radium isotopes may give information on the rates
and extent of surface-pore water mixing in an estuary.
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