Environmental Modelling and Software 122 (2019) 104523
R. Peridfiez et al,
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ig. 4. Example of water circulation obtained from an ocean model. It corresponds to the average surface circulation in March 2011. The model is FORA (Four-dimensional
/ariational Ocean ReAnalysis model; (Usui et al., 2016). This type of velocity vectors are used in Eulerian and Lagrangian dispersion models to evaluate advective transport of
-adionuclides in the water column, and often also diffusion coefficients.
POM, Priceton Ocean Model. POM'? was first described by Blum-
berg and Mellor (1987). It is a sigma coordinate (terrain-
following), free surface ocean model with embedded turbulence
and wave sub-models, as well as wet-dry capability. This model
has been used since the 1980s, and continues with innovative
new developments until today.
ROMS.!? The 3D baroclinic free-surface, terrain-following, primitive
equations (Haidvogel et al., 2000; Shchepetkin and McWilliams,
2009) are solved. The model, widely used for different appli-
sations, includes ice and sediment transport modules, and the
two-way nesting package AGRIF. Model equations are evaluated
using orthogonal curvilinear coordinates in the horizontal and
terrain-following coordinates in the vertical.
SELFE/SCHISM. The 3D primitive equation model SELFE (Zhang and
Battista, 2008; Roland et al., 2012) renamed now as SCHISM'*
is an open-source community supported modelling system with
an embedded wave model and a sediment transport model as
well. This model is based on unstructured grids and localized
sigma coordinates with shaved cell (LSC?), designed for seamless
simulation of 3D baroclinic circulation across the scales.
These models were used in many radionuclide transport calculations
’e.g. Kobayashi et al., 2007; Miyazawa et al., 2012; Tsumune et al,,
2012, 2013; Periäfez et al., 2016b; Maderich et al., 2017).
3.4. Water/sediment interactions and other processes
Radionuclide exchange between the dissolved and solid phases is a
significant process in the transport of non-conservative radionuclides in
he marine environment. A good general review is given in the book by
Duursma and Carroll (1996). Water-sediment interactions are schemat-
jcally shown in Fig. 5 (Maderich et al., 2017). In the water column,
12 http://www.ecepo.odu.edu/POMWEB/.
13 https://www.myroms.org/
14 http://cerm.vims.edu/schism/.
radionuclides in the dissolved and particulate phases are transported by
currents (advection processes) and turbulent diffusion. Radionuclides
in the dissolved phase interact with the particulate phase in suspended
sediments and bottom deposits. Exchange of activity between the dis-
solved and particulate phases is described by adsorption/desorption
processes. Settling of contaminated suspended sediments and bottom
erosion result in radionuclide exchanges between the bottom and sus-
pended sediment. The transfer of activity between the water column
and the pore water in the bottom sediment is governed by bottom
boundary layer turbulence regulated diffusional processes (Maderich
et al, 2017). The migration of activity in the sediments is due to
molecular diffusion, diffusion driven by bioturbation, bioirrigation and
also due to advection driven by surface waves and by subsurface
groundwater flow (Maderich et al., 2017). A basic microscopy theory
of radionuclide water/suspended sediment interactions was given by
Abril (1998).
Radionuclide transfers between water and sediments were initially
described in models in terms of the equilibrium distribution coefficient,
ky, of the considered radionuclide [as for instance in the models by
Abril and Garcia-Le6n (1993)]. The marine distribution coefficient for
a given radionuclide, k,, is defined (Carroll et al., 1999; Johansson
et al., 2001; IAEA, 2004; Takata et al., 2016; Periäfez et al., 2018)
as the ratio between the radionuclide concentration in the solid phase
(suspended matter or bed sediment) and the concentration in water
(dissolved phase):
C;
ka = Sr’
where C, and C,, are, respectively, radionuclide concentrations in the
solid (Bq kg!) and dissolved (Bq m7®) phases. Such concentrations
have to be at equilibrium, ie., after the partition of the radionuclide
between phases has reached equilibrium. This k, is measured in SI units
of m’kg-1, Table 1 summarizes recommended k, values (IAEA, 2004)
for ocean margin and open ocean and for a number of elements,
Thus, in the first models it was assumed that partition of the ra-
dionuclide between the liquid and solid (suspended matter and/or bed
sediments) achieves instantaneous equilibrium. From the radionuclide
concentration in water, knowing the radionuclide k,, concentration in