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The explicit bin-resolving microphysics model is an accurate moment-conserving
scheme, described in detail in Tzivion et al. [1987, 1989] and
Stevens et al. [1996a]. A brief description of the explicit microphysics
model is given below. In this scheme, both the mass and the number mixing
ratios are predicted for each bin. A total of 25 bins cover a drop spectrum
ranging from 1.56-504
(radius), with mass doubling from one bin to
the next. Predictive equations for both the mass and the number mixing
ratios in each bin require an additional 50 scalars for the liquid cloud
related processes: condensation/evaporation, collision-coalescence, droplet
activation from CCN, and sedimentation.
In some of our prior studies [Stevens et al., 1996a] a rather simple
drop activation scheme was implemented whereby CCN were assumed to
have a constant (in time and space) size distribution and activation was
calculated such that the the number of cloud drops was based
on the model-derived supersaturation but could not exceed the number
concentration of CCN. Thus, at each time step the drop concentration
Nd was incremented by an amount
![\begin{displaymath}\Delta N_d = {\rm max} [0, ~ N_{ccn} \int_{r_{cut}}^\infty f(r; r_g, \sigma_g) dr
- \sum_{k=1}^{25} N_k ]
\end{displaymath}](img4.gif) |
(1) |
where Nccn is the total CCN concentration, rcut is the
smallest radius of CCN activated at the ambient supersaturation S, rgis the median radius of CCN,
is the geometric standard deviation
of the CCN radii, and Nk is the number concentration of drops in size
bin k. In order to explore aerosol-cloud interactions one would ideally
like to model the size resolved aerosol spectrum [e.g.,
Feingold et al., 1996b]
as well as the drop size distribution response to the aerosol spectrum.
Due to the large computational expense of these simulations we opted for a
more simplified droplet activation scheme based on equation(1).
We assume that the CCN size distribution is constant throughout the model
domain (i.e., rg and
are constant), and that only Nccn
varies as one passes from the clean boundary layer to the rather polluted
air aloft. The representation of the aerosol is reduced to prognosing
Nccn, rather than a set of parameters that describe the full distribution
of CCN particles. For the goals of our study, we feel that this
representation is sufficient, although we recognize that variations in both the
size distribution and chemical composition of the particles may have
significant impact under certain circumstances [Feingold et al., 1999].
Note that outside of cloud the prognosed field Nccn is the
number concentration of CCN in cm-3 whereas within the cloud, it
represents the potential number of drops that can be activated, and not the
number concentration of unscavenged CCN.
The latter can easily be calculated as
|
Nunscavenged = Nccn - Nd
|
(2) |
Unlike Feingold et al. [1996b], CCN particles are not tracked within
drops and the current simplified treatment has an inherent assumption that
the CCN concentration would be unmodified (in both number and size)
on complete evaporation of
drops. For clouds with very weak collision-coalescence such as the cases
examined here, this is quite reasonable.
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