In Sendai, Japan 2000 SPIE Proceedings
Obtaining Calibrated Marine Aerosol Extinction Measurements Using
Horizontal Lidar Measurements, Differential Lidar-Target Measurements and A
Polar Nephelometer.
University of Hawaii
School of Ocean and Earth Science and Technology
Hawaii Institute of Geophysics and Planetology
Honolulu, Hawaii
Lidars are ideal for mapping the spatial distribution
of aerosol concentrations, however efforts to convert the lidar measurements
into estimates of the aerosol extinction or scattering coefficient are usually
complicated. The difficulties arise from the uncertainty in the aerosol
backscatter-to-extinction ratio and the lidar calibration. In marine conditions
with little absorption, the aerosol backscatter-to-extinction ratio is
identical to the aerosol phase function/4π at 180 degrees (backscatter) .
Uncertainty in the lidar calibration is another source of uncertainty, which
can change with time depending on the state of the optics (clean or dirty).
Here we investigate several techniques to obtain calibrated aerosol extinction
coefficient values. The first approach uses horizontal lidar measurements over
the open ocean where the atmosphere is horizontally homogeneous. The lidar
calibration or aerosol phase function is adjusted until the derived aerosol
extinction coefficients are flat with distance. Modeling shows that this
provides correct aerosol extinction values. A second approach uses a target to
reflect the lidar beam at different distances. The aerosol extinction is
derived from the differential transmission measurements. As an independent
measurement, the aerosol phase function and scattering coefficients can be
measured with a polar nephelometer.
Keywords: Lidar calibration, aerosol extinction, aerosol phase function, target calibration
For
a mono-static lidar systems the lidar equation can be written as
(1)
where n(r) is
the photoelectrons (signal) received from distance r and range bin Dr. Eo is the laser pulse
energy at wavelength l. The detector quantum
efficiency is dl, h is Planck’s constant, c is the speed of light,
A is the telescope effective area, and b(r) is the back scattering coefficient at range
r. In the second form of Eq. 1, C
is an overall lidar calibration coefficient, σs(r) is the total
scattering coefficient at range r, and
is the weighted phase
function (for 180 degree scattering angle) at range r. T(r)2
is the atmospheric transmission term to range r and is given by
(2)
The extinction coefficient (se(r))
is the sum of the scattering and absorption coefficients (ss(r)+
sa(r)). The scattering coefficient, ss(r),
is the sum of the aerosol and molecular scattering coefficients (sas (r)+sms(r)).
The absorption coefficient is also due to aerosol absorption and molecular
absorption (saa (r)+sma(r)).
The molecular absorption coefficient (sma(r))
is often negligible because lidar wavelengths are chosen where little
atmospheric absorption occurs. The aerosol phase function in Eq. 1 is the
weighted average of the aerosol and molecular phase functions given by
(3)
where
is the molecular
phase function at range r,
is the aerosol phase function at range r,
is the molecular scattering coefficient at range r,
is the aerosol
scattering coefficient at range r. In using Eq. 1-3 we would like to derive the
aerosol extinction coefficients.
Unfortunately both the
aerosol phase function and lidar calibration are also typically not known. Due
to these difficulties, numerous inversion techniques have been proposed. As
summarized by Reagan et al. (1989), these include the slope method (Collis,
1966), modeled transmission method (Russell et al., 1979), slant path method
(Sandford, 1967), and various methods using a relationship between extinction
and backscatter (Hitschfeld and Bordan, 1954, Fernald et al., 1972, Klett,
1981). Klett also proposed using a known value of the aerosol scattering at a
distant point and solving for the along-path extinction with a backward
stepping approach, which he showed to be more stable than the forward stepping
approach. This approach was found to be very sensitive to the lidar
calibration and the power law relation
between the backscattering coefficient and the extinction coefficient (Hughes
et al., 1985). If the aerosols are horizontally homogeneous then horizontal or
slant measurements can be used to provide boundary values to constrain the
aerosol extinction coefficients (Zhang and Hu, 1997) and even to estimate the
aerosol phase function (Young et al., 1993). Porter et al. (2000) used a
forward stepping approach to derive the aerosol scattering coefficient for open
ocean marine air. In this paper we will expand on the Porter et al. approach to
include absorbing aerosol and discuss several other methods.
The Porter et al. (2000)
forward stepping method of deriving aerosol scattering coefficients is
described. The forward stepping lidar inversion begins by assuming a fixed
aerosol transmission, Ta(r), from the lidar out to range, r~300 m to
step past the near field region where the scattered light cannot be properly
focused on the detector. The molecular transmission, Tm(r),
from the lidar out to the same starting point is calculated based on pressure
and temperature. Beyond this near-field region the inversion is begun by
calculating the aerosol scattering coefficient in the next sample bin at distance
r (r-Dr /2 to r+Dr/2) using
(4)
where equations (1)-(3) have
been combined and solved for the aerosol scattering coefficient. The aerosol
transmission (due to absorption and scattering) from the lidar to the bin is
given by Ta(r)=Ta(r-Dr) DTa(r).
is calculated using the aerosol extinction calculated in eq.
(4). Similarly a new molecular transmission, is calculated by Tm(r)
= Tm(r-Dr) DTm(r)
where
. The molecular scattering coefficient is computed at the
proper pressure and temperature following Lenoble (1993) using the hypsometric
equation for the height dependence. Next a new aerosol scattering coefficient is
calculated in the next sample bin using eq. (5) again. The process is repeated
out to the end of the lidar measurement. A schematic of the forward stepping
approach is given in Fig. 1.

Figure 1. Chart of forward
stepping algorithm.
This forward stepping approach has no restriction on the decreasing transmission and can accumulate large error at longer distances. The error comes from using an incorrect aerosol phase function (at 180 degrees) or wrong lidar calibration (Hughes et al., 1985). Here it is assumed that the lidar is properly aligned and the laser beam is within the collection cone of the receiver optics.
In order to test this forward
stepping approach, we generate pseudo-lidar data by using eq. (1)-(3). For the
model lidar data, the aerosol phase function (phase function at 180 degrees)
value was set to 0.65, to represent marine sea salt. The aerosol scattering
coefficient was set to 5x10-5 m-1. The aerosol absorption
coefficient was set to 0. The aerosol is assumed to be horizontally
homogeneous. The lidar calibration C is set to a fixed value. The
molecular scattering coefficient was set to 1.211x10-5 m-1
corresponding to surface pressure (1013 mb) and 532 nm wavelength. Figure 2
shows the modeled lidar return signal from a horizontal lidar measurement with
homogeneous aerosol. The lidar signal has been plotted versus the aerosol
optical thickness and the distance is shown on the right side. The relationship between the lidar signal
and the 1/r2 term (scaled to fit on the same plot) is also
shown as a function of optical thickness. Noise has also been introduced to
simulate digitization and electronic noise.
Using
the forward stepping approach described above, the aerosol scattering
coefficient is derived from the model-generated data using correct and
incorrect values of the aerosol phase function (at 180 degree). These results
are shown in Fig. 3, where it can be seen that the error increases with
distance when wrong values of the phase function are used. As expected, using
the correct aerosol phase function value, yields the correct aerosol scattering
coefficient (5x10-5 m-1) at all distances. Greater error
results if the aerosol phase function is underestimated than if overestimated.
If the aerosol phase function is overestimated the drop-off with range is not
so strong and might appear as a straight line if measurements are not made to
large enough optical depths. Using incorrect values for the lidar calibration
value (C) cause similar errors to those shown in Figure 3. In fact,
incorrect lidar calibration and incorrect aerosol phase function values can be
combined to produce derived extinction values which are constant with range and
have the correct extinction value.

Figure 2. Pseudo lidar signal generated from Eq. 1
as a function of aerosol optical depth.

Figure 3. Aerosol
extinction coefficient derived from forward stepping approach.
The
calculations done above have assumed no aerosol absorption. Figure 4 shows the
results when the aerosol absorption is included in the generation of the lidar
data. For these test the aerosol scattering and absorption coefficient values
were set to 5x10-5m-1
(aerosol single
scatter albedo of 0.5). In the inversion the aerosol were assumed to be only
scattering with no absorption. It can be seen that the derived values are not
constant with range and are less than the correct value. If the aerosol phase
function is manually adjusted so that the derived scattering coefficients are
constant with range (Fig. 5)

Figure 4 Aerosol extinction
coefficients derived from forward stepping approach.

Figure 5. Aerosol extinction coefficients derived from
forward stepping approach.
then
the derived extinction values are correct (10e-5 m-1) but
an incorrect aerosol phase function value (0.323) must be used.
When
aerosol absorption is present in the lidar data and is not used in the forward
stepping inversion (as Fig. 5), the ratio of the aerosol single scatter albedo
is equal to the ratio of the phase function required to obtain constant
extinction values with distance over the correct phase function. From the
examples shown in Figs. 3-5, it can be
seen that varying either the aerosol phase or the lidar calibration (Porter et
al., 2000) can adjust the derived aerosol extinction values so that they are
constant with range. When this is done the resulting extinction values are
correct for both absorbing and non-absorbing aerosol.
4.
TARGET
CALIBRATION APPROACH
Equation
1 can be rearrange into the following equation
(5)

Equation 5 has the form of a straight line and
can be plotted with
(y values) plotted
versus r (x values). The slope of the data is then
, and the zero intercept is
(Reagan, 1995). While
this approach is excellent for deriving the extinction coefficient (
), it is difficult to derive the lidar calibration, C,
because the backscattering coefficient, β(r), is often unknown due to uncertainty in the aerosol
properties. As a modification to this
approach, we have begun testing a new method to calibrate our lidar using a
moving target and measuring the return pulse from the target. In this case, the
backscattering coefficient is due to the properties of the target, which is
presumably well known. Therefore, the
lidar calibration can be derived by fitting a line to the data and
extrapolating the line back to the zero intercept.
Figure
6. Lidar signal measured from a dark Spectralon target at different distances.
Figure
6 shows our preliminary lidar measurements made using a dark spectralon target
at different distances. It can be seen that the signal is strongly attenuated
in the near field. This near field effect is expected due to the central
obstruction in our Schmidt-Cassegrain mono-static lidar (Sharma et. al., 1998;
Lienert, et al., 1999). Past approximately 75 m the target signal appears to
drops off with roughly a 1/r2 dependence but continues to be
affected by the near field effect as well. Based on modeling studies our lidar
system we estimate that the target measurements need to be made at a distance
greater than 300 m to avoid any significant near field effects. We will be
carrying out additional test with this promising approach.
5.
POLAR NEPHELOMETER METHOD

For non-absorbing aerosol, an additional way to
test our lidar measurements is to measure the aerosol phase function and
scattering coefficient. Doherty et al. (1989) have made measurements of the
aerosol phase function at backscattering angles in a closed system. We are
currently developing two open-air polar nephelometers, which will measure the
aerosol phase function and scattering coefficient. These systems are
improvements over our earlier CW system (Porter et al., 1997). The new systems
use an Nd-YAG pulsed laser with light at 1064, 532 and 355 nm. Either a PMT or
APD detector is used depending on wavelength. Angular measurements are made
every 1-degree (2-178 degrees) with our larger ground based system and every 6
degrees (6-174 degrees) with our aircraft system. Figure 7 shows some
measurements made a Bellows Beach in Hawaii. These test measurements were made
before the system was complete and include both polarization components of
polarized laser light scattered from the aerosol. Both systems are currently
under final modifications and we expect to begin making measurements soon.
Figure 7. Aerosol phase
function measurements at a coastal site.
6.
CONCLUSION
While
calibration of Mie-Rayleigh lidars is challenging, various techniques do exist
to convert the measurements into standard optical values such as extinction and
scattering coefficients. We have found that the horizontal method is very
useful and easy to implement and can give accuracies better than 25%. Although
the target method has promise, it requires measurements over a long distance to
avoid near field effects on the lidar calibration. Finally, the addition of new
instruments such as the open air polar nephelometers will provide important
validation data sets such the aerosol phase function and aerosol scattering
coefficient near the lidar site.
We would like to thank Steve
Ackleson and Ron Ferek for their support. The work carried out here was funded
by an ONR grant # N00014-96-1-0317.
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