The Raman method for lidar water vapor profiling uses
Raman-shifted backscatter from atmospheric water vapor and nitrogen
to retrieve water vapor mixing ratio q(r)
at a distance r as:
where and is a term correcting for the differential
atmospheric transmission at the water vapor and nitrogen Raman wavelengths. The
parameter
, known as the lidar calibration constant, is
actually a complex function of distance and wavelength and can be presented as:
(2)
where: MX and nX are the molecular mass and the number density of species X (air denotes dry air), σX(λ,r) is the Raman cross-section of species X, and OX(r) TX(λ,r) and ηX (r, λ) are respectively the overlap, the instrument transmission function, and the PMT efficiency of the Raman channel X.
The calibration
constant is commonly obtained by comparison of a lidar profile to data from a
reference instrument: a collocated radiosonde, a microwave radiometer, or a GPS
receiver. The thus derived calibration constant has low accuracy mostly because
of the limited accuracy of the reference instruments. Another essential
drawback of this calibration method is that the lidar and the reference
instrument nearly always sample different air masses with different time and
space resolutions, leading to additional systematic errors. Furthermore, the implicitly included atmospheric differential transmission , induces an additional systematic error.
In another approach, known as independent calibration, kH2O is calculated using Equation 2 from measured or modeled cross sections and instrumental parameters. The first applications of the method had low calibration accuracy mostly due to the low accuracy of the Raman cross-sections. Improvements in cross sections modeling allowed better accuracy but still the estimation of the instrumental functions is cumbersome, with limited accuracy and possibilities for systematic errors.
In the calibration
method, presented here, is derived using Equation 1 and
backscatter signals measured with the lidar receiver in a calibration cell
filled with a reference water vapor/air mixture. The reference mixture is prepared
gravimetrically. Since the preparation relays on fundamental principles and
basic units of measurements the reference mixture can be regarded as primary
humidity standard and the obtained in this way lidar calibration constant has
the potential to be traceable to national standards. The new calibration method
eliminates the unavoidable in the cross-calibration methods errors and
uncertainties induced by the reference instrument and by the calibration
procedure. Furthermore, the new method does not require modeling of the Raman cross
sections and estimation or measurement of the instrumental efficiencies, thus
avoiding the related systematic and random errors characteristic for the existing
independent calibration methods. Essential conditions for the successful
application of the method however, is the reduction to negligible levels the range
dependence of: a) the overlap functions ratio and b) the ratio of the integrals
in Equation 2. The High Spatial/Temporal Resolution Raman Lidar (HSTRRL) and
the Raman Lidar for Meteorological Observation (RALMO) built at the EPFL were
specially designed to satisfy the above mentioned conditions.
A lidar calibrated with the described method has the potential to become reference instrument for atmospheric profiling of water vapor and can be used for validation and calibration of other remote instruments for humidity measurements, such as microwave radiometer, balloon sondes, and GPS.
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