Jc. Lambert et al., Investigation of pole-to-pole performances of spaceborne atmospheric chemistry sensors with the NDSC, J ATMOS SCI, 56(2), 1999, pp. 176-193
Spaceborne atmospheric chemistry sensors provide unique access to the distr
ibution and variation of the concentration of many trace species on the glo
bal scale. However. since the measurements and the retrieval algorithms are
sensitive to a variety of instrumental as well as atmospheric sources of e
rror, they need to be validated carefully by correlative measurements. The
quality control and validation of satellite measurements on the global scal
e, as well as in the long term, is one of the goals of the Network for the
Detection of Stratospheric Change (NDSC). Started in 1991, at the present t
ime the NDSC includes five primary and two dozen complementary stations dis
tributed from the Arctic to the Antarctic, comprising a variety of instrume
nts such as UV-visible spectrometers, Fourier transform infrared spectromet
ers, lidars, and millimeter-wave radiometers.
After an overview of the main sources of uncertainty which could perturb th
e measurements from space, and of the ground-based data provided by the NDS
C for their validation, this paper will focus, as an example, on the measur
ement of total ozone by Earth Probe Total Ozone Mapping Spectrometers (TOMS
), ADEOS TOMS and ERS-2 Global Ozone Monitoring Experiment (GOME) and their
validations. The data recorded between summer 1996 and April 1997 by 16 Sy
steme d'Analyse par observations zenithales (SAOZ)NV-visible spectrometers
distributed over a range of latitudes from the Arctic to the Antarctic, and
by Dobson and Brewer spectrophotometers operating at selected sites of the
NDSC alpine and Antarctic stations, are used to investigate the solar zeni
th angle (SZA) dependence, the dispersion, the time-dependent drift, and th
e possible differences of sensitivity of the space-based sensors. Although
the comparison demonstrates an excellent agreement to within +/-2%-4% betwe
en all space- and ground-based instruments at northern middle latitudes, it
also reveals significant systematic features, such as a SZA dependence wit
h TOMS beyond 80 degrees, a seasonal SZA dependence with COME beyond 70 deg
rees, a systematic bias of a few percent between satellite and SAOZ observa
tions of low ozone columns in the southern Tropics, a difference in sensiti
vity to ozone between the COME and ground-based sensors at high latitudes,
and an interhemispheric difference of TOMS with the ground-based observatio
ns.