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Understanding the impact of aerosols on the earth's radiation budget and the long-term climate record requires consistent measurements of aerosol properties and radiative fluxes. The Clouds and the Earth's Radiant Energy System (CERES) Science Team combines satellite-based retrievals of aerosols, clouds, and radiative fluxes into Single Scanner Footprint (SSF) datasets from the Terra and Aqua satellites. Over ocean, two aerosol products are derived from the Moderate Resolution Imaging Spectroradiometer (MODIS) using different sampling and aerosol algorithms. The primary, or M, product is taken from the standard multispectral aerosol product developed by the MODIS aerosol group while a simpler, secondary [Advanced Very High Resolution Radiometer (AVHRR) like], or A, product is derived by the CERES Science Team using a different cloud clearing method and a single-channel aerosol algorithm. Two aerosol optical depths (AOD), [[tau].sub.a1] and [[tau].sub.a2], are derived from MODIS bands 1 (0.644 [micro]m) and 6 (l.632 [micro]m) resembling the AVHRR/3 channels 1 and 3A, respectively. On Aqua the retrievals are made in band 7 (2.119 [micro] m) because of poor quality data from band 6. The -respective Angstrom exponents can be derived from the values of [tau]. The A product serves as a backup for the M product. More importantly, the overlap of these aerosol products is essential for placing the 20 year heritage AVHRR aerosol record in the context of more advanced aerosol sensors and algorithms such as that used for the M product. This study documents the M and A products, highlighting their CERES SSF specifics. Based on 2 weeks of global Terra data, coincident M and A AODs are found to be strongly correlated in both bands. However. both domains in which the M and A aerosols are available, and the respective [tau]/[alpha] statistics significantly differ because of discrepancies in sampling due to differences in cloud and sun-glint screening. In both aerosol products, correlation is observed between the retrieved aerosol parameters ([tau]/[alpha]) and ambient cloud amount, with the dependence in the M product being more pronounced than in the A product.

For an 8-month period aerosol optical depth (AOD) is compared, derived over global oceans with five different retrieval algorithms applied to four satellite instruments flown on board three satellite platforms. The Advanced Very High Resolution Radiometer (AVHRR) was flown on hoard NOAA-14, the Ocean Color and Temperature Scanner (OCTS) and the Polarization and Directionality of the Earth's Reflectances (POLDER) on board the Advanced Earth Observing Satellite (ADEOS), and the Total Ozone Mapping Spectrometer (TOMS) on board the Earth Probe satellites. The aerosol data are presented on the same format and converted to the same wavelength in the comparison and can therefore be a useful tool in validation of global aerosol models, in particular models that can be driven with meteorological data for the November 1996 to June 1997 period studied here. Large uncertainties in the global mean AOD are found. There is at least a factor of 2 difference between the AOD from the retrievals. The largest uncertainties are found in the Southern Hemisphere, and the smallest differences mostly near the continents in the Northern Hemisphere. The largest relative differences are probably caused by differences in cloud screening.

Aerosol radiative forcing is a critical, though variable and uncertain, component of the global climate. Yet climate models rely on sparse information of the aerosol optical properties. In situ measurements, though important in many respects, seldom provide measurements of the undisturbed aerosol in the entire atmospheric column. Here, 8 yr of worldwide distributed data from the AERONET network of ground-based radiometers were used to remotely sense the aerosol absorption and other optical properties in several key locations. Established procedures for maintaining and calibrating the global network of radiometers, cloud screening, and inversion techniques allow for a consistent retrieval of the optical properties of aerosol in locations with varying emission sources and conditions. The multiyear, multi-instrument observations show robust differentiation in both the magnitude and spectral dependence of the absorption--a property driving aerosol climate forcing, for desert dust, biomass burning, urban-industrial, and marine aerosols. Moreover, significant variability of the absorption for the same aerosol type appearing due to different meteorological and source characteristics as well as different emission characteristics are observed. It is expected that this aerosol characterization will help refine aerosol optical models and reduce uncertainties in satellite observations of the global aerosol and in modeling aerosol impacts on climate.