SCIAMACHY (Scanning Imaging Absorption Spectrometer for Atmospheric Chartography) is a spectrometer designed to measure sunlight transmitted, reflected, and scattered by the earth's atmosphere or surface in the ultraviolet, visible, and near-infrared wavelength region (240-2380 nm) at moderate spectral resolution (0.2-1.5 nm, /⌬ ഠ 1000-10 000). SCIAMACHY will measure the earthshine radiance in limb and nadir viewing geometries and solar or lunar light transmitted through the atmosphere observed in occultation. The extraterrestrial solar irradiance and lunar radiance will be determined from observations of the sun and the moon above the atmosphere. The absorption, reflection, and scattering behavior of the atmosphere and the earth's surface is determined from comparison of earthshine radiance and solar irradiance. Inversion of the ratio of earthshine radiance and solar irradiance yields information about the amounts and distribution of important atmospheric constituents and the spectral reflectance (or albedo) of the earth's surface. SCIAMACHY was conceived to improve our knowledge and understanding of a variety of issues of importance for the chemistry and physics of the earth's atmosphere (troposphere, stratosphere, and mesosphere) and potential changes resulting from either increasing anthropogenic activity or the variability of natural phenomena. Topics of relevance for SCIAMACHY are R tropospheric pollution arising from industrial activity and biomass burning, R troposphere-stratosphere exchange processes, R stratospheric ozone chemistry focusing on the understanding of the ozone depletion in polar regions as well as in midlatitudes, and R solar variability and special events such as volcanic eruptions, and related regional and global phenomena. Inversion of the SCIAMACHY measurements enables the amounts and distribution of the atmospheric constituents O 3 , O 2 , O 2 (1 ⌬), O 4 , BrO, OClO, ClO, SO 2 , H 2 CO, NO, NO 2 , NO 3 , CO, CO 2 , CH 4 , H 2 O, N 2 O, and aerosol, as well as knowledge about the parameters pressure p, temperature T, radiation field, cloud cover, cloudtop height, and surface spectral reflectance to be determined. A special feature of SCIAMACHY is the combined limb-nadir measurement mode. The inversion of the combination of limb and nadir measurements will enable tropospheric column amounts of O 3 , NO 2 , BrO, CO, CH 4 , H 2 O, N 2 O, SO 2 , and H 2 CO to be determined.

Emissions from fossil fuel combustion and biomass burning reduce local air quality and affect global tropospheric chemistry. Nitrogen oxides are emitted by all combustion processes and play a key part in the photochemically induced catalytic production of ozone, which results in summer smog and has increased levels of tropospheric ozone globally. Release of nitrogen oxide also results in nitric acid deposition, and--at least locally--increases radiative forcing effects due to the absorption of downward propagating visible light. Nitrogen oxide concentrations in many industrialized countries are expected to decrease, but rapid economic development has the potential to increase significantly the emissions of nitrogen oxides in parts of Asia. Here we present the tropospheric column amounts of nitrogen dioxide retrieved from two satellite instruments GOME and SCIAMACHY over the years 1996-2004. We find substantial reductions in nitrogen dioxide concentrations over some areas of Europe and the USA, but a highly significant increase of about 50 per cent-with an accelerating trend in annual growth rate-over the industrial areas of China, more than recent bottom-up inventories suggest.

[1] We construct global budgets of atmospheric glyoxal and methylglyoxal with the goal of quantifying their potential for global secondary organic aerosol (SOA) formation via irreversible uptake by aqueous aerosols and clouds. We conduct a detailed simulation of glyoxal and methylglyoxal in the GEOS-Chem global 3-D chemical transport model including our best knowledge of source and sink processes. Our resulting best estimates of the global sources of glyoxal and methylglyoxal are 45 Tg a À1 and 140 Tg a À1 , respectively. Oxidation of biogenic isoprene contributes globally 47% of glyoxal and 79% of methylglyoxal. The second most important precursors are acetylene (mostly anthropogenic) for glyoxal and acetone (mostly biogenic) for methylglyoxal. Both acetylene and acetone have long lifetimes and provide a source of dicarbonyls in the free troposphere. Atmospheric lifetimes of glyoxal and methylglyoxal in the model are 2.9 h and 1.6 h, respectively, mostly determined by photolysis. Simulated dicarbonyl concentrations in continental surface air at northern midlatitudes are in the range 10-100 ppt, consistent with in situ measurements. On a global scale, the highest concentrations are over biomass burning regions, in agreement with glyoxal column observations from the SCIAMACHY satellite instrument. SCIAMACHY and a few ship cruises also suggest a large marine source of dicarbonyls missing from our model. The global source of SOA from the irreversible uptake of dicarbonyls in GEOS-Chem is 11 Tg C a À1 , including 2.6 Tg C a À1 from glyoxal and 8 Tg C a À1 from methylglyoxal; 90% of this source takes place in clouds. The magnitude of the global SOA source from dicarbonyls is comparable to that computed in GEOS-Chem from the standard mechanism involving reversible partitioning of semivolatile products from the oxidation of monoterpenes, sesquiterpenes, isoprene, and aromatics.

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