Search NASA⌕ Search

Engineering topics

Granier, C.

Publications and source records attributed to Granier, C..

Atmospheric Composition Change: Climate-Chemistry Interactions

Chemically active climate compounds are either primary compounds such as methane (CH4), removed by oxidation in the atmosphere, or secondary compounds such as ozone (O3), sulfate and organic aerosols, formed and removed in the atmosphere. Man-induced climate-chemistry interaction is a two-way process: Emissions of pollutants change the atmospheric composition contributing to climate change through the aforementioned climate components, and climate change, through changes in temperature, dynamics, the hydrological cycle, atmospheric stability, and biosphere-atmosphere interactions, affects the atmospheric composition and oxidation processes in the troposphere. Here we present progress in our understanding of processes of importance for climate-chemistry interactions, and their contributions to changes in atmospheric composition and climate forcing. A key factor is the oxidation potential involving compounds such as O3 and the hydroxyl radical (OH). Reported studies represent both current and future changes. Reported results include new estimates of radiative forcing based on extensive model studies of chemically active climate compounds such as O3, and of particles inducing both direct and indirect effects. Through EU projects such as ACCENT, QUANTIFY, and the AEROCOM project, extensive studies on regional and sector-wise differences in the impact on atmospheric distribution are performed. Studies have shown that land-based emissions have a different effect on climate than ship and aircraft emissions, and different measures are needed to reduce the climate impact. Several areas where climate change can affect the tropospheric oxidation process and the chemical composition are identified. This can take place through enhanced stratospheric-tropospheric exchange of ozone, more frequent periods with stable conditions favouring pollution build up over industrial areas, enhanced temperature-induced biogenic emissions, methane releases from permafrost thawing, and enhanced concentration through reduced biospheric uptake. During the last 510 years, new observational data have been made available and used for model validation and the study of atmospheric processes. Although there are significant uncertainties in the modelling of composition changes, access to new observational data has improved modelling capability. Emission scenarios for the coming decades have a large uncertainty range, in particular with respect to regional trends, leading to a significant uncertainty range in estimated regional composition changes and climate impact.

Atmosphere climate chemistry↗

Lidar detection of metallic species at the mesopause level

The measurement alkali species present in the atomic form at the mesopause level has been performed by lidar for more than ten years. Atomic and ionic calcium density profiles are obtained for 3 years by the same technique in the visible range, at 423 nm for atomic calcium, and 393 nm for ionic calcium Ca(+). The experimental set-up and the preliminary results have been presented elsewhere. The 423 nm wavelength is directly obtained by the emission of a dye laser pumped by the third harmonic of a Nd-YAG laser. For the generation of the 393 nm wavelength, frequency mixing was used: the emission at 624 nm of a dye laser pumped by the 2nd harmonic of a Nd-Yag laser is mixed with the fundamental infrared emission (remaining after frequency doubling), in a non-linear KDP crystal, which gives the 393 nm emission. The behavior of the two atomic species, calcium and sodium, which are in the same altitude range are compared. For 45% of the observations, no ionic calcium was detected: the ionic calcium abundance was thus below the detection threshold. Contrasting with the density profiles of the atomic species, sodium and calcium, the ionic calcium profile present important variations on small time scales. The main characteristics of theatomic and ionic calcium behaviors that can be deduced from the measurements made are given.

Granier, C.↗