ALBERT

Description: Every year, a dense smoke haze covers a large portion of South America originating from fires in the Amazon Basin and central parts of Brazil during the dry/biomass-burning season between August and October. Over a large portion of South America, the average aerosol optical depth at 550 nm exceeds 1.0 during the fire season while the background value during the rainy season is below 0.2. Biomass burning aerosol particles increase scattering and absorption of the incident solar radiation. The regional-scale aerosol layer reduces the amount of solar energy reaching the surface, cools the near surface air, and increases the diffuse radiation fraction over a large disturbed area of the Amazon rainforest. These factors affect the energy and CO2 fluxes at the surface. In this work, we applied a fully integrated atmospheric model to assess the impact of biomass burning aerosols in CO2 fluxes in the Amazon region during 2010. We address the effects of the attenuation of the global solar radiation and the enhancement of the diffuse solar radiation flux inside the vegetation canopy. Our results indicate that the biomass burning aerosols led to increases of about 27% of gross primary productivity of Amazonia, 10% of plant respiration and a decline in soil respiration of 3%. Consequently, in our model Amazonia, became a net carbon sink; net ecosystem exchange during September 2010 dropped from +101 to -104 TgC when the aerosol effects are considered, mainly due to the aerosol diffuse radiation effect. For the forest biome, our results point to a dominance of the diffuse radiation effect on CO2 fluxes, reaching a balance of 50% - 50% between the diffuse and direct aerosol effects for high aerosol loads. For C3 grasses and Savanna (cerrado), as expected, the contribution of the diffuse radiation effect is much lower, tending to zero with the increase of aerosol load. Taking all biomes together, our model shows the Amazon during the dry season, in the presence of high biomass burning aerosol loads, changing from being a source to being a sink of CO2 to the atmosphere.

Description: We present a new version of the Brazilian developments on the Regional Atmospheric Modeling System where different previous versions for weather, chemistry and carbon cycle were unified in a single integrated software system. The new version also has a new set of state-of-the-art physical parameterizations and greater computational parallel and memory usage efficiency. Together with the description of the main features are examples of the quality of the transport scheme for scalars, radiative fluxes on surface and model simulation of rainfall systems over South America in different spatial resolutions using a scale-aware convective parameterization. Besides, the simulation of the diurnal cycle of the convection and carbon dioxide concentration over the Amazon Basin, as well as carbon dioxide fluxes from biogenic processes over a large portion of South America are shown. Atmospheric chemistry examples present model performance in simulating near-surface carbon monoxide and ozone in Amazon Basin and Rio de Janeiro megacity. For tracer transport and dispersion, it is demonstrated the model capabilities to simulate the volcanic ash 3-d redistribution associated with the eruption of a Chilean volcano. Then, the gain of computational efficiency is described with some details. BRAMS has been applied for research and operational forecasting mainly in South America. Model results from the operational weather forecast of BRAMS on 5 km grid spacing in the Center for Weather Forecasting and Climate Studies, INPE/Brazil, since 2013 are used to quantify the model skill of near surface variables and rainfall. The scores show the reliability of BRAMS for the tropical and subtropical areas of South America. Requirements for keeping this modeling system competitive regarding on its functionalities and skills are discussed. At last, we highlight the relevant contribution of this work on the building up of a South American community of model developers.

Description: We present a characterization of the chemical composition of the atmosphere of the Brazilian Amazon rainforest based on trace gases measurements carried out during the South American Biomass Burning Analysis (SAMBBA) airborne experiment in September 2012. We analyzed the observations of the primary biomass burning emission tracers (carbon monoxide (CO) and nitrogen oxides (NOx)), ozone (O3), isoprene, and its main oxidation products, methyl vinyl ketone (MVK), methacrolein (MACR), and hydroxyhydroperoxides (ISOPOOH). The focus of SAMBBA was primarily on biomass burning emissions, but there were also several flights in areas of the Amazon forest not directly affected by biomass burning, revealing a background with a signature of biomass burning in the chemical composition due to long-range transport of biomass burning tracers from both Africa and the eastern part of Amazonia. We used the [MVK+MACR+ ISOPOOH]/[Isoprene] ratio and the hydroxyl radical (OH) indirect calculation to assess the oxidative capacity of the Amazon forest atmosphere. We compared the background regions (CO less than 150 ppbv), fresh and aged smoke plumes classified according to their photochemical age ([O3]/[CO]), to evaluate the impact of biomass burning emissions in the oxidative capacity of the Amazon forest atmosphere. We observed that biomass burning emissions disturb the isoprene oxidation reactions, especially for fresh plumes ([MVK+MACR+ISOPOOH]/[isoprene] = 7). The oxidation of isoprene is higher in fresh smoke plumes at lower altitudes (approx. 500 m) than in aged smoke plumes, anticipating near the surface a complex chain of oxidation reactions, which may be related to the secondary organic aerosols (SOA) formation. We proposed a refinement of the OH calculation based on the sequential reaction model, which considers vertical and horizontal transport for both biomass burning regimes and background environment. Our approach for the [OH] estimation resulted in values of the same order of magnitude of a recent observation in the Amazon rainforest [OH] congruent to 10(exp 6) (molecules cm(exp -3). During a fresh plume regime, the vertical profile of [OH] and [MVK+MACR+ISOPOOH]/[isoprene] ratio showed an evidence of an increase of the oxidizing power in the transition from PBL to cloud layer (1,000-1,500 m). These high values for [OH] (1.5 x 10(exp 6) molecules cm(exp -3) and [MVK+MACR+ISOPOOH]/[isoprene] (7.5) indicate a significant change above and inside of the cloud decks due to cloud edge effects on photolysis rates, which have a major impact on OH production rates.