Satellite imagery is formed by finite digital numbers representing a specific location of ground surface in which each matrix element is denominated as a picture element or pixel. The pixels represent the sensor measurements of spectral radiance. The radiance recorded in the satellite images is then an integrated sum of the radiances of all targets within the instantaneous field of view (IFOV) of the sensors. Therefore, the radiation detected is caused by a mixture of several different materials within the image pixels. For this reason, spectral unmixing has been used as a technique for analysing the mixture of components in remotely sensed images for almost 30 years. Different spectral unmixing approaches have been described in the literature. In recent years, many authors have proposed more complex models that permit obtaining a higher accuracy and use less computing time. Although the most widely used method consists of employing a single set of endmembers (typically three or four) on the whole image and using a constrained least squares method to perform the unmixing linearly, every different algorithm has its own merits and no single approach is optimal and applicable to all cases. Additionally, the number of applications using unmixing techniques is increasing. Spectral unmixing techniques are used mainly for providing information to monitor different natural resources (agricultural, forest, geological, etc.) and environmental problems (erosion, deforestation, plagues and disease, forest fires, etc.). This article is a comprehensive exploration of all of the major unmixing approaches and their applications.

Fires associated with land use and land cover changes release large amounts of aerosols and trace gases into the atmosphere. Although several inventories of biomass burning emissions cover Brazil, there are still considerable uncertainties and differences among them. While most fire emission inventories utilize the parameters of burned area, vegetation fuel load, emission factors, and other parameters to estimate the biomass burned and its associated emissions, several more recent inventories apply an alternative method based on fire radiative power (FRP) observations to estimate the amount of biomass burned and the corresponding emissions of trace gases and aerosols. The Brazilian Biomass Burning Emission Model (3BEM) and the Fire Inventory from NCAR (FINN) are examples of the first, while the Brazilian Biomass Burning Emission Model with FRP assimilation (3BEM_FRP) and the Global Fire Assimilation System (GFAS) are examples of the latter. These four biomass burning emission inventories were used during the South American Biomass Burning Analysis (SAMBBA) field campaign. This paper analyzes and inter-compared them, focusing on eight regions in Brazil and the time period of 1 September–31 October 2012. Aerosol optical thickness (AOT_550 nm) derived from measurements made by the Moderate Resolution Imaging Spectroradiometer (MODIS) operating on board the Terra and Aqua satellites is also applied to assess the inventories' consistency. The daily area-averaged pyrogenic carbon monoxide (CO) emission estimates exhibit significant linear correlations (r, p > 0.05 level, Student t test) between 3BEM and FINN and between 3BEM_ FRP and GFAS, with values of 0.86 and 0.85, respectively. These results indicate that emission estimates in this region derived via similar methods tend to agree with one other. However, they differ more from the estimates derived via the alternative approach. The evaluation of MODIS AOT_550 nm indicates that model simulation driven by 3BEM and FINN typically underestimate the smoke particle loading in the eastern region of Amazon forest, while 3BEM_FRP estimations to the area tend to overestimate fire emissions. The daily regional CO emission fluxes from 3BEM and FINN have linear correlation coefficients of 0.75–0.92, with typically 20–30 % higher emission fluxes in FINN. The daily regional CO emission fluxes from 3BEM_FRP and GFAS show linear correlation coefficients between 0.82 and 0.90, with a particularly strong correlation near the arc of deforestation in the Amazon rainforest. In this region, GFAS has a tendency to present higher CO emissions than 3BEM_FRP, while 3BEM_FRP yields more emissions in the area of soybean expansion east of the Amazon forest. Atmospheric aerosol optical thickness is simulated by using the emission inventories with two operational atmospheric chemistry transport models: the IFS from Monitoring Atmospheric Composition and Climate (MACC) and the Coupled Aerosol and Tracer Transport model to the Brazilian developments on the Regional Atmospheric Modelling System (CCATT-BRAMS). Evaluation against MODIS observations shows a good representation of the general patterns of the AOT_550 nm time series. However, the aerosol emissions from fires with particularly high biomass consumption still lead to an underestimation of the atmospheric aerosol load in both models.

We present a new version of the Brazilian developments on the Regional Atmospheric Modeling System (BRAMS), in which different previous versions for weather, chemistry, and carbon cycle were unified in a single integrated modeling system software. This new version also has a new set of state-of-the-art physical parameterizations and greater computational parallel and memory usage efficiency. The description of the main model features includes several examples illustrating the quality of the transport scheme for scalars, radiative fluxes on surface, and model simulation of rainfall systems over South America at different spatial resolutions using a scale aware convective parameterization. Additionally, 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 show the model performance in simulating near-surface carbon monoxide and ozone in the Amazon Basin and the megacity of Rio de Janeiro. For tracer transport and dispersion, the model capabilities to simulate the volcanic ash 3-D redistribution associated with the eruption of a Chilean volcano are demonstrated. The gain of computational efficiency is described in some detail. 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 both its functionalities and skills are discussed. Finally, we highlight the relevant contribution of this work to building a South American community of model developers.

Entre os elementos do sistema climático que influenciam as atividades socioeconômicas, a precipitação apresenta papel fundamental em áreas tropicais. Regiões como África e América do Sul apresentam uma escassez considerável de observações desta variável, uma vez que a rede de estações meteorológicas não cobre sistematicamente todo o território. Neste contexto, produtos de múltiplos sensores, algoritmos e modelos climáticos são utilizados cada vez mais para análises dos elementos atmosféricos, do clima e da influência da precipitação nas características ambientais. Assim, há uma demanda crescente de validação de produtos orbitais e de simulações numéricas de forma a dar suporte aos estudos da distribuição espacial e temporal da precipitação. Este estudo tem como objetivo principal analisar os dados mensais de precipitação do produto Climate Hazards Group InfraRed Precipitation with Stations (CHIRPS) e verificar sua similaridade com os dados de estações meteorológicas do conjunto de informações do Centro de Previsão de Tempo e Estudos Climáticos (CPTEC) do Instituto Nacional de Pesquisas Espaciais (INPE) e do Instituto Nacional de Meteorologia (INMET) para o território brasileiro para os anos de 1981 a 2011. Para avaliar o CHIRPS, foram utilizados dados de 183 estações meteorológicas do INMET/CPTEC. Os resultados indicam que todas as regiões políticas do Brasil apresentaram correlação linear alta entre as informações do INMET/CPTEC e CHIRPS (95,4 %), ainda, quando consideramos toda a área do Brasil, a correlação linear média entre os dados é de 97%, significativa a p<0,05, teste t-student. Espacialmente, o noroeste do estado do Amazonas e o sudoeste do Pará apresentaram as maiores diferenças entre o conjunto de dados. As estimativas do CHIRPS ajustadas linearmente com os dados do INMET/CPTEC apresentaram uma concordância mais acentuada.

The South American Biomass Burning Analysis (SAMBBA) field campaign took detailed in situ flight measurements of aerosol during the 2012 dry season to characterise biomass burning aerosol and improve understanding of its impacts on weather and climate. Developments have been made to the Weather Research and Forecast model with chemistry (WRF-Chem) model to improve the representation of biomass burning aerosol in the region, by coupling a sectional aerosol scheme to the plume-rise parameterisation. Brazilian Biomass Burning Emissions Model (3BEM) fire emissions are used, prepared using PREP-CHEM-SRC, and mapped to CBM-Z and MOSAIC species. Model results have been evaluated against remote sensing products, AERONET sites, and four case studies of flight measurements from the SAMBBA campaign. WRF-Chem predicted layers of elevated aerosol loadings (5–20 μg sm⁻³) of particulate organic matter at high altitude (6–8 km) over tropical forest regions, while flight measurements showed a sharp decrease above 2–4 km altitude. This difference was attributed to the plume-rise parameterisation overestimating injection height. The 3BEM emissions product was modified using estimates of active fire size and burned area for the 2012 fire season, which reduced the fire size. The enhancement factor for fire emissions was increased from 1.3 to 5 to retain reasonable aerosol optical depths (AODs). The smaller fire size lowered the injection height of the emissions, but WRF-Chem still showed elevated aerosol loadings between 4–5 km altitude. Over eastern cerrado (savannah-like) regions, both modelled and measured aerosol loadings decreased above approximately 4 km altitude. Compared with MODIS satellite data and AERONET sites, WRF-Chem represented AOD magnitude well (between 0.3–1.5) over western tropical forest fire regions in the first half of the campaign, but tended to over-predict them in the second half, when precipitation was more significant. Over eastern cerrado regions, WRF-Chem tended to under-predict AODs. Modelled aerosol loadings in the east were higher in the modified emission scenario. The primary organic matter to black carbon ratio was typically between 8–10 in WRF-Chem. This was lower than the western flight measurements (interquartile range of 11.6–15.7 in B734, 14.7–24.0 in B739), but similar to the eastern flight B742 (8.1–10.4). However, single scattering albedo was close to measured over the western flights (0.87–0.89 in model; 0.86–0.91 in flight B734, and 0.81–0.95 in flight B739 measurements) but too high over the eastern flight B742 (0.86–0.87 in model, 0.79–0.82 in measurements). This suggests that improvements are needed to both modelled aerosol composition and optical properties calculations in WRF-Chem.