scholarly journals Effect of dry-season biomass burning on Amazon basin aerosol concentrations and optical properties, 1992-1994

1996 ◽  
Vol 101 (D14) ◽  
pp. 19465-19481 ◽  
Author(s):  
B. N. Holben ◽  
A. Setzer ◽  
T. F. Eck ◽  
A. Pereira ◽  
I. Slutsker
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Amazon Basin ◽  
Dry Season

scholarly journals Biomass burning and urban emission impacts in the Andes Cordillera region based on in situ measurements from the Chacaltaya observatory, Bolivia (5240 m a.s.l.)

2019 ◽  
Vol 19 (23) ◽  
pp. 14805-14824
Author(s):  
Aurélien Chauvigné ◽  
Diego Aliaga ◽  
Karine Sellegri ◽  
Nadège Montoux ◽  
Radovan Krejci ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Light Absorption ◽  
Amazon Basin ◽  
Dry Season ◽  
La Paz ◽  
Extinction Coefficients ◽  
Aerosol Emission ◽  
El Alto ◽  
The Impact

Abstract. This study documents and analyses a 4-year continuous record of aerosol optical properties measured at the Global Atmosphere Watch (GAW) station of Chacaltaya (CHC; 5240 m a.s.l.), in Bolivia. Records of particle light scattering and particle light absorption coefficients are used to investigate how the high Andean Cordillera is affected by both long-range transport and by the fast-growing agglomeration of La Paz–El Alto, located approximately 20 km away and 1.5 km below the sampling site. The extended multi-year record allows us to study the properties of aerosol particles for different air mass types, during wet and dry seasons, also covering periods when the site was affected by biomass burning in the Bolivian lowlands and the Amazon Basin. The absorption, scattering, and extinction coefficients (median annual values of 0.74, 12.14, and 12.96 Mm−1 respectively) show a clear seasonal variation with low values during the wet season (0.57, 7.94, and 8.68 Mm−1 respectively) and higher values during the dry season (0.80, 11.23, and 14.51 Mm−1 respectively). The record is driven by variability at both seasonal and diurnal scales. At a diurnal scale, all records of intensive and extensive aerosol properties show a pronounced variation (daytime maximum, night-time minimum), as a result of the dynamic and convective effects. The particle light absorption, scattering, and extinction coefficients are on average 1.94, 1.49, and 1.55 times higher respectively in the turbulent thermally driven conditions than the more stable conditions, due to more efficient transport from the boundary layer. Retrieved intensive optical properties are significantly different from one season to the other, reflecting the changing aerosol emission sources of aerosol at a larger scale. Using the wavelength dependence of aerosol particle optical properties, we discriminated between contributions from natural (mainly mineral dust) and anthropogenic (mainly biomass burning and urban transport or industries) emissions according to seasons and local circulation. The main sources influencing measurements at CHC are from the urban area of La Paz–El Alto in the Altiplano and from regional biomass burning in the Amazon Basin. Results show a 28 % to 80 % increase in the extinction coefficients during the biomass burning season with respect to the dry season, which is observed in both tropospheric dynamic conditions. From this analysis, long-term observations at CHC provide the first direct evidence of the impact of biomass burning emissions of the Amazon Basin and urban emissions from the La Paz area on atmospheric optical properties at a remote site all the way to the free troposphere.

scholarly journals Biomass-burning and urban emission impacts in the Andes Cordillera region based on in-situ measurements from the Chacaltaya observatory, Bolivia (5240 m a.s.l.)

2019 ◽  
Author(s):  
Chauvigné Aurélien ◽  
Diego Aliaga ◽  
Marcos Andrade ◽  
Patrick Ginot ◽  
Radovan Krejci ◽  
...  
Keyword(s):  
Optical Properties ◽  
Aerosol Particle ◽  
Biomass Burning ◽  
Dry Season ◽  
Wet Season ◽  
Stable Layer ◽  
La Paz ◽  
Extinction Coefficients ◽  
El Alto

Abstract. We present the variability of aerosol particle optical properties measured at the global Atmosphere Watch (GAW) station Chacaltaya (5240 m a.s.l.). The in-situ mountain site is ideally located to study regional impacts of the densely populated urban area of La Paz/El Alto, and the intensive activity in the Amazonian basin. Four year measurements allow to study aerosol particle properties for distinct atmospheric conditions as stable and turbulent layers, different airmass origins, as well as for wet and dry seasons, including biomass-burning influenced periods. The absorption, scattering and extinction coefficients (median annual values of 0.74, 12.14 and 12.96 Mm−1 respectively) show a clear seasonal variation with low values during the wet season (0.57, 7.94 and 8.68 Mm−1 respectively) and higher values during the dry season (0.80, 11.23 and 14.51 Mm−1 respectively). These parameters also show a pronounced diurnal variation (maximum during daytime, minimum during night-time, as a result of the dynamic and convective effects of leading to lower atmospheric layers reaching the site during daytime. Retrieved intensive optical properties are significantly different from one season to the other, showing the influence of different sources of aerosols according to the season. Both intensive and extensive optical properties of aerosols were found to be different among the different atmospheric layers. The particle light absorption, scattering and extinction coefficients are in average 1.94, 1.49 and 1.55 times higher, respectively, in the turbulent layer compared to the stable layer. We observe that the difference is highest during the wet season and lowest during the dry season. Using wavelength dependence of aerosol particle optical properties, we discriminated contributions from natural (mainly mineral dust) and anthropogenic (mainly biomass-burning and urban transport or industries) emissions according to seasons and tropospheric layers. The main sources influencing measurements at CHC are arising from the urban area of La Paz/El Alto, and regional biomass-burning from the Amazonian basin. Results show a 28 % to 80 % increase of the extinction coefficients during the biomass-burning season with respect to the dry season, which is observed in both tropospheric layers. From this analyse, long-term observations at CHC provides the first direct evidence of the impact of emissions in the Amazonian basin on atmospheric optical properties far away from their sources, all the way to the stable layer.

scholarly journals Spectral dependence of aerosol light absorption over the Amazon Basin

2011 ◽  
Vol 11 (17) ◽  
pp. 8899-8912 ◽  
Author(s):  
L. V. Rizzo ◽  
A. L. Correia ◽  
P. Artaxo ◽  
A. S. Procópio ◽  
M. O. Andreae
Keyword(s):  
Spectral Range ◽  
Biomass Burning ◽  
Spectral Dependence ◽  
Amazon Basin ◽  
Dry Season ◽  
Negative Slope ◽  
Forest Site ◽  
Wet Season ◽  
Aerosol Absorption ◽  
The Impact

Abstract. In this study, we examine the spectral dependence of aerosol absorption at different sites and seasons in the Amazon Basin. The analysis is based on measurements performed during three intensive field experiments at a pasture site (Fazenda Nossa Senhora, Rondônia) and at a primary forest site (Cuieiras Reserve, Amazonas), from 1999 to 2004. Aerosol absorption spectra were measured using two Aethalometers: a 7-wavelength Aethalometer (AE30) that covers the visible (VIS) to near-infrared (NIR) spectral range, and a 2-wavelength Aethalometer (AE20) that measures absorption in the UV and in the NIR. As a consequence of biomass burning emissions, about 10 times greater absorption values were observed in the dry season in comparison to the wet season. Power law expressions were fitted to the measurements in order to derive the absorption Ångström exponent, defined as the negative slope of absorption versus wavelength in a log-log plot. At the pasture site, about 70 % of the absorption Ångström exponents fell between 1.5 and 2.5 during the dry season, indicating that biomass burning aerosols have a stronger spectral dependence than soot carbon particles. Ångström exponents decreased from the dry to the wet season, in agreement with the shift from biomass burning aerosols, predominant in the fine mode, to biogenic and dust aerosols, predominant in the coarse mode. The lowest absorption Ångström exponents (90 % of data below 1.5) were observed at the forest site during the dry season. Also, results indicate that low absorption coefficients were associated with low Ångström exponents. This finding suggests that biogenic aerosols from Amazonia have a weaker spectral dependence for absorption than biomass burning aerosols, contradicting our expectations of biogenic particles behaving as brown carbon. In a first order assessment, results indicate a small (<1 %) effect of variations in absorption Ångström exponents on 24-h aerosol forcings, at least in the spectral range of 450–880 nm. Further studies should be taken to assess the corresponding impact in the UV spectral range. The assumption that soot spectral properties represent all ambient light absorbing particles may cause a misjudgment of absorption towards the UV, especially in remote areas. Therefore, it is recommended to measure aerosol absorption at several wavelengths to accurately assess the impact of non-soot aerosols on climate and on photochemical atmospheric processes.

scholarly journals Sources of carbonaceous aerosol in the Amazon Basin

2010 ◽  
Vol 10 (12) ◽  
pp. 29923-29969 ◽  
Author(s):  
S. Gilardoni ◽  
E. Vignati ◽  
E. Marmer ◽  
F. Cavalli ◽  
C. Belis ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Amazon Basin ◽  
Elemental Carbon ◽  
Aerosol Particles ◽  
Dry Season ◽  
Carbonaceous Aerosol ◽  
Wet Season ◽  
Aerosol Mass ◽  
Aerosol Sources ◽  
Coarse Aerosol

Abstract. The quantification of sources of carbonaceous aerosol is important to understand their atmospheric concentrations and regulating processes and to study possible effects on climate and air quality, in addition to develop mitigation strategies. In the framework of the European Aerosol Cloud Climate Interaction (EUCAARI) project fine (Dp < 2.5 μm) and coarse (2.5 μm < Dp < 10 μm) aerosol particles were sampled from February to June (wet season) and from August to September (dry season) 2008 in the Central Amazon Basin. The mass of fine particles averaged 2.4 μg m−3 during the wet season and 4.2 μg m−3 during the dry season. The average coarse aerosol mass concentration during wet and dry periods was 7.9 and 7.6 μg m−3, respectively. The overall chemical composition of fine and coarse mass did not show any seasonality with the largest fraction of fine and coarse aerosol mass explained by organic carbon (OC); the average OC to mass ratio was 0.4 and 0.6 in fine and coarse aerosol modes, respectively. The mass absorbing cross section of soot was determined by comparison of elemental carbon and light absorption coefficient measurements and it was equal to 4.7 m2 g−1 at 637 nm. Carbon aerosol sources were identified by Positive Matrix Factorization (PMF) analysis of thermograms: 43% of fine total carbon mass was assigned to biomass burning, 34% to secondary organic aerosol (SOA), and 23% to volatile species that are difficult to apportion. In the coarse mode, primary biogenic aerosol particles (PBAP) dominated the carbonaceous aerosol mass. The results confirmed the importance of PBAP in forested areas. The source apportionment results were employed to evaluate the ability of global chemistry transport models to simulate carbonaceous aerosol sources in a regional tropical background site. The comparison showed an overestimation of elemental carbon (EC) by the TM5 model during the dry season and OC both during the dry and wet periods. The overestimation was likely due to the overestimation of biomass burning emission inventories and SOA production over tropical areas.

scholarly journals Variability of aerosol vertical distribution in the Sahel

2010 ◽  
Vol 10 (24) ◽  
pp. 12005-12023 ◽  
Author(s):  
O. Cavalieri ◽  
F. Cairo ◽  
F. Fierli ◽  
G. Di Donfrancesco ◽  
M. Snels ◽  
...  
Keyword(s):  
Optical Properties ◽  
West Africa ◽  
Vertical Distribution ◽  
Southern Hemisphere ◽  
Biomass Burning ◽  
Dry Season ◽  
Aerosol Transport ◽  
Air Masses ◽  
Monsoon Flow ◽  
Biomass Burning Aerosol

Abstract. In this work, we have studied the seasonal and inter-annual variability of the aerosol vertical distribution over Sahelian Africa for the years 2006, 2007 and 2008, characterizing the different kind of aerosols present in the atmosphere in terms of their optical properties observed by ground-based and satellite instruments, and their sources searched for by using trajectory analysis. This study combines data acquired by three ground-based micro lidar systems located in Banizoumbou (Niger), Cinzana (Mali) and M'Bour (Senegal) in the framework of the African Monsoon Multidisciplinary Analysis (AMMA), by the AEROsol RObotic NETwork (AERONET) sun-photometers and by the space-based Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) onboard the CALIPSO satellite (Cloud-Aerosol Lidar and Infrared Pathfinder Observations). During winter, the lower levels air masses arriving in the Sahelian region come mainly from North, North-West and from the Atlantic area, while in the upper troposphere air flow generally originates from West Africa, crossing a region characterized by the presence of large biomass burning sources. The sites of Cinzana, Banizoumbou and M'Bour, along a transect of aerosol transport from East to West, are in fact under the influence of tropical biomass burning aerosol emission during the dry season, as revealed by the seasonal pattern of the aerosol optical properties, and by back-trajectory studies. Aerosol produced by biomass burning are observed mainly during the dry season and are confined in the upper layers of the atmosphere. This is particularly evident for 2006, which was characterized by a large presence of biomass burning aerosols in all the three sites. Biomass burning aerosol is also observed during spring when air masses originating from North and East Africa pass over sparse biomass burning sources, and during summer when biomass burning aerosol is transported from the southern part of the continent by the monsoon flow. During summer months, the entire Sahelian region is under the influence of Saharan dust aerosols: the air masses in low levels arrive from West Africa crossing the Sahara desert or from the Southern Hemisphere crossing the Guinea Gulf while in the upper layers air masses still originate from North, North-East. The maximum of the desert dust activity is observed in this period which is characterized by large AOD (above 0.2) and backscattering values. It also corresponds to a maximum in the extension of the aerosol vertical distribution (up to 6 km of altitude). In correspondence, a progressive cleaning up of the lowermost layers of the atmosphere is occurring, especially evident in the Banizoumbou and Cinzana sites. Summer is in fact characterized by extensive and fast convective phenomena. Lidar profiles show at times large dust events loading the atmosphere with aerosol from the ground up to 6 km of altitude. These events are characterized by large total attenuated backscattering values, and alternate with very clear profiles, sometimes separated by only a few hours, indicative of fast removal processes occurring, likely due to intense convective and rain activity. The inter-annual variability in the three year monitoring period is not very significant. An analysis of the aerosol transport pathways, aiming at detecting the main source regions, revealed that air originated from the Saharan desert is present all year long and it is observed in the lower levels of the atmosphere at the beginning and at the end of the year. In the central part of the year it extends upward and the lower levels are less affected by air masses from Saharan desert when the monsoon flow carries air from the Guinea Gulf and the Southern Hemisphere inland.

scholarly journals Long term measurements of aerosol optical properties at a primary forest site in Amazonia

2013 ◽  
Vol 13 (5) ◽  
pp. 2391-2413 ◽  
Author(s):  
L. V. Rizzo ◽  
P. Artaxo ◽  
T. Müller ◽  
A. Wiedensohler ◽  
M. Paixão ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Dry Season ◽  
Primary Forest ◽  
Forest Site ◽  
Wet Season ◽  
Absorption Coefficients ◽  
Aerosol Forcing ◽  
Fine Mode

Abstract. A long term experiment was conducted in a primary forest area in Amazonia, with continuous in-situ measurements of aerosol optical properties between February 2008 and April 2011, comprising, to our knowledge, the longest database ever in the Amazon Basin. Two major classes of aerosol particles, with significantly different optical properties were identified: coarse mode predominant biogenic aerosols in the wet season (January–June), naturally released by the forest metabolism, and fine mode dominated biomass burning aerosols in the dry season (July–December), transported from regional fires. Dry particle median scattering coefficients at the wavelength of 550 nm increased from 6.3 Mm−1 to 22 Mm−1, whereas absorption at 637 nm increased from 0.5 Mm−1 to 2.8 Mm−1 from wet to dry season. Most of the scattering in the dry season was attributed to the predominance of fine mode (PM2) particles (40–80% of PM10 mass), while the enhanced absorption coefficients are attributed to the presence of light absorbing aerosols from biomass burning. As both scattering and absorption increased in the dry season, the single scattering albedo (SSA) did not show a significant seasonal variability, in average 0.86 ± 0.08 at 637 nm for dry aerosols. Measured particle optical properties were used to estimate the aerosol forcing efficiency at the top of the atmosphere. Results indicate that in this primary forest site the radiative balance was dominated by the cloud cover, particularly in the wet season. Due to the high cloud fractions, the aerosol forcing efficiency absolute values were below −3.5 W m−2 in 70% of the wet season days and in 46% of the dry season days. Besides the seasonal variation, the influence of out-of-Basin aerosol sources was observed occasionally. Periods of influence of the Manaus urban plume were detected, characterized by a consistent increase on particle scattering (factor 2.5) and absorption coefficients (factor 5). Episodes of biomass burning and mineral dust particles advected from Africa were observed between January and April, characterized by enhanced concentrations of crustal elements (Al, Si, Ti, Fe) and potassium in the fine mode. During these episodes, median particle absorption coefficients increased by a factor of 2, whereas median SSA values decreased by 7%, in comparison to wet season conditions.

scholarly journals Linking chemical composition and optical properties of biomass burning aerosols in Amazonia

2022 ◽  
Author(s):  
Milena Ponczek ◽  
Marco Aurélio de Menezes Franco ◽  
Samara Carbone ◽  
Luciana Varanda Rizzo ◽  
Djacinto Aparecido Monteiro dos Santos ◽  
...  
Keyword(s):  
Optical Properties ◽  
Chemical Composition ◽  
Field Experiment ◽  
Biomass Burning ◽  
Dry Season ◽  
Atmospheric Composition ◽  
Fine Mode ◽  
Fine Mode Aerosol ◽  
Aerosol Properties ◽  
Aerosol Chemical Composition

Biomass burning emissions in Amazonia changes the atmospheric composition and aerosol properties during the dry season. We investigated fine-mode aerosol chemical composition and optical properties at an intensive field experiment...

scholarly journals Long term measurements of aerosol optical properties at a pristine forest site in Amazonia

2012 ◽  
Vol 12 (9) ◽  
pp. 23333-23401 ◽  
Author(s):  
L. V. Rizzo ◽  
P. Artaxo ◽  
T. Müller ◽  
A. Wiedensohler ◽  
M. Paixão ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Dry Season ◽  
Forest Site ◽  
Wet Season ◽  
Absorption Coefficients ◽  
Aerosol Forcing ◽  
Fine Mode ◽  
Pristine Forest

Abstract. A long term experiment was conducted in a pristine area in the Amazon forest, with continuous in situ measurements of aerosol optical properties between February 2008 and April 2011, comprising, to our knowledge, the longest database ever in Amazonia. Two types of aerosol particles, with significantly different optical properties were identified: coarse mode predominant biogenic aerosols in the wet season (January–June), naturally released by the forest metabolism, and fine mode dominated biomass burning aerosols in the dry season (July–December), transported from regional fires. Dry particle median scattering coefficients at the wavelength of 550 nm increased from 6.3 Mm−1 to 22 Mm−1, whereas absorption at 637 nm increased from 0.5 Mm−1 to 2.8 Mm−1 from wet to dry season. Most of the scattering in the dry season was attributed to the predominance of fine mode particles (40–80% of PM10 mass), while the enhanced absorption coefficients are attributed to the presence of light absorbing aerosols from biomass burning. As both scattering and absorption increased in the dry season, the single scattering albedo (SSA) did not show a significant seasonal variability, in average 0.86 ± 0.08 at 637 nm for dry particles. Measured particle optical properties were used to estimate the aerosol forcing efficiency at the top of the atmosphere. Results indicate that in this pristine forest site the radiative balance was dominated by the cloud cover, or, in other words, the aerosol indirect effect predominated over the direct effect, particularly in the wet season. Due to the high cloud fractions, the aerosol forcing efficiency was below −3.5 W m−2 in 70% of the wet season days and in 46% of the dry season days. These values are lower than the ones reported in the literature, which are based on remote sensing data. Besides the seasonal variation, the influence of external aerosol sources was observed occasionally. Periods of influence of the Manaus urban plume were detected, characterized by a consistent increase on particle scattering (factor 2.5) and absorption coefficients (factor 5). Episodes of biomass burning and mineral dust particles advection from Africa were observed between January and April, characterized by enhanced concentrations of fine mode (PM2.0), crustal elements (Al, Si, Ti, Fe) and potassium. During these episodes, median particle absorption coefficients increased by a factor of 2, whereas median SSA values decreased by 7%, in comparison to wet season conditions.

scholarly journals Sources of carbonaceous aerosol in the Amazon basin

2011 ◽  
Vol 11 (6) ◽  
pp. 2747-2764 ◽  
Author(s):  
S. Gilardoni ◽  
E. Vignati ◽  
E. Marmer ◽  
F. Cavalli ◽  
C. Belis ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Amazon Basin ◽  
Elemental Carbon ◽  
Aerosol Particles ◽  
Dry Season ◽  
Carbonaceous Aerosol ◽  
Wet Season ◽  
Aerosol Mass ◽  
Aerosol Sources ◽  
Coarse Aerosol

Abstract. The quantification of sources of carbonaceous aerosol is important to understand their atmospheric concentrations and regulating processes and to study possible effects on climate and air quality, in addition to develop mitigation strategies. In the framework of the European Integrated Project on Aerosol Cloud Climate Interactions (EUCAARI) fine (Dp < 2.5 μm) and coarse (2.5 μm < Dp <10 μm) aerosol particles were sampled from February to June (wet season) and from August to September (dry season) 2008 in the central Amazon basin. The mass of fine particles averaged 2.4 μg m−3 during the wet season and 4.2 μg m−3 during the dry season. The average coarse aerosol mass concentration during wet and dry periods was 7.9 and 7.6 μg m−3, respectively. The overall chemical composition of fine and coarse mass did not show any seasonality with the largest fraction of fine and coarse aerosol mass explained by organic carbon (OC); the average OC to mass ratio was 0.4 and 0.6 in fine and coarse aerosol modes, respectively. The mass absorbing cross section of soot was determined by comparison of elemental carbon and light absorption coefficient measurements and it was equal to 4.7 m2 g−1 at 637 nm. Carbon aerosol sources were identified by Positive Matrix Factorization (PMF) analysis of thermograms: 44% of fine total carbon mass was assigned to biomass burning, 43% to secondary organic aerosol (SOA), and 13% to volatile species that are difficult to apportion. In the coarse mode, primary biogenic aerosol particles (PBAP) dominated the carbonaceous aerosol mass. The results confirmed the importance of PBAP in forested areas. The source apportionment results were employed to evaluate the ability of global chemistry transport models to simulate carbonaceous aerosol sources in a regional tropical background site. The comparison showed an overestimation of elemental carbon (EC) by the TM5 model during the dry season and OC both during the dry and wet periods. The overestimation was likely due to the overestimation of biomass burning emission inventories and SOA production over tropical areas.

scholarly journals Spectral dependence of aerosol light absorption over the Amazon Basin

2011 ◽  
Vol 11 (4) ◽  
pp. 11547-11577 ◽  
Author(s):  
L. V. Rizzo ◽  
A. L. Correia ◽  
P. Artaxo ◽  
A. S. Procópio ◽  
M. O. Andreae
Keyword(s):  
Biomass Burning ◽  
Spectral Dependence ◽  
Amazon Basin ◽  
Field Experiments ◽  
Dry Season ◽  
Negative Slope ◽  
Forest Site ◽  
Wet Season ◽  
Aerosol Absorption ◽  
The Impact

Abstract. In this study, we examine the spectral dependence of aerosol absorption at different sites and seasons in the Amazon Basin. The analysis is based on measurements performed during three intensive field experiments at a pasture site (Fazenda Nossa Senhora, Rondônia) and at a primary forest site (Cuieiras Reserve, Amazonas), from 1999 to 2004. Aerosol absorption spectra were measured using two Aethalometers: a 7-wavelength Aethalometer (AE30) that covers the visible (VIS) to near-infrared (NIR) spectral range, and a 2-wavelength Aethalometer (AE20) that measures absorption in the UV and in the visible. As a consequence of biomass burning emissions, about 10 times greater absorption values were observed in the dry season in comparison to the wet season. Power law expressions were fitted to the measurements in order to derive the Ångström exponent for absorption, defined as the negative slope of absorption vs. wavelength in a log-log plot. At the pasture site, about 70% of the Ångström exponents fell between 1.5 and 2.5 during the dry season, indicating that biomass burning aerosols have a stronger spectral dependence than soot carbon particles. Ångström exponents decreased from the dry to the wet season, in agreement with the shift from biomass burning aerosols, predominant in the fine mode, to biogenic and dust aerosols, predominant in the coarse mode. The lowest Ångström exponents (90% of data below 1.5) were observed at the forest site during the dry season. Also, results indicate that low absorption coefficients were associated with Ångström exponents below 1.0. This finding suggests that biogenic aerosols from Amazonia may have a weak spectral dependence for absorption, contradicting our expectations of biogenic particles behaving as brown carbon. Nevertheless, additional measurements should be taken in the future, to provide a complete picture of biogenic aerosol absorption spectral characteristics from different seasons and geographic locations. The assumption that soot spectral properties represent all ambient light absorbing particles may cause a misjudgment of absorption towards the UV, especially in remote areas. Therefore, it is recommended to measure aerosol absorption at several wavelengths from UV to near IR to accurately assess the impact of non-soot aerosols on climate and on photochemical atmospheric processes.

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