scholarly journals Optical closure for an aerosol column: Method, accuracy, and inferable properties applied to a biomass-burning aerosol and its radiative forcing

2002 ◽  
Vol 107 (D21) ◽  
pp. LAC 12-1-LAC 12-15 ◽  
Author(s):  
Markus Fiebig ◽  
Andreas Petzold ◽  
Ulla Wandinger ◽  
Manfred Wendisch ◽  
Christoph Kiemle ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Radiative Forcing ◽  
Column Method ◽  
Biomass Burning Aerosol ◽  
Method Accuracy

scholarly journals Intercomparison of biomass burning aerosol optical properties from in situ and remote-sensing instruments in ORACLES-2016

2019 ◽  
Vol 19 (14) ◽  
pp. 9181-9208 ◽  
Author(s):  
Kristina Pistone ◽  
Jens Redemann ◽  
Sarah Doherty ◽  
Paquita Zuidema ◽  
Sharon Burton ◽  
...  
Keyword(s):  
Optical Properties ◽  
Case Studies ◽  
Biomass Burning ◽  
Radiative Forcing ◽  
Measurement Techniques ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
Aerosol Optical Properties ◽  
Biomass Burning Aerosol

Abstract. The total effect of aerosols, both directly and on cloud properties, remains the biggest source of uncertainty in anthropogenic radiative forcing on the climate. Correct characterization of intensive aerosol optical properties, particularly in conditions where absorbing aerosol is present, is a crucial factor in quantifying these effects. The southeast Atlantic Ocean (SEA), with seasonal biomass burning smoke plumes overlying and mixing with a persistent stratocumulus cloud deck, offers an excellent natural laboratory to make the observations necessary to understand the complexities of aerosol–cloud–radiation interactions. The first field deployment of the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign was conducted in September of 2016 out of Walvis Bay, Namibia. Data collected during ORACLES-2016 are used to derive aerosol properties from an unprecedented number of simultaneous measurement techniques over this region. Here, we present results from six of the eight independent instruments or instrument combinations, all applied to measure or retrieve aerosol absorption and single-scattering albedo. Most but not all of the biomass burning aerosol was located in the free troposphere, in relative humidities typically ranging up to 60 %. We present the single-scattering albedo (SSA), absorbing and total aerosol optical depth (AAOD and AOD), and absorption, scattering, and extinction Ångström exponents (AAE, SAE, and EAE, respectively) for specific case studies looking at near-coincident and near-colocated measurements from multiple instruments, and SSAs for the broader campaign average over the month-long deployment. For the case studies, we find that SSA agrees within the measurement uncertainties between multiple instruments, though, over all cases, there is no strong correlation between values reported by one instrument and another. We also find that agreement between the instruments is more robust at higher aerosol loading (AOD400>0.4). The campaign-wide average and range shows differences in the values measured by each instrument. We find the ORACLES-2016 campaign-average SSA at 500 nm (SSA500) to be between 0.85 and 0.88, depending on the instrument considered (4STAR, AirMSPI, or in situ measurements), with the interquartile ranges for all instruments between 0.83 and 0.89. This is consistent with previous September values reported over the region (between 0.84 and 0.90 for SSA at 550nm). The results suggest that the differences observed in the campaign-average values may be dominated by instrument-specific spatial sampling differences and the natural physical variability in aerosol conditions over the SEA, rather than fundamental methodological differences.

scholarly journals Intercomparison of biomass burning aerosol optical properties from in-situ and remote-sensing instruments in ORACLES-2016

2019 ◽  
Author(s):  
Kristina Pistone ◽  
Jens Redemann ◽  
Sarah Doherty ◽  
Paquita Zuidema ◽  
Sharon Burton ◽  
...  
Keyword(s):  
Optical Properties ◽  
Case Studies ◽  
Biomass Burning ◽  
Radiative Forcing ◽  
Measurement Techniques ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
Aerosol Optical Properties ◽  
Biomass Burning Aerosol

Abstract. The total effect of aerosols, both directly and on cloud properties, remains the biggest source of uncertainty in anthropogenic radiative forcing on the climate. Correct characterization of intensive aerosol optical properties, particularly in conditions where absorbing aerosol is present, is a crucial factor in quantifying these effects. The Southeast Atlantic Ocean (SEA), with seasonal biomass burning smoke plumes overlying and mixing with a persistent stratocumulus cloud deck, offers an excellent natural laboratory to make the observations necessary to understand the complexities of aerosol-cloud-radiation interactions. The first field deployment of the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign was conducted in September of 2016 out of Walvis Bay, Namibia. Data collected during ORACLES-2016 are used to derive aerosol properties from an unprecedented number of simultaneous measurement techniques over this region. Here we present results from six of the eight independent instruments or instrument combinations, all applied to measure or retrieve aerosol absorption and single scattering albedo. Most but not all of the biomass-burning aerosol was located in the free troposphere, in relative humidities typically ranging up to 60 %. We present the single scattering albedo (SSA), absorbing and total aerosol optical depth (AOD and AAOD), and absorption, scattering, and extinction Ångström exponents (AAE, SAE, EAE) for specific case studies looking at near-coincident and -colocated measurements from multiple instruments, and SSAs for the broader campaign average over the monthlong deployment. For the case studies, we find that SSA agrees within the measurement uncertainties between multiple instruments, though, over all cases, there is no strong correlation between values reported by one instrument and another. We also find that agreement between the instruments is more robust at higher aerosol loading (AOD400 > 0.4). The campaign-wide average and range shows differences in the values measured by each instrument. We find the ORACLES-2016 campaign-average SSA at 500 nm (SSA500) to be between 0.85 and 0.88, depending on the instrument considered (4STAR, AirMSPI, or in situ measurements), with the inter-quartile ranges for all instruments between 0.83 and 0.89. This is consistent with previous September values reported over the region (between 0.84 and 0.90 for SSA at 550 nm). The results suggest that the differences observed in the campaign-average values may be dominated by instrument-specific spatial sampling differences and the natural physical variability in aerosol conditions over the SEA, rather than fundamental methodological differences.

scholarly journals Atmospheric aging enhances the ice nucleation ability of biomass-burning aerosol

2021 ◽  
Vol 7 (9) ◽  
pp. eabd3440
Author(s):  
Lydia G. Jahl ◽  
Thomas A. Brubaker ◽  
Michael J. Polen ◽  
Leif G. Jahn ◽  
Kerrigan P. Cain ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Radiative Forcing ◽  
Active Sites ◽  
Carbon Particle ◽  
Cloud Microphysics ◽  
Climate Forcing ◽  
Chemical Aging ◽  
Atmospheric Aging ◽  
Order Of Magnitude ◽  
Biomass Burning Aerosol

Ice-nucleating particles (INPs) in biomass-burning aerosol (BBA) that affect cloud glaciation, microphysics, precipitation, and radiative forcing were recently found to be driven by the production of mineral phases. BBA experiences extensive chemical aging as the smoke plume dilutes, and we explored how this alters the ice activity of the smoke using simulated atmospheric aging of authentic BBA in a chamber reactor. Unexpectedly, atmospheric aging enhanced the ice activity for most types of fuels and aging schemes. The removal of organic carbon particle coatings that conceal the mineral-based ice-active sites by evaporation or oxidation then dissolution can increase the ice activity by greater than an order of magnitude. This represents a different framework for the evolution of INPs from biomass burning where BBA becomes more ice active as it dilutes and ages, making a larger contribution to the INP budget, resulting cloud microphysics, and climate forcing than is currently considered.

Effects of atmospheric transformations of the organic fraction of biomass burning aerosol on the radiative forcing: a box model analysis

2021 ◽  
Author(s):  
Igor B. Konovalov ◽  
Nikolai A. Golovushkin ◽  
Tatyana B. Zhuravleva ◽  
Ilmir M. Nastrdinov ◽  
Daria A. Lvova ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Radiative Forcing ◽  
Model Analysis ◽  
Box Model ◽  
Organic Fraction ◽  
Biomass Burning Aerosol

scholarly journals Biomass combustion produces ice-active minerals in biomass-burning aerosol and bottom ash

2020 ◽  
Vol 117 (36) ◽  
pp. 21928-21937
Author(s):  
Leif G. Jahn ◽  
Michael J. Polen ◽  
Lydia G. Jahl ◽  
Thomas A. Brubaker ◽  
Joshua Somers ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Atmospheric Chemistry ◽  
Radiative Forcing ◽  
Combustion Process ◽  
Bottom Ash ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Biomass Combustion ◽  
Inorganic Elements ◽  
Biomass Burning Aerosol

Ice nucleation and the resulting cloud glaciation are significant atmospheric processes that affect the evolution of clouds and their properties including radiative forcing and precipitation, yet the sources and properties of atmospheric ice nucleants are poorly constrained. Heterogeneous ice nucleation caused by ice-nucleating particles (INPs) enables cloud glaciation at temperatures above the homogeneous freezing regime that starts near −35 °C. Biomass burning is a significant global source of atmospheric particles and a highly variable and poorly understood source of INPs. The nature of these INPs and how they relate to the fuel composition and its combustion are critical gaps in our understanding of the effects of biomass burning on the environment and climate. Here we show that the combustion process transforms inorganic elements naturally present in the biomass (not soil or dust) to form potentially ice-active minerals in both the bottom ash and emitted aerosol particles. These particles possess ice-nucleation activities high enough to be relevant to mixed-phase clouds and are active over a wide temperature range, nucleating ice at up to −13 °C. Certain inorganic elements can thus serve as indicators to predict the production of ice nucleants from the fuel. Combustion-derived minerals are an important but understudied source of INPs in natural biomass-burning aerosol emissions in addition to lofted primary soil and dust particles. These discoveries and insights should advance the realistic incorporation of biomass-burning INPs into atmospheric cloud and climate models. These mineral components produced in biomass-burning aerosol should also be studied in relation to other atmospheric chemistry processes, such as facilitating multiphase chemical reactions and nutrient availability.

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