Technique for determination of the single scattering albedo of submicron aerosol in the approximation of lognormal size distribution of black carbon

2016 ◽  
Author(s):  
V. S. Kozlov ◽  
M. V. Panchenko ◽  
V. V. Pol'kin ◽  
S. A. Terpugova
Keyword(s):  
Size Distribution ◽  
Black Carbon ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
Submicron Aerosol ◽  
Lognormal Size Distribution

scholarly journals Impact of long-range transport over the Atlantic Ocean on Saharan dust optical and microphysical properties

2017 ◽  
Author(s):  
Cristian Velasco-Merino ◽  
David Mateos ◽  
Carlos Toledano ◽  
Joseph M. Prospero ◽  
Jack Molinie ◽  
...  
Keyword(s):  
Atlantic Ocean ◽  
Size Distribution ◽  
Mineral Dust ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
West African ◽  
Asymmetry Factor ◽  
Caribbean Basin ◽  
Air Mass ◽  
Aerosol Properties

Abstract. Mineral dust aerosol can be a major driver of aerosol climatology in regions distant from the sources. This study addresses the change of columnar aerosol properties when mineral dust arrives to the Caribbean Basin after transport from Africa over the Atlantic Ocean. We use data from NASA Aerosol Robotic Network (AERONET) sites in five Caribbean and two West African sites to characterize changes in aerosol properties: aerosol optical depth, size distribution, single scattering albedo, and refractive indexes. After obtaining local aerosol climatology in each area, the air mass connections between West Africa and Caribbean Basin have been investigated by means of air mass back trajectories. Over the period 1996–2014 we identify 3174 connection days, on average, 167 connection days per year. Among these, 1162 pairs of data present aerosol data in Caribbean sites with corresponding aerosol observations in Western Africa sites ~5–7 days before. Of these 1162 days, 484 meet the criteria to be characterized as mineral dust outbreaks. Based on these days we observe the following changes in aerosol-related properties in transiting the Atlantic: AOD decreases about 0.16 or −30 %; the volume particle size distribution shape shows no changes; single scattering albedo, refractive indexes, and asymmetry factor remain unchanged; the difference in the effective radius in West African area with respect to Caribbean Basin is between 0 and +0.3 µm; and half of the analyzed cases present predominance of non-spherical particles in both areas.

scholarly journals Vertical profiles of submicron aerosol single scattering albedo over the Indian region immediately before monsoon onset and during its development: research from the SWAAMI field campaign

2020 ◽  
Vol 20 (6) ◽  
pp. 4031-4046
Author(s):  
Mohanan R. Manoj ◽  
Sreedharan K. Satheesh ◽  
Krishnaswamy K. Moorthy ◽  
Hugh Coe
Keyword(s):  
Active Phase ◽  
Single Scattering ◽  
Monsoon Onset ◽  
Single Scattering Albedo ◽  
Transfer Model ◽  
Heating Rates ◽  
Atmospheric Measurements ◽  
Middle Troposphere ◽  
Submicron Aerosol ◽  
Aerosol Absorption

Abstract. Vertical structures of aerosol single scattering albedo (SSA), from near the surface through the free troposphere, have been estimated for the first time at distinct geographical locations over the Indian mainland and adjoining oceans, using in situ measurements of aerosol scattering and absorption coefficients aboard the Facility for Airborne Atmospheric Measurements (FAAM) BAe-146 aircraft during the South West Asian Aerosol Monsoon Interactions (SWAAMI) campaign from June to July 2016. These are used to examine the spatial variation of SSA profiles and also to characterize its transformation from just prior to the onset of Indian Summer Monsoon (June 2016) to its active phase (July 2016). Very strong aerosol absorption, with SSA values as low as 0.7, persisted in the lower altitudes (<3 km) over the Indo-Gangetic Plains (IGP), prior to the monsoon onset, with a west-to-east gradient; lower values occurred in the north-western arid regions, peaking in the central IGP and somewhat decreasing towards the eastern end. During the active phase of the monsoon, the SSA is found to increase remarkably, indicating far less absorption. Nevertheless, significant aerosol absorption persisted in the lower and middle troposphere over the IGP. Inputting these SSA and extinction profiles into a radiative transfer model, we examined the effects of using height-resolved information in estimating atmospheric heating rates due to aerosols, over similar estimates made using a single columnar value. It was noted that use of a single SSA value leads to an underestimation (overestimation) of the heating rates over regions with low (high) SSA, emphasizing the importance of height-resolved information. Further, the use of realistic profiles showed significant heating of the atmosphere by submicron aerosol absorption at the middle troposphere, which may have strong implications for clouds and climate.

scholarly journals The Ångström Exponent and Single-Scattering Albedo of Black Carbon: Effects of Different Coating Materials

Atmosphere ◽  
2020 ◽  
Vol 11 (10) ◽  
pp. 1103
Author(s):  
Jie Luo ◽  
Yongming Zhang ◽  
Qixing Zhang
Keyword(s):  
Black Carbon ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
Optical Measurements ◽  
Coating Materials ◽  
Total Size ◽  
Angstrom Exponent ◽  
Ångström Exponent ◽  
Mixing States ◽  
Ångstrom Exponent

In this work, the absorption Ångström exponent (AAE), extinction Ångström exponent (EAE), and single-scattering albedo (SSA) of black carbon (BC) with different coating materials are numerically investigated. BC with different coating materials can provide explanations for the small AAE, small EAE, and large AAE observed in the atmosphere, which is difficult to be explained by bare BC aggregate models. The addition of organic carbon (OC) does not necessarily increase AAE due to the transformation of BC morphologies and the existence of non-absorbing OC. The addition of coating materials does also not necessarily decrease EAE. While the addition of coating materials can increase the total size of BC-containing particles, the effective refractive index can be modified by introducing the coating materials, so increases the EAE. We found that it is not possible to differentiate between thinly- and heavily-coated BC based on EAE or AAE alone. On the other hand, SSA is much less sensitive to the size and can provide much more information for distinguishing heavily-coated BC from thinly-coated BC. For BC with different coating materials and mixing states, AAE, EAE, and SSA show rather different sensitivities to particle size and composition ratios, and their spectral-dependences also exhibit distinct differences. Different AAE and EAE trends with BC/OC ratio were also found for BC with different coating materials and mixing states. Furthermore, we also found empirical fittings for AAE, EAE, SSA, and optical cross-sections, which may be useful for retrieving the size information based on the optical measurements.

scholarly journals Parameterization of single-scattering albedo (SSA) and absorption Ångström exponent (AAE) with EC / OC for aerosol emissions from biomass burning

2016 ◽  
Vol 16 (15) ◽  
pp. 9549-9561 ◽  
Author(s):  
Rudra P. Pokhrel ◽  
Nick L. Wagner ◽  
Justin M. Langridge ◽  
Daniel A. Lack ◽  
Thilina Jayarathne ◽  
...  
Keyword(s):  
Black Carbon ◽  
Biomass Burning ◽  
Single Scattering ◽  
Emission Factors ◽  
Single Scattering Albedo ◽  
Biomass Fuels ◽  
Brown Carbon ◽  
Pearson's R ◽  
Biomass Burning Aerosol ◽  
Pearson’S R

Abstract. Single-scattering albedo (SSA) and absorption Ångström exponent (AAE) are two critical parameters in determining the impact of absorbing aerosol on the Earth's radiative balance. Aerosol emitted by biomass burning represent a significant fraction of absorbing aerosol globally, but it remains difficult to accurately predict SSA and AAE for biomass burning aerosol. Black carbon (BC), brown carbon (BrC), and non-absorbing coatings all make substantial contributions to the absorption coefficient of biomass burning aerosol. SSA and AAE cannot be directly predicted based on fuel type because they depend strongly on burn conditions. It has been suggested that SSA can be effectively parameterized via the modified combustion efficiency (MCE) of a biomass burning event and that this would be useful because emission factors for CO and CO2, from which MCE can be calculated, are available for a large number of fuels. Here we demonstrate, with data from the FLAME-4 experiment, that for a wide variety of globally relevant biomass fuels, over a range of combustion conditions, parameterizations of SSA and AAE based on the elemental carbon (EC) to organic carbon (OC) mass ratio are quantitatively superior to parameterizations based on MCE. We show that the EC ∕ OC ratio and the ratio of EC ∕ (EC + OC) both have significantly better correlations with SSA than MCE. Furthermore, the relationship of EC ∕ (EC + OC) with SSA is linear. These improved parameterizations are significant because, similar to MCE, emission factors for EC (or black carbon) and OC are available for a wide range of biomass fuels. Fitting SSA with MCE yields correlation coefficients (Pearson's r) of  ∼  0.65 at the visible wavelengths of 405, 532, and 660 nm while fitting SSA with EC / OC or EC / (EC + OC) yields a Pearson's r of 0.94–0.97 at these same wavelengths. The strong correlation coefficient at 405 nm (r =  0.97) suggests that parameterizations based on EC / OC or EC / (EC + OC) have good predictive capabilities even for fuels in which brown carbon absorption is significant. Notably, these parameterizations are effective for emissions from Indonesian peat, which have very little black carbon but significant brown carbon (SSA  =  0.990 ± 0.001 at 532 and 660 nm, SSA  =  0.937 ± 0.011 at 405 nm). Finally, we demonstrate that our parameterization based on EC / (EC + OC) accurately predicts SSA during the first few hours of plume aging with data from Yokelson et al. (2009) gathered during a biomass burning event in the Yucatán Peninsula of Mexico.

scholarly journals Vertical profiles of light absorption and scattering associated with black-carbon particle fractions in the springtime Arctic above 79° N

2019 ◽  
Author(s):  
W. Richard Leaitch ◽  
John K. Kodros ◽  
Megan D. Willis ◽  
Sarah Hanna ◽  
Hannes Schulz ◽  
...  
Keyword(s):  
Optical Properties ◽  
Absorption Coefficient ◽  
Black Carbon ◽  
Light Absorption ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
The Arctic ◽  
Vertical Profiles ◽  
Near Surface ◽  
Arctic Atmosphere

Abstract. Despite the potential importance of black carbon (BC) to radiative forcing of the Arctic atmosphere, vertically-resolved measurements of the particle light scattering coefficient (Bsp) and light absorption coefficient (Bap) in the springtime Arctic atmosphere are infrequent, especially measurements at latitudes at or above 80oN. Here, relationships among vertically-distributed aerosol optical properties Bap, Bsp, and single scattering albedo or SSA), particle microphysics and particle chemistry are examined for a region of the Canadian archipelago between 79.9oN and 83.4oN from near the surface to 500 hPa. Airborne data collected during April, 2015, are combined with ground-based observations from the observatory at Alert, Nunavut and simulations from the GEOS-Chem-TOMAS model (Kodros et al., 2018) to increase our knowledge of the effects of BC on light absorption in the Arctic troposphere. The results are constrained for Bsp less than 15 Mm-1, which represent 98% of the observed Bsp, because the single scattering albedo (SSA) has a tendency to be lower at lower Bsp, resulting in a larger relative contribution to Arctic warming. At 18.4 m2 g-1, the average BC mass absorption coefficient (MAC) from the combined airborne and Alert observations is substantially higher than the two averaged modelled MAC values (9.5 m2 g-1 and 7.0 m2 g-1) for two different internal mixing assumptions, the latter of which is based on previous observations. The higher observed MAC value may be explained by an underestimation of BC and possible differences in BC microphysics and morphologies between the observations and model. We present Bap and SSA based on the assumption that Bap is overestimated in the observations in addition to the assumption that the higher MAC is explained. Median values of the measured Bap, rBC and organic component of particles all increase by a factor of 1.8±0.1 going from near-surface to 750 hPa, and values higher than the surface persist to 600 hPa. Modelled BC, organics, and Bap agree with the near-surface measurements, but do not reproduce the higher values observed between 900 hPa and 600 hPa. The differences between modelled and observed optical properties follow the same trend as the differences between the modelled and observed concentrations of the carbonaceous components (black and organic). Some discrepancies in the model may be due to the use of a relatively low imaginary refractive index of BC as well as by the ejection of biomass burning particles only into the boundary layer at sources. For the assumption of the higher observed MAC value, the SSA range between 0.88 and 0.94, which is significantly lower than other recent estimates for the Arctic, in part reflecting the constraint of Bsp <15 Mm-1. The large uncertainties in measuring optical properties and BC as well as the large differences between measured and modelled values, here and in the literature, argue for improved measurements of BC and light absorption by BC as well as more vertical profiles of aerosol chemistry, microphysics, and other optical properties in the Arctic.

scholarly journals Closure on the single scattering albedo in the WRF-Chem framework using data from the MILAGRO campaign

2009 ◽  
Vol 9 (1) ◽  
pp. 5009-5054
Author(s):  
J. C. Barnard ◽  
J. D. Fast ◽  
G. Paredes-Miranda ◽  
W. P. Arnott
Keyword(s):  
Optical Properties ◽  
Black Carbon ◽  
Chemical Properties ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
Aerosol Optical Properties ◽  
Mean Values ◽  
Coarse Mode ◽  
Fine Mode ◽  
Using Data

Abstract. Data from the MILAGRO field campaign, which took place in the Mexico City Metropolitan Area (MCMA) during March 2006, is used to perform a closure experiment between aerosol chemical properties and aerosol optical properties. Measured aerosol chemical properties, obtained from the MILAGRO T1 site, are fed to two different "chemical to optical properties" modules. One module uses a sectional approach and is identical to that used in the WRF-Chem model, while the other is based on a modal approach. This modal code is employed as an independent check on the WRF-Chem module. Both modules compute aerosol optical properties and, in particular, the single-scattering albedo, ϖ0, as a function of time. The single-scattering albedos are compared to independent measurements obtained from a photoacoustic spectrometer (PAS). Because chemical measurements of the aerosol coarse mode were not available, and the inlet of the PAS could not ingest aerosols larger than about 2 to 3 μm, we focus here on the fine-mode ϖ0. At 870 nm, the wavelength of the PAS measurements, the agreement between the computed (modal and WRF-Chem) and observed fine-mode ϖ0, averaged over the course of the campaign, is reasonably good. The observed ϖ0 value is 0.77, while for both modules, the calculated value was 0.75 resulting in a difference of 0.02 between observations and both computational approaches. This difference is less than the uncertainty of the observed ϖ0 values (6%, or 0.05), and therefore "closure" is achieved, at least for mean values. After adjusting some properties of black carbon absorption and mass concentration within plausible uncertainty limits, the two modules simulate well the diurnal variation of ϖ0, and the absorption coefficient, Babs, but are less successful in calculating the variation of the scattering coefficient, Bscat. This difficulty is probably caused by the presence of larger particles during the day when windblown dust is ubiquitous; this dust likely increases the proportion of large particles introduced into the PAS. The dust also contributes to a very large aerosol mass loading in the coarse mode, and neglect of the coarse mode may cause significant errors, estimated to be as large as 0.07, in the calculation and measurement of ambient ϖ0. Finally, the observed ϖ0 is compared to the ϖ0 computed by the full WRF-Chem model, which includes prognostic aerosol chemistry. Unlike the results discussed above, a comparison between observed and simulated ϖ0 values reveals major differences. This large discrepancy is probably due, in part, to poor characterization of emissions near the T1 site, particularly black carbon emissions.

scholarly journals Scattering and absorption by aerosols during EUCAARI-LONGREX: can airborne measurements and models agree?

2011 ◽  
Vol 11 (6) ◽  
pp. 18487-18525 ◽  
Author(s):  
E. J. Highwood ◽  
M. J. Northway ◽  
G. R. McMeeking ◽  
W. T. Morgan ◽  
D. Liu ◽  
...  
Keyword(s):  
Optical Properties ◽  
Black Carbon ◽  
Single Scattering ◽  
Temporal Variations ◽  
Mie Scattering ◽  
Single Scattering Albedo ◽  
Chemical Components ◽  
Atmospheric Measurements ◽  
Data Set ◽  
Airborne Measurements

Abstract. Scattering and absorption by aerosol in anthropogenically perturbed air masses over Europe has been measured using instrumentation flown on the UK's BAe-146-301 large Atmospheric Research Aircraft (ARA) operated by the Facility for Airborne Atmospheric Measurements (FAAM) on 14 flights during the EUCAARI-LONGREX campaign in May 2008. The geographical and temporal variations of the derived shortwave optical properties of aerosol are presented. Values of single scattering albedo of dry aerosol at 550 nm varied considerably over the data set from 0.86 to near unity. Dry aerosol optical depths ranged from 0.03 to 0.24. An optical properties closure study comparing calculations from composition data and Mie scattering code with the measured properties is presented. Very good agreement (to within 30 %) can be achieved for scattering, but the modelling of absorption is shown to be sensitive to the refractive indices chosen for organic aerosols, and to a lesser extent black carbon. Agreement with the measured absorption can only be achieved if organic carbon is assumed to be only weakly absorbing. Hygroscopic growth curves derived from the wet nephelometer indicate moderate water uptake by the aerosol with a campaign mean f(RH) value (change in scattering) of 1.3 at 80 % relative humidity. This value is consistent with the major chemical components of the aerosol measured by the aerosol mass spectrometer (AMS), which are primarily mixed organics and nitrate and some sulphate. As expected the effect of humidity is to raise the single scattering albedo, and to increase the aerosol optical depth. This study represents an important new body of data regarding European aerosol amounts, composition and optical properties and additionally demonstrates the importance of airborne measurements of black carbon mass and aerosol hygroscopicity.

scholarly journals Investigation of gaseous and particulate emissions from various marine vessel types measured on the banks of the Elbe in Northern Germany

2013 ◽  
Vol 13 (7) ◽  
pp. 3603-3618 ◽  
Author(s):  
J.-M. Diesch ◽  
F. Drewnick ◽  
T. Klimach ◽  
S. Borrmann
Keyword(s):  
Size Distribution ◽  
Black Carbon ◽  
Particle Number ◽  
Trace Gases ◽  
Identification System ◽  
Particulate Emissions ◽  
Submicron Aerosol ◽  
Nucleation Mode ◽  
Aerosol Mass ◽  
Diameter Range

Abstract. Measurements of the ambient aerosol, various trace gases and meteorological quantities using a mobile laboratory (MoLa) were performed on the banks of the Lower Elbe in an emission control area (ECA) which is passed by numerous private and commercial marine vessels reaching and leaving the port of Hamburg, Germany. From 25–29 April 2011 a total of 178 vessels were probed at a distance of about 0.8–1.2 km with high temporal resolution. 139 ship emission plumes were of sufficient quality to be analyzed further and to determine emission factors (EFs). Concentrations of aerosol number and mass as well as polycyclic aromatic hydrocarbons (PAH) and black carbon were measured in PM1 and size distribution instruments covered the diameter range from 6 nm up to 32 μm. The chemical composition of the non-refractory submicron aerosol was measured by means of an Aerosol Mass Spectrometer (Aerodyne HR-ToF-AMS). Gas phase species analyzers monitored various trace gases (O3, SO2, NO, NO2, CO2) in the air and a weather station provided wind, precipitation, solar radiation data and other quantities. Together with ship information for each vessel obtained from Automatic Identification System (AIS) broadcasts a detailed characterization of the individual ship types and of features affecting gas and particulate emissions is provided. Particle number EFs (average 2.6e+16 # kg−1) and PM1 mass EFs (average 2.4 g kg−1) tend to increase with the fuel sulfur content. Observed PM1 composition of the vessel emissions was dominated by organic matter (72%), sulfate (22%) and black carbon (6%) while PAHs only account for 0.2% of the submicron aerosol mass. Measurements of gaseous components showed an increase of SO2 (average EF: 7.7 g kg−1) and NOx (average EF: 53 g kg−1) while O3 decreased when a ship plume reached the sampling site. The particle number size distributions of the vessels are generally characterized by a bimodal size distribution, with the nucleation mode in the 10–20 nm diameter range and a combustion aerosol mode centered at about 35 nm while particles \\textgreater 1 μm were not found. "High particle number emitters" are characterized by a dominant nucleation mode. By contrast, increased particle concentrations around 150 nm primarily occurred for "high black carbon emitters". Classifying the vessels according to their gross tonnage shows a decrease of the number, black carbon and PAH EFs while EFs of SO2, NO, NO2, NOx, AMS species (particulate organics, sulfate) and PM1 mass concentration increase with increasing gross tonnages.

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