Aerosol optical properties in the marine boundary layer during the First Aerosol Characterization Experiment (ACE 1) and the underlying chemical and physical aerosol properties

1998 ◽  
Vol 103 (D13) ◽  
pp. 16547-16563 ◽  
Author(s):  
P. K. Quinn ◽  
D. J. Coffman ◽  
V. N. Kapustin ◽  
T. S. Bates ◽  
D. S. Covert
2001 ◽  
Vol 32 (8) ◽  
pp. 933-955 ◽  
Author(s):  
J Kuśmierczyk-Michulec ◽  
M Schulz ◽  
S Ruellan ◽  
O Krüger ◽  
E Plate ◽  
...  

2018 ◽  
Vol 176 ◽  
pp. 08011 ◽  
Author(s):  
Fábio J. S. Lopes ◽  
Juan Luis Guerrero-Rascado ◽  
Jose A. Benavent-Oltra ◽  
Roberto Román ◽  
Gregori A. Moreira ◽  
...  

During the period of August-September 2016 an intensive campaign was carried out to assess aerosol properties in São Paulo-Brazil aiming to detect long-range aerosol transport events and to characterize the instrument regarding data quality. Aerosol optical properties retrieved by the GALION - LALINET SPU lidar station and collocated AERONET sunphotometer system are presented as extinction/ backscatter vertical profiles with microphysical products retrieved with GRASP inversion algorithm.


2002 ◽  
Vol 107 (D21) ◽  
pp. LAC 5-1-LAC 5-15 ◽  
Author(s):  
U. Bundke ◽  
G. Hänel ◽  
H. Horvath ◽  
W. Kaller ◽  
S. Seidl ◽  
...  

2018 ◽  
Vol 18 (23) ◽  
pp. 17615-17635 ◽  
Author(s):  
Guangjie Zheng ◽  
Yang Wang ◽  
Allison C. Aiken ◽  
Francesca Gallo ◽  
Michael P. Jensen ◽  
...  

Abstract. The response of marine low cloud systems to changes in aerosol concentration represents one of the largest uncertainties in climate simulations. Major contributions to this uncertainty are derived from poor understanding of aerosol under natural conditions and the perturbation by anthropogenic emissions. The eastern North Atlantic (ENA) is a region of persistent but diverse marine boundary layer (MBL) clouds, whose albedo and precipitation are highly susceptible to perturbations in aerosol properties. In this study, we examine MBL aerosol properties, trace gas mixing ratios, and meteorological parameters measured at the Atmospheric Radiation Measurement Climate Research Facility's ENA site on Graciosa Island, Azores, Portugal, during a 3-year period from 2015 to 2017. Measurements impacted by local pollution on Graciosa Island and during occasional intense biomass burning and dust events are excluded from this study. Submicron aerosol size distribution typically consists of three modes: Aitken (At, diameter Dp<∼100 nm), accumulation (Ac, Dp within ∼100 to ∼300 nm), and larger accumulation (LA, Dp>∼300 nm) modes, with average number concentrations (denoted as NAt, NAc, and NLA below) of 330, 114, and 14 cm−3, respectively. NAt, NAc, and NLA show contrasting seasonal variations, suggesting different sources and removal processes. NLA is dominated by sea spray aerosol (SSA) and is higher in winter and lower in summer. This is due to the seasonal variations of SSA production, in-cloud coalescence scavenging, and dilution by entrained free troposphere (FT) air. In comparison, SSA typically contributes a relatively minor fraction to NAt (10 %) and NAc (21 %) on an annual basis. In addition to SSA, sources of Ac-mode particles include entrainment of FT aerosols and condensation growth of Aitken-mode particles inside the MBL, while in-cloud coalescence scavenging is the major sink of NAc. The observed seasonal variation of NAc, being higher in summer and lower in winter, generally agrees with the steady-state concentration estimated from major sources and sinks. NAt is mainly controlled by entrainment of FT aerosol, coagulation loss, and growth of Aitken-mode particles into the Ac-mode size range. Our calculation suggests that besides the direct contribution from entrained FT Ac-mode particles, growth of entrained FT Aitken-mode particles in the MBL also represent a substantial source of cloud condensation nuclei (CCN), with the highest contribution potentially reaching 60 % during summer. The growth of Aitken-mode particles to CCN size is an expected result of the condensation of sulfuric acid, a product from dimethyl sulfide oxidation, suggesting that ocean ecosystems may have a substantial influence on MBL CCN populations in the ENA.


1990 ◽  
Vol 95 (D4) ◽  
pp. 3659 ◽  
Author(s):  
W. A. Hoppel ◽  
J. W. Fitzgerald ◽  
G. M. Frick ◽  
R. E. Larson ◽  
E. J. Mack

2020 ◽  
Vol 20 (19) ◽  
pp. 11491-11526 ◽  
Author(s):  
Yohei Shinozuka ◽  
Pablo E. Saide ◽  
Gonzalo A. Ferrada ◽  
Sharon P. Burton ◽  
Richard Ferrare ◽  
...  

Abstract. In the southeast Atlantic, well-defined smoke plumes from Africa advect over marine boundary layer cloud decks; both are most extensive around September, when most of the smoke resides in the free troposphere. A framework is put forth for evaluating the performance of a range of global and regional atmospheric composition models against observations made during the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) airborne mission in September 2016. A strength of the comparison is a focus on the spatial distribution of a wider range of aerosol composition and optical properties than has been done previously. The sparse airborne observations are aggregated into approximately 2∘ grid boxes and into three vertical layers: 3–6 km, the layer from cloud top to 3 km, and the cloud-topped marine boundary layer. Simulated aerosol extensive properties suggest that the flight-day observations are reasonably representative of the regional monthly average, with systematic deviations of 30 % or less. Evaluation against observations indicates that all models have strengths and weaknesses, and there is no single model that is superior to all the others in all metrics evaluated. Whereas all six models typically place the top of the smoke layer within 0–500 m of the airborne lidar observations, the models tend to place the smoke layer bottom 300–1400 m lower than the observations. A spatial pattern emerges, in which most models underestimate the mean of most smoke quantities (black carbon, extinction, carbon monoxide) on the diagonal corridor between 16∘ S, 6∘ E, and 10∘ S, 0∘ E, in the 3–6 km layer, and overestimate them further south, closer to the coast, where less aerosol is present. Model representations of the above-cloud aerosol optical depth differ more widely. Most models overestimate the organic aerosol mass concentrations relative to those of black carbon, and with less skill, indicating model uncertainties in secondary organic aerosol processes. Regional-mean free-tropospheric model ambient single scattering albedos vary widely, between 0.83 and 0.93 compared with in situ dry measurements centered at 0.86, despite minimal impact of humidification on particulate scattering. The modeled ratios of the particulate extinction to the sum of the black carbon and organic aerosol mass concentrations (a mass extinction efficiency proxy) are typically too low and vary too little spatially, with significant inter-model differences. Most models overestimate the carbonaceous mass within the offshore boundary layer. Overall, the diversity in the model biases suggests that different model processes are responsible. The wide range of model optical properties requires further scrutiny because of their importance for radiative effect estimates.


2018 ◽  
Author(s):  
Guangjie Zheng ◽  
Yang Wang ◽  
Allison C. Aiken ◽  
Francesca Gallo ◽  
Mike Jensen ◽  
...  

Abstract. The response of marine low cloud systems to changes in aerosol concentration represents one of the largest uncertainties in climate simulations. Major contributions to this uncertainty derive from poor understanding of aerosol under natural conditions and the perturbation by anthropogenic emissions. The Eastern North Atlantic (ENA) is a region of persistent but diverse marine boundary layer (MBL) clouds, whose albedo and precipitation are highly susceptible to perturbations in aerosol properties. In this study, we examine MBL aerosol properties, trace gas mixing ratios, and meteorological parameters measured at the Atmospheric Radiation Measurement Climate Research Facility’s ENA site on Graciosa Island, Azores, Portugal from 2015 to 2017. Measurements impacted by local pollutions on Graciosa Island and during occasional intense biomass burning and dust events are excluded from this analysis. Submicron aerosol size distribution typically consists of three modes: Aitken (At), Accumulation (Ac), and Larger Accumulation (LA) modes, with average number concentrations (denoted as NAt, NAc and NLA below) of 330, 114, and 14 cm−3, respectively. NAt, NAc and NLA show contrasting seasonal variations, suggesting different sources and removal processes. NLA is dominated by sea spray aerosol (SSA), and is higher in winter and lower in summer. This is due to the seasonal variations of SSA production, coalescence scavenging, and dilution by entrained free troposphere (FT) air. In comparison, SSA typically contributes a relatively minor fraction to NAt (10 %) and NAc (21 %) on an annual basis. In addition to SSA, sources of Ac mode particles include entrainment of FT aerosols and condensation growth of At mode particles inside MBL, while coalescence scavenging is the major sink of NAc. The observed seasonal variation of NAc, being higher in summer and lower in winter, generally agrees with the estimate based on the major sources and sink. NAt is mainly controlled by entrainment of FT aerosol, coagulation loss, and growth of At mode particles into Ac mode size range. Our calculation suggests besides the direct contribution from entrained FT Ac mode particles, growth of entrained FT At mode particles in the MBL also represent a substantial source of cloud condensation nuclei (CCN), with the highest contribution potentially reaching nearly 60 % during summer. The growth of At mode particles to CCN size is expected a result of the condensation of sulfuric acid from dimethyl sulfide oxidation, suggesting that ocean ecosystems may have a substantial influence on MBL CCN populations in ENA.


2018 ◽  
Author(s):  
Dongxiang Wang ◽  
Dominika Szczepanik ◽  
Iwona S. Stachlewska

Abstract. PollyXT Raman Polarization Lidar observations were performed at the Remote Sensing laboratory in Warsaw (52.2109° N, 20.9826° E), Poland, in the framework of the European Aerosol Research Lidar Network (EARLINET) and the Aerosols, Clouds and Trace gases Research Infrastructure (ACTRIS). Data collected in July, August and September of 2013, 2015 and 2016 were analysed using the classical Raman approach. In total 202 sets of profiles of the particle extinction and backscatter coefficient, and linear particle depolarization ratio at 355 nm and 532 nm were derived for statistical investigations (EARLINET/ACTRIS Data Base). The main analysis was focused on intensive optical properties obtained within aerosol boundary layer (ABL). The interrelationships of different optical properties inside ABL are discussed for different periods: entire day, nocturnal time and sunrise/sunset time. In addition, the lidar derived boundary layer optical properties were compared with the columnar daytime aerosol properties derived from radiometer (MFR-7, PolandAOD-NET) and photometer (C318, AERONET). Relationships of these and surface in-situ measurements of particulate matter with an aerodynamic diameter


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