skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Assessing Radiative Impacts of African Smoke Aerosols Over the Southeastern Atlantic Ocean
Abstract Biomass burning smoke aerosols are efficient at attenuating incoming solar radiation. The Layered Atlantic Smoke Interactions with Clouds campaign was conducted from June 2016 to October 2017. The U. S. Department of Energy mobile Atmospheric Radiation Measurement site located on Ascension Island (AMF‐ASI) identified several instances of smoke plume intrusions. Increases in surface and column measurements of aerosol loading were directly related to increases in fine mode fraction, number concentrations of aerosols (Na), and cloud condensation nuclei (NCCN). During periods of weak lower tropospheric stability, smoke particles were more likely to be advected downward either by boundary layer turbulence or cloud top entrainment under non‐overcast sky conditions. Backward trajectory analysis illustrated that smoke aerosols reaching the AMF‐ASI site were fine mode, less aged, strongly absorbing, and had shorter boundary layer trajectories while longer boundary layer trajectories denoted mixtures of weakly absorbing smoke and coarse mode marine aerosols. The most polluted smoke cases of August 2016 and 2017 revealed a notable contrast in radiative forcing per unit aerosol optical depth or radiative forcing efficiency (ΔFeff) at the top of the atmosphere (TOA) and near‐surface (BOA). The weakly (strongly) absorbing 2016 cases exhibited weaker (stronger) ΔFeffat the TOA and BOA suggesting a warming (cooling) effect within the boundary layer. The 2017 cases featured the strongest ΔFeffsuggesting more of a cooling effect at the TOA and BOA due to mixing of fresh smoke with marine aerosols during transport.  more » « less
Award ID(s):
2031752
PAR ID:
10501503
Author(s) / Creator(s):
 ;  ;  ;  ;  ;  ;  ;  
Publisher / Repository:
DOI PREFIX: 10.1029
Date Published:
Journal Name:
Earth and Space Science
Volume:
11
Issue:
4
ISSN:
2333-5084
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Aerosols and their radiative properties play an integral part in understanding Earth’s climate. It is becoming increasingly common to examine aerosol’s radiative impacts on a regional scale. The primary goal of this research is to explore the impacts of regional aerosol’s forcing at the surface and top-of-atmosphere (TOA) in the south-eastern U.S. by using a 1-D radiative transfer model. By using test cases that are representative of conditions common to this region, an estimate of aerosol forcing can be compared to other results. Speciation data and aerosol layer analysis provide the basis for the modeling. Results indicate that the region experiences TOA cooling year-round, where the winter has TOA forcings between −2.8 and −5 W/m2, and the summer has forcings between −5 and −15 W/m2 for typical atmospheric conditions. Surface level forcing efficiencies are greater than those estimated for the TOA for all cases considered i.e., urban and non-urban background conditions. One potential implication of this research is that regional aerosol mixtures have effects that are not well captured in global climate model estimates, which has implications for a warming climate where all radiative inputs are not well characterized, thus increasing the ambiguity in determining regional climate impacts. 
    more » « less
  2. null (Ed.)
    Abstract. The aerosol indirect effect on cloud microphysical and radiative propertiesis one of the largest uncertainties in climate simulations. In order toinvestigate the aerosol–cloud interactions, a total of 16 low-level stratuscloud cases under daytime coupled boundary-layer conditions are selectedover the southern Great Plains (SGP) region of the United States. Thephysicochemical properties of aerosols and their impacts on cloudmicrophysical properties are examined using data collected from theDepartment of Energy Atmospheric Radiation Measurement (ARM) facility at the SGP site. The aerosol–cloud interaction index (ACIr) is used to quantify the aerosol impacts with respect to cloud-droplet effective radius. The mean value of ACIr calculated from all selected samples is0.145±0.05 and ranges from 0.09 to 0.24 at a range of cloudliquid water paths (LWPs; LWP=20–300 g m−2). The magnitude of ACIr decreases with an increasing LWP, which suggests a diminished cloud microphysical response to aerosol loading, presumably due to enhanced condensational growth processes and enlarged particle sizes. The impact of aerosols with different light-absorbing abilities on the sensitivity of cloud microphysical responses is also investigated. In the presence of weak light-absorbing aerosols, the low-level clouds feature a higher number concentration of cloud condensation nuclei (NCCN) and smaller effective radii (re), while the opposite is true for strong light-absorbing aerosols. Furthermore, the mean activation ratio of aerosols to CCN (NCCN∕Na) for weakly (strongly) absorbing aerosols is 0.54 (0.45), owing to the aerosol microphysical effects, particularly the different aerosol compositions inferred by their absorptive properties. In terms of the sensitivity of cloud-droplet number concentration (Nd) to NCCN, the fraction of CCN that converted to cloud droplets (Nd∕NCCN) for the weakly (strongly) absorptive regime is 0.69 (0.54). The measured ACIr values in the weakly absorptive regime arerelatively higher, indicating that clouds have greater microphysicalresponses to aerosols, owing to the favorable thermodynamic condition. Thereduced ACIr values in the strongly absorptive regime are due to the cloud-layer heating effect induced by strong light-absorbing aerosols. Consequently, we expect larger shortwave radiative cooling effects from clouds in the weakly absorptive regime than those in the strongly absorptive regime. 
    more » « less
  3. Abstract Controls on pristine aerosol over the Southern Ocean (SO) are critical for constraining the strength of global aerosol indirect forcing. Observations of summertime SO clouds and aerosols in synoptically varied conditions during the 2018 SOCRATES aircraft campaign reveal novel mechanisms influencing pristine aerosol‐cloud interactions. The SO free troposphere (3–6 km) is characterized by widespread, frequent new particle formation events contributing to much larger concentrations (≥1,000 mg−1) of condensation nuclei (diameters > 0.01 μm) than in typical sub‐tropical regions. Synoptic‐scale uplift in warm conveyor belts and sub‐polar vortices lifts marine biogenic sulfur‐containing gases to free‐tropospheric environments favorable for generating Aitken‐mode aerosol particles (0.01–0.1 μm). Free‐tropospheric Aitken particles subside into the boundary layer, where they grow in size to dominate the sulfur‐based cloud condensation nuclei (CCN) driving SO cloud droplet number concentrations (Nd ∼ 60–100 cm−3). Evidence is presented for a hypothesized Aitken‐buffering mechanism which maintains persistently high summertime SONdagainst precipitation removal through CCN replenishment from activation and growth of boundary layer Aitken particles. Nudged hindcasts from the Community Atmosphere Model (CAM6) are found to underpredict Aitken and accumulation mode aerosols andNd, impacting summertime cloud brightness and aerosol‐cloud interactions and indicating incomplete representations of aerosol mechanisms associated with ocean biology. 
    more » « less
  4. Abstract Deposition of aerosols to the surface ocean is an important factor affecting primary production in the surface ocean. However, the sources and fluxes of aerosols and associated trace elements remain poorly defined. Aerosol210Pb,210Po, and7Be data were collected on US GEOTRACES cruise GP15 (Pacific Meridional Transect, 152°W; 2018).210Pb fluxes are low close to the Alaskan margin, increase to a maximum at ∼43°N, then decrease to lower values. There is good agreement between210Pb fluxes and long‐term land‐based fluxes during the SEAREX program (1970–1980s), as well as between GP15 and GP16 (East Pacific Zonal Transect, 12°S; 2013) at adjacent stations. A normalized fractionf(7Be,210Pb) is used to discern aerosols with upper (highf) versus lower (lowf) troposphere sources. Alaskan/North Pacific aerosols show significant continental influence while equatorial/South Pacific aerosols are supplied to the marine boundary layer from the upper troposphere. Lithogenic trace elements Al and Ti show inverse correlations withf(7Be,210Pb), supporting a continental boundary layer provenance while anthropogenic Pb shows no clear relationship withf(7Be,210Pb). All but four samples have210Po/210Pb activity ratios <0.2 suggesting short aerosol residence time. Among the four samples (210Po/210Pb = 0.42–0.88), two suggest an upper troposphere source and longer aerosol residence time while the remaining two cannot be explained by long aerosol residence time nor a significant component of dust. We hypothesize that enrichments of210Po in them are linked to Po enrichments in the sea surface microlayer, possibly through Po speciation as a dissolved organic or dimethyl polonide species. 
    more » « less
  5. Abstract Marine cloud brightening (MCB) is proposed to offset global warming by emitting sea salt aerosols to the tropical marine boundary layer, which increases aerosol and cloud albedo. Sea salt aerosol is the main source of tropospheric reactive chlorine (Cly) and bromine (Bry). The effects of additional sea salt on atmospheric chemistry have not been explored. We simulate sea salt aerosol injections for MCB under two scenarios (212–569 Tg/a) in the GEOS‐Chem global chemical transport model, only considering their impacts as a halogen source. Globally, tropospheric Clyand Bryincrease (20–40%), leading to decreased ozone (−3 to −6%). Consequently, OH decreases (−3 to −5%), which increases the methane lifetime (3–6%). Our results suggest that the chemistry of the additional sea salt leads to minor total radiative forcing compared to that of the sea salt aerosol itself (~2%) but may have potential implications for surface ozone pollution in tropical coastal regions. 
    more » « less