An official website of the United States government
Abstract Rapid warming is likely increasing primary production and wildfire occurrence in the Arctic. Projected changes in carbonaceous aerosols during the summer will impact atmospheric chemistry and climate, but our understanding of these processes is limited by sparse observations. Here, we characterize carbonaceous aerosol in Alaska, USA: Toolik Field Station in the Interior and the Atmospheric Radiation Measurement facility at Utqiaġvik on the Arctic coast, during the summers of 2022 and 2023. We estimated PM2.5and PM10concentrations using laser light scattering (PurpleAir sensors) and examined total carbon (TC) and its organic carbon (OC) and elemental carbon (EC) fractions in total suspended particles (TSP). We investigated the dominant sources of carbonaceous aerosol using air mass backward‐trajectories from the NOAA HYSPLIT model and radiocarbon source apportionment of TC. TC concentrations were about twice as high in the Interior compared to the coast, with contemporary sources dominating at both Toolik (95%–99%) and Utqiaġvik (86%–89%) over minor contributions from fossil sources. Elevated PM, TC, OC, and EC concentrations coincided with major boreal forest fire activity in North America that brought smoke to the region. The radiocarbon signature of EC measured at Toolik during these wildfire events indicated that over 90% of the EC came from contemporary sources. Our measurements demonstrate the potential for Arctic aerosol concentrations to respond significantly to climate warming‐induced changes to the landscape and emphasize the need for continuous atmospheric monitoring to advance our understanding of this rapidly changing environment.
more »
« less
This content will become publicly available on August 1, 2026
Analyzing Aerosol Properties of Air Parcels Above Boone, NC, During the 2023 Summer Canadian Wildfire Season
ABSTRACT Air mass source regions and meteorological factors significantly influenced aerosol loading along air mass trajectories over Boone, North Carolina, between June 1, 2023, to August 31, 2023. This study examines the impact of northeast Canadian wildfires on aerosol loading, quantified by the particle light scattering coefficients at 550 nm measured at the NOAA Federated Aerosol Monitoring site at Appalachian State University (APP). Using NOAA’s HYSPLIT trajectory model, hourly back trajectories originating at 500 meters above ground level at APP were analyzed over a 96-hour timespan and categorized into four aerosol loading classifications based on the aerosol light scattering coefficient at 550 nm measured at APP. All air parcel trajectories originating in eastern Canada were associated with the high and very high aerosol load classifications. Statistical analysis shows that wildfire-sourced parcels exhibit elevated temperatures and variability in solar flux. The findings establish a link between Canadian wildfire activity and increased aerosol loading in Boone, NC, emphasizing the relationships between source region, transport dynamics, and atmospheric conditions. These results provide a framework for further exploration of aerosol source regions and their broader environmental impacts.
more »
« less
- Award ID(s):
- 2320510
- PAR ID:
- 10632668
- Publisher / Repository:
- United States Library of Congress
- Date Published:
- Journal Name:
- American journal of undergraduate research
- ISSN:
- 2375-8732
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Rapid warming is likely increasing primary production and wildfire occurrence in the Arctic. Projected changes in the abundance and composition of carbonaceous aerosols during the summer are likely to impact atmospheric chemistry and climate, but our understanding of these processes is limited by sparse observations. Here, we characterize carbonaceous aerosol at two field sites, Toolik Field Station in the Interior and the Atmospheric Radiation Measurement facility at Utqiaġvik on the Arctic coast of Alaska, USA, through the summers of 2022 and 2023. We estimated particulate matter ≤2.5 micrometers (PM2.5) and particulate matter ≤10 micrometers (PM10) using laser light scattering (PurpleAir sensors) and examined total carbon (TC) and its organic carbon (OC) and elemental carbon (EC) fractions in total suspended particles (TSP). We also investigated the dominant sources of carbonaceous aerosol using air mass backward-trajectories from the National Oceanic and Atmospheric Administration (NOAA) Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model and radiocarbon source apportionment of TC. We found TC concentrations were about twice as high in the Interior than on the coast and that modern sources were the dominant sources of carbonaceous aerosol at both Toolik (95–99%) and Utqiaġvik (86–89%), with minor contributions from fossil sources. Periods of significantly elevated PM, TC, OC, and EC concentrations coincided with major boreal forest fire activity in North America that brought smoke to the region. The radiocarbon signature of EC measured at Toolik during these wildfire smoke events indicated that over 90% of the EC originated from modern sources. Our measurements demonstrate changing aerosol concentrations in the Arctic during the summer, and emphasize the need for continuous atmospheric monitoring to evaluate and advance our understanding of this rapidly changing atmospheric environment. (Manuscript in prep)more » « less
-
Rapid warming is likely increasing primary production and wildfire occurrence in the Arctic. Projected changes in the abundance and composition of carbonaceous aerosols during the summer are likely to impact atmospheric chemistry and climate, but our understanding of these processes is limited by sparse observations. Here, we characterize carbonaceous aerosol at two field sites, Toolik Field Station in the Interior and the Atmospheric Radiation Measurement facility at Utqiaġvik on the Arctic coast of Alaska, USA, through the summers of 2022 and 2023. We estimated particulate matter ≤2.5 micrometers (PM2.5) and particulate matter ≤10 micrometers (PM10) using laser light scattering (PurpleAir sensors) and examined total carbon (TC) and its organic carbon (OC) and elemental carbon (EC) fractions in total suspended particles (TSP). We also investigated the dominant sources of carbonaceous aerosol using air mass backward-trajectories from the National Oceanic and Atmospheric Administration (NOAA) Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model and radiocarbon source apportionment of TC. We found TC concentrations were about twice as high in the Interior than on the coast and that modern sources were the dominant sources of carbonaceous aerosol at both Toolik (95–99%) and Utqiaġvik (86–89%), with minor contributions from fossil sources. Periods of significantly elevated PM, TC, OC, and EC concentrations coincided with major boreal forest fire activity in North America that brought smoke to the region. The radiocarbon signature of EC measured at Toolik during these wildfire smoke events indicated that over 90% of the EC originated from modern sources. Our measurements demonstrate changing aerosol concentrations in the Arctic during the summer, and emphasize the need for continuous atmospheric monitoring to evaluate and advance our understanding of this rapidly changing atmospheric environment. (Manuscript in prep)more » « less
-
Abstract. Twelve months of measurements collected during the Two-ColumnAerosol Project field campaign at Cape Cod, Massachusetts, which started inthe summer of 2012, were used to investigate aerosol physical, optical, andchemical properties and their influences on the dependence of clouddevelopment on thermodynamic (i.e., lower tropospheric stability, LTS)conditions. Relationships between aerosol loading and cloud properties underdifferent dominant air-mass conditions and the magnitude of the firstindirect effect (FIE), as well as the sensitivity of the FIE to differentaerosol compositions, are examined. The seasonal variation in aerosol numberconcentration (Na) was not consistent with variations in aerosoloptical properties (i.e., scattering coefficient, σs, andcolumnar aerosol optical depth). Organics were found to have a largecontribution to small particle sizes. This contribution decreased during theparticle growth period. Under low-aerosol-loading conditions, the liquidwater path (LWP) and droplet effective radius (DER) significantly increasedwith increasing LTS, but, under high-aerosol-loading conditions, LWP and DERchanged little, indicating that aerosols significantly weakened thedependence of cloud development on LTS. The reduction in LWP and DER fromlow- to high-aerosol-loading conditions was greater in stable environments,suggesting that clouds under stable conditions are more susceptible toaerosol perturbations than those under more unstable conditions. Highaerosol loading weakened the increase in DER as LWP increased andstrengthened the increase in cloud optical depth (COD) with increasing LWP,resulting in changes in the interdependence of cloud properties. Under bothcontinental and marine air-mass conditions, high aerosol loading cansignificantly increase COD and decrease LWP and DER, narrowing theirdistributions. Magnitudes of the FIE estimated under continental air-massconditions ranged from 0.07±0.03 to 0.26±0.09 with a meanvalue of 0.16±0.03 and showed an increasing trend as LWP increased.The calculated FIE values for aerosols with a low fraction of organics aregreater than those for aerosols with a high fraction of organics. Thisimplies that clouds over regions dominated by aerosol particles containingmostly inorganics are more susceptible to aerosol perturbations, resultingin larger climate forcing, than clouds over regions dominated by organicaerosol particles.more » « less
-
Abstract. Light absorbing organic carbon, or brown carbon (BrC), can be a significantcontributor to the visible light absorption budget. However, the sources ofBrC and the contributions of BrC to light absorption are not wellunderstood. Biomass burning is thought to be a major source of BrC.Therefore, as part of the WE-CAN (Western Wildfire Experiment for CloudChemistry, Aerosol Absorption and Nitrogen) study, BrC absorption data werecollected on board the National Science Foundation/National Center for Atmospheric Research (NSF/NCAR) C-130 aircraft as it intercepted smoke fromwildfires in the western US in July–August 2018. BrC absorptionmeasurements were obtained in near real-time using two techniques. The firstcoupled a particle-into-liquid sampler (PILS) with a liquid waveguidecapillary cell and a total organic carbon analyzer for measurements ofwater-soluble BrC absorption and WSOC (water-soluble organic carbon). Thesecond employed a custom-built photoacoustic aerosol absorption spectrometer(PAS) to measure total absorption at 405 and 660 nm. The PAS BrC absorption at 405 nm (PAS total Abs 405 BrC) was calculated by assuming the absorption determined by the PAS at 660 nm was equivalent to the black carbon (BC) absorption and the BC aerosol absorption Ångström exponent was 1. Data from the PILS and PAS were combined to investigate the water-soluble vs. total BrC absorption at 405 nm in the various wildfire plumes sampled during WE-CAN. WSOC, PILS water-soluble Abs 405, and PAS total Abs 405 tracked each other in and out of the smoke plumes. BrC absorption was correlated with WSOC (R2 value for PAS =0.42 and PILS =0.60) and CO (carbon monoxide) (R2 value for PAS =0.76 and PILS =0.55) for all wildfires sampled. The PILS water-soluble Abs 405 was corrected for thenon-water-soluble fraction of the aerosol using the calculated UHSAS(ultra-high-sensitivity aerosol spectrometer) aerosol mass. The correctedPILS water-soluble Abs 405 showed good closure with the PAS total Abs 405BrC with a factor of ∼1.5 to 2 difference. This differencewas explained by particle vs. bulk solution absorption measured by the PASvs. PILS, respectively, and confirmed by Mie theory calculations. DuringWE-CAN, ∼ 45 % (ranging from 31 % to 65 %) of the BrCabsorption was observed to be due to water-soluble species. The ratio of BrC absorption to WSOC or ΔCO showed no clear dependence on firedynamics or the time since emission over 9 h.more » « less
