TY - JOUR
T1 - Quantifying Scavenging Efficiencies of Different Aerosol Species and Size-Resolved Volume Concentrations in Tropical Convective Clouds over the West Pacific
AU - Hilario, Miguel Ricardo A.
AU - Barth, Mary
AU - Bennett, Ryan
AU - Crosbie, Ewan
AU - Digangi, Joshua P.
AU - Diskin, Glenn S.
AU - Lorenzo, Genevieve Rose
AU - Rutledge, Steven
AU - Martin, Melissa Yang
AU - Ziemba, Luke
AU - Sorooshian, Armin
N1 - Publisher Copyright:
© 2025 American Meteorological Society.
PY - 2025/2
Y1 - 2025/2
N2 - In-cloud aerosol scavenging remains a large source of model uncertainty, affecting capabilities to capture the aerosol lifetime and impacts on air quality and climate. While past work quantified aerosol scavenging efficiencies (SEs) in midlatitude mixed-phase deep convection, SEs are less well known for shallower convection. We used aircraft data over the tropical west Pacific to calculate SEs for three marine cumuli of different top heights (3-7 km MSL) using a simple entrainment model and measurements of the cloud outflow and nearby clear air. Across cases, efficient scavenging was observed for sulfate (>86%) and black carbon (70%-80%), while organic aerosols (53%-60%) and nitrate (61.5%) were moderately scavenged. Ammonium had a wide SE range (53%-87%). SEs of aerosol volume concentration showed near-total removal of aerosols with diameters greater than 100 nm (>92%) and inefficient removal for aerosols with diameters less than 100 nm (30%-50%), associated with the preferential activation and removal of larger particles. Mass-based SEs did not differ substantially between tropical cumuli and midlatitude deep convection, attributed to the negligible mass activated at higher supersaturations. The efficient scavenging of black carbon (BC) can be explained by an enhanced hygroscopic fraction of BC based on model results from the Community Earth System Model, version 2 (CESM2), Community Atmosphere Model with Chemistry, suggesting the internal mixing of BC with more soluble species during long-range transport through the marine atmosphere. The estimates of BC SEs provide direct evidence of substantial BC removal in convection as inferred by previous work and should motivate improvements in chemical transport models.
AB - In-cloud aerosol scavenging remains a large source of model uncertainty, affecting capabilities to capture the aerosol lifetime and impacts on air quality and climate. While past work quantified aerosol scavenging efficiencies (SEs) in midlatitude mixed-phase deep convection, SEs are less well known for shallower convection. We used aircraft data over the tropical west Pacific to calculate SEs for three marine cumuli of different top heights (3-7 km MSL) using a simple entrainment model and measurements of the cloud outflow and nearby clear air. Across cases, efficient scavenging was observed for sulfate (>86%) and black carbon (70%-80%), while organic aerosols (53%-60%) and nitrate (61.5%) were moderately scavenged. Ammonium had a wide SE range (53%-87%). SEs of aerosol volume concentration showed near-total removal of aerosols with diameters greater than 100 nm (>92%) and inefficient removal for aerosols with diameters less than 100 nm (30%-50%), associated with the preferential activation and removal of larger particles. Mass-based SEs did not differ substantially between tropical cumuli and midlatitude deep convection, attributed to the negligible mass activated at higher supersaturations. The efficient scavenging of black carbon (BC) can be explained by an enhanced hygroscopic fraction of BC based on model results from the Community Earth System Model, version 2 (CESM2), Community Atmosphere Model with Chemistry, suggesting the internal mixing of BC with more soluble species during long-range transport through the marine atmosphere. The estimates of BC SEs provide direct evidence of substantial BC removal in convection as inferred by previous work and should motivate improvements in chemical transport models.
KW - Aerosol-cloud interaction
KW - Aerosols
KW - Aerosols/particulates
KW - Primary aerosol
KW - Secondary inorganic aerosol
KW - Secondary organic aerosol
UR - https://www.scopus.com/pages/publications/85219578732
UR - https://www.scopus.com/pages/publications/85219578732#tab=citedBy
U2 - 10.1175/JAS-D-24-0064.1
DO - 10.1175/JAS-D-24-0064.1
M3 - Article
AN - SCOPUS:85219578732
SN - 0022-4928
VL - 82
SP - 267
EP - 282
JO - Journal of the Atmospheric Sciences
JF - Journal of the Atmospheric Sciences
IS - 2
ER -