Wintertime new particle formation and its contribution to cloud condensation nuclei in the Northeastern United States
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Published:2020-03-03
Issue:4
Volume:20
Page:2591-2601
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ISSN:1680-7324
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Container-title:Atmospheric Chemistry and Physics
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language:en
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Short-container-title:Atmos. Chem. Phys.
Author:
Yu FangqunORCID, Luo GanORCID, Nair Arshad ArjunanORCID, Schwab James J.ORCID, Sherman James P., Zhang Yanda
Abstract
Abstract. Atmospheric particles can act as cloud condensation
nuclei (CCN) and modify cloud properties and precipitation and thus
indirectly impact the hydrological cycle and climate. New particle formation
(NPF or nucleation), frequently observed at locations around the globe, is
an important source of ultrafine particles and CCN in the atmosphere. In
this study, wintertime NPF over the Northeastern United States (NEUS) is
simulated with WRF-Chem coupled with a size-resolved (sectional) advanced
particle microphysics (APM) model. Model-simulated variations in particle
number concentrations during a 2-month period (November–December 2013)
are in agreement with corresponding measurements taken at Pinnacle State
Park (PSP), New York, and Appalachian State University (APP), North Carolina.
We show that, even during wintertime, regional nucleation occurs and
contributes significantly to ultrafine-particle and CCN number
concentrations over the NEUS. The model shows that, due to low biogenic
emissions during this period, wintertime regional nucleation is solely
controlled by inorganic species and the newly developed ternary ion-mediated
nucleation scheme is able to capture the variations in observed particle
number concentrations (ranging from ∼200 to 20 000 cm−3)
at both PSP and APP. Total particle and CCN number concentrations
dramatically increase following NPF events and have the highest values over the Ohio Valley region, where elevated [SO2] is sustained by power plants.
Secondary particles dominate particle number abundance over the NEUS, and
their fraction increases with altitude from ≳85 % near the surface to ≳95 % in the upper
troposphere. The secondary fraction of CCN also increases with altitude,
from 20 %–50 % in the lower boundary layer to 50 %–60 % in the middle
troposphere to 70 %–85 % in the upper troposphere.
Publisher
Copernicus GmbH
Subject
Atmospheric Science
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