Measurement report: A 1-year study to estimate maritime contributions to PM10 in a coastal area in northern France
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Published:2023-08-04
Issue:15
Volume:23
Page:8607-8622
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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:
Ledoux FrédéricORCID, Roche Cloé, Delmaire Gilles, Roussel Gilles, Favez Olivier, Fadel MarcORCID, Courcot Dominique
Abstract
Abstract. This work focuses on filling the knowledge gap associated
with the contribution of natural and anthropogenic marine emissions to PM10 concentrations
in northern France. For this purpose, a 1-year measurement and sampling
campaign for PM10 has been conducted at a French coastal site situated
at the Strait of Dover. The characterization of PM10 samples
was performed considering major and trace elements, water-soluble ions,
organic carbon (OC), elemental carbon (EC), and organic markers of biomass
burning and primary biogenic emissions. Furthermore, the source
apportionment of PM10 was achieved using the constrained weighted non-negative matrix factorization (CW-NMF) model. The annual
average PM10 was 24.3 µg m−3, with six species contributing 69 % of its mass (NO3-, OC, SO42-, Cl−,
Na+, and NH4+). The source apportionment of PM10 led to
the identification of 9 sources. On average yearly, fresh and aged sea salts contributed 37 % of PM10, while secondary nitrate and sulfate contributed 42 %,
biomass burning contributed 8 %, and heavy-fuel-oil (HFO) combustion from shipping
emissions contributed almost 5 %. Additionally,
monthly evolution of the sources' contribution evidenced different behaviors
with high contributions of secondary nitrate and biomass burning during
winter. In the summer season, 15-times-higher concentrations for HFO
combustion (July compared to January) and the predominance of aged sea salts
versus fresh sea salts were observed.The concentration-weighted trajectory model showed
that the sources contributing more than 80 % of PM10 at Cap
Gris-Nez are of regional and/or long-range origins, with the North Sea and
the English Channel as hotspots for natural and anthropogenic marine
emissions and Belgium, the Netherlands, and the west of Germany as hotspots
for secondary inorganic aerosols.
Publisher
Copernicus GmbH
Subject
Atmospheric Science
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