TY - JOUR
T1 - Tracing human footprint and the fate of atmospheric polycyclic aromatic hydrocarbons over the Pearl River Estuary, China
T2 - Importance of particle size
AU - Lao, Jia Yong
AU - Li, Ting Yu
AU - Wu, Rongben
AU - Ruan, Yuefei
AU - Zeng, Eddy Y.
AU - Wu, Jiaxue
AU - Lam, Paul K.S.
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/5/1
Y1 - 2021/5/1
N2 - Few studies have focus on size-segregated particulate polycyclic aromatic hydrocarbons (PAHs) in the oceanic atmosphere. To better understand the impacts of anthropogenic activities on atmospheric PAHs, a heavily human-impacted estuary, the Pearl River Estuary (PRE), was chosen as a case study. We collected gaseous and size-segregated particulate samples of ambient air at two sites in the PRE, as well as from the exhaust emissions of the cruise ship used in the sampling campaign. In addition, surface seawater samples were collected. Size distribution patterns of high molecular-weight (HMW) particulate PAHs were bimodal at one site and unimodal at the other, suggesting PAHs at the former site were derived not only from long-range atmospheric transport but also from local sources. Gas–particle partition coefficients of HMW PAHs in size-segregated particles varied with particle sizes, mostly higher in fine particles (<1.8 μm). Dry deposition flux of Σ23PAHs (defined as the sum of 23 PAHs) was contributed mainly from coarse particles (>1.8 μm), and HMW PAHs with lower dry deposition velocities could be transported farther away. With respect to air–water exchange, lower MW PAHs tended to have net volatilization, whereas higher MW PAHs were likely to have net deposition. This study sheds new lights on the origins and fate of atmospheric PAHs over the PRE, and suggests the emissions of maritime traffics should be regulated. Collected near the metropolitan regions, atmospheric PAHs over the PRE were highly affected by anthropogenic activities, especially for HMW PAHs, which could pose a long-lasting impact to the oceanic atmosphere and marine organisms.
AB - Few studies have focus on size-segregated particulate polycyclic aromatic hydrocarbons (PAHs) in the oceanic atmosphere. To better understand the impacts of anthropogenic activities on atmospheric PAHs, a heavily human-impacted estuary, the Pearl River Estuary (PRE), was chosen as a case study. We collected gaseous and size-segregated particulate samples of ambient air at two sites in the PRE, as well as from the exhaust emissions of the cruise ship used in the sampling campaign. In addition, surface seawater samples were collected. Size distribution patterns of high molecular-weight (HMW) particulate PAHs were bimodal at one site and unimodal at the other, suggesting PAHs at the former site were derived not only from long-range atmospheric transport but also from local sources. Gas–particle partition coefficients of HMW PAHs in size-segregated particles varied with particle sizes, mostly higher in fine particles (<1.8 μm). Dry deposition flux of Σ23PAHs (defined as the sum of 23 PAHs) was contributed mainly from coarse particles (>1.8 μm), and HMW PAHs with lower dry deposition velocities could be transported farther away. With respect to air–water exchange, lower MW PAHs tended to have net volatilization, whereas higher MW PAHs were likely to have net deposition. This study sheds new lights on the origins and fate of atmospheric PAHs over the PRE, and suggests the emissions of maritime traffics should be regulated. Collected near the metropolitan regions, atmospheric PAHs over the PRE were highly affected by anthropogenic activities, especially for HMW PAHs, which could pose a long-lasting impact to the oceanic atmosphere and marine organisms.
KW - Air–water exchange flux
KW - Gas–particle partitioning
KW - Particle dry deposition
KW - Polycyclic aromatic hydrocarbons (PAHs)
KW - Size distribution
UR - http://www.scopus.com/inward/record.url?scp=85102322124&partnerID=8YFLogxK
U2 - 10.1016/j.scitotenv.2020.144267
DO - 10.1016/j.scitotenv.2020.144267
M3 - Article
C2 - 33429282
AN - SCOPUS:85102322124
SN - 0048-9697
VL - 767
JO - Science of the Total Environment
JF - Science of the Total Environment
M1 - 144267
ER -