Fate of organophosphate esters from the Northwestern Pacific to the Southern Ocean: Occurrence, distribution, and fugacity model simulation

•TCEP and TCPP were dominant in the seawater and atmosphere from the northwest Pacific to the Southern Ocean.•Dry and wet deposition were two main processes influenced the air-seawater transport of OPEs in the Ross Sea.•Ross Sea has played the role of a "sink" of OPEs in summer. Eleven org...

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Veröffentlicht in:Journal of environmental sciences (China) 2024-03, Vol.137, p.347-357
Hauptverfasser: Shi, Tengda, Li, Ruijing, Fu, Jie, Hou, Chao, Gao, Hui, Cheng, Guanjie, Zhang, Haibo, Jin, Shuaichen, Kong, Liang, Na, Guangshui
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Sprache:eng
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Zusammenfassung:•TCEP and TCPP were dominant in the seawater and atmosphere from the northwest Pacific to the Southern Ocean.•Dry and wet deposition were two main processes influenced the air-seawater transport of OPEs in the Ross Sea.•Ross Sea has played the role of a "sink" of OPEs in summer. Eleven organophosphate esters (OPEs) in the air and seawater were investigated from the northwestern Pacific Ocean to the Southern Ocean during the 2018 Chinese 34th Antarctic Scientific Expedition. The concentration of total OPEs ranged from 164.82 to 3501.79 pg/m3 in air and from 4.54 to 70.09 ng/L in seawater. Two halogenated OPEs, tri(chloropropyl) phosphate (TCPP) and tri (2-chloroethyl) phosphate (TCEP), were generally more abundant than the non-halogenated OPEs. A level III fugacity model was developed to simulate the transfer and fate of seven OPEs in the air and seawater regions of the central Ross Sea. The model results indicate that OPEs are transferred from the air to the seawater in the central Ross Sea in summer, during which the Ross Sea acts as a final OPE sink. Dry and wet deposition dominated the processes involving OPE transfer to seawater. The OPE degradation process was also found to be more pervasive in the atmosphere than in the seawater region. These findings highlights the importance of long-range transport of OPEs and their air–seawater interface behavior in the Antarctic.
ISSN:1001-0742
1878-7320
DOI:10.1016/j.jes.2023.03.001