TY - JOUR
T1 - Field evidence and modeling validation of biogeochemical controls on the deposition of persistent organic pollutants in the deep ocean
AU - Liu, Mengyang
AU - Zheng, Haowen
AU - Li, Hongliang
AU - Chen, Fajin
AU - Lou, Linghao
AU - Wang, Weimin
AU - Zhang, Haifeng
AU - Chen, Chunqing
AU - Ye, Jiandong
AU - Yan, Meng
AU - Leung, Kenneth M.Y.
AU - Cai, Minggang
PY - 2024/12/5
Y1 - 2024/12/5
N2 - Deposition in the deep ocean plays a crucial role in the global sink of persistent organic pollutants (POPs), yet observation-based assessments of their biogeochemical cycling are scarce. In this study, surface sediments were collected from deep sea of the Eastern Indian Ocean (2161–4545 m) and analyzed for organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs). Long-range atmospheric transport was identified as the dominant pathway for OCPs (36.7–762.0 pg/g) and PCBs (25.5–110.0 pg/g) to reach the basin area from surrounding agricultural, manufacturing, and combustion emissions. Besides the TOC-dependent deposition, unique hydrodynamic conditions in the mid-ocean ridge might influence the transport and accumulation of POPs by altering their resuspension and repartitioning processes. Results of the machine learning analysis suggested that logKOW, TOC content, and pollutant residence time in the ocean are important parameters in determining PCB concentrations in the Indian Ocean. Additionally, concentrations of POPs generally exhibited logarithmic relationships with microplastic abundances, indicating that microplastics act as potential carriers for transporting these pollutants to deep-sea sediments. This study revealed the biogeochemical controls on the deposition of OCPs and PCBs in the Indian Ocean by combining field observation and model simulation. Given the rapid rate of surface warming and various biogeochemical responses in the Indian Ocean, it is recommended to conduct long-term, high-resolution field observations to understand the dynamic fate of POPs in these changing ocean environments. © 2024 Elsevier B.V.
AB - Deposition in the deep ocean plays a crucial role in the global sink of persistent organic pollutants (POPs), yet observation-based assessments of their biogeochemical cycling are scarce. In this study, surface sediments were collected from deep sea of the Eastern Indian Ocean (2161–4545 m) and analyzed for organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs). Long-range atmospheric transport was identified as the dominant pathway for OCPs (36.7–762.0 pg/g) and PCBs (25.5–110.0 pg/g) to reach the basin area from surrounding agricultural, manufacturing, and combustion emissions. Besides the TOC-dependent deposition, unique hydrodynamic conditions in the mid-ocean ridge might influence the transport and accumulation of POPs by altering their resuspension and repartitioning processes. Results of the machine learning analysis suggested that logKOW, TOC content, and pollutant residence time in the ocean are important parameters in determining PCB concentrations in the Indian Ocean. Additionally, concentrations of POPs generally exhibited logarithmic relationships with microplastic abundances, indicating that microplastics act as potential carriers for transporting these pollutants to deep-sea sediments. This study revealed the biogeochemical controls on the deposition of OCPs and PCBs in the Indian Ocean by combining field observation and model simulation. Given the rapid rate of surface warming and various biogeochemical responses in the Indian Ocean, it is recommended to conduct long-term, high-resolution field observations to understand the dynamic fate of POPs in these changing ocean environments. © 2024 Elsevier B.V.
KW - Bay of Bengal
KW - Marine sediments
KW - Ninetyeast Ridge
KW - Persistent toxic substances (PTSs)
KW - Random Forest Model
UR - https://www.scopus.com/pages/publications/85208981474
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85208981474&origin=recordpage
U2 - 10.1016/j.jhazmat.2024.136395
DO - 10.1016/j.jhazmat.2024.136395
M3 - RGC 21 - Publication in refereed journal
SN - 0304-3894
VL - 480
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
M1 - 136395
ER -