4.8 Article

Compound-specific radiocarbon reveals sources and land-sea transport of polycyclic aromatic hydrocarbons in an urban estuary

期刊

WATER RESEARCH
卷 198, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2021.117134

关键词

Compound-specific radiocarbon analysis; Perylene; Sediment; C-14 signature; Coastal current; End-member mixing model

资金

  1. National Natural Science Foundation of China (NSFC) [41276066, 41877474]
  2. China Scholarship Council (CSC)

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The study utilized a compound-specific radiocarbon approach to evaluate the sources and land-sea transport of PAHs in urban estuaries, highlighting the significant contribution of fossil fuels to PAHs in the Jiulong River Estuary and Western Taiwan Strait. Furthermore, the quantification of perylene transport through the estuarine-coastal system using C-14 transport models revealed the impacts of fluvial erosions and ocean currents on its signature changes from one location to another. This compound-specific C-14 method and PAH transport model provide valuable insights for accurately assessing the land-sea transport and burial of organic pollutants in estuarine-coastal sedimentary systems.
As typical chemical indicators of the Anthropocene, polycyclic aromatic hydrocarbons (PAHs) and their environmental behavior in urban estuaries can reveal the influence of anthropogenic activities on coastal zones worldwide. In contrast to conventional approaches based on concentration datasets, we provide a compound-specific radiocarbon (C-14) perspective to quantitatively evaluate the sources and land-sea transport of PAHs in an estuarine-coastal surficial sedimentary system impacted by anthropogenic activities and coastal currents. Compound-specific C-14 of PAHs and their C-14 end-member mixing models showed that 67-73% of fluoranthene and pyrene and 76-80% of five- and six-ring PAHs in the Jiulong River Estuary (JRE, China) originated from fossil fuels (e.g., coal, oil spill, and petroleum-related emissions). In the adjacent Western Taiwan Strait (WTS), the contributions of fossil fuel to these PAH groups were higher at 74-79% and 84-87%, respectively. Furthermore, as a significant biomarker for source allocation of terrigenous organic matter, perylene, a typical five-ring PAH, and its land-sea transport from the basin through the JRE and finally to the WTS was quantitatively evaluated based on the C-14 transport models. In the JRE, fluvial erosions and anthropogenic emissions affected the C-14 signature of perylene (Delta C-14(perylene), -535 +/- 5 parts per thousand) with contributions of > 38% and < 62%, respectively. From the JRE to the WTS, the decreased Delta C-14(perylene) (-735 +/- 4 parts per thousand) could be attributed to the long-range transport of ocean current-driven perylene (-919 +/- 53 parts per thousand) with a contribution of 53 +/- 8 parts per thousand. This compound-specific C-14 approach and PAH transport model help provide a valuable reference for accurately quantifying land-sea transport and burial of organic pollutants in estuarine-coastal sedimentary systems. (C) 2021 Elsevier Ltd. All rights reserved.

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