Wet deposition of persistent organic pollutants (POPs) in Izmir, Turkey


ÇETİN B., ODABAŞI M., BAYRAM A.

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, vol.23, no.9, pp.9227-9236, 2016 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 23 Issue: 9
  • Publication Date: 2016
  • Doi Number: 10.1007/s11356-016-6183-6
  • Journal Name: ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.9227-9236
  • Keywords: Persistent organic pollutants (POPs), Wet deposition, Dry deposition, POLYCYCLIC AROMATIC-HYDROCARBONS, POLYBROMINATED DIPHENYL ETHERS, POLYCHLORINATED-BIPHENYLS PCBS, AIR-WATER EXCHANGE, ORGANOCHLORINE PESTICIDES, ATMOSPHERIC DEPOSITION, DRY DEPOSITION, SURFACE WATERS, SOIL EXCHANGE, GAS-EXCHANGE
  • Dokuz Eylül University Affiliated: Yes

Abstract

Concentrations of several polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), and polybrominated diphenyl ethers (PBDEs) were measured in precipitation (n = 33) at a suburban site in Izmir, Turkey. Total (dissolved + particle) volume weighted mean (VWM) concentrations for Sigma(16)PAHs, Sigma(18)PCBs, Sigma(17)OCPs, and Sigma 7PBDEs were 785, 19.2, 50.5, and 29.6 ng l(-1), respectively. Low molecular weight (LMW) compounds (acenaphthylene, fluorene, phenanthrene) and congeners (PCB-18, 28, and 31) dominated the PAH and PCB concentrations, respectively. For PBDEs, BDE-209, and for OCPs, chlorpyrifos, a currently used pesticide, were the predominant compounds. Annual Sigma 7PBDEs flux was 18.74 mu g m(-2) year(-1). PBDE fluxes were mainly in dissolved phase for all congeners except BDE-209 which had comparable proportions in both phases. Annual flux for Sigma(16)PAHs was 497.4 mu g m(-2) year(-1); higher molecular weight (MW) PAH fluxes had comparable amounts in both phases while lower MW ones were mostly in dissolved phase. Wet deposition fluxes for Sigma(18)PCBs and Sigma(17)OCPs were 9.40 and 31.94 mu g m(-2) year(-1), respectively, and they were predominantly in dissolved phase. Wet deposition fluxes were compared to previously measured annual dry deposition fluxes at the study site to determine their relative contributions to annual total (dry particle + wet) deposition. Dry deposition was the major removal mechanism for most of the PAHs and PCBs contributing >80 % to total (wet + dry) deposition. However, both processes were comparable for PBDEs. Wet deposition was the predominant process for some OCPs such as alpha-chlordane, gamma-chlordane, and trans-nonachlor while both processes were comparable for chlorpyrifos and heptachlor epoxide.