Organophosphorus flame retardants (OPFRs) in the seawater and sediments of the Qinzhou Bay, Northern Beibu Gulf: Occurrence, distribution, and ecological risks.
The occurrence, distributions, and ecological risks of 11 organophosphate flame retardants (OPFRs) were investigated in the seawater and sediment samples from the Qinzhou Bay. The Σ11OPFRs in the surface seawater and sediments ranged from 150 to 885 ng/L and from <the limit of quantification (LOQ) to 32.2 ng/g dw, respectively, with high levels of OPFRs in the industrialized and port areas. Tris (2-chloro-propyl) phosphate (TCIPP), tris (2-chloroethyl) phosphate (TCEP), and tri-n-butyl phosphate (TNBP) were the dominant OPFRs in the surface seawater and sediments. The Σ11OPFRs concentrations in the sediment core ranged 1.2-18.6 ng/g dw and the vertical trends showed a recent increase of OPFRs emissions, especially for TNBP and triphenyl phosphate (TPHP). Risk assessment revealed that individual OPFR could pose low to medium ecological risks, but the risk from the mixture of OPFRs on aquatic organisms requires more attention.
Zhang L
，Lu L
，Zhu W
，Yang B
，Lu D
，Dan SF
，Zhang S
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Community-level risk assessments on organophosphate esters in the sediments from the Bohai Sea of China based on multimodal species sensitivity distributions coupled with the equilibrium partitioning method.
Organophosphate esters (OPEs), increasingly used as alternatives to brominated flame retardants, are ubiquitous in the global aquatic environment. Despite their potential toxicological impact on ecosystems, community-level risk assessments for OPEs in sediments remain scarce. This study investigated OPE occurrences and composition characteristics in the Bohai Sea's sediments and appraised both individual and joint ecological risks posed by characteristic OPE homologs using ten commonly used species sensitivity distribution (SSD) models, integrating acute-to-chronic conversion and phase equilibrium partitioning. OPEs were detected across all sediment samples, with total concentrations ranging from 0.213 ng/g dry weight (dw) to 91.1 ng/g dw. The predominant congeners included tri-n-butyl phosphate (TnBP), triisobutyl phosphate (TiBP), tri(2-ethylhexyl) phosphate, tris(2-chloroethyl) phosphate (TCEP), tris(1-chloro-2-propyl) phosphate (TCPP), tris(1, 3-dichloro-2-propyl) phosphate (TDCIPP), and triphenylphosphine oxide. Best-fit SSD models varied among TnBP, TiBP, TCEP, TCPP, and TDCIPP, demonstrating Sigmoid, Burr III, Sigmoid, Burr III, and Burr III, respectively. The same parametric model demonstrated variability in the fitting process for different OPE congeners, which also happened to the fitting results of ten parametric models for the same specific characteristic congener, underscoring the necessity of employing multiple models for precise community-level risk assessments. Hazard concentrations for a 5% cumulative probability were 0.116 mg/L, 2.88 mg/L, 1.30 mg/L, 1.44 mg/L, and 1.85 mg/L for each respective congener. The resulting risk quotients (RQ) and overall hazard index (HI) were selected as criteria to assess the individual and joint ecological risks of OPEs in sediments from the Bohai Sea, respectively. RQ and HI were both below 0.1, indicating a low risk to the local ecosystems. Multi-model SSD analysis could provide refined data for community-level risk evaluation, offering valuable insights for the development of evidence-based environmental standards and pollution control strategies.
Quan T
，Huang C
，Yao Z
，Liu Z
，Ma X
，Han D
，Qi Y
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Organophosphate flame retardants (OPFRs) in water and sediment: Occurrence, distribution, and hotspots of contamination of Lake Shihwa, Korea.
Contamination by organophosphate flame retardants (OPFRs) is an emerging concern in aquatic environments. Concentrations of 18 OPFRs were measured in water and sediments collected from the artificial Lake Shihwa. OPFR concentrations in sediments measured in this study were the highest reported worldwide, implying severe OPFR contamination. The highest concentrations of OPFRs were found in creeks taken near industrial complexes, and OPFR concentrations decreased with increasing distance from creeks to inshore or offshore lake waters. On-going OPFR contamination by wastewater treatment plant (WWTP) discharge was evidenced by the clear decrease in OPFRs in water samples collected moving away from WWTP outfall. TBEP and TEP were dominant in water samples, while TDCPP and TCPP were dominant in sediment samples. Differences in contamination profiles with sample matrices are likely due to hydrophobicity of individual OPFRs. Non-parametric multidimensional scaling ordination showed that OPFR contamination was affected by pollution inflow and proximity to industrial complexes.
Lee S
，Cho HJ
，Choi W
，Moon HB
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