PubMed · 1434440
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D Holenstein. 1992. [Buying--with ecological conscience].. https://pubmed.ncbi.nlm.nih.gov/1434440/
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Organophosphate esters (OPEs), widely used as flame retardants and plasticizers, have been increasingly detected in aquatic environments. However, investigations of their distribution in high-altitude plateau lakes remain scarce. Identifying and quantifying the sources and associated risks of OPEs are crucial for subsequent water environment management. In this study, an integrated source-risk analysis approach was employed by combining the Positive Matrix Factorization (PMF) model, the Geodetector (GD) model, and risk quotient (RQ). Analysis of 14 OPEs in surface waters of the Dianchi Lake Basin (DLB) revealed 12 detectable compounds, with total OPEs concentrations (ΣOPEs) ranging from not detected (ND)-64.6 ng/L during the wet season and ND-35.8 ng/L during the dry season. Elevated ΣOPEs were primarily observed at inflow sites in the northern part of the lake and in urban rivers. Source apportionment indicated four major contributing sources: agricultural films containing flame-retardant and plasticizer additives, traffic-related particulate emissions, releases from household and personal care products, and industrial production and applications of flame retardants in plastics, electronics, and related products (the predominant source). The ecological impact caused by OPEs ranges from no risk to low risk, with tris(2-chloroethyl) phosphate emitted from industrial source being the primary driver of potential environmental risk. These findings highlight the necessity of prioritizing industrial sources in future management strategies. Overall, this study provides a methodological framework for source apportionment and risk assessment of OPEs and offers scientific evidence to support environmental management of OPEs in the DLB.
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Waters entering the St. Lawrence River from Lake Ontario and from the Ottawa River have been sampled on a quaternary basis between March 1995 and October 1996. Mercury, iron, manganese, organic carbon and other chemical parameters have been determined in the filtered water (< 0.5 micron) and suspended particles (> 0.5 micron). Average total mercury concentrations (+/- standard deviation, number of determinations) in filtered samples were 1.3 +/- 0.9 pM (39) at the mouth of Lake Ontario and 4.0 +/- 2.3 pM (54) at the outlet of the Ottawa River. The respective average concentrations in suspended particles were 1.1 +/- 0.4 (39) and 0.6 +/- 0.2 (55) nmol g-1. Partial correlation analyses reveal that in the fraction < 0.5 micron--which seems to consist of a significant fraction of colloids--mercury was significantly linked to iron, while in the particulate phase, mercury was related to manganese. Mercury was not correlated with organic carbon. A sorption model on iron and manganese hydroxides is proposed to explain these observations.