PubMed · 10111092
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1991. Update: formaldehyde.. https://pubmed.ncbi.nlm.nih.gov/10111092/
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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.
The quantity of the long lived (half-life 15.7 million years) radioactive isotope 129I in the pre-nuclear age ocean was approximately 100 kg. Various nuclear related activities, including weapons testing, nuclear fuel reprocessing, Chernobyl and other authorized or non-authorized dumping of radioactive waste have increased the ocean inventory of 129I by more than one order of magnitude. The most important of these sources are the direct marine discharges from the commercial reprocessing facilities at La Hague (France) and Sellafield (UK) which have discharged approximately 1640 kg in the English Channel, and approximately 720 kg in the Irish Sea, respectively. We discuss how this 129I can be used as both a 'pathway' and 'transit time' tracer in the North Atlantic and Arctic oceans, as well as a parameter for distinguishing between reprocessed and non-reprocessed nuclear waste in the ocean, and as a proxy for the transport and dilution of other soluble pollutants input to the North Sea.
More than 660 synthetic aperture radar (SAR) images acquired over the southern Baltic Sea, the North Sea, and the Gulf of Lion in the Mediterranean Sea by the Second European Remote Sensing Satellite (ERS-2) have been analyzed since December 1996 with respect to radar signatures of marine pollution and other phenomena causing similar signatures. First results of our analysis reveal that the seas are most polluted along the main shipping routes. The sizes of the detected oil spills vary between < 0.1 km2 and > 56 km2. SAR images acquired during descending (morning) and ascending (evening) satellite passes show different percentages of oil pollution, because most of this pollution occurs during night time and is still visible on the SAR images acquired in the morning time. Moreover, we found a higher amount of oil spills on SAR images acquired during summer (April-September) than on SAR images acquired during winter (October-March). We attribute this finding to the higher mean wind speed encountered in all three test areas during winter. By using an ERS-2 SAR image of the North Sea test area we show how the reduction of the normalized radar backscattering cross section (NRCS) by an oil spill depends on wind speed.