Historical record of polychlorinated biphenyls in a sediment core from Lake Biwa, Japan: Significance of unintentional emission and weathering signals revealed by full congener-specific analysis.

The occurrence of 209 PCB congeners was determined in a sediment core dated between 1930 and 2019 from Lake Biwa, a typical temperate monomictic lake in Japan. Concentrations of total PCBs ranged from 5.3 to 48 ng/g dry weight (dw), showing a highest peak at the 1960s to 1970s. The temporal trend of total PCBs in this sediment core generally matched with Japanese PCB production and emission pattern (i.e., increasing from the 1950s, peaking at 1970, and gradually decreasing since 1972). The vertical PCB profiles in our core were affected by physical mixing and bioturbation. By using a detailed and comprehensive analytical method, we have found elevated concentrations and special historical profiles of several congeners such as CB-7, -11, -47/48/75, -51, -68, and -209, which are still rarely included in routine PCB analysis. Some tetra-CB congeners like CB-47/48/75, -51, and -68 showed their concentration peaks at the early 2010s, which may be unintentionally produced during polymer manufacturing processes. PCB homolog- and congener-specific profiles in our sediment core samples have experienced weathering with higher proportions of penta- and hexa-CBs as compared to the Kanechlor usage pattern (i.e., dominated by tri- and tetra-CBs). Both intentional (i.e., technical mixtures) and unintentional (e.g., PCB-containing polymers and pigments) sources of PCBs were suggested from congener-specific analysis.

Determination of brominated flame retardants including polybrominated diphenyl ethers, pentabromoethylbenzene, hexabromobiphenyl, and decabromodiphenyl ethane in sediment samples: Validation of a rapid and efficient clean-up method and application to a sediment core from Lake Biwa, Japan.

The development of rapid and efficient analytical method for the determination of legacy and current-use brominated flame retardants (BFRs) has been performed due to environmental concern related to these pollutants. In the present study, we used an automated clean-up device equipped with pre-packed micro-column sets (containing sulfuric acid impregnated silica gel and silver-modified alumina) to develop an effective purification method for polybrominated diphenyl ethers (PBDEs), pentabromoethylbenzene, hexabromobiphenyl, and decabromodiphenyl ethane (DBDPE) in sediment extracts. Matrix-spiked sediments (n = 6) and the Standard Reference Material® 1944 samples (n = 6) were tested. Our method showed acceptable accuracy, repeatability, and sensitivity for almost all the target compounds with reduced processing time, labor requirement, and solvent amounts as compared to conventional clean-up method (e.g., sulfuric acid treatment and self-packed chromatographic columns). The validated method was applied to sediment core samples (n = 16) collected in 2019 from Lake Biwa, the largest lake in Japan. PBDEs were detected in sediment samples of 0-13 cm depth (dated between 1990 and 2019) at relatively low concentrations (median 5.7; range 2.6-9.4 ng/g dry weight). PBDE profiles were dominated by BDE-209, which accounted for 91 ± 10% of total PBDEs. Among other BFRs, only DBDPE was found in sediment layers of 0-9 cm depth (deposited between 2005 and 2019). DBDPE concentrations ranged from 0.43 to 1.6 (median 0.71) ng/g and showed increasing trend toward shallower depths.

Contamination levels and temporal trends of legacy and current-use brominated flame retardants in a dated sediment core from Beppu Bay, southwestern Japan.

Contamination levels and temporal trends of polybrominated diphenyl ethers (PBDEs) and some alternative brominated flame retardants (BFRs) were examined in a dated sediment core from the deepest part of the Beppu Bay, southwestern Japan. PBDEs were found in the upper layers of 0-15 cm depth at concentrations ranging from 5200 to 32,600 pg g-1 with the peak estimated at 1995. Decabromodiphenyl ether (BDE-209) was the most abundant congener, accounting for 96% in average of total PBDEs. The vertical profile of BDE-209 observed in our sediment core generally agreed with the historical pattern of domestic demand of commercial deca-BDE mixtures in Japan, and perfectly matched with maximum stock of these products (i.e., 42,000 tons in 1995). Among alternative BFRs, only decabromodiphenyl ethane (DBDPE), a replacement of deca-BDE, was found at significant levels with concentrations of 69-850 pg g-1 in sediment layers dated between 1991 and 2011. Ratios of DBDPE to BDE-209 gradually increased during this period, implying opposite trends of these two compounds and the role of DBDPE as a deca-BDE's alternative. The occurrence of deca-BDE components in sediments may pose medium risk to benthic aquatic life, while the ecological risk of other PBDE homologs and DBDPE was negligible.

Characterization of mono- to deca-chlorinated biphenyls in a well-preserved sediment core from Beppu Bay, Southwestern Japan: Historical profiles, emission sources, and inventory.

Contamination levels and profiles of mono- to deca-chlorinated biphenyls (PCBs) were characterized in a sediment core dated in 1954-2011 from Beppu Bay, southwestern Japan, providing a comprehensive and detailed picture on the environmental occurrence, temporal trends, and emission sources of these pollutants in the study area. Concentrations of total PCBs in the core ranged from 3.5 to 150 (median 15) ng g-1 dry weight and exhibited depth profile matching with Japanese PCB production and emission patterns (i.e., drastically increasing from the early 1960s, peaking in 1970, and then rapidly decreasing). Origin of PCBs in the studied samples largely associated with Kanechlor mixtures (e.g., KC-300 and KC-400), especially for sediment layers dated between the mid-1960s and early 1970s (i.e., the intensive PCB production period in Japan). In addition, dechlorination and weathering signals and emerging inputs of PCBs were also observed in deeper and shallower sediment segments with notable proportions of some unique congeners such as CB-47/48/51 and CB-11, respectively. Historical fluxes of PCBs in our samples showed quite similar vertical shape as concentrations. In the context of national implementation for complete treatment of PCB-containing waste until 2024, further investigations on spatiotemporal trends and environmental loads of PCBs in Japan are necessary.