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Updated: Jul 14, 2026

Development of Sulfidogenic Sludge from Marine Sediments and Trichloroethylene Reduction in an Upflow Anaerobic Sludge Blanket Reactor
Published on: October 15, 2015
Time trends in sources and dechlorination pathways of dioxins in agrochemically contaminated sediments
Minori Uchimiya1, Shigeki Masunaga
1Graduate School of Environment and Information Sciences, Yokohama National University, 79-7 Tokiwadai, Hodogaya, Yokohama 240-8501, Japan. uchimiya@ynu.ac.jp
Abstract:
Although polychlorinated dibenzo-p-dioxins and dibezofurans (PCDD/Fs) are considered recalcitrant toward biotic and abiotic degradation processes, laboratory studies indicated lateral dechlorination pathways (removal of 2,3,7,8-substituted chlorines) as possible natural remediation strategies under highly reducing conditions prevailing in contaminated sediments. Previous principal component analysis (PCA) of PCDD/Fs in Japanese sediments left unidentified a factor characterized by penta- to octa- homologues fully chlorinated at 1,2,6,9-positions (1,2,6,9-pattern). In the present study, we reexamined PCDD/Fs in sediment cores from urban (Tokyo Bay) and remote (Lake Shinji) areas of Japan using positive matrix factorization (PMF) and revealed a lateral dechlorination fingerprint exhibiting the 1,2,6,9-pattern. Relative molar concentrations of putative lateral dechlorination products linearly increased with sediment depth, suggesting that decades of reaction resulted in the accumulation of hepta- and hexa- chlorinated lateral dechlorination products in the bottom sediment layers. Times required for in situ formation of dechlorination products were estimated to be at least 27.8 +/- 17.9 year(mole %)(-1) in Lake Shinji and 4.7 +/- 0.5 year(mole %)(-1) in Tokyo Bay (both for the formation of 1,2,3,4,6,7,9-HpCDD) and are significantly longer than the dechlorination pathways observed in the laboratory.
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