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Untargeted Screening and Distribution of Organo-Bromine Compounds in Sediments of Lake Michigan.

TitleUntargeted Screening and Distribution of Organo-Bromine Compounds in Sediments of Lake Michigan.
Publication TypeJournal Article
Year of Publication2016
AuthorsPeng, H, Chen, C, Cantin, J, Saunders, DMV, Sun, J, Tang, S, Codling, G, Hecker, M, Wiseman, S, Jones, PD, Li, A, Rockne, KJ, Sturchio, NC, Giesy, JP
JournalEnviron Sci Technol
Volume50
Issue1
Pagination321-30
Date Published2016 Jan 05
ISSN1520-5851
KeywordsBromine Compounds, Environmental Monitoring, Geologic Sediments, Halogenated Diphenyl Ethers, Hydrocarbons, Brominated, Lakes, Michigan, Water Pollutants, Chemical
Abstract

Previously unreported natural and synthetic organo-bromine compounds (NSOBCs) have been found to contribute more than 99% of total organic bromine (TOB) in environmental matrices. We recently developed a novel untargeted method (data-independent precursor isolation and characteristic fragment, DIPIC-Frag) and identified ∼2000 NSOBCs in two sediments from Lake Michigan. In this study, this method was used to investigate the distributions of these NSOBCs in 23 surficial samples and 24 segments of a sediment core from Lake Michigan. NSOBCs were detected in all 23 surficial samples and exhibited 10- to 100-fold variations in peak abundance among locations. The pattern of distributions of NSOBCs was correlated with depth of the water column (r(2) = 0.61, p < 0.001). Hierarchical cluster analysis showed that sediments in close proximity exhibited similar profiles of NSOBCs. Distributions of NSOBCs in 24 segments of a sediment core dated from 1766 to 2008 were investigated, and samples from similar depths exhibited similar profiles of NSOBCs. NSOBCs were grouped into four clusters (soft-cluster analysis) with different temporal trends of abundances. 515 and 768 of the NSOBCs were grouped into cluster 1 and cluster 3 with increasing temporal trends, especially since 1950, indicating that abundances of these compounds might have been affected by human activities.

DOI10.1021/acs.est.5b04709
Alternate JournalEnviron. Sci. Technol.
PubMed ID26618527
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