Halogenated organic compounds in archived whale oil : a pre-industrial record

Author Posting. © The Authors, 2006. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Environmental Pollution 145 (2007): 668-671, doi:10.1016/j.envpol.2006.08.022.To provide additional evidence that several halogenated organic compounds (HOCs) found in environmental samples are natural and not industrially produced, we analyzed an archived whale oil sample collected in 1921 from the last voyage of the whaling ship Charles W. Morgan. This sample, which predates large-scale industrial manufacture of HOCs, contained two methoxylated polybrominated diphenyl ethers (MeO-PBDEs), five halogenated methyl bipyrroles (MBPs), one halogenated dimethyl bipyrrole (DMBP), and one dimethoxylated polybrominated biphenyl (diMeO-PBB). This result indicates, at least in part, a natural source of the latter compounds. Capsule Nine halogenated organic compounds have been detected in archived whale oil from the 1920s.This work was supported by the National Science Foundation (OCE-0221181 and OCE-0550486), the Woods Hole Oceanographic Institution (WHOI) Ocean Life Institute and the Postdoctoral Scholar Program at WHOI (with funding from The Camille and Henry Dreyfus Foundation, Inc. and The J. Seward Johnson Fund)

Identification of highly brominated analogues of Q1 in marine mammals

Author Posting. © The Authors, 2005. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Environmental Pollution 144 (2006): 336-344, doi:10.1016/j.envpol.2005.10.052.Three novel halogenated organic compounds (HOCs) have been identified in the blubber of marine mammals from coastal New England with the molecular formulae C9H3N2Br6Cl, C9H3N2Br7, and C9H4N2Br5Cl. They were identified using high and low resolution electron ionization (EI) and electron capture negative ionization (ECNI) gas chromatography mass spectrometry (GCMS) and appear to be highly brominated analogues of Q1, a heptachlorinated HOC that has been suspected to be naturally-produced. These new compounds were found in Atlantic white sided dolphin (Lagenorhynchus acutus), bottlenose dolphin (Tursiops truncatus), common dolphin (Delphinus delphis), Risso’s dolphin (Grampus griseus), harbor porpoise (Phocoena phocoena), beluga whale (Delphinapterus leucas), fin whale (Balaenoptera physalus), grey seal (Halichoerus grypus), harp seal (Phoca groenlandica) and a potential food source (Loligo pealei) with concentrations as high as 2.7 μg/g (lipid weight). The regiospecificity of C9H3N2Br6Cl is suggestive of a biogenic origin. Debromination of C9H3N2Br6Cl may be significant in the formation of C9H4N2Br5Cl.This work was supported by the National Science Foundation (OCE-0221181), the Woods Hole Oceanographic Institution (WHOI) Ocean Life Institute, the Postdoctoral Scholar Program at WHOI (with funding from The Camille and Henry Dreyfus Foundation, Inc. and The J. Seward Johnson Fund) (ELT) and The Island Foundation, Inc (BEP)

Natural 14C in Saccoglossus bromophenolosus compared to 14C in surrounding sediments

Author Posting. © Inter-Research, 2006. This article is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Marine Ecology Progress Series 324 (2006): 167-172, doi:10.3354/meps324167.The natural radiocarbon (14C) content of whole, gut voided Saccoglossus bromophenolosus collected in Lowes Cove, Maine, USA, was compared with that of a non-voided worm, sectioned individuals, and the natural product 2,4-dibromophenol (2,4-DBP) isolated from S. bromophenolosus. In all cases, the 14C content was greater than that of the sediment from which the enteropneusts were collected. The 14C content of 2 polychaetes, Glycera dibranchiata and Clymenella torquata, also collected from Lowes Cove, were similarly enriched in 14C compared to the bulk sediment. These results show that all 3 species consumed recently fixed carbon that was much newer than organic carbon in the bulk sediment. The value (+10.4‰) obtained for 2,4-DBP isolated from S. bromophenolosus in this study differs from that reported in a previous study (–170‰). The discrepancy is attributed to methodological differences. The importance of selecting an appropriate method when isolating compounds for natural abundance 14C analysis is discussed.This work was supported by the National Science Foundation (OCE-0221181) and the Postdoctoral Scholar Program at Woods Hole Oceanographic Institution (with funding provided by the Camille and Henry Dreyfus Foundation and the J. Seward Johnson Fund, awarded to E.L.T.)

Transport and release of chemicals from plastics to the environment and to wildlife

Plastics debris in the marine environment, including resin pellets, fragments and microscopic plastic fragments, contain organic contaminants, including polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons, petroleum hydrocarbons, organochlorine pesticides (2,2′-bis(p-chlorophenyl)-1,1,1-trichloroethane, hexachlorinated hexanes), polybrominated diphenylethers, alkylphenols and bisphenol A, at concentrations from sub ng g–1 to µg g–1. Some of these compounds are added during plastics manufacture, while others adsorb from the surrounding seawater. Concentrations of hydrophobic contaminants adsorbed on plastics showed distinct spatial variations reflecting global pollution patterns. Model calculations and experimental observations consistently show that polyethylene accumulates more organic contaminants than other plastics such as polypropylene and polyvinyl chloride. Both a mathematical model using equilibrium partitioning and experimental data have demonstrated the transfer of contaminants from plastic to organisms. A feeding experiment indicated that PCBs could transfer from contaminated plastics to streaked shearwater chicks. Plasticizers, other plastics additives and constitutional monomers also present potential threats in terrestrial environments because they can leach from waste disposal sites into groundwater and/or surface waters. Leaching and degradation of plasticizers and polymers are complex phenomena dependent on environmental conditions in the landfill and the chemical properties of each additive. Bisphenol A concentrations in leachates from municipal waste disposal sites in tropical Asia ranged from sub µg l–1 to mg l–1 and were correlated with the level of economic development