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dc.contributor.authorTotten, Lisa A.-
dc.contributor.authorGigliotti, Cari L.-
dc.contributor.authorVanRy, Daryl A.-
dc.contributor.authorOffenberg, John H.-
dc.contributor.authorNelson, Eric D.-
dc.contributor.authorDachs, Jordi-
dc.contributor.authorReinfelder, John R.-
dc.contributor.authorEisenreich, Steven J.-
dc.date.accessioned2009-09-01T12:37:00Z-
dc.date.available2009-09-01T12:37:00Z-
dc.date.issued2004-03-25-
dc.identifier.citationEnvironmental Science and Technology 38(9): 2568-2573 (2004)en_US
dc.identifier.issn0013-936X-
dc.identifier.urihttp://hdl.handle.net/10261/16527-
dc.description6 pages, 3 figures, 1 table.-- PMID: 15180052 [PubMed].-- Printed version published May 1, 2004.-- Supporting information available at: http://pubs.acs.org/doi/suppl/10.1021/es034878cen_US
dc.description.abstractThe first estimates of atmospheric deposition fluxes of polychlorinated biphenyls (PCBs) to the Hudson River Estuary are presented. Concentrations of PCBs were measured in air, aerosol, and precipitation at nine sites representing a variety of land-use regimes at regular intervals from October 1997 through May 2001. Highest concentrations in the gas phase were observed at urban sites such as Camden and Jersey City (∑PCB concentrations averaged 3250 and 1260 pg m-3, respectively). In great portions of the state encompassing forested, coastal, and suburban environments, gas-phase ∑PCB concentrations were essentially the same (averaging 150−220 pg m-3). This spatial trend suggests that atmospheric PCBs arise from highly localized, urban sources which influence atmospheric concentrations and deposition fluxes over a distance of a few tens of kilometers. Atmospheric ∑PCB deposition fluxes (gas absorption + dry particle deposition + wet deposition) ranged from 7.3 to 340 μg m-2 yr-1 and increased with proximity to urban areas. While the magnitude of the fluxes increased with urbanization, the relative proportions of wet, dry, and gaseous deposition remained largely constant. Because the Hudson River Estuary is adjacent to urban areas such as Jersey City, it is subject to higher depositional fluxes of PCBs. These depositional fluxes are at least 2−10 times those estimated for the Chesapeake Bay and Lake Michigan. Inputs of PCBs to the Hudson River Estuary from the upper Hudson River and from wastewater treatment plants are 8−18 times atmospheric inputs, and volatilization of PCBs from the estuary exceeds atmospheric deposition of low molecular weight PCBs.en_US
dc.description.sponsorshipThis research was supported by the New Jersey Department of Environmental Protection and the National Sea Grant College Program of the U.S. Department of Commerce's National Oceanic and Atmospheric Administration under NOAA Grant No. NA76-RG0091 (NJSG-01454). This research was also funded in part by a grant from the Hudson River Foundation (Project Officer Dennis Suzskowski) and the New Jersey Agricultural Experiment Station.en_US
dc.format.extent22195 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsclosedAccessen_US
dc.subjectPolychlorinated biphenylsen_US
dc.subjectPCBsen_US
dc.subjectAtmospheric concentrationsen_US
dc.subjectAtmospheric depositionen_US
dc.subjectHudson River Estuaryen_US
dc.titleAtmospheric concentrations and deposition of polychorinated biphenyls to the Hudson River Estuaryen_US
dc.typeartículoen_US
dc.identifier.doi10.1021/es034878c-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1021/es034878cen_US
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairetypeartículo-
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