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dc.contributor.advisorChristopher M. Reddy.en_US
dc.contributor.authorWhite, Helen Ken_US
dc.contributor.otherWoods Hole Oceanographic Institution.en_US
dc.date.accessioned2007-11-15T19:51:23Z
dc.date.available2007-11-15T19:51:23Z
dc.date.copyright2006en_US
dc.date.issued2006en_US
dc.identifier.urihttp://dspace.mit.edu/handle/1721.1/34566en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/34566
dc.descriptionThesis (Ph. D.)--Joint Program in Oceanography (Massachusetts Institute of Technology, Dept. of Earth, Atmospheric, and Planetary Sciences; and the Woods Hole Oceanographic Institution), 2006.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractTo provide a new perspective on the fate of both natural organic matter and hydrophobic organic contaminants (HOCs) in marine sediments, we have investigated the relationship between radiocarbon (14C) age and the different modes of association in aquatic sediments and soils. Radiocarbon is a sensitive tracer of OM provenance, with variations in its natural abundance reflecting the age and origin of material. The main objective has been to determine the significance of these associations, and to assess how they affect the transport, bioavailability, preservation and residence times of organic compounds in the environment. Our results indicate that the majority of HOCs that persist in marine sediments are solvent-extractable and incorporation into insoluble sediment residues is not quantitatively significant. For pristine sediments, systematic variations in 14C content are observed between different chemically defined sedimentary organic fractions. These variations are dependent on organic matter inputs and/or the affects of diagenesis. Our observations also provide evidence for the protection of labile marine carbon by chemical binding.en_US
dc.description.abstract(cont.) Finally, the persistence of n-alkanes from biogenic sources compared to those derived from petroleum indicates that protective matrix association can play a crucial role in determining the long-term fate of a compound. Overall, it is clear that both natural organic compounds and HOCs can undergo very different fates depending on their mode of introduction to, and physical disposition in environmental matrices.en_US
dc.description.statementofresponsibilityby Helen K. White.en_US
dc.format.extent204 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/34566en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectJoint Program in Oceanography.en_US
dc.subjectEarth, Atmospheric, and Planetary Sciences.en_US
dc.subjectWoods Hole Oceanographic Institution.en_US
dc.subject.lcshMarine sedimentsen_US
dc.subject.lcshCarbon compoundsen_US
dc.titleIsotopic constraints on the sources and associations of organic compounds in marine sedimentsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentJoint Program in Oceanographyen_US
dc.contributor.departmentWoods Hole Oceanographic Institutionen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences
dc.identifier.oclc71196529en_US


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