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Spatial trends of total mercury (THg) exposure, and the role of intestinal helminths on its distribution within piscivorous mammalian hosts

dc.contributor.authorMcGrew, Ashley Kaye, author
dc.contributor.authorBallweber, Lora R., advisor
dc.contributor.authorSalman, Mo D., advisor
dc.contributor.authorO'Hara, Todd M., committee member
dc.contributor.authorClements, Will H., committee member
dc.date.accessioned2007-01-03T08:20:40Z
dc.date.available2007-01-03T08:20:40Z
dc.date.issued2011
dc.description.abstractThis research project is unique in that it has explored the interface of three broad disciplines: ecology, toxicology, and parasitology. The primary objectives were to determine the role of gastrointestinal (GI) helminths in total mercury (THg) distribution within piscivorous mammalian hosts, and explore the complex interactions that exist within the host GI tract. The project was designed to address these objectives in two pinniped populations: Alaskan ice seals (Phoca largha and Phoca hispida), and California sea lions (Zalophus californianus). Initially, Alaskan gray wolves (Canis lupus) were selected as a reference species for this project, as these animals represent a mammalian definitive host, occupying a top trophic position in a terrestrial food web; nevertheless, preliminary findings demonstrated a subset of these wolves to be subsisting, at least in part, on prey sources of marine origin. Therefore, the project was expanded to include the Alaskan gray wolves as an additional "piscivorous" host for study. At necropsy, host tissues and GI tracts were collected. During GI tract processing, intestinal helminths were removed, weighed, and either saved for identification, or frozen for further analyses. Host tissues (e.g. liver, kidney, cardiac muscle, skeletal muscle), GI lumen contents, and parasites were then analyzed for THg concentrations and stable isotope values (C, N, and S). In Alaskan gray wolves, THg concentrations, and δ13C, δ15N and δ34S isotope values, provided four separate measures supporting the contention that Alaskan gray wolves, with access to marine resources, are relying on piscivory or exploitation of other organisms of marine origin. THg uptake was demonstrated to occur in these animals, and the toxicant-parasite interactions that exist within the GI tract may ultimately affect the host-toxicant interface. The interactions described depend not only on type of parasite and specific toxicant, but also on the complex ecological-like interactions within the host's body. In pinnipeds, parasites were shown to effectively bioaccumulate and/or biomagnify mercury (Hg) within the host GI tract. Within-parasite THg concentrations were not necessarily associated with concentrations in host lumen contents, or host liver and kidney. These data demonstrated that THg distribution in the host is affected by the presence of parasites; consequently, bioavailability of this toxicant to the host may also be affected. A design has been proposed for building an agent-based model, to further explore the interactions described in these studies. This framework will provide a foundation for future work focused on the ecotoxicoparasitology of other related systems.
dc.format.mediumborn digital
dc.format.mediumdoctoral dissertations
dc.identifierMcGrew_colostate_0053A_10861.pdf
dc.identifierETDF2011400255MIPA
dc.identifier.urihttp://hdl.handle.net/10217/70450
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectanisakid
dc.subjectbioaccumulation
dc.subjectmercury
dc.subjectstable isotopes
dc.subject.lcshCorynosoma
dc.titleSpatial trends of total mercury (THg) exposure, and the role of intestinal helminths on its distribution within piscivorous mammalian hosts
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineMicrobiology, Immunology, and Pathology
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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