The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis
Thesis (M.Sc.)--Memorial University of Newfoundland, 1999. Chemistry Bibliography: leaves 118-130 In the context of a multidisciplinary study to determine current and past ecosystem health, sterols were analyzed in plankton, settling particles and sediments from Trinity Bay, Newfoundland by saponifi...
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ftmemorialunivdc:oai:collections.mun.ca:theses3/25311 2023-05-15T17:23:32+02:00 The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis Hudson, Edward D., 1972- Memorial University of Newfoundland. Dept. of Chemistry Canada--Newfoundland and Labrador--Trinity Bay 1999 xiii, 135 leaves : ill., map Image/jpeg; Application/pdf http://collections.mun.ca/cdm/ref/collection/theses3/id/25311 eng eng Electronic Theses and Dissertations (19.41 MB) -- http://collections.mun.ca/PDFs/theses/Hudson_EdwardD.pdf a1393724 http://collections.mun.ca/cdm/ref/collection/theses3/id/25311 The author retains copyright ownership and moral rights in this thesis. Neither the thesis nor substantial extracts from it may be printed or otherwise reproduced without the author's permission. Paper copy kept in the Centre for Newfoundland Studies, Memorial University Libraries Sterols--Analysis Seawater--Sterol content--Newfoundland and Labrador--Trinity Bay Text Electronic thesis or dissertation 1999 ftmemorialunivdc 2015-08-06T19:17:45Z Thesis (M.Sc.)--Memorial University of Newfoundland, 1999. Chemistry Bibliography: leaves 118-130 In the context of a multidisciplinary study to determine current and past ecosystem health, sterols were analyzed in plankton, settling particles and sediments from Trinity Bay, Newfoundland by saponification, derivatization to their TMS ethers and GC and GC/MS. Plankton net tow samples and settling particles contained C27 and C28 sterols typical of marine plankton. However, higher plant C28 and C29 sterols were prominent in sediments from both in-shore and off-shore sites, indicating an appreciable terrestrial contribution to sedimentary organic carbon and either degradation or effective recycling of marine sterols. No decrease in total or individual sterols was observed down the cores, suggesting good overall preservation. The fecal sterol coprostanol was not detected in offshore sediments, net tow material or settling particles, and was present only at low levels in certain in-shore sedimentary horizons. This suggests that sewage discharges in rural Newfoundland are being efficiently degraded or dispersed. -- Total free sterols in the samples were determined by Iatroscan TLC-FTD on Chromarods, a widely-used method which effectively separates and quantifies lipid classes but provides no further information on the species in each class. Thus, a new method (TLC- Pyrolysis-GC/MS) was developed in which lipid bands are desorbed directly from the silica Chromarod surface into a GC/MS for analysis. Twelve lipid classes were either desorbed without further treatment, converted to trimethylsilyl derivatives on the Chromarod, or analyzed following in situ thermochemolysis with tetramethylammonium hydroxide. The method's utility was demonstrated with lipids from settling particles, especially where TLC bands contained more than one lipid class (wax/steryl esters, acetone-mobile polar lipids). Wax esters up to C42 were detected, with alkyl and acyl distributions consistent with a zooplankton source. The wax ester/steryl ester band contained no more than 8% steryl esters, suggesting that their contribution to this band is minimal but that their contribution to total sterols may be significant. The free sterol carbon number distribution in settling particles as determined by TLC-Pyrolysis-GC/MS matched that as determined by individual molecular species analysis (predominantly C27). By extending the scope of Iatroscan TLC-FID, the new method should have applications in many fields besides marine environmental studies viz. food science, biomedical science and petroleum analysis. Thesis Newfoundland studies University of Newfoundland Memorial University of Newfoundland: Digital Archives Initiative (DAI) Canada Fid ENVELOPE(-65.939,-65.939,-68.664,-68.664) Fid The ENVELOPE(-65.939,-65.939,-68.664,-68.664) Newfoundland |
institution |
Open Polar |
collection |
Memorial University of Newfoundland: Digital Archives Initiative (DAI) |
op_collection_id |
ftmemorialunivdc |
language |
English |
topic |
Sterols--Analysis Seawater--Sterol content--Newfoundland and Labrador--Trinity Bay |
spellingShingle |
Sterols--Analysis Seawater--Sterol content--Newfoundland and Labrador--Trinity Bay Hudson, Edward D., 1972- The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
topic_facet |
Sterols--Analysis Seawater--Sterol content--Newfoundland and Labrador--Trinity Bay |
description |
Thesis (M.Sc.)--Memorial University of Newfoundland, 1999. Chemistry Bibliography: leaves 118-130 In the context of a multidisciplinary study to determine current and past ecosystem health, sterols were analyzed in plankton, settling particles and sediments from Trinity Bay, Newfoundland by saponification, derivatization to their TMS ethers and GC and GC/MS. Plankton net tow samples and settling particles contained C27 and C28 sterols typical of marine plankton. However, higher plant C28 and C29 sterols were prominent in sediments from both in-shore and off-shore sites, indicating an appreciable terrestrial contribution to sedimentary organic carbon and either degradation or effective recycling of marine sterols. No decrease in total or individual sterols was observed down the cores, suggesting good overall preservation. The fecal sterol coprostanol was not detected in offshore sediments, net tow material or settling particles, and was present only at low levels in certain in-shore sedimentary horizons. This suggests that sewage discharges in rural Newfoundland are being efficiently degraded or dispersed. -- Total free sterols in the samples were determined by Iatroscan TLC-FTD on Chromarods, a widely-used method which effectively separates and quantifies lipid classes but provides no further information on the species in each class. Thus, a new method (TLC- Pyrolysis-GC/MS) was developed in which lipid bands are desorbed directly from the silica Chromarod surface into a GC/MS for analysis. Twelve lipid classes were either desorbed without further treatment, converted to trimethylsilyl derivatives on the Chromarod, or analyzed following in situ thermochemolysis with tetramethylammonium hydroxide. The method's utility was demonstrated with lipids from settling particles, especially where TLC bands contained more than one lipid class (wax/steryl esters, acetone-mobile polar lipids). Wax esters up to C42 were detected, with alkyl and acyl distributions consistent with a zooplankton source. The wax ester/steryl ester band contained no more than 8% steryl esters, suggesting that their contribution to this band is minimal but that their contribution to total sterols may be significant. The free sterol carbon number distribution in settling particles as determined by TLC-Pyrolysis-GC/MS matched that as determined by individual molecular species analysis (predominantly C27). By extending the scope of Iatroscan TLC-FID, the new method should have applications in many fields besides marine environmental studies viz. food science, biomedical science and petroleum analysis. |
author2 |
Memorial University of Newfoundland. Dept. of Chemistry |
format |
Thesis |
author |
Hudson, Edward D., 1972- |
author_facet |
Hudson, Edward D., 1972- |
author_sort |
Hudson, Edward D., 1972- |
title |
The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
title_short |
The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
title_full |
The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
title_fullStr |
The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
title_full_unstemmed |
The biogeochemistry of sterols in Trinity Bay, Newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
title_sort |
biogeochemistry of sterols in trinity bay, newfoundland, and a new method (thin layer chromatography-pyrolysis-gas chromatography-mass spectrometry) for their analysis |
publishDate |
1999 |
url |
http://collections.mun.ca/cdm/ref/collection/theses3/id/25311 |
op_coverage |
Canada--Newfoundland and Labrador--Trinity Bay |
long_lat |
ENVELOPE(-65.939,-65.939,-68.664,-68.664) ENVELOPE(-65.939,-65.939,-68.664,-68.664) |
geographic |
Canada Fid Fid The Newfoundland |
geographic_facet |
Canada Fid Fid The Newfoundland |
genre |
Newfoundland studies University of Newfoundland |
genre_facet |
Newfoundland studies University of Newfoundland |
op_source |
Paper copy kept in the Centre for Newfoundland Studies, Memorial University Libraries |
op_relation |
Electronic Theses and Dissertations (19.41 MB) -- http://collections.mun.ca/PDFs/theses/Hudson_EdwardD.pdf a1393724 http://collections.mun.ca/cdm/ref/collection/theses3/id/25311 |
op_rights |
The author retains copyright ownership and moral rights in this thesis. Neither the thesis nor substantial extracts from it may be printed or otherwise reproduced without the author's permission. |
_version_ |
1766113056041992192 |