The Hirnantian mass extinction was the second largest of the Phanerozoic. A global sea level fall resulting from a glaciation on Gondwanaland caused significant changes in ocean circulation patterns and nutrient cycling that is recorded as a worldwide positive δ13C excursion.<p>
In chapter 2, carbon and nitrogen isotope profiles were reconstructed from two North American carbonate platforms in Nevada and one in the Yukon with the purpose of gaining a better understanding of proximal to proximal gradients in δ13C values from Hirnantian epeiric seaway sediment. Positive δ13C excursions are recorded in bulk inorganic and organic carbon fractions from all three sections, and in graptolite periderms from one section. A larger positive excursion is recorded in the proximal sediment (7) compared to proximal sediment (3-4). This gradient appears to reflect differences in surface water dissolved inorganic carbon δ13C values across epeiric seas. These findings are consistent with the carbonate weathering hypothesis, that predicts larger positive δ13C shifts in proximal settings of tropical epeiric seas resulting from changes in the local carbon weathering flux caused by the exposure of vast areas of carbonate sediment during glacioeustatic sea level fall and restricted shelf circulation. A 2 positive excursion in δ15N is interpreted to result from increased ocean ventilation, greater partitioning of atmospheric oxygen into downwelling surface waters, oxygen minimum zone shrinkage, and declining denitrification rates. This allowed for upwelling of recycled nitrogen with high 15N values into the photic zone that forced exported organic matter from the photic zone to higher 15N values, consistent with the observed positive shift in 15N during the Hirnantian glaciation. This study presents a conceptual model to explain secular changes in δ13C and δ15N during the transition from a greenhouse to icehouse climate.<p>
The second focus of this research, presented in chapter 3, was on improving the chemical and analytical methods for δ18O analysis of biogenic apatites. The technique applies cation exchange chromatography that allows for small sample sizes of apatite (200 µg) to be used for chemical conversion to Ag3PO4. The precision (0.15, 1) of δ18O analysis obtained using a Thermal Conversion Elemental Analyser Continuous Flow Isotope Ratio Mass Spectrometer (TC/EA CF-IRMS), and the ability to collect multipe isotopes (O, Ca, Sr, REE) using a cation exchange column, makes this technique valuable for high-resolution, multi-isotope studies of biogenic apatites.
| Identifer | oai:union.ndltd.org:USASK/oai:usask.ca:etd-01072009-152505 |
| Date | 10 March 2009 |
| Creators | LaPorte, Dan F |
| Contributors | Mangano, Gabriela, Holmden, Chris, Buatois, Luis, Ansdell, Kevin M., Patterson, William P. |
| Publisher | University of Saskatchewan |
| Source Sets | University of Saskatchewan Library |
| Language | English |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://library.usask.ca/theses/available/etd-01072009-152505/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Saskatchewan or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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