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A New Insight into the Geochemistry ...

Fakhraee, Mojtaba.

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A New Insight into the Geochemistry of Sulfur in Low Sulfate Environments.

Record Type:	Electronic resources : Monograph/item
Title/Author:	A New Insight into the Geochemistry of Sulfur in Low Sulfate Environments./
Author:	Fakhraee, Mojtaba.
Published:	Ann Arbor : ProQuest Dissertations & Theses, : 2018,
Description:	241 p.
Notes:	Source: Dissertations Abstracts International, Volume: 80-05, Section: B.
Contained By:	Dissertations Abstracts International80-05B.
Subject:	Geobiology. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10930536
ISBN:	9780438565661

A New Insight into the Geochemistry of Sulfur in Low Sulfate Environments.
Fakhraee, Mojtaba.

A New Insight into the Geochemistry of Sulfur in Low Sulfate Environments. - Ann Arbor : ProQuest Dissertations & Theses, 2018 - 241 p.

Source: Dissertations Abstracts International, Volume: 80-05, Section: B.

Thesis (Ph.D.)--University of Minnesota, 2018.

This item must not be sold to any third party vendors.

As an essential element for life, sulfur plays an important role in the biosphere, hydrosphere, atmosphere and lithosphere. Studies of sulfur cycling have been traditionally concentrated on modern marine environments with 28mM of sulfate, yet its importance in low sulfate environments such as large freshwater systems as well as the oceans of the geologic past (>0.5 billion years ago) cannot be neglected. This thesis, through modeling and theoretical approach, aims to provide a new insight into several aspects of sulfur cycling in low sulfate environments. For example, it is widely assumed that water-column sulfate is the main sulfur source to fuel microbial sulfate reaction in sediments. While this assumption may be justified in high-sulfate environments such as modern seawater, I show that in low-sulfate environments mineralization of organic sulfur compounds can be an important source of sulfate and sedimentary sulfide. The results in this thesis indicate that in low sulfate environments (50%) of sulfate reduction. Extrapolating the results to Archean oceans with tens of µM of sulfate, modeling results reveal that sulfite generated by mineralization of organic sulfur could fuel microbial S reduction in the absence of ambient sulfate, and hydrogen sulfide generated by mineralization of reduced organic S compounds could provide a pathway to pyrite that bypassed the microbial reduction of sulfate or sulfite. Reproducing isotopic records in the sedimentary sulfides from the rock record, modeling results show that in the low sulfate (<10 µM) environment of the Archean oceans (2.5-4 billion years ago), oxygen could have accumulated to up to 25 µM, while being consistent with the sulfur isotopic composition in Neoarchean rocks. A mass balance model coupled to a sediment diagenesis model suggests that seawater sulfate concentrations during the Proterozoic Eon (0.5-2.4 billion years ago) remained below 1.5% of modern values (<500 µM), and possibly as low as 100 µM. Using exploratory modeling of sulfur cycling, I also constrain the geochemical factors that control the fluxes of methylmercury from modern freshwater sediments. Modeling results identify oxygen, sulfate, and organic matter as leading geochemical parameters. They also suggest a critical level of oxygen at the sediment water interface, below which methylation rate dominates demethylation rate, resulting in an efflux of methylmercury into overlying water.

ISBN: 9780438565661Subjects--Topical Terms:

549918
Geobiology.

A New Insight into the Geochemistry of Sulfur in Low Sulfate Environments.
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506 $a This item must not be sold to any third party vendors.
520 $a As an essential element for life, sulfur plays an important role in the biosphere, hydrosphere, atmosphere and lithosphere. Studies of sulfur cycling have been traditionally concentrated on modern marine environments with 28mM of sulfate, yet its importance in low sulfate environments such as large freshwater systems as well as the oceans of the geologic past (>0.5 billion years ago) cannot be neglected. This thesis, through modeling and theoretical approach, aims to provide a new insight into several aspects of sulfur cycling in low sulfate environments. For example, it is widely assumed that water-column sulfate is the main sulfur source to fuel microbial sulfate reaction in sediments. While this assumption may be justified in high-sulfate environments such as modern seawater, I show that in low-sulfate environments mineralization of organic sulfur compounds can be an important source of sulfate and sedimentary sulfide. The results in this thesis indicate that in low sulfate environments (50%) of sulfate reduction. Extrapolating the results to Archean oceans with tens of µM of sulfate, modeling results reveal that sulfite generated by mineralization of organic sulfur could fuel microbial S reduction in the absence of ambient sulfate, and hydrogen sulfide generated by mineralization of reduced organic S compounds could provide a pathway to pyrite that bypassed the microbial reduction of sulfate or sulfite. Reproducing isotopic records in the sedimentary sulfides from the rock record, modeling results show that in the low sulfate (<10 µM) environment of the Archean oceans (2.5-4 billion years ago), oxygen could have accumulated to up to 25 µM, while being consistent with the sulfur isotopic composition in Neoarchean rocks. A mass balance model coupled to a sediment diagenesis model suggests that seawater sulfate concentrations during the Proterozoic Eon (0.5-2.4 billion years ago) remained below 1.5% of modern values (<500 µM), and possibly as low as 100 µM. Using exploratory modeling of sulfur cycling, I also constrain the geochemical factors that control the fluxes of methylmercury from modern freshwater sediments. Modeling results identify oxygen, sulfate, and organic matter as leading geochemical parameters. They also suggest a critical level of oxygen at the sediment water interface, below which methylation rate dominates demethylation rate, resulting in an efflux of methylmercury into overlying water.
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