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Evaluation of Anaerobic Biodegradation of Organic Carbon Extracted from Aquifer Sediment

Abstract

dc:description.abstract

In conjunction with ongoing studies to develop a method for quantifying potentially biodegradable organic carbon (Rectanus et al 2005), this research was conducted to evaluate the extent to which organic carbon extracted using this method will biodegrade in anaerobic environments. The ultimate goal is to use this method for the evaluation of chloroethene contaminated sites in order to estimate the long-term sustainability of monitored natural attenuation (MNA) as a remediation strategy. Although relatively recalcitrant under aerobic conditions, the breakdown of chlorinated solvents primarily occurs through the anaerobic process of reductive dechlorination. The biodegradation of organic carbon in these anaerobic environments drives the system to reducing conditions conducive for reductive dechlorination. The extraction procedure developed by Rectanus et al. (2005) has been tested in several series of aerobic bioassays to determine the biodegradable fraction of carbon extracted. This study seeks to show that the carbon removed from the sediment by this extraction process will also degrade in anaerobic environments. Three aquifer sediment samples characterized by low, medium, and high carbon concentrations were taken from Naval Submarine Base Kings Bay, Georgia. Two sites were also sampled from Naval Amphibious Base Little Creek, Virginia. MLS20 is a site located inside of a chloroethene plume, and MLS10 is located outside of the plume. For approximately 12 weeks aqueous total organic carbon (TOC), headspace carbon dioxide (CO2), volatile fatty acids (VFAs), and headspace hydrogen concentrations were monitored for evidence of the biodegradation of organic carbon. Although few VFAs were observed throughout the experiments, their presence as early as 8 days after inoculation indicated that the bioassays were anaerobic. The fewest VFAs were seen in the MLS20 bioassays, while the most VFAs were observed in the MLS10 bioassays. MLS20 exhibited low levels of TOC loss and the low VFA levels indicate that complex organic matter was not highly degraded in these bioassays. The higher level of VFAs observed in MLS10 bioassays corresponded with little TOC degradation, indicating that although more complex organics were being broken down, conditions were not reduced enough to further oxidize the organic carbon. As much as 50% TOC loss was observed in the Kings Bay bioassays with few VFAs detected. Loss of TOC was accompanied by CO₂ generation which provides supporting evidence that organic carbon was being oxidized. Hydrogen was observed in the bioassays, suggesting that VFAs resulting from organic carbon breakdown were being oxidized. This indicates that organic carbon removed from sediment using the extraction process is biodegraded anaerobically and could lead to conditions capable of sustaining reductive dechlorination.

Degree

thesis:*
Name thesis:degree_name
Master of Science
Level thesis:degree_level
masters
Discipline thesis:degree_discipline
Environmental Sciences and Engineering
Department dc:contributor.department
Environmental Sciences and Engineering
Grantor dc:publisher
Virginia Tech
Year dc:date.issued
2006

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Kelly, Catherine Aileen
Chairs dc:contributor.committeechair
  • Widdowson, Mark A.
  • Novak, John T.
Committee member dc:contributor.committeemember
  • Vikesland, Peter J.

Subjects

dc:subject × 4

Rights

dc:rights
Statement dc:rights
  • In Copyright

Identifiers

dc:identifier.*
Dc Identifier Other
etd-09202006-140436
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/44888

Chain of custody

source
Harvested from
Virginia Tech
Base URL
vtechworks.lib.vt.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Kelly, Catherine Aileen. Evaluation of Anaerobic Biodegradation of Organic Carbon Extracted from Aquifer Sediment. masters thesis, Virginia Tech, 2006. http://hdl.handle.net/10919/44888