DOE/NETL Methane Hydrate Projects
Reconstructing Paleo-SMT Positions on the Cascadia Margin Using Magnetic Susceptibility Last Reviewed 1/2/2015


The goal of this project is to provide the gas hydrate community with a proven, geologically well-preserved proxy for paleo- sulfate-methane transition (SMT) reconstructions using magnetic susceptibility (χ) and grain size measurements to track diagenetic changes that are associated with the anaerobic oxidation of methane.  To achieve this goal, this project aims to (1) reconstruct the paleo-positions of the (SMT) using a  magnetic susceptibility (χ) and grain size proxy approach in gas hydrate-bearing sediment cores collected on the Cascadia continental margin during ODP Leg 204 and Integrated Ocean Drilling Program (IODP) Exp. 311, and (2) utilize gas hydrate systems specific CrunchFlow reactive transport modules to ultimately model the required methane and sulfate fluxes that best explain the paleo-positions of the SMT at sites on both the northern and central Cascadia margin. These data will be utilized to understand the natural variability in the flux of methane and sulfate implicit from the SMT migration history on the Cascadia margin. These data will also be used to assess whether this approach can be utilized on a future coring expedition to reconstruct the modern and recent past fluxes of methane and sulfate at a site located near the upper hydrate stability boundary, i.e., the region in marine gas hydrate systems that is the most susceptible to environmental change.

University of New Hampshire (UNH), Durham, NH 03824-3585

Methane in marine sediments, often existing ephemerally as gas hydrate, constitutes one of the largest reservoirs of natural gas on Earth, and fluxes of methane in marine sediments may be an important component in the global carbon cycle. Tracking changes in past methane flux, however, remains difficult as there are few available proxies that persist through geologic time.

Modern methane fluxes, as constrained by porewater geochemistry, provide a snapshot of the present-day SMT. Other proxies of SMT positions such as zones of authigenic barite can provide only a partial record of paleo-SMT positions because barites can easily dissolve in the stratigraphy below the most recent SMT [Von Breymann et al., 1992; Dickens, 2001]. Extraction of biomarkers from methanotrophic bacteria preserved in the sediments [e.g., Hinrichs, 2001; Gontharet et al., 2009] can also provide a record of past methane venting, but these compounds are often not well preserved in the sediment record. In an effort to better understand the dynamic response of gas hydrate systems and their potential impact on sea-floor stability, ocean ecology, and global climate, researchers intend to reconstruct the paleo-positions of the SMT at three sites on the Cascadia margin. This reconstruction will utilize a multi-proxy approach based on magnetic susceptibility to observe the dynamic behavior of the SMT through glacial-interglacial timescales.

Recent work by UNH on the Indian continental margin [Phillips et al., 2012] shows that magnetic susceptibility (χ), constrained by magnetic properties, and integrated with core sedimentology (including grain size), authigenic mineralogy, and porewater geochemistry, can be used to track the paleo-positions of the SMT.  As others have documented [e.g. Kasten et al., 1998 and Riedinger et al., 2005], anaerobic oxidation of methane (AOM) at the SMT can result in dissolution of existing ferrimagnetic minerals (e.g., magnetite) and precipitation of authigenic carbonate, pyrite, and magnetic iron sulfide minerals (e.g., pyrrhotite and greigite), altering the original χ of the bulk sediment.  The dissolution of magnetic iron oxides and the re-precipitation of magnetic and non-magnetic iron sulfides [Canfield and Berner, 1987] occurs during hydrogen sulfide production at the SMT during either AOM [Kasten et al., 1998] or sulfate reduction via organic matter oxidation [Passier et al., 1996].  In anoxic marine sediments under reducing conditions, magnetite is more resistant to dissolution than other iron oxides and oxyhydroxides, but more prone to dissolution than iron (Fe) bound in silicate minerals [Canfield et al. 1992].  Thus, if sediments with magnetic mineralogy dominated by magnetite have depleted zones of χ indicating dissolution of magnetite and re-precipitation of Fe-sulfides, the drawdown in χ likely indicates a long-term paleo-position of the SMT.

By identifying intervals where χ has been reduced by the pyritization of magnetite due to anaerobic oxidation of methane at present and past SMT positions, and by constraining sulfate fluxes influenced by sedimentation rate, past changes in methane flux can be tracked. A transport and reaction model like CrunchFlow, involving these fluxes and magnetite dissolution kinetics, can be used to link the migration history of the SMT to the χ record. The approach being developed in this project—using cores from the Cascadia margin—has potential application to several, if not most, methane-bearing marine sequences globally, where significant magnetic iron oxides exist in the primary depositional record. By reconstructing the history of past methane and sulfate fluxes, predictive models describing how modern gas hydrate systems will respond to short- and long-timescale environmental changes can be developed.

Accomplishments (most recent listed first)

  • UNH researchers at the IODP Gulf Coast Repository in College Station used an X-ray fluorescence (XRF) core scanner to obtain XRF elemental measurements of the upper ~100 meters of sediment at each Cascadia Margin site (1249, 1252, and 1325) because it provides high sampling resolution (mm to cm scale) core measurements of major chemical elements (e.g., Al, Si, P, S, K, Ca, Ti, Mn, Fe, Sr, Zr, Ba, Rb) in marine sediments cores. From these element distributions, the Zr/Rb ratio was examined as a high-resolution proxy for grain size. The remaining elements observed in the XRF data were used to track primary and secondary mineral phases throughout the cores. IRM measurements have been completed and interpreted to identify intervals containing magnetic iron sulfides and determine how they relate to the χ record.
  • Bulk and lithogenic grain size measurements have been completed for each site. Before being measured, sediment grains were treated with hydrogen peroxide and hydrochloric acid to remove biogenic components that dilute lithogenic components. The lithogenic-dominant grain size was used to calibrate the Zr/Rb record. Carbon, hydrogen, nitrogen, and sulfur (CHNS) analysis is complete, and the sulfur data were used to determine where magnetic or non-magnetic iron sulfides have been precipitated. Samples collected for constructing the age model were processed by freeze drying and sieving. Benthic foraminifers were selected and analyzed for stable isotopic analysis (Oregon State University Stable Isotope Laboratory), and planktonic foraminifers were selected for radiocarbon analysis (Woods Hole Oceanographic Institution National Ocean Sciences Accelerator Mass Spectrometry Facility). The age model was used to constrain sedimentation and mass-accumulation rates of organic carbon in order to constrain geochemical modeling
  • Sediment age models were developed using oxygen isotope stratigraphy and radiocarbon age dates.
  • The XRF, magnetic susceptibility, grain size, isothermal remanent magnetism (IRM), and sulfur data were integrated to determine intervals of magnetic susceptibility drawdown at Sites 1249, 1252, and 1325. The Zr/Rb pattern was used to predict primary detrital magnetic susceptibility.  The difference between the modeled primary and actual magnetic susceptibility was used to calculate magnetite loss and pyrite sulfur gain.  The predicted sulfur precipitation matches closely to that of actual measured sulfur. Our approach successfully identified intervals of diagenetic dissolution of magnetic susceptibility that may represent past prolonged positions of the SMT. These results were presented by a PhD student at the Gordon Research Conference on Natural Gas Hydrate Systems in Galveston, TX, March 23–28, 2014.
  • XRF elemental core scans have been completed for the records at sites 1249, 1252, and 1325 using the XRF core scanner at the IODP core repository in College Station, TX. A PhD. graduate student learned how to operate the XRF core scanner and successfully collected XRF data from sedimentary records during a first visit to the facility in February 2013 and completed this work during a second trip in June (2013).
  • CHNS measurements were completed for Site 1249 to complement existing CHNS data from sites 1249 and 1325. These data show downcore variation in organic and inorganic carbon, nitrogen, and sulfur at a 1 m resolution.
  • IRM measurements were completed for Site 1325 to complement existing data at sites 1249 and 1252. These data show downcore variation in the dominant magnetic mineral assemblages (magnetite and magnetic iron sulfides) at a resolution of 2 m.
  • Sediment samples from the cores were requested via a sample request document sent to the IODP core repository in College Station, TX. This request was approved and the samples were collected by the curatorial staff and shipped to UNH. These samples are being used for grain size analysis, CHNS elemental analysis, magnetic mineralogy, and age models.
  • A Malvern Mastersizer 2000 laser particle size analyzer was purchased, installed, and is currently operating in the sedimentology lab at UNH. The project team has established and tested sediment type specific protocols and began testing pre-treatment procedures (to eliminate inorganic and organic carbon) to obtain the lithogenic-only grain size distributions in the samples. Bulk grain size measurements have been completed for sites 1252, 1249, and 1325.

Current Status (January 2015)
The project research has been completed and a final report is being developed.

Project Start: October 1, 2012
Project End: September 30, 2014

Project Cost Information:
DOE Contribution: $188,073 
Performer Contribution: $53,621

Contact Information:
NETL – John Terneus ( or 304-285-4254)
University of New Hampshire – Joel Johnson ( or 603-862-4080)

Additional Information

Quarterly Research Performance Progress Report [PDF-142KB] - Period ending 12-31-2012

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