Contributors | Affiliation | Role |
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Teske, Andreas | University of North Carolina at Chapel Hill (UNC-Chapel Hill) | Principal Investigator |
Joye, Samantha B. | University of Georgia (UGA) | Co-Principal Investigator |
Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Methodology: Porewater Methane concentrations were determined by headspace Gas Chromatography - flame ionization detection, and d13C signatures of methane were determined by Gas Chromatography coupled to Mass Spectrometry, using a Finnigan MAT Delta S isotope ratio Mass Spectrometer inlet system.
Sampling and Analytical Procedures: For combined concentration and δ13C analysis of methane, 2 ml sediment subsamples were added to 30 ml serum vials containing 2 ml of 1 M sodium hydroxide solution, sealed with thick butyl rubber stoppers, crimped with aluminum seals and stored at 4°C. Due to shipping problems and a resulting shortage of serum vials, only selected sediment cores were sampled for methane. Since cores were retrieved unpressurized, outgassing may have impacted in particular the measurements of methane concentrations near and above saturation, 1.5 mM. After the cruise, the methane samples were analyzed by headspace gas chromatography-flame ionization detection (GC-FID) at Florida State University (Magen et al., 2014). Gas samples were analyzed for δ13C by injecting 0.1 to 0.5 ml of sample into a gas chromatograph interfaced to a Finnigan MAT Delta S isotope ratio Mass Spectrometer inlet system as previously described (Chanton and Liptay 2000). Values are reported in the per mil (‰) notation relative to Vienna Pee Dee Belemnite (VPDB). Sampling site names are based on Teske et al. 2016 and Teske et al. 2021.
Known Problems/Issues: Problems with Mexican customs and the agent used by WHOI at the time have resulted in limited availability of sampling gear and sampling vials on the ship. Transport problems during the return trip have caused sample losses among the porewater samples, which are evident in occasional gaps in porewater profiles or short profiles.
BCO-DMO Processing:
- added Site_Name column;
- renamed columns to comply with BCO-DMO naming conventions;
- added columns for Lat, Lon, and Depth_Dive from separate file provided by data submitter.
File |
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porewater_methane.csv (Comma Separated Values (.csv), 6.18 KB) MD5:50c30fc1fe470f9a29e38d2e4ff9ab8f Primary data file for dataset ID 842974 |
Parameter | Description | Units |
Site_Name | Site/location name | unitless |
Site | Site number | unitless |
Depth_Dive | Depth of sample collection | meters (m) |
Lat | Latitude of sampling location | decimal degrees North |
Lon | Longitude of sampling location | decimal degrees East |
Depth | Core depth | centimeters (cm) |
del_CH4 | delCH4 | per mil |
del_CH4_Std_Dev | Standard deviation of del_CH4 | per mil |
Conc_CH4_pcnt | CH4 concentration, percent | percent (%) |
Conc_CH4_ppm | CH4 concentration, parts per million | parts per million (ppm) |
Conc_CH4_mM | CH4 concentration, millimolar | millimolar (mM) |
Dataset-specific Instrument Name | |
Generic Instrument Name | Flame Ionization Detector |
Dataset-specific Description | Methane samples were analyzed by headspace gas chromatography-flame ionization detection (GC-FID). |
Generic Instrument Description | A flame ionization detector (FID) is a scientific instrument that measures the concentration of organic species in a gas stream. It is frequently used as a detector in gas chromatography. Standalone FIDs can also be used in applications such as landfill gas monitoring, fugitive emissions monitoring and internal combustion engine emissions measurement in stationary or portable instruments. |
Dataset-specific Instrument Name | |
Generic Instrument Name | Gas Chromatograph |
Dataset-specific Description | Methane samples were analyzed by headspace gas chromatography-flame ionization detection (GC-FID). |
Generic Instrument Description | Instrument separating gases, volatile substances, or substances dissolved in a volatile solvent by transporting an inert gas through a column packed with a sorbent to a detector for assay. (from SeaDataNet, BODC) |
Dataset-specific Instrument Name | Finnigan MAT Delta S isotope ratio Mass Spectrometer |
Generic Instrument Name | Isotope-ratio Mass Spectrometer |
Generic Instrument Description | The Isotope-ratio Mass Spectrometer is a particular type of mass spectrometer used to measure the relative abundance of isotopes in a given sample (e.g. VG Prism II Isotope Ratio Mass-Spectrometer). |
Dataset-specific Instrument Name | Alvin pushcore |
Generic Instrument Name | Push Corer |
Generic Instrument Description | Capable of being performed in numerous environments, push coring is just as it sounds. Push coring is simply pushing the core barrel (often an aluminum or polycarbonate tube) into the sediment by hand. A push core is useful in that it causes very little disturbance to the more delicate upper layers of a sub-aqueous sediment.
Description obtained from: http://web.whoi.edu/coastal-group/about/how-we-work/field-methods/coring/ |
Website | |
Platform | R/V Atlantis |
Report | |
Start Date | 2016-12-09 |
End Date | 2016-12-27 |
Website | |
Platform | HOV Alvin |
Report | |
Start Date | 2016-12-09 |
End Date | 2016-12-27 |
Description | Alvin dives conducted at Guyamas Basin on R/V Atlantis cruise AT37-06. |
Description from NSF award abstract:
Hydrothermally active sediments in the Guaymas Basin are dominated by novel microbial communities that catalyze important biogeochemical processes in these seafloor ecosystems. This project will investigate genomic potential, physiological capabilities and biogeochemical roles of key uncultured organisms from Guaymas sediments, especially the high-temperature anaerobic methane oxidizers that occur specifically in hydrothermally active sediments (ANME-1Guaymas). The study will focus on their role in carbon transformations, but also explore their potential involvement in sulfur and nitrogen transformations. First-order research topics include quantifying anaerobic methane oxidation under high temperature,in situ concentrations of phosphorus and methane , and with alternate electron acceptors; sulfate and sulfur-dependent microbial pathways and isotopic signatures under these conditions; and nitrogen transformations in methane-oxidizing microbial communities, hydrothermal mats and sediments.
This integrated biogeochemical and microbiological research will explore the pathways of and environmental controls on the consumption and production of methane, other alkanes, inorganic carbon, organic acids and organic matter that fuel the Guaymas sedimentary microbial ecosystem. The hydrothermal sediments of Guaymas Basin provide a spatially compact, high-activity location for investigating novel modes of methane cycling and carbon assimilation into microbial biomass. In the case of anaerobic methane oxidation, the high temperature and pressure tolerance of Guaymas Basin methane-oxidizing microbial communities, and their potential to uncouple from the dominant electron acceptor sulfate, vastly increase the predicted subsurface habitat space and biogeochemical role for anaerobic microbial methanotrophy in global deep subsurface diagenesis. Further, microbial methane production and oxidation interlocks with syulfur and nitrogen transformations, which will be explored at the organism and process level in hydrothermal sediment microbial communities and mats of Guaymas Basin. In general, first-order research tasks (rate measurements, radiotracer incorporation studies, genomes, in situ microgradients) define the key microbial capabilities, pathways and processes that mediate chemical exchange between the subsurface hydrothermal/seeps and deep ocean waters.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) | |
NSF Division of Ocean Sciences (NSF OCE) |