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  • Center for Marine Environmental Sciences; MARUM  (6)
  • FISH–secondary ion MS
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  • 1
    Publication Date: 2022-05-25
    Description: Author Posting. © National Academy of Sciences, 2006. This article is posted here by permission of National Academy of Sciences for personal use, not for redistribution. The definitive version was published in Proceedings of the National Academy of Sciences 103 (2006): 3846-3851, doi:10.1073/pnas.0600035103.
    Description: Studies of deeply buried, sedimentary microbial communities and associated biogeochemical processes during Ocean Drilling Program Leg 201 showed elevated prokaryotic cell numbers in sediment layers where methane is consumed anaerobically at the expense of sulfate. Here, we show that extractable archaeal rRNA, selecting only for active community members in these ecosystems, is dominated by sequences of uncultivated Archaea affiliated with the Marine Benthic Group B and the Miscellaneous Crenarchaeotal Group, whereas known methanotrophic Archaea are not detectable. Carbon flow reconstructions based on stable isotopic compositions of whole archaeal cells, intact archaeal membrane lipids, and other sedimentary carbon pools indicate that these Archaea assimilate sedimentary organic compounds other than methane even though methanotrophy accounts for a major fraction of carbon cycled in these ecosystems. Oxidation of methane by members of Marine Benthic Group B and the Miscellaneous Crenarchaeotal Group without assimilation of methane–carbon provides a plausible explanation. Maintenance energies of these subsurface communities appear to be orders of magnitude lower than minimum values known from laboratory observations, and ecosystem-level carbon budgets suggest that community turnover times are on the order of 100–2,000 years. Our study provides clues about the metabolic functionality of two cosmopolitan groups of uncultured Archaea.
    Description: This work was supported by Deutsche Forschungsgemeinschaft (to J.S.L., R.A., M.E., and K.-U.H. at Research Center for Ocean Margins and Grant Hi 616/4 to K.U.-H.); National Aeronautics and Space Administration Astrobiology Institute Grants NNA04CC06A (to J.E.B. and C.H.H. at Pennsylvania State University), NCC 2-1275 (to M.A.L., K.G.L., K.B.S., H.F.F., A.T., and K.-U.H. at the University of Rhode Island), and NCC 2-1054 (to M.L.S. and A.T. at the Marine Biological Laboratory); the G. Unger Vetlesen Foundation; U.S. Department of Energy Grant DE-FG02-93ER20117; and NSF Grant MCB03-48492. J.F.B. was supported by NSF Integrative Graduate Education and Research Traineeship Program Grant DGE-9972759 and a Schlanger fellowship from the Joint Oceanographic Institutions (JOI). M.A.L. was supported in part by postcruise support from JOI.
    Keywords: Anaerobic methanotrophy ; Deep biosphere ; FISH–secondary ion MS ; Intact polar lipids ; Stable carbon isotopes
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: 1901480 bytes
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  • 2
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    PANGAEA
    In:  Supplement to: Zhuang, Guang-Chao; Lin, Yu-Shih; Elvert, Marcus; Heuer, Verena B; Hinrichs, Kai-Uwe (2014): Gas chromatographic analysis of methanol and ethanol in marine sediment pore waters: Validation and implementation of three pretreatment techniques. Marine Chemistry, 160, 82-90, https://doi.org/10.1016/j.marchem.2014.01.011
    Publication Date: 2023-03-03
    Description: Low-molecular-weight (LMW) alcohols are produced during the microbial degradation of organic matter from precursors such as lignin, pectin, and carbohydrates. The biogeochemical behavior of these alcohols in marine sediment is poorly constrained but potentially central to carbon cycling. Little is known about LMW alcohols in sediment pore waters because of their low concentrations and high water miscibility, both of which pose substantial analytical challenges. In this study, three alternative methods were adapted for the analysis of trace amounts of methanol and ethanol in small volumes of saline pore waters: direct aqueous injection (DAI), solid-phase microextraction (SPME), and purge and trap (P&T) in combination with gas chromatography (GC) coupled to either a flame ionization detector (FID) or a mass spectrometer (MS). Key modifications included the desalination of samples prior to DAI, the use of a threaded midget bubbler to purge small-volume samples under heated conditions and the addition of salt during P&T. All three methods were validated for LMW alcohol analysis, and the lowest detection limit (60 nM and 40 nM for methanol and ethanol, respectively) was achieved with the P&T technique. With these methods, ambient concentrations of volatile alcohols were determined for the first time in marine sediment pore waters of the Black Sea and the Gulf of Mexico. A strong correlation between the two compounds was observed and tentatively interpreted as being controlled by similar sources and sinks at the examined stations.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 3
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    PANGAEA
    In:  Supplement to: Zhuang, Guang-Chao; Lin, Yu-Shih; Bowles, Marshall W; Heuer, Verena B; Lever, Mark A; Elvert, Marcus; Hinrichs, Kai-Uwe (2017): Distribution and isotopic composition of trimethylamine, dimethylsulfide and dimethylsulfoniopropionate in marine sediments. Marine Chemistry, 196, 35-46, https://doi.org/10.1016/j.marchem.2017.07.007
    Publication Date: 2023-03-03
    Description: Methylated amines and sulfides are ubiquitous organic nitrogen and sulfur compounds in the marine environment and could serve as important energy substrates to methanogens inhabiting anoxic sediments. However, their abundance and isotopic values remain largely unconstrained in marine sediments. In this study, we investigated the distribution of trimethylamine (TMA), dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) in Aarhus Bay, Denmark and provided the first report for their stable carbon isotopic composition. Simultaneous measurement of those two compounds in small volumes of pore waters and sediments was accomplished with gas chromatography in combination with either a purge and trap system for quantification or a headspace method for carbon isotopic analysis. TMA in the solid phase (exchangeable pool, 0.3-6.6 µmol/kg wet sediment; base-extractable pool, 2-18 µmol/kg) was much more abundant than the dissolved pool (〈 20 nM), indicating strong adsorption of TMA to sediments. Likewise, total base-hydrolyzable DMS(P)t (including DMS and base-released DMS from DMSP) in sediment was at least three orders of magnitude higher (11-65 µmol/kg) than the dissolved pool of DMS(P)d in the pore water (including DMS and dissolved DMSP; 1-12 nM). TMA and DMS(P) contents in the solid phase peaked in the surface sediment, consistent with their phytodetrital origin. TMA was more 13C-depleted than DMS(P) (TMA: -36.4 per mil to -39.2 per mil; DMS: -18.6 per mil to -23.4 per mil), presumably due to different biological or biosynthetic origins of the respective methyl groups. Both compounds showed a downcore decrease in their solid-phase concentration, a feature that was attributed to microbial degradation, but progressive enrichment in 13C (up to 4 per mil) with depth was observed only for DMS(P). The considerable pool size of TMA and DMS(P) outlined in this study and geochemical evidence of their degradability suggested these two compounds could be potentially important substrates for methane production in sulfate-reducing environments.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 4
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    PANGAEA
    In:  Supplement to: Tamborrino, Leonardo; Himmler, Tobias; Elvert, Marcus; Conti, Daniel; Gualtieri, Alessandro F; Fontana, Daniela; Bohrmann, Gerhard (2019): Formation of tubular carbonate conduits at Athina mud volcano, eastern Mediterranean Sea. Marine and Petroleum Geology, 107, 20-31, https://doi.org/10.1016/j.marpetgeo.2019.05.003
    Publication Date: 2023-03-03
    Description: Tubular carbonate conduits (TCC) represent the termination of fluid plumbing systems in environments of hydrocarbon seepage and play a relevant role in the discharge of methane from sub-seafloor sediments to the water column. However, the biogeochemical reactions and biological activities involved in their formation are not fully understood. To address this, TCC samples were collected with a remotely operated vehicle from the seabed on the SW flank of the Athina mud volcano in the eastern Mediterranean Sea. Petrographic, mineralogical, stable carbon and oxygen isotope and lipid biomarker analyses were performed to elucidate the formation processes of the tubular carbonates. Clotted and fibrous aragonite form the internal lining of the cavities, while the outer portion of the tubes is formed by micritic Mg-calcite cementing hemipelagic sediment. 13C-depleted Mg-calcite and aragonite (as low as −14.4‰ V-PDB) and lipid biomarkers (archaeol, −89.8‰ V-PDB) indicate that carbonate precipitation was influenced by sulfate-dependent anaerobic oxidation of methane (AOM). AOM locally enhances aragonite precipitation, thereby facilitating early lithification of the conduits within the mud volcano sediments. The size and morphology of the TCC comparable with the buried portion of tubeworm colonies found in the proximity of the sampling site. However, our results suggest that TCC likely formed by the action of burrowing organism rather than being mineralizations of the tubeworm colonies. This study provides new insights into the interpretation and understanding of TCC, highlighting the role of macrofaunal activity in the formation of migration pathways for hydrocarbon-rich fluids on the flank of a mud volcano.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 5
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    PANGAEA
    In:  Supplement to: Elvert, Marcus; Pohlman, John W; Becker, Kevin W; Gaglioti, Benjamin V; Hinrichs, Kai-Uwe; Wooller, Matthew J (2016): Methane turnover and environmental change from Holocene lipid biomarker records in a thermokarst lake in Arctic Alaska. The Holocene, 26(11), 1766-1777, https://doi.org/10.1177/0959683616645942
    Publication Date: 2023-05-12
    Description: Arctic lakes and wetlands contribute a substantial amount of methane to the contemporary atmosphere, yet profound knowledge gaps remain regarding the intensity and climatic control of past methane emissions from this source. In this study, we reconstruct methane turnover and environmental conditions, including estimates of mean annual and summer temperature, from a thermokarst lake (Lake Qalluuraq) on the Arctic Coastal Plain of northern Alaska for the Holocene by using source-specific lipid biomarkers preserved in a radiocarbon-dated sediment core. Our results document a more prominent role for methane in the carbon cycle when the lake basin was an emergent fen habitat between ~12,300 and ~10,000 cal yr BP, a time period closely coinciding with the Holocene Thermal Maximum (HTM) in North Alaska. Enhanced methane turnover was stimulated by relatively warm temperatures, increased moisture, nutrient supply, and primary productivity. After ~10,000 cal yr BP, a thermokarst lake with abundant submerged mosses evolved, and through the mid-Holocene temperatures were approximately 3°C cooler. Under these conditions, organic matter decomposition was attenuated, which facilitated the accumulation of submerged mosses within a shallower Lake Qalluuraq. Reduced methane assimilation into biomass during the mid-Holocene suggests that thermokarst lakes are carbon sinks during cold periods. In the late-Holocene from ~2700 cal yr BP to the most recent time, however, temperatures and carbon deposition rose and methane oxidation intensified, indicating that more rapid organic matter decomposition and enhanced methane production could amplify climate feedback via potential methane emissions in the future.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 5 datasets
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  • 6
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    PANGAEA
    In:  Supplement to: Pittauer, Daniela; Roos, Per; Qiao, Jixin; Geibert, Walter; Elvert, Marcus; Fischer, Helmut W (2018): Pacific Proving Grounds radioisotope imprint in the Philippine Sea sediments. Journal of Environmental Radioactivity, 186, 131-141, https://doi.org/10.1016/j.jenvrad.2017.06.021
    Publication Date: 2023-06-08
    Description: Radionuclide concentrations were studied in sediment cores taken at the continental slope of the Philippine Sea off Mindanao Island in the equatorial Western Pacific. High resolution deposition records of anthropogenic radionuclides were collected at this site. Excess 210Pb together with excess 228Th and anthropogenic radionuclides provided information about accumulation rates. Concentrations of Am and Pu isotopes were detected by gamma spectrometry, alpha spectrometry and ICP-MS. The Pu ratios indicate a high portion (minimum of 60%) of Pu from the Pacific Proving Grounds (PPG). This implies that the transport of PPG derived plutonium with the Mindanao Current southward is similarly effective as the previously known transport towards the north with the Kuroshio Current. The record is compared to other studies from northwest Pacific marginal seas and Lombok basin in the Indonesian Archipelago. The sediment core top at site GeoB17409 was found to contain a 6 cm thick layer dominated by terrestrial organic matter, which was interpreted as a result of the 2012 Typhoon Pablo-related fast deposition.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 7
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    PANGAEA
    In:  Supplement to: Evans, Thomas W; Könneke, Martin; Lipp, Julius S; Adhikari, Rishi Ram; Taubner, Heidi; Elvert, Marcus; Hinrichs, Kai-Uwe (2018): Lipid biosynthesis of Nitrosopumilus maritimus dissected by lipid specific radioisotope probing (lipid-RIP) under contrasting ammonium supply. Geochimica et Cosmochimica Acta, 242, 51-63, https://doi.org/10.1016/j.gca.2018.09.001
    Publication Date: 2023-06-03
    Description: Ammonia-oxidizing archaea (AOA) are among the most abundant microbes in the oceans and are one of the major sources of glycerol dibiphytanyl glycerol tetraethers (GDGTs) in the water column and underlying sediments. However, little is known about the mechanistic steps during biosynthesis of GDGTs that form the basis of the TEX86 paleothermometer. Recent results showed that, apart from temperature, physiological factors such as growth stage and variations of the ammonium oxidation rate may affect the TEX86 temperature proxy. We performed a short term incubation experiment with radiolabeled 14C-bicarbonate to accurately trace the effect of high and low ammonium (NH4+) supply, on the production of individual membrane lipids by the AOA model organism Nitrosopumilus maritimus. The 14C incorporation during growth was monitored at five time intervals by liquid chromatography coupled to flow-through scintillation counting of the hydrolyzed membrane lipid extract, allowing a straight forward and sensitive on-line detection of 14C incorporation into archaeal lipids on time-scales lower than a single cell cycle. The experiments showed that low NH4+ supply results in higher cyclization of GDGTs with a preferential synthesis of crenarchaeol, whereas excess NH4+ led to predominant production of GDGT-0. Consequently, the cultures with a high NH4+ supply resulted in up to 10 °C lower estimated incubation temperatures than the cultures with low quantities of available NH4+ using the TEX86L calibration. Interestingly, a high relative production of archaeol was observed at the beginning of all experiments (up to 27%), independent of the NH4+ supply; likewise the degree of cyclization was initially lowest indicating delayed production of cycloalkylated derivatives. This pattern is consistent with N. maritimus synthesizing GDGTs by head-to-head condensation of two archaeol molecules and subsequent cyclization of the resulting acyclic tetraether. This study provides robust information on the biosynthesis of GDGTs in N. maritimus and advances our understanding of the influence of NH4+ supply on the TEX86 proxy.
    Keywords: Center for Marine Environmental Sciences; MARUM
    Type: Dataset
    Format: application/zip, 8 datasets
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