Woods Hole Oceanographic Institution

»Bioavailability of soil organic matter and microbial community dynamics upon permafrost thaw
»7000 years of virus-host molecular dynamics in the Black Sea
»Preservation potential of ancient DNA in Pleistocene marine sediments: Implications for paleoenvironmental reconstructions
»Source-specific variability in post-depositional DNA preservation with potential implications for DNA-based paleecological records
»Exploring preserved ancient dinoflagellalte and haptophyte DNA signatures to infer ecological and environmental conditions during sapropel S1 formation in the eastern Mediterranean
»Ancient DNA in lake sediment records
»Vertical distribution of metabolically active eukaryotes in the water column and sediments of the Black Sea
»DNA and lipid molecular stratigraphic records of haptophyte succession in the Black Sea during the Holocene
»Diversity of Archaea and potential for crenarchaeotal nitrification of group 1.1a in the rivers Rhine and TĂȘt
»Holocene sources of fossil BHPs
»An unusual 17[α],21[β](H)-bacteriohopanetetrol in Holocene sediments from Ace Lake (Antarctica)
»Holocene sources of organic matter in Antarctic fjord
»Variations in spatial and temporal distribution of Archaea in the North Sea
»Archaeal nitrifiers in the Black Sea
»Pleistocene Mediterranean sapropel DNA
»Rapid sulfurisation of highly branched isoprenoid (HBI) alkenes in sulfidic Holocene sediments
»Aerobic and anaerobic methanotrophs in the Black Sea water column
»Fossil DNA in Cretaceous Black Shales: Myth or Reality?
»Sulfur and methane cycling during the Holocene in Ace Lake (Antarctica)
»Ancient algal DNA in the Black Sea
»Archaeal nitrification in the ocean
»Characterization of microbial communities found in the human vagina by analysis of terminal restriction fragment length polymorphisms of 16S rRNA genes
»Biomarker and 16S rDNA evidence for anaerobic oxidation of methane and related carbonate precipitation in deep-sea mud volcanoes of the Sorokin Trough, Black Sea
»Temperature-dependent variation in the distribution of tetraether membrane lipids of marine Crenarchaeota: Implications for TEX86 paleothermometry
»Paleoecology of algae in Ace Lake
»Evolution of the methane cycle in Ace Lake (Antarctica) during the Holocene: Response of methanogens and methanotrophs to environmental change
»Ongoing modification of Mediterranean Pleistocene sapropels mediated by prokaryotes.
»Microbial communities in the chemocline of a hypersaline deep-sea basin (Urania basin, Mediterranean Sea)
»Functional exoenzymes as indicators of metabolically active bacteria in 124,000-year-old sapropel layers of the Eastern Mediterranean Sea
»Specific detection of different phylogenetic groups of chemocline bacteria based on PCR and denaturing gradient gel electrophoresis of 16S rRNA gene fragments
»Analysis of subfossil molecular remains of purple sulfur bacteria in a lake sediment
»Effects of nitrate availability and the presence of Glyceria maxima the composition and activity of the dissimilatory nitrate-reducing bacterial community
»Microbial activities and populations in upper sediment and sapropel layers

Coolen, M. J. L., E. C. Hopmans, W. I. C. Rijpstra, G. Muyzer, S. Schouten, J. K. Volkman and J. S. Sinninghe Damsté, Evolution of the methane cycle in Ace Lake (Antarctica) during the Holocene: Response of methanogens and methanotrophs to environmental change, Org. Geochem., 35(10), 1151-1167, 2004

Post-glacial Ace Lake (Vestfold Hills, Antarctica), which was initially a freshwater lake and then an open marine system, is currently a meromictic basin with anoxic, sulfidic and methane-saturated bottom waters. Lipid and 16S ribosomal RNA gene stratigraphy of up to 10,400-year-old sediment core samples from the lake revealed that these environmentally induced chemical and physical changes caused clear shifts in the species composition of archaea and aerobic methanotrophic bacteria. The combined presence of lipids specific for methanogenic archaea and molecular remains of aerobic methanotrophic bacteria (13C-depleted Δ8(14)-sterols and 16S rRNA genes) revealed that an active methane cycle occurred in Ace Lake during the last 3000 calendar years and that the extant methanotrophs were most likely introduced when it became a marine inlet (9400 y BP); rDNA sequences of known methanogens were only recovered from the oldest sediments deposited during the freshwater phase. The latter sequences showed 100% sequence similarity with Methanosarcinales species from freshwater environments and were the source of sn-2- and sn3-hydroxyarchaeols. Archaeal phylotypes related to uncultivated Archaea associated with various marine environments were recovered from the present-day anoxic water column and sediments deposited during the meromictic and marine period. Full text of article can be viewed here.

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