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  • 1
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A large fraction of globally produced methane is converted to CO2 by anaerobic oxidation in marine sediments. Strong geochemical evidence for net methane consumption in anoxic sediments is based on methane profiles, radiotracer experiments and stable carbon isotope data. ...
    Type of Medium: Electronic Resource
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  • 2
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    In:  Supplement to: Ravenschlag, Katrin; Sahm, Kerstin; Amann, Rudolf (2001): Quantitative molecular analysis of the microbial community in marine arctic sediments (Svalbard). Applied and Environmental Microbiology, 67(1), 387-395, https://doi.org/10.1128/AEM.67.1.387-395.2001
    Publication Date: 2023-07-10
    Description: Fluorescence in situ hybridization (FISH) with 16S rRNA-targeted oligonucleotide probes were used to investigate the phylogenetic composition of a marine Arctic sediment (Svalbard). Hybridization and microscopy counts of hybridized and 4',6'-diamidino-2-phenylindole (DAPI)-stained cells were performed as described previously from Snaidr et al. (1997, http://aem.asm.org/content/63/7/2884.full.pdf). Means were calculated from 10 to 20 randomly chosen fields on each filter section, corresponding to 800 to 1,000 DAPI-stained cells. Counting results were always corrected by subtracting signals observed with the probe NON338. Formamide concentrations are given in further details. FISH resulted in the detection of a large fraction of microbes living in the top 5 cm of the sediment. Up to 65.4% ± 7.5% of total DAPI cell counts hybridized to the bacterial probe EUB338, and up to 4.9% ± 1.5% hybridized to the archaeal probe ARCH915. Besides delta-proteobacterial sulfate-reducing bacteria (up to 16% 52) members of the Cytophaga-Flavobacterium cluster were the most abundant group detected in this sediment, accounting for up to 12.8% of total DAPI cell counts. Furthermore, members of the order Planctomycetales accounted for up to 3.9% of total cell counts. In accordance with previous studies, these findings support the hypothesis that these bacterial groups are not simply settling with organic matter from the pelagic zone but are indigenous to the anoxic zones of marine sediments. Members of the gamma-proteobacteria also constituted a significant fraction in this sediment (6.1% ± 2.5% of total cell counts). A new probe (GAM660) specific for sequences affiliated with free-living or endosymbiotic sulfur-oxidizing bacteria was developed. A significant number of cells was detected by this probe (2.1% ± 0.7% of total DAPI cell counts), showing no clear zonation along the vertical profile. Gram-positive bacteria and the beta-proteobacteria were near the detection limit in all sediments.
    Keywords: Archaea, targed with ARCH915 oligonucleotide FISH-probe; Bacteria, targeted with EUB338 l oligonucleotides FISH-probe; Core; CORE; Cytophaga-Flavobacterium cluster, targeted with CF319a oligonucleotide FISH-probe; DEPTH, sediment/rock; Epifluorescence microscopy after DAPI staining; Event label; Fluorescence in situ hybridization (FISH); Gammaproteobacteria, targeted with Gam42a oligonucleotide FISH-probe; Gammaproteobacteria, targeted with GAM660 oligonucleotide FISH-probe; Latitude of event; Longitude of event; Planctomycetales, targeted with PLA886 oligonucleotide FISH-probe; Prokaryotes, abundance as single cells; SBF_19980728; Smeerenburgfjorden, Svalbard
    Type: Dataset
    Format: text/tab-separated-values, 220 data points
    Location Call Number Limitation Availability
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  • 3
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    In:  Supplement to: Ravenschlag, Katrin; Sahm, Kerstin; Knoblauch, Christian; Jørgensen, Bo Barker; Amann, Rudolf I (2000): Community Structure, Cellular rRNA Content, and Activity of Sulfate-Reducing Bacteria in Marine Arctic Sediments. Applied and Environmental Microbiology, 66(8), 3592-3602, https://doi.org/10.1128/AEM.66.8.3592-3602.2000
    Publication Date: 2024-01-20
    Description: The community structure of sulfate-reducing bacteria (SRB) of a marine Arctic sediment (Smeerenburgfjorden, Svalbard) was characterized by both fluorescence in situ hybridization (FISH) by using group- and genus-specific 16S rRNA-targeted oligonucleotide probes. Samples stored in PBS-ethanol were diluted and treated by mild sonication. A 10-ml aliquot of a 1:40 dilution was filtered onto a 0.2-mm-pore-size type GTTP polycarbonate filter (Millipore, Eschborn, Germany). Hybridization and microscopic counting of hybridized and 49,69-diamidino-2-phenylindole (DAPI)-stained cells were performed as described previously from Snaidr et al. (1997, http://aem.asm.org/content/63/7/2884.full.pdf). Details of probes and formamide concentrations which were used are listed in futher details.. Means were calculated by using 10 to 20 randomly chosen fields for each filter section, which corresponded to 800 to 1,000 DAPI-stained cells. Counting results were always corrected by subtracting signals observed with probe NON338. The SRB community was dominated by members of the Desulfosarcina-Desulfococcus group. This group accounted for up to 73% of the SRB detected. The predominance was shown to be a common feature for different stations along the coast of Svalbard. In a top-to-bottom approach we aimed to further resolve the composition of this large group of SRB by using probes for cultivated genera. While this approach failed, directed cloning of probe-targeted genes encoding 16S rRNA was successful and resulted in sequences which were all affiliated with the Desulfosarcina-Desulfococcus group. A group of clone sequences (group SVAL1) most closely related to Desulfosarcina variabilis (91.2% sequence similarity) was dominant and was shown to be most abundant in situ, accounting for up to 54.8% of the total SRB detected.
    Keywords: Bacteria, sulfate reducing; Bacteria, targed with EUB338(I-III) oligonucleotide FISH-probe; Core; CORE; Date/Time of event; DEPTH, sediment/rock; Desulfobacterium spp., targeted with 221 oligonucleotides FISH-probe; Desulfobacter spp., targeted with DSB985 oligonucleotides FISH-probe; Desulfobulbus spp., targeted with 660 oligonucleotides FISH-probe; Desulforhopalus spp., targeted with DSR651 oligonucleotides FISH-probe; Desulfotalea spp., targeted with Sval428 oligonucleotides FISH-probe; Desulfovibrio spp., targeted with DSV698 oligonucleotides FISH-probe; Desulfuromonas spp., targeted with DRM432 oligonucleotides FISH-probe; Desulfusarcina/Desulfococcus, targeted with DSS658 oligonucleotide FISH-probe; Epifluorescence microscopy after DAPI staining; Event label; Fluorescence in situ hybridization (FISH); Latitude of event; Longitude of event; Prokaryotes, abundance as single cells; SBF_19980728; Smeerenburgfjorden, Svalbard; Svalbard clone group SVAL1, targeted with DSS225 oligonucleotide FISH-probe; Svalbard clones Sva0081/Sva0863, targeted with cl81-644 oligonucleotide FISH-probe
    Type: Dataset
    Format: text/tab-separated-values, 337 data points
    Location Call Number Limitation Availability
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