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Abundance of Prokaryotes in deep-sea sediments analyzed by CARD-FISH
We fixed 0.5 g aliquots of sediment with a 4% formaldehyde solution for 2-4 h, washed the fixed sediments three times with 1x phosphate-buffered saline (PBS), before storing... -
Niche differentiation of sulfur-oxidizing bacteria (SUP05) in submarine hydro...
Chemistry and microbial cell numbers of two bathy- (Brothers volcano; BrV-cone and northwest caldera; NWC) and a mesopelagic (Macauley volcano; McV) plumes on the Kermadec... -
Anaerobic methanotrophic archaea-2 and Desulfosarcina/Desulfococcus group in ...
The anaerobic oxidation of methane (AOM) with sulfate as terminal electron acceptor is mediated by consortia of methanotrophic archaea (ANME) and sulfate-reducing bacteria... -
Relative abundance of prokaryotes in bacterial mat covered cold seep sediment...
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(Table 1) In situ geochemical parameters of Lost Hammer sediment and overlyin...
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CARD-FISH cell counts of taxonomic bacterial and archaeal groups in Fram Stra...
With CARD-FISH we quantified 16 microbial taxonomic groups in different water depths, from surface to the deep sea. We investigated 11 stations in LTER-HAUSGARTEN and adjacent... -
CARD-FISH counts of the water column and sediment at HAUSGARTEN, Fram Strait
We determined the concentrations of different types of bacteria via Catalysed reporter deposition-fluorescence in situ hybridization (CARD-FISH) at different depths of the water... -
On-board sequencing of the microbial community of the South Pacific Gyre
Fluorescence in situ hybridization (FISH) with 16S rRNA-targeted oligonucleotide probes was used to investigate the phylogenetic composition of the seven most abundant bacterial... -
Relative abundance of prokaryotic picoplankton populations in the Atlantic Ocean
Members of the prokaryotic picoplankton are the main drivers of the biogeochemical cycles over large areas of the world's oceans. In order to ascertain changes in picoplankton... -
(Table T1) Total procaryotes, and living bacteria and archaea in black shales...
Subseafloor sediments harbor over half of all prokaryotic cells on Earth (Whitman et al., 1998). This immense number is calculated from numerous microscopic acridine orange... -
Relative abundance of prokaryotes in sediments of the Håkon Mosby mud volcano...
CARD-FISH was performed as previously described in Ruff et al., (2013; doi:10.1371/journal.pone.0072627) with the following modifications. 4-6 µl of 25-fold diluted sediment... -
Microbial community composition and bacterioplankton at time series station H...
A process of global importance in carbon cycling is the remineralization of algae biomass by heterotrophic bacteria, most notably during massive marine algae blooms. Such blooms... -
Microbial community in sediment of Gullfaks and Tommeliten methane seeps in t...
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Cell concentrations of five bacterial key groups in ice, water, and sediment ...
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CARD-FISH cell counts of Bacteria and Archaea in sediments of HAUSGARTEN, Fra...
We quantified Bacteria and Archaea, as well as 15 bacterial groups at various taxonomic ranks using catalyzed reporter deposition-fluorescence in situ hybridization (CARD-FISH)... -
Analysis of the microbial community composition with depth along the Atlantic...
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Composition of bacterioplankton in the North Atlantic subtropical gyre
Subtropical oceanic gyres are the most extensive biomes on Earth where SAR11 and Prochlorococcus bacterioplankton numerically dominate the surface waters depleted in inorganic... -
Chloroflexus spp. and Sulfurihydrogenibium spp. in microbial mats of the Naka...
Microbial mats develop in a wide range of aquatic habitats, such as geothermal hot springs, hypersaline ponds, marine cold seeps or hydrothermal vents. The Nakabusa hot spring... -
Verrucomicrobia in situ abundance and water chemistry in a humic lake during ...
Members of the highly diverse bacterial phylum Verrucomicrobia are globally distributed in various terrestrial and aquatic habitats. They are key players in soils, but little is...
