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Metadata und statistic analysis of archaeal and bacterial sequences originati...
DNA extraction was carried out as described on the MICROBIS project pages (http://icomm.mbl.edu/microbis ) using a commercially available extraction kit. We amplified the... -
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 in sediment of Gullfaks and Tommeliten methane seeps in t...
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Methane concentration, oxidation rates and abundance of bacteria during Maria...
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(Table 5) Abundance of chemo-organotrophic bacteria and their activity in sed...
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Seawater carbonate chemistry and ROS and EPS production of the Trichodesmium ...
The diazotrophic cyanobacterium Trichodesmium is thought to be a major contributor to the new N in the parts of the oligotrophic, subtropical and tropical oceans. In this study... -
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... -
Microbial community composition in sediments of the Hydrate Ridge (Cascadian ...
Cold seep environments such as sediments above outcropping hydrate at Hydrate Ridge (Cascadia margin off Oregon) are characterized by methane venting, high sulfide fluxes caused... -
Hydrochemical and microbiological properties of groundwater from pristine aqu...
The hydrochemistry and the microbial diversity of a pristine aquifer system near Garzweiler, Germany next to the open-pit lignite mine Garzweiler 1, were characterized.... -
Microbial community composition of sandy intertidal sediments of Sylt-Rømø Ba...
Molecular biological methods were used to investigate the microbial diversity and community structure in intertidal sandy sediments near the island of Sylt (Wadden Sea) at a... -
Archaeal and bacterial diversity at different sites as determined by 16S rRNA...
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Bacteria abundance and proportion of dividing cells ins sediment core POS317/...
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Tissue damage and tissue localisation of the bacteria Vibrio aestuarianus dur...
Histopathological damage and localisation of Vibrio aestuarianus in diverse oyster tissues were studied on experimentally infected animals by histology and immunohistochemistry... -
Community composition
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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 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)... -
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... -
PeECE III - Pelagic Ecosystem CO2 Enrichment Study, Raunefjord, Bergen, Norwa...
The effects of CO2-induced seawater acidification on plankton communities were also addressed in a series of 3 mesocosm experiments, called the Pelagic Ecosystem CO2 Enrichment... -
Bacillus cereus fatty acids during growth at different temperatures
This data set presents changes all along growth in fatty acids of three strains of the foodborne pathogenic bacteria Bacillus cereus, two mesophilic (ATCC 14579 and ATCC 10876)... -
Bacteria data from 2016 mesocosm experiment manipulating Si:N and copepod gra...
Phytoplankton, microzooplankton, copepod and dissolved nutrient data from a mesocosm experiment, which took place in summer 2016. A range of Si:N ratios and two levels of...