GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • ABYSS; Accession number, genetics; ARK-XXIX/2.2; Assessment of bacterial life and matter cycling in deep-sea surface sediments; beta-glucosidase activity; Cell counts, standard deviation; Chitobiase activity; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; HG_IV; Incubation duration; Multicorer with television; North Greenland Sea; Oxygen; Polarstern; Pressure; Prokaryotes, abundance as single cells; PS93/050-5/6; PS93.2; Replicates; Respiration rate, oxygen, sediment; Sample type; Station label; Treatment; TVMUC  (1)
  • ACUTE; Ammonia monooxygenase, amoA gene, relative abundance; Aquaculture practice in tropical coastal ecosystems - understanding ecological and socio-economic consequences; Core; DHC; Dissimilatory sulfate reductase, dsrA gene, relative abundance; Diver-held corer; Event label; Extraction: Mobio DNA Isolation Kit (Mo Bio Laboratories, Carlsbad, USA); Analysis: Shimadzu Biospec Nano microvolume spectrophotometer; FC; fish cage; Guiguiwanen_channel_S1; Guiguiwanen_channel_S3; marine aquaculture; Nitrite reductase, nirK gene, relative abundance; nutrient loading; OC; off cage site; Philippines; Site; Sulfur oxidizing multi-enzyme, gene soxB, relative abundance  (1)
  • ACUTE; after Aerts et al. (2015); after Clairborne (1985); after De Coen and Janssen (1997); Aquaculture practice in tropical coastal ecosystems - understanding ecological and socio-economic consequences; Available energy, per wet mass; Bradford method (1976); Bremen, Germany; Calculated; Calculated (sum of Protein, Carbohydrates, Lipids); Calculated according to Verslycke et al. (2004); Carbohydrates, per wet mass; Catalase activity, per protein mass; Cellular energy allocation; Chanos chanos, length; Chanos chanos, mass; Cortisol; DATE/TIME; described by Ellis and Goldberg (1971) and adapted to microplate usage by Lima et al. (2007); described by Vassault (1983) and adapted by Diamantino et al. (2001); Electron transport system activity, per wet mass; Experiment_Milkfish; Extraction of Lipids after Bligh & Dyer (1959); Fish, wet weighted; Fish measuring board; Hepatosomatic index; Isocitrate dehydrogenase activity, per protein mass; Laboratory experiment; Lactate dehydrogenase activity, per protein mass; Lipid peroxidation, per wet mass; Lipids, per wet mass; McCord and Fridovich (1969) with adaptation for measurements in microplates described by Lima et al. (2007); Ohkawa et al. (1979) and Bird and Draper (1984); Proteins, per wet mass; Sample ID; Sample material; Superoxide dismutase activity, unit per protein mass; Tank number; Time point, descriptive; Treatment: temperature description  (1)
Document type
Keywords
Publisher
Years
  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Hoffmann, Katy; Hassenrück, Christiane; Salman-Carvalho, Verena; Holtappels, Moritz; Bienhold, Christina (2017): Response of bacterial communities to different detritus compositions in Arctic deep-sea sediments. Frontiers in Microbiology, 8, 266, https://doi.org/10.3389/fmicb.2017.00266
    Publication Date: 2023-03-16
    Description: In a multidisciplinary ex situ experiment, benthic bacterial deep-sea communities from 2,500 m water depth at the Long-Term Ecological Research Observatory HAUSGARTEN (stationPS93/050-5 and 6), were retrieved using a TV-guided multiple corer. Surface sediments (0 - 2 cm) of 16 cores were mixed with sterile filtered deep-sea water to a final sediment dilution of 3.5 fold. The slurries were split and supplemented with five different types of habitat-related detritus: chitin, as the most abundant biopolymer in the oceans, and four different naturally occurring Arctic algae species, i.e. Thalassiosira weissflogii, Emiliania huxleyi, Bacillaria sp. and Melosira arctica. Incubations were performed in five replicates, at in situ temperature and at atmospheric pressure, as well as at in situ pressure of 250 atm. At the start of the incubation and after 23 days, changes in key community functions, i.e. extracellular enzymatic activity, oxygen respiration and secondary production of biomass (bacterial cell numbers and biomass), were assessed along with changes in the bacterial community composition based on 16S rRNA gene and 16S rRNA Illumina sequencing. In summary, differences in community structure and in the uptake and remineralization of carbon in the different treatments suggest an effect of organic matter quality on bacterial diversity as well as on carbon turnover at the seafloor.
    Keywords: ABYSS; Accession number, genetics; ARK-XXIX/2.2; Assessment of bacterial life and matter cycling in deep-sea surface sediments; beta-glucosidase activity; Cell counts, standard deviation; Chitobiase activity; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; HG_IV; Incubation duration; Multicorer with television; North Greenland Sea; Oxygen; Polarstern; Pressure; Prokaryotes, abundance as single cells; PS93/050-5/6; PS93.2; Replicates; Respiration rate, oxygen, sediment; Sample type; Station label; Treatment; TVMUC
    Type: Dataset
    Format: text/tab-separated-values, 1540 data points
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2023-02-23
    Description: Physicochemical parameters and relative abundance of selected nutrient cycling genes were measured in sediment and pore water samples taken from a fish farming area (Site S3 16◦23.097 N, 119◦55.551 E, depth 12.6m) and a control site (Site S1 16◦22.960 N, 119◦54.723 E, depth 15m) not influenced by fish farming. From each site, five pairs of cores representing five biological replicates were collected. One core from each pair was used for physicochemical analysis while the other cores were used for microbial community analysis. Samples from S1 were collected on 2017-06-10 and samples from S3 were collected the following day. Nitrogen (bacterial ammonia monooxygenase/ amoA and nitrite reductase/ nirK) and sulfur (dissimilatory sulfate reductase/ dsrA and sulfur oxidation/ soxB) cycling genes were quantified and normalized against the abundance of the 16S rRNA gene.
    Keywords: ACUTE; Ammonia monooxygenase, amoA gene, relative abundance; Aquaculture practice in tropical coastal ecosystems - understanding ecological and socio-economic consequences; Core; DHC; Dissimilatory sulfate reductase, dsrA gene, relative abundance; Diver-held corer; Event label; Extraction: Mobio DNA Isolation Kit (Mo Bio Laboratories, Carlsbad, USA); Analysis: Shimadzu Biospec Nano microvolume spectrophotometer; FC; fish cage; Guiguiwanen_channel_S1; Guiguiwanen_channel_S3; marine aquaculture; Nitrite reductase, nirK gene, relative abundance; nutrient loading; OC; off cage site; Philippines; Site; Sulfur oxidizing multi-enzyme, gene soxB, relative abundance
    Type: Dataset
    Format: text/tab-separated-values, 140 data points
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2024-03-20
    Description: Milkfish (Chanos chanos) is one of the most important aquaculture species in Asian countries. These teleost fish are traditionally cultured in outdoor-based systems and therefore have to cope with daily and/or seasonally changing environmental conditions. Temperature changes beyond the optimal range of a fish species are known to induce an endocrine stress response resulting in the release of cortisol via the hypothalamic-pituitary-interrenal axis. Moreover, (thermal) stress induces glucocorticoid-mediated changes in the fish's energy metabolism to cope with the stressor(s) and regain homeostasis. Long-term elevations of cortisol are known to be detrimental for fish performance. In this study, we investigated the stress response of juvenile milkfish, which were exposed to a gradual temperature increase of 1°C per day over 7 days in the range from 26°C to 33°C, followed by an exposure to constant 33°C for 21 days. We quantified ontogenetic (OG) and regenerated (RG) scale cortisol to evaluate chronic stress. To investigate metabolic implications and oxidative stress response, activity levels of key enzymes involved in metabolic (isocitrate dehydrogenase - IDH, lactate dehydrogenase - LDH, electron transfer system - ETS) and antioxidant (superoxide dismutase - SOD, catalase - CAT) related pathways were quantified. Furthermore, we measured available energy resources (protein, carbohydrates, lipids) and potential cellular damage due to oxidative stress (lipid peroxidation - LPO). Finally, changes in the gut microbiome of the milkfish related to the temperature stress were analyzed to elucidate their role in the stress response and interactions with physiological parameters. This study is part of the ACUTE project (AquaCUlture practice in Tropical coastal Ecosystems - Understanding ecological and socio-economic consequences) funded by the Leibniz Association grant SAW-2015-ZMT-4. It is associated with the following publications: Hanke et al., 2019 (doi:10.1016/j.aquaculture.2018.09.016) and Hassenrück et al., 2020 (doi:10.3390/microorganisms9010005). The final OTU table and statistical analysis scripts for Hassenrück et al., 2020 are supplied as further details to this data set.
    Keywords: ACUTE; after Aerts et al. (2015); after Clairborne (1985); after De Coen and Janssen (1997); Aquaculture practice in tropical coastal ecosystems - understanding ecological and socio-economic consequences; Available energy, per wet mass; Bradford method (1976); Bremen, Germany; Calculated; Calculated (sum of Protein, Carbohydrates, Lipids); Calculated according to Verslycke et al. (2004); Carbohydrates, per wet mass; Catalase activity, per protein mass; Cellular energy allocation; Chanos chanos, length; Chanos chanos, mass; Cortisol; DATE/TIME; described by Ellis and Goldberg (1971) and adapted to microplate usage by Lima et al. (2007); described by Vassault (1983) and adapted by Diamantino et al. (2001); Electron transport system activity, per wet mass; Experiment_Milkfish; Extraction of Lipids after Bligh & Dyer (1959); Fish, wet weighted; Fish measuring board; Hepatosomatic index; Isocitrate dehydrogenase activity, per protein mass; Laboratory experiment; Lactate dehydrogenase activity, per protein mass; Lipid peroxidation, per wet mass; Lipids, per wet mass; McCord and Fridovich (1969) with adaptation for measurements in microplates described by Lima et al. (2007); Ohkawa et al. (1979) and Bird and Draper (1984); Proteins, per wet mass; Sample ID; Sample material; Superoxide dismutase activity, unit per protein mass; Tank number; Time point, descriptive; Treatment: temperature description
    Type: Dataset
    Format: text/tab-separated-values, 2478 data points
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...