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  • 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)
  • Accession number, genetics; Ammonium; bloom; Continuous Segmented Flow Analyzer, SEAL Analytical, QuAAtro39; cyanobacteria; experiment; Experiment; gene expression; Laboratory; Nodularia spumigena; Nodularia spumigena, biomass as dry weight; Phosphate; phosphate limitation; Plate reader,TECAN, Infinite F200 PRO; polyphosphate; Polyphosphate/biomass as dry weight ratio; Salinity; Sample ID; Sampling date/time, experiment; Species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Strain; Time in days; Treatment: light:dark cycle; Treatment: light intensity; Treatment: nutrients; Treatment: temperature; Type of study; Uniform resource locator/link to reference  (1)
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  • 1
    Publication Date: 2024-01-26
    Description: Nodularia spumigena is a toxic, filamentous cyanobacterium capable to fix atmospheric nitrogen, which is often dominating cyanobacterial bloom events in the Baltic Sea and other aquatic systems worldwide. Phosphate (P) limitation has been considered as one environmental parameter that is somehow promoting the establishment of cyanobacterial mass developments. In the present study, we analyzed the response of Nodularia spumigena strain CCY9914 towards strong phosphorus limitation in an experimental approach. Pre-experimental and experimental incubations were performed at the Department of Plant Physiology (University of Rostock, Germany). Specifically, cultures were incubated under P-replete and P-deplete conditions for 21 days. The P-replete medium was composed as follows: 33% ASNIII and 67% BG11 medium mixture (as described by Hagemann et al., 2019), with 0.02 g L-1 K2HPO4 in the modified ASNIII (Rippka et al., 1979) and 0.00078 mg L-1 K2HPO4 in BG11 medium modified with 20 mM TES buffer to pH 8 (Rippka et al., 1979). Conversely, the P-deplete medium did not contain any additional P. Samples were collected after 3 hours (day 0), 7, 14 and 21 days from the start of the experiment to assess the variation of the following physiological parameters: biomass increase estimated by dry weight measurements and polyphosphate accumulation measured according to Martin et al. (2014). Additionally, ortho-phosphate and ammonium concentrations were measured in the medium to assess nutrient conditions during the course of the experiment. The experiment was repeated two times. During the second iteration of the experiment, samples from d7 and d14 were used for differential gene expression analysis (RNA-seq data available on Gene Expression Omnibus (GEO) accession GSE213384).
    Keywords: Accession number, genetics; Ammonium; bloom; Continuous Segmented Flow Analyzer, SEAL Analytical, QuAAtro39; cyanobacteria; experiment; Experiment; gene expression; Laboratory; Nodularia spumigena; Nodularia spumigena, biomass as dry weight; Phosphate; phosphate limitation; Plate reader,TECAN, Infinite F200 PRO; polyphosphate; Polyphosphate/biomass as dry weight ratio; Salinity; Sample ID; Sampling date/time, experiment; Species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Strain; Time in days; Treatment: light:dark cycle; Treatment: light intensity; Treatment: nutrients; Treatment: temperature; Type of study; Uniform resource locator/link to reference
    Type: Dataset
    Format: text/tab-separated-values, 874 data points
    Location Call Number Limitation Availability
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  • 2
    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
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