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Relative contribution of bacterial, fungal or plant essential amino acid to D...
Using Bayesion mixing models on mean-centered δ¹³C values of essential amino acids (eAA) extracted from Drosophila melanogaster flies and ontogenetic environments reared in a... -
Life-history traits, development time and dry weight upon eclosion of Drosoph...
In an experimental approach fruit and vegetable puree was inoculated with allochthonous and autochthonous fly fecal microbiota to record life-history parameters (time until... -
δ¹³C of amino acids extracted from Drosophila melanogaster and its ontogeneti...
Compound specific stable isotope analysis (CSIA) of amino acids (AA) extracted from flies, ontogenetic environments after fly eclosion and samples of environments prior to an... -
Abundance and biomass of macrofauna in the German Bight from 2012 to 2015
The long-term ecological research benthic monitoring comprises four representative permanent stations (SSd, Slt, FSd and WB) that have been sampled countinuously since 1969. The... -
Inorganic ion and metabolite concentrations in tissue of marine invertebrates...
Laboratory experiments were conducted in the climate chambers at GEOMAR Helmholtz Centre for Ocean Research Kiel in the time between March and November 2018. Experiments were... -
Fatty acid composition of zooplankton, fishes and sea birds from the northern...
Fatty acids were analyzed by gas chromatography using a DB-FFAP column of 30 m length and 0.25 mm inner diameter and a programmable temperature vaporizer injector. Following the... -
Effects of hypoxia and reoxygenation on the intermediary metabolites in the h...
This dataset has no description
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Effects of hypoxia and reoxygenation on the intermediary metabolites in the g...
This dataset has no description
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Seawater carbonate chemistry and physiological performance parameters of Carc...
Ocean acidification causes an accumulation of CO2 in marine organisms and leads to shifts in acid-base parameters. Acid-base regulation in gill breathers involves a net increase... -
(Table 3) Fatty acid and alcohol composition of Acartia bifilosa from Santala...
This dataset has no description
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(Table 2) Dry mass, lipid content and fatty acid composition of the amphipod ...
Fatty acids contributing <= 1.5% are combined under Others, unless they represent important biomarkers. -
(Table S4) Biomass of macroalgae and invertebrate species identified at vent ...
Please note, that values were originally given in gram dry weight per 2500 cm². The values were recalculated to g/m² by multiplying by 4. <0.04 is given as "+" (<0.01... -
(Table 4) Fatty acid and fatty alcohol compositions (mass %) of Oithona simil...
This dataset has no description
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(Table 1) Fatty acid and fatty alcohol compositions (mass %) of Pseudocalanus...
This dataset has no description
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(Table 2) Dry mass, total lipid and wax ester content as well as fatty acid a...
This dataset has no description
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(Table 3) Dry mass, lipid, carbon and nitrogen content and fatty acid composi...
T. longicornis females were sampled on 12 May 2005 and 5 May 2008 off the island of Helgoland. In 2008, approximately 300 healthy-looking T. longicornis females were incubated... -
(Table 2) Concentrations of adenosine triphosphate, adenosine diphosphate, an...
This dataset has no description
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(Table 3) Fatty acid composition of muscle tissue of demersal fish species sa...
For samples with N = 2 the values of the first and second sample are given. -
(Table 3) Proportions of the ten most abundant fatty acids in peracarid sampl...
For groups with specimen numbers = 2 minimum and maximum values are given. -
(Table 2) Fatty acid composition of prey species of Arctic walruses (Odobenus...
The levels of the non-methylene-interrupted (NMI) FAs 22:2Delta7.13 and 22:2Delta7.15 are relative to the total 100% of the 22 FA before.
