Alkenone analyses of sediment core MSM45/19_2
The presented data originates from the 1306cm long gravity core MSM45-19-2 (58°45.68 N, 61°56.25 W, 202m water depth) taken during R/V Maria S. Merian cruise MSM45 in August 2015 at 202 m water depth on the northern Labrador Shelf, northeast Canada, northwest Atlantic. In order to fully understand t...
| Main Authors: | , |
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| Format: | Dataset |
| Language: | English |
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PANGAEA
2022
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| Online Access: | https://doi.pangaea.de/10.1594/PANGAEA.945742 https://doi.org/10.1594/PANGAEA.945742 |
| Summary: | The presented data originates from the 1306cm long gravity core MSM45-19-2 (58°45.68 N, 61°56.25 W, 202m water depth) taken during R/V Maria S. Merian cruise MSM45 in August 2015 at 202 m water depth on the northern Labrador Shelf, northeast Canada, northwest Atlantic. In order to fully understand the dynamics that contributed to the establishment of modern Labrador Sea circulation, detailed reconstructions of the major paleoceanographic changes through the Holocene are critical. Therefore, this study aims to provide new information on bottom (i.e. subsurface) water mass composition as well as on changes in primary productivity and sea-ice conditions in the LC during the Holocene. Reconstructions are based on alkenone biomarker concentrations to provide a better understanding of the dynamics of different water masses that contributed to the establishment of modern Labrador Sea. circulation. Long-chain alkenones are biosynthesized by haptophytes (e.g. the coccolithophorid Emiliania huxleyi) living in surface waters. They consist of 37 carbon atoms with 2, 3, or 4 double bonds (C37:2, C37:3, and C37:4, respectively). Alkenone analyses were carried out at the Biomarker Laboratory at Kiel University. In total, 290 samples were analyzed in 5-cm intervals. Long-chained alkenones (C37) were extracted from 2 to 3 g of homogenized bulk sediment, using an Accelerated Solvent Extractor (Dionex ASE-200) with a mixture of 9:1 (v/v) of dichloromethane: methanol (DCM: MeOH) at 100°C and 100 bar N2 (g) pressure for 20 min. Extracts were cooled at −20°C and brought to near dryness by Syncore polyvap at 40°C and 490 mbar. For the identification and quantification of C37:2, C37:3, and C37:4 compounds, we used a multi-dimensional, double gas column chromatography (MD-GC) set up with two Agilent 6890 gas chromatographs (Etourneau et al., 2010). The addition of an internal standard prior to extraction (cholestane (C27H48) and hexatriacontane (C36H74)) allowed quantification of the three different compounds in nanograms per gram dry ... |
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