Zhuang, Guang-Chao; Lin, Yu-Shih; Bowles, Marshall W; Heuer, Verena B; Lever, Mark A; Elvert, Marcus; Hinrichs, Kai-Uwe (2018): Distribution and isotopic composition of trimethylamine, dimethylsulfide and dimethylsulfoniopropionate in sediment core M1 [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.888368, In supplement to: Zhuang, G-C et al. (2017): Distribution and isotopic composition of trimethylamine, dimethylsulfide and dimethylsulfoniopropionate in marine sediments. Marine Chemistry, 196, 35-46, https://doi.org/10.1016/j.marchem.2017.07.007
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Project(s):
Coverage:
Latitude: 56.117900 * Longitude: 10.346800
Minimum DEPTH, sediment/rock: 0.01 m * Maximum DEPTH, sediment/rock: 0.54 m
Event(s):
Parameter(s):
| # | Name | Short Name | Unit | Principal Investigator | Method/Device | Comment |
|---|---|---|---|---|---|---|
| 1 | DEPTH, sediment/rock | Depth sed | m | Zhuang, Guang-Chao | Geocode | |
| 2 | Sulfate | [SO4]2- | mmol/l | Zhuang, Guang-Chao | ||
| 3 | Methane | CH4 | mmol/l | Zhuang, Guang-Chao | ||
| 4 | δ13C, organic carbon | δ13C Corg | ‰ PDB | Zhuang, Guang-Chao | ||
| 5 | δ13C, methane | δ13C CH4 | ‰ PDB | Zhuang, Guang-Chao | ||
| 6 | Trimethylamine, exchangeable | TMA exch | µmol/kg | Zhuang, Guang-Chao | ||
| 7 | Trimethylamine, base-extractable | TMA b-ext | µmol/kg | Zhuang, Guang-Chao | ||
| 8 | Trimethylamine, δ13C | TMA δ13C | ‰ PDB | Zhuang, Guang-Chao | ||
| 9 | Dimethylsulfoniopropionate, dissolved | DMSP diss | nmol/l | Zhuang, Guang-Chao | ||
| 10 | Base-hydrolysable dimethylsulfoniopropionate | DMSPt | µmol/kg | Zhuang, Guang-Chao | ||
| 11 | Dimethylsulfoniopropionate, δ13C | DMSP δ13C | ‰ PDB | Zhuang, Guang-Chao |
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
134 data points
Data
| 1 Depth sed [m] | 2 [SO4]2- [mmol/l] | 3 CH4 [mmol/l] | 4 δ13C Corg [‰ PDB] | 5 δ13C CH4 [‰ PDB] | 6 TMA exch [µmol/kg] | 7 TMA b-ext [µmol/kg] | 8 TMA δ13C [‰ PDB] | 9 DMSP diss [nmol/l] | 10 DMSPt [µmol/kg] | 11 DMSP δ13C [‰ PDB] |
|---|---|---|---|---|---|---|---|---|---|---|
| 0.01 | 23.3 | 0.0013 | -21.3 | 5.3 | 14.9 | 12.3 | 64.8 | |||
| 0.03 | 22.7 | 0.0016 | -21.2 | 18.0 | 5.9 | 54.2 | ||||
| 0.05 | 22.6 | 0.0015 | -21.6 | 5.4 | 11.5 | 2.4 | 61.5 | |||
| 0.07 | 22.1 | 0.0024 | -21.4 | 2.7 | 11.6 | 56.8 | ||||
| 0.09 | 22.2 | -20.9 | 1.7 | 6.3 | 42.0 | |||||
| 0.11 | 21.9 | 0.0028 | -20.4 | 1.1 | 7.1 | 3.1 | 44.0 | |||
| 0.13 | 21.9 | 0.0033 | -20.2 | 0.8 | 5.8 | 41.0 | ||||
| 0.15 | 21.5 | 0.0032 | -18.9 | 0.6 | 4.6 | -38.1 | 2.1 | 36.7 | -21.9 | |
| 0.17 | 21.7 | 0.0037 | -18.1 | 0.5 | 4.8 | -39.3 | 2.8 | 35.4 | -21.1 | |
| 0.19 | 21.0 | 0.0042 | -18.0 | 0.5 | 3.2 | 2.6 | 31.6 | |||
| 0.22 | 20.9 | 0.0031 | -20.7 | 3.7 | -39.2 | 31.5 | -20.0 | |||
| 0.26 | 19.6 | 0.0047 | -18.0 | -43.5 | 0.4 | 3.2 | -38.1 | 3.6 | 26.8 | -20.0 |
| 0.30 | 19.2 | 0.0043 | -17.4 | -49.0 | 3.3 | 4.4 | 29.6 | |||
| 0.34 | 18.0 | 0.0070 | -18.9 | -48.2 | 0.4 | 2.5 | 24.6 | |||
| 0.38 | 16.7 | 0.0082 | -17.6 | -55.6 | 2.4 | -37.7 | 3.0 | 23.1 | -18.6 | |
| 0.42 | 15.9 | 0.0090 | -17.8 | -52.0 | 0.4 | 2.9 | 2.4 | 26.7 | ||
| 0.46 | 14.6 | 0.0103 | -17.7 | -55.2 | 2.2 | 6.8 | 21.6 | |||
| 0.50 | 13.6 | 0.0107 | -18.5 | -59.8 | 0.4 | 2.0 | 2.3 | 17.0 | ||
| 0.54 | 13.2 | -17.8 |