Martin, Bettina (2015): Stable isotopes (δ¹³C and d15N) in zooplankton from different transects in the northern Namibian upwelling area (Benguela Current System) during DISCOVERY 356 [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.846233
Always quote citation above when using data! You can download the citation in several formats below.
Related to:
Koppelmann, Rolf; Kullmann, Björn; Lahajnar, Niko; Martin, Bettina; Mohrholz, Volker (2013): Onshore-offshore distribution of Thecosomata (Gastropoda) in the Benguela Current upwelling region off Namibia: species diversity and trophic position. Journal of the Marine Biological Association of the United Kingdom, 93(06), 1625-1640, https://doi.org/10.1017/S0025315413000052
Project(s):
Funding:
Bundesministerium für Bildung und Forschung, Bonn (BMBF), grant/award no. 03F0650: Geochemistry and ecology of the Namibian upwelling system
Coverage:
Median Latitude: -20.758423 * Median Longitude: 11.953538 * South-bound Latitude: -23.071000 * West-bound Longitude: 9.661000 * North-bound Latitude: -18.283000 * East-bound Longitude: 13.536000
Date/Time Start: 2010-09-19T22:18:00 * Date/Time End: 2010-10-07T21:26:00
Minimum DEPTH, water: 12.5 m * Maximum DEPTH, water: 700.0 m
Event(s):
D356-15_3 * Latitude Start: -23.026000 * Longitude Start: 13.055000 * Latitude End: -23.055000 * Longitude End: 13.046000 * Date/Time Start: 2010-09-19T22:18:00 * Date/Time End: 2010-09-19T23:13:00 * Location: Benguela Upwelling * Campaign: D356 * Basis: Discovery (1962) * Method/Device: Double MOCNESS 333 (MOC-D-333)
D356-15_7 * Latitude Start: -23.041000 * Longitude Start: 13.035000 * Latitude End: -23.008000 * Longitude End: 13.035000 * Date/Time Start: 2010-09-20T05:21:00 * Date/Time End: 2010-09-20T06:17:00 * Location: Benguela Upwelling * Campaign: D356 * Basis: Discovery (1962) * Method/Device: Double MOCNESS 333 (MOC-D-333)
D356-16_3 * Latitude Start: -22.836000 * Longitude Start: 11.791000 * Latitude End: -23.046000 * Longitude End: 11.808000 * Date/Time Start: 2010-09-20T17:17:00 * Date/Time End: 2010-09-20T23:34:00 * Location: Benguela Upwelling * Campaign: D356 * Basis: Discovery (1962) * Method/Device: Double MOCNESS 333 (MOC-D-333)
Parameter(s):
| # | Name | Short Name | Unit | Principal Investigator | Method/Device | Comment |
|---|---|---|---|---|---|---|
| 1 | Event label | Event | Martin, Bettina | |||
| 2 | Latitude of event | Latitude | Martin, Bettina | |||
| 3 | Longitude of event | Longitude | Martin, Bettina | |||
| 4 | Date/Time of event | Date/Time | Martin, Bettina | |||
| 5 | Sample code/label | Sample label | Martin, Bettina | |||
| 6 | DEPTH, water | Depth water | m | Martin, Bettina | Geocode | |
| 7 | Taxon/taxa | Taxa | Martin, Bettina | |||
| 8 | Species | Species | Martin, Bettina | |||
| 9 | δ15N/14N ratio | δ15N/14N | Martin, Bettina | |||
| 10 | δ13C/12C ratio | δ13C/12C | Martin, Bettina |
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
424 data points
Data
| 1 Event | 2 Latitude | 3 Longitude | 4 Date/Time | 5 Sample label | 6 Depth water [m] | 7 Taxa | 8 Species | 9 δ15N/14N | 10 δ13C/12C |
|---|---|---|---|---|---|---|---|---|---|
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_R5 | 300.0 | Chaetognatha | S. decipiens | 9.164 | -20.841 |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_R5 | 300.0 | Chaetognatha | 6.814 | -19.906 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S. enflata | 9.794 | -19.805 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | 12.323 | -19.474 | ||
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S.zetesiois/planctonis | 11.992 | -18.151 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S.zetesiois/planctonis | 11.930 | -18.773 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | 10.890 | -19.874 | ||
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_R5 | 300.0 | Chaetognatha | 9.348 | -19.652 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_R5 | 300.0 | Chaetognatha | S. decipiens | 8.667 | -20.461 |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_R4 | 300.0 | Chaetognatha | 8.187 | -19.771 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_R5 | 300.0 | Chaetognatha | S. decipiens | 9.527 | -20.829 |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S. enflata | 9.035 | -21.915 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S.zetesiois/planctonis | 11.319 | -18.106 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | 10.005 | -21.257 | ||
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S.zetesiois/planctonis | 11.386 | -17.822 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S. enflata | 9.929 | -21.480 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | S. enflata | 11.265 | -20.804 | |
| D356-23_2 | -19.0330 | 10.3660 | 2010-09-27T09:40 | MOC-D-13_L1 + R1 | Chaetognatha | 11.087 | -20.442 | ||
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.270 | -19.931 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.648 | -19.402 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.253 | -19.004 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.634 | -19.323 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.765 | -19.647 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.437 | -20.083 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.380 | -20.269 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_L1 | 125.0 | Chaetognatha | 8.727 | -19.620 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R2 | 125.0 | Chaetognatha | 8.008 | -20.283 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R3 | 75.0 | Chaetognatha | 10.230 | -19.717 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R2 | 125.0 | Chaetognatha | 8.476 | -19.949 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R4 | 37.5 | Chaetognatha | 9.022 | -18.770 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R3 | 75.0 | Chaetognatha | 10.330 | -19.700 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R3 | 75.0 | Chaetognatha | 10.221 | -19.550 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R2 | 125.0 | Chaetognatha | 8.518 | -20.404 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R2 | 125.0 | Chaetognatha | 8.334 | -20.208 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R2 | 125.0 | Chaetognatha | 8.617 | -20.285 | |
| D356-25_6 | -19.0500 | 11.5410 | 2010-09-29T00:25 | MOC-D-16_R3 | 75.0 | Chaetognatha | 10.268 | -19.685 | |
| D356-27_7_1 | -18.9900 | 12.1860 | 2010-09-29T22:20 | MOC-D-18_R4 | 37.5 | Chaetognatha | S.minima | 10.176 | -20.735 |
| D356-27_7_1 | -18.9900 | 12.1860 | 2010-09-29T22:20 | MOC-D-18_R4 | 37.5 | Chaetognatha | S.minima | 10.379 | -20.534 |
| D356-27_7_1 | -18.9900 | 12.1860 | 2010-09-29T22:20 | MOC-D-18_R4 | 37.5 | Chaetognatha | S.minima | 10.309 | -20.792 |
| D356-27_7_1 | -18.9900 | 12.1860 | 2010-09-29T22:20 | MOC-D-18_R4 | 37.5 | Chaetognatha | S.minima | 10.020 | -20.534 |
| D356-27_7_1 | -18.9900 | 12.1860 | 2010-09-29T22:20 | MOC-D-18_R4 | 37.5 | Chaetognatha | S.minima | 10.054 | -20.371 |
| D356-27_7_1 | -18.9900 | 12.1860 | 2010-09-29T22:20 | MOC-D-18_R4 | 37.5 | Chaetognatha | S.minima | 10.171 | -20.573 |
| D356-29_8_1 | -18.9900 | 12.1910 | 2010-09-30T11:15 | MOC-D-20_L1 + R1 | 50.0 | Chaetognatha | S.enflata | 9.758 | -19.937 |
| D356-29_8_1 | -18.9900 | 12.1910 | 2010-09-30T11:15 | MOC-D-20_R2 | 75.0 | Chaetognatha | 9.574 | -20.375 | |
| D356-29_8_1 | -18.9900 | 12.1910 | 2010-09-30T11:15 | MOC-D-20_R2 | 75.0 | Chaetognatha | 9.833 | -20.166 | |
| D356-29_8_1 | -18.9900 | 12.1910 | 2010-09-30T11:15 | MOC-D-20_R2 | 75.0 | Chaetognatha | 9.476 | -20.206 | |
| D356-29_8_1 | -18.9900 | 12.1910 | 2010-09-30T11:15 | MOC-D-20_R3 | 37.5 | Chaetognatha | 9.224 | -20.165 | |
| D356-29_8_1 | -18.9900 | 12.1910 | 2010-09-30T11:15 | MOC-D-20_R4 | 12.5 | Chaetognatha | 9.614 | -20.470 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R2 | 700.0 | Chaetognatha | 10.105 | -18.908 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R2 | 700.0 | Chaetognatha | 10.470 | -19.166 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R2 | 700.0 | Chaetognatha | 11.068 | -19.303 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R3 | 500.0 | Chaetognatha | 8.966 | -17.025 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R3 | 500.0 | Chaetognatha | 9.693 | -19.472 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R3 | 500.0 | Chaetognatha | 9.574 | -19.328 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R4 | 300.0 | Chaetognatha | 7.384 | -19.343 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R4 | 300.0 | Chaetognatha | 7.506 | -19.230 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R5 | 300.0 | Chaetognatha | 6.996 | -19.788 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R5 | 150.0 | Chaetognatha | 7.907 | -19.394 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R5 | 150.0 | Chaetognatha | 8.605 | -19.034 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R6 | 75.0 | Chaetognatha | 6.357 | -20.127 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R6 | 75.0 | Chaetognatha | 6.346 | -20.120 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R7 | 12.5 | Chaetognatha | 6.769 | -20.292 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R8 | 12.5 | Chaetognatha | 6.171 | -19.712 | |
| D356-32_6 | -18.2830 | 10.8260 | 2010-10-02T14:19 | MOC-D-21_R8 | 12.5 | Chaetognatha | 6.046 | -19.863 | |
| D356-34_8 | -18.6560 | 10.6530 | 2010-10-03T17:11 | MOC-D-22_R7 | 36.0 | Chaetognatha | 7.650 | -22.362 | |
| D356-34_8 | -18.6560 | 10.6530 | 2010-10-03T17:11 | MOC-D-22_R5 | 36.0 | Chaetognatha | 8.569 | -22.624 | |
| D356-34_8 | -18.6560 | 10.6530 | 2010-10-03T17:11 | MOC-D-22_R5 | 36.0 | Chaetognatha | 7.468 | -22.727 | |
| D356-34_8 | -18.6560 | 10.6530 | 2010-10-03T17:11 | MOC-D-22_R1 | 20.0 | Chaetognatha | 8.533 | -21.558 | |
| D356-39_5 | -18.5910 | 9.6610 | 2010-10-05T08:12 | MOC-D-23_L1 + R1 | Chaetognatha | 6.899 | -21.089 | ||
| D356-39_5 | -18.5910 | 9.6610 | 2010-10-05T08:12 | MOC-D-23_L1 + R1 | Chaetognatha | 8.176 | -20.073 | ||
| D356-39_5 | -18.5910 | 9.6610 | 2010-10-05T08:12 | MOC-D-23_L1 + R1 | Chaetognatha | 7.924 | -20.911 | ||
| D356-39_5 | -18.5910 | 9.6610 | 2010-10-05T08:12 | MOC-D-23_L1 + R1 | Chaetognatha | 6.698 | -20.603 | ||
| D356-39_5 | -18.5910 | 9.6610 | 2010-10-05T08:12 | MOC-D-23_L1 + R1 | Chaetognatha | 7.956 | -20.916 | ||
| D356-39_5 | -18.5910 | 9.6610 | 2010-10-05T08:12 | MOC-D-23_L1 + R1 | Chaetognatha | 8.658 | -20.414 | ||
| D356-43_1 | -22.9840 | 13.0420 | 2010-10-07T20:36 | MOC-D-24_R1 | Chaetognatha | 10.098 | -19.606 | ||
| D356-43_1 | -22.9840 | 13.0420 | 2010-10-07T20:36 | MOC-D-24_R1 | Chaetognatha | 11.004 | -19.311 | ||
| D356-43_1 | -22.9840 | 13.0420 | 2010-10-07T20:36 | MOC-D-24_R1 | Chaetognatha | 10.442 | -19.363 | ||
| D356-43_1 | -22.9840 | 13.0420 | 2010-10-07T20:36 | MOC-D-24_R1 | Chaetognatha | 11.051 | -19.038 | ||
| D356-43_1 | -22.9840 | 13.0420 | 2010-10-07T20:36 | MOC-D-24_R1 | Chaetognatha | 9.658 | -19.589 | ||
| D356-16_3 | -22.8360 | 11.7910 | 2010-09-20T17:17 | MOC-D-08_ | Pteropoda | Clio pyramidiata | 4.965 | -21.484 | |
| D356-16_3 | -22.8360 | 11.7910 | 2010-09-20T17:17 | MOC-D-08_ | Pteropoda | Limacina inflata | 4.070 | -22.397 | |
| D356-16_3 | -22.8360 | 11.7910 | 2010-09-20T17:17 | MOC-D-08_ | Pteropoda | Diacria trispinosa | 4.638 | -20.517 | |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06+07_ | Pteropoda | Gymnosomata | 6.308 | -21.354 | |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06+07_ | Pteropoda | Clio pyramidiata | 5.085 | -21.210 | |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06+07_ | Pteropoda | Diacria trispinosa | 5.114 | -22.141 | |
| D356-17_4_1 | -23.0000 | 13.5000 | 2010-09-22T00:00 | MOC-D-10+11+12_ | Pteropoda | Diacria trispinosa | 5.252 | -22.760 | |
| D356-17_4_1 | -23.0000 | 13.5000 | 2010-09-22T00:00 | MOC-D-10+11+12_ | Pteropoda | Diacria rampali | 5.027 | -23.085 | |
| D356-17_4_1 | -23.0000 | 13.5000 | 2010-09-22T00:00 | MOC-D-10+11+12_ | Pteropoda | Clio pyramidiata | 5.894 | -23.612 | |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06_R8 | 37.5 | Thaliacea | Salpa fusiformis | 4.703 | -23.494 |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06_R8 | 37.5 | Thaliacea | Salpa fusiformis | 4.665 | -23.681 |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06_R8 | 37.5 | Thaliacea | Salpa fusiformis | 5.600 | -24.351 |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06_R7 | 75.0 | Thaliacea | Salpa fusiformis | 5.566 | -23.292 |
| D356-15_3 | -23.0260 | 13.0550 | 2010-09-19T22:18 | MOC-D-06_R7 | 75.0 | Thaliacea | Salpa fusiformis | 6.466 | -23.461 |
| D356-15_7 | -23.0410 | 13.0350 | 2010-09-20T05:21 | MOC-D-07_R9 | 12.5 | Thaliacea | Salpa fusiformis | 2.909 | -23.276 |
| D356-15_7 | -23.0410 | 13.0350 | 2010-09-20T05:21 | MOC-D-07_R9 | 12.5 | Thaliacea | Salpa fusiformis | 3.786 | -23.526 |
| D356-17_8 | -23.0560 | 13.5280 | 2010-09-22T07:37 | MOC-D-11_R9 | 12.5 | Thaliacea | Salpa fusiformis | 6.460 | -22.749 |
| D356-17_8 | -23.0560 | 13.5280 | 2010-09-22T07:37 | MOC-D-11_R9 | 12.5 | Thaliacea | Salpa fusiformis | 5.884 | -23.105 |