Risebrobakken, Bjørg; Dokken, Trond; Smedsrud, Lars Henrik; Andersson, Carin; Jansen, Eystein; Moros, Matthias; Ivanova, Elena V (2014): (Table 1) Age determination of Barents Sea sediment cores [dataset]. Bjerknes Centre for Climate Research, PANGAEA, https://doi.org/10.1594/PANGAEA.829724, Supplement to: Risebrobakken, B et al. (2011): Early Holocene temperature variability in the Nordic Seas: The role of oceanic heat advection versus changes in orbital forcing. Paleoceanography, 26(4), PA4206, https://doi.org/10.1029/2011PA002117
Always quote citation above when using data! You can download the citation in several formats below.
Abstract:
The separate roles of oceanic heat advection and orbital forcing on influencing early Holocene temperature variability in the eastern Nordic Seas is investigated. The effect of changing orbital forcing on the ocean temperatures is tested using the 1DICE model, and the 1DICE results are compared with new and previously published temperature reconstructions from a transect of five cores located underneath the pathway of Atlantic water, from the Faroe-Shetland Channel in the south to the Barents Sea in the north. The stronger early Holocene summer insolation at high northern latitudes increased the summer mixed layer temperatures, however, ocean temperatures underneath the summer mixed layer did not increase significantly. The absolute maximum in summer mixed layer temperatures occurred between 9 and 6 ka BP, representing the Holocene Thermal Maximum in the eastern Nordic Seas. In contrast, maximum in northward oceanic heat transport through the Norwegian Atlantic Current occurred approximately 10 ka BP. The maximum in oceanic heat transport at 10 ka BP occurred due to a major reorganization of the Atlantic Ocean circulation, entailing strong and deep rejuvenation of the Atlantic Meridional Overturning Circulation, combined with changes in the North Atlantic gyre dynamic causing enhanced transport of heat and salt into the Nordic Seas.
Related to:
Bakke, Jostein; Lie, Øyvind; Heegaard, E; Dokken, Trond; Haug, Gerald H; Birks, Hilary H; Dulski, Peter; Nilsen, Trygve (2009): Rapid oceanic and atmospheric changes during the Younger Dryas cold period. Nature Geoscience, 2(3), 202-205, https://doi.org/10.1038/ngeo439
Chistyakova, Natalia O; Ivanova, Elena V; Risebrobakken, Bjørg; Ovsepyan, E A; Ovsepyan, Ya S (2010): Reconstruction of the postglacial environments in the southwestern Barents Sea based on foraminiferal assemblages. Translated from Okeanologiya, 2010, 50(4), 608-617, Oceanology, 50(4), 573-581, https://doi.org/10.1134/S0001437010040132
Ivanova, Elena V; Ovsepyan, E A; Risebrobakken, Bjørg; Vetrov, Alexander A (2008): Downcore distribution of living calcareous foraminifera and stable isotopes in the western Barents Sea. Journal of Foraminiferal Research, 38(4), 337-356, https://doi.org/10.2113/gsjfr.38.4.337
Risebrobakken, Bjørg; Jansen, Eystein; Andersson, Carin; Mjelde, Eirik; Hevroy, Kjersti (2003): A high-resolution study of Holocene paleoclimatic and paleoceanographic changes in the Nordic Seas. Paleoceanography, 18(1), 1017, https://doi.org/10.1029/2002PA000764
Risebrobakken, Bjørg; Moros, Matthias; Ivanova, Elena V; Chistyakova, Natalia O; Rosenberg, Reinhild (2010): Climate and oceanographic variability in the SW Barents Sea during the Holocene. The Holocene, 20(4), 609-621, https://doi.org/10.1177/0959683609356586
Sarnthein, Michael; van Kreveld, Shirley A; Erlenkeuser, Helmut; Grootes, Pieter Meiert; Kucera, Michal; Pflaumann, Uwe; Schulz, Michael (2003): Centennial-to-millennial-scale periodicities of Holocene climate and sediment injections off western Barents shelf, 75°N. Boreas, 32(3), 447-461, https://doi.org/10.1111/j.1502-3885.2003.tb01227.x
Coverage:
Median Latitude: 70.853416 * Median Longitude: 16.902105 * South-bound Latitude: 62.374667 * West-bound Longitude: -0.980167 * North-bound Latitude: 78.924670 * East-bound Longitude: 41.882830
Date/Time Start: 1988-07-16T00:00:00 * Date/Time End: 1999-08-01T00:00:00
Minimum DEPTH, sediment/rock: 0.0250 m * Maximum DEPTH, sediment/rock: 8.1350 m
Event(s):
GIK23258-2 * Latitude: 74.998083 * Longitude: 13.968533 * Date/Time: 1988-07-16T00:00:00 * Elevation: -1768.0 m * Penetration: 10.5 m * Recovery: 9.32 m * Location: Arctic Ocean * Campaign: M7/2 * Basis: Meteor (1986) * Method/Device: Kasten corer (KAL)
MD95-2011 (MD952011) * Latitude: 66.969660 * Longitude: 7.639330 * Date/Time: 1995-06-08T00:00:00 * Elevation: -1048.0 m * Recovery: 17 m * Location: Voring Plateau * Campaign: MD101 (IMAGES I) * Basis: Marion Dufresne (1995) * Method/Device: Calypso Corer (CALYPSO) * Comment: XII Sections, Site location wrong, slumps. Bent core; liner imploded in the middle of the core; 30 cm of sediment of the top recovered in a 1/2 liner
MD99-2284 (3664N/S) * Latitude: 62.374667 * Longitude: -0.980167 * Date/Time: 1999-08-01T00:00:00 * Elevation: -1500.0 m * Recovery: 33.15 m * Location: N. Shetland channel * Campaign: MD114 (IMAGES V) * Basis: Marion Dufresne (1995) * Method/Device: Calypso Corer (CALYPSO)
Parameter(s):
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
888 data points
Data
| 1 Event | 2 Latitude | 3 Longitude | 4 Elevation [m] | 5 Lab label | 6 Depth sed [m] | 7 Dated material | 8 Age dated [ka] (Age, 14C AMS) | 9 Age dated std dev [±] (Age, 14C AMS) | 10 Age dated [ka] (#2, Age, 14C AMS) | 11 Age dated std dev [±] (#2, Age, 14C AMS) | 12 Res effect [a] | 13 Res effect std dev [±] | 14 Age min [ka] (1 sigma range, Age, 14C calib...) | 15 Age max [ka] (1 sigma range, Age, 14C calib...) | 16 Age min [ka] (#2, 1 sigma range, Age, 14C c...) | 17 Age max [ka] (#2, 1 sigma range, Age, 14C c...) | 18 Prob (relative) | 19 Cal age [ka BP] (Age, 14C calibrated) | 20 Cal age [ka BP] (#2, Age, 14C calibrated) | 21 Comment | 22 Reference |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-20001 | 0.0750 | Bulk foraminifera | 1.460 | 0.160 | 71 | 21 | 0.767 | 1.110 | 1.000 | 0.942 | Not used | This study | |||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | 0.1150 | Bulk foraminifera | 1.170 | 0.030 | 71 | 21 | 0.629 | 0.687 | 1.000 | 0.659 | This study | |||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-15134 | 0.1550 | Mollusc | 7.490 | 0.040 | 7.54 | 0.05 | 71 | 21 | 7.837 | 7.932 | 7.868 | 7.982 | 1.000 | 7.883 | 7.93 | Not used | This study |
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-20002 | 0.3100 | Bulk foraminifera | 3.305 | 0.030 | 71 | 21 | 2.988 | 3.123 | 1.000 | 3.055 | Not used | This study | |||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-36197 | 0.3650 | Bulk foraminifera | 3.135 | 0.035 | 71 | 21 | 2.767 | 2.874 | 1.000 | 2.830 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-20003 | 0.6100 | Bulk foraminifera | 3.425 | 0.035 | 71 | 21 | 3.163 | 3.292 | 1.000 | 3.223 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-20004 | 0.7900 | Bulk foraminifera | 4.180 | 0.035 | 71 | 21 | 4.900 | 4.224 | 1.000 | 4.163 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-36198 | 1.0050 | Bulk foraminifera | 5.240 | 0.050 | 71 | 21 | 5.472 | 5.580 | 1.000 | 5.528 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-15136 | 1.2600 | Snail/mollusc | 6.380 | 0.040 | 71 | 21 | 6.790 | 6.836 | 1.000 | 6.769 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-12699 | 1.4300 | Yoldia | 6.820 | 0.040 | 71 | 21 | 7.228 | 7.332 | 1.000 | 7.280 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-15137 | 1.6850 | Mollusc | 7.360 | 0.040 | 71 | 21 | 7.690 | 7.820 | 1.000 | 7.751 | This study | ||||||
| PSh-5157 | 78.9247 | 41.8828 | -461 | Poz-15138 | 2.2050 | Mollusc | 9.000 | 0.050 | 71 | 21 | 9.517 | 9.651 | 1.000 | 9.590 | This study | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-15130 | 0.0750 | Mollusc fragments, benthic foraminifera | ?0.102 | 71 | 21 | Ivanova et al. (2008) | |||||||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-20399 | 0.1417 | Lenticulina sp. | 0.635 | 0.030 | 71 | 21 | 0.174 | 0.258 | 0.788 | 0.197 | Ivanova et al. (2008) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-19995 | 0.2150 | Bulk foraminifera | 1.670 | 0.030 | 71 | 21 | 1.118 | 1.223 | 1.000 | 1.164 | Ivanova et al. (2008) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-19997 | 0.4050 | Bulk foraminifera | 2.845 | 0.030 | 71 | 21 | 2.426 | 2.630 | 1.000 | 2.508 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-20568 | 0.4550 | Bulk foraminifera | 4.960 | 0.040 | 71 | 21 | 5.132 | 5.287 | 1.000 | 5.204 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-15131 | 0.5050 | Mollusc fragments | 6.105 | 0.035 | 71 | 21 | 6.393 | 6.500 | 1.000 | 6.451 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-19998 | 0.6050 | Bulk foraminifera | 7.040 | 0.040 | 71 | 21 | 7.423 | 7.570 | 1.000 | 7.472 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-12701 | 0.6950 | Brachiopod | 7.500 | 0.040 | 71 | 21 | 7.844 | 7.939 | 1.000 | 7.892 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-19999 | 0.8650 | Bulk foraminifera | 8.550 | 0.050 | 71 | 21 | 9.100 | 9.171 | 1.000 | 9.103 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-15132 | 0.9950 | Mollusc fragments, benthic foraminifera, ostracode | 9.700 | 0.050 | 71 | 21 | 1.444 | 1.556 | 1.000 | 10.496 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-19991 | 1.2250 | Mollusc | 10.010 | 0.050 | 71 | 21 | 1.565 | 1.779 | 1.000 | 10.693 | Risebrobakken et al. (2010); Chistyakova et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-15133 | 1.3350 | Mollusc fragments | 10.290 | 0.050 | 71 | 21 | 11.290 | 11.196 | 1.000 | 11.100 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-12629 | 1.4850 | Astarte crenata | 10.360 | 0.050 | 71 | 21 | 11.118 | 11.217 | 1.000 | 11.165 | Risebrobakken et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-16594 | 2.4100 | Bulk benthic foraminifera | 12.150 | 0.070 | 71 | 21 | 13.450 | 13.660 | 1.000 | 13.515 | Risebrobakken et al. (2010); Chistyakova et al. (2010) | ||||||
| PSh-5159N | 71.0000 | 22.0000 | -422 | Poz-19992 | 3.3300 | Bulk benthic foraminifera | 13.550 | 0.070 | 71 | 21 | 15.486 | 16.227 | 0.961 | 15.813 | Risebrobakken et al. (2010); Chistyakova et al. (2010) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7648 | 0.2500 | Neogloboquadrina pachyderma s | 1.165 | 0.035 | 71 | 21 | 0.622 | 0.689 | 1.000 | 0.655 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7649 | 0.5100 | Neogloboquadrina pachyderma s | 2.555 | 0.030 | 71 | 21 | 2.710 | 2.210 | 1.000 | 2.145 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7650 | 0.6700 | Neogloboquadrina pachyderma s | 3.500 | 0.035 | 71 | 21 | 3.255 | 3.358 | 1.000 | 3.307 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7651 | 0.9300 | Neogloboquadrina pachyderma s | 4.825 | 0.040 | 71 | 21 | 4.889 | 5.670 | 1.000 | 5.002 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA11534 | 1.1800 | Neogloboquadrina pachyderma d | 6.140 | 0.070 | 71 | 21 | 6.440 | 6.581 | 1.000 | 6.495 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7653 | 1.5400 | Neogloboquadrina pachyderma s | 7.660 | 0.045 | 71 | 21 | 7.988 | 8.112 | 1.000 | 8.050 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7654 | 1.7700 | Neogloboquadrina pachyderma s | 8.380 | 0.045 | 71 | 21 | 8.796 | 8.969 | 1.000 | 8.872 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA8553 | 1.9200 | Neogloboquadrina pachyderma s | 8.760 | 0.040 | 71 | 21 | 9.312 | 9.426 | 1.000 | 9.368 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA11535 | 2.0700 | Neogloboquadrina pachyderma d | 8.955 | 0.055 | 71 | 21 | 9.473 | 9.599 | 1.000 | 9.541 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA9193 | 2.4100 | Neogloboquadrina pachyderma s | 9.330 | 0.070 | 71 | 21 | 9.996 | 1.186 | 0.927 | 10.074 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA8554 | 2.4900 | Neogloboquadrina pachyderma s | 9.235 | 0.050 | 71 | 21 | 9.880 | 1.950 | 1.000 | 9.965 | Not used | Sarnthein et al. (2003) | |||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA9354 | 2.5000 | Neogloboquadrina pachyderma s | 9.435 | 0.055 | 71 | 21 | 1.147 | 1.264 | 1.000 | 10.210 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7657 | 3.1500 | Neogloboquadrina pachyderma s | 10.980 | 0.070 | 200 | 50 | 12.500 | 12.365 | 1.000 | 12.216 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA7659 | 3.5500 | Neogloboquadrina pachyderma s | 12.010 | 0.055 | 71 | 21 | 13.295 | 13.490 | 1.000 | 13.359 | Sarnthein et al. (2003) | ||||||
| GIK23258-2 | 74.9981 | 13.9685 | -1768 | KIA 9354 | 3.9400 | Neogloboquadrina pachyderma s | 12.390 | 0.060 | 71 | 21 | 13.672 | 13.837 | 1.000 | 13.751 | Sarnthein et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8245 | 0.0500 | Neogloboquadrina pachyderma d | 1.020 | 0.100 | 0 | 0 | 0.519 | 0.665 | 1.000 | 0.600 | Not used | This study | |||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | GifA96471 | 0.1050 | Neogloboquadrina pachyderma d | 0.980 | 0.060 | 0 | 0 | 0.526 | 0.619 | 1.000 | 0.573 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 5600 | 0.2450 | Neogloboquadrina pachyderma d | 1.590 | 0.040 | 0 | 0 | 1.120 | 1.215 | 1.000 | 1.153 | Not used | Risebrobakken et al. (2003) | |||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 3925 | 0.3050 | Neogloboquadrina pachyderma d | 1.040 | 0.040 | 0 | 0 | 0.590 | 0.649 | 0.789 | 0.611 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 5601 | 0.4750 | Neogloboquadrina pachyderma d | 1.160 | 0.030 | 0 | 0 | 0.667 | 0.727 | 1.000 | 0.703 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8244 | 0.5550 | Neogloboquadrina pachyderma d | 1.530 | 0.090 | 0 | 0 | 0.976 | 1.174 | 1.000 | 1.085 | Not used | This study | |||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 3926 | 0.7050 | Neogloboquadrina pachyderma d | 1.460 | 0.050 | 0 | 0 | 0.941 | 1.570 | 1.000 | 1.008 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 6286 | 0.8950 | Neogloboquadrina pachyderma d | 1.590 | 0.030 | 0 | 0 | 0.740 | 0.838 | 1.000 | 0.796 | Not used | Risebrobakken et al. (2003) | |||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8246 | 1.0200 | Neogloboquadrina pachyderma d | 1.790 | 0.060 | 0 | 0 | 1.275 | 1.390 | 1.000 | 1.338 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 3927 | 1.3050 | Neogloboquadrina pachyderma d | 2.350 | 0.040 | 0 | 0 | 1.912 | 2.290 | 1.000 | 1.970 | Not used | Risebrobakken et al. (2003) | |||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 6287 | 1.5400 | Neogloboquadrina pachyderma d | 2.335 | 0.025 | 0 | 0 | 1.888 | 2.000 | 1.000 | 1.953 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | GifA96472 | 1.7050 | Neogloboquadrina pachyderma d | 2.620 | 0.060 | 0 | 0 | 2.190 | 2.360 | 1.000 | 2.301 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8242 | 2.2500 | Neogloboquadrina pachyderma d | 3.000 | 0.050 | 0 | 0 | 2.724 | 2.822 | 1.000 | 2.775 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8241 | 2.5000 | Neogloboquadrina pachyderma d | 3.380 | 0.070 | 0 | 0 | 3.162 | 3.339 | 1.000 | 3.246 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 10011 | 2.6950 | Neogloboquadrina pachyderma d | 3.820 | 0.035 | 0 | 0 | 3.711 | 3.823 | 1.000 | 3.769 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8240 | 3.0000 | Neogloboquadrina pachyderma d | 4.080 | 0.070 | 0 | 0 | 4.600 | 4.224 | 1.000 | 4.122 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 463 | 3.2050 | Neogloboquadrina pachyderma d | 4.330 | 0.050 | 0 | 0 | 4.396 | 4.526 | 1.000 | 4.464 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8238 | 4.5100 | Neogloboquadrina pachyderma d | 6.420 | 0.160 | 0 | 0 | 6.729 | 7.111 | 1.000 | 6.906 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA 464 | 5.2050 | Neogloboquadrina pachyderma d | 7.260 | 0.060 | 0 | 0 | 7.657 | 7.788 | 1.000 | 7.725 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8237 | 5.2850 | Neogloboquadrina pachyderma d | 7.690 | 0.110 | 0 | 0 | 8.350 | 8.274 | 1.000 | 8.154 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8236 | 5.3350 | ? | 8.530 | 0.160 | 0 | 0 | 8.988 | 9.377 | 1.000 | 9.154 | Not used | This study | |||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8235 | 5.4150 | ? | 8.280 | 0.140 | 0 | 0 | 8.618 | 8.994 | 1.000 | 8.822 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | Poz-8234 | 5.7050 | ? | 8.700 | 0.090 | 0 | 0 | 8.618 | 8.994 | 1.000 | 9.362 | This study | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | TUa-3315 | 7.0350 | Neogloboquadrina pachyderma s | 10.775 | 0.085 | 200 | 50 | 11.629 | 12.510 | 0.958 | 11.805 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | 7.0950 | Tephra | 12.170 | Vedde Ash | Risebrobakken et al. (2003) | |||||||||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | TUa-3316 | 7.3050 | Neogloboquadrina pachyderma s | 11.875 | 0.140 | 0 | 0 | 13.174 | 13.429 | 1.000 | 13.320 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA465 | 7.5050 | Neogloboquadrina pachyderma s | 12.220 | 0.090 | 0 | 0 | 13.578 | 13.752 | 0.788 | 13.635 | Risebrobakken et al. (2003) | ||||||
| MD95-2011 | 66.9697 | 7.6393 | -1048 | KIA3519 | 8.1350 | Neogloboquadrina pachyderma s | 13.450 | 0.090 | 0 | 0 | 15.247 | 15.969 | 0.926 | 15.760 | Dreger (1999) | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | KIA-10676 | 0.0250 | Neogloboquadrina pachyderma s | 1.690 | 0.030 | 0 | 0 | 1.222 | 1.283 | 1.000 | 1.251 | This study | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | Poz-10150 | 0.1950 | Neogloboquadrina pachyderma s | 3.515 | 0.035 | 0 | 0 | 3.355 | 3.438 | 1.000 | 3.399 | This study | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | Poz-10151 | 0.3650 | Neogloboquadrina pachyderma s | 5.295 | 0.035 | 0 | 0 | 5.610 | 5.686 | 1.000 | 5.649 | This study | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | Poz-10157 | 0.5350 | Neogloboquadrina pachyderma s | 7.300 | 0.040 | 0 | 0 | 7.770 | 7.814 | 1.000 | 7.762 | This study | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | Poz-33098 | 0.7150 | Neogloboquadrina pachyderma s | 7.940 | 0.070 | 0 | 0 | 8.334 | 8.476 | 1.000 | 8.405 | This study | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | TUa-3301 | 1.0050 | Neogloboquadrina pachyderma s | 8.680 | 0.085 | 0 | 0 | 9.261 | 9.451 | 1.000 | 9.343 | Bakke et al. (2009) | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | Poz-33098 | 1.6550 | Neogloboquadrina pachyderma s | 9.340 | 0.090 | 0 | 0 | 1.740 | 1.319 | 1.000 | 10.181 | This study | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | 1.8550 | Tephra | 10.350 | Saksurnavatn Ash | ||||||||||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | TUa-3302 | 2.1350 | Neogloboquadrina pachyderma s | 10.050 | 0.095 | 200 | 50 | 1.584 | 1.915 | 1.000 | 10.779 | Bakke et al. (2009) | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | TUa-3304 | 2.4950 | Neogloboquadrina pachyderma s | 10.700 | 0.090 | 200 | 50 | 11.546 | 11.874 | 0.723 | 11.654 | Bakke et al. (2009) | ||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | 3.6250 | Tephra | 12.170 | Vedde Ash | ||||||||||||||
| MD99-2284 | 62.3747 | -0.9802 | -1500 | Poz-29526 | 4.2350 | Neogloboquadrina pachyderma s | 11.440 | 0.080 | 0 | 0 | 12.799 | 12.986 | 0.733 | 12.912 | This study |