Barrett, Ruby (2025): Species level size-normalised weight data [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.973593, In: Barrett, R (2025): Planktic foraminifera size-normalised weight data and associated environmental data [dataset bundled publication]. PANGAEA, https://doi.org/10.1594/PANGAEA.973256
Always quote citation above when using data! You can download the citation in several formats below.
Published: 2025-01-13 • DOI registered: 2025-01-14
Abstract:
This dataset contains a compilation of published and new SNW data with corresponding sea surface (≤ 20 m) environmental data extracted from CMIP6 that are used in the species level Bayesian regression modelling.
Source:
Barker, S (2002): Planktonic foraminiferal proxies for temperature and pCO2 [dissertation]. University of Cambridge
Béjard, Thibauld M; Rigual-Hernández, Andrés S; Flores, José Abel; Tarruella, Javier P; Durrieu de Madron, Xavier; Cacho, Isabel; Haghipour, Neghar; Hunter, Aidan; Sierro, Francisco Javier (2023): Calcification response of planktic foraminifera to environmental change in the western Mediterranean Sea during the industrial era. Biogeosciences, 20(7), 1505-1528, https://doi.org/10.5194/bg-20-1505-2023
Marr, Julene P; Baker, Joel A; Carter, Lionel; Allan, Adrian S R; Dunbar, Gavin B; Bostock, Helen C (2011): Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean|. Paleoceanography, 26(2), PA2209, https://doi.org/10.1029/2010PA002059
Marshall, Brittney J; Thunell, Robert C; Henehan, Michael J; Astor, Yrene; Wejnert, Katherine (2013): Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series. Paleoceanography, 28(2), 363-376, https://doi.org/10.1002/palo.20034
Pallacks, Sven; Ziveri, Patrizia; Schiebel, Ralf; Vonhof, Hubert B; Rae, James W B; Littley, Eloise; Garcia-Orellana, Jordi; Langer, Gerald; Grelaud, Michaël; Martrat, Belen (2023): Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea. Communications Earth & Environment, 4(1), 301, https://doi.org/10.1038/s43247-023-00947-7
Qin, Bingbin; Li, Tiegang; Xiong, Zhifang; Algeo, Thomas J; Chang, Fengming (2017): Deepwater carbonate ion concentrations in the western tropical Pacific since 250 ka: Evidence for oceanic carbon storage and global climate influence. Paleoceanography, 32(4), 351-370, https://doi.org/10.1002/2016PA003039
Weinkauf, Manuel F G; Kunze, Jose G; Waniek, Joanna J; Kucera, Michal (2016): Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. PLoS ONE, 11(2), https://doi.org/10.1371/journal.pone.0148363
References:
Aze, Tracy; Ezard, Thomas H G; Purvis, Andy; Coxall, Helen K; Stewart, Duncan R M; Wade, Bridget S; Pearson, Paul N (2011): A phylogeny of Cenozoic macroperforate planktonic foraminifera from fossil data. Biological Reviews, 86(4), 900-927, https://doi.org/10.1111/j.1469-185X.2011.00178.x
Jiang, Li-Qing; Dunne, John; Carter, Brendan R; Tjiputra, Jerry; Terhaar, Jens; Sharp, Jonathan D; Olsen, Are; Alin, Simone; Bakker, Dorothee C E; Feely, Richard A; Gattuso, Jean-Pierre; Hogan, Patrick; Ilyina, Tatiana; Lange, Nico; Lauvset, Siv K; Lewis, Ernie R; Lovato, Tomas; Palmieri, Julien; Santana-Falcón, Yeray; Schwinger, Jörg; Séférian, Roland; Strand, Gary; Swart, Neil; Tanhua, Toste; Tsujino, Hiroyuki; Wanninkhof, Rik; Watanabe, Michio; Yamamoto, Akitomo; Ziehn, Tilo (2023): Global Surface Ocean Acidification Indicators From 1750 to 2100. Journal of Advances in Modeling Earth Systems, 15(3), e2022MS003563, https://doi.org/10.1029/2022MS003563
Funding:
Natural Environment Research Council (NERC), grant/award no. NE/S007504/1: NERC GW4+ DTP2 - a Great Western Alliance Doctoral Training Partnership
Coverage:
Median Latitude: 38.324119 * Median Longitude: 1.348481 * South-bound Latitude: -53.630000 * West-bound Longitude: -174.000000 * North-bound Latitude: 78.400000 * East-bound Longitude: 180.000000
Parameter(s):
License:
Creative Commons Attribution 4.0 International (CC-BY-4.0)
Status:
Curation Level: Basic curation (CurationLevelB)
Size:
10780 data points
Data
1 Author(s) | 2 Reference | 3 Sample ID | 4 Data type | 5 Elevation [m a.s.l.] | 6 Depth sed [m] (mbsf) | 7 Depth water [m] (maximum) | 8 Depth water [m] (minimum) | 9 Latitude | 10 Longitude | 11 Species UID | 12 Size fraction (The size of the sieves used t...) | 13 SNW [µg] (Measurement based weight appr...) | 14 Ecogroup (According to Aze et al. (2011)) | 15 [CO3]2- [µmol/kg] (Extracted from models in the ...) | 16 Sal (PSS-78, Extracted from models...) | 17 SST [°C] (Extracted from models in the ...) | 18 [PO4]3- [µmol/kg] (Extracted from models in the ...) | 19 PP C int [mol/m2/a] (Extracted from models in the ...) | 20 Basin (Ocean basin) |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 11B | Coretop | -2220.0 | 0.0 | 35.6 | -32.6 | Globigerina bulloides | 300-350 | 11.17645923 | Non-Symbiont Spinose | 261.0 | 36.288 | 20.692 | 0.13029598 | 11.19352174 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15B | Coretop | -2585.0 | 0.0 | 38.6 | -25.0 | Globigerina bulloides | 300-350 | 17.16153116 | Non-Symbiont Spinose | 244.0 | 36.051 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15aB | Coretop | -2738.0 | 0.0 | 38.9 | -25.0 | Globigerina bulloides | 300-350 | 18.8312159 | Non-Symbiont Spinose | 244.0 | 35.99 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 14B | Coretop | -2858.0 | 0.0 | 40.4 | -25.8 | Globigerina bulloides | 300-350 | 18.89876425 | Non-Symbiont Spinose | 234.0 | 35.869 | 17.265 | 0.20152946 | 14.4711826 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 9B | Coretop | -2026.0 | 0.0 | 40.8 | -27.5 | Globigerina bulloides | 300-350 | 18.77589295 | Non-Symbiont Spinose | 237.0 | 35.945 | 17.915 | 0.23714916 | 14.75367931 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 8B | Coretop | -3232.0 | 0.0 | 42.3 | -25.7 | Globigerina bulloides | 300-350 | 17.64127358 | Non-Symbiont Spinose | 231.0 | 35.941 | 16.38 | 0.24253952 | 14.57241899 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 13B | Coretop | -3133.0 | 0.0 | 42.9 | -25.3 | Globigerina bulloides | 300-350 | 19.20108102 | Non-Symbiont Spinose | 231.0 | 35.856 | 16.38 | 0.24022223 | 14.37514414 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 7B | Coretop | -2664.0 | 0.0 | 43.9 | -25.0 | Globigerina bulloides | 300-350 | 14.24234958 | Non-Symbiont Spinose | 230.0 | 35.709 | 16.338 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 12B | Coretop | -3052.0 | 0.0 | 44.1 | -24.9 | Globigerina bulloides | 300-350 | 16.65123685 | Non-Symbiont Spinose | 215.0 | 35.657 | 14.505 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 11B | Coretop | -3208.0 | 0.0 | 45.0 | -24.66 | Globigerina bulloides | 300-350 | 15.73458885 | Non-Symbiont Spinose | 231.0 | 35.863 | 16.175 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 11B | Coretop | -2741.0 | 0.0 | 45.4 | -25.4 | Globigerina bulloides | 300-350 | 13.89155712 | Non-Symbiont Spinose | 236.0 | 35.92 | 16.872 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 5B | Coretop | -3069.0 | 0.0 | 46.0 | -23.848 | Globigerina bulloides | 300-350 | 12.90803389 | Non-Symbiont Spinose | 224.0 | 35.731 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 8B | Coretop | -3393.0 | 0.0 | 46.2 | -23.715 | Globigerina bulloides | 300-350 | 13.84546959 | Non-Symbiont Spinose | 224.0 | 35.682 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 5B | Coretop | -3121.0 | 0.0 | 46.9 | -25.4 | Globigerina bulloides | 300-350 | 11.34036385 | Non-Symbiont Spinose | 227.0 | 35.768 | 15.731 | 0.34558492 | 12.43581229 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 9B | Coretop | -3074.0 | 0.0 | 48.4 | -25.1 | Globigerina bulloides | 300-350 | 13.91376548 | Non-Symbiont Spinose | 216.0 | 35.579 | 13.496 | 0.35420919 | 11.76409828 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 3B | Coretop | -3113.0 | 0.0 | 50.2 | -27.0 | Globigerina bulloides | 300-350 | 13.38103847 | Non-Symbiont Spinose | 211.0 | 35.012 | 13.845 | 0.32729929 | 10.64878986 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 7B | Coretop | -3013.0 | 0.0 | 50.5 | -26.5 | Globigerina bulloides | 300-350 | 13.0568807 | Non-Symbiont Spinose | 210.0 | 34.962 | 13.561 | 0.35298834 | 10.53125999 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 6B | Coretop | -3381.0 | 0.0 | 51.4 | -25.8 | Globigerina bulloides | 300-350 | 11.94848146 | Non-Symbiont Spinose | 188.0 | 35.194 | 11.187 | 0.35698403 | 10.60658247 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 2B | Coretop | -2731.0 | 0.0 | 53.1 | -20.798 | Globigerina bulloides | 300-350 | 12.65806764 | Non-Symbiont Spinose | 214.0 | 35.345 | 13.255 | 0.43018857 | 10.8645545 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 1B | Coretop | -2580.0 | 0.0 | 53.4 | -27.5 | Globigerina bulloides | 300-350 | 12.55077308 | Non-Symbiont Spinose | 199.0 | 34.79 | 11.449 | 0.45058216 | 10.50154811 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 5B | Coretop | -2812.0 | 0.0 | 53.6 | -27.1 | Globigerina bulloides | 300-350 | 12.65943261 | Non-Symbiont Spinose | 199.0 | 34.757 | 11.449 | 0.46918559 | 10.69622741 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 4B | Coretop | -2821.0 | 0.0 | 55.0 | -28.3 | Globigerina bulloides | 300-350 | 12.72121838 | Non-Symbiont Spinose | 175.0 | 34.921 | 9.688 | 0.5071466 | 10.91926445 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 3B | Coretop | -2819.0 | 0.0 | 56.4 | -27.8 | Globigerina bulloides | 300-350 | 11.49438575 | Non-Symbiont Spinose | 166.0 | 35.039 | 8.639 | 0.53353757 | 11.11399203 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 2B | Coretop | -2767.0 | 0.0 | 57.9 | -26.0 | Globigerina bulloides | 300-350 | 11.72351317 | Non-Symbiont Spinose | 176.0 | 34.977 | 9.698 | 0.57675681 | 11.97909612 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 1B | Coretop | -2911.0 | 0.0 | 58.5 | -20.493 | Globigerina bulloides | 300-350 | 11.81072925 | Non-Symbiont Spinose | 176.0 | 35.24 | 9.452 | 0.58786587 | 12.3979585 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 1B | Coretop | -2010.0 | 0.0 | 59.7 | -27.4 | Globigerina bulloides | 300-350 | 13.22920933 | Non-Symbiont Spinose | 171.0 | 35.052 | 8.57 | 0.65484188 | 11.77028595 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 15B | Coretop | -3271.0 | 0.0 | 30.5 | -36.95 | Globigerina inflata | 300-350 | 35.02201623 | Non-Symbiont Non-Spinose | 271.0 | 36.558 | 21.069 | 0.05398491 | 7.29490915 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 13B | Coretop | -2992.0 | 0.0 | 32.8 | -34.7 | Globigerina inflata | 300-350 | 31.95625419 | Non-Symbiont Non-Spinose | 266.0 | 36.471 | 20.301 | 0.07400047 | 9.62155778 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 17B | Coretop | -2934.0 | 0.0 | 35.4 | -29.4 | Globigerina inflata | 300-350 | 29.0092147 | Non-Symbiont Non-Spinose | 256.0 | 36.221 | 19.435 | 0.10293545 | 9.52483931 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 11B | Coretop | -2220.0 | 0.0 | 35.6 | -32.6 | Globigerina inflata | 300-350 | 32.82892957 | Non-Symbiont Non-Spinose | 261.0 | 36.288 | 20.692 | 0.13029598 | 11.19352174 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15B | Coretop | -2585.0 | 0.0 | 38.6 | -25.0 | Globigerina inflata | 300-350 | 31.0843826 | Non-Symbiont Non-Spinose | 244.0 | 36.051 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15aB | Coretop | -2738.0 | 0.0 | 38.9 | -25.0 | Globigerina inflata | 300-350 | 32.12091333 | Non-Symbiont Non-Spinose | 244.0 | 35.99 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 14B | Coretop | -2858.0 | 0.0 | 40.4 | -25.8 | Globigerina inflata | 300-350 | 32.21452327 | Non-Symbiont Non-Spinose | 234.0 | 35.869 | 17.265 | 0.20152946 | 14.4711826 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 9B | Coretop | -2026.0 | 0.0 | 40.8 | -27.5 | Globigerina inflata | 300-350 | 31.64195104 | Non-Symbiont Non-Spinose | 237.0 | 35.945 | 17.915 | 0.23714916 | 14.75367931 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 8B | Coretop | -3232.0 | 0.0 | 42.3 | -25.7 | Globigerina inflata | 300-350 | 31.52454747 | Non-Symbiont Non-Spinose | 231.0 | 35.941 | 16.38 | 0.24253952 | 14.57241899 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 13B | Coretop | -3133.0 | 0.0 | 42.9 | -25.3 | Globigerina inflata | 300-350 | 31.30100159 | Non-Symbiont Non-Spinose | 231.0 | 35.856 | 16.38 | 0.24022223 | 14.37514414 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 7B | Coretop | -2664.0 | 0.0 | 43.9 | -25.0 | Globigerina inflata | 300-350 | 30.19834986 | Non-Symbiont Non-Spinose | 230.0 | 35.709 | 16.338 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 12B | Coretop | -3052.0 | 0.0 | 44.1 | -24.9 | Globigerina inflata | 300-350 | 30.92188458 | Non-Symbiont Non-Spinose | 215.0 | 35.657 | 14.505 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 11B | Coretop | -3208.0 | 0.0 | 45.0 | -24.66 | Globigerina inflata | 300-350 | 29.29729485 | Non-Symbiont Non-Spinose | 231.0 | 35.863 | 16.175 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 11B | Coretop | -2741.0 | 0.0 | 45.4 | -25.4 | Globigerina inflata | 300-350 | 28.14296448 | Non-Symbiont Non-Spinose | 236.0 | 35.92 | 16.872 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 5B | Coretop | -3069.0 | 0.0 | 46.0 | -23.848 | Globigerina inflata | 300-350 | 29.97450967 | Non-Symbiont Non-Spinose | 224.0 | 35.731 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 8B | Coretop | -3393.0 | 0.0 | 46.2 | -23.715 | Globigerina inflata | 300-350 | 31.59870488 | Non-Symbiont Non-Spinose | 224.0 | 35.682 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 5B | Coretop | -3121.0 | 0.0 | 46.9 | -25.4 | Globigerina inflata | 300-350 | 25.77812753 | Non-Symbiont Non-Spinose | 227.0 | 35.768 | 15.731 | 0.34558492 | 12.43581229 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 9B | Coretop | -3074.0 | 0.0 | 48.4 | -25.1 | Globigerina inflata | 300-350 | 27.72564385 | Non-Symbiont Non-Spinose | 216.0 | 35.579 | 13.496 | 0.35420919 | 11.76409828 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 3B | Coretop | -3113.0 | 0.0 | 50.2 | -27.0 | Globigerina inflata | 300-350 | 26.06885195 | Non-Symbiont Non-Spinose | 211.0 | 35.012 | 13.845 | 0.32729929 | 10.64878986 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 7B | Coretop | -3013.0 | 0.0 | 50.5 | -26.5 | Globigerina inflata | 300-350 | 28.778226 | Non-Symbiont Non-Spinose | 210.0 | 34.962 | 13.561 | 0.35298834 | 10.53125999 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 6B | Coretop | -3381.0 | 0.0 | 51.4 | -25.8 | Globigerina inflata | 300-350 | 24.15430403 | Non-Symbiont Non-Spinose | 188.0 | 35.194 | 11.187 | 0.35698403 | 10.60658247 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 2B | Coretop | -2731.0 | 0.0 | 53.1 | -20.798 | Globigerina inflata | 300-350 | 24.50883041 | Non-Symbiont Non-Spinose | 214.0 | 35.345 | 13.255 | 0.43018857 | 10.8645545 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 1B | Coretop | -2580.0 | 0.0 | 53.4 | -27.5 | Globigerina inflata | 300-350 | 24.34175504 | Non-Symbiont Non-Spinose | 199.0 | 34.79 | 11.449 | 0.45058216 | 10.50154811 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 5B | Coretop | -2812.0 | 0.0 | 53.6 | -27.1 | Globigerina inflata | 300-350 | 25.24015208 | Non-Symbiont Non-Spinose | 199.0 | 34.757 | 11.449 | 0.46918559 | 10.69622741 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 4B | Coretop | -2821.0 | 0.0 | 55.0 | -28.3 | Globigerina inflata | 300-350 | 21.77035755 | Non-Symbiont Non-Spinose | 175.0 | 34.921 | 9.688 | 0.5071466 | 10.91926445 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 3B | Coretop | -2819.0 | 0.0 | 56.4 | -27.8 | Globigerina inflata | 300-350 | 19.43806847 | Non-Symbiont Non-Spinose | 166.0 | 35.039 | 8.639 | 0.53353757 | 11.11399203 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 2B | Coretop | -2767.0 | 0.0 | 57.9 | -26.0 | Globigerina inflata | 300-350 | 23.18836228 | Non-Symbiont Non-Spinose | 176.0 | 34.977 | 9.698 | 0.57675681 | 11.97909612 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 1B | Coretop | -2911.0 | 0.0 | 58.5 | -20.493 | Globigerina inflata | 300-350 | 20.7565368 | Non-Symbiont Non-Spinose | 176.0 | 35.24 | 9.452 | 0.58786587 | 12.3979585 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15B | Coretop | -2585.0 | 0.0 | 38.6 | -25.0 | Neogloboquadrina pachyderma | 250-300 | 10.04634956 | Non-Symbiont Non-Spinose | 244.0 | 36.051 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15aB | Coretop | -2738.0 | 0.0 | 38.9 | -25.0 | Neogloboquadrina pachyderma | 250-300 | 10.33217461 | Non-Symbiont Non-Spinose | 244.0 | 35.99 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 14B | Coretop | -2858.0 | 0.0 | 40.4 | -25.8 | Neogloboquadrina pachyderma | 250-300 | 11.97738122 | Non-Symbiont Non-Spinose | 234.0 | 35.869 | 17.265 | 0.20152946 | 14.4711826 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 12B | Coretop | -4085.0 | 0.0 | 40.6 | -20.118 | Neogloboquadrina pachyderma | 250-300 | 7.50112816 | Non-Symbiont Non-Spinose | 237.0 | 35.92 | 17.796 | 0.18828798 | 14.23368554 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 9B | Coretop | -2026.0 | 0.0 | 40.8 | -27.5 | Neogloboquadrina pachyderma | 250-300 | 11.41381598 | Non-Symbiont Non-Spinose | 237.0 | 35.945 | 17.915 | 0.23714916 | 14.75367931 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 8B | Coretop | -3232.0 | 0.0 | 42.3 | -25.7 | Neogloboquadrina pachyderma | 250-300 | 12.51207398 | Non-Symbiont Non-Spinose | 231.0 | 35.941 | 16.38 | 0.24253952 | 14.57241899 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 13B | Coretop | -3133.0 | 0.0 | 42.9 | -25.3 | Neogloboquadrina pachyderma | 250-300 | 10.26959012 | Non-Symbiont Non-Spinose | 231.0 | 35.856 | 16.38 | 0.24022223 | 14.37514414 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 7B | Coretop | -2664.0 | 0.0 | 43.9 | -25.0 | Neogloboquadrina pachyderma | 250-300 | 10.37907556 | Non-Symbiont Non-Spinose | 230.0 | 35.709 | 16.338 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 13B | Coretop | -4016.0 | 0.0 | 44.0 | -20.017 | Neogloboquadrina pachyderma | 250-300 | 8.63369751 | Non-Symbiont Non-Spinose | 224.0 | 35.721 | 15.345 | 0.25662878 | 14.73507213 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 12B | Coretop | -3052.0 | 0.0 | 44.1 | -24.9 | Neogloboquadrina pachyderma | 250-300 | 10.71378573 | Non-Symbiont Non-Spinose | 215.0 | 35.657 | 14.505 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 11B | Coretop | -3208.0 | 0.0 | 45.0 | -24.66 | Neogloboquadrina pachyderma | 250-300 | 10.1422331 | Non-Symbiont Non-Spinose | 231.0 | 35.863 | 16.175 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 11B | Coretop | -2741.0 | 0.0 | 45.4 | -25.4 | Neogloboquadrina pachyderma | 250-300 | 9.61669549 | Non-Symbiont Non-Spinose | 236.0 | 35.92 | 16.872 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 5B | Coretop | -3069.0 | 0.0 | 46.0 | -23.848 | Neogloboquadrina pachyderma | 250-300 | 11.11717969 | Non-Symbiont Non-Spinose | 224.0 | 35.731 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 8B | Coretop | -3393.0 | 0.0 | 46.2 | -23.715 | Neogloboquadrina pachyderma | 250-300 | 9.79436278 | Non-Symbiont Non-Spinose | 224.0 | 35.682 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 5B | Coretop | -3121.0 | 0.0 | 46.9 | -25.4 | Neogloboquadrina pachyderma | 250-300 | 9.67390565 | Non-Symbiont Non-Spinose | 227.0 | 35.768 | 15.731 | 0.34558492 | 12.43581229 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 4B | Coretop | -3945.0 | 0.0 | 47.2 | -21.387 | Neogloboquadrina pachyderma | 250-300 | 8.78783652 | Non-Symbiont Non-Spinose | 225.0 | 35.577 | 15.47 | 0.34217356 | 13.51080798 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 15B | Coretop | -4177.0 | 0.0 | 47.6 | -20.922 | Neogloboquadrina pachyderma | 250-300 | 9.13746447 | Non-Symbiont Non-Spinose | 223.0 | 35.543 | 15.524 | 0.36197874 | 12.70011472 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 3B | Coretop | -4479.0 | 0.0 | 47.7 | -20.808 | Neogloboquadrina pachyderma | 250-300 | 8.21690297 | Non-Symbiont Non-Spinose | 223.0 | 35.518 | 15.524 | 0.36197874 | 12.70011472 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 9B | Coretop | -3074.0 | 0.0 | 48.4 | -25.1 | Neogloboquadrina pachyderma | 250-300 | 9.5662173 | Non-Symbiont Non-Spinose | 216.0 | 35.579 | 13.496 | 0.35420919 | 11.76409828 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 3B | Coretop | -3113.0 | 0.0 | 50.2 | -27.0 | Neogloboquadrina pachyderma | 250-300 | 10.39381974 | Non-Symbiont Non-Spinose | 211.0 | 35.012 | 13.845 | 0.32729929 | 10.64878986 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 7B | Coretop | -3013.0 | 0.0 | 50.5 | -26.5 | Neogloboquadrina pachyderma | 250-300 | 10.48886683 | Non-Symbiont Non-Spinose | 210.0 | 34.962 | 13.561 | 0.35298834 | 10.53125999 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 6B | Coretop | -3381.0 | 0.0 | 51.4 | -25.8 | Neogloboquadrina pachyderma | 250-300 | 9.85297304 | Non-Symbiont Non-Spinose | 188.0 | 35.194 | 11.187 | 0.35698403 | 10.60658247 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 2B | Coretop | -2731.0 | 0.0 | 53.1 | -20.798 | Neogloboquadrina pachyderma | 250-300 | 8.46103777 | Non-Symbiont Non-Spinose | 214.0 | 35.345 | 13.255 | 0.43018857 | 10.8645545 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 1B | Coretop | -2580.0 | 0.0 | 53.4 | -27.5 | Neogloboquadrina pachyderma | 250-300 | 11.12583964 | Non-Symbiont Non-Spinose | 199.0 | 34.79 | 11.449 | 0.45058216 | 10.50154811 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 5B | Coretop | -2812.0 | 0.0 | 53.6 | -27.1 | Neogloboquadrina pachyderma | 250-300 | 9.38471142 | Non-Symbiont Non-Spinose | 199.0 | 34.757 | 11.449 | 0.46918559 | 10.69622741 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 4B | Coretop | -2821.0 | 0.0 | 55.0 | -28.3 | Neogloboquadrina pachyderma | 250-300 | 10.329404 | Non-Symbiont Non-Spinose | 175.0 | 34.921 | 9.688 | 0.5071466 | 10.91926445 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 3B | Coretop | -2819.0 | 0.0 | 56.4 | -27.8 | Neogloboquadrina pachyderma | 250-300 | 8.45000154 | Non-Symbiont Non-Spinose | 166.0 | 35.039 | 8.639 | 0.53353757 | 11.11399203 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 2B | Coretop | -2767.0 | 0.0 | 57.9 | -26.0 | Neogloboquadrina pachyderma | 250-300 | 8.56129913 | Non-Symbiont Non-Spinose | 176.0 | 34.977 | 9.698 | 0.57675681 | 11.97909612 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 1B | Coretop | -2911.0 | 0.0 | 58.5 | -20.493 | Neogloboquadrina pachyderma | 250-300 | 7.24884443 | Non-Symbiont Non-Spinose | 176.0 | 35.24 | 9.452 | 0.58786587 | 12.3979585 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 15B | Coretop | -3271.0 | 0.0 | 30.5 | -36.95 | Globorotalia truncatulinoides | 300-350 | 35.53494282 | Non-Symbiont Non-Spinose | 271.0 | 36.558 | 21.069 | 0.05398491 | 7.29490915 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 13B | Coretop | -2992.0 | 0.0 | 32.8 | -34.7 | Globorotalia truncatulinoides | 300-350 | 33.18332948 | Non-Symbiont Non-Spinose | 266.0 | 36.471 | 20.301 | 0.07400047 | 9.62155778 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 17B | Coretop | -2934.0 | 0.0 | 35.4 | -29.4 | Globorotalia truncatulinoides | 300-350 | 32.44852268 | Non-Symbiont Non-Spinose | 256.0 | 36.221 | 19.435 | 0.10293545 | 9.52483931 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 11B | Coretop | -2220.0 | 0.0 | 35.6 | -32.6 | Globorotalia truncatulinoides | 300-350 | 32.02066162 | Non-Symbiont Non-Spinose | 261.0 | 36.288 | 20.692 | 0.13029598 | 11.19352174 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15B | Coretop | -2585.0 | 0.0 | 38.6 | -25.0 | Globorotalia truncatulinoides | 300-350 | 29.83091957 | Non-Symbiont Non-Spinose | 244.0 | 36.051 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 15aB | Coretop | -2738.0 | 0.0 | 38.9 | -25.0 | Globorotalia truncatulinoides | 300-350 | 32.11226002 | Non-Symbiont Non-Spinose | 244.0 | 35.99 | 18.187 | 0.17618181 | 13.68781733 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 14B | Coretop | -2858.0 | 0.0 | 40.4 | -25.8 | Globorotalia truncatulinoides | 300-350 | 32.91628167 | Non-Symbiont Non-Spinose | 234.0 | 35.869 | 17.265 | 0.20152946 | 14.4711826 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 9B | Coretop | -2026.0 | 0.0 | 40.8 | -27.5 | Globorotalia truncatulinoides | 300-350 | 33.3391904 | Non-Symbiont Non-Spinose | 237.0 | 35.945 | 17.915 | 0.23714916 | 14.75367931 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 8B | Coretop | -3232.0 | 0.0 | 42.3 | -25.7 | Globorotalia truncatulinoides | 300-350 | 29.9550964 | Non-Symbiont Non-Spinose | 231.0 | 35.941 | 16.38 | 0.24253952 | 14.57241899 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 13B | Coretop | -3133.0 | 0.0 | 42.9 | -25.3 | Globorotalia truncatulinoides | 300-350 | 32.14452375 | Non-Symbiont Non-Spinose | 231.0 | 35.856 | 16.38 | 0.24022223 | 14.37514414 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T86 7B | Coretop | -2664.0 | 0.0 | 43.9 | -25.0 | Globorotalia truncatulinoides | 300-350 | 31.66886471 | Non-Symbiont Non-Spinose | 230.0 | 35.709 | 16.338 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 12B | Coretop | -3052.0 | 0.0 | 44.1 | -24.9 | Globorotalia truncatulinoides | 300-350 | 31.16095367 | Non-Symbiont Non-Spinose | 215.0 | 35.657 | 14.505 | 0.25796133 | 14.19485922 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 11B | Coretop | -3208.0 | 0.0 | 45.0 | -24.66 | Globorotalia truncatulinoides | 300-350 | 29.31928962 | Non-Symbiont Non-Spinose | 231.0 | 35.863 | 16.175 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 11B | Coretop | -2741.0 | 0.0 | 45.4 | -25.4 | Globorotalia truncatulinoides | 300-350 | 28.27912026 | Non-Symbiont Non-Spinose | 236.0 | 35.92 | 16.872 | 0.29858894 | 13.85012844 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 5B | Coretop | -3069.0 | 0.0 | 46.0 | -23.848 | Globorotalia truncatulinoides | 300-350 | 26.74965098 | Non-Symbiont Non-Spinose | 224.0 | 35.731 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T90 8B | Coretop | -3393.0 | 0.0 | 46.2 | -23.715 | Globorotalia truncatulinoides | 300-350 | 28.4383157 | Non-Symbiont Non-Spinose | 224.0 | 35.682 | 14.974 | 0.32388736 | 13.43295588 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 9B | Coretop | -3074.0 | 0.0 | 48.4 | -25.1 | Globorotalia truncatulinoides | 300-350 | 30.04374333 | Non-Symbiont Non-Spinose | 216.0 | 35.579 | 13.496 | 0.35420919 | 11.76409828 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | T88 6B | Coretop | -3381.0 | 0.0 | 51.4 | -25.8 | Globorotalia truncatulinoides | 300-350 | 26.39799457 | Non-Symbiont Non-Spinose | 188.0 | 35.194 | 11.187 | 0.35698403 | 10.60658247 | ATL | ||
Barker | Appendix 3, Planktonic foraminiferal proxies for temperature and pCO2. | NEAP 8K database | Sediment core | -2360.0 | 0.0 | 59.8 | -23.9 | Globigerina bulloides | 300-350 | 11.83641162 | Non-Symbiont Spinose | 177.0 | 35.149 | 9.071 | 0.62963029 | 12.13519015 | ATL | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.22478032 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B10 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.6388215 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B11 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 5.16725396 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B12 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.95772579 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB II 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.1740986 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 5.37587309 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.94625211 | Non-Symbiont Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.61300869 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.67892437 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.7318054 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 5.00270256 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VII 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.18072879 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.16110151 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VII 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.51483215 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB IX 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.12005354 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.1777316 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.34219039 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XI 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.02237817 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XI 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.54421514 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XI 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.22880739 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XII 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.96336036 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XII 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.02194624 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XII 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.43061472 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.20244758 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.4726332 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.78151641 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.78725579 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.7146846 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.38759973 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.85899513 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.83808595 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.80089453 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.08763324 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 4.4340755 | Non-Symbiont Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XXII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 3.55465105 | Non-Symbiont Spinose | 194.5950513 | 39.50077772 | 18.60218956 | 0.07801616 | 11.72752465 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B10 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.04706361 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B11 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.3473059 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B12 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.15372461 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B1 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.06279687 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B2 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.47079546 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.20680181 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 5.02873689 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B4 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.40313306 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B5 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.5661454 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B6 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.14938768 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VIII 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.00153828 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.36672829 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.90966163 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XII 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.1515914 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIII 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.31840616 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.84014534 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.33420184 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.58700571 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XV 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.83857487 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XV 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.10890619 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.85990959 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.58515568 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.38965673 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.72791362 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.42639305 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.42366426 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 5.08103288 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.95078071 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.06472217 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.17190791 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 5.0827253 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XXI 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 3.13462165 | Non-Symbiont Non-Spinose | 194.5950513 | 39.50077772 | 18.60218956 | 0.07801616 | 11.72752465 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 16.44071139 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 25.40903738 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B11 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 12.73133885 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB I2B12 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 14.72375574 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 17.36176636 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 17.94434625 | Non-Symbiont Non-Spinose | 204.4284311 | 39.39733699 | 17.86150606 | 0.11599651 | 11.57689551 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 15.83289661 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 24.4925591 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB III2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 22.82408935 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.16209757 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 16.17424591 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 14.49982599 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB V2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 13.43531268 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VII 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 17.23091236 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VII 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 28.48179628 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VII 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 31.06471527 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VIII 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 21.54985967 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VIII 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 17.63408796 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VIII 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.34231248 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB VIII 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.23483989 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB IX 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 17.94957203 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 22.58647235 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 27.02746876 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 21.84532755 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB X 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.1564068 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XI 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 12.89951675 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XII 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 16.77335061 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIII 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.6717965 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIII 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 33.78190899 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 33.29000172 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIII 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 25.54288194 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 29.58334346 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 22.18689135 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 16.01979364 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIV 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 16.4058488 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XV 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 27.352901 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XV 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 31.24673868 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XV 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 32.86671368 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 22.48673981 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 21.66726784 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.44181949 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 16.44723786 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 27.26456628 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVI 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 21.15875334 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 34.27188354 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVII 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 30.01184092 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 19.5532772 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 19.18979951 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 23.63407946 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XVIII 2B5 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 21.78231337 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIX 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 33.35802697 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIX 2B2 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 33.39604005 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIX 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 34.92220381 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XIX 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 31.05270436 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B1 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 18.15739328 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XX 2B3 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 22.95272479 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XXI 2B4 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 36.2975028 | Non-Symbiont Non-Spinose | 199.709257 | 39.37565826 | 18.28363333 | 0.09256227 | 10.59136733 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | NB XXI 2B6 | Sediment trap | 530 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 27.97070682 | Non-Symbiont Non-Spinose | 194.5950513 | 39.50077772 | 18.60218956 | 0.07801616 | 11.72752465 | MED | |||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | PLANIER CORE-TOP | Coretop | -1095.0 | 0.0 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 5.37100739 | Non-Symbiont Spinose | 238.9780501 | 39.45058746 | 18.06826938 | 0.11069427 | 9.62725074 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | PLANIER CORE-TOP | Coretop | -1095.0 | 0.0 | 42.989 | 5.121 | Globigerina bulloides | 250-300 | 5.00965139 | Non-Symbiont Spinose | 238.9780501 | 39.45058746 | 18.06826938 | 0.11069427 | 9.62725074 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | PLANIER CORE-TOP | Coretop | -1095.0 | 0.0 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.49412065 | Non-Symbiont Non-Spinose | 238.9780501 | 39.45058746 | 18.06826938 | 0.11069427 | 9.62725074 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | PLANIER CORE-TOP | Coretop | -1095.0 | 0.0 | 42.989 | 5.121 | Neogloboquadrina incompta | 200-250 | 4.5814014 | Non-Symbiont Non-Spinose | 238.9780501 | 39.45058746 | 18.06826938 | 0.11069427 | 9.62725074 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | PLANIER CORE-TOP | Coretop | -1095.0 | 0.0 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 34.3074154 | Non-Symbiont Non-Spinose | 238.9780501 | 39.45058746 | 18.06826938 | 0.11069427 | 9.62725074 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | PLANIER CORE-TOP | Coretop | -1095.0 | 0.0 | 42.989 | 5.121 | Globorotalia truncatulinoides | 400-500 | 36.81173261 | Non-Symbiont Non-Spinose | 238.9780501 | 39.45058746 | 18.06826938 | 0.11069427 | 9.62725074 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS0 - 0,5 cm | Sediment core | -990.0 | 0.005 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 4.84829468 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS0,5 - 1 cm | Sediment core | -990.0 | 0.01 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 4.46158592 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS1 - 1,5 cm | Sediment core | -990.0 | 0.015 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 4.88432296 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS1,5 - 2 cm | Sediment core | -990.0 | 0.02 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 4.87645293 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS2 - 3 cm | Sediment core | -990.0 | 0.03 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 4.7146898 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS3 - 4 cm | Sediment core | -990.0 | 0.04 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 4.56816556 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS4 - 5 cm | Sediment core | -990.0 | 0.05 | 42.2656 | 3.54 | Globigerina bulloides | 250-300 | 5.3159722 | Non-Symbiont Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS0 - 0,5 cm | Sediment core | -990.0 | 0.005 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 4.17155861 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS0,5 - 1 cm | Sediment core | -990.0 | 0.01 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 4.05130975 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS1 - 1,5 cm | Sediment core | -990.0 | 0.015 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 4.26065716 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS1,5 - 2 cm | Sediment core | -990.0 | 0.02 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 3.98251385 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS2 - 3 cm | Sediment core | -990.0 | 0.03 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 4.39751532 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS3 - 4 cm | Sediment core | -990.0 | 0.04 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 3.77425525 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS4 - 5 cm | Sediment core | -990.0 | 0.05 | 42.2656 | 3.54 | Neogloboquadrina incompta | 200-250 | 4.12536032 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS0 - 0,5 cm | Sediment core | -990.0 | 0.005 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 30.96300806 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS0,5 - 1 cm | Sediment core | -990.0 | 0.01 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 30.11250591 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS1 - 1,5 cm | Sediment core | -990.0 | 0.015 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 27.97823053 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS1,5 - 2 cm | Sediment core | -990.0 | 0.02 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 27.27063441 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS2 - 3 cm | Sediment core | -990.0 | 0.03 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 30.14901333 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS3 - 4 cm | Sediment core | -990.0 | 0.04 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 28.01581789 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
Bejard | Calcification response of planktic foraminifera to environmental change in the Western Mediterranean Sea during the industrial era | LACAZE-DUTHIERS4 - 5 cm | Sediment core | -990.0 | 0.05 | 42.2656 | 3.54 | Globorotalia truncatulinoides | 400-500 | 28.90249184 | Non-Symbiont Non-Spinose | 241.3525258 | 39.29777075 | 18.6024545 | 0.08441233 | 10.36767115 | MED | ||
New data | n/a | GIK23238-1 | Coretop | -981.0 | 0.0 | 67.0 | 7.8 | Neogloboquadrina pachyderma | 200-250 | 5.60744947 | Non-Symbiont Non-Spinose | 179.0 | 35.019 | 7.118 | 0.47371998 | 10.08141008 | ATL | ||
New data | n/a | GIK23239 | Coretop | -1529.0 | 0.0 | 67.5 | 8.4 | Neogloboquadrina pachyderma | 200-250 | 6.32308979 | Non-Symbiont Non-Spinose | 175.0 | 35.035 | 7.112 | 0.48700425 | 10.43818148 | ATL | ||
New data | n/a | GIK23243-2 | Coretop | -2721.0 | 0.0 | 69.4 | -6.5 | Neogloboquadrina pachyderma | 200-250 | 6.6115494 | Non-Symbiont Non-Spinose | 166.0 | 35.134 | 4.549 | 0.14009572 | 11.728758 | ATL | ||
New data | n/a | GIK23244-1 | Coretop | -2085.0 | 0.0 | 69.4 | -8.7 | Neogloboquadrina pachyderma | 200-250 | 6.76442136 | Non-Symbiont Non-Spinose | 174.0 | 35.027 | 5.382 | 0.53896508 | 5.64252924 | ATL | ||
New data | n/a | GIK23266-1 | Coretop | -2773.0 | 0.0 | 72.0 | 7.5 | Neogloboquadrina pachyderma | 200-250 | 6.45106211 | Non-Symbiont Non-Spinose | 167.0 | 35.052 | 5.295 | 0.53338337 | 8.18491921 | ATL | ||
New data | n/a | GIK23267-2 | Coretop | -2974.0 | 0.0 | 72.0 | 5.0 | Neogloboquadrina pachyderma | 200-250 | 6.38592834 | Non-Symbiont Non-Spinose | 180.0 | 34.964 | 5.474 | 0.53083783 | 7.85632454 | ATL | ||
New data | n/a | GIK23269-2 | Coretop | -2877.0 | 0.0 | 71.5 | 0.7 | Neogloboquadrina pachyderma | 200-250 | 5.84524894 | Non-Symbiont Non-Spinose | 171.0 | 35.043 | 5.52 | 0.53092742 | 7.22740295 | ATL | ||
New data | n/a | GIK23295-2 | Coretop | -2134.0 | 0.0 | 71.1 | -6.0 | Neogloboquadrina pachyderma | 200-250 | 6.2779022 | Non-Symbiont Non-Spinose | 176.0 | 34.766 | 3.319 | 0.14520795 | 17.20702089 | ATL | ||
New data | n/a | GIK233091 | Coretop | -1423.0 | 0.0 | 67.7 | 5.8 | Neogloboquadrina pachyderma | 200-250 | 7.20263695 | Non-Symbiont Non-Spinose | 167.0 | 34.948 | 6.519 | 0.50235999 | 10.6254375 | ATL | ||
New data | n/a | GIK23313-2 | Coretop | -961.0 | 0.0 | 67.0 | 7.8 | Neogloboquadrina pachyderma | 200-250 | 7.10607283 | Non-Symbiont Non-Spinose | 179.0 | 35.019 | 7.118 | 0.47371998 | 10.08141008 | ATL | ||
New data | n/a | GIK23364-6 | Coretop | -2794.0 | 0.0 | 70.5 | -4.0 | Neogloboquadrina pachyderma | 200-250 | 7.06992542 | Non-Symbiont Non-Spinose | 186.0 | 35.13 | 6.63 | 0.56251912 | 3.64355727 | ATL | ||
New data | n/a | GIK233651 | Coretop | -2795.0 | 0.0 | 70.5 | -2.0 | Neogloboquadrina pachyderma | 200-250 | 6.10075542 | Non-Symbiont Non-Spinose | 185.0 | 35.109 | 6.743 | 0.52790769 | 6.50608487 | ATL | ||
New data | n/a | GIK23373 | Coretop | -1338.0 | 0.0 | 67.0 | 2.9 | Neogloboquadrina pachyderma | 200-250 | 7.10642667 | Non-Symbiont Non-Spinose | 163.0 | 34.989 | 5.548 | 0.51615174 | 9.34255029 | ATL | ||
New data | n/a | GIK23398-2 | Coretop | -2224.0 | 0.0 | 76.4 | 9.0 | Neogloboquadrina pachyderma | 200-250 | 7.12995242 | Non-Symbiont Non-Spinose | 191.0 | 34.939 | 6.376 | 0.54615202 | 8.96614071 | ATL | ||
New data | n/a | GIK23402-2 | Coretop | -2439.0 | 0.0 | 68.7 | 0.2 | Neogloboquadrina pachyderma | 200-250 | 7.22019753 | Non-Symbiont Non-Spinose | 168.0 | 35.086 | 5.591 | 0.52831327 | 6.92328453 | ATL | ||
New data | n/a | PS1704 | Coretop | -1195.0 | 0.0 | 78.4 | 1.1 | Neogloboquadrina pachyderma | 200-250 | 6.95220432 | Non-Symbiont Non-Spinose | 202.0 | 34.298 | 1.615 | 0.56441928 | 3.96809077 | ATL | ||
New data | n/a | PS1707-1 | Coretop | -2118.0 | 0.0 | 72.6 | -13.8 | Neogloboquadrina pachyderma | 200-250 | 8.27944648 | Non-Symbiont Non-Spinose | 175.0 | 33.411 | 4.113 | 0.56550285 | 4.10478321 | ATL | ||
New data | n/a | PS1743-2 | Coretop | -1695.0 | 0.0 | 76.8 | -5.4 | Neogloboquadrina pachyderma | 200-250 | 9.5337176 | Non-Symbiont Non-Spinose | 245.0 | 36.1 | 19.326 | 0.54983494 | 5.35840782 | ATL | ||
New data | n/a | PS1918-2 | Coretop | -1174.0 | 0.0 | 75.0 | -12.4 | Neogloboquadrina pachyderma | 200-250 | 8.16046172 | Non-Symbiont Non-Spinose | 138.0 | 31.74 | -0.621 | 0.56054504 | 3.70911924 | ATL | ||
New data | n/a | PS2412-2 | Coretop | -583.0 | 0.0 | 76.6 | -7.5 | Neogloboquadrina pachyderma | 200-250 | 8.94302644 | Non-Symbiont Non-Spinose | 139.0 | 30.895 | -0.763 | 0.56062378 | 3.1542271 | ATL | ||
New data | n/a | PS2415-5 | Coretop | -375.0 | 0.0 | 77.7 | -14.1 | Neogloboquadrina pachyderma | 200-250 | 7.62494344 | Non-Symbiont Non-Spinose | 119.0 | 30.514 | -0.156 | 0.54909648 | 2.3035169 | ATL | ||
New data | n/a | PS2627-5 | Coretop | -2009.0 | 0.0 | 73.1 | -15.7 | Neogloboquadrina pachyderma | 200-250 | 7.78171076 | Non-Symbiont Non-Spinose | 159.0 | 32.854 | 0.555 | 0.56480897 | 4.01844051 | ATL | ||
New data | n/a | PS2644-2 | Coretop | -778.0 | 0.0 | 67.9 | -21.8 | Neogloboquadrina pachyderma | 200-250 | 6.68488928 | Non-Symbiont Non-Spinose | 175.0 | 34.806 | 4.833 | 0.5637484 | 5.52285081 | ATL | ||
New data | n/a | PS2646-2 | Coretop | -1115.0 | 0.0 | 68.6 | -21.5 | Neogloboquadrina pachyderma | 200-250 | 6.97724231 | Non-Symbiont Non-Spinose | 176.0 | 34.001 | 2.288 | 0.56114269 | 3.70131624 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 0.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.61743128 | Non-Symbiont Non-Spinose | 140.0 | 34.321 | 9.081 | 0.36486049 | 10.14796285 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 1.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.28065472 | Non-Symbiont Non-Spinose | 144.0 | 34.355 | 8.723 | 0.39623313 | 9.92348698 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 2.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.96084661 | Non-Symbiont Non-Spinose | 144.0 | 34.355 | 8.723 | 0.39623313 | 9.92348698 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 2.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.86540968 | Non-Symbiont Non-Spinose | 144.0 | 34.355 | 8.723 | 0.39623313 | 9.92348698 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 3.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.39177756 | Non-Symbiont Non-Spinose | 148.0 | 34.378 | 8.569 | 0.35685389 | 9.88093606 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 4.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.87301564 | Non-Symbiont Non-Spinose | 148.0 | 34.378 | 8.569 | 0.35685389 | 9.88093606 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 5.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.02130635 | Non-Symbiont Non-Spinose | 148.0 | 34.378 | 8.569 | 0.35685389 | 9.88093606 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 6.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.95617141 | Non-Symbiont Non-Spinose | 152.0 | 34.338 | 8.353 | 0.36846906 | 9.75651288 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 7.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.00920823 | Non-Symbiont Non-Spinose | 152.0 | 34.338 | 8.353 | 0.36846906 | 9.75651288 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 9.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.90799857 | Non-Symbiont Non-Spinose | 156.0 | 34.33 | 8.216 | 0.37357655 | 9.92231238 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 10.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.62536201 | Non-Symbiont Non-Spinose | 158.0 | 34.351 | 8.324 | 0.38729288 | 9.56848623 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 11.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.34820677 | Non-Symbiont Non-Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 12.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.41128205 | Non-Symbiont Non-Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 13.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.13903164 | Non-Symbiont Non-Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 14.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.10888475 | Non-Symbiont Non-Spinose | 158.0 | 34.339 | 8.21 | 0.41647122 | 10.18755082 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 15.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.70589679 | Non-Symbiont Non-Spinose | 158.0 | 34.339 | 8.21 | 0.41647122 | 10.18755082 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 15.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.17187582 | Non-Symbiont Non-Spinose | 161.0 | 34.293 | 8.024 | 0.44479069 | 9.89932765 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 16.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.13454343 | Non-Symbiont Non-Spinose | 161.0 | 34.293 | 8.024 | 0.44479069 | 9.89932765 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 16.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.38658015 | Non-Symbiont Non-Spinose | 161.0 | 34.293 | 8.024 | 0.44479069 | 9.89932765 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 17.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.9859283 | Non-Symbiont Non-Spinose | 160.0 | 34.288 | 8.027 | 0.39066131 | 10.04942838 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 17.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.49470356 | Non-Symbiont Non-Spinose | 160.0 | 34.288 | 8.027 | 0.39066131 | 10.04942838 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 18.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.15537298 | Non-Symbiont Non-Spinose | 160.0 | 34.288 | 8.027 | 0.39066131 | 10.04942838 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 18.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.86556053 | Non-Symbiont Non-Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 19.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.35473151 | Non-Symbiont Non-Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 20.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.91157124 | Non-Symbiont Non-Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 21.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.47053674 | Non-Symbiont Non-Spinose | 165.0 | 34.337 | 8.228 | 0.39926828 | 9.74302987 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 21.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.34916018 | Non-Symbiont Non-Spinose | 165.0 | 34.337 | 8.228 | 0.39926828 | 9.74302987 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 22.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.18463053 | Non-Symbiont Non-Spinose | 166.0 | 34.319 | 7.994 | 0.43583445 | 9.67406747 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 23.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.55033865 | Non-Symbiont Non-Spinose | 166.0 | 34.319 | 7.994 | 0.43583445 | 9.67406747 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 25.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.68138994 | Non-Symbiont Non-Spinose | 166.0 | 34.308 | 8.136 | 0.43741742 | 9.57454068 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 27.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.37091444 | Non-Symbiont Non-Spinose | 167.0 | 34.326 | 8.264 | 0.41581135 | 9.99099969 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 29.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.40079857 | Non-Symbiont Non-Spinose | 168.0 | 34.389 | 8.313 | 0.44449476 | 9.73991008 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 30.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.49288839 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 31.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.91417019 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 33.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.81994749 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 33.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.07951014 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 35.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.80576105 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 36.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 6.39022001 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 37.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.9280867 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 37.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.72677338 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 38.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.27200317 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 39.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.53683469 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 40.25 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.44295605 | Non-Symbiont Non-Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 41.75 | 63.80639 | 5.22444 | Neogloboquadrina incompta | 200-250 | 5.60078997 | Non-Symbiont Non-Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 3.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.28550141 | Non-Symbiont Spinose | 148.0 | 34.378 | 8.569 | 0.35685389 | 9.88093606 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 5.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.14957507 | Non-Symbiont Spinose | 148.0 | 34.378 | 8.569 | 0.35685389 | 9.88093606 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 5.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.15935409 | Non-Symbiont Spinose | 148.0 | 34.378 | 8.569 | 0.35685389 | 9.88093606 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 6.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.91057434 | Non-Symbiont Spinose | 152.0 | 34.338 | 8.353 | 0.36846906 | 9.75651288 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 7.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.27908659 | Non-Symbiont Spinose | 152.0 | 34.338 | 8.353 | 0.36846906 | 9.75651288 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 7.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.91313257 | Non-Symbiont Spinose | 156.0 | 34.33 | 8.216 | 0.37357655 | 9.92231238 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 8.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.81939581 | Non-Symbiont Spinose | 156.0 | 34.33 | 8.216 | 0.37357655 | 9.92231238 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 8.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.52695091 | Non-Symbiont Spinose | 156.0 | 34.33 | 8.216 | 0.37357655 | 9.92231238 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 9.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.52695091 | Non-Symbiont Spinose | 156.0 | 34.33 | 8.216 | 0.37357655 | 9.92231238 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 9.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.51684139 | Non-Symbiont Spinose | 156.0 | 34.33 | 8.216 | 0.37357655 | 9.92231238 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 10.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.82023411 | Non-Symbiont Spinose | 158.0 | 34.351 | 8.324 | 0.38729288 | 9.56848623 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 10.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.90158843 | Non-Symbiont Spinose | 158.0 | 34.351 | 8.324 | 0.38729288 | 9.56848623 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 11.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.77663469 | Non-Symbiont Spinose | 158.0 | 34.351 | 8.324 | 0.38729288 | 9.56848623 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 11.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.16278128 | Non-Symbiont Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 12.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.51077496 | Non-Symbiont Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 12.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.2237349 | Non-Symbiont Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 13.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.6169444 | Non-Symbiont Spinose | 158.0 | 34.337 | 8.246 | 0.40871352 | 9.50050555 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 13.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.84645442 | Non-Symbiont Spinose | 158.0 | 34.339 | 8.21 | 0.41647122 | 10.18755082 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 14.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.50457596 | Non-Symbiont Spinose | 158.0 | 34.339 | 8.21 | 0.41647122 | 10.18755082 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 14.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.14397809 | Non-Symbiont Spinose | 158.0 | 34.339 | 8.21 | 0.41647122 | 10.18755082 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 15.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.53320017 | Non-Symbiont Spinose | 158.0 | 34.339 | 8.21 | 0.41647122 | 10.18755082 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 15.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.88087819 | Non-Symbiont Spinose | 161.0 | 34.293 | 8.024 | 0.44479069 | 9.89932765 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 16.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.57287242 | Non-Symbiont Spinose | 161.0 | 34.293 | 8.024 | 0.44479069 | 9.89932765 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 16.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.50851491 | Non-Symbiont Spinose | 161.0 | 34.293 | 8.024 | 0.44479069 | 9.89932765 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 17.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.67897388 | Non-Symbiont Spinose | 160.0 | 34.288 | 8.027 | 0.39066131 | 10.04942838 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 17.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.88409672 | Non-Symbiont Spinose | 160.0 | 34.288 | 8.027 | 0.39066131 | 10.04942838 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 18.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.87343029 | Non-Symbiont Spinose | 160.0 | 34.288 | 8.027 | 0.39066131 | 10.04942838 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 18.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.95977493 | Non-Symbiont Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 19.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.91144792 | Non-Symbiont Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 19.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 7.34889894 | Non-Symbiont Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 20.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.42955535 | Non-Symbiont Spinose | 164.0 | 34.29 | 8.166 | 0.40696935 | 10.06454552 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 20.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.55709326 | Non-Symbiont Spinose | 165.0 | 34.337 | 8.228 | 0.39926828 | 9.74302987 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 21.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.56948471 | Non-Symbiont Spinose | 165.0 | 34.337 | 8.228 | 0.39926828 | 9.74302987 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 21.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.58499054 | Non-Symbiont Spinose | 165.0 | 34.337 | 8.228 | 0.39926828 | 9.74302987 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 22.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.58967068 | Non-Symbiont Spinose | 165.0 | 34.337 | 8.228 | 0.39926828 | 9.74302987 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 22.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.18670532 | Non-Symbiont Spinose | 166.0 | 34.319 | 7.994 | 0.43583445 | 9.67406747 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 23.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.35798715 | Non-Symbiont Spinose | 166.0 | 34.319 | 7.994 | 0.43583445 | 9.67406747 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 23.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.61047249 | Non-Symbiont Spinose | 166.0 | 34.319 | 7.994 | 0.43583445 | 9.67406747 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 24.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.7403952 | Non-Symbiont Spinose | 166.0 | 34.319 | 7.994 | 0.43583445 | 9.67406747 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 24.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.7403952 | Non-Symbiont Spinose | 166.0 | 34.308 | 8.136 | 0.43741742 | 9.57454068 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 25.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.40429198 | Non-Symbiont Spinose | 166.0 | 34.308 | 8.136 | 0.43741742 | 9.57454068 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 24.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.13180227 | Non-Symbiont Spinose | 166.0 | 34.308 | 8.136 | 0.43741742 | 9.57454068 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 26.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.23076681 | Non-Symbiont Spinose | 166.0 | 34.308 | 8.136 | 0.43741742 | 9.57454068 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 26.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.91666404 | Non-Symbiont Spinose | 167.0 | 34.326 | 8.264 | 0.41581135 | 9.99099969 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 27.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.53317684 | Non-Symbiont Spinose | 167.0 | 34.326 | 8.264 | 0.41581135 | 9.99099969 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 27.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.89962078 | Non-Symbiont Spinose | 167.0 | 34.326 | 8.264 | 0.41581135 | 9.99099969 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 28.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.38105457 | Non-Symbiont Spinose | 167.0 | 34.326 | 8.264 | 0.41581135 | 9.99099969 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 28.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.74041981 | Non-Symbiont Spinose | 168.0 | 34.389 | 8.313 | 0.44449476 | 9.73991008 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 29.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.50457596 | Non-Symbiont Spinose | 168.0 | 34.389 | 8.313 | 0.44449476 | 9.73991008 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 29.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.15590854 | Non-Symbiont Spinose | 168.0 | 34.389 | 8.313 | 0.44449476 | 9.73991008 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 30.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.88014502 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 30.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.76758885 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 31.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.50457596 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 31.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.66707981 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 32.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.70823108 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 32.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.68052963 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 33.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.9436682 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 33.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.94275636 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 33.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.56681922 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 34.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.65114518 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 35.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.86022188 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 35.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.09101047 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 36.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.56156271 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 36.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.08638364 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 37.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.86022188 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 37.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.21062 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 37.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.35391757 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 38.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.25112727 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 39.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.94970198 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 39.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.42973713 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 40.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.13811676 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 40.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.07344969 | Non-Symbiont Spinose | 169.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 41.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.45754021 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 41.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.95446982 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 42.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.50601084 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 42.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.27908659 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 43.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 10.01428698 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 43.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 9.25923161 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 44.25 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.51839336 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GS06-144-22-MC | Sediment core | -921.0 | 44.75 | 63.80639 | 5.22444 | Globigerina bulloides | 250-300 | 8.88885356 | Non-Symbiont Spinose | 175.0 | 34.326 | 8.216 | 0.45142168 | 9.16781776 | ATL | ||
New data | n/a | GeoB3804-2 | Coretop | -3882.0 | 0.0 | -30.743333 | -8.77 | Globigerinoides ruber | 300-350 | 18.87517614 | Symbiont Spinose | 239.0 | 35.804 | 16.927 | 0.13503281 | 7.45167595 | ATL | ||
New data | n/a | GeoB3803-1 | Coretop | -4173.0 | 0.0 | -30.348333 | -8.571667 | Globigerinoides ruber | 300-350 | 18.11770505 | Symbiont Spinose | 250.0 | 35.815 | 21.065 | 0.1345384 | 9.39829129 | ATL | ||
New data | n/a | GeoB3812-2 | Coretop | -4204.0 | 0.0 | -31.615 | -19.76 | Globigerinoides ruber | 300-350 | 18.1067342 | Symbiont Spinose | 244.0 | 35.879 | 17.458 | 0.11585642 | 6.24780954 | ATL | ||
New data | n/a | GeoB2913-4 | Coretop | -3621.0 | 0.0 | 29.11 | -15.4617 | Globigerinoides ruber | 300-350 | 20.77622448 | Symbiont Spinose | 260.0 | 36.619 | 20.269 | 0.11823883 | 11.34345436 | ATL | ||
New data | n/a | GeoB1403-2 | Coretop | -3692.0 | 0.0 | -1.198333 | -11.711667 | Globigerinoides ruber | 300-350 | 13.66010447 | Symbiont Spinose | 265.0 | 35.802 | 25.596 | 0.11697148 | 21.04705785 | ATL | ||
New data | n/a | GeoB1802-10 | Coretop | -3603.0 | 0.0 | 29.176667 | -15.405 | Globigerinoides ruber | 300-350 | 19.94265026 | Symbiont Spinose | 260.0 | 36.799 | 20.269 | 0.11823883 | 11.34345436 | ATL | ||
New data | n/a | GeoB3603-1 | Coretop | -2851.0 | 0.0 | -35.121667 | 17.533333 | Globigerinoides ruber | 300-350 | 20.66725787 | Symbiont Spinose | 260.0 | 35.511 | 19.619 | 0.24903457 | 22.22107671 | ATL | ||
New data | n/a | GeoB1721-4 | Coretop | -3079.0 | 0.0 | -29.175 | 13.088333 | Globigerinoides ruber | 300-350 | 18.31807952 | Symbiont Spinose | 237.0 | 35.397 | 17.622 | 0.57374181 | 21.39131439 | ATL | ||
New data | n/a | GeoB1726-2 | Coretop | -1006.0 | 0.0 | -30.27 | 3.261667 | Globigerinoides ruber | 300-350 | 24.4761405 | Symbiont Spinose | 246.0 | 35.729 | 19.25 | 0.15516494 | 9.97101556 | ATL | ||
New data | n/a | GeoB2911-2 | Coretop | -4020.0 | 0.0 | 11.503333 | -21.04 | Globigerinoides ruber | 300-350 | 8.1940725 | Symbiont Spinose | 266.0 | 35.504 | 24.999 | 0.07359414 | 16.36436256 | ATL | ||
New data | n/a | GeoB3809-1 | Coretop | -3470.0 | 0.0 | -31.053333 | -16.33 | Globigerinoides ruber | 300-350 | 19.01936553 | Symbiont Spinose | 237.0 | 35.702 | 16.03 | 0.11859489 | 5.48967723 | ATL | ||
New data | n/a | GeoB1015-3 | Coretop | -1650.0 | 0.0 | -11.7738 | 12.8385 | Globigerinoides ruber | 300-350 | 11.83819311 | Symbiont Spinose | 222.0 | 35.703 | 21.113 | 0.2645909 | 18.05296772 | ATL | ||
New data | n/a | GeoB5133-3 | Coretop | -3660.0 | 0.0 | -19.086667 | -10.191667 | Globigerinoides ruber | 300-350 | 17.83251707 | Symbiont Spinose | 272.0 | 36.485 | 25.239 | 0.14133149 | 11.79093097 | ATL | ||
New data | n/a | GeoB1034-1 | Coretop | -3731.0 | 0.0 | -21.721667 | 5.43 | Globigerinoides ruber | 300-350 | 20.58865043 | Symbiont Spinose | 244.0 | 35.657 | 21.168 | 0.45894185 | 15.21271955 | ATL | ||
New data | n/a | GeoB3810-2 | Coretop | -3810.0 | 0.0 | -31.133333 | -16.838333 | Globigerinoides ruber | 300-350 | 18.48561516 | Symbiont Spinose | 237.0 | 35.867 | 16.03 | 0.11681119 | 5.397742 | ATL | ||
New data | n/a | GeoB3807-1 | Coretop | -2515.0 | 0.0 | -30.75 | -13.198333 | Globigerinoides ruber | 300-350 | 22.84963265 | Symbiont Spinose | 238.0 | 35.75 | 16.445 | 0.12498948 | 5.67264728 | ATL | ||
New data | n/a | GeoB5121-2 | Coretop | -3486.0 | 0.0 | -24.183333 | -12.021667 | Globigerinoides ruber | 300-350 | 20.70316754 | Symbiont Spinose | 281.0 | 36.784 | 24.943 | 0.1505637 | 8.18880946 | ATL | ||
New data | n/a | GeoB1808-7 | Coretop | -3385.0 | 0.0 | -5.803333 | -9.398333 | Globigerinoides ruber | 300-350 | 13.76945638 | Symbiont Spinose | 267.0 | 36.204 | 26.214 | 0.08383765 | 14.16504714 | ATL | ||
New data | n/a | GeoB2912-2 | Coretop | -4136.0 | 0.0 | 21.28 | -20.708333 | Globigerinoides ruber | 300-350 | 12.9637781 | Symbiont Spinose | 259.0 | 36.488 | 20.969 | 0.27260081 | 22.65815494 | ATL | ||
New data | n/a | GeoB1404-8 | Coretop | -3988.0 | 0.0 | -0.078333 | -10.778333 | Globigerinoides ruber | 300-350 | 12.87008766 | Symbiont Spinose | 259.0 | 35.899 | 24.391 | 0.07305675 | 11.49996233 | ATL | ||
New data | n/a | GeoB6011-2 | Coretop | -993.0 | 0.0 | 30.315 | -10.2883 | Globigerinoides ruber | 300-350 | 19.44901357 | Symbiont Spinose | 245.0 | 35.94 | 19.852 | 0.11995584 | 20.86115905 | ATL | ||
New data | n/a | GeoB3915-1 | Coretop | -3127.0 | 0.0 | -2.28 | -38.015 | Globigerinoides ruber | 300-350 | 16.66332619 | Symbiont Spinose | 283.0 | 36.302 | 26.709 | 0.07534127 | 9.30299802 | ATL | ||
New data | n/a | GeoB5142-2 | Coretop | -3946.0 | 0.0 | -19.088333 | -17.145 | Globigerinoides ruber | 300-350 | 18.76072976 | Symbiont Spinose | 283.0 | 36.853 | 25.772 | 0.11648273 | 7.53303942 | ATL | ||
New data | n/a | GeoB3804-2 | Coretop | -3882.0 | 0.0 | -30.743333 | -8.77 | Globorotalia truncatulinoides | 300-350 | 30.69597604 | Non-Symbiont Non-Spinose | 239.0 | 35.804 | 16.927 | 0.13503281 | 7.45167595 | ATL | ||
New data | n/a | GeoB3803-1 | Coretop | -4173.0 | 0.0 | -30.348333 | -8.571667 | Globorotalia truncatulinoides | 300-350 | 27.52463245 | Non-Symbiont Non-Spinose | 239.0 | 35.791 | 16.927 | 0.13127706 | 7.67691485 | ATL | ||
New data | n/a | GeoB3812-2 | Coretop | -4204.0 | 0.0 | -31.615 | -19.76 | Globorotalia truncatulinoides | 300-350 | 26.75838 | Non-Symbiont Non-Spinose | 244.0 | 35.879 | 17.458 | 0.11585642 | 6.24780954 | ATL | ||
New data | n/a | GeoB2913-4 | Coretop | -3621.0 | 0.0 | 29.11 | -15.4617 | Globorotalia truncatulinoides | 300-350 | 27.68749264 | Non-Symbiont Non-Spinose | 260.0 | 36.619 | 20.269 | 0.11823883 | 11.34345436 | ATL | ||
New data | n/a | GeoB1403-2 | Coretop | -3692.0 | 0.0 | -1.198333 | -11.711667 | Globorotalia truncatulinoides | 300-350 | 25.60090456 | Non-Symbiont Non-Spinose | 265.0 | 35.802 | 25.596 | 0.11697148 | 21.04705785 | ATL | ||
New data | n/a | GeoB1802-10 | Coretop | -3603.0 | 0.0 | 29.176667 | -15.405 | Globorotalia truncatulinoides | 300-350 | 31.67727265 | Non-Symbiont Non-Spinose | 260.0 | 36.799 | 20.269 | 0.11823883 | 11.34345436 | ATL | ||
New data | n/a | GeoB3603-1 | Coretop | -2851.0 | 0.0 | -35.121667 | 17.533333 | Globorotalia truncatulinoides | 300-350 | 24.22936438 | Non-Symbiont Non-Spinose | 260.0 | 35.511 | 19.619 | 0.24903457 | 22.22107671 | ATL | ||
New data | n/a | GeoB1721-4 | Coretop | -3079.0 | 0.0 | -29.175 | 13.088333 | Globorotalia truncatulinoides | 300-350 | 21.06703127 | Non-Symbiont Non-Spinose | 237.0 | 35.397 | 17.622 | 0.57374181 | 21.39131439 | ATL | ||
New data | n/a | GeoB1726-2 | Coretop | -1006.0 | 0.0 | -30.27 | 3.261667 | Globorotalia truncatulinoides | 300-350 | 25.36975152 | Non-Symbiont Non-Spinose | 246.0 | 35.729 | 19.25 | 0.15516494 | 9.97101556 | ATL | ||
New data | n/a | GeoB3809-1 | Coretop | -3470.0 | 0.0 | -31.053333 | -16.33 | Globorotalia truncatulinoides | 300-350 | 29.29477222 | Non-Symbiont Non-Spinose | 237.0 | 35.702 | 16.03 | 0.11859489 | 5.48967723 | ATL | ||
New data | n/a | GeoB5133-3 | Coretop | -3660.0 | 0.0 | -19.086667 | -10.191667 | Globorotalia truncatulinoides | 300-350 | 24.5739302 | Non-Symbiont Non-Spinose | 272.0 | 36.485 | 25.239 | 0.14133149 | 11.79093097 | ATL | ||
New data | n/a | GeoB1034-1 | Coretop | -3731.0 | 0.0 | -21.721667 | 5.43 | Globorotalia truncatulinoides | 300-350 | 25.3333114 | Non-Symbiont Non-Spinose | 244.0 | 35.657 | 21.168 | 0.45894185 | 15.21271955 | ATL | ||
New data | n/a | GeoB3810-2 | Coretop | -3810.0 | 0.0 | -31.133333 | -16.838333 | Globorotalia truncatulinoides | 300-350 | 29.79300714 | Non-Symbiont Non-Spinose | 237.0 | 35.867 | 16.03 | 0.11681119 | 5.397742 | ATL | ||
New data | n/a | GeoB3807-1 | Coretop | -2515.0 | 0.0 | -30.75 | -13.198333 | Globorotalia truncatulinoides | 300-350 | 27.93626809 | Non-Symbiont Non-Spinose | 238.0 | 35.75 | 16.445 | 0.12498948 | 5.67264728 | ATL | ||
New data | n/a | GeoB5121-2 | Coretop | -3486.0 | 0.0 | -24.183333 | -12.021667 | Globorotalia truncatulinoides | 300-350 | 30.03931934 | Non-Symbiont Non-Spinose | 281.0 | 36.784 | 24.943 | 0.1505637 | 8.18880946 | ATL | ||
New data | n/a | GeoB1729-2 | Coretop | -4401.0 | 0.0 | -28.891667 | 1.001667 | Globorotalia truncatulinoides | 300-350 | 25.47165377 | Non-Symbiont Non-Spinose | 250.0 | 35.815 | 21.065 | 0.1345384 | 9.39829129 | ATL | ||
New data | n/a | GeoB2912-2 | Coretop | -4136.0 | 0.0 | 21.28 | -20.708333 | Globorotalia truncatulinoides | 300-350 | 26.61687616 | Non-Symbiont Non-Spinose | 259.0 | 36.488 | 20.969 | 0.27260081 | 22.65815494 | ATL | ||
New data | n/a | GeoB1404-8 | Coretop | -3988.0 | 0.0 | -0.078333 | -10.778333 | Globorotalia truncatulinoides | 300-350 | 28.19637129 | Non-Symbiont Non-Spinose | 259.0 | 35.899 | 24.391 | 0.07305675 | 11.49996233 | ATL | ||
New data | n/a | GeoB6011-2 | Coretop | -993.0 | 0.0 | 30.315 | -10.2883 | Globorotalia truncatulinoides | 300-350 | 34.53150286 | Non-Symbiont Non-Spinose | 245.0 | 35.94 | 19.852 | 0.11995584 | 20.86115905 | ATL | ||
New data | n/a | GeoB5142-2 | Coretop | -3946.0 | 0.0 | -19.088333 | -17.145 | Globorotalia truncatulinoides | 300-350 | 31.13155295 | Non-Symbiont Non-Spinose | 283.0 | 36.853 | 25.772 | 0.11648273 | 7.53303942 | ATL | ||
New data | n/a | GeoB3804-2 | Coretop | -3882.0 | 0.0 | -30.743333 | -8.77 | Orbulina universa | 300-350 | 13.15460629 | Symbiont Spinose | 239.0 | 35.804 | 16.927 | 0.13503281 | 7.45167595 | ATL | ||
New data | n/a | GeoB3803-1 | Coretop | -4173.0 | 0.0 | -30.348333 | -8.571667 | Orbulina universa | 300-350 | 13.35515593 | Symbiont Spinose | 239.0 | 35.791 | 16.927 | 0.13127706 | 7.67691485 | ATL | ||
New data | n/a | GeoB3812-2 | Coretop | -4204.0 | 0.0 | -31.615 | -19.76 | Orbulina universa | 300-350 | 13.88493577 | Symbiont Spinose | 244.0 | 35.879 | 17.458 | 0.11585642 | 6.24780954 | ATL | ||
New data | n/a | GeoB1802-10 | Coretop | -3603.0 | 0.0 | 29.176667 | -15.405 | Orbulina universa | 300-350 | 14.63794955 | Symbiont Spinose | 260.0 | 36.799 | 20.269 | 0.11823883 | 11.34345436 | ATL | ||
New data | n/a | GeoB3603-1 | Coretop | -2851.0 | 0.0 | -35.121667 | 17.533333 | Orbulina universa | 300-350 | 17.96152682 | Symbiont Spinose | 260.0 | 35.511 | 19.619 | 0.24903457 | 22.22107671 | ATL | ||
New data | n/a | GeoB1721-4 | Coretop | -3079.0 | 0.0 | -29.175 | 13.088333 | Orbulina universa | 300-350 | 16.45103255 | Symbiont Spinose | 237.0 | 35.397 | 17.622 | 0.57374181 | 21.39131439 | ATL | ||
New data | n/a | GeoB1726-2 | Coretop | -1006.0 | 0.0 | -30.27 | 3.261667 | Orbulina universa | 300-350 | 22.03385267 | Symbiont Spinose | 246.0 | 35.729 | 19.25 | 0.15516494 | 9.97101556 | ATL | ||
New data | n/a | GeoB3809-1 | Coretop | -3470.0 | 0.0 | -31.053333 | -16.33 | Orbulina universa | 300-350 | 17.43836006 | Symbiont Spinose | 237.0 | 35.702 | 16.03 | 0.11859489 | 5.48967723 | ATL | ||
New data | n/a | GeoB1715-3 | Coretop | -4095.0 | 0.0 | -26.47 | 11.638333 | Orbulina universa | 300-350 | 9.55957278 | Symbiont Spinose | 230.0 | 35.321 | 17.708 | 0.78272045 | 20.33793763 | ATL | ||
New data | n/a | GeoB5133-3 | Coretop | -3660.0 | 0.0 | -19.086667 | -10.191667 | Orbulina universa | 300-350 | 14.10622559 | Symbiont Spinose | 272.0 | 36.485 | 25.239 | 0.14133149 | 11.79093097 | ATL | ||
New data | n/a | GeoB1034-1 | Coretop | -3731.0 | 0.0 | -21.721667 | 5.43 | Orbulina universa | 300-350 | 14.40238622 | Symbiont Spinose | 244.0 | 35.657 | 21.168 | 0.45894185 | 15.21271955 | ATL | ||
New data | n/a | GeoB3810-2 | Coretop | -3810.0 | 0.0 | -31.133333 | -16.838333 | Orbulina universa | 300-350 | 16.37322718 | Symbiont Spinose | 237.0 | 35.867 | 16.03 | 0.11681119 | 5.397742 | ATL | ||
New data | n/a | GeoB3807-1 | Coretop | -2515.0 | 0.0 | -30.75 | -13.198333 | Orbulina universa | 300-350 | 13.09396135 | Symbiont Spinose | 238.0 | 35.75 | 16.445 | 0.12498948 | 5.67264728 | ATL | ||
New data | n/a | GeoB5121-2 | Coretop | -3486.0 | 0.0 | -24.183333 | -12.021667 | Orbulina universa | 300-350 | 14.06681806 | Symbiont Spinose | 281.0 | 36.784 | 24.943 | 0.1505637 | 8.18880946 | ATL | ||
New data | n/a | GeoB6011-2 | Coretop | -993.0 | 0.0 | 30.315 | -10.2883 | Orbulina universa | 300-350 | 17.59571317 | Symbiont Spinose | 245.0 | 35.94 | 19.852 | 0.11995584 | 20.86115905 | ATL | ||
New data | n/a | GeoB3915-1 | Coretop | -3127.0 | 0.0 | -2.28 | -38.015 | Orbulina universa | 300-350 | 8.20829909 | Symbiont Spinose | 283.0 | 36.302 | 26.709 | 0.07534127 | 9.30299802 | ATL | ||
New data | n/a | GeoB5142-2 | Coretop | -3946.0 | 0.0 | -19.088333 | -17.145 | Orbulina universa | 300-350 | 14.57615779 | Symbiont Spinose | 283.0 | 36.853 | 25.772 | 0.11648273 | 7.53303942 | ATL | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | P71 | Coretop | -125.0 | 0.0 | -33.86 | 174.69 | Globigerina bulloides | 300-350 | 8.2670625 | Non-Symbiont Spinose | 251.0 | 35.666 | 19.569 | 0.17908345 | 12.52544669 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | P81 | Coretop | -125.0 | 0.0 | -34.02 | 173.51 | Globigerina bulloides | 300-350 | 7.48368212 | Non-Symbiont Spinose | 243.0 | 35.573 | 18.213 | 0.1829129 | 12.71518356 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | S793 | Coretop | -125.0 | 0.0 | -36.32 | 176.8 | Globigerina bulloides | 300-350 | 5.36728677 | Non-Symbiont Spinose | 243.0 | 35.617 | 17.755 | 0.19130388 | 12.91789944 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | P69 | Coretop | -75.0 | 0.0 | -40.4 | 178.0 | Globigerina bulloides | 300-350 | 6.47664407 | Non-Symbiont Spinose | 227.0 | 35.327 | 14.489 | 0.26215788 | 13.28899943 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | S938 | Coretop | -75.0 | 0.0 | -40.03 | 180.0 | Globigerina bulloides | 300-350 | 6.05205018 | Non-Symbiont Spinose | 224.0 | 35.342 | 14.079 | 0.24847013 | 15.34149425 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | R623 | Coretop | -125.0 | 0.0 | -43.2 | -174.0 | Globigerina bulloides | 300-350 | 8.63744025 | Non-Symbiont Spinose | 201.0 | 34.682 | 12.596 | 0.37154336 | 14.14411848 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | Q220 | Coretop | -125.0 | 0.0 | -44.29 | 174.98 | Globigerina bulloides | 300-350 | 12.66621795 | Non-Symbiont Spinose | 194.0 | 34.474 | 11.381 | 0.5018871 | 15.45372284 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | F111 | Coretop | -125.0 | 0.0 | -48.95 | 174.98 | Globigerina bulloides | 300-350 | 16.45529412 | Non-Symbiont Spinose | 179.0 | 34.296 | 9.734 | 1.08752872 | 9.94353835 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | D178 | Coretop | -125.0 | 0.0 | -51.72 | 169.83 | Globigerina bulloides | 300-350 | 13.98539043 | Non-Symbiont Spinose | 168.0 | 34.41 | 8.58 | 1.16886253 | 7.58515152 | PAC | ||
Marr | Ecological and temperature controls on Mg/Ca ratios of Globigerina bulloides from the southwest Pacific Ocean | B32 | Coretop | -125.0 | 0.0 | -53.63 | 169.87 | Globigerina bulloides | 300-350 | 15.48742015 | Non-Symbiont Spinose | 165.0 | 34.322 | 7.949 | 1.1860309 | 7.16784887 | PAC | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR19_9 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 19.69866667 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR19_12 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 21.51735849 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR20_9 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 18.22248588 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR20_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 18.62649351 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR22_1 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 21.47114754 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR22_4 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 19.00236025 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR22_9 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 17.5035443 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR22_12 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 18.83421384 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR23_2 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 20.08977273 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR23_7 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 20.41916084 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR23_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 22.21753623 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR24_4 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 19.96311688 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR25_1 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 17.32136126 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR25_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Globigerinoides ruber | 355-650 | 20.46796117 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR18_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 38.87776157 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR19_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 42.27307692 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR20_9 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 36.26124758 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR20_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 35.8460499 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR21_8 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 37.22536825 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR22_1 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 40.73546585 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR22_13 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 36.84858974 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR23_2 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 45.25434867 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR23_7 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 41.57842576 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR23_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 41.58191181 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR25_2 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 40.93362832 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR25_8 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 43.01927335 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Marshall | Planktonic foraminiferal area density as a proxy for carbonate ion concentration: A calibration study using the Cariaco Basin ocean time series | CAR25_11 | Sediment trap | 410 | 150 | 10.5 | -65.51667 | Trilobatus sacculifer | 425-850 | 41.35846154 | Symbiont Spinose | 221.0 | 33.551 | 28.11 | 0.10706841 | 18.28400756 | ATL | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS1 | Coretop | -3778.0 | 0.0 | 15.51667 | 134.96667 | Trilobatus sacculifer | 350-400 | 25.48556007 | Symbiont Spinose | 283.0 | 34.458 | 27.843 | 0.02550518 | 3.23964463 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS2 | Coretop | -3364.0 | 0.0 | 15.45 | 135.05 | Trilobatus sacculifer | 350-400 | 30.07198209 | Symbiont Spinose | 283.0 | 34.624 | 28.039 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS3 | Coretop | -3262.0 | 0.0 | 15.08333 | 134.53333 | Trilobatus sacculifer | 350-400 | 31.37095951 | Symbiont Spinose | 283.0 | 34.625 | 27.843 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS4 | Coretop | -3052.0 | 0.0 | 14.78333 | 134.53333 | Trilobatus sacculifer | 350-400 | 32.71254723 | Symbiont Spinose | 281.0 | 34.616 | 27.754 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS6 | Coretop | -2632.0 | 0.0 | 13.45 | 134.78333 | Trilobatus sacculifer | 350-400 | 35.72550452 | Symbiont Spinose | 279.0 | 34.541 | 27.718 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS7 | Coretop | -3420.0 | 0.0 | 13.15 | 135.95 | Trilobatus sacculifer | 350-400 | 30.57560198 | Symbiont Spinose | 279.0 | 34.541 | 27.963 | 0.02658917 | 3.77393162 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS8 | Coretop | -3920.0 | 0.0 | 13.13333 | 135.43333 | Trilobatus sacculifer | 350-400 | 27.43380383 | Symbiont Spinose | 279.0 | 34.317 | 27.963 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS9 | Coretop | -3680.0 | 0.0 | 13.36667 | 134.98333 | Trilobatus sacculifer | 350-400 | 30.68207424 | Symbiont Spinose | 279.0 | 36.296 | 27.718 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS10 | Coretop | -3556.0 | 0.0 | 12.91667 | 135.4 | Trilobatus sacculifer | 350-400 | 30.45843312 | Symbiont Spinose | 277.0 | 34.429 | 28.071 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS2 | Coretop | -3364.0 | 0.0 | 15.45 | 135.05 | Neogloboquadrina dutertrei | 350-400 | 32.34399465 | Faculative Non-Spinose | 283.0 | 34.624 | 28.039 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS3 | Coretop | -3262.0 | 0.0 | 15.08333 | 134.53333 | Neogloboquadrina dutertrei | 350-400 | 34.69530101 | Faculative Non-Spinose | 283.0 | 34.625 | 27.843 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS4 | Coretop | -3052.0 | 0.0 | 14.78333 | 134.53333 | Neogloboquadrina dutertrei | 350-400 | 33.53375753 | Faculative Non-Spinose | 281.0 | 34.616 | 27.754 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS6 | Coretop | -2632.0 | 0.0 | 13.45 | 134.78333 | Neogloboquadrina dutertrei | 350-400 | 38.0852467 | Faculative Non-Spinose | 279.0 | 34.541 | 27.718 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS7 | Coretop | -3420.0 | 0.0 | 13.15 | 135.95 | Neogloboquadrina dutertrei | 350-400 | 34.35184104 | Faculative Non-Spinose | 279.0 | 34.541 | 27.963 | 0.02658917 | 3.77393162 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS8 | Coretop | -3920.0 | 0.0 | 13.13333 | 135.43333 | Neogloboquadrina dutertrei | 350-400 | 29.41758642 | Faculative Non-Spinose | 279.0 | 34.317 | 27.963 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS9 | Coretop | -3680.0 | 0.0 | 13.36667 | 134.98333 | Neogloboquadrina dutertrei | 350-400 | 32.20535998 | Faculative Non-Spinose | 279.0 | 36.296 | 27.718 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS10 | Coretop | -3556.0 | 0.0 | 12.91667 | 135.4 | Neogloboquadrina dutertrei | 350-400 | 33.24772454 | Faculative Non-Spinose | 277.0 | 34.429 | 28.071 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS1 | Coretop | -3778.0 | 0.0 | 15.51667 | 134.96667 | Pulleniatina obliquiloculata | 350-400 | 38.02988915 | Faculative Non-Spinose | 283.0 | 34.458 | 27.843 | 0.02550518 | 3.23964463 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS2 | Coretop | -3364.0 | 0.0 | 15.45 | 135.05 | Pulleniatina obliquiloculata | 350-400 | 41.85738817 | Faculative Non-Spinose | 283.0 | 34.624 | 28.039 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS3 | Coretop | -3262.0 | 0.0 | 15.08333 | 134.53333 | Pulleniatina obliquiloculata | 350-400 | 42.47992542 | Faculative Non-Spinose | 283.0 | 34.625 | 27.843 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS4 | Coretop | -3052.0 | 0.0 | 14.78333 | 134.53333 | Pulleniatina obliquiloculata | 350-400 | 37.63114608 | Faculative Non-Spinose | 281.0 | 34.616 | 27.754 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS5 | Coretop | -3924.0 | 0.0 | 13.98333 | 134.96667 | Pulleniatina obliquiloculata | 350-400 | 32.875 | Faculative Non-Spinose | 281.0 | 34.616 | 27.754 | 0.02584209 | 3.25385618 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS6 | Coretop | -2632.0 | 0.0 | 13.45 | 134.78333 | Pulleniatina obliquiloculata | 350-400 | 44.36750177 | Faculative Non-Spinose | 279.0 | 34.541 | 27.718 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS7 | Coretop | -3420.0 | 0.0 | 13.15 | 135.95 | Pulleniatina obliquiloculata | 350-400 | 39.40509606 | Faculative Non-Spinose | 279.0 | 34.541 | 27.963 | 0.02658917 | 3.77393162 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS8 | Coretop | -3920.0 | 0.0 | 13.13333 | 135.43333 | Pulleniatina obliquiloculata | 350-400 | 37.50433088 | Faculative Non-Spinose | 279.0 | 34.317 | 27.963 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS9 | Coretop | -3680.0 | 0.0 | 13.36667 | 134.98333 | Pulleniatina obliquiloculata | 350-400 | 38.23693167 | Faculative Non-Spinose | 279.0 | 36.296 | 27.718 | 0.02663818 | 3.78781358 | PAC | ||
Qin | Deepwater carbonate ion concentrations in the western tropical Pacific since 250?ka: Evidence for oceanic carbon storage and global climate influence | SS10 | Coretop | -3556.0 | 0.0 | 12.91667 | 135.4 | Pulleniatina obliquiloculata | 350-400 | 35.46759093 | Faculative Non-Spinose | 277.0 | 34.429 | 28.071 | 0.02663818 | 3.78781358 | PAC | ||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-02 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 4.42634669 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-03 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 4.59693573 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-04 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 4.85525154 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-05 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 3.90849268 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-06 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 4.3930466 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-07 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 3.88632047 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-08 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 3.37377989 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-09 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 2.97715039 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-10 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 5.48095908 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-11 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 5.8056513 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-13 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 4.54021095 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-14 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 2.9404503 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-15 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 4.46586268 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-16 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 5.07415195 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-17 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 3.53249616 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-18 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerina bulloides | 200-300 | 3.69835589 | Non-Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-02 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 7.75114063 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-03 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 7.04322013 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-04 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 8.62089612 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-05 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 4.14770344 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-06 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 7.83510209 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-07 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 6.33946655 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-08 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 7.9994061 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-09 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 9.08629523 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-10 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 7.46698974 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-11 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 7.59307778 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-12 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 6.61020943 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-13 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 4.81325814 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-14 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 2.71948188 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-15 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 5.67825959 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-16 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 5.37101295 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-17 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 6.66450555 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-18 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides elongatus | 200-250 | 4.89296572 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-02 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 5.0933734 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-03 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 5.18486218 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-04 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 5.16536907 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-05 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 4.18168237 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-06 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 4.31439194 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-08 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 4.37264489 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-09 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 7.46308181 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-10 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 5.20093537 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-11 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 5.87587498 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-12 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 4.85115692 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-13 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 3.94797529 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-14 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 2.42259693 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-15 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 3.97394246 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-16 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 3.9321868 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-17 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 4.70633317 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Weinkauf | Seasonal Variation in Shell Calcification of Planktonic Foraminifera in the NE Atlantic Reveals Species-Specific Response to Temperature, Productivity, and Optimum Growth Conditions. | 276-22-18 | Sediment trap | 2000 | 33.0 | -22.0 | Globigerinoides ruber | 200-250 | 4.38687311 | Symbiont Spinose | 218.0 | 36.492 | 19.843 | 0.09148754 | 7.02221006 | ATL | |||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.015 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 15.99 | Symbiont Spinose | 202.7134087 | 40.08920612 | 20.65221338 | 0.04606142 | 9.01755643 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.035 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.61 | Symbiont Spinose | 206.889648 | 39.94776637 | 20.31347344 | 0.05127673 | 8.74687145 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.055 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 16.17 | Symbiont Spinose | 212.2988583 | 39.96925869 | 19.9323592 | 0.0637929 | 9.29267924 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.075 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 15.78 | Symbiont Spinose | 216.5281994 | 40.02250652 | 19.60085628 | 0.05723632 | 9.55380388 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.095 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 14.91 | Symbiont Spinose | 216.5281994 | 40.02250652 | 19.60085628 | 0.05723632 | 9.55380388 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.115 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.68 | Symbiont Spinose | 221.1132024 | 39.93988326 | 19.54987013 | 0.05878456 | 9.20974529 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.135 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.79 | Symbiont Spinose | 222.8535809 | 39.956018 | 19.34209782 | 0.05547644 | 9.30448141 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.155 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.32 | Symbiont Spinose | 224.8892888 | 39.9190965 | 19.82054704 | 0.05390925 | 8.45555925 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.175 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 16.74 | Symbiont Spinose | 224.8892888 | 39.9190965 | 19.82054704 | 0.05390925 | 8.45555925 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.195 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 18.61 | Symbiont Spinose | 228.7388932 | 40.07091093 | 19.94982794 | 0.0554158 | 9.54403705 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.215 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.51 | Symbiont Spinose | 230.0449227 | 40.07280951 | 19.88745685 | 0.05602869 | 9.84607246 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.235 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 18.78 | Symbiont Spinose | 233.1158681 | 40.06877686 | 19.90695542 | 0.05623492 | 8.42599864 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.255 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 19.56 | Symbiont Spinose | 234.2824555 | 39.96992378 | 19.84711401 | 0.0667098 | 9.67344495 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.275 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 19.96 | Symbiont Spinose | 235.5869099 | 40.13205674 | 19.71863167 | 0.06060983 | 9.76196693 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.295 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 18.01 | Symbiont Spinose | 237.3533007 | 40.0441534 | 20.07351573 | 0.06671972 | 8.95196347 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.315 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 19.4 | Symbiont Spinose | 237.0102674 | 39.98271503 | 19.7638833 | 0.05488042 | 8.27143056 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.335 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 20.1 | Symbiont Spinose | 238.3020849 | 40.0175484 | 19.7944488 | 0.05281774 | 9.4498828 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.355 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 18.29 | Symbiont Spinose | 239.0889112 | 40.0532896 | 19.71844238 | 0.0591671 | 9.32870515 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.375 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.68 | Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.395 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 18.56 | Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.415 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 19.44 | Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.435 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 19.02 | Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.455 | 37.71 | 12.40553 | Globigerinoides elongatus | 250-300 | 17.97 | Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.015 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.06 | Non-Symbiont Spinose | 202.7134087 | 40.08920612 | 20.65221338 | 0.04606142 | 9.01755643 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.035 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.12 | Non-Symbiont Spinose | 206.889648 | 39.94776637 | 20.31347344 | 0.05127673 | 8.74687145 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.055 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.21 | Non-Symbiont Spinose | 212.2988583 | 39.96925869 | 19.9323592 | 0.0637929 | 9.29267924 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.075 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.22 | Non-Symbiont Spinose | 216.5281994 | 40.02250652 | 19.60085628 | 0.05723632 | 9.55380388 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.095 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.48 | Non-Symbiont Spinose | 216.5281994 | 40.02250652 | 19.60085628 | 0.05723632 | 9.55380388 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.115 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 8.25 | Non-Symbiont Spinose | 221.1132024 | 39.93988326 | 19.54987013 | 0.05878456 | 9.20974529 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.135 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.63 | Non-Symbiont Spinose | 222.8535809 | 39.956018 | 19.34209782 | 0.05547644 | 9.30448141 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.155 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.73 | Non-Symbiont Spinose | 224.8892888 | 39.9190965 | 19.82054704 | 0.05390925 | 8.45555925 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.175 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.55 | Non-Symbiont Spinose | 224.8892888 | 39.9190965 | 19.82054704 | 0.05390925 | 8.45555925 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.195 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.46 | Non-Symbiont Spinose | 228.7388932 | 40.07091093 | 19.94982794 | 0.0554158 | 9.54403705 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.215 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.15 | Non-Symbiont Spinose | 230.0449227 | 40.07280951 | 19.88745685 | 0.05602869 | 9.84607246 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.235 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.43 | Non-Symbiont Spinose | 233.1158681 | 40.06877686 | 19.90695542 | 0.05623492 | 8.42599864 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.255 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.98 | Non-Symbiont Spinose | 234.2824555 | 39.96992378 | 19.84711401 | 0.0667098 | 9.67344495 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.275 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 12.38 | Non-Symbiont Spinose | 235.5869099 | 40.13205674 | 19.71863167 | 0.06060983 | 9.76196693 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.295 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 12.8 | Non-Symbiont Spinose | 237.3533007 | 40.0441534 | 20.07351573 | 0.06671972 | 8.95196347 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.315 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.74 | Non-Symbiont Spinose | 237.0102674 | 39.98271503 | 19.7638833 | 0.05488042 | 8.27143056 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.335 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.52 | Non-Symbiont Spinose | 238.3020849 | 40.0175484 | 19.7944488 | 0.05281774 | 9.4498828 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.355 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.43 | Non-Symbiont Spinose | 239.0889112 | 40.0532896 | 19.71844238 | 0.0591671 | 9.32870515 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.375 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.32 | Non-Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.395 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 10.67 | Non-Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.415 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.68 | Non-Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.435 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.86 | Non-Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S7-c2 | Sediment core | -281.1 | 0.455 | 37.71 | 12.40553 | Globigerina bulloides | 250-300 | 11.8 | Non-Symbiont Spinose | 240.9832926 | 40.06080036 | 20.04472184 | 0.06293916 | 9.24051747 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.005 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 12.95 | Symbiont Spinose | 213.39338 | 36.74427916 | 20.8868199 | 0.52081497 | 6.2358038 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.015 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 11.34 | Symbiont Spinose | 226.774422 | 36.69117343 | 19.9918723 | 0.55146011 | 4.76298212 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.025 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 11.44 | Symbiont Spinose | 231.6704544 | 36.68367456 | 20.03003027 | 0.55728952 | 4.54881055 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.035 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 13.75 | Symbiont Spinose | 233.1795041 | 36.6234712 | 19.74596901 | 0.57009373 | 4.45350616 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.045 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 13.23 | Symbiont Spinose | 234.9870164 | 36.64935964 | 20.24643857 | 0.54091367 | 5.70260702 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.055 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 13.3 | Symbiont Spinose | 235.5304769 | 36.62997157 | 20.19512001 | 0.55697663 | 5.51723259 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.065 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.75 | Symbiont Spinose | 242.2665058 | 36.70662696 | 20.2638135 | 0.54378772 | 4.85030934 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.075 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 12.63 | Symbiont Spinose | 245.6989018 | 36.70572513 | 19.9248719 | 0.54184955 | 5.21004112 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.085 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.43 | Symbiont Spinose | 250.4106644 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.095 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.9 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.105 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 16.02 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.115 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 15.0 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.125 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 13.97 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.135 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 15.85 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.145 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.02 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.155 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.84 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.165 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.85 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.175 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 15.81 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.185 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 16.14 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.195 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.14 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.205 | 36.07 | -4.1104 | Globigerinoides elongatus | 250-300 | 14.69 | Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.005 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 6.82 | Non-Symbiont Spinose | 217.0039723 | 36.6650624 | 20.42393035 | 0.53094412 | 4.68410553 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.015 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 8.66 | Non-Symbiont Spinose | 226.774422 | 36.69117343 | 19.9918723 | 0.55146011 | 4.76298212 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.025 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 8.03 | Non-Symbiont Spinose | 231.6704544 | 36.68367456 | 20.03003027 | 0.55728952 | 4.54881055 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.035 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 8.99 | Non-Symbiont Spinose | 233.1795041 | 36.6234712 | 19.74596901 | 0.57009373 | 4.45350616 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.045 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 9.79 | Non-Symbiont Spinose | 234.9870164 | 36.64935964 | 20.24643857 | 0.54091367 | 5.70260702 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.055 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 10.33 | Non-Symbiont Spinose | 238.0483328 | 36.82029893 | 20.3634435 | 0.54085748 | 5.45941156 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.065 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 9.49 | Non-Symbiont Spinose | 242.2665058 | 36.70662696 | 20.2638135 | 0.54378772 | 4.85030934 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.075 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 10.13 | Non-Symbiont Spinose | 245.6989018 | 36.70572513 | 19.9248719 | 0.54184955 | 5.21004112 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.085 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 8.55 | Non-Symbiont Spinose | 250.4106644 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.105 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 9.91 | Non-Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.125 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 9.16 | Non-Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.145 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 8.16 | Non-Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.165 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 9.22 | Non-Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.185 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 10.41 | Non-Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S3-c1 | Sediment core | -1136.7 | 0.205 | 36.07 | -4.1104 | Globigerina bulloides | 250-300 | 6.97 | Non-Symbiont Spinose | 257.0370059 | 36.9554512 | 20.52603283 | 0.53628372 | 5.54630069 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0075 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 14.75 | Symbiont Spinose | 204.6987135 | 38.68494463 | 19.4346771 | 0.05818551 | 12.44709909 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0125 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 13.39 | Symbiont Spinose | 204.6987135 | 38.68494463 | 19.4346771 | 0.05818551 | 12.44709909 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0175 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.88 | Symbiont Spinose | 204.6987135 | 38.68494463 | 19.4346771 | 0.05818551 | 12.44709909 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0225 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 14.02 | Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0275 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 11.88 | Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0325 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 11.3 | Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0375 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 15.3 | Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0475 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 15.45 | Symbiont Spinose | 213.5793918 | 38.71561708 | 18.79052723 | 0.07278427 | 12.38351766 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0525 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.77 | Symbiont Spinose | 217.9495112 | 38.66455288 | 18.75944935 | 0.07089518 | 12.31929687 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0575 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.56 | Symbiont Spinose | 217.9495112 | 38.66455288 | 18.75944935 | 0.07089518 | 12.31929687 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0625 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 20.02 | Symbiont Spinose | 217.9495112 | 38.66455288 | 18.75944935 | 0.07089518 | 12.31929687 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0675 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.51 | Symbiont Spinose | 219.2311111 | 38.66861111 | 18.47377868 | 0.07253906 | 12.10316258 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0725 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.56 | Symbiont Spinose | 219.2311111 | 38.66861111 | 18.47377868 | 0.07253906 | 12.10316258 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0775 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.82 | Symbiont Spinose | 221.3187171 | 38.60893707 | 18.92916968 | 0.06069644 | 11.06126988 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0825 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.13 | Symbiont Spinose | 221.3187171 | 38.60893707 | 18.92916968 | 0.06069644 | 11.06126988 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0875 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.82 | Symbiont Spinose | 221.3187171 | 38.60893707 | 18.92916968 | 0.06069644 | 11.06126988 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0925 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 20.21 | Symbiont Spinose | 223.6588365 | 38.69211197 | 18.98112578 | 0.06234491 | 11.30676786 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0975 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.55 | Symbiont Spinose | 223.6588365 | 38.69211197 | 18.98112578 | 0.06234491 | 11.30676786 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1025 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.03 | Symbiont Spinose | 225.6597418 | 38.78335304 | 19.1169029 | 0.05541583 | 11.39833142 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1075 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.68 | Symbiont Spinose | 225.6597418 | 38.78335304 | 19.1169029 | 0.05541583 | 11.39833142 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1125 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.3 | Symbiont Spinose | 227.2949945 | 38.75101487 | 18.80541803 | 0.05791055 | 11.16398105 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1175 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.71 | Symbiont Spinose | 227.2949945 | 38.75101487 | 18.80541803 | 0.05791055 | 11.16398105 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1225 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.23 | Symbiont Spinose | 229.8537831 | 38.65446501 | 19.00579304 | 0.06336623 | 11.83586804 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1275 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.78 | Symbiont Spinose | 233.6457163 | 38.74484259 | 19.16467861 | 0.06713797 | 10.66250167 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1325 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.68 | Symbiont Spinose | 231.9838271 | 38.6594924 | 18.81594992 | 0.05648476 | 11.10427295 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1375 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.28 | Symbiont Spinose | 234.7487065 | 38.76315991 | 18.81420882 | 0.05514138 | 10.97801375 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1425 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.1 | Symbiont Spinose | 237.3611608 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1475 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 20.73 | Symbiont Spinose | 237.3611608 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1525 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.69 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1575 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.01 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1625 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.58 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1675 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.73 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1725 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.28 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1775 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 20.2 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1825 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.26 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1875 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.54 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1925 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.95 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1975 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.21 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2025 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 15.92 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2075 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.22 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2125 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.81 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2175 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.15 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2225 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.25 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2275 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.06 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2325 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.42 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2375 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.39 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2425 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.55 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2475 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.75 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2525 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 15.23 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2575 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.3 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2625 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.23 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2675 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.49 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2725 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.31 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2775 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.3 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2825 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.03 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2875 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.96 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2925 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.93 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3025 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.09 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3075 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.4 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3125 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.98 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3175 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.82 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3225 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.76 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3275 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.89 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3325 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.03 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3375 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.5 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3425 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 16.81 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3475 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.73 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3525 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.69 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3575 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.63 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3625 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 18.3 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3675 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 17.95 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3775 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 20.6 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3825 | 41.11 | 2.382 | Globigerinoides elongatus | 250-300 | 19.14 | Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0025 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.03 | Non-Symbiont Spinose | 200.2370002 | 38.74871995 | 19.78039633 | 0.05638773 | 12.67550814 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0075 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.13 | Non-Symbiont Spinose | 204.6987135 | 38.68494463 | 19.4346771 | 0.05818551 | 12.44709909 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0125 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.48 | Non-Symbiont Spinose | 204.6987135 | 38.68494463 | 19.4346771 | 0.05818551 | 12.44709909 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0175 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.57 | Non-Symbiont Spinose | 204.6987135 | 38.68494463 | 19.4346771 | 0.05818551 | 12.44709909 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0225 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.34 | Non-Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0275 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.89 | Non-Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0325 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 14.01 | Non-Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0375 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.42 | Non-Symbiont Spinose | 210.4097736 | 38.72236716 | 19.04954716 | 0.06912181 | 12.18184858 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0425 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.82 | Non-Symbiont Spinose | 213.5793918 | 38.71561708 | 18.79052723 | 0.07278427 | 12.38351766 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0475 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.77 | Non-Symbiont Spinose | 213.5793918 | 38.71561708 | 18.79052723 | 0.07278427 | 12.38351766 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0525 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.11 | Non-Symbiont Spinose | 217.9495112 | 38.66455288 | 18.75944935 | 0.07089518 | 12.31929687 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0575 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.33 | Non-Symbiont Spinose | 217.9495112 | 38.66455288 | 18.75944935 | 0.07089518 | 12.31929687 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0625 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.45 | Non-Symbiont Spinose | 217.9495112 | 38.66455288 | 18.75944935 | 0.07089518 | 12.31929687 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0675 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.41 | Non-Symbiont Spinose | 219.2311111 | 38.66861111 | 18.47377868 | 0.07253906 | 12.10316258 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0725 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.14 | Non-Symbiont Spinose | 219.2311111 | 38.66861111 | 18.47377868 | 0.07253906 | 12.10316258 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0775 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.85 | Non-Symbiont Spinose | 221.3187171 | 38.60893707 | 18.92916968 | 0.06069644 | 11.06126988 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0825 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.24 | Non-Symbiont Spinose | 221.3187171 | 38.60893707 | 18.92916968 | 0.06069644 | 11.06126988 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0875 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.06 | Non-Symbiont Spinose | 221.3187171 | 38.60893707 | 18.92916968 | 0.06069644 | 11.06126988 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0925 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.02 | Non-Symbiont Spinose | 223.6588365 | 38.69211197 | 18.98112578 | 0.06234491 | 11.30676786 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.0975 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.67 | Non-Symbiont Spinose | 223.6588365 | 38.69211197 | 18.98112578 | 0.06234491 | 11.30676786 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1025 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.8 | Non-Symbiont Spinose | 225.6597418 | 38.78335304 | 19.1169029 | 0.05541583 | 11.39833142 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1075 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.96 | Non-Symbiont Spinose | 225.6597418 | 38.78335304 | 19.1169029 | 0.05541583 | 11.39833142 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1125 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.09 | Non-Symbiont Spinose | 227.2949945 | 38.75101487 | 18.80541803 | 0.05791055 | 11.16398105 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1175 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.68 | Non-Symbiont Spinose | 227.2949945 | 38.75101487 | 18.80541803 | 0.05791055 | 11.16398105 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1225 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.89 | Non-Symbiont Spinose | 229.8537831 | 38.65446501 | 19.00579304 | 0.06336623 | 11.83586804 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1275 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.72 | Non-Symbiont Spinose | 233.6457163 | 38.74484259 | 19.16467861 | 0.06713797 | 10.66250167 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1325 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.93 | Non-Symbiont Spinose | 231.9838271 | 38.6594924 | 18.81594992 | 0.05648476 | 11.10427295 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1375 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.39 | Non-Symbiont Spinose | 234.7487065 | 38.76315991 | 18.81420882 | 0.05514138 | 10.97801375 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1425 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.46 | Non-Symbiont Spinose | 237.3611608 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1475 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.42 | Non-Symbiont Spinose | 237.3611608 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1525 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.58 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.1775 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.98 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2025 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.15 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2225 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 13.49 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2425 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.1 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2625 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 11.89 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.2825 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 13.08 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3075 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 13.37 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3575 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 12.57 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED | ||
Pallack | Anthropogenic acidification of surface waters drives decreased biogenic calcification in the Mediterranean Sea | MedSeA-S23-c1 | Sediment core | -1156.0 | 0.3825 | 41.11 | 2.382 | Globigerina bulloides | 250-300 | 10.79 | Non-Symbiont Spinose | 243.7738889 | 38.83550491 | 19.26721975 | 0.06881365 | 10.97672288 | MED |