Articles | Volume 13, issue 1
https://doi.org/10.5194/bg-13-211-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Special issue:
https://doi.org/10.5194/bg-13-211-2016
© Author(s) 2016. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
15 Jan 2016
Research article |
| 15 Jan 2016
Millennial changes in North Atlantic oxygen concentrations
B. A. A. Hoogakker
CORRESPONDING AUTHOR
Department of Earth Sciences, University of Oxford, Oxford, OX1 3AN,
UK
D. J. R. Thornalley
Department of Geography, University College London, London, WC1E 6BT,
UK
S. Barker
School of Earth and Ocean Sciences, Cardiff University, Cardiff, CF10
3AT, UK
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B. A. A. Hoogakker, R. S. Smith, J. S. Singarayer, R. Marchant, I. C. Prentice, J. R. M. Allen, R. S. Anderson, S. A. Bhagwat, H. Behling, O. Borisova, M. Bush, A. Correa-Metrio, A. de Vernal, J. M. Finch, B. Fréchette, S. Lozano-Garcia, W. D. Gosling, W. Granoszewski, E. C. Grimm, E. Grüger, J. Hanselman, S. P. Harrison, T. R. Hill, B. Huntley, G. Jiménez-Moreno, P. Kershaw, M.-P. Ledru, D. Magri, M. McKenzie, U. Müller, T. Nakagawa, E. Novenko, D. Penny, L. Sadori, L. Scott, J. Stevenson, P. J. Valdes, M. Vandergoes, A. Velichko, C. Whitlock, and C. Tzedakis
Clim. Past, 12, 51–73, https://doi.org/10.5194/cp-12-51-2016, https://doi.org/10.5194/cp-12-51-2016, 2016
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In this paper we use two climate models to test how Earth’s vegetation responded to changes in climate over the last 120 000 years, looking at warm interglacial climates like today, cold ice-age glacial climates, and intermediate climates. The models agree well with observations from pollen, showing smaller forested areas and larger desert areas during cold periods. Forests store most terrestrial carbon; the terrestrial carbon lost during cold climates was most likely relocated to the oceans.
Nico Wunderling, Anna S. von der Heydt, Yevgeny Aksenov, Stephen Barker, Robbin Bastiaansen, Victor Brovkin, Maura Brunetti, Victor Couplet, Thomas Kleinen, Caroline H. Lear, Johannes Lohmann, Rosa Maria Roman-Cuesta, Sacha Sinet, Didier Swingedouw, Ricarda Winkelmann, Pallavi Anand, Jonathan Barichivich, Sebastian Bathiany, Mara Baudena, John T. Bruun, Cristiano M. Chiessi, Helen K. Coxall, David Docquier, Jonathan F. Donges, Swinda K. J. Falkena, Ann Kristin Klose, David Obura, Juan Rocha, Stefanie Rynders, Norman Julius Steinert, and Matteo Willeit
Earth Syst. Dynam., 15, 41–74, https://doi.org/10.5194/esd-15-41-2024, https://doi.org/10.5194/esd-15-41-2024, 2024
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This paper maps out the state-of-the-art literature on interactions between tipping elements relevant for current global warming pathways. We find indications that many of the interactions between tipping elements are destabilizing. This means that tipping cascades cannot be ruled out on centennial to millennial timescales at global warming levels between 1.5 and 2.0 °C or on shorter timescales if global warming surpasses 2.0 °C.
Nil Irvalı, Ulysses S. Ninnemann, Are Olsen, Neil L. Rose, David J. R. Thornalley, Tor L. Mjell, and François Counillon
EGUsphere, https://doi.org/10.5194/egusphere-2023-2845, https://doi.org/10.5194/egusphere-2023-2845, 2023
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Marine sediments are excellent archives for reconstructing past changes in climate and ocean circulation. Yet, dating uncertainties, particularly during the 20th century, pose major challenges. Here we propose a novel chronostratigraphic approach that uses anthropogenic signals, such as the oceanic 13C Suess effect and spheroidal carbonaceous fly ash particles, to reduce age model uncertainties in high-resolution marine archives over the 20th century.
Zhiyi Jiang, Chris Brierley, David Thornalley, and Sophie Sax
Clim. Past, 19, 107–121, https://doi.org/10.5194/cp-19-107-2023, https://doi.org/10.5194/cp-19-107-2023, 2023
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This work looks at a series of model simulations of two past warm climates. We focus on the deep overturning circulation in the Atlantic Ocean. We show that there are no robust changes in the overall strength of the circulation. We also show that the circulation hardly plays a role in changes in the surface climate across the globe.
Chris M. Brierley, Anni Zhao, Sandy P. Harrison, Pascale Braconnot, Charles J. R. Williams, David J. R. Thornalley, Xiaoxu Shi, Jean-Yves Peterschmitt, Rumi Ohgaito, Darrell S. Kaufman, Masa Kageyama, Julia C. Hargreaves, Michael P. Erb, Julien Emile-Geay, Roberta D'Agostino, Deepak Chandan, Matthieu Carré, Partrick J. Bartlein, Weipeng Zheng, Zhongshi Zhang, Qiong Zhang, Hu Yang, Evgeny M. Volodin, Robert A. Tomas, Cody Routson, W. Richard Peltier, Bette Otto-Bliesner, Polina A. Morozova, Nicholas P. McKay, Gerrit Lohmann, Allegra N. Legrande, Chuncheng Guo, Jian Cao, Esther Brady, James D. Annan, and Ayako Abe-Ouchi
Clim. Past, 16, 1847–1872, https://doi.org/10.5194/cp-16-1847-2020, https://doi.org/10.5194/cp-16-1847-2020, 2020
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This paper provides an initial exploration and comparison to climate reconstructions of the new climate model simulations of the mid-Holocene (6000 years ago). These use state-of-the-art models developed for CMIP6 and apply the same experimental set-up. The models capture several key aspects of the climate, but some persistent issues remain.
James A. Menking, Edward J. Brook, Sarah A. Shackleton, Jeffrey P. Severinghaus, Michael N. Dyonisius, Vasilii Petrenko, Joseph R. McConnell, Rachael H. Rhodes, Thomas K. Bauska, Daniel Baggenstos, Shaun Marcott, and Stephen Barker
Clim. Past, 15, 1537–1556, https://doi.org/10.5194/cp-15-1537-2019, https://doi.org/10.5194/cp-15-1537-2019, 2019
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An ice core from Taylor Glacier, Antarctica, spans a period ~ 70 000 years ago when Earth entered the last ice age. Chemical analyses of the ice and air bubbles allow for an independent determination of the ages of the ice and gas bubbles. The difference between the age of the ice and the bubbles at any given depth, called ∆age, is unusually high in the Taylor Glacier core compared to the Taylor Dome ice core situated to the south. This implies a dramatic accumulation gradient between the sites.
Jamie D. Wilson, Stephen Barker, Neil R. Edwards, Philip B. Holden, and Andy Ridgwell
Biogeosciences, 16, 2923–2936, https://doi.org/10.5194/bg-16-2923-2019, https://doi.org/10.5194/bg-16-2923-2019, 2019
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The remains of plankton rain down from the surface ocean to the deep ocean, acting to store CO2 in the deep ocean. We used a model of biology and ocean circulation to explore the importance of this process in different regions of the ocean. The amount of CO2 stored in the deep ocean is most sensitive to changes in the Southern Ocean. As plankton in the Southern Ocean are likely those most impacted by future climate change, the amount of CO2 they store in the deep ocean could also be affected.
B. A. A. Hoogakker, R. S. Smith, J. S. Singarayer, R. Marchant, I. C. Prentice, J. R. M. Allen, R. S. Anderson, S. A. Bhagwat, H. Behling, O. Borisova, M. Bush, A. Correa-Metrio, A. de Vernal, J. M. Finch, B. Fréchette, S. Lozano-Garcia, W. D. Gosling, W. Granoszewski, E. C. Grimm, E. Grüger, J. Hanselman, S. P. Harrison, T. R. Hill, B. Huntley, G. Jiménez-Moreno, P. Kershaw, M.-P. Ledru, D. Magri, M. McKenzie, U. Müller, T. Nakagawa, E. Novenko, D. Penny, L. Sadori, L. Scott, J. Stevenson, P. J. Valdes, M. Vandergoes, A. Velichko, C. Whitlock, and C. Tzedakis
Clim. Past, 12, 51–73, https://doi.org/10.5194/cp-12-51-2016, https://doi.org/10.5194/cp-12-51-2016, 2016
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In this paper we use two climate models to test how Earth’s vegetation responded to changes in climate over the last 120 000 years, looking at warm interglacial climates like today, cold ice-age glacial climates, and intermediate climates. The models agree well with observations from pollen, showing smaller forested areas and larger desert areas during cold periods. Forests store most terrestrial carbon; the terrestrial carbon lost during cold climates was most likely relocated to the oceans.
J. D. Wilson, A. Ridgwell, and S. Barker
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We explore whether ocean model transport rates, in the form of a transport matrix, can be used to estimate remineralisation rates from dissolved nutrient concentrations and infer vertical fluxes of particulate organic carbon. Estimated remineralisation rates are significantly sensitive to uncertainty in the observations and the modelled circulation. The remineralisation of dissolved organic matter is an additional source of uncertainty when inferring vertical fluxes from remineralisation rates.
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Biogeosciences, 19, 1195–1209, https://doi.org/10.5194/bg-19-1195-2022, https://doi.org/10.5194/bg-19-1195-2022, 2022
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Size measurements of the planktonic foraminifer Globorotalia menardii and related forms are used to investigate the shell-size evolution for the last 8 million years in the eastern tropical Atlantic Ocean. Long-term changes in the shell size coincide with major climatic, palaeogeographic and palaeoceanographic changes and suggest the occurrence of a new G. menardii type in the Atlantic Ocean ca. 2 million years ago.
Nele Manon Vollmar, Karl-Heinz Baumann, Mariem Saavedra-Pellitero, and Iván Hernández-Almeida
Biogeosciences, 19, 585–612, https://doi.org/10.5194/bg-19-585-2022, https://doi.org/10.5194/bg-19-585-2022, 2022
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Práxedes Muñoz, Lorena Rebolledo, Laurent Dezileau, Antonio Maldonado, Christoph Mayr, Paola Cárdenas, Carina B. Lange, Katherine Lalangui, Gloria Sanchez, Marco Salamanca, Karen Araya, Ignacio Jara, Gabriel Easton, and Marcel Ramos
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The cell size, degree of calcification and growth rates of coccolithophores impact their role in the carbon cycle and may also influence their adaptation to environmental change. Combining insights from culture experiments and the fossil record, we show that the selection for smaller cells over the past 15 Myr has been a common adaptive trait among different lineages. However, heavily calcified species maintained a more stable biogeochemical output than the ancestral lineage of E. huxleyi.
Niels J. de Winter, Clemens V. Ullmann, Anne M. Sørensen, Nicolas Thibault, Steven Goderis, Stijn J. M. Van Malderen, Christophe Snoeck, Stijn Goolaerts, Frank Vanhaecke, and Philippe Claeys
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Hannah M. Palmer, Tessa M. Hill, Peter D. Roopnarine, Sarah E. Myhre, Katherine R. Reyes, and Jonas T. Donnenfield
Biogeosciences, 17, 2923–2937, https://doi.org/10.5194/bg-17-2923-2020, https://doi.org/10.5194/bg-17-2923-2020, 2020
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Modern climate change is causing expansions of low-oxygen zones, with detrimental impacts to marine life. To better predict future ocean oxygen change, we study past expansions and contractions of low-oxygen zones using microfossils of seafloor organisms. We find that, along the San Diego margin, the low-oxygen zone expanded into more shallow water in the last 400 years, but the conditions within and below the low-oxygen zone did not change significantly in the last 1500 years.
Yuanyuan Hong, Moriaki Yasuhara, Hokuto Iwatani, and Briony Mamo
Biogeosciences, 16, 585–604, https://doi.org/10.5194/bg-16-585-2019, https://doi.org/10.5194/bg-16-585-2019, 2019
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This study analyzed microfaunal assemblages in surface sediments from 52 sites in Hong Kong marine waters. We selected 18 species for linear regression modeling to statistically reveal the relationship between species distribution and environmental factors. These results show environmental preferences of commonly distributed species on Asian coasts, providing a robust baseline for past environmental reconstruction of the broad Asian region using microfossils in sediment cores.
Jorge Domingo Carrillo-Briceño, Zoneibe Luz, Austin Hendy, László Kocsis, Orangel Aguilera, and Torsten Vennemann
Biogeosciences, 16, 33–56, https://doi.org/10.5194/bg-16-33-2019, https://doi.org/10.5194/bg-16-33-2019, 2019
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By combining taxonomy and geochemistry, we corroborated the described paleoenvironments from a Neogene fossiliferous deposit of South America. Shark teeth specimens were used for taxonomic identification and as proxies for geochemical analyses. With a multidisciplinary approach we refined the understanding about the paleoenvironmental setting and the paleoecological characteristics of the studied groups, in our case, for the bull shark and its incursions into brackish waters.
Anna Binczewska, Bjørg Risebrobakken, Irina Polovodova Asteman, Matthias Moros, Amandine Tisserand, Eystein Jansen, and Andrzej Witkowski
Biogeosciences, 15, 5909–5928, https://doi.org/10.5194/bg-15-5909-2018, https://doi.org/10.5194/bg-15-5909-2018, 2018
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Primary productivity is an important factor in the functioning and structuring of the coastal ecosystem. Thus, two sediment cores from the Skagerrak (North Sea) were investigated in order to obtain a comprehensive picture of primary productivity changes during the last millennium and identify associated forcing factors (e.g. anthropogenic, climate). The cores were dated and analysed for palaeoproductivity proxies and palaeothermometers.
Sami A. Jokinen, Joonas J. Virtasalo, Tom Jilbert, Jérôme Kaiser, Olaf Dellwig, Helge W. Arz, Jari Hänninen, Laura Arppe, Miia Collander, and Timo Saarinen
Biogeosciences, 15, 3975–4001, https://doi.org/10.5194/bg-15-3975-2018, https://doi.org/10.5194/bg-15-3975-2018, 2018
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Oxygen deficiency is a major environmental problem deteriorating seafloor habitats especially in the coastal ocean with large human impact. Here we apply a wide set of chemical and physical analyses to a 1500-year long sediment record and show that, although long-term climate variability has modulated seafloor oxygenation in the coastal northern Baltic Sea, the oxygen loss over the 20th century is unprecedentedly severe, emphasizing the need to reduce anthropogenic nutrient input in the future.
Saúl González-Lemos, José Guitián, Miguel-Ángel Fuertes, José-Abel Flores, and Heather M. Stoll
Biogeosciences, 15, 1079–1091, https://doi.org/10.5194/bg-15-1079-2018, https://doi.org/10.5194/bg-15-1079-2018, 2018
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Changes in atmospheric carbon dioxide affect ocean chemistry and the ability of marine organisms to manufacture shells from calcium carbonate. We describe a technique to obtain more reproducible measurements of the thickness of calcium carbonate shells made by microscopic marine algae called coccolithophores, which will allow researchers to compare how the shell thickness responds to variations in ocean chemistry in the past and present.
Ulrich Kotthoff, Jeroen Groeneveld, Jeanine L. Ash, Anne-Sophie Fanget, Nadine Quintana Krupinski, Odile Peyron, Anna Stepanova, Jonathan Warnock, Niels A. G. M. Van Helmond, Benjamin H. Passey, Ole Rønø Clausen, Ole Bennike, Elinor Andrén, Wojciech Granoszewski, Thomas Andrén, Helena L. Filipsson, Marit-Solveig Seidenkrantz, Caroline P. Slomp, and Thorsten Bauersachs
Biogeosciences, 14, 5607–5632, https://doi.org/10.5194/bg-14-5607-2017, https://doi.org/10.5194/bg-14-5607-2017, 2017
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We present reconstructions of paleotemperature, paleosalinity, and paleoecology from the Little Belt (Site M0059) over the past ~ 8000 years and evaluate the applicability of numerous proxies. Conditions were lacustrine until ~ 7400 cal yr BP. A transition to brackish–marine conditions then occurred within ~ 200 years. Salinity proxies rarely allowed quantitative estimates but revealed congruent results, while quantitative temperature reconstructions differed depending on the proxies used.
Shuichang Zhang, Xiaomei Wang, Huajian Wang, Emma U. Hammarlund, Jin Su, Yu Wang, and Donald E. Canfield
Biogeosciences, 14, 2133–2149, https://doi.org/10.5194/bg-14-2133-2017, https://doi.org/10.5194/bg-14-2133-2017, 2017
Liza M. Roger, Annette D. George, Jeremy Shaw, Robert D. Hart, Malcolm Roberts, Thomas Becker, Bradley J. McDonald, and Noreen J. Evans
Biogeosciences, 14, 1721–1737, https://doi.org/10.5194/bg-14-1721-2017, https://doi.org/10.5194/bg-14-1721-2017, 2017
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The shell compositions of bivalve species from south Western Australia are described here to better understand the factors involved in their formation. The shell composition can be used to reconstruct past environmental conditions, but certain species manifest an offset compared to the environmental parameters measured. As shown here, shells that experience the same conditions can present different compositions in relation to structure, organic composition and environmental conditions.
Johan Vellekoop, Lineke Woelders, Sanem Açikalin, Jan Smit, Bas van de Schootbrugge, Ismail Ö. Yilmaz, Henk Brinkhuis, and Robert P. Speijer
Biogeosciences, 14, 885–900, https://doi.org/10.5194/bg-14-885-2017, https://doi.org/10.5194/bg-14-885-2017, 2017
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The Cretaceous–Paleogene boundary, ~ 66 Ma, is characterized by a mass extinction. We studied groups of both surface-dwelling and bottom-dwelling organisms to unravel the oceanographic consequences of these extinctions. Our integrated records indicate that a reduction of the transport of organic matter to the sea floor resulted in enhanced recycling of nutrients in the upper water column and decreased food supply at the sea floor in the first tens of thousands of years after the extinctions.
Johan Renaudie
Biogeosciences, 13, 6003–6014, https://doi.org/10.5194/bg-13-6003-2016, https://doi.org/10.5194/bg-13-6003-2016, 2016
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Marine planktonic diatoms are today both the main silica and carbon exporter to the deep sea. However, 50 million years ago, radiolarians were the main silica exporter and diatoms were a rare, geographically restricted group. Quantification of their rise to dominance suggest that diatom abundance is primarily controlled by the continental weathering and has a negative feedback, observable on a geological timescale, on the carbon cycle.
Jelena Vidović, Rafał Nawrot, Ivo Gallmetzer, Alexandra Haselmair, Adam Tomašových, Michael Stachowitsch, Vlasta Ćosović, and Martin Zuschin
Biogeosciences, 13, 5965–5981, https://doi.org/10.5194/bg-13-5965-2016, https://doi.org/10.5194/bg-13-5965-2016, 2016
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We studied the ecological history of the Gulf of Trieste. Before the 20th century, the only activity here was ore mining, releasing high amounts of mercury into its northern part, Panzano Bay. Mercury did not cause changes to microorganisms, as it is not bioavailable. In the 20th century, agriculture caused nutrient enrichment in the bay and increased diversity of microorganisms. Industrial activities increased the concentrations of pollutants, causing only minor changes to microorganisms.
Aurélie Penaud, Frédérique Eynaud, Antje Helga Luise Voelker, and Jean-Louis Turon
Biogeosciences, 13, 5357–5377, https://doi.org/10.5194/bg-13-5357-2016, https://doi.org/10.5194/bg-13-5357-2016, 2016
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This paper presents new analyses conducted at high resolution in the Gulf of Cadiz over the last 50 ky. Palaeohydrological changes in these subtropical latitudes are discussed through dinoflagellate cyst assemblages but also dinocyst transfer function results, implying sea surface temperature and salinity as well as annual productivity reconstructions. This study is thus important for our understanding of past and future productivity regimes, also implying consequences on the biological pump.
William Hardy, Aurélie Penaud, Fabienne Marret, Germain Bayon, Tania Marsset, and Laurence Droz
Biogeosciences, 13, 4823–4841, https://doi.org/10.5194/bg-13-4823-2016, https://doi.org/10.5194/bg-13-4823-2016, 2016
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Our approach is based on a multi-proxy study from a core collected off the Congo River and discusses surface oceanic conditions (upwelling cells, river-induced upwelling), land–sea interactions and terrestrial erosion and in particular enables us to spatially constrain the migration of atmospheric systems. This paper thus presents new data highlighting, with the highest resolution ever reached in this region, the great correlation between phytoplanktonic organisms and monsoonal mechanisms.
Philippine Campagne, Xavier Crosta, Sabine Schmidt, Marie Noëlle Houssais, Olivier Ther, and Guillaume Massé
Biogeosciences, 13, 4205–4218, https://doi.org/10.5194/bg-13-4205-2016, https://doi.org/10.5194/bg-13-4205-2016, 2016
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Diatoms and biomarkers have been recently used for palaeoclimate reconstructions in the Southern Ocean. Few sediment-based ecological studies have investigated their relationships with environmental conditions. Here, we compare high-resolution sedimentary records with meteorological data to study relationships between our proxies and recent atmospheric and sea surface changes. Our results indicate that coupled wind pattern and sea surface variability act as the proximal forcing at that scale.
Niels A. G. M. van Helmond, Appy Sluijs, Nina M. Papadomanolaki, A. Guy Plint, Darren R. Gröcke, Martin A. Pearce, James S. Eldrett, João Trabucho-Alexandre, Ireneusz Walaszczyk, Bas van de Schootbrugge, and Henk Brinkhuis
Biogeosciences, 13, 2859–2872, https://doi.org/10.5194/bg-13-2859-2016, https://doi.org/10.5194/bg-13-2859-2016, 2016
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Over the past decades large changes have been observed in the biogeographical dispersion of marine life resulting from climate change. To better understand present and future trends it is important to document and fully understand the biogeographical response of marine life during episodes of environmental change in the geological past.
Here we investigate the response of phytoplankton, the base of the marine food web, to a rapid cold spell, interrupting greenhouse conditions during the Cretaceous.
Thomas C. Brachert, Markus Reuter, Stefan Krüger, Julia Kirkerowicz, and James S. Klaus
Biogeosciences, 13, 1469–1489, https://doi.org/10.5194/bg-13-1469-2016, https://doi.org/10.5194/bg-13-1469-2016, 2016
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We present stable isotope proxy data and calcification records from fossil reef corals. The corals investigated derive from the Florida carbonate platform and are of middle Pliocene to early Pleistocene age. From the data we infer an environment subject to intermittent upwelling on annual to decadal timescales. Calcification rates were enhanced during periods of upwelling. This is likely an effect of dampened SSTs during the upwelling.
M. Hermoso, I. Z. X. Chan, H. L. O. McClelland, A. M. C. Heureux, and R. E. M. Rickaby
Biogeosciences, 13, 301–312, https://doi.org/10.5194/bg-13-301-2016, https://doi.org/10.5194/bg-13-301-2016, 2016
B. Metcalfe, W. Feldmeijer, M. de Vringer-Picon, G.-J. A. Brummer, F. J. C. Peeters, and G. M. Ganssen
Biogeosciences, 12, 4781–4807, https://doi.org/10.5194/bg-12-4781-2015, https://doi.org/10.5194/bg-12-4781-2015, 2015
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Iron biogeochemical budgets during the natural ocean fertilisation experiment KEOPS-2 showed that complex circulation and transport pathways were responsible for differences in the mode and strength of iron supply, with vertical supply dominant on the plateau and lateral supply dominant in the plume. The exchange of iron between dissolved, biogenic and lithogenic pools was highly dynamic, resulting in a decoupling of iron supply and carbon export and controlling the efficiency of fertilisation.
J. P. D'Olivo, M. T. McCulloch, S. M. Eggins, and J. Trotter
Biogeosciences, 12, 1223–1236, https://doi.org/10.5194/bg-12-1223-2015, https://doi.org/10.5194/bg-12-1223-2015, 2015
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The boron isotope composition in the skeleton of massive Porites corals from the central Great Barrier Reef is used to reconstruct the seawater pH over the 1940-2009 period. The long-term decline in the coral-reconstructed seawater pH is in close agreement with estimates based on the CO2 uptake by surface waters due to rising atmospheric levels. We also observed a significant relationship between terrestrial runoff data and the inshore coral boron isotopes records.
J. Schönfeld, W. Kuhnt, Z. Erdem, S. Flögel, N. Glock, M. Aquit, M. Frank, and A. Holbourn
Biogeosciences, 12, 1169–1189, https://doi.org/10.5194/bg-12-1169-2015, https://doi.org/10.5194/bg-12-1169-2015, 2015
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Today’s oceans show distinct mid-depth oxygen minima while whole oceanic basins became transiently anoxic in the Mesozoic. To constrain past bottom-water oxygenation, we compared sediments from the Peruvian OMZ with the Cenomanian OAE 2 from Morocco. Corg accumulation rates in laminated OAE 2 sections match Holocene rates off Peru. Laminated deposits are found at oxygen levels of < 7µmol kg-1; crab burrows appear at 10µmol kg-1 today, both defining threshold values for palaeoreconstructions.
S. C. Löhr and M. J. Kennedy
Biogeosciences, 11, 4971–4983, https://doi.org/10.5194/bg-11-4971-2014, https://doi.org/10.5194/bg-11-4971-2014, 2014
R. Hoffmann, J. A. Schultz, R. Schellhorn, E. Rybacki, H. Keupp, S. R. Gerden, R. Lemanis, and S. Zachow
Biogeosciences, 11, 2721–2739, https://doi.org/10.5194/bg-11-2721-2014, https://doi.org/10.5194/bg-11-2721-2014, 2014
T. J. Algeo, P. A. Meyers, R. S. Robinson, H. Rowe, and G. Q. Jiang
Biogeosciences, 11, 1273–1295, https://doi.org/10.5194/bg-11-1273-2014, https://doi.org/10.5194/bg-11-1273-2014, 2014
C. Berger, K. J. S. Meier, H. Kinkel, and K.-H. Baumann
Biogeosciences, 11, 929–944, https://doi.org/10.5194/bg-11-929-2014, https://doi.org/10.5194/bg-11-929-2014, 2014
T. Caley, S. Zaragosi, J. Bourget, P. Martinez, B. Malaizé, F. Eynaud, L. Rossignol, T. Garlan, and N. Ellouz-Zimmermann
Biogeosciences, 10, 7347–7359, https://doi.org/10.5194/bg-10-7347-2013, https://doi.org/10.5194/bg-10-7347-2013, 2013
N. Preto, C. Agnini, M. Rigo, M. Sprovieri, and H. Westphal
Biogeosciences, 10, 6053–6068, https://doi.org/10.5194/bg-10-6053-2013, https://doi.org/10.5194/bg-10-6053-2013, 2013
I. Polovodova Asteman, K. Nordberg, and H. L. Filipsson
Biogeosciences, 10, 1275–1290, https://doi.org/10.5194/bg-10-1275-2013, https://doi.org/10.5194/bg-10-1275-2013, 2013
J.-E. Tesdal, E. D. Galbraith, and M. Kienast
Biogeosciences, 10, 101–118, https://doi.org/10.5194/bg-10-101-2013, https://doi.org/10.5194/bg-10-101-2013, 2013
L. Durantou, A. Rochon, D. Ledu, G. Massé, S. Schmidt, and M. Babin
Biogeosciences, 9, 5391–5406, https://doi.org/10.5194/bg-9-5391-2012, https://doi.org/10.5194/bg-9-5391-2012, 2012
C. A. Grove, J. Zinke, T. Scheufen, J. Maina, E. Epping, W. Boer, B. Randriamanantsoa, and G.-J. A. Brummer
Biogeosciences, 9, 3063–3081, https://doi.org/10.5194/bg-9-3063-2012, https://doi.org/10.5194/bg-9-3063-2012, 2012
D. Wall-Palmer, M. B. Hart, C. W. Smart, R. S. J. Sparks, A. Le Friant, G. Boudon, C. Deplus, and J. C. Komorowski
Biogeosciences, 9, 309–315, https://doi.org/10.5194/bg-9-309-2012, https://doi.org/10.5194/bg-9-309-2012, 2012
S. F. Rella and M. Uchida
Biogeosciences, 8, 3545–3553, https://doi.org/10.5194/bg-8-3545-2011, https://doi.org/10.5194/bg-8-3545-2011, 2011
M. C. Nash, U. Troitzsch, B. N. Opdyke, J. M. Trafford, B. D. Russell, and D. I. Kline
Biogeosciences, 8, 3331–3340, https://doi.org/10.5194/bg-8-3331-2011, https://doi.org/10.5194/bg-8-3331-2011, 2011
A. Penaud, F. Eynaud, A. Voelker, M. Kageyama, F. Marret, J. L. Turon, D. Blamart, T. Mulder, and L. Rossignol
Biogeosciences, 8, 2295–2316, https://doi.org/10.5194/bg-8-2295-2011, https://doi.org/10.5194/bg-8-2295-2011, 2011
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Short summary
Models predict a decrease in future ocean O2, driven by surface water warming and freshening in the polar regions, causing a reduction in ocean circulation. Here we assess this effect in the past, focussing on the response of deep and intermediate waters from the North Atlantic during large-scale ice rafting and millennial-scale cooling events of the last glacial.
Our assessment agrees with the models but also highlights the importance of biological processes driving ocean O2 change.
Models predict a decrease in future ocean O2, driven by surface water warming and freshening in...
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