Articles | Volume 10, issue 11
https://doi.org/10.5194/bg-10-7347-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-10-7347-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
15 Nov 2013
Research article |
| 15 Nov 2013
Southern Hemisphere imprint for Indo-Asian summer monsoons during the last glacial period as revealed by Arabian Sea productivity records
T. Caley
Université Bordeaux, CNRS, EPOC, UMR5805, 33400 Talence, France
Section Climate Change and Landscape Dynamics, Dept. of Earth Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands
S. Zaragosi
Université Bordeaux, CNRS, EPOC, UMR5805, 33400 Talence, France
J. Bourget
School of Earth and Environment, CPGCO2, University of Western Australia, 35 Stirling Highway, Crawley 6009, Australia
P. Martinez
Université Bordeaux, CNRS, EPOC, UMR5805, 33400 Talence, France
B. Malaizé
Université Bordeaux, CNRS, EPOC, UMR5805, 33400 Talence, France
F. Eynaud
Université Bordeaux, CNRS, EPOC, UMR5805, 33400 Talence, France
L. Rossignol
Université Bordeaux, CNRS, EPOC, UMR5805, 33400 Talence, France
T. Garlan
Service Hydrographique et Océanographique de la Marine, Cellule Sédimentologie, 13 Rue du Chatellier, BP30316 29603 Brest cedex, France
N. Ellouz-Zimmermann
IFPEN, 1 and 4 Avenue de Bois Préau, 92852 Rueil-Malmaison, France
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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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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.
B. A. A. Hoogakker, D. J. R. Thornalley, and S. Barker
Biogeosciences, 13, 211–221, https://doi.org/10.5194/bg-13-211-2016, https://doi.org/10.5194/bg-13-211-2016, 2016
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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.
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
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
D. Gallego-Torres, F. Martinez-Ruiz, P. A. Meyers, A. Paytan, F. J. Jimenez-Espejo, and M. Ortega-Huertas
Biogeosciences, 8, 415–431, https://doi.org/10.5194/bg-8-415-2011, https://doi.org/10.5194/bg-8-415-2011, 2011
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