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Volume 11, issue 10
Biogeosciences, 11, 2721–2739, 2014
https://doi.org/10.5194/bg-11-2721-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-11-2721-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
Biogeosciences, 11, 2721–2739, 2014
https://doi.org/10.5194/bg-11-2721-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-11-2721-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
Research article 22 May 2014
Research article | 22 May 2014
Non-invasive imaging methods applied to neo- and paleo-ontological cephalopod research
R. Hoffmann et al.
Related subject area
Paleobiogeoscience: Marine Record
A 15-million-year-long record of phenotypic evolution in the heavily calcified coccolithophore Helicosphaera and its biogeochemical implications
Shell chemistry of the boreal Campanian bivalve Rastellum diluvianum (Linnaeus, 1767) reveals temperature seasonality, growth rates and life cycle of an extinct Cretaceous oyster
Southern California margin benthic foraminiferal assemblages record recent centennial-scale changes in oxygen minimum zone
Baseline for ostracod-based northwestern Pacific and Indo-Pacific shallow-marine paleoenvironmental reconstructions: ecological modeling of species distributions
Neogene Caribbean elasmobranchs: diversity, paleoecology and paleoenvironmental significance of the Cocinetas Basin assemblage (Guajira Peninsula, Colombia)
Coastal primary productivity changes over the last millennium: a case study from the Skagerrak (North Sea)
A 1500-year multiproxy record of coastal hypoxia from the northern Baltic Sea indicates unprecedented deoxygenation over the 20th century
Technical note: An empirical method for absolute calibration of coccolith thickness
Reconstructing Holocene temperature and salinity variations in the western Baltic Sea region: a multi-proxy comparison from the Little Belt (IODP Expedition 347, Site M0059)
The oxic degradation of sedimentary organic matter 1400 Ma constrains atmospheric oxygen levels
Geochemical and microstructural characterisation of two species of cool-water bivalves (Fulvia tenuicostata and Soletellina biradiata) from Western Australia
Ecological response to collapse of the biological pump following the mass extinction at the Cretaceous–Paleogene boundary
Quantifying the Cenozoic marine diatom deposition history: links to the C and Si cycles
Anthropogenically induced environmental changes in the northeastern Adriatic Sea in the last 500 years (Panzano Bay, Gulf of Trieste)
Palaeohydrological changes over the last 50 ky in the central Gulf of Cadiz: complex forcing mechanisms mixing multi-scale processes
Dinocyst assemblage constraints on oceanographic and atmospheric processes in the eastern equatorial Atlantic over the last 44 kyr
Sedimentary response to sea ice and atmospheric variability over the instrumental period off Adélie Land, East Antarctica
Equatorward phytoplankton migration during a cold spell within the Late Cretaceous super-greenhouse
Upwellings mitigated Plio-Pleistocene heat stress for reef corals on the Florida platform (USA)
Millennial changes in North Atlantic oxygen concentrations
Vanishing coccolith vital effects with alleviated carbon limitation
Late Pleistocene glacial–interglacial shell-size–isotope variability in planktonic foraminifera as a function of local hydrography
Coral records of reef-water pH across the central Great Barrier Reef, Australia: assessing the influence of river runoff on inshore reefs
Records of past mid-depth ventilation: Cretaceous ocean anoxic event 2 vs. Recent oxygen minimum zones
Organomineral nanocomposite carbon burial during Oceanic Anoxic Event 2
Icehouse–greenhouse variations in marine denitrification
Changes in calcification of coccoliths under stable atmospheric CO2
Southern Hemisphere imprint for Indo-Asian summer monsoons during the last glacial period as revealed by Arabian Sea productivity records
The calcareous nannofossil Prinsiosphaera achieved rock-forming abundances in the latest Triassic of western Tethys: consequences for the δ13C of bulk carbonate
The Little Ice Age: evidence from a sediment record in Gullmar Fjord, Swedish west coast
Nitrogen isotopes in bulk marine sediment: linking seafloor observations with subseafloor records
Quantitative reconstruction of sea-surface conditions over the last 150 yr in the Beaufort Sea based on dinoflagellate cyst assemblages: the role of large-scale atmospheric circulation patterns
Spatial linkages between coral proxies of terrestrial runoff across a large embayment in Madagascar
Pteropods from the Caribbean Sea: variations in calcification as an indicator of past ocean carbonate saturation
Sedimentary organic matter and carbonate variations in the Chukchi Borderland in association with ice sheet and ocean-atmosphere dynamics over the last 155 kyr
First discovery of dolomite and magnesite in living coralline algae and its geobiological implications
Assessment of sea surface temperature changes in the Gulf of Cadiz during the last 30 ka: implications for glacial changes in the regional hydrography
Productivity patterns and N-fixation associated with Pliocene-Holocene sapropels: paleoceanographic and paleoecological significance
Twentieth century δ13C variability in surface water dissolved inorganic carbon recorded by coralline algae in the northern North Pacific Ocean and the Bering Sea
The enigmatic ichnofossil Tisoa siphonalis and widespread authigenic seep carbonate formation during the Late Pliensbachian in southern France
Hypoxia and cyanobacteria blooms - are they really natural features of the late Holocene history of the Baltic Sea?
Heavy metal incorporation in foraminiferal calcite: results from multi-element enrichment culture experiments with Ammonia tepida
Technical Note: On methodologies for determining the size-normalised weight of planktic foraminifera
Increase in water column denitrification during the last deglaciation: the influence of oxygen demand in the eastern equatorial Pacific
Historical records of coastal eutrophication-induced hypoxia
Luka Šupraha and Jorijntje Henderiks
Biogeosciences, 17, 2955–2969, https://doi.org/10.5194/bg-17-2955-2020, https://doi.org/10.5194/bg-17-2955-2020, 2020
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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
Biogeosciences, 17, 2897–2922, https://doi.org/10.5194/bg-17-2897-2020, https://doi.org/10.5194/bg-17-2897-2020, 2020
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In this study, we present a detailed investigation of the chemical composition of 12 specimens of very well preserved, 78-million-year-old oyster shells from southern Sweden. The chemical data show how the oysters grew, the environment in which they lived and how old they became and also provide valuable information about which chemical measurements we can use to learn more about ancient climate and environment from such shells. In turn, this can help improve climate reconstructions and models.
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.
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
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
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
B. Williams, J. Halfar, R. S. Steneck, U. G. Wortmann, S. Hetzinger, W. Adey, P. Lebednik, and M. Joachimski
Biogeosciences, 8, 165–174, https://doi.org/10.5194/bg-8-165-2011, https://doi.org/10.5194/bg-8-165-2011, 2011
B. van de Schootbrugge, D. Harazim, K. Sorichter, W. Oschmann, J. Fiebig, W. Püttmann, M. Peinl, F. Zanella, B. M. A. Teichert, J. Hoffmann, A. Stadnitskaia, and Y. Rosenthal
Biogeosciences, 7, 3123–3138, https://doi.org/10.5194/bg-7-3123-2010, https://doi.org/10.5194/bg-7-3123-2010, 2010
L. Zillén and D. J. Conley
Biogeosciences, 7, 2567–2580, https://doi.org/10.5194/bg-7-2567-2010, https://doi.org/10.5194/bg-7-2567-2010, 2010
D. Munsel, U. Kramar, D. Dissard, G. Nehrke, Z. Berner, J. Bijma, G.-J. Reichart, and T. Neumann
Biogeosciences, 7, 2339–2350, https://doi.org/10.5194/bg-7-2339-2010, https://doi.org/10.5194/bg-7-2339-2010, 2010
C. J. Beer, R. Schiebel, and P. A. Wilson
Biogeosciences, 7, 2193–2198, https://doi.org/10.5194/bg-7-2193-2010, https://doi.org/10.5194/bg-7-2193-2010, 2010
P. Martinez and R. S. Robinson
Biogeosciences, 7, 1–9, https://doi.org/10.5194/bg-7-1-2010, https://doi.org/10.5194/bg-7-1-2010, 2010
A. J. Gooday, F. Jorissen, L. A. Levin, J. J. Middelburg, S. W. A. Naqvi, N. N. Rabalais, M. Scranton, and J. Zhang
Biogeosciences, 6, 1707–1745, https://doi.org/10.5194/bg-6-1707-2009, https://doi.org/10.5194/bg-6-1707-2009, 2009
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