Articles | Volume 10, issue 4
https://doi.org/10.5194/bg-10-2331-2013
© 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-10-2331-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
08 Apr 2013
Research article |
| 08 Apr 2013
Response of halocarbons to ocean acidification in the Arctic
F. E. Hopkins
Plymouth Marine Laboratory, Plymouth, UK
S. A. Kimmance
Plymouth Marine Laboratory, Plymouth, UK
J. A. Stephens
Plymouth Marine Laboratory, Plymouth, UK
R. G. J. Bellerby
Norwegian Institute for Water Research, Bergen, Norway
Uni Bjerknes Centre, Uni Research AS, Bergen, Norway
Geophysical Institute, University of Bergen, Bergen, Norway
C. P. D. Brussaard
Royal Netherlands Institute for Sea Research (NIOZ), Texel, the Netherlands
J. Czerny
Helmholtz Centre for Ocean Research (GEOMAR), Kiel, Germany
K. G. Schulz
Helmholtz Centre for Ocean Research (GEOMAR), Kiel, Germany
S. D. Archer
Plymouth Marine Laboratory, Plymouth, UK
Bigelow Laboratory for Ocean Sciences, Maine, USA
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Charlotte Eich, Mathijs van Manen, J. Scott P. McCain, Loay J. Jabre, Willem H. van de Poll, Jinyoung Jung, Sven B. E. H. Pont, Hung-An Tian, Indah Ardiningsih, Gert-Jan Reichart, Erin M. Bertrand, Corina P. D. Brussaard, and Rob Middag
Biogeosciences, 21, 4637–4663, https://doi.org/10.5194/bg-21-4637-2024, https://doi.org/10.5194/bg-21-4637-2024, 2024
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Phytoplankton growth in the Southern Ocean (SO) is often limited by low iron (Fe) concentrations. Sea surface warming impacts Fe availability and can affect phytoplankton growth. We used shipboard Fe clean incubations to test how changes in Fe and temperature affect SO phytoplankton. Their abundances usually increased with Fe addition and temperature increase, with Fe being the major factor. These findings imply potential shifts in ecosystem structure, impacting food webs and elemental cycling.
Laura Marín-Samper, Javier Arístegui, Nauzet Hernández-Hernández, Joaquín Ortiz, Stephen D. Archer, Andrea Ludwig, and Ulf Riebesell
Biogeosciences, 21, 2859–2876, https://doi.org/10.5194/bg-21-2859-2024, https://doi.org/10.5194/bg-21-2859-2024, 2024
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Our planet is facing a climate crisis. Scientists are working on innovative solutions that will aid in capturing the hard to abate emissions before it is too late. Exciting research reveals that ocean alkalinity enhancement, a key climate change mitigation strategy, does not harm phytoplankton, the cornerstone of marine ecosystems. Through meticulous study, we may have uncovered a positive relationship: up to a specific limit, enhancing ocean alkalinity boosts photosynthesis by certain species.
Librada Ramírez, Leonardo J. Pozzo-Pirotta, Aja Trebec, Víctor Manzanares-Vázquez, José L. Díez, Javier Arístegui, Ulf Riebesell, Stephen D. Archer, and María Segovia
EGUsphere, https://doi.org/10.5194/egusphere-2024-847, https://doi.org/10.5194/egusphere-2024-847, 2024
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We studied the potential effects of increasing ocean alkalinity on a natural plankton community in subtropical waters of the Atlantic near Gran Canaria, Spain. Alkalinity is the capacity of water to resist acidification and plankton are usually microscopic plants (phytoplankton) and animals (zooplankton), often less than 2,5 cm in length. This study suggests that increasing ocean alkalinity did not have a significant negative impact on the studied plankton community.
Hans van Haren, Corina P. D. Brussaard, Loes J. A. Gerringa, Mathijs H. van Manen, Rob Middag, and Ruud Groenewegen
Ocean Sci., 17, 301–318, https://doi.org/10.5194/os-17-301-2021, https://doi.org/10.5194/os-17-301-2021, 2021
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Changes in ocean temperature may affect vertical density stratification, which may hamper turbulent exchange and thus nutrient availability for phytoplankton growth. To quantify varying physical conditions, we sampled the upper 500 m along 17 ± 5° W between [30, 63]° N in summer. South to north, temperature decreased with stratification while turbulence and nutrient fluxes remained constant, likely due to internal waves breaking and little affected by the physical process of global warming.
Xiaoshuang Li, Richard Garth James Bellerby, Jianzhong Ge, Philip Wallhead, Jing Liu, and Anqiang Yang
Geosci. Model Dev., 13, 5103–5117, https://doi.org/10.5194/gmd-13-5103-2020, https://doi.org/10.5194/gmd-13-5103-2020, 2020
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We have developed an ANN model to predict pH using 11 cruise datasets from 2013 to 2017,
demonstrated its reliability using three cruise datasets during 2018 and applied it to
retrieve monthly pH for the period 2000 to 2016 on the East China Sea shelf using the
ANN model in combination with input variables from the Changjiang biology Finite-Volume
Coastal Ocean Model. This approach may be a valuable tool for understanding the seasonal
variation of pH in poorly observed regions.
Frances E. Hopkins, Philip D. Nightingale, John A. Stephens, C. Mark Moore, Sophie Richier, Gemma L. Cripps, and Stephen D. Archer
Biogeosciences, 17, 163–186, https://doi.org/10.5194/bg-17-163-2020, https://doi.org/10.5194/bg-17-163-2020, 2020
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We investigated the effects of ocean acidification (OA) on the production of climate active gas dimethylsulfide (DMS) in polar waters. We found that polar DMS production was unaffected by OA – in contrast to temperate waters, where large increases in DMS occurred. The regional differences in DMS response may reflect natural variability in community adaptation to ambient carbonate chemistry and should be taken into account in predicting the influence of future DMS emissions on Earth's climate.
Laura F. Korte, Franziska Pausch, Scarlett Trimborn, Corina P. D. Brussaard, Geert-Jan A. Brummer, Michèlle van der Does, Catarina V. Guerreiro, Laura T. Schreuder, Chris I. Munday, and Jan-Berend W. Stuut
Biogeosciences Discuss., https://doi.org/10.5194/bg-2018-484, https://doi.org/10.5194/bg-2018-484, 2018
Revised manuscript not accepted
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This paper shows the differences of nutrient release after dry and wet Saharan dust deposition in the tropical North Atlantic Ocean at 12° N. Incubation experiments were conducted along an east-west transect. Large differences were observed between both deposition types with wet deposition being the dominant source of phosphate, silicate, and iron. Both deposition types suggest that Saharan dust particles might be incorporated into marine snow aggregates and act as ballast mineral.
Sergio Balzano, Julie Lattaud, Laura Villanueva, Sebastiaan W. Rampen, Corina P. D. Brussaard, Judith van Bleijswijk, Nicole Bale, Jaap S. Sinninghe Damsté, and Stefan Schouten
Biogeosciences, 15, 5951–5968, https://doi.org/10.5194/bg-15-5951-2018, https://doi.org/10.5194/bg-15-5951-2018, 2018
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We tried to identify the microbes which biosynthesize a class of lipids widespread in seawater, the long chain alkyl diols (LCDs). We could not find any microorganism likely involved in the production of LCDs. The amounts of LCDs found are too high to be produced by living organisms and are likely to be part of the refractory organic matter persisting for long periods in the water column.
Nicole J. Bale, Tracy A. Villareal, Ellen C. Hopmans, Corina P. D. Brussaard, Marc Besseling, Denise Dorhout, Jaap S. Sinninghe Damsté, and Stefan Schouten
Biogeosciences, 15, 1229–1241, https://doi.org/10.5194/bg-15-1229-2018, https://doi.org/10.5194/bg-15-1229-2018, 2018
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Associations between diatoms and N-fixing cyanobacteria (diatom–diazotroph associations, DDAs) play an important role in the N cycle of the tropical North Atlantic. Heterocysts are the site of N fixation and contain unique glycolipids. We measured these glycolipids in the water column and surface sediment from the tropical North Atlantic. We found a significant correlation between the concentration of glycolipid and of DDAs, strengthening their application as biomarkers.
Katharine J. Crawfurd, Santiago Alvarez-Fernandez, Kristina D. A. Mojica, Ulf Riebesell, and Corina P. D. Brussaard
Biogeosciences, 14, 3831–3849, https://doi.org/10.5194/bg-14-3831-2017, https://doi.org/10.5194/bg-14-3831-2017, 2017
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Carbon dioxide (CO2) is increasing in the atmosphere and oceans. To simulate future conditions we manipulated CO2 concentrations of natural Baltic seawater in 55 m3 bags in situ. We saw increased growth rates and abundances of the smallest-sized eukaryotic phytoplankton and reduced abundances of other phytoplankton with increased CO2. Viral and bacterial abundances were also affected. This would lead to more carbon recycling in the surface water and affect marine food webs and the carbon cycle.
Thomas Hornick, Lennart T. Bach, Katharine J. Crawfurd, Kristian Spilling, Eric P. Achterberg, Jason N. Woodhouse, Kai G. Schulz, Corina P. D. Brussaard, Ulf Riebesell, and Hans-Peter Grossart
Biogeosciences, 14, 1–15, https://doi.org/10.5194/bg-14-1-2017, https://doi.org/10.5194/bg-14-1-2017, 2017
Kristian Spilling, Kai G. Schulz, Allanah J. Paul, Tim Boxhammer, Eric P. Achterberg, Thomas Hornick, Silke Lischka, Annegret Stuhr, Rafael Bermúdez, Jan Czerny, Kate Crawfurd, Corina P. D. Brussaard, Hans-Peter Grossart, and Ulf Riebesell
Biogeosciences, 13, 6081–6093, https://doi.org/10.5194/bg-13-6081-2016, https://doi.org/10.5194/bg-13-6081-2016, 2016
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We performed an experiment in the Baltic Sea in order to investigate the consequences of the increasing CO2 levels on biological processes in the free water mass. There was more accumulation of organic carbon at high CO2 levels. Surprisingly, this was caused by reduced loss processes (respiration and bacterial production) in a high-CO2 environment, and not by increased photosynthetic fixation of CO2. Our carbon budget can be used to better disentangle the effects of ocean acidification.
Alison L. Webb, Emma Leedham-Elvidge, Claire Hughes, Frances E. Hopkins, Gill Malin, Lennart T. Bach, Kai Schulz, Kate Crawfurd, Corina P. D. Brussaard, Annegret Stuhr, Ulf Riebesell, and Peter S. Liss
Biogeosciences, 13, 4595–4613, https://doi.org/10.5194/bg-13-4595-2016, https://doi.org/10.5194/bg-13-4595-2016, 2016
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This paper presents concentrations of several trace gases produced by the Baltic Sea phytoplankton community during a mesocosm experiment with five different CO2 levels. Average concentrations of dimethylsulphide were lower in the highest CO2 mesocosms over a 6-week period, corresponding to previous mesocosm experiment results. No dimethylsulfoniopropionate was detected due to a methodological issue. Concentrations of iodine- and bromine-containing halocarbons were unaffected by increasing CO2.
Douwe S. Maat, Nicole J. Bale, Ellen C. Hopmans, Jaap S. Sinninghe Damsté, Stefan Schouten, and Corina P. D. Brussaard
Biogeosciences, 13, 1667–1676, https://doi.org/10.5194/bg-13-1667-2016, https://doi.org/10.5194/bg-13-1667-2016, 2016
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This study shows that the phytoplankter Micromonas pusilla alters its lipid composition when the macronutrient phosphate is in low supply. This reduction in phospholipids is directly dependent on the strength of the limitation. Furthermore we show that, when M. pusilla is infected by viruses, lipid remodeling is lower. The study was carried out to investigate how phytoplankton and its viruses are affected by environmental factors and how this affects food web dynamics.
J. Brandsma, T. R. Sutton, J. M. Herniman, J. E. Hunter, T. E. G. Biggs, C. Evans, C. P. D. Brussaard, A. D. Postle, T. J. Jenkins, and G. J. Langley
Biogeosciences Discuss., https://doi.org/10.5194/bg-2016-13, https://doi.org/10.5194/bg-2016-13, 2016
Manuscript not accepted for further review
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Marine phytoplankton fix around 1 billion tonnes of carbon as lipid biomass each year. We present a new method for analysing complex lipid mixtures from phytoplankton biomass using supercritical fluid technology which has better resolution and is several times faster than existing methods. Thus, it enables larger-scale and more in-depth studies of phytoplankton lipid metabolism, the way it is controlled by ecological and environmental processes, and its impact on global biogeochemistry.
C. J. Daniels, A. J. Poulton, M. Esposito, M. L. Paulsen, R. Bellerby, M. St John, and A. P. Martin
Biogeosciences, 12, 2395–2409, https://doi.org/10.5194/bg-12-2395-2015, https://doi.org/10.5194/bg-12-2395-2015, 2015
E. Jeansson, R. G. J. Bellerby, I. Skjelvan, H. Frigstad, S. R. Ólafsdóttir, and J. Olafsson
Biogeosciences, 12, 875–885, https://doi.org/10.5194/bg-12-875-2015, https://doi.org/10.5194/bg-12-875-2015, 2015
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Long-term mean monthly fluxes of carbon and nutrients to the surface layer of the Iceland Sea are presented. From these fluxes we estimate primary production based on newly added nitrate (i.e. new production) and net community production (NCP). The annual new production in the Iceland Sea is estimated to 0.45±0.09mol N/m2/yr, and the net annual NCP to 7.3±1.0mol C/m2/yr. The typical C:N ratio during biological uptake is 9.0, challenging the Redfield C:N as the conversion factor in the area.
F. E. Hopkins and S. D. Archer
Biogeosciences, 11, 4925–4940, https://doi.org/10.5194/bg-11-4925-2014, https://doi.org/10.5194/bg-11-4925-2014, 2014
Y. Artioli, J. C. Blackford, G. Nondal, R. G. J. Bellerby, S. L. Wakelin, J. T. Holt, M. Butenschön, and J. I. Allen
Biogeosciences, 11, 601–612, https://doi.org/10.5194/bg-11-601-2014, https://doi.org/10.5194/bg-11-601-2014, 2014
D. S. Maat, N. J. Bale, E. C. Hopmans, A.-C. Baudoux, J. S. Sinninghe Damsté, S. Schouten, and C. P. D. Brussaard
Biogeosciences, 11, 185–194, https://doi.org/10.5194/bg-11-185-2014, https://doi.org/10.5194/bg-11-185-2014, 2014
F. Ziska, B. Quack, K. Abrahamsson, S. D. Archer, E. Atlas, T. Bell, J. H. Butler, L. J. Carpenter, C. E. Jones, N. R. P. Harris, H. Hepach, K. G. Heumann, C. Hughes, J. Kuss, K. Krüger, P. Liss, R. M. Moore, A. Orlikowska, S. Raimund, C. E. Reeves, W. Reifenhäuser, A. D. Robinson, C. Schall, T. Tanhua, S. Tegtmeier, S. Turner, L. Wang, D. Wallace, J. Williams, H. Yamamoto, S. Yvon-Lewis, and Y. Yokouchi
Atmos. Chem. Phys., 13, 8915–8934, https://doi.org/10.5194/acp-13-8915-2013, https://doi.org/10.5194/acp-13-8915-2013, 2013
A. Silyakova, R. G. J. Bellerby, K. G. Schulz, J. Czerny, T. Tanaka, G. Nondal, U. Riebesell, A. Engel, T. De Lange, and A. Ludvig
Biogeosciences, 10, 4847–4859, https://doi.org/10.5194/bg-10-4847-2013, https://doi.org/10.5194/bg-10-4847-2013, 2013
W. H. van de Poll, G. Kulk, K. R. Timmermans, C. P. D. Brussaard, H. J. van der Woerd, M. J. Kehoe, K. D. A. Mojica, R. J. W. Visser, P. D. Rozema, and A. G. J. Buma
Biogeosciences, 10, 4227–4240, https://doi.org/10.5194/bg-10-4227-2013, https://doi.org/10.5194/bg-10-4227-2013, 2013
C. Motegi, T. Tanaka, J. Piontek, C. P. D. Brussaard, J.-P. Gattuso, and M. G. Weinbauer
Biogeosciences, 10, 3285–3296, https://doi.org/10.5194/bg-10-3285-2013, https://doi.org/10.5194/bg-10-3285-2013, 2013
J. Czerny, K. G. Schulz, T. Boxhammer, R. G. J. Bellerby, J. Büdenbender, A. Engel, S. A. Krug, A. Ludwig, K. Nachtigall, G. Nondal, B. Niehoff, A. Silyakova, and U. Riebesell
Biogeosciences, 10, 3109–3125, https://doi.org/10.5194/bg-10-3109-2013, https://doi.org/10.5194/bg-10-3109-2013, 2013
S. D. Archer, S. A. Kimmance, J. A. Stephens, F. E. Hopkins, R. G. J. Bellerby, K. G. Schulz, J. Piontek, and A. Engel
Biogeosciences, 10, 1893–1908, https://doi.org/10.5194/bg-10-1893-2013, https://doi.org/10.5194/bg-10-1893-2013, 2013
A. Engel, C. Borchard, J. Piontek, K. G. Schulz, U. Riebesell, and R. Bellerby
Biogeosciences, 10, 1291–1308, https://doi.org/10.5194/bg-10-1291-2013, https://doi.org/10.5194/bg-10-1291-2013, 2013
C. P. D. Brussaard, A. A. M. Noordeloos, H. Witte, M. C. J. Collenteur, K. Schulz, A. Ludwig, and U. Riebesell
Biogeosciences, 10, 719–731, https://doi.org/10.5194/bg-10-719-2013, https://doi.org/10.5194/bg-10-719-2013, 2013
T. Tanaka, S. Alliouane, R. G. B. Bellerby, J. Czerny, A. de Kluijver, U. Riebesell, K. G. Schulz, A. Silyakova, and J.-P. Gattuso
Biogeosciences, 10, 315–325, https://doi.org/10.5194/bg-10-315-2013, https://doi.org/10.5194/bg-10-315-2013, 2013
K. G. Schulz, R. G. J. Bellerby, C. P. D. Brussaard, J. Büdenbender, J. Czerny, A. Engel, M. Fischer, S. Koch-Klavsen, S. A. Krug, S. Lischka, A. Ludwig, M. Meyerhöfer, G. Nondal, A. Silyakova, A. Stuhr, and U. Riebesell
Biogeosciences, 10, 161–180, https://doi.org/10.5194/bg-10-161-2013, https://doi.org/10.5194/bg-10-161-2013, 2013
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Biogeosciences, 21, 5495–5515, https://doi.org/10.5194/bg-21-5495-2024, https://doi.org/10.5194/bg-21-5495-2024, 2024
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Mana Gharun, Ankit Shekhar, Jingfeng Xiao, Xing Li, and Nina Buchmann
Biogeosciences, 21, 5481–5494, https://doi.org/10.5194/bg-21-5481-2024, https://doi.org/10.5194/bg-21-5481-2024, 2024
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Makcim L. De Sisto and Andrew H. MacDougall
Biogeosciences, 21, 4853–4873, https://doi.org/10.5194/bg-21-4853-2024, https://doi.org/10.5194/bg-21-4853-2024, 2024
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Outi Kinnunen, Leif Backman, Juha Aalto, Tuula Aalto, and Tiina Markkanen
Biogeosciences, 21, 4739–4763, https://doi.org/10.5194/bg-21-4739-2024, https://doi.org/10.5194/bg-21-4739-2024, 2024
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Climate change is expected to increase the risk of forest fires. Ecosystem process model simulations are used to project changes in fire occurrence in Fennoscandia under six climate projections. The findings suggest a longer fire season, more fires, and an increase in burnt area towards the end of the century.
Jo Cook, Clare Brewster, Felicity Hayes, Nathan Booth, Sam Bland, Pritha Pande, Samarthia Thankappan, Håkan Pleijel, and Lisa Emberson
Biogeosciences, 21, 4809–4835, https://doi.org/10.5194/bg-21-4809-2024, https://doi.org/10.5194/bg-21-4809-2024, 2024
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Niels Suitner, Giulia Faucher, Carl Lim, Julieta Schneider, Charly A. Moras, Ulf Riebesell, and Jens Hartmann
Biogeosciences, 21, 4587–4604, https://doi.org/10.5194/bg-21-4587-2024, https://doi.org/10.5194/bg-21-4587-2024, 2024
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Milagros Rico, Paula Santiago-Díaz, Guillermo Samperio-Ramos, Melchor González-Dávila, and Juana Magdalena Santana-Casiano
Biogeosciences, 21, 4381–4394, https://doi.org/10.5194/bg-21-4381-2024, https://doi.org/10.5194/bg-21-4381-2024, 2024
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Changes in pH generate stress conditions, either because high pH drastically decreases the availability of trace metals such as Fe(II), a restrictive element for primary productivity, or because reactive oxygen species are increased with low pH. The metabolic functions and composition of microalgae can be affected. These modifications in metabolites are potential factors leading to readjustments in phytoplankton community structure and diversity and possible alteration in marine ecosystems.
Jo Cook, Durgesh Singh Yadav, Felicity Hayes, Nathan Booth, Sam Bland, Pritha Pande, Samarthia Thankappan, and Lisa Emberson
EGUsphere, https://doi.org/10.5194/egusphere-2024-2968, https://doi.org/10.5194/egusphere-2024-2968, 2024
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Ozone (O3) pollution reduces wheat yields and quality in India, affecting amino acids essential for nutrition, like lysine and methionine. Here, we improve the DO3SE-CropN model to simulate wheat’s protective processes against O3 and their impact on protein and amino acid concentrations. While the model captures O3-induced yield losses, it underestimates amino acid reductions. Further research is needed to refine the model, enabling future risk assessments of O3's impact on yields and nutrition.
James A. King, James Weber, Peter Lawrence, Stephanie Roe, Abigail L. S. Swann, and Maria Val Martin
Biogeosciences, 21, 3883–3902, https://doi.org/10.5194/bg-21-3883-2024, https://doi.org/10.5194/bg-21-3883-2024, 2024
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Tackling climate change by adding, restoring, or enhancing forests is gaining global support. However, it is important to investigate the broader implications of this. We used a computer model of the Earth to investigate a future where tree cover expanded as much as possible. We found that some tropical areas were cooler because of trees pumping water into the atmosphere, but this also led to soil and rivers drying. This is important because it might be harder to maintain forests as a result.
Benoît Pasquier, Mark Holzer, and Matthew A. Chamberlain
Biogeosciences, 21, 3373–3400, https://doi.org/10.5194/bg-21-3373-2024, https://doi.org/10.5194/bg-21-3373-2024, 2024
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How do perpetually slower and warmer oceans sequester carbon? Compared to the preindustrial state, we find that biological productivity declines despite warming-stimulated growth because of a lower nutrient supply from depth. This throttles the biological carbon pump, which still sequesters more carbon because it takes longer to return to the surface. The deep ocean is isolated from the surface, allowing more carbon from the atmosphere to pass through the ocean without contributing to biology.
Rebecca Chloe Evans and H. Damon Matthews
EGUsphere, https://doi.org/10.5194/egusphere-2024-1810, https://doi.org/10.5194/egusphere-2024-1810, 2024
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To mitigate our impact on the climate, research suggests that we will need to both drastically reduce emissions and perform carbon dioxide removal (CDR). We simulated future climates under three emissions scenarios, in which we removed some carbon from the air and put it into agricultural soil at varying rates. We found that agricultural CDR is much more effective at reducing global temperatures if done in a low emissions scenario and at a high rate, and it becomes less effective with time.
Stéphane Doléac, Marina Lévy, Roy El Hourany, and Laurent Bopp
EGUsphere, https://doi.org/10.5194/egusphere-2024-1820, https://doi.org/10.5194/egusphere-2024-1820, 2024
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Phytoplankton net primary production (NPP) is influenced by many processes, and their representation varies across Earth-system models. This leads to differing projections for NPP's future under climate change, especially in the North Atlantic. To address this, we identified and assessed the processes controlling NPP in each model. This assessment helped us select the most reliable models, significantly improving NPP projections in the region.
Matthew A. Chamberlain, Tilo Ziehn, and Rachel M. Law
Biogeosciences, 21, 3053–3073, https://doi.org/10.5194/bg-21-3053-2024, https://doi.org/10.5194/bg-21-3053-2024, 2024
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This paper explores the climate processes that drive increasing global average temperatures in zero-emission commitment (ZEC) simulations despite decreasing atmospheric CO2. ACCESS-ESM1.5 shows the Southern Ocean to continue to warm locally in all ZEC simulations. In ZEC simulations that start after the emission of more than 1000 Pg of carbon, the influence of the Southern Ocean increases the global temperature.
Luna J. J. Geerts, Astrid Hylén, and Filip J. R. Meysman
EGUsphere, https://doi.org/10.5194/egusphere-2024-1824, https://doi.org/10.5194/egusphere-2024-1824, 2024
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Coastal enhanced silicate weathering (CESW) with olivine is a promising method for capturing CO2 from the atmosphere, yet studies in field conditions are lacking. We bridge the gap between theoretical studies and the real-world environment by estimating the predictability of CESW parameters and identifying aspects to consider when applying CESW. A major source of uncertainty is the lack of experimental studies with sediment, which can heavily influence the speed and efficiency of CO2 drawdown.
Shuaifeng Song, Xuezhen Zhang, and Xiaodong Yan
Biogeosciences, 21, 2839–2858, https://doi.org/10.5194/bg-21-2839-2024, https://doi.org/10.5194/bg-21-2839-2024, 2024
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We mapped the distribution of future potential afforestation regions based on future high-resolution climate data and climate–vegetation models. After considering the national afforestation policy and climate change, we found that the future potential afforestation region was mainly located around and to the east of the Hu Line. This study provides a dataset for exploring the effects of future afforestation.
Tianfei Xue, Jens Terhaar, A. E. Friederike Prowe, Thomas L. Frölicher, Andreas Oschlies, and Ivy Frenger
Biogeosciences, 21, 2473–2491, https://doi.org/10.5194/bg-21-2473-2024, https://doi.org/10.5194/bg-21-2473-2024, 2024
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Phytoplankton play a crucial role in marine ecosystems. However, climate change's impact on phytoplankton biomass remains uncertain, particularly in the Southern Ocean. In this region, phytoplankton biomass within the water column is likely to remain stable in response to climate change, as supported by models. This stability arises from a shallower mixed layer, favoring phytoplankton growth but also increasing zooplankton grazing due to phytoplankton concentration near the surface.
Kinga Kulesza and Agata Hościło
Biogeosciences, 21, 2509–2527, https://doi.org/10.5194/bg-21-2509-2024, https://doi.org/10.5194/bg-21-2509-2024, 2024
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We present coherence and time lags in spectral response of three vegetation types in the European temperate zone to the influencing meteorological factors and teleconnection indices for the period 2002–2022. Vegetation condition in broadleaved forest, coniferous forest and pastures was measured with MODIS NDVI and EVI, and the coherence between NDVI and EVI and meteorological elements was described using the methods of wavelet coherence and Pearson’s linear correlation with time lag.
Anton Lokshin, Daniel Palchan, and Avner Gross
Biogeosciences, 21, 2355–2365, https://doi.org/10.5194/bg-21-2355-2024, https://doi.org/10.5194/bg-21-2355-2024, 2024
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Ash particles from wildfires are rich in phosphorus (P), a crucial nutrient that constitutes a limiting factor in 43 % of the world's land ecosystems. We hypothesize that wildfire ash could directly contribute to plant nutrition. We find that fire ash application boosts the growth of plants, but the only way plants can uptake P from fire ash is through the foliar uptake pathway and not through the roots. The fertilization impact of fire ash was also maintained under elevated levels of CO2.
Nina Bednaršek, Greg Pelletier, Hanna van de Mortel, Marisol García-Reyes, Richard Feely, and Andrew Dickson
EGUsphere, https://doi.org/10.5194/egusphere-2024-947, https://doi.org/10.5194/egusphere-2024-947, 2024
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The environmental impacts of ocean alkalinity enhancement (OAE) are unknown. A conceptual framework was developed showing 40 % of species to respond positively, 20 % negatively and 40 % with neutral response upon alkalinity addition. Biological thresholds were found between 10 to 500 µmol/kg NaOH addition, emphasizing lab experiments to be conducted at lower dosages. A precautionary approach is warranted to avoid potential risks.
Marcus Breil, Vanessa K. M. Schneider, and Joaquim G. Pinto
Biogeosciences, 21, 811–824, https://doi.org/10.5194/bg-21-811-2024, https://doi.org/10.5194/bg-21-811-2024, 2024
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The general impact of afforestation on the regional climate conditions in Europe during the period 1986–2015 is investigated. For this purpose, a regional climate model simulation is performed, in which afforestation during this period is considered, and results are compared to a simulation in which this is not the case. Results show that afforestation had discernible impacts on the climate change signal in Europe, which may have mitigated the local warming trend, especially in summer in Europe.
Ali Asaadi, Jörg Schwinger, Hanna Lee, Jerry Tjiputra, Vivek Arora, Roland Séférian, Spencer Liddicoat, Tomohiro Hajima, Yeray Santana-Falcón, and Chris D. Jones
Biogeosciences, 21, 411–435, https://doi.org/10.5194/bg-21-411-2024, https://doi.org/10.5194/bg-21-411-2024, 2024
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Carbon cycle feedback metrics are employed to assess phases of positive and negative CO2 emissions. When emissions become negative, we find that the model disagreement in feedback metrics increases more strongly than expected from the assumption that the uncertainties accumulate linearly with time. The geographical patterns of such metrics over land highlight that differences in response between tropical/subtropical and temperate/boreal ecosystems are a major source of model disagreement.
Mana Gharun, Ankit Shekhar, Lukas Hörtnagl, Luana Krebs, Nicola Arriga, Mirco Migliavacca, Marilyn Roland, Bert Gielen, Leonardo Montagnani, Enrico Tomelleri, Ladislav Šigut, Matthias Peichl, Peng Zhao, Marius Schmidt, Thomas Grünwald, Mika Korkiakoski, Annalea Lohila, and Nina Buchmann
EGUsphere, https://doi.org/10.5194/egusphere-2023-2964, https://doi.org/10.5194/egusphere-2023-2964, 2024
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Effect of winter warming on forest CO2 fluxes has rarely been investigated. We tested the effect of the warm winter in 2020 on the forest CO2 fluxes across 14 sites in Europe and found that in colder sites net ecosystem productivity (NEP) declined during the warm winter, while in the warmer sites NEP increased. Warming leads to increased respiration fluxes but if not translated into a direct warming of the soil might not enhance productivity, if the soil within the rooting zone remains frozen.
Flora Desmet, Matthias Münnich, and Nicolas Gruber
Biogeosciences, 20, 5151–5175, https://doi.org/10.5194/bg-20-5151-2023, https://doi.org/10.5194/bg-20-5151-2023, 2023
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Ocean acidity extremes in the upper 250 m depth of the northeastern Pacific rapidly increase with atmospheric CO2 rise, which is worrisome for marine organisms that rapidly experience pH levels outside their local environmental conditions. Presented research shows the spatiotemporal heterogeneity in this increase between regions and depths. In particular, the subsurface increase is substantially slowed down by the presence of mesoscale eddies, often not resolved in Earth system models.
Philipp Suessle, Jan Taucher, Silvan Goldenberg, Moritz Baumann, Kristian Spilling, Andrea Noche-Ferreira, Mari Vanharanta, and Ulf Riebesell
EGUsphere, https://doi.org/10.5194/egusphere-2023-2800, https://doi.org/10.5194/egusphere-2023-2800, 2023
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Ocean alkalinity enhancement (OAE) is a negative emission technology which may alter marine communities and the particle export they drive. Here, impacts of carbonate-based OAE on the flux and attenuation of sinking particles in an oligotrophic plankton community are presented. Whilst biological parameters remained unaffected, abiotic carbonate precipitation occurred. Among counteracting OAE’s efficiency, it influenced mineral ballasting and particle sinking velocities, requiring monitoring.
Geneviève W. Elsworth, Nicole S. Lovenduski, Kristen M. Krumhardt, Thomas M. Marchitto, and Sarah Schlunegger
Biogeosciences, 20, 4477–4490, https://doi.org/10.5194/bg-20-4477-2023, https://doi.org/10.5194/bg-20-4477-2023, 2023
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Anthropogenic climate change will influence marine phytoplankton over the coming century. Here, we quantify the influence of anthropogenic climate change on marine phytoplankton internal variability using an Earth system model ensemble and identify a decline in global phytoplankton biomass variance with warming. Our results suggest that climate mitigation efforts that account for marine phytoplankton changes should also consider changes in phytoplankton variance driven by anthropogenic warming.
Olivia Haas, Iain Colin Prentice, and Sandy P. Harrison
Biogeosciences, 20, 3981–3995, https://doi.org/10.5194/bg-20-3981-2023, https://doi.org/10.5194/bg-20-3981-2023, 2023
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We quantify the impact of CO2 and climate on global patterns of burnt area, fire size, and intensity under Last Glacial Maximum (LGM) conditions using three climate scenarios. Climate change alone did not produce the observed LGM reduction in burnt area, but low CO2 did through reducing vegetation productivity. Fire intensity was sensitive to CO2 but strongly affected by changes in atmospheric dryness. Low CO2 caused smaller fires; climate had the opposite effect except in the driest scenario.
Rebecca M. Varney, Sarah E. Chadburn, Eleanor J. Burke, Simon Jones, Andy J. Wiltshire, and Peter M. Cox
Biogeosciences, 20, 3767–3790, https://doi.org/10.5194/bg-20-3767-2023, https://doi.org/10.5194/bg-20-3767-2023, 2023
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This study evaluates soil carbon projections during the 21st century in CMIP6 Earth system models. In general, we find a reduced spread of changes in global soil carbon in CMIP6 compared to the previous CMIP5 generation. The reduced CMIP6 spread arises from an emergent relationship between soil carbon changes due to change in plant productivity and soil carbon changes due to changes in turnover time. We show that this relationship is consistent with false priming under transient climate change.
Claudia Hinrichs, Peter Köhler, Christoph Völker, and Judith Hauck
Biogeosciences, 20, 3717–3735, https://doi.org/10.5194/bg-20-3717-2023, https://doi.org/10.5194/bg-20-3717-2023, 2023
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This study evaluated the alkalinity distribution in 14 climate models and found that most models underestimate alkalinity at the surface and overestimate it in the deeper ocean. It highlights the need for better understanding and quantification of processes driving alkalinity distribution and calcium carbonate dissolution and the importance of accounting for biases in model results when evaluating potential ocean alkalinity enhancement experiments.
Yonghong Zheng, Huanfeng Shen, Rory Abernethy, and Rob Wilson
Biogeosciences, 20, 3481–3490, https://doi.org/10.5194/bg-20-3481-2023, https://doi.org/10.5194/bg-20-3481-2023, 2023
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Investigations in central and western China show that tree ring inverted latewood intensity expresses a strong positive relationship with growing-season temperatures, indicating exciting potential for regions south of 30° N that are traditionally not targeted for temperature reconstructions. Earlywood BI also shows good potential to reconstruct hydroclimate parameters in some humid areas and will enhance ring-width-based hydroclimate reconstructions in the future.
Stefano Potter, Sol Cooperdock, Sander Veraverbeke, Xanthe Walker, Michelle C. Mack, Scott J. Goetz, Jennifer Baltzer, Laura Bourgeau-Chavez, Arden Burrell, Catherine Dieleman, Nancy French, Stijn Hantson, Elizabeth E. Hoy, Liza Jenkins, Jill F. Johnstone, Evan S. Kane, Susan M. Natali, James T. Randerson, Merritt R. Turetsky, Ellen Whitman, Elizabeth Wiggins, and Brendan M. Rogers
Biogeosciences, 20, 2785–2804, https://doi.org/10.5194/bg-20-2785-2023, https://doi.org/10.5194/bg-20-2785-2023, 2023
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Here we developed a new burned-area detection algorithm between 2001–2019 across Alaska and Canada at 500 m resolution. We estimate 2.37 Mha burned annually between 2001–2019 over the domain, emitting 79.3 Tg C per year, with a mean combustion rate of 3.13 kg C m−2. We found larger-fire years were generally associated with greater mean combustion. The burned-area and combustion datasets described here can be used for local- to continental-scale applications of boreal fire science.
V. Rachel Chimuka, Claude-Michel Nzotungicimpaye, and Kirsten Zickfeld
Biogeosciences, 20, 2283–2299, https://doi.org/10.5194/bg-20-2283-2023, https://doi.org/10.5194/bg-20-2283-2023, 2023
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We propose a new method to quantify carbon cycle feedbacks under negative CO2 emissions. Our method isolates the lagged carbon cycle response to preceding positive emissions from the response to negative emissions. Our findings suggest that feedback parameters calculated with the novel approach are larger than those calculated with the conventional approach whereby carbon cycle inertia is not corrected for, with implications for the effectiveness of carbon dioxide removal in reducing CO2 levels.
Marcus Breil, Annabell Weber, and Joaquim G. Pinto
Biogeosciences, 20, 2237–2250, https://doi.org/10.5194/bg-20-2237-2023, https://doi.org/10.5194/bg-20-2237-2023, 2023
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A promising strategy for mitigating burdens of heat extremes in Europe is to replace dark coniferous forests with brighter deciduous forests. The consequence of this would be reduced absorption of solar radiation, which should reduce the intensities of heat periods. In this study, we show that deciduous forests have a certain cooling effect on heat period intensities in Europe. However, the magnitude of the temperature reduction is quite small.
Gesche Blume-Werry, Jonatan Klaminder, Eveline J. Krab, and Sylvain Monteux
Biogeosciences, 20, 1979–1990, https://doi.org/10.5194/bg-20-1979-2023, https://doi.org/10.5194/bg-20-1979-2023, 2023
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Northern soils store a lot of carbon. Most research has focused on how this carbon storage is regulated by cold temperatures. However, it is soil organisms, from minute bacteria to large earthworms, that decompose the organic material. Novel soil organisms from further south could increase decomposition rates more than climate change does and lead to carbon losses. We therefore advocate for including soil organisms when predicting the fate of soil functions in warming northern ecosystems.
Koramanghat Unnikrishnan Jayakrishnan and Govindasamy Bala
Biogeosciences, 20, 1863–1877, https://doi.org/10.5194/bg-20-1863-2023, https://doi.org/10.5194/bg-20-1863-2023, 2023
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Afforestation and reducing fossil fuel emissions are two important mitigation strategies to reduce the amount of global warming. Our work shows that reducing fossil fuel emissions is relatively more effective than afforestation for the same amount of carbon removed from the atmosphere. However, understanding of the processes that govern the biophysical effects of afforestation should be improved before considering our results for climate policy.
Jens Hartmann, Niels Suitner, Carl Lim, Julieta Schneider, Laura Marín-Samper, Javier Arístegui, Phil Renforth, Jan Taucher, and Ulf Riebesell
Biogeosciences, 20, 781–802, https://doi.org/10.5194/bg-20-781-2023, https://doi.org/10.5194/bg-20-781-2023, 2023
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CO2 can be stored in the ocean via increasing alkalinity of ocean water. Alkalinity can be created via dissolution of alkaline materials, like limestone or soda. Presented research studies boundaries for increasing alkalinity in seawater. The best way to increase alkalinity was found using an equilibrated solution, for example as produced from reactors. Adding particles for dissolution into seawater on the other hand produces the risk of losing alkalinity and degassing of CO2 to the atmosphere.
Damian L. Arévalo-Martínez, Amir Haroon, Hermann W. Bange, Ercan Erkul, Marion Jegen, Nils Moosdorf, Jens Schneider von Deimling, Christian Berndt, Michael Ernst Böttcher, Jasper Hoffmann, Volker Liebetrau, Ulf Mallast, Gudrun Massmann, Aaron Micallef, Holly A. Michael, Hendrik Paasche, Wolfgang Rabbel, Isaac Santos, Jan Scholten, Katrin Schwalenberg, Beata Szymczycha, Ariel T. Thomas, Joonas J. Virtasalo, Hannelore Waska, and Bradley A. Weymer
Biogeosciences, 20, 647–662, https://doi.org/10.5194/bg-20-647-2023, https://doi.org/10.5194/bg-20-647-2023, 2023
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Groundwater flows at the land–ocean transition and the extent of freshened groundwater below the seafloor are increasingly relevant in marine sciences, both because they are a highly uncertain term of biogeochemical budgets and due to the emerging interest in the latter as a resource. Here, we discuss our perspectives on future research directions to better understand land–ocean connectivity through groundwater and its potential responses to natural and human-induced environmental changes.
Morgan Sparey, Peter Cox, and Mark S. Williamson
Biogeosciences, 20, 451–488, https://doi.org/10.5194/bg-20-451-2023, https://doi.org/10.5194/bg-20-451-2023, 2023
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Accurate climate models are vital for mitigating climate change; however, projections often disagree. Using Köppen–Geiger bioclimate classifications we show that CMIP6 climate models agree well on the fraction of global land surface that will change classification per degree of global warming. We find that 13 % of land will change climate per degree of warming from 1 to 3 K; thus, stabilising warming at 1.5 rather than 2 K would save over 7.5 million square kilometres from bioclimatic change.
Huanhuan Wang, Chao Yue, and Sebastiaan Luyssaert
Biogeosciences, 20, 75–92, https://doi.org/10.5194/bg-20-75-2023, https://doi.org/10.5194/bg-20-75-2023, 2023
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This study provided a synthesis of three influential methods to quantify afforestation impact on surface temperature. Results showed that actual effect following afforestation was highly dependent on afforestation fraction. When full afforestation is assumed, the actual effect approaches the potential effect. We provided evidence the afforestation faction is a key factor in reconciling different methods and emphasized that it should be considered for surface cooling impacts in policy evaluation.
Ryan S. Padrón, Lukas Gudmundsson, Laibao Liu, Vincent Humphrey, and Sonia I. Seneviratne
Biogeosciences, 19, 5435–5448, https://doi.org/10.5194/bg-19-5435-2022, https://doi.org/10.5194/bg-19-5435-2022, 2022
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The answer to how much carbon land ecosystems are projected to remove from the atmosphere until 2100 is different for each Earth system model. We find that differences across models are primarily explained by the annual land carbon sink dependence on temperature and soil moisture, followed by the dependence on CO2 air concentration, and by average climate conditions. Our insights on why each model projects a relatively high or low land carbon sink can help to reduce the underlying uncertainty.
Julian Gutt, Stefanie Arndt, David Keith Alan Barnes, Horst Bornemann, Thomas Brey, Olaf Eisen, Hauke Flores, Huw Griffiths, Christian Haas, Stefan Hain, Tore Hattermann, Christoph Held, Mario Hoppema, Enrique Isla, Markus Janout, Céline Le Bohec, Heike Link, Felix Christopher Mark, Sebastien Moreau, Scarlett Trimborn, Ilse van Opzeeland, Hans-Otto Pörtner, Fokje Schaafsma, Katharina Teschke, Sandra Tippenhauer, Anton Van de Putte, Mia Wege, Daniel Zitterbart, and Dieter Piepenburg
Biogeosciences, 19, 5313–5342, https://doi.org/10.5194/bg-19-5313-2022, https://doi.org/10.5194/bg-19-5313-2022, 2022
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Long-term ecological observations are key to assess, understand and predict impacts of environmental change on biotas. We present a multidisciplinary framework for such largely lacking investigations in the East Antarctic Southern Ocean, combined with case studies, experimental and modelling work. As climate change is still minor here but is projected to start soon, the timely implementation of this framework provides the unique opportunity to document its ecological impacts from the very onset.
Daniel François, Adina Paytan, Olga Maria Oliveira de Araújo, Ricardo Tadeu Lopes, and Cátia Fernandes Barbosa
Biogeosciences, 19, 5269–5285, https://doi.org/10.5194/bg-19-5269-2022, https://doi.org/10.5194/bg-19-5269-2022, 2022
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Our analysis revealed that under the two most conservative acidification projections foraminifera assemblages did not display considerable changes. However, a significant decrease in species richness was observed when pH decreases to 7.7 pH units, indicating adverse effects under high-acidification scenarios. A micro-CT analysis revealed that calcified tests of Archaias angulatus were of lower density in low pH, suggesting no acclimation capacity for this species.
Leander Moesinger, Ruxandra-Maria Zotta, Robin van der Schalie, Tracy Scanlon, Richard de Jeu, and Wouter Dorigo
Biogeosciences, 19, 5107–5123, https://doi.org/10.5194/bg-19-5107-2022, https://doi.org/10.5194/bg-19-5107-2022, 2022
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The standardized vegetation optical depth index (SVODI) can be used to monitor the vegetation condition, such as whether the vegetation is unusually dry or wet. SVODI has global coverage, spans the past 3 decades and is derived from multiple spaceborne passive microwave sensors of that period. SVODI is based on a new probabilistic merging method that allows the merging of normally distributed data even if the data are not gap-free.
Rebecca M. Varney, Sarah E. Chadburn, Eleanor J. Burke, and Peter M. Cox
Biogeosciences, 19, 4671–4704, https://doi.org/10.5194/bg-19-4671-2022, https://doi.org/10.5194/bg-19-4671-2022, 2022
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Soil carbon is the Earth’s largest terrestrial carbon store, and the response to climate change represents one of the key uncertainties in obtaining accurate global carbon budgets required to successfully militate against climate change. The ability of climate models to simulate present-day soil carbon is therefore vital. This study assesses soil carbon simulation in the latest ensemble of models which allows key areas for future model development to be identified.
Laurent Bopp, Olivier Aumont, Lester Kwiatkowski, Corentin Clerc, Léonard Dupont, Christian Ethé, Thomas Gorgues, Roland Séférian, and Alessandro Tagliabue
Biogeosciences, 19, 4267–4285, https://doi.org/10.5194/bg-19-4267-2022, https://doi.org/10.5194/bg-19-4267-2022, 2022
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The impact of anthropogenic climate change on the biological production of phytoplankton in the ocean is a cause for concern because its evolution could affect the response of marine ecosystems to climate change. Here, we identify biological N fixation and its response to future climate change as a key process in shaping the future evolution of marine phytoplankton production. Our results show that further study of how this nitrogen fixation responds to environmental change is essential.
Negar Vakilifard, Richard G. Williams, Philip B. Holden, Katherine Turner, Neil R. Edwards, and David J. Beerling
Biogeosciences, 19, 4249–4265, https://doi.org/10.5194/bg-19-4249-2022, https://doi.org/10.5194/bg-19-4249-2022, 2022
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To remain within the Paris climate agreement, there is an increasing need to develop and implement carbon capture and sequestration techniques. The global climate benefits of implementing negative emission technologies over the next century are assessed using an Earth system model covering a wide range of plausible climate states. In some model realisations, there is continued warming after emissions cease. This continued warming is avoided if negative emissions are incorporated.
Marco Reale, Gianpiero Cossarini, Paolo Lazzari, Tomas Lovato, Giorgio Bolzon, Simona Masina, Cosimo Solidoro, and Stefano Salon
Biogeosciences, 19, 4035–4065, https://doi.org/10.5194/bg-19-4035-2022, https://doi.org/10.5194/bg-19-4035-2022, 2022
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Future projections under the RCP8.5 and RCP4.5 emission scenarios of the Mediterranean Sea biogeochemistry at the end of the 21st century show different levels of decline in nutrients, oxygen and biomasses and an acidification of the water column. The signal intensity is stronger under RCP8.5 and in the eastern Mediterranean. Under RCP4.5, after the second half of the 21st century, biogeochemical variables show a recovery of the values observed at the beginning of the investigated period.
Charly A. Moras, Lennart T. Bach, Tyler Cyronak, Renaud Joannes-Boyau, and Kai G. Schulz
Biogeosciences, 19, 3537–3557, https://doi.org/10.5194/bg-19-3537-2022, https://doi.org/10.5194/bg-19-3537-2022, 2022
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This research presents the first laboratory results of quick and hydrated lime dissolution in natural seawater. These two minerals are of great interest for ocean alkalinity enhancement, a strategy aiming to decrease atmospheric CO2 concentrations. Following the dissolution of these minerals, we identified several hurdles and presented ways to avoid them or completely negate them. Finally, we proceeded to various simulations in today’s oceans to implement the strategy at its highest potential.
Taraka Davies-Barnard, Sönke Zaehle, and Pierre Friedlingstein
Biogeosciences, 19, 3491–3503, https://doi.org/10.5194/bg-19-3491-2022, https://doi.org/10.5194/bg-19-3491-2022, 2022
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Biological nitrogen fixation is the largest natural input of new nitrogen onto land. Earth system models mainly represent global total terrestrial biological nitrogen fixation within observational uncertainties but overestimate tropical fixation. The model range of increase in biological nitrogen fixation in the SSP3-7.0 scenario is 3 % to 87 %. While biological nitrogen fixation is a key source of new nitrogen, its predictive power for net primary productivity in models is limited.
Niel Verbrigghe, Niki I. W. Leblans, Bjarni D. Sigurdsson, Sara Vicca, Chao Fang, Lucia Fuchslueger, Jennifer L. Soong, James T. Weedon, Christopher Poeplau, Cristina Ariza-Carricondo, Michael Bahn, Bertrand Guenet, Per Gundersen, Gunnhildur E. Gunnarsdóttir, Thomas Kätterer, Zhanfeng Liu, Marja Maljanen, Sara Marañón-Jiménez, Kathiravan Meeran, Edda S. Oddsdóttir, Ivika Ostonen, Josep Peñuelas, Andreas Richter, Jordi Sardans, Páll Sigurðsson, Margaret S. Torn, Peter M. Van Bodegom, Erik Verbruggen, Tom W. N. Walker, Håkan Wallander, and Ivan A. Janssens
Biogeosciences, 19, 3381–3393, https://doi.org/10.5194/bg-19-3381-2022, https://doi.org/10.5194/bg-19-3381-2022, 2022
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In subarctic grassland on a geothermal warming gradient, we found large reductions in topsoil carbon stocks, with carbon stocks linearly declining with warming intensity. Most importantly, however, we observed that soil carbon stocks stabilised within 5 years of warming and remained unaffected by warming thereafter, even after > 50 years of warming. Moreover, in contrast to the large topsoil carbon losses, subsoil carbon stocks remained unaffected after > 50 years of soil warming.
Roberto Pilli, Ramdane Alkama, Alessandro Cescatti, Werner A. Kurz, and Giacomo Grassi
Biogeosciences, 19, 3263–3284, https://doi.org/10.5194/bg-19-3263-2022, https://doi.org/10.5194/bg-19-3263-2022, 2022
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To become carbon neutral by 2050, the European Union (EU27) forest C sink should increase to −450 Mt CO2 yr-1. Our study highlights that under current management practices (i.e. excluding any policy scenario) the forest C sink of the EU27 member states and the UK may decrease to about −250 Mt CO2eq yr-1 in 2050. The expected impacts of future climate change, however, add a considerable uncertainty, potentially nearly doubling or halving the sink associated with forest management.
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