Articles | Volume 11, issue 1
https://doi.org/10.5194/bg-11-33-2014
© Author(s) 2014. 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-11-33-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
04 Jan 2014
Research article |
| 04 Jan 2014
The iron budget in ocean surface waters in the 20th and 21st centuries: projections by the Community Earth System Model version 1
K. Misumi
Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, 1646 Abiko, Abiko, Chiba 270-1194, Japan
K. Lindsay
Climate and Global Dynamics Division, National Center for Atmospheric Research, P.O. Box 3000, Boulder, CO 80307-3000, USA
J. K. Moore
Department of Earth System Science, University of California at Irvine; 3214 Croul Hall, Irvine, CA 92697-3100, USA
S. C. Doney
Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution; 266 Woods Hole Rd., MS# 25, Woods Hole, MA 02543-1050, USA
F. O. Bryan
Climate and Global Dynamics Division, National Center for Atmospheric Research, P.O. Box 3000, Boulder, CO 80307-3000, USA
D. Tsumune
Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, 1646 Abiko, Abiko, Chiba 270-1194, Japan
Y. Yoshida
Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, 1646 Abiko, Abiko, Chiba 270-1194, Japan
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Global NPP and EP are reduced considerably for RCP8.5. Negative response of NPP and EP to stratification increases reflects a bottom-up control. Models with dynamic phytoplankton community structure show larger declines in EP than in NPP driven by phytoplankton community composition shifts. Projections of the NPP response to climate change depend on the phytoplankton community structure, the efficiency of the biological pump and the levels of regenerated production.
Charlotte Laufkötter, Meike Vogt, Nicolas Gruber, Olivier Aumont, Laurent Bopp, Scott C. Doney, John P. Dunne, Judith Hauck, Jasmin G. John, Ivan D. Lima, Roland Seferian, and Christoph Völker
Biogeosciences, 13, 4023–4047, https://doi.org/10.5194/bg-13-4023-2016, https://doi.org/10.5194/bg-13-4023-2016, 2016
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We compare future projections in marine export production, generated by four ecosystem models under IPCC's high-emission scenario RCP8.5. While all models project decreases in export, they differ strongly regarding the drivers. The formation of sinking particles of organic matter is the most uncertain process with models not agreeing on either magnitude or the direction of change. Changes in diatom concentration are a strong driver for export in some models but of low significance in others.
Allison H. Baker, Yong Hu, Dorit M. Hammerling, Yu-heng Tseng, Haiying Xu, Xiaomeng Huang, Frank O. Bryan, and Guangwen Yang
Geosci. Model Dev., 9, 2391–2406, https://doi.org/10.5194/gmd-9-2391-2016, https://doi.org/10.5194/gmd-9-2391-2016, 2016
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Software quality assurance is critical to detecting errors in large, complex climate simulation codes. We focus on ocean model simulation data in the context of an ensemble-based statistical consistency testing approach developed for atmospheric data. Because ocean and atmosphere models have differing characteristics, we develop a new statistical tool to evaluate ocean model simulation data that provide a simple, subjective, and systematic way to detect errors and instil model confidence.
Roland Séférian, Marion Gehlen, Laurent Bopp, Laure Resplandy, James C. Orr, Olivier Marti, John P. Dunne, James R. Christian, Scott C. Doney, Tatiana Ilyina, Keith Lindsay, Paul R. Halloran, Christoph Heinze, Joachim Segschneider, Jerry Tjiputra, Olivier Aumont, and Anastasia Romanou
Geosci. Model Dev., 9, 1827–1851, https://doi.org/10.5194/gmd-9-1827-2016, https://doi.org/10.5194/gmd-9-1827-2016, 2016
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This paper explores how the large diversity in spin-up protocols used for ocean biogeochemistry in CMIP5 models contributed to inter-model differences in modeled fields. We show that a link between spin-up duration and skill-score metrics emerges from both individual IPSL-CM5A-LR's results and an ensemble of CMIP5 models. Our study suggests that differences in spin-up protocols constitute a source of inter-model uncertainty which would require more attention in future intercomparison exercises.
J. E. Rheuban, S. Williamson, J. E. Costa, D. M. Glover, R. W. Jakuba, D. C. McCorkle, C. Neill, T. Williams, and S. C. Doney
Biogeosciences, 13, 253–265, https://doi.org/10.5194/bg-13-253-2016, https://doi.org/10.5194/bg-13-253-2016, 2016
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We analysed 22 years of water quality data collected through a citizen science program focused on Buzzards Bay, MA. We found that summertime water temperatures warmed by nearly 2C and chlorophyll a nearly doubled across Buzzards Bay from 1992-2013. Although water quality worsened over time, nutrient concentrations remained largely the same in many places. Warming or altered rainfall patterns from a changing climate may partially offset benefits achieved by reducing nutrients.
C. Laufkötter, M. Vogt, N. Gruber, M. Aita-Noguchi, O. Aumont, L. Bopp, E. Buitenhuis, S. C. Doney, J. Dunne, T. Hashioka, J. Hauck, T. Hirata, J. John, C. Le Quéré, I. D. Lima, H. Nakano, R. Seferian, I. Totterdell, M. Vichi, and C. Völker
Biogeosciences, 12, 6955–6984, https://doi.org/10.5194/bg-12-6955-2015, https://doi.org/10.5194/bg-12-6955-2015, 2015
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We analyze changes in marine net primary production (NPP) and its drivers for the 21st century in 9 marine ecosystem models under the RCP8.5 scenario. NPP decreases in 5 models and increases in 1 model; 3 models show no significant trend. The main drivers include stronger nutrient limitation, but in many models warming-induced increases in phytoplankton growth outbalance the nutrient effect. Temperature-driven increases in grazing and other loss processes cause a net decrease in biomass and NPP.
C. Hauri, S. C. Doney, T. Takahashi, M. Erickson, G. Jiang, and H. W. Ducklow
Biogeosciences, 12, 6761–6779, https://doi.org/10.5194/bg-12-6761-2015, https://doi.org/10.5194/bg-12-6761-2015, 2015
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Evaluation of a unique 20-year-long time series of inorganic carbon and nutrient observations from the West Antarctic Peninsula region shows that summertime biological productivity and meltwater input drive a large range of surface aragonite saturation states from values < 1 (undersaturated) up to 3.9. Even though we did not detect any statistically significant long-term trends, ongoing ocean acidification and freshwater input may soon induce more unfavorable conditions than seen today.
N. S. Lovenduski, M. C. Long, and K. Lindsay
Biogeosciences, 12, 6321–6335, https://doi.org/10.5194/bg-12-6321-2015, https://doi.org/10.5194/bg-12-6321-2015, 2015
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We investigate variability in surface ocean carbonate chemistry using output from a 1000-year control simulation of an Earth System Model. We find that the detection timescale for trends is strongly influenced by the variability. As the scientific community seeks to detect the anthropogenic influence on ocean carbonate chemistry, these results will aid the interpretation of trends calculated from spatially and temporally sparse observations.
R. Arruda, P. H. R. Calil, A. A. Bianchi, S. C. Doney, N. Gruber, I. Lima, and G. Turi
Biogeosciences, 12, 5793–5809, https://doi.org/10.5194/bg-12-5793-2015, https://doi.org/10.5194/bg-12-5793-2015, 2015
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We investigate surface ocean pCO2 and air-sea CO2 fluxes climatological variability through biogeochemical modeling in the southwestern Atlantic Ocean. Surface ocean pCO2 spatio-temporal variability was found to be controlled mainly by temperature and Dissolved Inorganic Carbon (DIC). Biological production, physical transport and solubility are the main controlling processes. With different behaviors on subtropical and subantarctic open ocean, and on inner/outer continental shelves.
R. H. R. Stanley, W. J. Jenkins, S. C. Doney, and D. E. Lott III
Biogeosciences, 12, 5199–5210, https://doi.org/10.5194/bg-12-5199-2015, https://doi.org/10.5194/bg-12-5199-2015, 2015
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A long-standing enigma in oceanography is the process in which nutrients are supplied to the sunlit zone of the low nutrient regions of the ocean. In this work, we present one approach for quantifying the physical supply of nitrate to the euphotic zone in the Sargasso Sea through the use of gas tracers. We find that the nitrate supplied is more than enough to support the rates of net community production (balance of photosynthesis respiration) observed.
A. Jahn, K. Lindsay, X. Giraud, N. Gruber, B. L. Otto-Bliesner, Z. Liu, and E. C. Brady
Geosci. Model Dev., 8, 2419–2434, https://doi.org/10.5194/gmd-8-2419-2015, https://doi.org/10.5194/gmd-8-2419-2015, 2015
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Carbon isotopes have been added to the ocean model of the Community Earth System Model version 1 (CESM1). This paper describes the details of how the abiotic 14C tracer and the biotic 13C and 14C tracers were added to the existing ocean model of the CESM. In addition, it shows the first results of the new model features compared to observational data for the 1990s.
B. F. Jonsson, S. Doney, J. Dunne, and M. L. Bender
Biogeosciences, 12, 681–695, https://doi.org/10.5194/bg-12-681-2015, https://doi.org/10.5194/bg-12-681-2015, 2015
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We compare how two global circulation models simulate biological production over the year with observations. Note that models simulate the range of biological production and biomass well but fail with regard to timing and regional structures. This is probably because the physics in the models are wrong, especially vertical processes such as mixed layer dynamics.
S. Sitch, P. Friedlingstein, N. Gruber, S. D. Jones, G. Murray-Tortarolo, A. Ahlström, S. C. Doney, H. Graven, C. Heinze, C. Huntingford, S. Levis, P. E. Levy, M. Lomas, B. Poulter, N. Viovy, S. Zaehle, N. Zeng, A. Arneth, G. Bonan, L. Bopp, J. G. Canadell, F. Chevallier, P. Ciais, R. Ellis, M. Gloor, P. Peylin, S. L. Piao, C. Le Quéré, B. Smith, Z. Zhu, and R. Myneni
Biogeosciences, 12, 653–679, https://doi.org/10.5194/bg-12-653-2015, https://doi.org/10.5194/bg-12-653-2015, 2015
R. T. Letscher, J. K. Moore, Y.-C. Teng, and F. Primeau
Biogeosciences, 12, 209–221, https://doi.org/10.5194/bg-12-209-2015, https://doi.org/10.5194/bg-12-209-2015, 2015
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Marine DOM is known to exhibit stoichiometry depleted in N and P compared with POM, suggesting variable production and remineralization stoichiometry for C, N, and P within marine DOM cycling. We utilize marine DOM observations and an inverse tracer modeling framework to optimize DOM cycling parameters for the BEC biogeochemistry ocean model of the CESM, finding a variable stoichiometry with faster turnover of P > N > C superior to the commonly assumed Redfield stoichiometry for marine DOM.
M. Gehlen, R. Séférian, D. O. B. Jones, T. Roy, R. Roth, J. Barry, L. Bopp, S. C. Doney, J. P. Dunne, C. Heinze, F. Joos, J. C. Orr, L. Resplandy, J. Segschneider, and J. Tjiputra
Biogeosciences, 11, 6955–6967, https://doi.org/10.5194/bg-11-6955-2014, https://doi.org/10.5194/bg-11-6955-2014, 2014
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This study evaluates potential impacts of pH reductions on North Atlantic deep-sea ecosystems in response to latest IPCC scenarios.Multi-model projections of pH changes over the seafloor are analysed with reference to a critical threshold based on palaeo-oceanographic studies, contemporary observations and model results. By 2100 under the most severe IPCC CO2 scenario, pH reductions occur over ~23% of deep-sea canyons and ~8% of seamounts – including seamounts proposed as marine protected areas.
S. Wang, D. Bailey, K. Lindsay, J. K. Moore, and M. Holland
Biogeosciences, 11, 4713–4731, https://doi.org/10.5194/bg-11-4713-2014, https://doi.org/10.5194/bg-11-4713-2014, 2014
C. Le Quéré, G. P. Peters, R. J. Andres, R. M. Andrew, T. A. Boden, P. Ciais, P. Friedlingstein, R. A. Houghton, G. Marland, R. Moriarty, S. Sitch, P. Tans, A. Arneth, A. Arvanitis, D. C. E. Bakker, L. Bopp, J. G. Canadell, L. P. Chini, S. C. Doney, A. Harper, I. Harris, J. I. House, A. K. Jain, S. D. Jones, E. Kato, R. F. Keeling, K. Klein Goldewijk, A. Körtzinger, C. Koven, N. Lefèvre, F. Maignan, A. Omar, T. Ono, G.-H. Park, B. Pfeil, B. Poulter, M. R. Raupach, P. Regnier, C. Rödenbeck, S. Saito, J. Schwinger, J. Segschneider, B. D. Stocker, T. Takahashi, B. Tilbrook, S. van Heuven, N. Viovy, R. Wanninkhof, A. Wiltshire, and S. Zaehle
Earth Syst. Sci. Data, 6, 235–263, https://doi.org/10.5194/essd-6-235-2014, https://doi.org/10.5194/essd-6-235-2014, 2014
I. D. Lima, P. J. Lam, and S. C. Doney
Biogeosciences, 11, 1177–1198, https://doi.org/10.5194/bg-11-1177-2014, https://doi.org/10.5194/bg-11-1177-2014, 2014
Y.-W. Luo, I. D. Lima, D. M. Karl, C. A. Deutsch, and S. C. Doney
Biogeosciences, 11, 691–708, https://doi.org/10.5194/bg-11-691-2014, https://doi.org/10.5194/bg-11-691-2014, 2014
M. Ishii, R. A. Feely, K. B. Rodgers, G.-H. Park, R. Wanninkhof, D. Sasano, H. Sugimoto, C. E. Cosca, S. Nakaoka, M. Telszewski, Y. Nojiri, S. E. Mikaloff Fletcher, Y. Niwa, P. K. Patra, V. Valsala, H. Nakano, I. Lima, S. C. Doney, E. T. Buitenhuis, O. Aumont, J. P. Dunne, A. Lenton, and T. Takahashi
Biogeosciences, 11, 709–734, https://doi.org/10.5194/bg-11-709-2014, https://doi.org/10.5194/bg-11-709-2014, 2014
V. V. S. S. Sarma, A. Lenton, R. M. Law, N. Metzl, P. K. Patra, S. Doney, I. D. Lima, E. Dlugokencky, M. Ramonet, and V. Valsala
Biogeosciences, 10, 7035–7052, https://doi.org/10.5194/bg-10-7035-2013, https://doi.org/10.5194/bg-10-7035-2013, 2013
M. Vogt, T. Hashioka, M. R. Payne, E. T. Buitenhuis, C. Le Quéré, S. Alvain, M. N. Aita, L. Bopp, S. C. Doney, T. Hirata, I. Lima, S. Sailley, and Y. Yamanaka
Biogeosciences Discuss., https://doi.org/10.5194/bgd-10-17193-2013, https://doi.org/10.5194/bgd-10-17193-2013, 2013
Revised manuscript has not been submitted
T. Hashioka, M. Vogt, Y. Yamanaka, C. Le Quéré, E. T. Buitenhuis, M. N. Aita, S. Alvain, L. Bopp, T. Hirata, I. Lima, S. Sailley, and S. C. Doney
Biogeosciences, 10, 6833–6850, https://doi.org/10.5194/bg-10-6833-2013, https://doi.org/10.5194/bg-10-6833-2013, 2013
L. Bopp, L. Resplandy, J. C. Orr, S. C. Doney, J. P. Dunne, M. Gehlen, P. Halloran, C. Heinze, T. Ilyina, R. Séférian, J. Tjiputra, and M. Vichi
Biogeosciences, 10, 6225–6245, https://doi.org/10.5194/bg-10-6225-2013, https://doi.org/10.5194/bg-10-6225-2013, 2013
D. Tsumune, T. Tsubono, M. Aoyama, M. Uematsu, K. Misumi, Y. Maeda, Y. Yoshida, and H. Hayami
Biogeosciences, 10, 5601–5617, https://doi.org/10.5194/bg-10-5601-2013, https://doi.org/10.5194/bg-10-5601-2013, 2013
E. T. Buitenhuis, M. Vogt, R. Moriarty, N. Bednaršek, S. C. Doney, K. Leblanc, C. Le Quéré, Y.-W. Luo, C. O'Brien, T. O'Brien, J. Peloquin, R. Schiebel, and C. Swan
Earth Syst. Sci. Data, 5, 227–239, https://doi.org/10.5194/essd-5-227-2013, https://doi.org/10.5194/essd-5-227-2013, 2013
A. Lenton, B. Tilbrook, R. M. Law, D. Bakker, S. C. Doney, N. Gruber, M. Ishii, M. Hoppema, N. S. Lovenduski, R. J. Matear, B. I. McNeil, N. Metzl, S. E. Mikaloff Fletcher, P. M. S. Monteiro, C. Rödenbeck, C. Sweeney, and T. Takahashi
Biogeosciences, 10, 4037–4054, https://doi.org/10.5194/bg-10-4037-2013, https://doi.org/10.5194/bg-10-4037-2013, 2013
C. Le Quéré, R. J. Andres, T. Boden, T. Conway, R. A. Houghton, J. I. House, G. Marland, G. P. Peters, G. R. van der Werf, A. Ahlström, R. M. Andrew, L. Bopp, J. G. Canadell, P. Ciais, S. C. Doney, C. Enright, P. Friedlingstein, C. Huntingford, A. K. Jain, C. Jourdain, E. Kato, R. F. Keeling, K. Klein Goldewijk, S. Levis, P. Levy, M. Lomas, B. Poulter, M. R. Raupach, J. Schwinger, S. Sitch, B. D. Stocker, N. Viovy, S. Zaehle, and N. Zeng
Earth Syst. Sci. Data, 5, 165–185, https://doi.org/10.5194/essd-5-165-2013, https://doi.org/10.5194/essd-5-165-2013, 2013
M. Aoyama, M. Uematsu, D. Tsumune, and Y. Hamajima
Biogeosciences, 10, 3067–3078, https://doi.org/10.5194/bg-10-3067-2013, https://doi.org/10.5194/bg-10-3067-2013, 2013
C. Beaulieu, S. A. Henson, Jorge L. Sarmiento, J. P. Dunne, S. C. Doney, R. R. Rykaczewski, and L. Bopp
Biogeosciences, 10, 2711–2724, https://doi.org/10.5194/bg-10-2711-2013, https://doi.org/10.5194/bg-10-2711-2013, 2013
S. Khatiwala, T. Tanhua, S. Mikaloff Fletcher, M. Gerber, S. C. Doney, H. D. Graven, N. Gruber, G. A. McKinley, A. Murata, A. F. Ríos, and C. L. Sabine
Biogeosciences, 10, 2169–2191, https://doi.org/10.5194/bg-10-2169-2013, https://doi.org/10.5194/bg-10-2169-2013, 2013
R. Wanninkhof, G. -H. Park, T. Takahashi, C. Sweeney, R. Feely, Y. Nojiri, N. Gruber, S. C. Doney, G. A. McKinley, A. Lenton, C. Le Quéré, C. Heinze, J. Schwinger, H. Graven, and S. Khatiwala
Biogeosciences, 10, 1983–2000, https://doi.org/10.5194/bg-10-1983-2013, https://doi.org/10.5194/bg-10-1983-2013, 2013
U. Schuster, G. A. McKinley, N. Bates, F. Chevallier, S. C. Doney, A. R. Fay, M. González-Dávila, N. Gruber, S. Jones, J. Krijnen, P. Landschützer, N. Lefèvre, M. Manizza, J. Mathis, N. Metzl, A. Olsen, A. F. Rios, C. Rödenbeck, J. M. Santana-Casiano, T. Takahashi, R. Wanninkhof, and A. J. Watson
Biogeosciences, 10, 607–627, https://doi.org/10.5194/bg-10-607-2013, https://doi.org/10.5194/bg-10-607-2013, 2013
C. Hauri, N. Gruber, M. Vogt, S. C. Doney, R. A. Feely, Z. Lachkar, A. Leinweber, A. M. P. McDonnell, M. Munnich, and G.-K. Plattner
Biogeosciences, 10, 193–216, https://doi.org/10.5194/bg-10-193-2013, https://doi.org/10.5194/bg-10-193-2013, 2013
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Consistency of global carbon budget between concentration- and emission-driven historical experiments simulated by CMIP6 Earth system models and suggestions for improved simulation of CO2 concentration
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Impact of winter warming on CO2 fluxes in evergreen needleleaf forests
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Long-term impacts of global temperature stabilization and overshoot on exploited marine species
Modelling ozone-induced changes in wheat amino acids and protein quality using a process-based crop model
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Mapping the future afforestation distribution of China constrained by a national afforestation plan and climate change
Southern Ocean phytoplankton under climate change: a shifting balance of bottom-up and top-down control
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Direct foliar phosphorus uptake from wildfire ash
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Experiments of the efficacy of tree ring blue intensity as a climate proxy in central and western China
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Quantifying land carbon cycle feedbacks under negative CO2 emissions
The potential of an increased deciduous forest fraction to mitigate the effects of heat extremes in Europe
Ideas and perspectives: Alleviation of functional limitations by soil organisms is key to climate feedbacks from arctic soils
A comparison of the climate and carbon cycle effects of carbon removal by afforestation and an equivalent reduction in fossil fuel emissions
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Reconciling different approaches to quantifying land surface temperature impacts of afforestation using satellite observations
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Tomohiro Hajima, Michio Kawamiya, Akihiko Ito, Kaoru Tachiiri, Chris D. Jones, Vivek Arora, Victor Brovkin, Roland Séférian, Spencer Liddicoat, Pierre Friedlingstein, and Elena Shevliakova
Biogeosciences, 22, 1447–1473, https://doi.org/10.5194/bg-22-1447-2025, https://doi.org/10.5194/bg-22-1447-2025, 2025
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This study analyzes atmospheric CO2 concentrations and global carbon budgets simulated by multiple Earth system models, using several types of simulations (CO2 concentration- and emission-driven experiments). We successfully identified problems with regard to the global carbon budget in each model. We also found urgent issues with regard to land use change CO2 emissions that should be solved in the latest generation of models.
Nicolas Picard, Noël Fonton, Faustin Boyemba Bosela, Adeline Fayolle, Joël Loumeto, Gabriel Ngua Ayecaba, Bonaventure Sonké, Olga Diane Yongo Bombo, Hervé Martial Maïdou, and Alfred Ngomanda
Biogeosciences, 22, 1413–1426, https://doi.org/10.5194/bg-22-1413-2025, https://doi.org/10.5194/bg-22-1413-2025, 2025
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Allometric equations predict tree biomass and are crucial for estimating forest carbon storage, thus assessing the role of forests in climate change mitigation. Usually, these equations are selected based on tree-level predictive performance. However, we evaluated the model performance at plot and forest levels, finding it varies with plot size. This has significant implications for reducing uncertainty in biomass estimates at these levels.
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
Biogeosciences, 22, 1393–1411, https://doi.org/10.5194/bg-22-1393-2025, https://doi.org/10.5194/bg-22-1393-2025, 2025
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The effect of winter warming on forest CO2 fluxes has rarely been investigated. We tested the effect of the warm winter of 2020 on the forest CO2 fluxes across 14 sites in Europe and found that the net ecosystem productivity (NEP) across most sites declined during the warm winter due to increased respiration fluxes.
Yu Shang, Jingmin Qiu, Yuxi Weng, Xin Wang, Di Zhang, Yuwei Zhou, Juntian Xu, and Futian Li
Biogeosciences, 22, 1203–1214, https://doi.org/10.5194/bg-22-1203-2025, https://doi.org/10.5194/bg-22-1203-2025, 2025
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Research on the influences of dynamic pH on the marine ecosystem is still in its infancy. We manipulated the culturing pH to simulate pH fluctuation and found lower pH could increase eicosapentaenoic acid and docosahexaenoic acid production with unaltered growth and photosynthesis in two marine diatoms. It is important to consider pH variation for more accurate predictions regarding the consequences of acidification in coastal waters.
Anne L. Morée, Fabrice Lacroix, William W. L. Cheung, and Thomas L. Frölicher
Biogeosciences, 22, 1115–1133, https://doi.org/10.5194/bg-22-1115-2025, https://doi.org/10.5194/bg-22-1115-2025, 2025
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Using novel Earth system model simulations and applying the Aerobic Growth Index, we show that only about half of the habitat loss for marine species is realized when temperature stabilization is initially reached. The maximum habitat loss happens over a century after peak warming in a temperature overshoot scenario peaking at 2 °C before stabilizing at 1.5 °C. We also emphasize that species adaptation may be key in mitigating the long-term impacts of temperature stabilization and overshoot.
Jo Cook, Durgesh Singh Yadav, Felicity Hayes, Nathan Booth, Sam Bland, Pritha Pande, Samarthia Thankappan, and Lisa Emberson
Biogeosciences, 22, 1035–1056, https://doi.org/10.5194/bg-22-1035-2025, https://doi.org/10.5194/bg-22-1035-2025, 2025
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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.
Stéphane Doléac, Marina Lévy, Roy El Hourany, and Laurent Bopp
Biogeosciences, 22, 841–862, https://doi.org/10.5194/bg-22-841-2025, https://doi.org/10.5194/bg-22-841-2025, 2025
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The marine biogeochemistry components of Coupled Model Intercomparison Project phase 6 (CMIP6) models vary widely in their process representations. Using an innovative bioregionalization of the North Atlantic, we reveal that this model diversity largely drives the divergence in net primary production projections under a high-emission scenario. The identification of the most mechanistically realistic models allows for a substantial reduction in projection uncertainty.
Nina Bednaršek, Hanna van de Mortel, Greg Pelletier, Marisol García-Reyes, Richard A. Feely, and Andrew G. Dickson
Biogeosciences, 22, 473–498, https://doi.org/10.5194/bg-22-473-2025, https://doi.org/10.5194/bg-22-473-2025, 2025
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The environmental impacts of ocean alkalinity enhancement (OAE) are unknown. Our synthesis, based on 68 collected studies with 84 unique species, shows that 35 % of species respond positively, 26 % respond negatively, and 39 % show a neutral response to alkalinity addition. Biological thresholds were found from 50 to 500 µmol kg−1 NaOH addition. A precautionary approach is warranted to avoid potential risks, while current regulatory framework needs improvements to assure safe biological limits.
Luna J. J. Geerts, Astrid Hylén, and Filip J. R. Meysman
Biogeosciences, 22, 355–384, https://doi.org/10.5194/bg-22-355-2025, https://doi.org/10.5194/bg-22-355-2025, 2025
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Marine enhanced rock weathering (mERW) 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 mERW parameters and identifying aspects to consider when applying mERW. A major source of uncertainty is the lack of experimental studies with sediment, which can heavily influence the speed and efficiency of CO2 drawdown.
Philipp Suessle, Jan Taucher, Silvan Urs Goldenberg, Moritz Baumann, Kristian Spilling, Andrea Noche-Ferreira, Mari Vanharanta, and Ulf Riebesell
Biogeosciences, 22, 71–86, https://doi.org/10.5194/bg-22-71-2025, https://doi.org/10.5194/bg-22-71-2025, 2025
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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.
Thuy Huu Nguyen, Thomas Gaiser, Jan Vanderborght, Andrea Schnepf, Felix Bauer, Anja Klotzsche, Lena Lärm, Hubert Hüging, and Frank Ewert
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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Leaf water potential was at certain thresholds, depending on soil type, water treatment, and weather conditions. In rainfed plots, the lower water availability in the stony soil resulted in fewer roots with a higher root tissue conductance than the silty soil. In the silty soil, higher stress in the rainfed soil led to more roots with a lower root tissue conductance than in the irrigated plot. Crop responses to water stress can be opposite, depending on soil water conditions that are compared.
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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In 2022, Europe's forests faced unprecedented dry conditions. Our study aimed to understand how different forest types respond to extreme drought. Using meteorological data and satellite imagery, we compared 2022 with two previous extreme years, 2003 and 2018. Despite less severe drought in 2022, forests showed a 30 % greater decline in photosynthesis compared to 2018 and 60 % more than 2003. This suggests an alarming level of vulnerability of forests across Europe to more frequent droughts.
Qi Zheng, Johannes J. Viljoen, Xuerong Sun, and Robert J. W. Brewin
EGUsphere, https://doi.org/10.5194/egusphere-2024-3502, https://doi.org/10.5194/egusphere-2024-3502, 2024
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Phytoplankton contribute to half of Earth’s primary production, but not a lot is known about subsurface phytoplankton, living at the base of the sunlit ocean. We develop a two-layered box model to simulate phytoplankton seasonal and interannual variations in different depth layers of the ocean. Our model captures seasonal and long-term trends of the two layers, explaining how they respond to a warming ocean, furthering our understanding of how phytoplankton are responding to climate change.
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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The remaining carbon budget (RCB) represents the allowable future CO2 emissions before a temperature target is reached. Understanding the uncertainty in the RCB is critical for effective climate regulation and policy-making. One major source of uncertainty is the representation of the carbon cycle in Earth system models. We assessed how nutrient limitation affects the estimation of the RCB. We found a reduction in the estimated RCB when nutrient limitation is taken into account.
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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At ground level, the air pollutant ozone (O3) damages wheat yield and quality. We modified the DO3SE-Crop model to simulate O3 effects on wheat quality and identified onset of leaf death as the key process affecting wheat quality upon O3 exposure. This aligns with expectations, as the onset of leaf death aids nutrient transfer from leaves to grains. Breeders should prioritize wheat varieties resistant to protein loss from delayed leaf death, to maintain yield and quality under O3 exposure.
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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Recent studies described the precipitation of carbonates as a result of alkalinity enhancement in seawater, which could adversely affect the carbon sequestration potential of ocean alkalinity enhancement (OAE) approaches. By conducting experiments in natural seawater, this study observed uniform patterns during the triggered runaway carbonate precipitation, which allow the prediction of safe and efficient local application levels of OAE scenarios.
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.
Christine Kaufhold, Matteo Willeit, Bo Liu, and Andrey Ganopolski
EGUsphere, https://doi.org/10.5194/egusphere-2024-2976, https://doi.org/10.5194/egusphere-2024-2976, 2024
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This study simulates long-term future climate scenarios to examine how long CO2 emissions will persist in the atmosphere. It shows that the effectiveness of carbon removal processes varies with the amount emitted. The removal of CO2 through silicate weathering is faster than previously thought, leading to a quicker reduction over time. The combined behaviour of different carbon cycle processes emphasizes the need to include all of them in models, as to better predict long-term atmospheric CO2.
Anton Lokshin, Daniel Palchan, Elnatan Golan, Ran Erel, Daniele Andronico, and Avner Gross
EGUsphere, https://doi.org/10.5194/egusphere-2024-2531, https://doi.org/10.5194/egusphere-2024-2531, 2024
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Our research explores how chickpea plants can absorb essential nutrients like phosphorus, iron, and nickel directly from dust deposited on their leaves, in addition to uptake through their roots. This process was particularly effective under higher levels of atmospheric CO2, leading to increased plant growth. By using Nd isotopic tools, we traced the nutrients from dust and found that certain leaf traits enhance this uptake. This discovery may become increasingly important as CO2 levels rise.
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.
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.
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.
Lucia S. Layritz, Konstantin Gregor, Andreas Krause, Stefan Kruse, Ben F. Meyer, Tom A. M. Pugh, and Anja Rammig
EGUsphere, https://doi.org/10.5194/egusphere-2024-1028, https://doi.org/10.5194/egusphere-2024-1028, 2024
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Disturbances (e.g. fire) can change which species grow in a forest, affecting water, carbon, energy flows, and the climate. They are expected to increase with climate change, but it is uncertain by how much. We studied how future climate and disturbances might impact vegetation with a simulation model. Our findings highlight the importance of considering both factors, with future disturbance patterns posing significant uncertainty. More research is needed to understand their future development.
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.
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.
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
Short summary
Short summary
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.
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