Articles | Volume 8, issue 3
https://doi.org/10.5194/bg-8-771-2011
© Author(s) 2011. 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-8-771-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Effects of changes in carbonate chemistry speciation on Coccolithus braarudii: a discussion of coccolithophorid sensitivities
S. A. Krug
Leibniz Institute of Marine Sciences (IFM-GEOMAR), Düsternbrooker Weg 20, 24105 Kiel, Germany
K. G. Schulz
Leibniz Institute of Marine Sciences (IFM-GEOMAR), Düsternbrooker Weg 20, 24105 Kiel, Germany
U. Riebesell
Leibniz Institute of Marine Sciences (IFM-GEOMAR), Düsternbrooker Weg 20, 24105 Kiel, Germany
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39 citations as recorded by crossref.
- Growth response of Emiliania huxleyi to ocean alkalinity enhancement G. Faucher et al. https://doi.org/10.5194/bg-22-405-2025
- Predicting coccolithophore rain ratio responses to calcite saturation state S. Fielding https://doi.org/10.3354/meps10657
- Editorial preface to special issue: Biocalcifier resilience and response during Phanerozoic global climate changes C. Bottini & G. Crippa https://doi.org/10.1016/j.palaeo.2025.113106
- Changes in calcification of coccoliths under stable atmospheric CO2 C. Berger et al. https://doi.org/10.5194/bg-11-929-2014
- Phytoplankton Blooms at Increasing Levels of Atmospheric Carbon Dioxide: Experimental Evidence for Negative Effects on Prymnesiophytes and Positive on Small Picoeukaryotes K. Schulz et al. https://doi.org/10.3389/fmars.2017.00064
- The role of ocean acidification in Emiliania huxleyi coccolith thinning in the Mediterranean Sea K. Meier et al. https://doi.org/10.5194/bg-11-2857-2014
- Low sensitivity of a heavily calcified coccolithophore under increasing CO2: the case study of Helicosphaera carteri S. Bianco et al. https://doi.org/10.5194/bg-22-1821-2025
- The requirement for calcification differs between ecologically important coccolithophore species C. Walker et al. https://doi.org/10.1111/nph.15272
- High nitrate to phosphorus regime attenuates negative effects of rising pCO2 on total population carbon accumulation B. Matthiessen et al. https://doi.org/10.5194/bg-9-1195-2012
- Stable isotope fractionation of strontium in coccolithophore calcite: Influence of temperature and carbonate chemistry M. Müller et al. https://doi.org/10.1111/gbi.12276
- Environmental controls on coccolithophore calcification J. Raven & K. Crawfurd https://doi.org/10.3354/meps09993
- Differential impacts of pH on growth, physiology, and elemental stoichiometry across three coccolithophore species N. Chauhan & R. Rickaby https://doi.org/10.1002/lno.12738
- Multispecies expression of coccolithophore vital effects with changing CO2 concentrations and pH in the laboratory with insights for reconstructing CO2 levels in geological history G. Le Guevel et al. https://doi.org/10.5194/bg-22-2287-2025
- High temperature decreases the PIC / POC ratio and increases phosphorus requirements in Coccolithus pelagicus (Haptophyta) A. Gerecht et al. https://doi.org/10.5194/bg-11-3531-2014
- Trace metal limitations (Co, Zn) increase PIC/POC ratio in coccolithophore Emiliania huxleyi M. Boye et al. https://doi.org/10.1016/j.marchem.2017.03.006
- A coastal coccolithophore maintains pH homeostasis and switches carbon sources in response to ocean acidification Y. Liu et al. https://doi.org/10.1038/s41467-018-04463-7
- Temperature Modulates Coccolithophorid Sensitivity of Growth, Photosynthesis and Calcification to Increasing Seawater pCO2 S. Sett et al. https://doi.org/10.1371/journal.pone.0088308
- Influence of temperature and CO2 on the strontium and magnesium composition of coccolithophore calcite M. Müller et al. https://doi.org/10.5194/bg-11-1065-2014
- Carbon fixation of a temperate plankton community in response to calcium- and silicate-based Ocean Alkalinity Enhancement using air-sea gas exchange measurements J. Schneider et al. https://doi.org/10.5194/bg-23-137-2026
- Population-specific responses in physiological rates of Emiliania huxleyi to a broad CO2 range Y. Zhang et al. https://doi.org/10.5194/bg-15-3691-2018
- Reviews and Syntheses: Responses of coccolithophores to ocean acidification: a meta-analysis J. Meyer & U. Riebesell https://doi.org/10.5194/bg-12-1671-2015
- Ocean acidification in a geoengineering context P. Williamson & C. Turley https://doi.org/10.1098/rsta.2012.0167
- Physiology regulates the relationship between coccosphere geometry and growth phase in coccolithophores R. Sheward et al. https://doi.org/10.5194/bg-14-1493-2017
- Coccolithogenesis In Scyphosphaera apsteinii (Prymnesiophyceae) B. Drescher et al. https://doi.org/10.1111/j.1529-8817.2012.01227.x
- Dissolved Inorganic Carbon Inventory and CO2Sequestration in Ureolytic Biocalcification Process withBacillus Pasteurii B. Mahanty et al. https://doi.org/10.1080/01490451.2013.819051
- Dissecting the impact of CO2 and pH on the mechanisms of photosynthesis and calcification in the coccolithophore Emiliania huxleyi L. Bach et al. https://doi.org/10.1111/nph.12225
- Phosphorus availability modifies carbon production in Coccolithus pelagicus (Haptophyta) A. Gerecht et al. https://doi.org/10.1016/j.jembe.2015.06.019
- A comparison of species specific sensitivities to changing light and carbonate chemistry in calcifying marine phytoplankton N. Gafar et al. https://doi.org/10.1038/s41598-019-38661-0
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- Increasing coccolith calcification during CO2 rise of the penultimate deglaciation (Termination II) K. Meier et al. https://doi.org/10.1016/j.marmicro.2014.07.001
- Influence of CO<sub>2</sub> and nitrogen limitation on the coccolith volume of <I>Emiliania huxleyi</I> (Haptophyta) M. Müller et al. https://doi.org/10.5194/bg-9-4155-2012
- Cascading effects augment the direct impact of CO2 on phytoplankton growth in a biogeochemical model M. Seifert et al. https://doi.org/10.1525/elementa.2021.00104
- Quantifying the Atmospheric CO2 Forcing Effect on Surface Ocean pCO2 in the North Pacific Subtropical Gyre in the Past Two Decades S. Chen et al. https://doi.org/10.3389/fmars.2021.636881
- Productivity response of calcareous nannoplankton to Eocene Thermal Maximum 2 (ETM2) M. Dedert et al. https://doi.org/10.5194/cp-8-977-2012
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- Reduced H+channel activity disrupts pH homeostasis and calcification in coccolithophores at low ocean pH D. Kottmeier et al. https://doi.org/10.1073/pnas.2118009119
- Covariation of metabolic rates and cell size in coccolithophores G. Aloisi https://doi.org/10.5194/bg-12-4665-2015
- Coccolithophore particulate inorganic and organic carbon ratios: An evaluation of acid decalcification methods M. Cox et al. https://doi.org/10.1002/lom3.70051
- Particulate inorganic to organic carbon production as a predictor for coccolithophorid sensitivity to ongoing ocean acidification N. Gafar et al. https://doi.org/10.1002/lol2.10105
39 citations as recorded by crossref.
- Growth response of Emiliania huxleyi to ocean alkalinity enhancement G. Faucher et al. https://doi.org/10.5194/bg-22-405-2025
- Predicting coccolithophore rain ratio responses to calcite saturation state S. Fielding https://doi.org/10.3354/meps10657
- Editorial preface to special issue: Biocalcifier resilience and response during Phanerozoic global climate changes C. Bottini & G. Crippa https://doi.org/10.1016/j.palaeo.2025.113106
- Changes in calcification of coccoliths under stable atmospheric CO2 C. Berger et al. https://doi.org/10.5194/bg-11-929-2014
- Phytoplankton Blooms at Increasing Levels of Atmospheric Carbon Dioxide: Experimental Evidence for Negative Effects on Prymnesiophytes and Positive on Small Picoeukaryotes K. Schulz et al. https://doi.org/10.3389/fmars.2017.00064
- The role of ocean acidification in Emiliania huxleyi coccolith thinning in the Mediterranean Sea K. Meier et al. https://doi.org/10.5194/bg-11-2857-2014
- Low sensitivity of a heavily calcified coccolithophore under increasing CO2: the case study of Helicosphaera carteri S. Bianco et al. https://doi.org/10.5194/bg-22-1821-2025
- The requirement for calcification differs between ecologically important coccolithophore species C. Walker et al. https://doi.org/10.1111/nph.15272
- High nitrate to phosphorus regime attenuates negative effects of rising pCO2 on total population carbon accumulation B. Matthiessen et al. https://doi.org/10.5194/bg-9-1195-2012
- Stable isotope fractionation of strontium in coccolithophore calcite: Influence of temperature and carbonate chemistry M. Müller et al. https://doi.org/10.1111/gbi.12276
- Environmental controls on coccolithophore calcification J. Raven & K. Crawfurd https://doi.org/10.3354/meps09993
- Differential impacts of pH on growth, physiology, and elemental stoichiometry across three coccolithophore species N. Chauhan & R. Rickaby https://doi.org/10.1002/lno.12738
- Multispecies expression of coccolithophore vital effects with changing CO2 concentrations and pH in the laboratory with insights for reconstructing CO2 levels in geological history G. Le Guevel et al. https://doi.org/10.5194/bg-22-2287-2025
- High temperature decreases the PIC / POC ratio and increases phosphorus requirements in Coccolithus pelagicus (Haptophyta) A. Gerecht et al. https://doi.org/10.5194/bg-11-3531-2014
- Trace metal limitations (Co, Zn) increase PIC/POC ratio in coccolithophore Emiliania huxleyi M. Boye et al. https://doi.org/10.1016/j.marchem.2017.03.006
- A coastal coccolithophore maintains pH homeostasis and switches carbon sources in response to ocean acidification Y. Liu et al. https://doi.org/10.1038/s41467-018-04463-7
- Temperature Modulates Coccolithophorid Sensitivity of Growth, Photosynthesis and Calcification to Increasing Seawater pCO2 S. Sett et al. https://doi.org/10.1371/journal.pone.0088308
- Influence of temperature and CO2 on the strontium and magnesium composition of coccolithophore calcite M. Müller et al. https://doi.org/10.5194/bg-11-1065-2014
- Carbon fixation of a temperate plankton community in response to calcium- and silicate-based Ocean Alkalinity Enhancement using air-sea gas exchange measurements J. Schneider et al. https://doi.org/10.5194/bg-23-137-2026
- Population-specific responses in physiological rates of Emiliania huxleyi to a broad CO2 range Y. Zhang et al. https://doi.org/10.5194/bg-15-3691-2018
- Reviews and Syntheses: Responses of coccolithophores to ocean acidification: a meta-analysis J. Meyer & U. Riebesell https://doi.org/10.5194/bg-12-1671-2015
- Ocean acidification in a geoengineering context P. Williamson & C. Turley https://doi.org/10.1098/rsta.2012.0167
- Physiology regulates the relationship between coccosphere geometry and growth phase in coccolithophores R. Sheward et al. https://doi.org/10.5194/bg-14-1493-2017
- Coccolithogenesis In Scyphosphaera apsteinii (Prymnesiophyceae) B. Drescher et al. https://doi.org/10.1111/j.1529-8817.2012.01227.x
- Dissolved Inorganic Carbon Inventory and CO2Sequestration in Ureolytic Biocalcification Process withBacillus Pasteurii B. Mahanty et al. https://doi.org/10.1080/01490451.2013.819051
- Dissecting the impact of CO2 and pH on the mechanisms of photosynthesis and calcification in the coccolithophore Emiliania huxleyi L. Bach et al. https://doi.org/10.1111/nph.12225
- Phosphorus availability modifies carbon production in Coccolithus pelagicus (Haptophyta) A. Gerecht et al. https://doi.org/10.1016/j.jembe.2015.06.019
- A comparison of species specific sensitivities to changing light and carbonate chemistry in calcifying marine phytoplankton N. Gafar et al. https://doi.org/10.1038/s41598-019-38661-0
- Growth of the coccolithophore Emiliania huxleyi in light- and nutrient-limited batch reactors: relevance for the BIOSOPE deep ecological niche of coccolithophores L. Perrin et al. https://doi.org/10.5194/bg-13-5983-2016
- Increasing coccolith calcification during CO2 rise of the penultimate deglaciation (Termination II) K. Meier et al. https://doi.org/10.1016/j.marmicro.2014.07.001
- Influence of CO<sub>2</sub> and nitrogen limitation on the coccolith volume of <I>Emiliania huxleyi</I> (Haptophyta) M. Müller et al. https://doi.org/10.5194/bg-9-4155-2012
- Cascading effects augment the direct impact of CO2 on phytoplankton growth in a biogeochemical model M. Seifert et al. https://doi.org/10.1525/elementa.2021.00104
- Quantifying the Atmospheric CO2 Forcing Effect on Surface Ocean pCO2 in the North Pacific Subtropical Gyre in the Past Two Decades S. Chen et al. https://doi.org/10.3389/fmars.2021.636881
- Productivity response of calcareous nannoplankton to Eocene Thermal Maximum 2 (ETM2) M. Dedert et al. https://doi.org/10.5194/cp-8-977-2012
- Species-specific calcite production reveals Coccolithus pelagicus as the key calcifier in the Arctic Ocean C. Daniels et al. https://doi.org/10.3354/meps11820
- Reduced H+channel activity disrupts pH homeostasis and calcification in coccolithophores at low ocean pH D. Kottmeier et al. https://doi.org/10.1073/pnas.2118009119
- Covariation of metabolic rates and cell size in coccolithophores G. Aloisi https://doi.org/10.5194/bg-12-4665-2015
- Coccolithophore particulate inorganic and organic carbon ratios: An evaluation of acid decalcification methods M. Cox et al. https://doi.org/10.1002/lom3.70051
- Particulate inorganic to organic carbon production as a predictor for coccolithophorid sensitivity to ongoing ocean acidification N. Gafar et al. https://doi.org/10.1002/lol2.10105
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