148 citations as recorded by crossref.

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18. Regulation of calcification site pH is a polyphyletic but not always governing response to ocean acidification Y. Liu et al. https://doi.org/10.1126/sciadv.aax1314
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20. Climate engineering by mimicking natural dust climate control: the iron salt aerosol method F. Oeste et al. https://doi.org/10.5194/esd-8-1-2017
21. Haplo-diplontic life cycle expands coccolithophore niche J. de Vries et al. https://doi.org/10.5194/bg-18-1161-2021
22. The representation of alkalinity and the carbonate pump from CMIP5 to CMIP6 Earth system models and implications for the carbon cycle A. Planchat et al. https://doi.org/10.5194/bg-20-1195-2023
23. Coastal Phytoplankton Response to Acidification and Warming Under Differing Levels of Nutrient Availability C. Law et al. https://doi.org/10.3390/microorganisms14050989
24. The DIC carbon isotope evolutions during CO2 bubbling: Implications for ocean acidification laboratory culture H. Zhang et al. https://doi.org/10.3389/fmars.2022.1045634
25. High levels of solar radiation offset impacts of ocean acidification on calcifying and non-calcifying strains of Emiliania huxleyi P. Jin et al. https://doi.org/10.3354/meps12042
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27. Distribution of extant coccolithophores from the northwest continental shelf of India during the summer monsoon M. Chowdhury et al. https://doi.org/10.1080/00318884.2022.2037340
28. Intracellular nanoscale architecture as a master regulator of calcium carbonate crystallization in marine microalgae Y. Kadan et al. https://doi.org/10.1073/pnas.2025670118
29. Long-term dynamics of adaptive evolution in a globally important phytoplankton species to ocean acidification L. Schlüter et al. https://doi.org/10.1126/sciadv.1501660
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34. Seasonal variability of the carbonate system and coccolithophore Emiliania huxleyi at a Scottish Coastal Observatory monitoring site P. León et al. https://doi.org/10.1016/j.ecss.2018.01.011
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38. Short-term effects of winter warming and acidification on phytoplankton growth and mortality: more losers than winners in a temperate coastal lagoon R. Domingues et al. https://doi.org/10.1007/s10750-021-04672-0
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42. Human Versus Natural Influences on Climate and Biodiversity: The Carbon Dioxide Connection W. Davis https://doi.org/10.3390/sci7040152
43. Coccolithophore Abundance, Degree of Calcification, and Their Contribution to Particulate Inorganic Carbon in the South China Sea X. Jin et al. https://doi.org/10.1029/2021JG006657
44. Independence of nutrient limitation and carbon dioxide impacts on the Southern Ocean coccolithophore Emiliania huxleyi M. Müller et al. https://doi.org/10.1038/ismej.2017.53
45. Microzooplankton grazing responds to simulated ocean acidification indirectly through changes in prey cellular characteristics M. Olson et al. https://doi.org/10.3354/meps12716
46. Meta-analysis reveals responses of coccolithophores and diatoms to warming J. Wang et al. https://doi.org/10.1016/j.marenvres.2023.106275
47. Carbonate system and acidification of the Adriatic Sea C. Cantoni et al. https://doi.org/10.1016/j.marchem.2024.104462
48. Effects of temperature and pH on the growth, calcification, and biomechanics of two species of articulated coralline algae R. Guenther et al. https://doi.org/10.3354/meps14166
49. Influence of Hydrodynamic Regime on Living Coccolithophores in the Cretan Sea and South Cretan Area (Eastern Mediterranean) M. Dimiza et al. https://doi.org/10.3390/jmse14050517
50. Increased Biogenic Calcification and Burial Under Elevated pCO2 During the Miocene: A Model‐Data Comparison W. Si et al. https://doi.org/10.1029/2022GB007541
51. Palaeoenvironmental vs. evolutionary control on size variation of coccoliths across the Lower-Middle Jurassic J. Ferreira et al. https://doi.org/10.1016/j.palaeo.2016.10.029
52. Uncertain fate of pelagic calcifying protists: a cellular perspective on a changing ocean A. Shemi et al. https://doi.org/10.1093/ismejo/wraf007
53. Day length as a key factor moderating the response of coccolithophore growth to elevated pCO2 L. Bretherton et al. https://doi.org/10.1002/lno.11115
54. Coccolithophore calcification is independent of carbonate chemistry in the tropical ocean E. Marañón et al. https://doi.org/10.1002/lno.10295
55. Meta‐analysis suggests negative, but pCO2‐specific, effects of ocean acidification on the structural and functional properties of crustacean biomaterials K. Siegel et al. https://doi.org/10.1002/ece3.8922
56. Reduced growth with increased quotas of particulate organic and inorganic carbon in the coccolithophore Emiliania huxleyi under future ocean climate change conditions Y. Zhang et al. https://doi.org/10.5194/bg-17-6357-2020
57. H+ -driven increase in CO2 uptake and decrease in HCO3− uptake explain coccolithophores' acclimation responses to ocean acidification D. Kottmeier et al. https://doi.org/10.1002/lno.10352
58. 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
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63. Estimates of the Direct Effect of Seawater pH on the Survival Rate of Species Groups in the California Current Ecosystem D. Busch et al. https://doi.org/10.1371/journal.pone.0160669
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66. Ocean acidification effects on haploid and diploid Emiliania huxleyi strains: Why changes in cell size matter M. Brady Olson et al. https://doi.org/10.1016/j.jembe.2016.12.008
67. Coccolithophore community response to increasing pCO2 in Mediterranean oligotrophic waters A. Oviedo et al. https://doi.org/10.1016/j.ecss.2015.12.007
68. Effects of elevated pCO2 on the response of coccolithophore Emiliania huxleyi to prolonged darkness L. Gao et al. https://doi.org/10.1080/17451000.2023.2169463
69. Ocean acidification research in the Mediterranean Sea: Status, trends and next steps A. Hassoun et al. https://doi.org/10.3389/fmars.2022.892670
70. Technical note: A comparison of methods for estimating coccolith mass C. Valença et al. https://doi.org/10.5194/bg-21-1601-2024
71. Large impact of light on alkenone-inferred temperatures from continuous cultures of the coccolithophore Gephyrocapsa (Emiliania) huxleyi under nutrient limitation J. Sachs & M. Wolhowe https://doi.org/10.1016/j.gca.2025.12.057
72. Surface ocean carbon dioxide during the Atlantic Meridional Transect (1995–2013); evidence of ocean acidification V. Kitidis et al. https://doi.org/10.1016/j.pocean.2016.08.005
73. Ocean warming, not acidification, controlled coccolithophore response during past greenhouse climate change S. Gibbs et al. https://doi.org/10.1130/G37273.1
74. Coccolithophore calcification studied by single-cell impedance cytometry: Towards single-cell PIC:POC measurements D. de Bruijn et al. https://doi.org/10.1016/j.bios.2020.112808
75. Calcification of an estuarine coccolithophore increases with ocean acidification when subjected to diurnally fluctuating carbonate chemistry M. White et al. https://doi.org/10.3354/meps12639
76. Physiological responses of a coccolithophore to multiple environmental drivers P. Jin et al. https://doi.org/10.1016/j.marpolbul.2019.06.032
77. Coccolithophore calcification: Changing paradigms in changing oceans C. Brownlee et al. https://doi.org/10.1016/j.actbio.2020.07.050
78. Orbital-scale variability in the contribution of foraminifera and coccolithophores to pelagic carbonate production P. Cornuault et al. https://doi.org/10.5194/bg-22-7973-2025
79. Ocean warming modulates the effects of acidification on Emiliania huxleyi calcification and sinking S. Milner et al. https://doi.org/10.1002/lno.10292
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82. The Phenomenon Of Emiliania Huxleyi In Aspects Of Global Climate And The Ecology Of The World Ocean D. Pozdnyakov et al. https://doi.org/10.24057/2071-9388-2020-214
83. The carbonate pump feedback on alkalinity and the carbon cycle in the 21st century and beyond A. Planchat et al. https://doi.org/10.5194/esd-15-565-2024
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