59 citations as recorded by crossref.

1. Change in coccolith size and morphology due to response to temperature and salinity in coccolithophore Emiliania huxleyi (Haptophyta) isolated from the Bering and Chukchi seas K. Saruwatari et al. https://doi.org/10.5194/bg-13-2743-2016
2. Technical note: A comparison of methods for estimating coccolith mass C. Valença et al. https://doi.org/10.5194/bg-21-1601-2024
3. 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
4. Decrease in coccolithophore calcification and CO2 since the middle Miocene C. Bolton et al. https://doi.org/10.1038/ncomms10284
5. Coccolithophore community response to increasing pCO2 in Mediterranean oligotrophic waters A. Oviedo et al. https://doi.org/10.1016/j.ecss.2015.12.007
6. Modulating ion-binding at macromolecular interfaces during (bio)mineralization: A snapshot review for calcium carbonate and calcium phosphate systems B. Knight & C. McCutchin https://doi.org/10.1557/s43580-024-00860-x
7. Environmental controls on the Emiliania huxleyi calcite mass M. Horigome et al. https://doi.org/10.5194/bg-11-2295-2014
8. Control of Biogenic Nanocrystal Formation in Biomineralization L. Addadi et al. https://doi.org/10.1002/ijch.201500038
9. Coccolith volume of the Southern Ocean coccolithophore Emiliania huxleyi as a possible indicator for palaeo‐cell volume M. Müller et al. https://doi.org/10.1111/gbi.12414
10. High‐Resolution Coccolithophore Morphological Changes in Response to Orbital Forcings During the Early Oligocene R. Ma et al. https://doi.org/10.1029/2022GC010746
11. On culture artefacts in coccolith morphology G. Langer et al. https://doi.org/10.1007/s10152-012-0328-x
12. Influence of plankton community structure on the sinking velocity of marine aggregates L. Bach et al. https://doi.org/10.1002/2016GB005372
13. Nannoplankton malformation during the Paleocene-Eocene Thermal Maximum and its paleoecological and paleoceanographic significance T. Bralower & J. Self-Trail https://doi.org/10.1002/2016PA002980
14. Enhancing Gephyrocapsa huxleyi growth with recycled calcium from oyster shells G. Pierluigi et al. https://doi.org/10.1007/s44473-026-00107-7
15. Multiple carbonate system parameters independently govern shell formation in a marine mussel A. Ninokawa et al. https://doi.org/10.1038/s43247-024-01440-5
16. 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
17. Nutritional response of a coccolithophore to changing pH and temperature R. Johnson et al. https://doi.org/10.1002/lno.12204
18. Effect of phosphorus limitation on coccolith morphology and element ratios in Mediterranean strains of the coccolithophore Emiliania huxleyi A. Oviedo et al. https://doi.org/10.1016/j.jembe.2014.04.021
19. Over-calcified forms of the coccolithophore Emiliania huxleyi in high-CO2 waters are not preadapted to ocean acidification P. von Dassow et al. https://doi.org/10.5194/bg-15-1515-2018
20. Limited variability in the phytoplankton Emiliania huxleyi since the pre-industrial era in the Subantarctic Southern Ocean A. Rigual-Hernández et al. https://doi.org/10.1016/j.ancene.2020.100254
21. Coccolithophore responses to environmental variability in the South China Sea: species composition and calcite content X. Jin et al. https://doi.org/10.5194/bg-13-4843-2016
22. High-CO2 Levels Rather than Acidification Restrict Emiliania huxleyi Growth and Performance V. Vázquez et al. https://doi.org/10.1007/s00248-022-02035-3
23. A critical trade-off between nitrogen quota and growth allows Coccolithus braarudii life cycle phases to exploit varying environment J. de Vries et al. https://doi.org/10.5194/bg-21-1707-2024
24. Coccolithophore Assemblage Dynamics and Emiliania huxleyi Morphological Patterns During Three Sampling Campaigns Between 2017 and 2019 in the South Aegean Sea (Greece, NE Mediterranean) P. Penales et al. https://doi.org/10.3390/geosciences15070268
25. Technical Note: Weight approximation of coccoliths using a circular polarizer and interference colour derived retardation estimates – (The CPR Method) J. Bollmann https://doi.org/10.5194/bg-11-1899-2014
26. 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
27. Simulated ocean acidification reveals winners and losers in coastal phytoplankton L. Bach et al. https://doi.org/10.1371/journal.pone.0188198
28. Emiliania huxleyi—Bacteria Interactions under Increasing CO2 Concentrations J. Barcelos e Ramos et al. https://doi.org/10.3390/microorganisms10122461
29. The response of calcifying plankton to climate change in the Pliocene C. Davis et al. https://doi.org/10.5194/bg-10-6131-2013
30. Mass and Fine‐Scale Morphological Changes Induced by Changing Seawater pH in the Coccolith Gephyrocapsa oceanica M. Hermoso & F. Minoletti https://doi.org/10.1029/2018JG004535
31. Effects of CO2 concentration on a late summer surface sea ice community A. McMinn et al. https://doi.org/10.1007/s00227-017-3102-4
32. Zooplankton fecal pellets, marine snow, phytodetritus and the ocean’s biological pump J. Turner https://doi.org/10.1016/j.pocean.2014.08.005
33. Calcareous plankton response to orbital and millennial-scale climate changes across the Middle Pleistocene in the western Mediterranean A. Girone et al. https://doi.org/10.1016/j.palaeo.2013.09.005
34. Interannual changes of austral summer coccolithophore assemblages and southward expanse in the Southern Indian Ocean S. Patil et al. https://doi.org/10.1016/j.dsr2.2020.104765
35. Plastic pollution impacts on marine carbon biogeochemistry L. Galgani & S. Loiselle https://doi.org/10.1016/j.envpol.2020.115598
36. Variability in the organic ligands released by <em>Emiliania huxleyi</em> under simulated ocean acidification conditions G. Samperio-Ramos et al. https://doi.org/10.3934/environsci.2017.6.788
37. Phenotypic Variability in the Coccolithophore Emiliania huxleyi S. Blanco-Ameijeiras et al. https://doi.org/10.1371/journal.pone.0157697
38. Influence of CO&lt;sub&gt;2&lt;/sub&gt; and nitrogen limitation on the coccolith volume of &lt;I&gt;Emiliania huxleyi&lt;/I&gt; (Haptophyta) M. Müller et al. https://doi.org/10.5194/bg-9-4155-2012
39. On the potential role of marine calcifiers in glacial‐interglacial dynamics A. Omta et al. https://doi.org/10.1002/gbc.20060
40. 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
41. Reduction in size of the calcifying phytoplankton Calcidiscus leptoporus to environmental changes between the Holocene and modern Subantarctic Southern Ocean A. Rigual-Hernández et al. https://doi.org/10.3389/fmars.2023.1159884
42. The Effect of cytoskeleton inhibitors on coccolith morphology in Coccolithus braarudii and Scyphosphaera apsteinii G. Langer et al. https://doi.org/10.1111/jpy.13303
43. Impact of trace metal concentrations on coccolithophore growth and morphology: laboratory simulations of Cretaceous stress G. Faucher et al. https://doi.org/10.5194/bg-14-3603-2017
44. Coccolith mass and morphology of different Emiliania huxleyi morphotypes: A critical examination using Canary Islands material S. Linge Johnsen et al. https://doi.org/10.1371/journal.pone.0230569
45. Diurnally fluctuatingpCO2 enhances growth of a coastal strain ofEmiliania huxleyiunder future-projected ocean acidification conditions F. Li et al. https://doi.org/10.1093/icesjms/fsab036
46. 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
47. Solar UV Irradiances Modulate Effects of Ocean Acidification on the Coccolithophorid Emiliania huxleyi K. Xu & K. Gao https://doi.org/10.1111/php.12363
48. Globally enhanced calcification across the coccolithophore Gephyrocapsa complex during the mid-Brunhes interval A. González-Lanchas et al. https://doi.org/10.1016/j.quascirev.2023.108375
49. Temperature affects the morphology and calcification of Emiliania huxleyi strains A. Rosas-Navarro et al. https://doi.org/10.5194/bg-13-2913-2016
50. 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
51. High resolution spatial analyses of trace elements in coccoliths reveal new insights into element incorporation in coccolithophore calcite C. Bottini et al. https://doi.org/10.1038/s41598-020-66503-x
52. Ocean warming modulates the effects of acidification on Emiliania huxleyi calcification and sinking S. Milner et al. https://doi.org/10.1002/lno.10292
53. A unifying concept of coccolithophore sensitivity to changing carbonate chemistry embedded in an ecological framework L. Bach et al. https://doi.org/10.1016/j.pocean.2015.04.012
54. Covariation of metabolic rates and cell size in coccolithophores G. Aloisi https://doi.org/10.5194/bg-12-4665-2015
55. Effects of elevated CO2 on growth, calcification, and spectral dependence of photoinhibition in the coccolithophore Emiliania huxleyi (Prymnesiophyceae)1 M. Lorenzo et al. https://doi.org/10.1111/jpy.12885
56. Changes in calcification of coccoliths under stable atmospheric CO2 C. Berger et al. https://doi.org/10.5194/bg-11-929-2014
57. Strain-specific morphological response of the dominant calcifying phytoplankton species Emiliania huxleyi to salinity change C. Gebühr et al. https://doi.org/10.1371/journal.pone.0246745
58. Assessing the potential of amino acid 13C patterns as a carbon source tracer in marine sediments: effects of algal growth conditions and sedimentary diagenesis T. Larsen et al. https://doi.org/10.5194/bg-12-4979-2015
59. 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