56 citations as recorded by crossref.

1. Calcareous Nannofossil Response to Climate Variability During the Middle Pleistocene Transition in the Northwest Pacific Ocean (Ocean Drilling Program Leg 198 Site 1209) C. Lupi et al. https://doi.org/10.1029/2018PA003488
2. Evolution of Mutation Rate in Astronomically Large Phytoplankton Populations M. Krasovec et al. https://doi.org/10.1093/gbe/evaa131
3. Eocene emergence of highly calcifying coccolithophores despite declining atmospheric CO2 L. Claxton et al. https://doi.org/10.1038/s41561-022-01006-0
4. 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
5. A global compilation of coccolithophore calcification rates C. Daniels et al. https://doi.org/10.5194/essd-10-1859-2018
6. 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
7. The role of the cytoskeleton in biomineralisation in haptophyte algae G. Durak et al. https://doi.org/10.1038/s41598-017-15562-8
8. High‐Resolution Coccolithophore Morphological Changes in Response to Orbital Forcings During the Early Oligocene R. Ma et al. https://doi.org/10.1029/2022GC010746
9. Seasonal patterns of coccolithophores in the ultra-oligotrophic South-East Levantine Basin, Eastern Mediterranean Sea S. Keuter et al. https://doi.org/10.1016/j.marmicro.2022.102153
10. Microfossil evidence for trophic changes during the Eocene–Oligocene transition in the South Atlantic (ODP Site 1263, Walvis Ridge) M. Bordiga et al. https://doi.org/10.5194/cp-11-1249-2015
11. Two-year seasonality (2017, 2018), export and long-term changes in coccolithophore communities in the subtropical ecosystem of the Gulf of Aqaba, Red Sea S. Keuter et al. https://doi.org/10.1016/j.dsr.2022.103919
12. Dimethylsulfoniopropionate (DMSP) and dimethyl sulfide (DMS) cycling across contrasting biological hotspots of the New Zealand subtropical front M. Lizotte et al. https://doi.org/10.5194/os-13-961-2017
13. 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
14. Factors controlling coccolithophore biogeography in the Southern Ocean C. Nissen et al. https://doi.org/10.5194/bg-15-6997-2018
15. Contrasting species-specific stress response to environmental pH determines the fate of coccolithophores in future oceans N. Chauhan et al. https://doi.org/10.1016/j.marpolbul.2024.117136
16. Phosphorus availability modifies carbon production in Coccolithus pelagicus (Haptophyta) A. Gerecht et al. https://doi.org/10.1016/j.jembe.2015.06.019
17. Atlantic sediments reveal interacting environmental and physiological controls on coccolithophore calcite production A. González-Lanchas et al. https://doi.org/10.1038/s41467-026-73162-5
18. Adaptive evolution in the coccolithophore Gephyrocapsa oceanica following 1,000 generations of selection under elevated CO2 S. Tong et al. https://doi.org/10.1111/gcb.14065
19. Microbe‐Mediated Extracellular and Intracellular Mineralization: Environmental, Industrial, and Biotechnological Applications W. Qin et al. https://doi.org/10.1002/adma.201907833
20. Why marine phytoplankton calcify F. Monteiro et al. https://doi.org/10.1126/sciadv.1501822
21. 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
22. 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
23. Biological carbon pump in the ocean and phytoplankton structure L. Pautova & V. Silkin https://doi.org/10.33624/2587-9367-2019-1(3)-1-12
24. The effect of temperature and salinity on DMSP production in Gephyrocapsa oceanica (Isochrysidales, Coccolithophyceae) S. Larsen & J. Beardall https://doi.org/10.1080/00318884.2023.2170636
25. Size-dependent dynamics of the internal carbon pool drive isotopic vital effects in calcifying phytoplankton N. Chauhan & R. Rickaby https://doi.org/10.1016/j.gca.2024.03.033
26. Cellular morphological trait dataset for extant coccolithophores from the Atlantic Ocean R. Sheward et al. https://doi.org/10.1038/s41597-024-03544-1
27. Coccolith size rules – What controls the size of coccoliths during coccolithogenesis? B. Suchéras-Marx et al. https://doi.org/10.1016/j.marmicro.2021.102080
28. The Biological Calcium Carbonate Pump in the Norwegian and Barents Seas: Regulation Mechanisms L. Pautova et al. https://doi.org/10.1134/S1028334X20010079
29. 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
30. A role for diatom-like silicon transporters in calcifying coccolithophores G. Durak et al. https://doi.org/10.1038/ncomms10543
31. The influence of environmental variability on the biogeography of coccolithophores and diatoms in the Great Calcite Belt H. Smith et al. https://doi.org/10.5194/bg-14-4905-2017
32. An Extracellular Polysaccharide-Rich Organic Layer Contributes to Organization of the Coccosphere in Coccolithophores C. Walker et al. https://doi.org/10.3389/fmars.2018.00306
33. The requirement for calcification differs between ecologically important coccolithophore species C. Walker et al. https://doi.org/10.1111/nph.15272
34. Coccolithophore Distribution in the Western Black Sea in the Summer of 2016 M. Dimiza et al. https://doi.org/10.3390/d15121194
35. Meta-analysis reveals responses of coccolithophores and diatoms to warming J. Wang et al. https://doi.org/10.1016/j.marenvres.2023.106275
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. A Bacterial Pathogen Displaying Temperature-Enhanced Virulence of the Microalga Emiliania huxleyi T. Mayers et al. https://doi.org/10.3389/fmicb.2016.00892
38. Species-specific differential dissolution morphology of selected coccolithophore species: an experimental study G. Langer et al. https://doi.org/10.5194/bg-23-1795-2026
39. A multifunctional organelle coordinates phagocytosis and chlorophagy in a marine eukaryote phytoplankton Scyphosphaera apsteinii J. Koester et al. https://doi.org/10.1111/nph.20388
40. Characterization of a Time-Domain Dual Lifetime Referencing pCO2 Optode and Deployment as a High-Resolution Underway Sensor across the High Latitude North Atlantic Ocean J. Clarke et al. https://doi.org/10.3389/fmars.2017.00396
41. The role of coccolithophore calcification in bioengineering their environment K. Flynn et al. https://doi.org/10.1098/rspb.2016.1099
42. A Model Simulation of the Adaptive Evolution through Mutation of the Coccolithophore Emiliania huxleyi Based on a Published Laboratory Study K. Denman https://doi.org/10.3389/fmars.2016.00286
43. 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
44. Ocean warming modulates the effects of acidification on Emiliania huxleyi calcification and sinking S. Milner et al. https://doi.org/10.1002/lno.10292
45. Role for Atlantic inflows and sea ice loss on shifting phytoplankton blooms in the Barents Sea L. Oziel et al. https://doi.org/10.1002/2016JC012582
46. 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
47. Growth and mortality of coccolithophores during spring in a temperate Shelf Sea (Celtic Sea, April 2015) K. Mayers et al. https://doi.org/10.1016/j.pocean.2018.02.024
48. IOD-ENSO interaction with natural coccolithophore assemblages in the tropical eastern Indian Ocean H. Liu et al. https://doi.org/10.1016/j.pocean.2021.102545
49. First Assessment of Coccolithophore-Driven Carbonate Flux in the Ulleung Basin, East Sea (Sea of Japan) S. An et al. https://doi.org/10.1007/s12601-025-00243-9
50. Allometry of carbon and nitrogen content and growth rate in a diverse range of coccolithophores N. Villiot et al. https://doi.org/10.1093/plankt/fbab038
51. The Ecology, Biogeochemistry, and Optical Properties of Coccolithophores W. Balch https://doi.org/10.1146/annurev-marine-121916-063319
52. Coccolithophore growth and calcification in a changing ocean K. Krumhardt et al. https://doi.org/10.1016/j.pocean.2017.10.007
53. 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
54. Phytoplankton dynamics in contrasting early stage North Atlantic spring blooms: composition, succession, and potential drivers C. Daniels et al. https://doi.org/10.5194/bg-12-2395-2015
55. Coccolithophore Cell Biology: Chalking Up Progress A. Taylor et al. https://doi.org/10.1146/annurev-marine-122414-034032
56. 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