58 citations as recorded by crossref.

1. EVOLUTIONARY RESPONSES OF A COCCOLITHOPHORIDGEPHYROCAPSA OCEANICATO OCEAN ACIDIFICATION P. Jin et al. https://doi.org/10.1111/evo.12112
2. Effects of CO2 and iron availability on phytoplankton and eubacterial community compositions in the northwest subarctic Pacific H. Endo et al. https://doi.org/10.1016/j.jembe.2012.11.003
3. Comment on ''Effects of long-term high CO2 exposure on two species of coccolithophore'' by Müller et al. (2010) S. Collins https://doi.org/10.5194/bg-7-2199-2010
4. Effect of ocean acidification on marine phytoplankton and biogeochemical cycles K. Sugie & T. Yoshimura https://doi.org/10.5928/kaiyou.20.5_101
5. EXPERIMENTAL EVOLUTION MEETS MARINE PHYTOPLANKTON T. Reusch & P. Boyd https://doi.org/10.1111/evo.12035
6. Nitrogen source and pCO2 synergistically affect carbon allocation, growth and morphology of the coccolithophore Emiliania huxleyi: potential implications of ocean acidification for the carbon cycle S. Lefebvre et al. https://doi.org/10.1111/j.1365-2486.2011.02575.x
7. Simulating CO2 leakages from CCS to determine Zn toxicity using the marine microalgae Pleurochrysis roscoffensis E. Bautista- Chamizo et al. https://doi.org/10.1016/j.chemosphere.2015.09.041
8. Adaptive responses of free‐living and symbiotic microalgae to simulated future ocean conditions W. Chan et al. https://doi.org/10.1111/gcb.15546
9. Environmental controls on the growth, photosynthetic and calcification rates of a Southern Hemisphere strain of the coccolithophore Emiliania huxleyi Y. Feng et al. https://doi.org/10.1002/lno.10442
10. Lower Salinity Leads to Improved Physiological Performance in the Coccolithophorid Emiliania huxleyi, Which Partly Ameliorates the Effects of Ocean Acidification J. Xu et al. https://doi.org/10.3389/fmars.2020.00704
11. Interacting effects of ocean acidification and warming on growth and DMS‐production in the haptophyte coccolithophore Emiliania huxleyi H. Arnold et al. https://doi.org/10.1111/gcb.12105
12. Dissolution Rates of Biogenic Carbonates in Natural Seawater at Different pCO2 Conditions: A Laboratory Study M. Pickett & A. Andersson https://doi.org/10.1007/s10498-015-9261-3
13. 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
14. SHORT- VERSUS LONG-TERM RESPONSES TO CHANGING CO2IN A COASTAL DINOFLAGELLATE BLOOM: IMPLICATIONS FOR INTERSPECIFIC COMPETITIVE INTERACTIONS AND COMMUNITY STRUCTURE A. Tatters et al. https://doi.org/10.1111/evo.12029
15. Global coccolithophore diversity: Drivers and future change C. O’Brien et al. https://doi.org/10.1016/j.pocean.2015.10.003
16. Calcification response of a key phytoplankton family to millennial-scale environmental change H. McClelland et al. https://doi.org/10.1038/srep34263
17. 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
18. Exploring aberrant bivalve shell ultrastructure and geochemistry as proxies for past sea water acidification S. Hahn et al. https://doi.org/10.1111/sed.12107
19. Sensitivity of pelagic calcification to ocean acidification R. Gangstø et al. https://doi.org/10.5194/bg-8-433-2011
20. Decreased photosynthesis and growth with reduced respiration in the model diatom Phaeodactylum tricornutum grown under elevated CO2 over 1800 generations F. Li et al. https://doi.org/10.1111/gcb.13501
21. Response of the calcifying coccolithophore Emiliania huxleyi to low pH/high pCO2: from physiology to molecular level S. Richier et al. https://doi.org/10.1007/s00227-010-1580-8
22. A Voltage-Gated H+ Channel Underlying pH Homeostasis in Calcifying Coccolithophores A. Taylor et al. https://doi.org/10.1371/journal.pbio.1001085
23. Short- and long-term conditioning of a temperate marine diatom community to acidification and warming A. Tatters et al. https://doi.org/10.1098/rstb.2012.0437
24. Environmental controls on the Emiliania huxleyi calcite mass M. Horigome et al. https://doi.org/10.5194/bg-11-2295-2014
25. Emiliania huxleyi increases calcification but not expression of calcification-related genes in long-term exposure to elevated temperature and p CO 2 I. Benner et al. https://doi.org/10.1098/rstb.2013.0049
26. Experimental strategies to assess the biological ramifications of multiple drivers of global ocean change—A review P. Boyd et al. https://doi.org/10.1111/gcb.14102
27. Influence of post‐Tehuano oceanographic processes in the dynamics of the CO2 system in the Gulf of Tehuantepec, Mexico C. Chapa‐Balcorta et al. https://doi.org/10.1002/2015JC011249
28. The requirement for calcification differs between ecologically important coccolithophore species C. Walker et al. https://doi.org/10.1111/nph.15272
29. 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
30. Differing responses of three Southern Ocean Emiliania huxleyi ecotypes to changing seawater carbonate chemistry M. Müller et al. https://doi.org/10.3354/meps11309
31. The role of preconditioning in ocean acidification experiments: a test with the intertidal isopodParadella dianae P. Munguia & B. Alenius https://doi.org/10.1080/10236244.2013.788287
32. Evolution, Microbes, and Changing Ocean Conditions S. Collins et al. https://doi.org/10.1146/annurev-marine-010318-095311
33. Community interactions dampen acidification effects in a coastal plankton system D. Rossoll et al. https://doi.org/10.3354/meps10352
34. Phytoplankton community responses to iron and CO2 enrichment in different biogeochemical regions of the Southern Ocean H. Endo et al. https://doi.org/10.1007/s00300-017-2130-3
35. Environmental controls on coccolithophore calcification J. Raven & K. Crawfurd https://doi.org/10.3354/meps09993
36. Reduced resilience of a globally distributed coccolithophore to ocean acidification: Confirmed up to 2000 generations P. Jin & K. Gao https://doi.org/10.1016/j.marpolbul.2015.12.039
37. Predicting coccolithophore rain ratio responses to calcite saturation state S. Fielding https://doi.org/10.3354/meps10657
38. 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
39. Ocean acidification has different effects on the production of dimethylsulfide and dimethylsulfoniopropionate measured in cultures of Emiliania huxleyi and a mesocosm study: a comparison of laboratory monocultures and community interactions A. Webb et al. https://doi.org/10.1071/EN14268
40. Resilience of Emiliania huxleyi to future changes in subantarctic waters E. Armstrong et al. https://doi.org/10.1371/journal.pone.0284415
41. Development of environmental impact monitoring protocol for offshore carbon capture and storage (CCS): A biological perspective H. Kim et al. https://doi.org/10.1016/j.eiar.2015.11.004
42. Influence of changing carbonate chemistry on morphology and weight of coccoliths formed by Emiliania huxleyi L. Bach et al. https://doi.org/10.5194/bg-9-3449-2012
43. Biogeochemical response of Emiliania huxleyi (PML B92/11) to elevated CO2 and temperature under phosphorous limitation: A chemostat study C. Borchard et al. https://doi.org/10.1016/j.jembe.2011.10.004
44. 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
45. Human Versus Natural Influences on Climate and Biodiversity: The Carbon Dioxide Connection W. Davis https://doi.org/10.3390/sci7040152
46. 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
47. Variation in plastic responses of a globally distributed picoplankton species to ocean acidification E. Schaum et al. https://doi.org/10.1038/nclimate1774
48. Calcareous nannofossil response to the Weissert episode (Early Cretaceous): Implications for palaeoecological and palaeoceanographic reconstructions S. Duchamp-Alphonse et al. https://doi.org/10.1016/j.marmicro.2014.10.002
49. Phenotypic plasticity and evolutionary demographic responses to climate change: taking theory out to the field L. Chevin et al. https://doi.org/10.1111/j.1365-2435.2012.02043.x
50. Biological impacts of ocean acidification: a postgraduate perspective on research priorities S. Garrard et al. https://doi.org/10.1007/s00227-012-2033-3
51. Algal and aquatic plant carbon concentrating mechanisms in relation to environmental change J. Raven et al. https://doi.org/10.1007/s11120-011-9632-6
52. Calcification in the planktonic foraminifera Globigerina bulloides linked to phosphate concentrations in surface waters of the North Atlantic Ocean D. Aldridge et al. https://doi.org/10.5194/bg-9-1725-2012
53. EFFECTS ON MARINE ALGAE OF CHANGED SEAWATER CHEMISTRY WITH INCREASING ATMOSPHERIC CO₂ J. Raven https://doi.org/10.3318/BIOE.2011.01
54. 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
55. Comparative effects of seawater acidification on microalgae: Single and multispecies toxicity tests E. Bautista-Chamizo et al. https://doi.org/10.1016/j.scitotenv.2018.08.225
56. Will temperature and salinity changes exacerbate the effects of seawater acidification on the marine microalga Phaeodactylum tricornutum? E. Bautista-Chamizo et al. https://doi.org/10.1016/j.scitotenv.2018.03.314
57. 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
58. Ocean acidification affects physiology of coccolithophore Emiliania huxleyi and weakens its mechanical resistance to copepods H. Xu et al. https://doi.org/10.1016/j.marenvres.2023.106232