Articles | Volume 18, issue 3
https://doi.org/10.5194/bg-18-1161-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/bg-18-1161-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
16 Feb 2021
Research article |
| 16 Feb 2021
| 16 Feb 2021
Haplo-diplontic life cycle expands coccolithophore niche
Joost de Vries
CORRESPONDING AUTHOR
BRIDGE, School of Geographical Sciences, University of Bristol, University Road, Bristol BS8 1SS, UK
Marine Biological Association, The Laboratory, Citadel Hill, Plymouth PL1 2PB, UK
Fanny Monteiro
BRIDGE, School of Geographical Sciences, University of Bristol, University Road, Bristol BS8 1SS, UK
Glen Wheeler
Marine Biological Association, The Laboratory, Citadel Hill, Plymouth PL1 2PB, UK
Alex Poulton
The Lyell Centre for Earth & Marine Science & Technology, Heriot-Watt University, Edinburgh EH14 4BA, UK
Jelena Godrijan
Division for Marine and Environmental Research, Ruđer Bošković
Institute, Bijenička cesta 54, 10000 Zagreb, Croatia
Federica Cerino
Oceanography Section, Istituto Nazionale di Oceanografia e di Geofisica Sperimentale – OGS, via Piccard 54, 34151 Trieste, Italy
Elisa Malinverno
Department of Earth and Environmenal Sciences, University of Milano-Bicocca, Piazza della Scienza 4, 20126 Milan, Italy
Consorzio Nazionale Interuniversitario per le Scienze del Mare – CoNISMa, Piazzale Flaminio 9, 00196 Rome, Italy
Gerald Langer
Marine Biological Association, The Laboratory, Citadel Hill, Plymouth PL1 2PB, UK
Colin Brownlee
Marine Biological Association, The Laboratory, Citadel Hill, Plymouth PL1 2PB, UK
School of Ocean and Earth Science, University of Southampton, Southampton SO14 3ZH, UK
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Cited
16 citations as recorded by crossref.
- A critical trade-off between nitrogen quota and growth allows Coccolithus braarudii life cycle phases to exploit varying environment J. de Vries et al. 10.5194/bg-21-1707-2024
- Phagocytosis in Marine Coccolithophore Gephyrocapsa huxleyi: Comparison between Calcified and Non-Calcified Strains J. Ye et al. 10.3390/biology13050310
- Evolutionary Rates in the Haptophyta: Exploring Molecular and Phenotypic Diversity J. Henderiks et al. 10.3390/jmse10060798
- Allometry of carbon and nitrogen content and growth rate in a diverse range of coccolithophores N. Villiot et al. 10.1093/plankt/fbab038
- Novel combination coccospheres fromHelicosphaeraspp indicate complex relationships between species D. Sturm et al. 10.1093/plankt/fbac044
- Distribution of extant coccolithophores from the northwest continental shelf of India during the summer monsoon M. Chowdhury et al. 10.1080/00318884.2022.2037340
- Haploid Helps Phaeocystis Globosa Distribute to Deeper Dim Water, as Evidenced by Growth and Photosynthetic Physiology J. Zhuang et al. 10.3389/fmars.2022.902330
- A multi‐level exploration of the relationship between temperature and species diversity: Two cases of marine phytoplankton J. Gao & Q. Su 10.1002/ece3.9584
- Contrasting species-specific stress response to environmental pH determines the fate of coccolithophores in future oceans N. Chauhan et al. 10.1016/j.marpolbul.2024.117136
- Spatial variation in key functional traits of Mediterranean fucoid algae: Insights from Cystoseira sensu lato intertidal canopies L. Cannarozzi et al. 10.1016/j.ecss.2023.108524
- Silicon drives the evolution of complex crystal morphology in calcifying algae T. Mock 10.1111/nph.17507
- CASCADE: Dataset of extant coccolithophore size, carbon content and global distribution J. de Vries et al. 10.1038/s41597-024-03724-z
- Novel heterococcolithophores, holococcolithophores and life cycle combinations from the families Syracosphaeraceae and Papposphaeraceae and the genus <i>Florisphaera</i> S. Keuter et al. 10.5194/jm-40-75-2021
- Osmotrophy of dissolved organic carbon by coccolithophores in darkness J. Godrijan et al. 10.1111/nph.17819
- Distinct physiological responses ofCoccolithus braarudiilife cycle phases to light intensity and nutrient availability G. Langer et al. 10.1080/09670262.2022.2056925
- Different photosynthetic responses of haploid and diploid Emiliania huxleyi (Prymnesiophyceae) to high light and ultraviolet radiation Z. Ruan et al. 10.1186/s40643-023-00660-5
15 citations as recorded by crossref.
- A critical trade-off between nitrogen quota and growth allows Coccolithus braarudii life cycle phases to exploit varying environment J. de Vries et al. 10.5194/bg-21-1707-2024
- Phagocytosis in Marine Coccolithophore Gephyrocapsa huxleyi: Comparison between Calcified and Non-Calcified Strains J. Ye et al. 10.3390/biology13050310
- Evolutionary Rates in the Haptophyta: Exploring Molecular and Phenotypic Diversity J. Henderiks et al. 10.3390/jmse10060798
- Allometry of carbon and nitrogen content and growth rate in a diverse range of coccolithophores N. Villiot et al. 10.1093/plankt/fbab038
- Novel combination coccospheres fromHelicosphaeraspp indicate complex relationships between species D. Sturm et al. 10.1093/plankt/fbac044
- Distribution of extant coccolithophores from the northwest continental shelf of India during the summer monsoon M. Chowdhury et al. 10.1080/00318884.2022.2037340
- Haploid Helps Phaeocystis Globosa Distribute to Deeper Dim Water, as Evidenced by Growth and Photosynthetic Physiology J. Zhuang et al. 10.3389/fmars.2022.902330
- A multi‐level exploration of the relationship between temperature and species diversity: Two cases of marine phytoplankton J. Gao & Q. Su 10.1002/ece3.9584
- Contrasting species-specific stress response to environmental pH determines the fate of coccolithophores in future oceans N. Chauhan et al. 10.1016/j.marpolbul.2024.117136
- Spatial variation in key functional traits of Mediterranean fucoid algae: Insights from Cystoseira sensu lato intertidal canopies L. Cannarozzi et al. 10.1016/j.ecss.2023.108524
- Silicon drives the evolution of complex crystal morphology in calcifying algae T. Mock 10.1111/nph.17507
- CASCADE: Dataset of extant coccolithophore size, carbon content and global distribution J. de Vries et al. 10.1038/s41597-024-03724-z
- Novel heterococcolithophores, holococcolithophores and life cycle combinations from the families Syracosphaeraceae and Papposphaeraceae and the genus <i>Florisphaera</i> S. Keuter et al. 10.5194/jm-40-75-2021
- Osmotrophy of dissolved organic carbon by coccolithophores in darkness J. Godrijan et al. 10.1111/nph.17819
- Distinct physiological responses ofCoccolithus braarudiilife cycle phases to light intensity and nutrient availability G. Langer et al. 10.1080/09670262.2022.2056925
Discussed (final revised paper)
Latest update: 23 Dec 2024
Short summary
Coccolithophores are important calcifying phytoplankton with an overlooked life cycle. We compile a global dataset of marine coccolithophore abundance to investigate the environmental characteristics of each life cycle phase. We find that both phases contribute to coccolithophore abundance and that their different environmental preference increases coccolithophore habitat. Accounting for the life cycle of coccolithophores is thus crucial for understanding their ecology and biogeochemical impact.
Coccolithophores are important calcifying phytoplankton with an overlooked life cycle. We...
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