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| Auteurs principaux: | , |
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| Format: | Dataset Open Access |
| Langue: | en |
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PANGAEA
2018
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| Accès en ligne: | https://doi.org/10.1594/PANGAEA.924611 |
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| _version_ | 1867171023179218944 |
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| author | Gafar, Natasha A Schulz, Kai Georg |
| author_facet | Gafar, Natasha A Schulz, Kai Georg |
| collection | Datos científicos de ciencias marinas y ambientales |
| contents | Coccolithophore responses to changes in carbonate chemistry speciation such as CO2 and H+ are highly modulated by light intensity and temperature. Here, we fit an analytical equation, accounting for simultaneous changes in carbonate chemistry speciation, light and temperature, to published and original data for Emiliania huxleyi, and compare the projections with those for Gephyrocapsa oceanica. Based on our analysis, the two most common bloom-forming species in present-day coccolithophore communities appear to be adapted for a similar fundamental light niche but slightly different ones for temperature and CO2, with E. huxleyi having a tolerance to lower temperatures and higher CO2 levels than G. oceanica. Based on growth rates, a dominance of E. huxleyi over G. oceanica is projected below temperatures of 22 °C at current atmospheric CO2 levels. This is similar to a global surface sediment compilation of E. huxleyi and G. oceanica coccolith abundances suggesting temperature-dependent dominance shifts. For a future Representative Concentration Pathway (RCP) 8.5 climate change scenario (1000 µatm fCO2), we project a CO2 driven niche contraction for G. oceanica to regions of even higher temperatures. However, the greater sensitivity of G. oceanica to increasing CO2 is partially mitigated by increasing temperatures. Finally, we compare satellite-derived particulate inorganic carbon estimates in the surface ocean with a recently proposed metric for potential coccolithophore success on the community level, i.e. the temperature-, light- and carbonate-chemistry-dependent CaCO3 production potential (CCPP). Based on E. huxleyi alone, as there was interestingly a better correlation than when in combination with G. oceanica, and excluding the Antarctic province from the analysis, we found a good correlation between CCPP and satellite-derived particulate inorganic carbon (PIC) with an R2 of 0.73, p < 0.01 and a slope of 1.03 for austral winter/boreal summer and an R2 of 0.85, p < 0.01 and a slope of 0.32 for austral summer/boreal winter. |
| format | Dataset Open Access |
| id | pangaea_https___doi_org_10_1594_PANGAEA_924611 |
| institution | PANGAEA |
| language | en |
| publishDate | 2018 |
| publisher | PANGAEA |
| record_format | pangaea |
| spellingShingle | Seawater carbonate chemistry and particulate organic and inorganic carbon, growth of Emiliania huxleyi Gafar, Natasha A Schulz, Kai Georg Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Bottles or small containers/Aquaria (<20 L); Calcification/Dissolution; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, per cell; Carbon, organic, particulate, production per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Coast and continental shelf; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Haptophyta; Hydrogen ion; Irradiance; Laboratory experiment; Light; North Atlantic; OA-ICC; Ocean acidification; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH, total scale; Phytoplankton; Primary production/Photosynthesis; Registration number of species; Salinity; Single species; Species; Temperate; Temperature, water; Type; Uniform resource locator/link to reference Coccolithophore responses to changes in carbonate chemistry speciation such as CO2 and H+ are highly modulated by light intensity and temperature. Here, we fit an analytical equation, accounting for simultaneous changes in carbonate chemistry speciation, light and temperature, to published and original data for Emiliania huxleyi, and compare the projections with those for Gephyrocapsa oceanica. Based on our analysis, the two most common bloom-forming species in present-day coccolithophore communities appear to be adapted for a similar fundamental light niche but slightly different ones for temperature and CO2, with E. huxleyi having a tolerance to lower temperatures and higher CO2 levels than G. oceanica. Based on growth rates, a dominance of E. huxleyi over G. oceanica is projected below temperatures of 22 °C at current atmospheric CO2 levels. This is similar to a global surface sediment compilation of E. huxleyi and G. oceanica coccolith abundances suggesting temperature-dependent dominance shifts. For a future Representative Concentration Pathway (RCP) 8.5 climate change scenario (1000 µatm fCO2), we project a CO2 driven niche contraction for G. oceanica to regions of even higher temperatures. However, the greater sensitivity of G. oceanica to increasing CO2 is partially mitigated by increasing temperatures. Finally, we compare satellite-derived particulate inorganic carbon estimates in the surface ocean with a recently proposed metric for potential coccolithophore success on the community level, i.e. the temperature-, light- and carbonate-chemistry-dependent CaCO3 production potential (CCPP). Based on E. huxleyi alone, as there was interestingly a better correlation than when in combination with G. oceanica, and excluding the Antarctic province from the analysis, we found a good correlation between CCPP and satellite-derived particulate inorganic carbon (PIC) with an R2 of 0.73, p < 0.01 and a slope of 1.03 for austral winter/boreal summer and an R2 of 0.85, p < 0.01 and a slope of 0.32 for austral summer/boreal winter. |
| title | Seawater carbonate chemistry and particulate organic and inorganic carbon, growth of Emiliania huxleyi |
| topic | Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Bottles or small containers/Aquaria (<20 L); Calcification/Dissolution; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, inorganic, particulate, production per cell; Carbon, organic, particulate, per cell; Carbon, organic, particulate, production per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Coast and continental shelf; Emiliania huxleyi; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Haptophyta; Hydrogen ion; Irradiance; Laboratory experiment; Light; North Atlantic; OA-ICC; Ocean acidification; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH, total scale; Phytoplankton; Primary production/Photosynthesis; Registration number of species; Salinity; Single species; Species; Temperate; Temperature, water; Type; Uniform resource locator/link to reference |
| url | https://doi.org/10.1594/PANGAEA.924611 |