Testing the direct effect of CO2 concentration on a bloom of the coccolithophorid Emiliania huxleyi in mesocosm experiments

By A. Engel, I. Zondervan, K. Aerts, L. Beaufort, A. Benthien, L. Chou, B. Delille, Jean-Pierre Gattuso, J. Harlay, Christina Heemann and 8 more. 2005

313 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/e26fc13be483ebd8921a7a6dfa5b81140d373b54

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Citations in the corpus

Responses of marine benthic microalgae to elevated CO2 (2011, unknown): “…al. 2005; IPCC 2007), so research into the effects that these chemical changes may have on primary producers has predominately focused on calciﬁers (Engel et al. 2005; Langer et al. 2009; Martin and Gattuso 2009), although work is also now emerging on the effects of elevated CO 2 on…”
Mesocosm Experiments as a Tool for Ecological Climate-Change Research (2013, background): “Ecotrons, several of which are now under construction in a range of countries (e.g. Germany, France, Norway, and Belgium), are highly instrumented sets of chambers designed for ecosystem research under controlled (usually confined) environmental conditions, which allow the simultaneous manipulation ”
Interactive effects of increased pCO2, temperature and irradiance on the marine coccolithophore Emiliania huxleyi (Prymnesiophyceae) (2008, background): “huxleyi , mostly focusing on the influence of CO 2 enrichment (Riebesell et al , 2000 ; Zondervan et al , 2001 , 2002 ; Riebesell, 2004 ; Engel et al , 2005 ).”
CO2 control of Trichodesmium N2 fixation, photosynthesis, growth rates, and elemental ratios: Implications for past, present, and future ocean biogeochemistry (2007, background): “Similar enhancement of N2 fixation at elevated pCO2 was also reported for the IMS Trichodesmium strain by Levitan et al. (2007). Genomic evidence suggests that this strain possesses homologues for genes encoding a low-affinity HCO 3 transport system (BicA) and a low affinity form of the NDH-1 comple”
Phenotypic plasticity and evolutionary demographic responses to climate change: taking theory out to the field (2013, background): “Both processes respond plastically to pH, carbon and other nutrient levels (Engel et al. 2005; Lefebvre et al. 2012); in particular, the production of particulate inorganic carbon (PIC) is reduced in CO2-enriched environments, as a consequence of acidification.”
Climate change and Australian marine life (2007, background): “…et al. 1993, Kurihara et al. 2004, Michaelidis et al. 2005, Berge et al. 2006; 42Riebesell et al. 2000, Antia et al. 2001, Tortell et al. 2002, Engel et al. 2005; 43Orr et al. 2005; 44See Hoegh-Guldberg 2004; 45Guinotte et al. 2006, Raven et al. 2005; 46Dawson & Dennison 1996; 47Moorthy &…”
Meta-analysis reveals negative yet variable effects of ocean acidification on marine organisms. (2010, background): “Yet there is variation in the efficiency of CCMs, and marine phytoplankton with less efficient CCMs have shown the capacity to increase photosynthetic rates in carbon and nutrient replete conditions (Rost & Riebesell 2004; Engel et al. 2005; Riebesell et al. 2007).”
Coupling of heterotrophic bacteria to phytoplankton bloom development at different pCO 2 levels: a mesocosm study (2008, background): “Whereas BPP of attached bacteria dramatically increased at the peak of the bloom and remained high during the breakdown of the bloom, BPP of free-living bacteria strongly increased after the phytoplankton bloom and reached its maximum when phytoplankton biomass was low but POC, PON, and POP still hi”
ELEVATED ATMOSPHERIC CARBON DIOXIDE INCREASES ORGANIC CARBON FIXATION BY EMILIANIA HUXLEYI (HAPTOPHYTA), UNDER NUTRIENT‐LIMITED HIGH‐LIGHT CONDITIONS 1 (2005, background): “Recently, Engel et al. (2005) found that net specific growth rate of E. huxleyi, the rate of calcification per cell, and the elemental stoichiometry of uptake and production processes were sensitive to changes in [CO2].”
Environmental controls on coccolithophore calcification (2012, background): “Likewise in natural waters, E. huxleyi was found in greater numbers by Feng et al. (2009) and in lower numbers by Engel et al. (2005), but in both cases, PIC l−1 was reduced.”