CO2 concentrating mechanisms in algae: mechanisms, environmental modulation, and evolution.

By M. Giordano, John Beardall, J. Raven. Annual Review of Plant Biology, 2005

1,525 citations recorded by the source corpus.

Subfields: Molecular Biology, Oceanography, Renewable Energy, Sustainability and the Environment

View Paper: https://www.semanticscholar.org/paper/f301964421743eada604689470a8e65efdebe374

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

1. J. Raven
2. D. Ort
3. John Beardall
4. Xinguang Zhu
5. S. Long
6. Z. Finkel
7. A. Irwin
8. Mark E. Warner

In Oceanography

1. J. Raven
2. U. Riebesell
3. D. Thornton
4. Raphael M. Kudela
5. W. Cochlan
6. B. Rost
7. Mark E. Warner
8. V. Trainer

In Renewable Energy, Sustainability and the Environment

1. J. Raven
2. John Beardall
3. A. Irwin
4. D. Thornton
5. B. Rost
6. U. Riebesell
7. Z. Finkel
8. V. Fabry

Citations in the corpus

• The future of seaweed aquaculture in a rapidly changing world (2017, background): “, 2012) as they generally express active CO2 concentrating mechanisms (CCMs) (Giordano et al., 2005).”
• Use of sodium bicarbonate to stimulate triacylglycerol accumulation in the chlorophyte Scenedesmus sp. and the diatom Phaeodactylum tricornutum (2012, background): “Recently, there have been a number of reviews focused on inorganic carbon use and carbon concentrating mechanisms in microalgae (Colman et al. 2002; Giordano et al. 2005; Kaplan and Reinhold 1999; Moroney and Somanchi 1999; Moroney and Ynalvez 2007; Raven 2010).”
• Effects of elevated CO2 and phosphorus supply on growth, photosynthesis and nutrient uptake in the marine macroalga Gracilaria lemaneiformis (Rhodophyta). (2010, background): “High CO2 levels generally enhance photosynthesis in many species due to the diffusion of more CO2 from the external bulk medium to the active site of Rubisco, although most of them possess CO2 concentrating mechanisms (CCMs) and mainly utilize HCO3 (Giordano et al. 2005).”
• Arctic microbial community dynamics influenced by elevated CO2 levels (2012, background): “Diffusion of CO 2 is typically not expected to limit photosynthesis in the very small-sized phytoplankton (Giordano et al., 2005), although CCMs were identified for the pico-phytoplankter Micromonas pusilla (Worden et al., 2009).”
• Bio-mitigation of carbon dioxide using microalgal systems: Advances and perspectives (2017, background): “Organic compounds must be small enough to move across the cell walls and are then converted to lipids and other metabolites through respiration pathways such as pentose phosphate pathway (PPP) [2,25].”
• The age of Rubisco: the evolution of oxygenic photosynthesis (2007, background): “In typical cyanobacteria, there are extremely effective carbon concentrating mechanisms, including both bicarbonate transporters and CO 2 uptake systems (Badger & Price, 2003; Badger et al ., 2005; Giordano et al., 2005).”
• Climate change and ocean acidification effects on seagrasses and marine macroalgae (2013, methodology): “Although the method and degree of HCO3 usage may well impact the response of a species to rising CO2, the mechanisms and critical values that saturate Rubisco with CO2 and lower their dependence on a CCM are not well understood (Giordano et al., 2005; Raven, 2010, 2011; Raven et al., 2011).”
• Poleward expansion of the coccolithophore Emiliania huxleyi (2014, background): “But diatoms (Giordano et al., 2005) and other coccolithophore species (Moolna and Rickaby, 2012) may be better adapted to low CO2 due to more efficient carbon acquisition than E. huxleyi (Rost and Riebesell, 2004).”
• Macroalgal responses to ocean acidification depend on nutrient and light levels (2015, background): “The ways in which ocean acidification affects communities of primary producers are likely to vary regionally, depending on the species present and abiotic factors such as temperature, light and nutrient availability (Giordano et al., 2005; Brodie et al., 2014; Hofmann et al., 2014).”
• Differential effects of ocean acidification on growth and photosynthesis among phylotypes of Symbiodinium (Dinophyceae) (2011, background): “CCMs generally differ in their design and efficiency between algal species (Tortell 2000; Giordano et al. 2005); thus, it is conceivable that some Symbiodinium phylotypes possess less efficient CCMs (relying to a greater extent on the passive, diffusive uptake of CO2(aq)) than others.”
• Harmful algal blooms and climate change: Learning from the past and present to forecast the future (2015, background): “CO2 enrichment is expected to relieve the energy requirements of carbon concentrating mechanisms (CCM) and particularly benefit those species having Form II Rubisco (ribulose-1,5-bis-phosphate carboxylase-oxygenase), which has a low affinity for CO2 (Beardall et al., 2009; Giordano et al., 2005; Rav”
• The effect of elevated CO2 on growth and competition in experimental phytoplankton communities (2011, background): “However, most phytoplankton, both marine and freshwater, have active carbon concentration mechanisms (CCMs) which allow the uptake of bicarbonate and its conversion to CO2 (Giordano et al., 2005).”
• Diversity of carbon use strategies in a kelp forest community: implications for a high CO2 ocean (2011, background): “A minority of marine macroalgae use dissolved CO2 entering the cells by diffusion as the carbon source for photosynthesis (Maberly, 1990; Maberly et al., 1992; Beardall & Giordano, 2002; Raven et al., 2002a, b; Raven, 2003; Giordano et al., 2005).”