Abstract:Ocean acidification in response to rising atmospheric CO2 partial pressures is widely expected to reduce calcification by marine organisms. From the mid-Mesozoic, coccolithophores have been major calcium carbonate producers in the world's oceans, today accounting for about a third of the total marine CaCO3 production. Here, we present laboratory evidence that calcification and net primary production in the coccolithophore species Emiliania huxleyi are significantly increased by high CO2 partial pressures. Fiel… Show more
“…The projected rate of change in ocean CO 2 chemistry leaves little time for organisms to evolve adaptations. While some species may be CO 2 -insensitive or able to adapt (e.g., Miller et al, 2009), the energetic costs of achieving net shell growth and preventing dissolution in conditions of aragonite under-saturation will likely have other impacts on overall growth rates, predation, metabolism or reproduction, as observed in organisms from other regions (e.g., Iglesias-Rodriguez et al, 2008;Fabry et al, 2008;Wood et al, 2008;Tunnicliffe et al, 2009).…”
The article presents a study that investigates on the importance of identifying and quantifying planetary boundaries to prevent human activities in affecting environmental condition. The author states the industrial revolution and advancement in human civilization has caused the unstability of the environmental state that is less conducive for humans to live and affect their health condition. The author notes that planetary boundaries served a control variables to secure the safety of its citizen as well as protect the environment from shifting to dangerous levels. It also cites the different planetary boundaries, along with its impact on climate change and Earth system degradation
“…The projected rate of change in ocean CO 2 chemistry leaves little time for organisms to evolve adaptations. While some species may be CO 2 -insensitive or able to adapt (e.g., Miller et al, 2009), the energetic costs of achieving net shell growth and preventing dissolution in conditions of aragonite under-saturation will likely have other impacts on overall growth rates, predation, metabolism or reproduction, as observed in organisms from other regions (e.g., Iglesias-Rodriguez et al, 2008;Fabry et al, 2008;Wood et al, 2008;Tunnicliffe et al, 2009).…”
The article presents a study that investigates on the importance of identifying and quantifying planetary boundaries to prevent human activities in affecting environmental condition. The author states the industrial revolution and advancement in human civilization has caused the unstability of the environmental state that is less conducive for humans to live and affect their health condition. The author notes that planetary boundaries served a control variables to secure the safety of its citizen as well as protect the environment from shifting to dangerous levels. It also cites the different planetary boundaries, along with its impact on climate change and Earth system degradation
“…Many studies focused on the effects of ocean acidification on coccolithophore (Riebesell et al, 2000;Feng et al, 2008;Iglesias-Rodriguez et al, 2008;De Bodt et al, 2010), but few considered the role of UVR in natural conditions (Gao et al, 2009). Our results indicate that reduced calcification in E. huxleyi made the cells more vulnerable when they are exposed to excessive light energy even without UVR considered, since reduced calcification led to downregualated photoprotective capability.…”
Abstract. Changes in calcification of coccolithophores may affect their photosynthetic responses to both, ultraviolet radiation (UVR, 280-400 nm) and temperature. We operated semi-continuous cultures of Emiliania huxleyi (strain CS-369) at reduced (0.1 mM, LCa) and ambient (10 mM, HCa) Ca 2+ concentrations and, after 148 generations, we exposed cells to six radiation treatments (>280, >295, >305, >320, >350 and >395 nm by using Schott filters) and two temperatures (20 and 25 • C) to examine photosynthesis and calcification responses. Overall, our study demonstrated that: (1) decreased calcification resulted in a down regulation of photoprotective mechanisms (i.e., as estimated via non-photochemical quenching, NPQ), pigments contents and photosynthetic carbon fixation; (2) calcification (C) and photosynthesis (P ) (as well as their ratio) have different responses related to UVR with cells grown under the high Ca 2+ concentration being more resistant to UVR than those grown under the low Ca 2+ level; (3) elevated temperature increased photosynthesis and calcification of E. huxleyi grown at high Ca 2+ concentrations whereas decreased both processes in low Ca 2+ grown cells. Therefore, a decrease in calcification rates in E. huxleyi is expected to decrease photosynthesis rates, resulting in a negative feedback that further reduces calcification.
“…For example, a number of studies have investigated the consequences of reduced pH for calcifying phytoplankton (Table 1). Results by a number of laboratories suggest negative effects of higher CO 2 /lower pH on coccolithophore cultures (Riebesell et al, 2000(Riebesell et al, , 2007 but at least two studies indicate enhanced calcification under elevated CO 2 (Langer et al, 2006;Iglesias-Rodriguez et al, 2008). Ridgwell et al (2009) have suggested that some of these differences may be due to strain variations in the cultures used for these experiments; or there may be experimental design consequences resulting from the procedures used to adjust the pH .…”
Section: Ocean Acidification and Microbesmentioning
The pH of the surface ocean is changing as a result of increases in atmospheric carbon dioxide (CO2), and there are concerns about potential impacts of lower pH and associated alterations in seawater carbonate chemistry on the biogeochemical processes in the ocean. However, it is important to place these changes within the context of pH in the present-day ocean, which is not constant; it varies systematically with season, depth and along productivity gradients. Yet this natural variability in pH has rarely been considered in assessments of the effect of ocean acidification on marine microbes. Surface pH can change as a consequence of microbial utilization and production of carbon dioxide, and to a lesser extent other microbially mediated processes such as nitrification. Useful comparisons can be made with microbes in other aquatic environments that readily accommodate very large and rapid pH change. For example, in many freshwater lakes, pH changes that are orders of magnitude greater than those projected for the twenty second century oceans can occur over periods of hours. Marine and freshwater assemblages have always experienced variable pH conditions. Therefore, an appropriate null hypothesis may be, until evidence is obtained to the contrary, that major biogeochemical processes in the oceans other than calcification will not be fundamentally different under future higher CO2/lower pH conditions.
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