scholarly journals Concomitant ocean acidification and increasing total alkalinity at a coastal site in the NW Mediterranean Sea (2007-2015)

2016 ◽  
Author(s):  
Lydia Kapsenberg ◽  
Samir Alliouane ◽  
Frédéric Gazeau ◽  
Laure Mousseau ◽  
Jean-Pierre Gattuso
Keyword(s):  
Ocean Acidification ◽  
Mediterranean Sea ◽  
Dissolved Inorganic Carbon ◽  
Coastal Ocean ◽  
Total Alkalinity ◽  
Global Ocean ◽  
Coastal Zones ◽  
Carbonate Chemistry ◽  
Nw Mediterranean ◽  
Nw Mediterranean Sea

Abstract. Monitoring of global ocean change is necessary in coastal zones due to their physical and biological complexity. Here, we document changes in coastal carbonate chemistry at the coastal time-series station, Point B, in the NW Mediterranean Sea from 2007 through 2015 at 1 and 50 m. The rate of surface ocean acidification (−0.0028 ± 0.0003 units pHT yr−1) was faster-than-expected based on atmospheric carbon dioxide forcing alone. Changes in carbonate chemistry were predominantly driven by an increase in total dissolved inorganic carbon (CT, +2.97 ± 0.20 μmol kg−1 yr−1), > 50 % of which was buffered by a synchronous increase in total alkalinity (AT, +2.08 ± 0.19 μmol kg−1 yr−1). The increase in AT was unrelated to salinity and its cause remains to be identified. Interestingly, concurrent increases in AT and CT were most rapid from May to July. Changes at 50 m were slower compared to 1 m. It seems therefore likely that changes in coastal AT cycling via a shallow coastal process gave rise to these observations. This study exemplifies the importance of understanding coastal ocean acidification through localized biogeochemical cycling that extends beyond simple air-sea gas exchange dynamics, in order to make relevant predictions about future coastal ocean change and ecosystem function.

scholarly journals The role of ocean acidification in <i>Emiliania huxleyi</i> coccolith thinning in the Mediterranean Sea

2014 ◽  
Vol 11 (10) ◽  
pp. 2857-2869 ◽  
Author(s):  
K. J. S. Meier ◽  
L. Beaufort ◽  
S. Heussner ◽  
P. Ziveri
Keyword(s):  
Ocean Acidification ◽  
Mediterranean Sea ◽  
Abundant Species ◽  
Emiliania Huxleyi ◽  
Carbonate Chemistry ◽  
Carbonate Production ◽  
Surface Ocean ◽  
Nw Mediterranean ◽  
Seawater Carbonate Chemistry

Abstract. Ocean acidification is a result of the uptake of anthropogenic CO2 from the atmosphere into the ocean and has been identified as a major environmental and economic threat. The release of several thousands of petagrams of carbon over a few hundred years will have an overwhelming effect on surface ocean carbon reservoirs. The recorded and anticipated changes in seawater carbonate chemistry will presumably affect global oceanic carbonate production. Coccolithophores as the primary calcifying phytoplankton group, and especially Emiliania huxleyi as the most abundant species have shown a reduction of calcification at increased CO2 concentrations for the majority of strains tested in culture experiments. A reduction of calcification is associated with a decrease in coccolith weight. However, the effect in monoclonal cultures is relatively small compared to the strong variability displayed in natural E. huxleyi communities, as these are a mix of genetically and sometimes morphologically distinct types. Average coccolith weight is likely influenced by the variability in seawater carbonate chemistry in different parts of the world's oceans and on glacial/interglacial time scales due to both physiological effects and morphotype selectivity. An effect of the ongoing ocean acidification on E. huxleyi calcification has so far not been documented in situ. Here, we analyze E. huxleyi coccolith weight from the NW Mediterranean Sea in a 12-year sediment trap series, and surface sediment and sediment core samples using an automated recognition and analyzing software. Our findings clearly show (1) a continuous decrease in the average coccolith weight of E. huxleyi from 1993 to 2005, reaching levels below pre-industrial (Holocene) and industrial (20th century) values recorded in the sedimentary record and (2) seasonal variability in coccolith weight that is linked to the coccolithophore productivity. The observed long-term decrease in coccolith weight is most likely a result of the changes in the surface ocean carbonate system. Our results provide the first indications of an in situ impact of ocean acidification on coccolithophore weight in a natural E. huxleyi population, even in the highly alkaline Mediterranean Sea.

scholarly journals Current estimates of K<sub>1</sub>* and K<sub>2</sub>* appear inconsistent with measured CO<sub>2</sub> system parameters in cold oceanic regions

Ocean Science ◽  
2020 ◽  
Vol 16 (4) ◽  
pp. 847-862 ◽  
Author(s):  
Olivier Sulpis ◽  
Siv K. Lauvset ◽  
Mathilde Hagens
Keyword(s):  
Surface Water ◽  
Ocean Acidification ◽  
Carbonic Acid ◽  
Dissolved Inorganic Carbon ◽  
Dissociation Constants ◽  
Total Alkalinity ◽  
Global Ocean ◽  
Polar Regions ◽  
Carbonate System ◽  
System Variables

Abstract. Seawater absorption of anthropogenic atmospheric carbon dioxide (CO2) has led to a range of changes in carbonate chemistry, collectively referred to as ocean acidification. Stoichiometric dissociation constants used to convert measured carbonate system variables (pH, pCO2, dissolved inorganic carbon, total alkalinity) into globally comparable parameters are crucial for accurately quantifying these changes. The temperature and salinity coefficients of these constants have generally been experimentally derived under controlled laboratory conditions. Here, we use field measurements of carbonate system variables taken from the Global Ocean Data Analysis Project version 2 and the Surface Ocean CO2 Atlas data products to evaluate the temperature dependence of the carbonic acid stoichiometric dissociation constants. By applying a novel iterative procedure to a large dataset of 948 surface-water, quality-controlled samples where four carbonate system variables were independently measured, we show that the set of equations published by Lueker et al. (2000), currently preferred by the ocean acidification community, overestimates the stoichiometric dissociation constants at temperatures below about 8 ∘C. We apply these newly derived temperature coefficients to high-latitude Argo float and cruise data to quantify the effects on surface-water pCO2 and calcite saturation states. These findings highlight the critical implications of uncertainty in stoichiometric dissociation constants for future projections of ocean acidification in polar regions and the need to improve knowledge of what causes the CO2 system inconsistencies in cold waters.

scholarly journals CO<sub>2</sub> perturbation experiments: similarities and differences between dissolved inorganic carbon and total alkalinity manipulations

2009 ◽  
Vol 6 (10) ◽  
pp. 2145-2153 ◽  
Author(s):  
K. G. Schulz ◽  
J. Barcelos e Ramos ◽  
R. E. Zeebe ◽  
U. Riebesell
Keyword(s):  
Ocean Acidification ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Total Alkalinity ◽  
Calcium Carbonate Precipitation ◽  
Carbonate Chemistry ◽  
Carbonate System ◽  
Experimental Conditions ◽  
Saturation State ◽  
Basic Approaches

Abstract. Increasing atmospheric carbon dioxide (CO2) through human activities and invasion of anthropogenic CO2 into the surface ocean alters the seawater carbonate chemistry, increasing CO2 and bicarbonate (HCO3−) at the expense of carbonate ion (CO32−) concentrations. This redistribution in the dissolved inorganic carbon (DIC) pool decreases pH and carbonate saturation state (Ω). Several components of the carbonate system are considered potential key variables influencing for instance calcium carbonate precipitation in marine calcifiers such as coccolithophores, foraminifera, corals, mollusks and echinoderms. Unravelling the sensitivities of marine organisms and ecosystems to CO2 induced ocean acidification (OA) requires well-controlled experimental setups and accurate carbonate system manipulations. Here we describe and analyse the chemical changes involved in the two basic approaches for carbonate chemistry manipulation, i.e. changing DIC at constant total alkalinity (TA) and changing TA at constant DIC. Furthermore, we briefly introduce several methods to experimentally manipulate DIC and TA. Finally, we examine responses obtained with both approaches using published results for the coccolithophore Emiliania huxleyi. We conclude that under most experimental conditions in the context of ocean acidification DIC and TA manipulations yield similar changes in all parameters of the carbonate system, which implies direct comparability of data obtained with the two basic approaches for CO2 perturbation.

Copepod response to ocean acidification in a low nutrient-low chlorophyll environment in the NW Mediterranean Sea

2017 ◽  
Vol 186 ◽  
pp. 152-162 ◽  
Author(s):  
S. Zervoudaki ◽  
E. Krasakopoulou ◽  
T. Moutsopoulos ◽  
M. Protopapa ◽  
S. Marro ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
Mediterranean Sea ◽  
Nw Mediterranean ◽  
Nw Mediterranean Sea

scholarly journals Current estimates of K<sub>1</sub><sup>*</sup> and K<sub>2</sub><sup>*</sup> appear inconsistent with measured CO<sub>2</sub> system parameters in cold oceanic regions

2020 ◽  
Author(s):  
Olivier Sulpis ◽  
Siv K. Lauvset ◽  
Mathilde Hagens
Keyword(s):  
Surface Water ◽  
Ocean Acidification ◽  
Carbonic Acid ◽  
Dissolved Inorganic Carbon ◽  
Dissociation Constants ◽  
Total Alkalinity ◽  
Global Ocean ◽  
Polar Regions ◽  
Carbonate System ◽  
System Variables

Abstract. Seawater absorption of anthropogenic atmospheric carbon dioxide (CO2) has led to a range of changes in carbonate chemistry, collectively referred to as ocean acidification. Stoichiometric dissociation constants used to convert measured carbonate system variables (pH, pCO2, dissolved inorganic carbon, total alkalinity) into globally comparable parameters are crucial for accurately quantifying these changes. The temperature and salinity coefficients of these constants have generally been experimentally derived under controlled laboratory conditions. Here, we use field measurements of carbonate system variables taken from the Global Ocean Data Analysis Project version 2 and the Surface Ocean CO2 Atlas databases to evaluate the temperature dependence of the carbonic acid stoichiometric dissociation constants. By applying a novel iterative procedure to a large dataset of 948 surface-water, quality-controlled samples where four carbonate system variables were independently measured, we show that the set of equations published by Lueker et al. (2000), currently preferred by the ocean acidification community, overestimates the stoichiometric dissociation constants at low temperatures, below ~ 8 °C. We apply these newly derived temperature coefficients to high-latitude Argo float and cruise data to quantify the effects on surface-water pCO2 and calcite saturation states. These findings highlight the critical implications of uncertainty in stoichiometric dissociation constants for future projections of ocean acidification in polar regions, and the need to improve knowledge of what causes the CO2 system inconsistencies in cold waters.

scholarly journals Coastal ocean acidification and increasing total alkalinity in the northwestern Mediterranean Sea

Ocean Science ◽  
2017 ◽  
Vol 13 (3) ◽  
pp. 411-426 ◽  
Author(s):  
Lydia Kapsenberg ◽  
Samir Alliouane ◽  
Frédéric Gazeau ◽  
Laure Mousseau ◽  
Jean-Pierre Gattuso
Keyword(s):  
Time Series ◽  
Ocean Acidification ◽  
Mediterranean Sea ◽  
Temporal Resolution ◽  
Total Alkalinity ◽  
Carbonate Chemistry ◽  
Deconvolution Analysis ◽  
Northwestern Mediterranean Sea ◽  
Coastal Acidification ◽  
Northwestern Mediterranean

Abstract. Coastal time series of ocean carbonate chemistry are critical for understanding how global anthropogenic change manifests in near-shore ecosystems. Yet, they are few and have low temporal resolution. At the time series station Point B in the northwestern Mediterranean Sea, seawater was sampled weekly from 2007 through 2015, at 1 and 50 m, and analyzed for total dissolved inorganic carbon (CT) and total alkalinity (AT). Parameters of the carbonate system such as pH (pHT, total hydrogen ion scale) were calculated and a deconvolution analysis was performed to identify drivers of change. The rate of surface ocean acidification was −0.0028 ± 0.0003 units pHT yr−1. This rate is larger than previously identified open-ocean trends due to rapid warming that occurred over the study period (0.072 ± 0.022 °C yr−1). The total pHT change over the study period was of similar magnitude as the diel pHT variability at this site. The acidification trend can be attributed to atmospheric carbon dioxide (CO2) forcing (59 %, 2.08 ± 0.01 ppm CO2 yr−1) and warming (41 %). Similar trends were observed at 50 m but rates were generally slower. At 1 m depth, the increase in atmospheric CO2 accounted for approximately 40 % of the observed increase in CT (2.97 ± 0.20 µmol kg−1 yr−1). The remaining increase in CT may have been driven by the same unidentified process that caused an increase in AT (2.08 ± 0.19 µmol kg−1 yr−1). Based on the analysis of monthly trends, synchronous increases in CT and AT were fastest in the spring–summer transition. The driving process of the interannual increase in AT has a seasonal and shallow component, which may indicate riverine or groundwater influence. This study exemplifies the importance of understanding changes in coastal carbonate chemistry through the lens of biogeochemical cycling at the land–sea interface. This is the first coastal acidification time series providing multiyear data at high temporal resolution. The data confirm rapid warming in the Mediterranean Sea and demonstrate coastal acidification with a synchronous increase in total alkalinity.

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