scholarly journals Carbonate chemistry in the microenvironment within cyanobacterial aggregates under present‐day and future p CO 2 levels

2021 ◽  
Author(s):  
Meri Eichner ◽  
Dieter Wolf‐Gladrow ◽  
Helle Ploug
Keyword(s):  
Carbonate Chemistry ◽  
Cyanobacterial Aggregates

Calcification of an estuarine coccolithophore increases with ocean acidification when subjected to diurnally fluctuating carbonate chemistry

2018 ◽  
Vol 601 ◽  
pp. 59-76
Author(s):  
MM White ◽  
DT Drapeau ◽  
LC Lubelczyk ◽  
VC Abel ◽  
BC Bowler ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
Carbonate Chemistry

scholarly journals Thermal stress reduces pocilloporid coral resilience to ocean acidification by impairing control over calcifying fluid chemistry

2021 ◽  
Vol 7 (2) ◽  
pp. eaba9958
Author(s):  
Maxence Guillermic ◽  
Louise P. Cameron ◽  
Ilian De Corte ◽  
Sambuddha Misra ◽  
Jelle Bijma ◽  
...  
Keyword(s):  
Thermal Stress ◽  
Ocean Acidification ◽  
Pocillopora Damicornis ◽  
Carbonate Chemistry ◽  
Negative Interaction ◽  
Saturation State ◽  
Stylophora Pistillata ◽  
Coral Calcification ◽  
Influence Of Temperature On ◽  
Different Time Scales

The combination of thermal stress and ocean acidification (OA) can more negatively affect coral calcification than an individual stressors, but the mechanism behind this interaction is unknown. We used two independent methods (microelectrode and boron geochemistry) to measure calcifying fluid pH (pHcf) and carbonate chemistry of the corals Pocillopora damicornis and Stylophora pistillata grown under various temperature and pCO2 conditions. Although these approaches demonstrate that they record pHcf over different time scales, they reveal that both species can cope with OA under optimal temperatures (28°C) by elevating pHcf and aragonite saturation state (Ωcf) in support of calcification. At 31°C, neither species elevated these parameters as they did at 28°C and, likewise, could not maintain substantially positive calcification rates under any pH treatment. These results reveal a previously uncharacterized influence of temperature on coral pHcf regulation—the apparent mechanism behind the negative interaction between thermal stress and OA on coral calcification.

The role of tides on the carbonate chemistry of a coastal polynya in the south-eastern Weddell Sea

2021 ◽  
Author(s):  
Elise Droste ◽  
Melchor González Dávila ◽  
Juana Magdalena Santana Casiano ◽  
Mario Hoppema ◽  
Gerd Rohardt ◽  
...  
Keyword(s):  
Southern Ocean ◽  
Weddell Sea ◽  
Water Masses ◽  
Total Alkalinity ◽  
The South ◽  
Carbonate Chemistry ◽  
Large Variability ◽  
South Eastern ◽  
Coastal Polynya ◽  
Eastern Weddell Sea

<p>Tides have a large impact on coastal polynyas around Antarctica. We investigate the effect of semi-diurnal tidal cycles on the seawater carbonate chemistry in a coastal polynya hugging the Ekström Ice Shelf in the south-eastern Weddell Sea. This region experiences some of the strongest tides in the Southern Ocean. We assess the implications for the contribution of coastal polynyas to the carbon dioxide (CO<sub>2</sub>) air-sea flux of the Weddell Sea.</p><p>Two site visits, in January 2015 and January 2019, are intercompared in terms of the dissolved inorganic carbon (DIC) concentration, total alkalinity, pH, and CO<sub>2</sub> partial pressure (pCO<sub>2</sub>). The tides induce large variability in the carbonate chemistry of the coastal polynya in the austral summer: DIC concentrations vary between 2174 and 2223 umol kg<sup>-1</sup>.</p><p>The tidal fluctuation in the DIC concentration can swing the polynya from a sink to a source of atmospheric CO<sub>2 </sub>on a semi-diurnal timescale. We attribute these changes to the mixing of different water masses. The amount of variability induced by tides depends on – and is associated with – large scale oceanographic and biogeochemical processes that affect the characteristics and presence of the water masses being mixed, such as the rate of sea ice melt.</p><p>Sampling strategies in Antarctic coastal polynyas should always take tidal influences into account. This would help to reduce biases in our understanding of how coastal polynyas contribute to the CO<sub>2</sub> uptake by the Southern Ocean.</p>

scholarly journals Revisiting carbonate chemistry controls on planktic foraminifera Mg /  Ca: implications for sea surface temperature and hydrology shifts over the Paleocene–Eocene Thermal Maximum and Eocene–Oligocene transition

2016 ◽  
Vol 12 (4) ◽  
pp. 819-835 ◽  
Author(s):  
David Evans ◽  
Bridget S. Wade ◽  
Michael Henehan ◽  
Jonathan Erez ◽  
Wolfgang Müller
Keyword(s):  
Laser Ablation ◽  
Inductively Coupled Plasma ◽  
Data Sets ◽  
Carbonate Chemistry ◽  
Surface Hydrology ◽  
Planktic Foraminifera ◽  
Inductively Coupled ◽  
Accurate Picture ◽  
Thermal Maximum ◽  
The Relationship

Abstract. Much of our knowledge of past ocean temperatures comes from the foraminifera Mg / Ca palaeothermometer. Several nonthermal controls on foraminifera Mg incorporation have been identified, of which vital effects, salinity, and secular variation in seawater Mg / Ca are the most commonly considered. Ocean carbonate chemistry is also known to influence Mg / Ca, yet this is rarely examined as a source of uncertainty, either because (1) precise pH and [CO32−] reconstructions are sparse or (2) it is not clear from existing culture studies how a correction should be applied. We present new culture data of the relationship between carbonate chemistry and Mg / Ca for the surface-dwelling planktic species Globigerinoides ruber and compare our results to data compiled from existing studies. We find a coherent relationship between Mg / Ca and the carbonate system and argue that pH rather than [CO32−] is likely to be the dominant control. Applying these new calibrations to data sets for the Paleocene–Eocene Thermal Maximum (PETM) and Eocene–Oligocene transition (EOT) enables us to produce a more accurate picture of surface hydrology change for the former and a reassessment of the amount of subtropical precursor cooling for the latter. We show that pH-adjusted Mg / Ca and δ18O data sets for the PETM are within error of no salinity change and that the amount of precursor cooling over the EOT has been previously underestimated by  ∼ 2 °C based on Mg / Ca. Finally, we present new laser-ablation data of EOT-age Turborotalia ampliapertura from St. Stephens Quarry (Alabama), for which a solution inductively coupled plasma mass spectrometry (ICPMS) Mg / Ca record is available (Wade et al., 2012). We show that the two data sets are in excellent agreement, demonstrating that fossil solution and laser-ablation data may be directly comparable. Together with an advancing understanding of the effect of Mg / Casw, the coherent picture of the relationship between Mg / Ca and pH that we outline here represents a step towards producing accurate and quantitative palaeotemperatures using this proxy.

scholarly journals Modelling coral calcification accounting for the impacts of coral bleaching and ocean acidification

2015 ◽  
Vol 12 (9) ◽  
pp. 2607-2630 ◽  
Author(s):  
C. Evenhuis ◽  
A. Lenton ◽  
N. E. Cantin ◽  
J. M. Lough
Keyword(s):  
Ocean Acidification ◽  
Arrhenius Equation ◽  
Sea Surface ◽  
Carbonate Chemistry ◽  
Reef Environment ◽  
Local Environments ◽  
Trade Offs ◽  
Coral Reef Environment ◽  
Coral Health ◽  
Rates Of Growth

Abstract. Coral reefs are diverse ecosystems that are threatened by rising CO2 levels through increases in sea surface temperature and ocean acidification. Here we present a new unified model that links changes in temperature and carbonate chemistry to coral health. Changes in coral health and population are explicitly modelled by linking rates of growth, recovery and calcification to rates of bleaching and temperature-stress-induced mortality. The model is underpinned by four key principles: the Arrhenius equation, thermal specialisation, correlated up- and down-regulation of traits that are consistent with resource allocation trade-offs, and adaption to local environments. These general relationships allow this model to be constructed from a range of experimental and observational data. The performance of the model is assessed against independent data to demonstrate how it can capture the observed response of corals to stress. We also provide new insights into the factors that determine calcification rates and provide a framework based on well-known biological principles to help understand the observed global distribution of calcification rates. Our results suggest that, despite the implicit complexity of the coral reef environment, a simple model based on temperature, carbonate chemistry and different species can give insights into how corals respond to changes in temperature and ocean acidification.

scholarly journals Environmental controls on the <i>Emiliania huxleyi</i> calcite mass

2014 ◽  
Vol 11 (8) ◽  
pp. 2295-2308 ◽  
Author(s):  
M. T. Horigome ◽  
P. Ziveri ◽  
M. Grelaud ◽  
K.-H. Baumann ◽  
G. Marino ◽  
...  
Keyword(s):  
Seawater Temperature ◽  
World Ocean ◽  
Environmental Parameters ◽  
Abundant Species ◽  
Emiliania Huxleyi ◽  
Ion Concentration ◽  
Carbonate Chemistry ◽  
Environmental Controls ◽  
Carbonate Ion ◽  
Phosphate Availability

Abstract. Although ocean acidification is expected to impact (bio) calcification by decreasing the seawater carbonate ion concentration, [CO32−], there is evidence of nonuniform response of marine calcifying plankton to low seawater [CO32−]. This raises questions about the role of environmental factors other than acidification and about the complex physiological responses behind calcification. Here we investigate the synergistic effect of multiple environmental parameters, including seawater temperature, nutrient (nitrate and phosphate) availability, and carbonate chemistry on the coccolith calcite mass of the cosmopolitan coccolithophore Emiliania huxleyi, the most abundant species in the world ocean. We use a suite of surface (late Holocene) sediment samples from the South Atlantic and southwestern Indian Ocean taken from depths lying above the modern lysocline (with the exception of eight samples that are located at or below the lysocline). The coccolith calcite mass in our results presents a latitudinal distribution pattern that mimics the main oceanographic features, thereby pointing to the potential importance of seawater nutrient availability (phosphate and nitrate) and carbonate chemistry (pH and pCO2) in determining coccolith mass by affecting primary calcification and/or the geographic distribution of E. huxleyi morphotypes. Our study highlights the importance of evaluating the combined effect of several environmental stressors on calcifying organisms to project their physiological response(s) in a high-CO2 world and improve interpretation of paleorecords.

scholarly journals Evaluation of a semi-automatic system for long-term seawater carbonate chemistry manipulation

2013 ◽  
Vol 86 (4) ◽  
pp. 443-451 ◽  
Author(s):  
RODRIGO TORRES ◽  
PATRICIO H MANRIQUEZ ◽  
CRISTIAN DUARTE ◽  
JORGE M NAVARRO ◽  
NELSON A LAGOS ◽  
...  
Keyword(s):  
Automatic System ◽  
Carbonate Chemistry ◽  
Seawater Carbonate Chemistry
Sign in / Sign up

Export Citation Format

Share Document