scholarly journals Ocean acidification studies and the uncertainties relevance on measurements of marine carbonate system properties

2018 ◽  
Vol 66 (2) ◽  
pp. 234-242 ◽  
Author(s):  
Adriana Rodrigues Perretti ◽  
Ana Cecília Rizzatti de Albergaria-Barbosa ◽  
Rodrigo Kerr ◽  
Leticia Cotrim da Cunha
2012 ◽  
Vol 9 (11) ◽  
pp. 15541-15565 ◽  
Author(s):  
R. G. J. Bellerby ◽  
A. Silyakova ◽  
G. Nondal ◽  
D. Slagstad ◽  
J. Czerny ◽  
...  

Abstract. A major, potential stressor of marine systems is the changing water chemistry following increasing seawater carbon dioxide concentration (CO2), commonly termed ocean acidification. In order to understand how an Arctic pelagic ecosystem may respond to future CO2, a deliberate ocean acidification and nutrient perturbation study was undertaken in an Arctic fjord. The initial setting and evolution of seawater carbonate chemistry were investigated. Additions of carbon dioxide resulted in a wide range of ocean acidification scenarios. This study documents the changes to the CO2 system throughout the study following net biological consumption and gas exchange with the atmosphere. In light of the common practice of extrapolating results to cover regions away from experimental conditions, a modelling study was also performed to assess the representativeness, in the context of the simulated present and future carbonate system, of the experimental study region to both the near and wider Arctic region. The mesocosm experiment represented the range of simulated marine carbonate system for the coming century and beyond (pCO2 to 1420 μatm) and thus extrapolations may be appropriate to ecosystems exhibiting similar levels of CO2 system drivers. However, as the regional ocean acidification was very heterogenous and did not follow changes in atmospheric CO2, care should be taken in extrapolating the mesocosm response to other regions based on atmospheric CO2 scenarios.


2020 ◽  
Vol 221 ◽  
pp. 103783 ◽  
Author(s):  
Mehdia Asma Keraghel ◽  
Ferial Louanchi ◽  
Mohamed Zerrouki ◽  
Malik Aït Kaci ◽  
Nadira Aït-Ameur ◽  
...  

2020 ◽  
Vol 71 (3) ◽  
pp. 263 ◽  
Author(s):  
Catriona L. Hurd ◽  
John Beardall ◽  
Steeve Comeau ◽  
Christopher E. Cornwall ◽  
Jonathan N Havenhand ◽  
...  

‘Multiple drivers’ (also termed ‘multiple stressors’) is the term used to describe the cumulative effects of multiple environmental factors on organisms or ecosystems. Here, we consider ocean acidification as a multiple driver because many inorganic carbon parameters are changing simultaneously, including total dissolved inorganic carbon, CO2, HCO3–, CO32–, H+ and CaCO3 saturation state. With the rapid expansion of ocean acidification research has come a greater understanding of the complexity and intricacies of how these simultaneous changes to the seawater carbonate system are affecting marine life. We start by clarifying key terms used by chemists and biologists to describe the changing seawater inorganic carbon system. Then, using key groups of non-calcifying (fish, seaweeds, diatoms) and calcifying (coralline algae, coccolithophores, corals, molluscs) organisms, we consider how various physiological processes are affected by different components of the carbonate system.


2016 ◽  
Vol 74 (4) ◽  
pp. 926-928 ◽  
Author(s):  
Paul McElhany

The ocean acidification (OA) literature is replete with laboratory studies that report species sensitivity to seawater carbonate chemistry in experimental treatments as an “effect of OA”. I argue that this is unintentionally misleading, since these studies do not actually demonstrate an effect of OA but rather show sensitivity to CO2. Documenting an effect of OA involves showing a change in a species (e.g. population abundance or distribution) as a consequence of anthropogenic changes in marine carbonate chemistry. To date, there have been no unambiguous demonstrations of a population level effect of anthropogenic OA, as that term is defined by the IPCC.


2020 ◽  
Author(s):  
Maria Teresa Guerra ◽  
Carlos Rocha

<p>Organic and inorganic whole system metabolism for two Irish coastal areas were compared to evaluate carbonate system resilience to acidification. The two systems are characterized by contrasting watershed input types and composition. Kinvara Bay is fed by Submarine Groundwater Discharge (SGD) derived from a karstic catchment while Killary Harbour is fed by river discharge draining a siliciclastic catchment. Freshwater sources to sea have distinct Total Alkalinity (TA) and Dissolved Inorganic Carbon (DIC) concentrations, higher and lower than the open ocean, respectively, but both evidence seasonally variable low pH, ranging from 6.20 to 7.50. Retention of TA and DIC was calculated for the two areas using LOICZ methodology. In Kinvara bay, annually averaged retention of DIC was greater than for TA (5 × 10<sup>4</sup> and 1.5 × 10<sup>5</sup> mol d<sup>-1</sup>), suggesting the system is acidifying further. Conversely, Killary Harbour shows negative TA and DIC retention, with DIC:TA <1, suggesting an internal buffer against ocean acidification is operating.</p><p>Net Community Production (NCP) was calculated for both systems using Dissolved Oxygen data. Subsequently, we estimated Net Community Calcification (NCC) from the ratio between TA and DIC. NCP was always positive in Killary Harbour with an average of 318 mmol O<sub>2</sub> m<sup>-2 </sup>d<sup>-1</sup> (equivalent to 89 mol C m<sup>-2</sup> y<sup>-1</sup>). However, Kinvara Bay shows relatively lower positive NCP in spring and summer (average of 46 mmol O<sub>2</sub> m<sup>-2</sup> d<sup>-1</sup>), but negative NCP in autumn and winter. Therefore, Kinvara Bay’s Total Organic Carbon (TOC) production was low, at ~21 g m<sup>-2</sup> y<sup>-1</sup> and not enough to overcome acidification driven by the SGD source composition. These results emphasize the complexity of interactions between the drivers of coastal acidification rate, affecting our ability to accurately assess the resilience of the carbonate system in these areas to ocean acidification pressure in the future.</p>


2012 ◽  
Vol 9 (11) ◽  
pp. 4441-4454 ◽  
Author(s):  
S. Hohn ◽  
A. Merico

Abstract. Rising atmospheric CO2 concentrations due to anthropogenic emissions induce changes in the carbonate chemistry of the oceans and, ultimately, a drop in ocean pH. This acidification process can harm calcifying organisms like coccolithophores, molluscs, echinoderms, and corals. It is expected that ocean acidification in combination with other anthropogenic stressors will cause a severe decline in coral abundance by the end of this century, with associated disastrous effects on reef ecosystems. Despite the growing importance of the topic, little progress has been made with respect to modelling the impact of acidification on coral calcification. Here we present a model for a coral polyp that simulates the carbonate system in four different compartments: the seawater, the polyp tissue, the coelenteron, and the calcifying fluid. Precipitation of calcium carbonate takes place in the metabolically controlled calcifying fluid beneath the polyp tissue. The model is adjusted to a state of activity as observed by direct microsensor measurements in the calcifying fluid. We find that a transport mechanism for bicarbonate is required to supplement carbon into the calcifying fluid because CO2 diffusion alone is not sufficient to sustain the observed calcification rates. Simulated CO2 perturbation experiments reveal decreasing calcification rates under elevated pCO2 despite the strong metabolic control of the calcifying fluid. Diffusion of CO2 through the tissue into the calcifying fluid increases with increasing seawater pCO2, leading to decreased aragonite saturation in the calcifying fluid. Our modelling study provides important insights into the complexity of the calcification process at the organism level and helps to quantify the effect of ocean acidification on corals.


2021 ◽  
Vol 13 (2) ◽  
pp. 777-808
Author(s):  
Luke Gregor ◽  
Nicolas Gruber

Abstract. Ocean acidification has profoundly altered the ocean's carbonate chemistry since preindustrial times, with potentially serious consequences for marine life. Yet, no long-term, global observation-based data set exists that allows us to study changes in ocean acidification for all carbonate system parameters over the last few decades. Here, we fill this gap and present a methodologically consistent global data set of all relevant surface ocean parameters, i.e., dissolved inorganic carbon (DIC), total alkalinity (TA), partial pressure of CO2 (pCO2), pH, and the saturation state with respect to mineral CaCO3 (Ω) at a monthly resolution over the period 1985 through 2018 at a spatial resolution of 1∘×1∘. This data set, named OceanSODA-ETHZ, was created by extrapolating in time and space the surface ocean observations of pCO2 (from the Surface Ocean CO2 Atlas, SOCAT) and total alkalinity (TA; from the Global Ocean Data Analysis Project, GLODAP) using the newly developed Geospatial Random Cluster Ensemble Regression (GRaCER) method (code available at https://doi.org/10.5281/zenodo.4455354, Gregor, 2021). This method is based on a two-step (cluster-regression) approach but extends it by considering an ensemble of such cluster regressions, leading to improved robustness. Surface ocean DIC, pH, and Ω were then computed from the globally mapped pCO2 and TA using the thermodynamic equations of the carbonate system. For the open ocean, the cluster-regression method estimates pCO2 and TA with global near-zero biases and root mean squared errors of 12 µatm and 13 µmol kg−1, respectively. Taking into account also the measurement and representation errors, the total uncertainty increases to 14 µatm and 21 µmol kg−1, respectively. We assess the fidelity of the computed parameters by comparing them to direct observations from GLODAP, finding surface ocean pH and DIC global biases of near zero, as well as root mean squared errors of 0.023 and 16 µmol kg−1, respectively. These uncertainties are very comparable to those expected by propagating the total uncertainty from pCO2 and TA through the thermodynamic computations, indicating a robust and conservative assessment of the uncertainties. We illustrate the potential of this new data set by analyzing the climatological mean seasonal cycles of the different parameters of the surface ocean carbonate system, highlighting their commonalities and differences. Further, this data set provides a novel constraint on the global- and basin-scale trends in ocean acidification for all parameters. Concretely, we find for the period 1990 through 2018 global mean trends of 8.6 ± 0.1 µmol kg−1 per decade for DIC, −0.016 ± 0.000 per decade for pH, 16.5 ± 0.1 µatm per decade for pCO2, and −0.07 ± 0.00 per decade for Ω. The OceanSODA-ETHZ data can be downloaded from https://doi.org/10.25921/m5wx-ja34 (Gregor and Gruber, 2020).


2021 ◽  
Vol 3 ◽  
Author(s):  
Daniel J. Burt ◽  
Friederike Fröb ◽  
Tatiana Ilyina

Ocean Alkalinity Enhancement (OAE) simultaneously mitigates atmospheric concentrations of CO2 and ocean acidification; however, no previous studies have investigated the response of the non-linear marine carbonate system sensitivity to alkalinity enhancement on regional scales. We hypothesise that regional implementations of OAE can sequester more atmospheric CO2 than a global implementation. To address this, we investigate physical regimes and alkalinity sensitivity as drivers of the carbon-uptake potential response to global and different regional simulations of OAE. In this idealised ocean-only set-up, total alkalinity is enhanced at a rate of 0.25 Pmol a-1 in 75-year simulations using the Max Planck Institute Ocean Model coupled to the HAMburg Ocean Carbon Cycle model with pre-industrial atmospheric forcing. Alkalinity is enhanced globally and in eight regions: the Subpolar and Subtropical Atlantic and Pacific gyres, the Indian Ocean and the Southern Ocean. This study reveals that regional alkalinity enhancement has the capacity to exceed carbon uptake by global OAE. We find that 82–175 Pg more carbon is sequestered into the ocean when alkalinity is enhanced regionally and 156 PgC when enhanced globally, compared with the background-state. The Southern Ocean application is most efficient, sequestering 12% more carbon than the Global experiment despite OAE being applied across a surface area 40 times smaller. For the first time, we find that different carbon-uptake potentials are driven by the surface pattern of total alkalinity redistributed by physical regimes across areas of different carbon-uptake efficiencies. We also show that, while the marine carbonate system becomes less sensitive to alkalinity enhancement in all experiments globally, regional responses to enhanced alkalinity vary depending upon the background concentrations of dissolved inorganic carbon and total alkalinity. Furthermore, the Subpolar North Atlantic displays a previously unexpected alkalinity sensitivity increase in response to high total alkalinity concentrations.


2021 ◽  
Author(s):  
Matthew P. Humphreys ◽  
Ernie R. Lewis ◽  
Jonathan D. Sharp ◽  
Denis Pierrot

Abstract. Oceanic dissolved inorganic carbon (TC) is the largest pool of carbon that interacts considerably with the atmosphere on human timescales. Oceanic TC is increasing through uptake of anthropogenic carbon dioxide (CO2), and seawater pH is decreasing as a consequence. Both the exchange of CO2 between ocean and atmosphere and the pH response are governed by a set of parameters that interact through chemical equilibria, collectively known as the marine carbonate system. To investigate these processes, at least two of the marine carbonate system's parameters are typically measured – most commonly, two from TC, total alkalinity (AT), pH, and seawater CO2 fugacity (fCO2; or its partial pressure, pCO2, or its dry-air mole fraction, xCO2) – from which the remaining parameters can be calculated and the equilibrium state of seawater solved. Several software tools exist to carry out these calculations, but no fully functional and rigorously validated tool was previously available for Python, a popular scientific programming language. Here, we present PyCO2SYS, a Python package intended to fill this capability gap. We describe the elements of PyCO2SYS that have been inherited from the existing CO2SYS family of software and explain subsequent adjustments and improvements. For example, PyCO2SYS uses automatic differentiation to solve the marine carbonate system and calculate chemical buffer factors, ensuring that the effect of every solute and reaction is accurately included in all its results. We validate PyCO2SYS with internal consistency tests and comparisons against other software, showing that PyCO2SYS produces results that are either virtually identical or different for known reasons, with the differences negligible for all practical purposes. We discuss new insights that arose during the development process, for example that the marine carbonate system cannot be unambiguously solved from the total alkalinity and carbonate ion parameter pair. Finally, we consider potential future developments to PyCO2SYS and discuss the outlook for this and other software for solving the marine carbonate system. The code for PyCO2SYS is distributed via GitHub (https://github.com/mvdh7/PyCO2SYS) under the GNU General Public License v3, archived on Zenodo (Humphreys et al., 2021), and documented online (https://PyCO2SYS.readthedocs.io).


2017 ◽  
Author(s):  
Celeste Sánchez-Noguera ◽  
Ines Stuhldreier ◽  
Jorge Cortés ◽  
Carlos Jiménez ◽  
Álvaro Morales ◽  
...  

Abstract. Numerous experiments have shown that ocean acidification impedes coral calcification, but knowledge about in situ reef ecosystem response to ocean acidification is still scarce. Bahía Culebra, situated at the northern Pacific coast of Costa Rica, is a location naturally exposed to acidic conditions due to the Papagayo seasonal upwelling. We measured pH and pCO2 in situ during two non-upwelling seasons (June 2012, May–June 2013), with a high temporal resolution of every 15 and 30 min, respectively, using two Submersible Autonomous Moored Instruments (SAMI-pH, SAMI-CO2). These results were compared with published data from the upwelling season 2009. Findings revealed that the carbonate system in Bahía Culebra shows a high temporal variability. Incoming offshore waters drive inter- and intra-seasonal changes. Lowest pH (7.8) and highest pCO2 (658.3 µatm) values measured during a cold-water intrusion event in the non-upwelling season were similar to those minimum values reported from upwelling season (pH = 7.8, pCO2 = 643.5 µatm), unveiling that natural acidification occurs sporadically also in non-upwelling season. This affects the interaction of photosynthesis, respiration, calcification, and carbonate dissolution and the resulting diel cycle of pH and pCO2 in the reefs of Bahía Culebra. During non-upwelling season, the aragonite saturation state (Ωa) rises to values of > 3.3 and enhances calcification. Aragonite saturation state values during upwelling season falls below 2.5, hampering calcification and coral growth. Low reef accretion in Bahía Culebra indicates high erosion rates and that these reefs grow on the verge of their ecological tolerance. The Ωa threshold values for coral growth, derived from the correlation between Ωa and coral linear extension rates, suggest that future ocean acidification will threaten reefs in Bahía Culebra. These data contribute to build a better understanding of the carbonate system dynamics and coral reefs key response (e.g. coral growth) to natural low-pH conditions, in upwelling areas in the Eastern Tropical Pacific and beyond.


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