scholarly journals Effect of ocean acidification on the benthic foraminifera <i>Ammonia</i> sp. is caused by a decrease in carbonate ion concentration

2013 ◽  
Vol 10 (10) ◽  
pp. 6185-6198 ◽  
Author(s):  
N. Keul ◽  
G. Langer ◽  
L. J. de Nooijer ◽  
J. Bijma

Abstract. About 30% of the anthropogenically released CO2 is taken up by the oceans; such uptake causes surface ocean pH to decrease and is commonly referred to as ocean acidification (OA). Foraminifera are one of the most abundant groups of marine calcifiers, estimated to precipitate ca. 50 % of biogenic calcium carbonate in the open oceans. We have compiled the state of the art literature on OA effects on foraminifera, because the majority of OA research on this group was published within the last three years. Disparate responses of this important group of marine calcifiers to OA were reported, highlighting the importance of a process-based understanding of OA effects on foraminifera. We cultured the benthic foraminifer Ammonia sp. under a range of carbonate chemistry manipulation treatments to identify the parameter of the carbonate system causing the observed effects. This parameter identification is the first step towards a process-based understanding. We argue that [CO32−] is the parameter affecting foraminiferal size-normalized weights (SNWs) and growth rates. Based on the presented data, we can confirm the strong potential of Ammonia sp. foraminiferal SNW as a [CO32−] proxy.

2013 ◽  
Vol 10 (1) ◽  
pp. 1147-1176 ◽  
Author(s):  
N. Keul ◽  
G. Langer ◽  
L. J. de Nooijer ◽  
J. Bijma

Abstract. About 30% of the anthropogenically released CO2 is taken up by the oceans, which causes surface ocean pH to decrease and is commonly referred to as Ocean Acidification (OA). Foraminifera are one of the most abundant groups of marine calcifiers, estimated to precipitate ca. 50% of biogenic calcium carbonate in the open oceans. We have compiled the state of the art of OA effects on foraminifera, because the majority of OA research on this group was published within the last 3 yr. Disparate responses of this important group of marine calcifiers to OA were reported, highlighting the importance of a process based understanding of OA effects on foraminifera. The benthic foraminifer Ammonia sp. was cultured using two carbonate chemistry manipulation approaches: While pH and carbonate ions where varied in one, pH was kept constant in the other while carbonate ion concentration varied. This allows the identification of teh parameter of the parameter of the carbonate system causing observed effects. This parameter identification is the first step towards a process based understanding. We argue that [CO32−] is the parameter affecting foraminiferal size normalized weights (SNW) and growth rates and based on the presented data we can confirm the strong potential of foraminiferal SNW as a [CO32−] proxy.


2010 ◽  
Vol 3 (1) ◽  
pp. 109-130 ◽  
Author(s):  
A.-M. Nisumaa ◽  
S. Pesant ◽  
R. G. J. Bellerby ◽  
B. Delille ◽  
J. Middelburg ◽  
...  

Abstract. The uptake of anthropogenic CO2 by the oceans has led to a rise in the oceanic partial pressure of CO2, and to a decrease in pH and carbonate ion concentration. This modification of the marine carbonate system is referred to as ocean acidification. Numerous papers report the effects of ocean acidification on marine organisms and communities but few have provided details concerning full carbonate chemistry and complementary observations. Additionally, carbonate system variables are often reported in different units, calculated using different sets of dissociation constants and on different pH scales. Hence the direct comparison of experimental results has been problematic and often misleading. The need was identified to (1) gather data on carbonate chemistry, biological and biogeochemical properties, and other ancillary data from published experimental data, (2) transform the information into common framework, and (3) make data freely available. The present paper is the outcome of an effort to integrate ocean carbonate chemistry data from the literature which has been supported by the European Network of Excellence for Ocean Ecosystems Analysis (EUR-OCEANS) and the European Project on Ocean Acidification (EPOCA). A total of 166 papers were identified, 86 contained enough information to readily compute carbonate chemistry variables, and 67 datasets were archived at PANGAEA – The Publishing Network for Geoscientific &amp; Environmental Data. This data compilation is regularly updated as an ongoing mission of EPOCA. Data access: http://doi.pangaea.de/10.1594/PANGAEA.735138


2010 ◽  
Vol 2 (2) ◽  
pp. 167-175 ◽  
Author(s):  
A.-M. Nisumaa ◽  
S. Pesant ◽  
R. G. J. Bellerby ◽  
B. Delille ◽  
J. J. Middelburg ◽  
...  

Abstract. The uptake of anthropogenic CO2 by the oceans has led to a rise in the oceanic partial pressure of CO2, and to a decrease in pH and carbonate ion concentration. This modification of the marine carbonate system is referred to as ocean acidification. Numerous papers report the effects of ocean acidification on marine organisms and communities but few have provided details concerning full carbonate chemistry and complementary observations. Additionally, carbonate system variables are often reported in different units, calculated using different sets of dissociation constants and on different pH scales. Hence the direct comparison of experimental results has been problematic and often misleading. The need was identified to (1) gather data on carbonate chemistry, biological and biogeochemical properties, and other ancillary data from published experimental data, (2) transform the information into common framework, and (3) make data freely available. The present paper is the outcome of an effort to integrate ocean carbonate chemistry data from the literature which has been supported by the European Network of Excellence for Ocean Ecosystems Analysis (EUR-OCEANS) and the European Project on Ocean Acidification (EPOCA). A total of 185 papers were identified, 100 contained enough information to readily compute carbonate chemistry variables, and 81 data sets were archived at PANGAEA – The Publishing Network for Geoscientific &amp; Environmental Data. This data compilation is regularly updated as an ongoing mission of EPOCA. Data access: http://doi.pangaea.de/10.1594/PANGAEA.735138


2013 ◽  
Vol 26 (5) ◽  
pp. 1764-1771 ◽  
Author(s):  
Katsumi Matsumoto ◽  
Ben McNeil

Abstract It is now well understood that the global surface ocean, whose pH has been reduced by ~0.1 in response to rising atmospheric CO2 since industrialization, will continue to become more acidic as fossil fuel CO2 emissions escalate. However, it is unclear how uncertainties in climate sensitivity to future CO2 emissions will alter the manifestation of ocean acidification. Using an earth system model of intermediate complexity, this study performs a set of simulations that varies equilibrium climate sensitivity by 1.0°–4.5°C for a given CO2 emissions scenario and finds two unexpected and decoupled responses. First, the greater the climate sensitivity, the larger the surface mixed layer acidification signal but the smaller the subsurface acidification. However, taken throughout the ocean, the highest climate sensitivity will paradoxically cause greater global warming while buffering whole-ocean pH by up to 24% on centennial time scales. Second, this study finds a large decoupling between pH and carbonate ion concentration in surface waters whereby these chemical properties show opposite effects under variable climate sensitivity. For every 1°C increase in climate sensitivity, the surface ocean pH reduction grows by 4%, while surface ocean carbonate ion reduction shrinks by 2%. The chemical and spatial decoupling found here highlights the importance of distinguishing the biological impacts of pH and aragonite saturation and understanding the spatial extent of important calcifying biomes so as to truly understand the long-term impacts of ocean acidification.


2010 ◽  
Vol 7 (2) ◽  
pp. 1707-1726 ◽  
Author(s):  
C. J. M. Hoppe ◽  
G. Langer ◽  
S. D. Rokitta ◽  
D. A. Wolf-Gladrow ◽  
B. Rost

Abstract. Seawater carbonate chemistry is typically calculated from two measured parameters. Depending on the choice of these input parameters, discrepancies in calculated pCO2 have been recognized by marine chemists, but the significance of this phenomenon for CO2 perturbation experiments has so far not been determined. To mimic different pCO2 scenarios, two common perturbation methods for seawater carbonate chemistry (changing either DIC or TA) were applied using state-of-the-art protocols and equipment. The carbonate system was over-constrained by measuring DIC, TA, pH, and pCO2. Calculated pCO2 matched measured pCO2 if pH and TA or pH and DIC were chosen as input parameters, whereas pCO2 calculated from TA and DIC was considerably lower than measured values. This has important implications for CO2 perturbation experiments. First, calculated pCO2 values may not be comparable if different input parameters were used. Second, responses of organisms to acidification may be overestimated when using TA and DIC for calculations. This is especially troublesome for experiments with calcifiers, as carbonate ion concentration and thus calcite or aragonite saturation state are overestimated. We suggest refraining from measuring TA and DIC only and rather include pH as input parameter for carbonate chemistry calculations.


2014 ◽  
Vol 11 (8) ◽  
pp. 2295-2308 ◽  
Author(s):  
M. T. Horigome ◽  
P. Ziveri ◽  
M. Grelaud ◽  
K.-H. Baumann ◽  
G. Marino ◽  
...  

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.


2021 ◽  
Author(s):  
Laurie Charrieau ◽  
Katsunori Kimoto ◽  
Delphine Dissard ◽  
Beatrice Below ◽  
Kazuhiko Fujita ◽  
...  

&lt;p&gt;Ocean acidification is a consequence of current anthropogenic climate changes.&amp;#160;The concomitant decrease in pH and carbonate ion concentration in sea water may have severe impacts on calcifying organisms. Coral reefs are among the first ecosystems recognized vulnerable to ocean acidification. Within&amp;#160;coral reefs, large benthic foraminifera (LBF) are major calcium carbonate producers.&lt;/p&gt;&lt;p&gt;The aim of this study was to evaluate the effects of varying&amp;#160;pH on&amp;#160;survival and calcification of the&amp;#160;symbiont-bearing LBF species &lt;em&gt;Peneroplis&lt;/em&gt; spp.&amp;#160;We performed culture experiments to study their&amp;#160;resistance to ocean acidification conditions,&amp;#160;as well as their resilience once placed back under open ocean pH (7.9).&lt;/p&gt;&lt;p&gt;After three&amp;#160;days, small signs of test decalcification were observed on specimens kept at pH 7.4, and severe test decalcification was observed on specimens kept at pH 6.9, with the inner organic lining clearly appearing.&amp;#160;After 32 days under pH 7.4, similar strongly decalcified specimens were observed. All the specimens were alive&amp;#160;at the end of the experiment. This result demonstrates the&amp;#160;resistance of &lt;em&gt;Peneroplis &lt;/em&gt;spp.&amp;#160;to an acidified pH, at least on a short period of time.&lt;/p&gt;&lt;p&gt;After being partially decalcified, some of the living specimens were placed back at pH 7.9. After one month, the majority of the specimens showed recalcification&amp;#160;features, mostly by addition of new chambers.&amp;#160;The trace elements concentrations of the newly formed chambers were analysed by LA-ICPMS. Interestingly, more chambers were added when food was given, which&amp;#160;highlights the crucial role of energy source in the&amp;#160;recalcification process. Moreover, the newly formed chambers were most of the time abnormal, and the general structure&amp;#160;of the tests was altered, with potential impacts on reproduction and in situ survival. In conclusion, if symbiont-bearing LBF show some resistance and resilience to&amp;#160;lowered pH&amp;#160;conditions, they&amp;#160;will remain&amp;#160;strongly affected by ocean acidification.&lt;/p&gt;


2014 ◽  
Vol 11 (10) ◽  
pp. 2857-2869 ◽  
Author(s):  
K. J. S. Meier ◽  
L. Beaufort ◽  
S. Heussner ◽  
P. Ziveri

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.


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).


2012 ◽  
Vol 9 (2) ◽  
pp. 1781-1792 ◽  
Author(s):  
C. J. M. Hoppe ◽  
G. Langer ◽  
S. D. Rokitta ◽  
D. A. Wolf-Gladrow ◽  
B. Rost

Abstract. The growing field of ocean acidification research is concerned with the investigation of organisms' responses to increasing pCO2 values. One important approach in this context is culture work using seawater with adjusted CO2 levels. As aqueous pCO2 is difficult to measure directly in small scale experiments, it is generally calculated from two other measured parameters of the carbonate system (often AT, CT or pH). Unfortunately, the overall uncertainties of measured and subsequently calculated values are often unknown. Especially under high pCO2, this can become a severe problem with respect to the interpretation of physiological and ecological data. In the few datasets from ocean acidification research where all three of these parameters were measured, pCO2 values calculated from AT and CT are typically about 30 % lower (i.e. ~300 μatm at a target pCO2 of 1000 μatm) than those calculated from AT and pH or CT and pH. This study presents and discusses these discrepancies as well as likely consequences for the ocean acidification community. Until this problem is solved, one has to consider that calculated parameters of the carbonate system (e.g. pCO2, calcite saturation state) may not be comparable between studies, and that this may have important implications for the interpretation of CO2 perturbation experiments.


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