scholarly journals Growth response of calcifying marine epibionts to biogenic pH fluctuations and global ocean acidification scenarios

2020 ◽  
Author(s):  
Mildred Jessica Johnson ◽  
Laura Margarethe Hennigs ◽  
Yvonne Sawall ◽  
Christian Pansch ◽  
Marlene Wall
2015 ◽  
Vol 12 (8) ◽  
pp. 5907-5940
Author(s):  
T. P. Sasse ◽  
B. I. McNeil ◽  
R. J. Matear ◽  
A. Lenton

Abstract. Ocean acidification is a predictable consequence of rising atmospheric carbon dioxide (CO2), and is highly likely to impact the entire marine ecosystem – from plankton at the base to fish at the top. Factors which are expected to be impacted include reproductive health, organism growth and species composition and distribution. Predicting when critical threshold values will be reached is crucial for projecting the future health of marine ecosystems and for marine resources planning and management. The impacts of ocean acidification will be first felt at the seasonal scale, however our understanding how seasonal variability will influence rates of future ocean acidification remains poorly constrained due to current model and data limitations. To address this issue, we first quantified the seasonal cycle of aragonite saturation state utilizing new data-based estimates of global ocean surface dissolved inorganic carbon and alkalinity. This seasonality was then combined with earth system model projections under different emissions scenarios (RCPs 2.6, 4.5 and 8.5) to provide new insights into future aragonite under-saturation onset. Under a high emissions scenario (RCP 8.5), our results suggest accounting for seasonality will bring forward the initial onset of month-long under-saturation by 17 years compared to annual-mean estimates, with differences extending up to 35 ± 17 years in the North Pacific due to strong regional seasonality. Our results also show large-scale under-saturation once atmospheric CO2 reaches 486 ppm in the North Pacific and 511 ppm in the Southern Ocean independent of emission scenario. Our results suggest that accounting for seasonality is critical to projecting the future impacts of ocean acidification on the marine environment.


2021 ◽  
Vol 8 ◽  
Author(s):  
Emily Rowlands ◽  
Tamara Galloway ◽  
Matthew Cole ◽  
Ceri Lewis ◽  
Victoria Peck ◽  
...  

In aquatic environments, plastic pollution occurs concomitantly with anthropogenic climate stressors such as ocean acidification. Within the Southern Ocean, Antarctic krill (Euphausia Superba) support many marine predators and play a key role in the biogeochemical cycle. Ocean acidification and plastic pollution have been acknowledged to hinder Antarctic krill development and physiology in singularity, however potential multi-stressor effects of plastic particulates coupled with ocean acidification are unexplored. Furthermore, Antarctic krill may be especially vulnerable to plastic pollution due to their close association with sea-ice, a known plastic sink. Here, we investigate the behaviour of nanoplastic [spherical, aminated (NH2), and yellow-green fluorescent polystyrene nanoparticles] in Antarctic seawater and explore the single and combined effects of nanoplastic (160 nm radius, at a concentration of 2.5 μg ml–1) and ocean acidification (pCO2 ∼900, pHT 7.7) on the embryonic development of Antarctic krill. Gravid female krill were collected in the Atlantic sector of the Southern Ocean (North Scotia Sea). Produced eggs were incubated at 0.5 °C in four treatments (control, nanoplastic, ocean acidification and the multi-stressor scenario of nanoplastic presence, and ocean acidification) and their embryonic development after 6 days, at the incubation endpoint, was determined. We observed that negatively charged nanoplastic particles suspended in seawater from the Scotia Sea aggregated to sizes exceeding the nanoscale after 24 h (1054.13 ± 53.49 nm). Further, we found that the proportion of embryos developing through the early stages to reach at least the limb bud stage was highest in the control treatment (21.84%) and lowest in the multi-stressor treatment (13.17%). Since the biological thresholds to any stressors can be altered by the presence of additional stressors, we propose that future nanoplastic ecotoxicology studies should consider the changing global ocean under future climate scenarios for assessments of their impact and highlight that determining the behaviour of nanoplastic particles used in incubation studies is critical to determining their toxicity.


2014 ◽  
Vol 161 (7) ◽  
pp. 1687-1696 ◽  
Author(s):  
Rebecca K. James ◽  
Christopher D. Hepburn ◽  
Christopher E. Cornwall ◽  
Christina M. McGraw ◽  
Catriona L. Hurd

2018 ◽  
Vol 15 (6) ◽  
pp. 1843-1862 ◽  
Author(s):  
Andrés S. Rigual Hernández ◽  
José A. Flores ◽  
Francisco J. Sierro ◽  
Miguel A. Fuertes ◽  
Lluïsa Cros ◽  
...  

Abstract. The Southern Ocean is experiencing rapid and relentless change in its physical and biogeochemical properties. The rate of warming of the Antarctic Circumpolar Current exceeds that of the global ocean, and the enhanced uptake of carbon dioxide is causing basin-wide ocean acidification. Observational data suggest that these changes are influencing the distribution and composition of pelagic plankton communities. Long-term and annual field observations on key environmental variables and organisms are a critical basis for predicting changes in Southern Ocean ecosystems. These observations are particularly needed, since high-latitude systems have been projected to experience the most severe impacts of ocean acidification and invasions of allochthonous species. Coccolithophores are the most prolific calcium-carbonate-producing phytoplankton group playing an important role in Southern Ocean biogeochemical cycles. Satellite imagery has revealed elevated particulate inorganic carbon concentrations near the major circumpolar fronts of the Southern Ocean that can be attributed to the coccolithophore Emiliania huxleyi. Recent studies have suggested changes during the last decades in the distribution and abundance of Southern Ocean coccolithophores. However, due to limited field observations, the distribution, diversity and state of coccolithophore populations in the Southern Ocean remain poorly characterised. We report here on seasonal variations in the abundance and composition of coccolithophore assemblages collected by two moored sediment traps deployed at the Antarctic zone south of Australia (2000 and 3700 m of depth) for 1 year in 2001–2002. Additionally, seasonal changes in coccolith weights of E. huxleyi populations were estimated using circularly polarised micrographs analysed with C-Calcita software. Our findings indicate that (1) coccolithophore sinking assemblages were nearly monospecific for E. huxleyi morphotype B/C in the Antarctic zone waters in 2001–2002; (2) coccoliths captured by the traps experienced weight and length reduction during summer (December–February); (3) the estimated annual coccolith weight of E. huxleyi at both sediment traps (2.11 ± 0.96 and 2.13 ± 0.91 pg at 2000 and 3700 m) was consistent with previous studies for morphotype B/C in other Southern Ocean settings (Scotia Sea and Patagonian shelf); and (4) coccolithophores accounted for approximately 2–5 % of the annual deep-ocean CaCO3 flux. Our results are the first annual record of coccolithophore abundance, composition and degree of calcification in the Antarctic zone. They provide a baseline against which to monitor coccolithophore responses to changes in the environmental conditions expected for this region in coming decades.


2015 ◽  
Vol 12 (103) ◽  
pp. 20141227 ◽  
Author(s):  
Susan C. Fitzer ◽  
Wenzhong Zhu ◽  
K. Elizabeth Tanner ◽  
Vernon R. Phoenix ◽  
Nicholas A. Kamenos ◽  
...  

Ocean acidification (OA) and the resultant changing carbonate saturation states is threatening the formation of calcium carbonate shells and exoskeletons of marine organisms. The production of biominerals in such organisms relies on the availability of carbonate and the ability of the organism to biomineralize in changing environments. To understand how biomineralizers will respond to OA the common blue mussel, Mytilus edulis , was cultured at projected levels of p CO 2 (380, 550, 750, 1000 µatm) and increased temperatures (ambient, ambient plus 2°C). Nanoindentation (a single mussel shell) and microhardness testing were used to assess the material properties of the shells. Young's modulus ( E ), hardness ( H ) and toughness ( K IC ) were measured in mussel shells grown in multiple stressor conditions. OA caused mussels to produce shell calcite that is stiffer (higher modulus of elasticity) and harder than shells grown in control conditions. The outer shell (calcite) is more brittle in OA conditions while the inner shell (aragonite) is softer and less stiff in shells grown under OA conditions. Combining increasing ocean p CO 2 and temperatures as projected for future global ocean appears to reduce the impact of increasing p CO 2 on the material properties of the mussel shell. OA may cause changes in shell material properties that could prove problematic under predation scenarios for the mussels; however, this may be partially mitigated by increasing temperature.


PLoS ONE ◽  
2015 ◽  
Vol 10 (10) ◽  
pp. e0140394 ◽  
Author(s):  
Michael Y. Roleda ◽  
Christopher E. Cornwall ◽  
Yuanyuan Feng ◽  
Christina M. McGraw ◽  
Abigail M. Smith ◽  
...  

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).


Ocean Science ◽  
2020 ◽  
Vol 16 (4) ◽  
pp. 847-862 ◽  
Author(s):  
Olivier Sulpis ◽  
Siv K. Lauvset ◽  
Mathilde Hagens

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.


Author(s):  
M. Debora Iglesias-Rodriguez ◽  
Kenneth R.N. Anthony ◽  
Jella Bijma ◽  
Andrew G. Dickson ◽  
Scott C. Doney ◽  
...  

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