scholarly journals Integrated Assessment of Ocean Acidification Risks to Pteropods in the Northern High Latitudes: Regional Comparison of Exposure, Sensitivity and Adaptive Capacity

2021 ◽  
Vol 8 ◽  
Author(s):  
Nina Bednaršek ◽  
Kerry-Ann Naish ◽  
Richard A. Feely ◽  
Claudine Hauri ◽  
Katsunori Kimoto ◽  
...  
Keyword(s):  
Species Diversity ◽  
Ocean Acidification ◽  
Adaptive Capacity ◽  
Bering Sea ◽  
Ecosystem Change ◽  
Subpolar Gyre ◽  
Saturation State ◽  
Spatial Connectivity ◽  
Integrated Risk ◽  
Amundsen Gulf

Exposure to the impact of ocean acidification (OA) is increasing in high-latitudinal productive habitats. Pelagic calcifying snails (pteropods), a significant component of the diet of economically important fish, are found in high abundance in these regions. Pteropods have thin shells that readily dissolve at low aragonite saturation state (Ωar), making them susceptible to OA. Here, we conducted a first integrated risk assessment for pteropods in the Eastern Pacific subpolar gyre, the Gulf of Alaska (GoA), Bering Sea, and Amundsen Gulf. We determined the risk for pteropod populations by integrating measures of OA exposure, biological sensitivity, and resilience. Exposure was based on physical-chemical hydrographic observations and regional biogeochemical model outputs, delineating seasonal and decadal changes in carbonate chemistry conditions. Biological sensitivity was based on pteropod morphometrics and shell-building processes, including shell dissolution, density and thickness. Resilience and adaptive capacity were based on species diversity and spatial connectivity, derived from the particle tracking modeling. Extensive shell dissolution was found in the central and western part of the subpolar gyre, parts of the Bering Sea, and Amundsen Gulf. We identified two distinct morphotypes: L. helicina helicina and L. helicina pacifica, with high-spired and flatter shells, respectively. Despite the presence of different morphotypes, genetic analyses based on mitochondrial haplotypes identified a single species, without differentiation between the morphological forms, coinciding with evidence of widespread spatial connectivity. We found that shell morphometric characteristics depends on omega saturation state (Ωar); under Ωar decline, pteropods build flatter and thicker shells, which is indicative of a certain level of phenotypic plasticity. An integrated risk evaluation based on multiple approaches assumes a high risk for pteropod population persistence with intensification of OA in the high latitude eastern North Pacific because of their known vulnerability, along with limited evidence of species diversity despite their connectivity and our current lack of sufficient knowledge of their adaptive capacity. Such a comprehensive understanding would permit improved prediction of ecosystem change relevant to effective fisheries resource management, as well as a more robust foundation for monitoring ecosystem health and investigating OA impacts in high-latitudinal habitats.

scholarly journals Ocean carbonate system variability in the North Atlantic Subpolar surface water (1993–2017)

2019 ◽  
Author(s):  
Coraline Leseurre ◽  
Claire Lo Monaco ◽  
Gilles Reverdin ◽  
Nicolas Metzl ◽  
Jonathan Fin ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
North Atlantic ◽  
Surface Waters ◽  
Total Alkalinity ◽  
Subpolar Gyre ◽  
Saturation State ◽  
The North ◽  
Anthropogenic Co2 ◽  
North Atlantic Subpolar Gyre ◽  
The North Atlantic

Abstract. The North Atlantic is one of the major sinks for anthropogenic CO2. In this study, we investigate the evolution of CO2 uptake and ocean acidification in the North Atlantic Subpolar Gyre (50° N–64° N) using repeated observations collected over the last three decades in the framework of the long-term monitoring program SURATLANT (SURveillance de l'ATLANTique). Data obtained between 1993 and 1997 suggest an important reduction in the capacity of the ocean to absorb CO2 from the atmosphere during summer, due to a rapid increase in the fugacity of CO2 (fCO2) in surface waters (5 times faster than the increase in the atmosphere). This was associated with a rapid decrease in surface pH (of the order of −0.014/yr) and was mainly driven by a significant warming and increase in DIC. Similar trends are observed between 2001 and 2007 during both summer and winter with a mean decrease of pH between −0.006/yr and −0.013/yr. These rapid trends are mainly explained by a significant warming of surface waters, a decrease in alkalinity during summer and an increase in DIC during winter. On the contrary, data obtained during the last decade (2008–2017) show a stagnation of surface fCO2 (increasing the ocean sink for CO2) and pH. These recent trends are explained by the cooling of surface waters, a small decrease of total alkalinity and the near-stagnation of dissolved inorganic carbon. Overall our results show that the uptake of CO2 and ocean acidification in the North Atlantic Subpolar Gyre is substantially impacted by multi-decadal variability, in addition to the accumulation of anthropogenic CO2. As a consequence, the future evolution of air-sea CO2 fluxes, pH and the saturation state of surface waters with regards to aragonite and calcite remain highly uncertain in this region.

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.

scholarly journals Metabolic cost of calcification in bivalve larvae under experimental ocean acidification

2016 ◽  
Vol 74 (4) ◽  
pp. 941-954 ◽  
Author(s):  
Christina A. Frieder ◽  
Scott L. Applebaum ◽  
T.-C. Francis Pan ◽  
Dennis Hedgecock ◽  
Donal T. Manahan
Keyword(s):  
Ocean Acidification ◽  
Climate Change Impacts ◽  
Metabolic Cost ◽  
Shell Formation ◽  
Metabolic Demand ◽  
Shell Size ◽  
Saturation State ◽  
Shell Mass ◽  
Energy Limitation ◽  
Endogenous Reserves

Abstract Physiological increases in energy expenditure frequently occur in response to environmental stress. Although energy limitation is often invoked as a basis for decreased calcification under ocean acidification, energy-relevant measurements related to this process are scant. In this study we focus on first-shell (prodissoconch I) formation in larvae of the Pacific oyster, Crassostrea gigas. The energy cost of calcification was empirically derived to be ≤ 1.1 µJ (ng CaCO3)−1. Regardless of the saturation state of aragonite (2.77 vs. 0.77), larvae utilize the same amount of total energy to complete first-shell formation. Even though there was a 56% reduction of shell mass and an increase in dissolution at aragonite undersaturation, first-shell formation is not energy limited because sufficient endogenous reserves are available to meet metabolic demand. Further studies were undertaken on larvae from genetic crosses of pedigreed lines to test for variance in response to aragonite undersaturation. Larval families show variation in response to ocean acidification, with loss of shell size ranging from no effect to 28%. These differences show that resilience to ocean acidification may exist among genotypes. Combined studies of bioenergetics and genetics are promising approaches for understanding climate change impacts on marine organisms that undergo calcification.

scholarly journals Benthic buffers and boosters of ocean acidification on coral reefs

2013 ◽  
Vol 10 (7) ◽  
pp. 4897-4909 ◽  
Author(s):  
K. R. N. Anthony ◽  
G. Diaz-Pulido ◽  
N. Verlinden ◽  
B. Tilbrook ◽  
A. J. Andersson
Keyword(s):  
Ocean Acidification ◽  
Benthic Communities ◽  
Time Of Day ◽  
High Flow ◽  
Net Community Production ◽  
Reef Environment ◽  
Saturation State ◽  
Low Co2 ◽  
Coral Reef Environment ◽  
Community Production

Abstract. Ocean acidification is a threat to marine ecosystems globally. In shallow-water systems, however, ocean acidification can be masked by benthic carbon fluxes, depending on community composition, seawater residence time, and the magnitude and balance of net community production (NCP) and calcification (NCC). Here, we examine how six benthic groups from a coral reef environment on Heron Reef (Great Barrier Reef, Australia) contribute to changes in the seawater aragonite saturation state (Ωa). Results of flume studies using intact reef habitats (1.2 m by 0.4 m), showed a hierarchy of responses across groups, depending on CO2 level, time of day and water flow. At low CO2 (350–450 μatm), macroalgae (Chnoospora implexa), turfs and sand elevated Ωa of the flume water by around 0.10 to 1.20 h−1 – normalised to contributions from 1 m2 of benthos to a 1 m deep water column. The rate of Ωa increase in these groups was doubled under acidification (560–700 μatm) and high flow (35 compared to 8 cm s−1). In contrast, branching corals (Acropora aspera) increased Ωa by 0.25 h−1 at ambient CO2 (350–450 μatm) during the day, but reduced Ωa under acidification and high flow. Nighttime changes in Ωa by corals were highly negative (0.6–0.8 h−1) and exacerbated by acidification. Calcifying macroalgae (Halimeda spp.) raised Ωa by day (by around 0.13 h−1), but lowered Ωa by a similar or higher amount at night. Analyses of carbon flux contributions from benthic communities with four different compositions to the reef water carbon chemistry across Heron Reef flat and lagoon indicated that the net lowering of Ωa by coral-dominated areas can to some extent be countered by long water-residence times in neighbouring areas dominated by turfs, macroalgae and carbonate sand.

scholarly journals Benthic buffers and boosters of ocean acidification on coral reefs

2013 ◽  
Vol 10 (2) ◽  
pp. 1831-1865 ◽  
Author(s):  
K. R. N. Anthony ◽  
G. Diaz-Pulido ◽  
N. Verlinden ◽  
B. Tilbrook ◽  
A. J. Andersson
Keyword(s):  
Ocean Acidification ◽  
Time Of Day ◽  
High Flow ◽  
Net Community Production ◽  
Reef Environment ◽  
Saturation State ◽  
Low Co2 ◽  
Coral Reef Environment ◽  
Co2 Level ◽  
Community Production

Abstract. Ocean acidification is a threat to marine ecosystems globally. In shallow-water systems, however, ocean acidification can be masked by benthic carbon fluxes, depending on community composition, seawater residence time, and the magnitude and balance of net community production (pn) and calcification (gn). Here, we examine how six benthic groups from a coral reef environment on Heron Reef (Great Barrier Reef, Australia) contribute to changes in seawater aragonite saturation state (Ωa). Results of flume studies showed a hierarchy of responses across groups, depending on CO2 level, time of day and water flow. At low CO2 (350–450 μatm), macroalgae (Chnoospora implexa), turfs and sand elevated Ωa of the flume water by around 0.10 to 1.20 h−1 – normalised to contributions from 1 m2 of benthos to a 1 m deep water column. The rate of Ωa increase in these groups was doubled under acidification (560–700 μatm) and high flow (35 compared to 8 cm s−1). In contrast, branching corals (Acropora aspera) increased Ωa by 0.25 h−1 at ambient CO2 (350–450 μatm) during the day, but reduced Ωa under acidification and high flow. Nighttime changes in Ωa by corals were highly negative (0.6–0.8 h−1) and exacerbated by acidification. Calcifying macroalgae (Halimeda spp.) raised Ωa by day (by around 0.13 h−1), but lowered Ωa by a similar or higher amount at night. Analyses of carbon flux contributions from four different benthic compositions to the reef water carbon chemistry across Heron Reef flat and lagoon indicated that the net lowering of Ωa by coral-dominated areas can to some extent be countered by long water residence times in neighbouring areas dominated by turfs, macroalgae and potentially sand.

scholarly journals Quantifying the influence of CO<sub>2</sub> seasonality on future ocean acidification

2015 ◽  
Vol 12 (8) ◽  
pp. 5907-5940
Author(s):  
T. P. Sasse ◽  
B. I. McNeil ◽  
R. J. Matear ◽  
A. Lenton
Keyword(s):  
Ocean Acidification ◽  
North Pacific ◽  
Dissolved Inorganic Carbon ◽  
Marine Ecosystem ◽  
Global Ocean ◽  
Saturation State ◽  
The North ◽  
Data Limitations ◽  
The Future ◽  
The North Pacific

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.

scholarly journals Shell mineralogy of a foundational marine species, Mytilus californianus, over half a century in a changing ocean

2021 ◽  
Vol 118 (3) ◽  
pp. e2004769118
Author(s):  
Elizabeth M. Bullard ◽  
Ivan Torres ◽  
Tianqi Ren ◽  
Olivia A. Graeve ◽  
Kaustuv Roy
Keyword(s):  
Ocean Acidification ◽  
Historical Data ◽  
Mineralogical Composition ◽  
Marine Species ◽  
Mytilus Californianus ◽  
Negative Effects ◽  
Saturation State ◽  
Long Term Changes ◽  
Time Periods

Anthropogenic warming and ocean acidification are predicted to negatively affect marine calcifiers. While negative effects of these stressors on physiology and shell calcification have been documented in many species, their effects on shell mineralogical composition remains poorly known, especially over longer time periods. Here, we quantify changes in the shell mineralogy of a foundation species, Mytilus californianus, under 60 y of ocean warming and acidification. Using historical data as a baseline and a resampling of present-day populations, we document a substantial increase in shell calcite and decrease in aragonite. These results indicate that ocean pH and saturation state, not temperature or salinity, play a strong role in mediating the shell mineralogy of this species and reveal long-term changes in this trait under ocean acidification.

scholarly journals Ocean carbonate system variability in the North Atlantic Subpolar surface water (1993–2017)

2020 ◽  
Vol 17 (9) ◽  
pp. 2553-2577
Author(s):  
Coraline Leseurre ◽  
Claire Lo Monaco ◽  
Gilles Reverdin ◽  
Nicolas Metzl ◽  
Jonathan Fin ◽  
...  
Keyword(s):  
Surface Water ◽  
Ocean Acidification ◽  
North Atlantic ◽  
Subpolar Gyre ◽  
The North ◽  
Short Period ◽  
North Atlantic Subpolar Gyre ◽  
The North Atlantic ◽  
Co2 Sink

Abstract. The North Atlantic is one of the major ocean sinks for natural and anthropogenic atmospheric CO2. Given the variability of the circulation, convective processes or warming–cooling recognized in the high latitudes in this region, a better understanding of the CO2 sink temporal variability and associated acidification needs a close inspection of seasonal, interannual to multidecadal observations. In this study, we investigate the evolution of CO2 uptake and ocean acidification in the North Atlantic Subpolar Gyre (50–64∘ N) using repeated observations collected over the last 3 decades in the framework of the long-term monitoring program SURATLANT (SURveillance de l'ATLANTique). Over the full period (1993–2017) pH decreases (−0.0017 yr−1) and fugacity of CO2 (fCO2) increases (+1.70 µatm yr−1). The trend of fCO2 in surface water is slightly less than the atmospheric rate (+1.96 µatm yr−1). This is mainly due to dissolved inorganic carbon (DIC) increase associated with the anthropogenic signal. However, over shorter periods (4–10 years) and depending on the season, we detect significant variability investigated in more detail in this study. Data obtained between 1993 and 1997 suggest a rapid increase in fCO2 in summer (up to +14 µatm yr−1) that was driven by a significant warming and an increase in DIC for a short period. Similar fCO2 trends are observed between 2001 and 2007 during both summer and winter, but, without significant warming detected, these trends are mainly explained by an increase in DIC and a decrease in alkalinity. This also leads to a pH decrease but with contrasting trends depending on the region and season (between −0.006 and −0.013 yr−1). Conversely, data obtained during the last decade (2008–2017) in summer show a cooling of surface waters and an increase in alkalinity, leading to a strong decrease in surface fCO2 (between −4.4 and −2.3 µatm yr−1; i.e., the ocean CO2 sink increases). Surprisingly, during summer, pH increases up to +0.0052 yr−1 in the southern subpolar gyre. Overall, our results show that, in addition to the accumulation of anthropogenic CO2, the temporal changes in the uptake of CO2 and ocean acidification in the North Atlantic Subpolar Gyre present significant multiannual variability, not clearly directly associated with the North Atlantic Oscillation (NAO). With such variability it is uncertain to predict the near-future evolution of air–sea CO2 fluxes and pH in this region. Thus, it is highly recommended to maintain long-term observations to monitor these properties in the next decade.

scholarly journals Coral calcifying fluid aragonite saturation states derived from Raman spectroscopy

2017 ◽  
Vol 14 (22) ◽  
pp. 5253-5269 ◽  
Author(s):  
Thomas M. DeCarlo ◽  
Juan P. D'Olivo ◽  
Taryn Foster ◽  
Michael Holcomb ◽  
Thomas Becker ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
High Resolution ◽  
Ocean Acidification ◽  
Environmental Changes ◽  
Isotope Geochemistry ◽  
Strong Dependence ◽  
Saturation State ◽  
Minimal Sample ◽  
Biomineralization Process ◽  
Elevated Co2 And Temperature

Abstract. Quantifying the saturation state of aragonite (ΩAr) within the calcifying fluid of corals is critical for understanding their biomineralization process and sensitivity to environmental changes including ocean acidification. Recent advances in microscopy, microprobes, and isotope geochemistry enable the determination of calcifying fluid pH and [CO32−], but direct quantification of ΩAr (where ΩAr =  [CO32−][Ca2+]∕Ksp) has proved elusive. Here we test a new technique for deriving ΩAr based on Raman spectroscopy. First, we analysed abiogenic aragonite crystals precipitated under a range of ΩAr from 10 to 34, and we found a strong dependence of Raman peak width on ΩAr with no significant effects of other factors including pH, Mg∕Ca partitioning, and temperature. Validation of our Raman technique for corals is difficult because there are presently no direct measurements of calcifying fluid ΩAr available for comparison. However, Raman analysis of the international coral standard JCp-1 produced ΩAr of 12.3 ± 0.3, which we demonstrate is consistent with published skeletal Mg∕Ca, Sr∕Ca, B∕Ca, δ11B, and δ44Ca data. Raman measurements are rapid ( ≤  1 s), high-resolution ( ≤  1 µm), precise (derived ΩAr ± 1 to 2 per spectrum depending on instrument configuration), accurate ( ±2 if ΩAr < 20), and require minimal sample preparation, making the technique well suited for testing the sensitivity of coral calcifying fluid ΩAr to ocean acidification and warming using samples from natural and laboratory settings. To demonstrate this, we also show a high-resolution time series of ΩAr over multiple years of growth in a Porites skeleton from the Great Barrier Reef, and we evaluate the response of ΩAr in juvenile Acropora cultured under elevated CO2 and temperature.

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