scholarly journals The recent state and variability of the carbonate system of the Canadian Arctic in the context of ocean acidification

2020 ◽  
Author(s):  
Alexis Beaupré-Laperrière ◽  
Alfonso Mucci ◽  
Helmuth Thomas
Keyword(s):  
Ocean Acidification ◽  
Arctic Ocean ◽  
Surface Waters ◽  
Canadian Arctic ◽  
Buffering Capacity ◽  
The Arctic ◽  
Carbonate Mineral ◽  
Potential Threat ◽  
Carbonate System ◽  
The Arctic Ocean

Abstract. Ocean acidification driven by the uptake of anthropogenic CO2 by the surface oceans constitutes a potential threat to the health of marine ecosystems around the globe. The Arctic Ocean is particularly vulnerable to acidification due to its relatively low buffering capacity and, thus, is an ideal region to study the progression and effects of acidification before they become globally widespread. The appearance of undersaturated surface waters with respect to the carbonate mineral aragonite (ΩA 

scholarly journals The Arctic Ocean marine carbon cycle: evaluation of air-sea CO<sub>2</sub> exchanges, ocean acidification impacts and potential feedbacks

2009 ◽  
Vol 6 (4) ◽  
pp. 6695-6747 ◽  
Author(s):  
N. R. Bates ◽  
J. T. Mathis
Keyword(s):  
Gas Exchange ◽  
Carbon Cycle ◽  
Sea Ice ◽  
Ocean Acidification ◽  
Arctic Ocean ◽  
Surface Waters ◽  
The Arctic ◽  
Subsurface Water ◽  
Phytoplankton Primary Production ◽  
The Arctic Ocean

Abstract. At present, although seasonal sea-ice cover mitigates atmosphere-ocean gas exchange, the Arctic Ocean takes up carbon dioxide (CO2) on the order of −65 to −175 Tg C year−1, contributing 5–14% to the global balance of CO2 sinks and sources. Because of this, the Arctic Ocean is an important influence on the global carbon cycle, with the marine carbon cycle and atmosphere-ocean CO2 exchanges sensitive to Arctic Ocean and global climate change feedbacks. In the near-term, further sea-ice loss and increases in phytoplankton growth rates are expected to increase the uptake of CO2 by Arctic surface waters, although mitigated somewhat by surface warming in the Arctic. Thus, the capacity of the Arctic Ocean to uptake CO2 is expected to alter in response to environmental changes driven largely by climate. These changes are likely to continue to modify the physics, biogeochemistry, and ecology of the Arctic Ocean in ways that are not yet fully understood. In surface waters, sea-ice melt, river runoff, cooling and uptake of CO2 through air-sea gas exchange combine to decrease the calcium carbonate (CaCO3) mineral saturation states (Ω) of seawater that is counteracted by seasonal phytoplankton primary production (PP). Biological processes drive divergent trajectories for Ω in surface and subsurface waters of Arctic shelves with subsurface water experiencing undersaturation with respect to aragonite and calcite. Thus, in response to increased sea-ice loss, warming and enhanced phytoplankton PP, the benthic ecosystem of the Arctic shelves are expected to be negatively impacted by the biological amplification of ocean acidification. This in turn reduces the ability of many species to produce CaCO3 shells or tests with profound implications for Arctic marine ecosystems.

scholarly journals The recent state and variability of the carbonate system of the Canadian Arctic Archipelago and adjacent basins in the context of ocean acidification

2020 ◽  
Vol 17 (14) ◽  
pp. 3923-3942
Author(s):  
Alexis Beaupré-Laperrière ◽  
Alfonso Mucci ◽  
Helmuth Thomas
Keyword(s):  
Ocean Acidification ◽  
Dissolved Inorganic Carbon ◽  
Canadian Arctic ◽  
Canada Basin ◽  
The Arctic ◽  
Canadian Arctic Archipelago ◽  
Potential Threat ◽  
Carbonate System ◽  
System Parameters ◽  
Spatial Coverage

Abstract. Ocean acidification driven by the uptake of anthropogenic CO2 by the surface oceans constitutes a potential threat to the health of marine ecosystems around the globe. The Arctic Ocean is particularly vulnerable to acidification and thus is an ideal region to study the progression and effects of acidification before they become globally widespread. The appearance of undersaturated surface waters with respect to the carbonate mineral aragonite (ΩA<1), an important threshold beyond which the calcification and growth of some marine organisms might be hindered, has recently been documented in the Canada Basin and adjacent Canadian Arctic Archipelago (CAA), a dynamic region with an inherently strong variability in biogeochemical processes. Nonetheless, few of these observations were made in the last 5 years and the spatial coverage in the latter region is poor. We use a dataset of carbonate system parameters measured in the CAA and its adjacent basins (Canada Basin and Baffin Bay) from 2003 to 2016 to describe the recent state of these parameters across the Canadian Arctic and investigate the amplitude and sources of the system's variability over more than a decade. Our findings reveal that, in the summers of 2014 to 2016, the ocean surface across our study area served as a net CO2 sink and was partly undersaturated with respect to aragonite in the Canada Basin and the Queen Maud Gulf, the latter region exhibiting undersaturation over its entire water column at some locations. We estimate, using measurements made across several years, that approximately a third of the interannual variability in surface dissolved inorganic carbon (DIC) concentrations in the CAA results from fluctuations in biological activity. In consideration of the system's variability resulting from these fluctuations, we derive times of emergence of the anthropogenic ocean acidification signal for carbonate system parameters in the study area.

scholarly journals The Arctic Ocean marine carbon cycle: evaluation of air-sea CO<sub>2</sub> exchanges, ocean acidification impacts and potential feedbacks

2009 ◽  
Vol 6 (11) ◽  
pp. 2433-2459 ◽  
Author(s):  
N. R. Bates ◽  
J. T. Mathis
Keyword(s):  
Gas Exchange ◽  
Carbon Cycle ◽  
Sea Ice ◽  
Ocean Acidification ◽  
Arctic Ocean ◽  
Surface Waters ◽  
Environmental Changes ◽  
The Arctic ◽  
Phytoplankton Primary Production ◽  
The Arctic Ocean

Abstract. At present, although seasonal sea-ice cover mitigates atmosphere-ocean gas exchange, the Arctic Ocean takes up carbon dioxide (CO2) on the order of −66 to −199 Tg C year−1 (1012 g C), contributing 5–14% to the global balance of CO2 sinks and sources. Because of this, the Arctic Ocean has an important influence on the global carbon cycle, with the marine carbon cycle and atmosphere-ocean CO2 exchanges sensitive to Arctic Ocean and global climate change feedbacks. In the near-term, further sea-ice loss and increases in phytoplankton growth rates are expected to increase the uptake of CO2 by Arctic Ocean surface waters, although mitigated somewhat by surface warming in the Arctic. Thus, the capacity of the Arctic Ocean to uptake CO2 is expected to alter in response to environmental changes driven largely by climate. These changes are likely to continue to modify the physics, biogeochemistry, and ecology of the Arctic Ocean in ways that are not yet fully understood. In surface waters, sea-ice melt, river runoff, cooling and uptake of CO2 through air-sea gas exchange combine to decrease the calcium carbonate (CaCO3) mineral saturation states (Ω) of seawater while seasonal phytoplankton primary production (PP) mitigates this effect. Biological amplification of ocean acidification effects in subsurface waters, due to the remineralization of organic matter, is likely to reduce the ability of many species to produce CaCO3 shells or tests with profound implications for Arctic marine ecosystems

scholarly journals Regional variability of acidification in the Arctic: a sea of contrasts

2014 ◽  
Vol 11 (2) ◽  
pp. 293-308 ◽  
Author(s):  
E. E. Popova ◽  
A. Yool ◽  
Y. Aksenov ◽  
A. C. Coward ◽  
T. R. Anderson
Keyword(s):  
Climate Change ◽  
Primary Production ◽  
Arctic Ocean ◽  
Canadian Arctic ◽  
Atmospheric Co2 ◽  
The Arctic ◽  
Canadian Arctic Archipelago ◽  
Regional Variability ◽  
The Arctic Ocean ◽  
The Impact

Abstract. The Arctic Ocean is a region that is particularly vulnerable to the impact of ocean acidification driven by rising atmospheric CO2, with potentially negative consequences for calcifying organisms such as coccolithophorids and foraminiferans. In this study, we use an ocean-only general circulation model, with embedded biogeochemistry and a comprehensive description of the ocean carbon cycle, to study the response of pH and saturation states of calcite and aragonite to rising atmospheric pCO2 and changing climate in the Arctic Ocean. Particular attention is paid to the strong regional variability within the Arctic, and, for comparison, simulation results are contrasted with those for the global ocean. Simulations were run to year 2099 using the RCP8.5 (an Intergovernmental Panel on Climate Change (IPCC) Fifth Assessment Report (AR5) scenario with the highest concentrations of atmospheric CO2). The separate impacts of the direct increase in atmospheric CO2 and indirect effects via impact of climate change (changing temperature, stratification, primary production and freshwater fluxes) were examined by undertaking two simulations, one with the full system and the other in which atmospheric CO2 was prevented from increasing beyond its preindustrial level (year 1860). Results indicate that the impact of climate change, and spatial heterogeneity thereof, plays a strong role in the declines in pH and carbonate saturation (Ω) seen in the Arctic. The central Arctic, Canadian Arctic Archipelago and Baffin Bay show greatest rates of acidification and Ω decline as a result of melting sea ice. In contrast, areas affected by Atlantic inflow including the Greenland Sea and outer shelves of the Barents, Kara and Laptev seas, had minimal decreases in pH and Ω because diminishing ice cover led to greater vertical mixing and primary production. As a consequence, the projected onset of undersaturation in respect to aragonite is highly variable regionally within the Arctic, occurring during the decade of 2000–2010 in the Siberian shelves and Canadian Arctic Archipelago, but as late as the 2080s in the Barents and Norwegian seas. We conclude that, for future projections of acidification and carbonate saturation state in the Arctic, regional variability is significant and needs to be adequately resolved, with particular emphasis on reliable projections of the rates of retreat of the sea ice, which are a major source of uncertainty.

scholarly journals Model constraints on the anthropogenic carbon budget of the Arctic Ocean

2019 ◽  
Vol 16 (11) ◽  
pp. 2343-2367 ◽  
Author(s):  
Jens Terhaar ◽  
James C. Orr ◽  
Marion Gehlen ◽  
Christian Ethé ◽  
Laurent Bopp
Keyword(s):  
Ocean Acidification ◽  
Arctic Ocean ◽  
Lower Limit ◽  
Ocean Circulation ◽  
The Arctic ◽  
Model Resolution ◽  
Lateral Transport ◽  
The Arctic Ocean ◽  
Anthropogenic Carbon ◽  
The Difference

Abstract. The Arctic Ocean is projected to experience not only amplified climate change but also amplified ocean acidification. Modeling future acidification depends on our ability to simulate baseline conditions and changes over the industrial era. Such centennial-scale changes require a global model to account for exchange between the Arctic and surrounding regions. Yet the coarse resolution of typical global models may poorly resolve that exchange as well as critical features of Arctic Ocean circulation. Here we assess how simulations of Arctic Ocean storage of anthropogenic carbon (Cant), the main driver of open-ocean acidification, differ when moving from coarse to eddy-admitting resolution in a global ocean-circulation–biogeochemistry model (Nucleus for European Modeling of the Ocean, NEMO; Pelagic Interactions Scheme for Carbon and Ecosystem Studies, PISCES). The Arctic's regional storage of Cant is enhanced as model resolution increases. While the coarse-resolution model configuration ORCA2 (2∘) stores 2.0 Pg C in the Arctic Ocean between 1765 and 2005, the eddy-admitting versions ORCA05 and ORCA025 (1∕2∘ and 1∕4∘) store 2.4 and 2.6 Pg C. The difference in inventory between model resolutions that is accounted for is only from their divergence after 1958, when ORCA2 and ORCA025 were initialized with output from the intermediate-resolution configuration (ORCA05). The difference would have been larger had all model resolutions been initialized in 1765 as was ORCA05. The ORCA025 Arctic Cant storage estimate of 2.6 Pg C should be considered a lower limit because that model generally underestimates observed CFC-12 concentrations. It reinforces the lower limit from a previous data-based approach (2.5 to 3.3 Pg C). Independent of model resolution, there was roughly 3 times as much Cant that entered the Arctic Ocean through lateral transport than via the flux of CO2 across the air–sea interface. Wider comparison to nine earth system models that participated in the Coupled Model Intercomparison Project Phase 5 (CMIP5) reveals much larger diversity of stored Cant and lateral transport. Only the CMIP5 models with higher lateral transport obtain Cant inventories that are close to the data-based estimates. Increasing resolution also enhances acidification, e.g., with greater shoaling of the Arctic's average depth of the aragonite saturation horizon during 1960–2012, from 50 m in ORCA2 to 210 m in ORCA025. Even higher model resolution would likely further improve such estimates, but its prohibitive costs also call for other more practical avenues for improvement, e.g., through model nesting, addition of coastal processes, and refinement of subgrid-scale parameterizations.

Recent changes in the exchange of sea ice between the Arctic Ocean and the Canadian Arctic Archipelago

2013 ◽  
Vol 118 (7) ◽  
pp. 3595-3607 ◽  
Author(s):  
Stephen E. L. Howell ◽  
Trudy Wohlleben ◽  
Mohammed Dabboor ◽  
Chris Derksen ◽  
Alexander Komarov ◽  
...  
Keyword(s):  
Sea Ice ◽  
Arctic Ocean ◽  
Canadian Arctic ◽  
The Arctic ◽  
Canadian Arctic Archipelago ◽  
The Arctic Ocean

Dissolved Neodymium Isotopes Trace Origin and Spatiotemporal Evolution of Modern Arctic Sea Ice

2020 ◽  
Author(s):  
Georgi Laukert ◽  
Dorothea Bauch ◽  
Ilka Peeken ◽  
Thomas Krumpen ◽  
Kirstin Werner ◽  
...  
Keyword(s):  
Sea Ice ◽  
Arctic Ocean ◽  
Surface Waters ◽  
Ice Cores ◽  
Arctic Sea Ice ◽  
The Arctic ◽  
Spatiotemporal Evolution ◽  
Arctic Sea ◽  
The Arctic Ocean ◽  
Ice Floes

&lt;p&gt;The lifetime and thickness of Arctic sea ice have markedly decreased in the recent past. This affects Arctic marine ecosystems and the biological pump, given that sea ice acts as platform and transport medium of marine and atmospheric nutrients. At the same time sea ice reduces light penetration to the Arctic Ocean and restricts ocean/atmosphere exchange. In order to understand the ongoing changes and their implications, reconstructions of source regions and drift trajectories of Arctic sea ice are imperative. Automated ice tracking approaches based on satellite-derived sea-ice motion products (e.g. ICETrack) currently perform well in dense ice fields, but provide limited information at the ice edge or in poorly ice-covered areas. Radiogenic neodymium (Nd) isotopes (&amp;#949;&lt;sub&gt;Nd&lt;/sub&gt;) have the potential to serve as a chemical tracer of sea-ice provenance and thus may provide information beyond what can be expected from satellite-based assessments. This potential results from pronounced &amp;#949;&lt;sub&gt;Nd&lt;/sub&gt; differences between the distinct marine and riverine sources, which feed the surface waters of the different sea-ice formation regions. We present the first dissolved (&lt; 0.45 &amp;#181;m) Nd isotope and concentration data obtained from optically clean Arctic first- and multi-year sea ice (ice cores) collected from different ice floes across the Fram Strait during the RV POLARSTERN cruise PS85 in 2014. Our data confirm the preservation of the seawater &amp;#949;&lt;sub&gt;Nd&lt;/sub&gt;signatures in sea ice despite low Nd concentrations (on average ~ 6 pmol/kg) resulting from efficient brine rejection. The large range in &amp;#949;&lt;sub&gt;Nd&lt;/sub&gt; signatures (~ -10 to -30) mirrors that of surface waters in various parts of the Arctic Ocean, indicating that differences between ice floes but also between various sections in an individual ice core reflect the origin and evolution of the sea ice over time. Most ice cores have &amp;#949;&lt;sub&gt;Nd&lt;/sub&gt; signatures of around -10, suggesting that the sea ice was formed in well-mixed waters in the central Arctic Ocean and transported directly to the Fram Strait via the Transpolar Drift. Some ice cores, however, also revealed highly unradiogenic signatures (&amp;#949;&lt;sub&gt;Nd&lt;/sub&gt; &lt; ~ -15) in their youngest (bottom) sections, which we attribute to incorporation of meltwater from Greenland into newly grown sea ice layers. Our new approach facilitates the reconstruction of the origin and spatiotemporal evolution of isolated sea-ice floes in the future Arctic.&lt;/p&gt;

scholarly journals Monitoring and assessment of ocean acidification in the Arctic Ocean-A scoping paper

2010 ◽  
Author(s):  
Lisa L. Robbins ◽  
Kimberly K. Yates ◽  
Richard Feely ◽  
Victoria Fabry
Keyword(s):  
Ocean Acidification ◽  
Arctic Ocean ◽  
The Arctic ◽  
The Arctic Ocean

scholarly journals Macroalgae contribute to nested mosaics of pH variability in a subarctic fjord

2015 ◽  
Vol 12 (16) ◽  
pp. 4895-4911 ◽  
Author(s):  
D. Krause-Jensen ◽  
C. M. Duarte ◽  
I. E. Hendriks ◽  
L. Meire ◽  
M. E. Blicher ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
Arctic Ocean ◽  
Boundary Layers ◽  
Total Alkalinity ◽  
The Arctic ◽  
Kelp Forests ◽  
Coastal Habitats ◽  
Saturation State ◽  
The Arctic Ocean ◽  
Diffusive Boundary

Abstract. The Arctic Ocean is considered the most vulnerable ecosystem to ocean acidification, and large-scale assessments of pH and the saturation state for aragonite (Ωarag) have led to the notion that the Arctic Ocean is already close to a corrosive state. In high-latitude coastal waters the regulation of pH and Ωarag is, however, far more complex than offshore because increased biological activity and input of glacial meltwater affect pH. Effects of ocean acidification on calcifiers and non-calcifying phototrophs occupying coastal habitats cannot be derived from extrapolation of current and forecasted offshore conditions, but they require an understanding of the regimes of pH and Ωarag in their coastal habitats. To increase knowledge of the natural variability in pH in the Arctic coastal zone and specifically to test the influence of benthic vegetated habitats, we quantified pH variability in a Greenland fjord in a nested-scale approach. A sensor array logging pH, O2, PAR, temperature and salinity was applied on spatial scales ranging from kilometre scale across the horizontal extension of the fjord; to 100 m scale vertically in the fjord, 10–100 m scale between subtidal habitats with and without kelp forests and between vegetated tidal pools and adjacent vegetated shores; and to centimetre to metre scale within kelp forests and millimetre scale across diffusive boundary layers of macrophyte tissue. In addition, we assessed the temporal variability in pH on diurnal and seasonal scales. Based on pH measurements combined with point samples of total alkalinity, dissolved inorganic carbon and relationships to salinity, we also estimated variability in Ωarag. Results show variability in pH and Ωarag of up to 0.2–0.3 units at several scales, i.e. along the horizontal and vertical extension of the fjord, between seasons and on a diel basis in benthic habitats and within 1 m3 of kelp forest. Vegetated intertidal pools exhibited extreme diel pH variability of > 1.5 units and macrophyte diffusive boundary layers a pH range of up to 0.8 units. Overall, pelagic and benthic metabolism was an important driver of pH and Ωarag producing mosaics of variability from low levels in the dark to peak levels at high irradiance generally appearing favourable for calcification. We suggest that productive coastal environments may form niches of high pH in a future acidified Arctic Ocean.

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