scholarly journals Air-ice carbon pathways inferred from a sea ice tank experiment

Elem Sci Anth ◽  
2016 ◽  
Vol 4 ◽  
Author(s):  
Marie Kotovitch ◽  
Sébastien Moreau ◽  
Jiayun Zhou ◽  
Martin Vancoppenolle ◽  
Gerhard S. Dieckmann ◽  
...  
Keyword(s):  
Sea Ice ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Bubble Nucleation ◽  
Atmospheric Co2 ◽  
The Arctic ◽  
Gas Bubble ◽  
Co2 Fluxes ◽  
Carbon Cycle Model ◽  
Ice Growth

Abstract Given rapid sea ice changes in the Arctic Ocean in the context of climate warming, better constraints on the role of sea ice in CO2 cycling are needed to assess the capacity of polar oceans to buffer the rise of atmospheric CO2 concentration. Air-ice CO2 fluxes were measured continuously using automated chambers from the initial freezing of a sea ice cover until its decay during the INTERICE V experiment at the Hamburg Ship Model Basin. Cooling seawater prior to sea ice formation acted as a sink for atmospheric CO2, but as soon as the first ice crystals started to form, sea ice turned to a source of CO2, which lasted throughout the whole ice growth phase. Once ice decay was initiated by warming the atmosphere, the sea ice shifted back again to a sink of CO2. Direct measurements of outward ice-atmosphere CO2 fluxes were consistent with the depletion of dissolved inorganic carbon in the upper half of sea ice. Combining measured air-ice CO2 fluxes with the partial pressure of CO2 in sea ice, we determined strongly different gas transfer coefficients of CO2 at the air-ice interface between the growth and the decay phases (from 2.5 to 0.4 mol m−2 d−1 atm−1). A 1D sea ice carbon cycle model including gas physics and carbon biogeochemistry was used in various configurations in order to interpret the observations. All model simulations correctly predicted the sign of the air-ice flux. By contrast, the amplitude of the flux was much more variable between the different simulations. In none of the simulations was the dissolved gas pathway strong enough to explain the large fluxes during ice growth. This pathway weakness is due to an intrinsic limitation of ice-air fluxes of dissolved CO2 by the slow transport of dissolved inorganic carbon in the ice. The best means we found to explain the high air-ice carbon fluxes during ice growth is an intense yet uncertain gas bubble efflux, requiring sufficient bubble nucleation and upwards rise. We therefore call for further investigation of gas bubble nucleation and transport in sea ice.

scholarly journals Inorganic carbon fluxes on the Mackenzie Shelf of the Beaufort Sea

2017 ◽  
Author(s):  
Jacoba Mol ◽  
Helmuth Thomas ◽  
Paul G. Myers ◽  
Xianmin Hu ◽  
Alfonso Mucci
Keyword(s):  
Sea Ice ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Beaufort Sea ◽  
Total Alkalinity ◽  
The Arctic ◽  
Surface Mixed Layer ◽  
Saturation State ◽  
Carbon Transfer ◽  
Mackenzie Shelf

Abstract. The Mackenzie Shelf in the southeastern Beaufort Sea is a region that has experienced large changes in the past several decades as warming, sea-ice loss, and increased river discharge have altered carbon cycling. Upwelling and downwelling events are common on the shelf, caused by strong, fluctuating along-shore winds, resulting in cross-shelf Ekman transport, and an alternating estuarine and anti-estuarine circulation. Downwelling carries inorganic carbon and other remineralization products off the shelf and into the deep basin for possible long-term storage in the world oceans. Upwelling carries dissolved inorganic carbon (DIC) and nutrient-rich waters from the Pacific-origin upper halocline layer (UHL) onto the shelf. Profiles of DIC and total alkalinity (TA) taken in August and September of 2014 are used to investigate the cycling of inorganic carbon on the Mackenzie Shelf. The along-shore transport of water and the cross-shelf transport of inorganic carbon are quantified using velocity field output from a simulation of the Arctic and Northern Hemisphere Atlantic (ANHA4) configuration of the Nucleus of European Modelling of the Ocean (NEMO) framework. A strong upwelling event prior to sampling on the Mackenzie Shelf is analyzed and the resulting influence on the carbonate system, including the saturation state of waters with respect to aragonite and pH, is investigated. TA and the oxygen isotope ratio of water (δ18O) are used to examine water-mass distributions in the study area and to investigate the influence of Pacific Water, Mackenzie River freshwater, and sea-ice melt on carbon dynamics and air-sea fluxes of carbon dioxide (CO2) in the surface mixed layer. Understanding carbon transfer in this seasonally dynamic environment is key to quantify the importance of Arctic shelf regions to the global carbon cycle and provide a basis for understanding how it will respond to the aforementioned climate-induced changes.

scholarly journals Estimates of ikaite export from sea ice to the underlying seawater in a sea ice–seawater mesocosm

2016 ◽  
Vol 10 (5) ◽  
pp. 2173-2189 ◽  
Author(s):  
Nicolas-Xavier Geilfus ◽  
Ryan J. Galley ◽  
Brent G. T. Else ◽  
Karley Campbell ◽  
Tim Papakyriakou ◽  
...  
Keyword(s):  
Sea Ice ◽  
Water Column ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Carbon Dynamics ◽  
Total Alkalinity ◽  
Main Process ◽  
Saturation State ◽  
Ice Growth ◽  
Ice Melt

Abstract. The precipitation of ikaite and its fate within sea ice is still poorly understood. We quantify temporal inorganic carbon dynamics in sea ice from initial formation to its melt in a sea ice–seawater mesocosm pool from 11 to 29 January 2013. Based on measurements of total alkalinity (TA) and total dissolved inorganic carbon (TCO2), the main processes affecting inorganic carbon dynamics within sea ice were ikaite precipitation and CO2 exchange with the atmosphere. In the underlying seawater, the dissolution of ikaite was the main process affecting inorganic carbon dynamics. Sea ice acted as an active layer, releasing CO2 to the atmosphere during the growth phase, taking up CO2 as it melted and exporting both ikaite and TCO2 into the underlying seawater during the whole experiment. Ikaite precipitation of up to 167 µmolkg−1 within sea ice was estimated, while its export and dissolution into the underlying seawater was responsible for a TA increase of 64–66 µmolkg−1 in the water column. The export of TCO2 from sea ice to the water column increased the underlying seawater TCO2 by 43.5 µmolkg−1, suggesting that almost all of the TCO2 that left the sea ice was exported to the underlying seawater. The export of ikaite from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased vertical connectivity in sea ice due to the upward percolation of seawater and meltwater flushing during sea ice melt. Based on the change in TA in the water column around the onset of sea ice melt, more than half of the total ikaite precipitated in the ice during sea ice growth was still contained in the ice when the sea ice began to melt. Ikaite crystal dissolution in the water column kept the seawater pCO2 undersaturated with respect to the atmosphere in spite of increased salinity, TA and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying seawater can potentially hamper the effect of oceanic acidification on the aragonite saturation state (Ωaragonite) in fall and in winter in ice-covered areas, at the time when Ωaragonite is smallest.

scholarly journals Inorganic carbon fluxes on the Mackenzie Shelf of the Beaufort Sea

2018 ◽  
Vol 15 (4) ◽  
pp. 1011-1027 ◽  
Author(s):  
Jacoba Mol ◽  
Helmuth Thomas ◽  
Paul G. Myers ◽  
Xianmin Hu ◽  
Alfonso Mucci
Keyword(s):  
Sea Ice ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Beaufort Sea ◽  
Total Alkalinity ◽  
The Arctic ◽  
Surface Mixed Layer ◽  
Carbon Transfer ◽  
Mackenzie Shelf ◽  
Upwelling Event

Abstract. The Mackenzie Shelf in the southeastern Beaufort Sea is a region that has experienced large changes in the past several decades as warming, sea-ice loss, and increased river discharge have altered carbon cycling. Upwelling and downwelling events are common on the shelf, caused by strong, fluctuating along-shore winds, resulting in cross-shelf Ekman transport, and an alternating estuarine and anti-estuarine circulation. Downwelling carries dissolved inorganic carbon (DIC) and other remineralization products off the shelf and into the deep basin for possible long-term storage in the world's oceans. Upwelling carries DIC and nutrient-rich waters from the Pacific-origin upper halocline layer (UHL) onto the shelf. Profiles of DIC and total alkalinity (TA) taken in August and September of 2014 are used to investigate the cycling of carbon on the Mackenzie Shelf. The along-shore transport of water and the cross-shelf transport of DIC are quantified using velocity field output from a simulation of the Arctic and Northern Hemisphere Atlantic (ANHA4) configuration of the Nucleus of European Modelling of the Ocean (NEMO) framework. A strong upwelling event prior to sampling on the Mackenzie Shelf took place, bringing CO2-rich (elevated pCO2) water from the UHL onto the shelf bottom. The maximum on-shelf DIC flux was estimated at 16.9×103 mol C d−1 m−2 during the event. The maximum on-shelf transport of DIC through the upwelling event was found to be 65±15×10-3 Tg C d−1. TA and the oxygen isotope ratio of water (δ18O-H2O) are used to examine water-mass distributions in the study area and to investigate the influence of Pacific Water, Mackenzie River freshwater, and sea-ice melt on carbon dynamics and air–sea fluxes of carbon dioxide (CO2) in the surface mixed layer. Understanding carbon transfer in this seasonally dynamic environment is key to quantify the importance of Arctic shelf regions to the global carbon cycle and provide a basis for understanding how it will respond to the aforementioned climate-induced changes.

scholarly journals Assessment of the sea-ice carbon pump: Insights from a three-dimensional ocean-sea-ice biogeochemical model (NEMO-LIM-PISCES)

Elem Sci Anth ◽  
2016 ◽  
Vol 4 ◽  
Author(s):  
Sébastien Moreau ◽  
Martin Vancoppenolle ◽  
Laurent Bopp ◽  
Oliver Aumont ◽  
Gurvan Madec ◽  
...  
Keyword(s):  
Carbon Cycle ◽  
Sea Ice ◽  
General Circulation ◽  
Circulation Model ◽  
Total Alkalinity ◽  
The Arctic ◽  
Global Ocean ◽  
Biogeochemical Model ◽  
Co2 Fluxes ◽  
Ice Growth

Abstract The role of sea ice in the carbon cycle is minimally represented in current Earth System Models (ESMs). Among potentially important flaws, mentioned by several authors and generally overlooked during ESM design, is the link between sea-ice growth and melt and oceanic dissolved inorganic carbon (DIC) and total alkalinity (TA). Here we investigate whether this link is indeed an important feature of the marine carbon cycle misrepresented in ESMs. We use an ocean general circulation model (NEMO-LIM-PISCES) with sea-ice and marine carbon cycle components, forced by atmospheric reanalyses, adding a first-order representation of DIC and TA storage and release in/from sea ice. Our results suggest that DIC rejection during sea-ice growth releases several hundred Tg C yr−1 to the surface ocean, of which < 2% is exported to depth, leading to a notable but weak redistribution of DIC towards deep polar basins. Active carbon processes (mainly CaCO3 precipitation but also ice-atmosphere CO2 fluxes and net community production) increasing the TA/DIC ratio in sea-ice modified ocean-atmosphere CO2 fluxes by a few Tg C yr−1 in the sea-ice zone, with specific hemispheric effects: DIC content of the Arctic basin decreased but DIC content of the Southern Ocean increased. For the global ocean, DIC content increased by 4 Tg C yr−1 or 2 Pg C after 500 years of model run. The simulated numbers are generally small compared to the present-day global ocean annual CO2 sink (2.6 ± 0.5 Pg C yr−1). However, sea-ice carbon processes seem important at regional scales as they act significantly on DIC redistribution within and outside polar basins. The efficiency of carbon export to depth depends on the representation of surface-subsurface exchanges and their relationship with sea ice, and could differ substantially if a higher resolution or different ocean model were used.

scholarly journals Seasonal marine carbon system processes in an Arctic coastal landfast sea ice environment observed with an innovative underwater sensor platform

Elem Sci Anth ◽  
2021 ◽  
Vol 9 (1) ◽  
Author(s):  
P. J. Duke ◽  
B. G. T. Else ◽  
S. F. Jones ◽  
S. Marriot ◽  
M. M. M. Ahmed ◽  
...  
Keyword(s):  
Sea Ice ◽  
Phytoplankton Bloom ◽  
Dissolved Inorganic Carbon ◽  
Set Covering ◽  
The Arctic ◽  
Data Set ◽  
Saturation State ◽  
Ice Growth ◽  
Sensor Platform ◽  
Carbon System

Studying carbon dioxide in the ocean helps to understand how the ocean will be impacted by climate change and respond to increasing fossil fuel emissions. The marine carbonate system is not well characterized in the Arctic, where challenging logistics and extreme conditions limit observations of atmospheric CO2 flux and ocean acidification. Here, we present a high-resolution marine carbon system data set covering the complete cycle of sea-ice growth and melt in an Arctic estuary (Nunavut, Canada). This data set was collected through three consecutive yearlong deployments of sensors for pH and partial pressure of CO2 in seawater (pCO2sw) on a cabled underwater observatory. The sensors were remarkably stable compared to discrete samples: While corrections for offsets were required in some instances, we did not observe significant drift over the deployment periods. Our observations revealed a strong seasonality in this marine carbon system. Prior to sea-ice formation, air–sea gas exchange and respiration were the dominant processes, leading to increasing pCO2sw and reduced aragonite saturation state (ΩAr). During sea-ice growth, water column respiration and brine rejection (possibly enriched in dissolved inorganic carbon, relative to alkalinity, due to ikaite precipitation in sea ice) drove pCO2sw to supersaturation and lowered ΩAr to < 1. Shortly after polar sunrise, the ecosystem became net autotrophic, returning pCO2sw to undersaturation. The biological community responsible for this early switch to autotrophy (well before ice algae or phytoplankton blooms) requires further investigation. After sea-ice melt initiated, an under-ice phytoplankton bloom strongly reduced aqueous carbon (chlorophyll-a max of 2.4 µg L–1), returning ΩAr to > 1 after 4.5 months of undersaturation. Based on simple extrapolations of anthropogenic carbon inventories, we suspect that this seasonal undersaturation would not have occurred naturally. At ice breakup, the sensor platform recorded low pCO2sw (230 µatm), suggesting a strong CO2 sink during the open water season.

scholarly journals Impacts of ikaite export from sea ice to the underlying seawater in a sea ice-seawater mesocosm

2016 ◽  
Author(s):  
N.-X Geilfus ◽  
R. J. Galley ◽  
B. G. T. Else ◽  
T. Papakyriakou ◽  
O. Crabeck ◽  
...  
Keyword(s):  
Sea Ice ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Open Water ◽  
Carbon Dynamics ◽  
Co2 Exchange ◽  
Total Alkalinity ◽  
Main Process ◽  
Saturation State ◽  
Ice Growth

Abstract. Ikaite precipitation within sea ice could act as a significant sink for atmospheric CO2. However, the fate of these ikaite crystals is still poorly understood. We quantify temporal inorganic carbon dynamics from initial sea ice formation from open water to its melt during a month-long experiment in a sea ice-seawater mesocosm pool. Within sea ice, ikaite precipitation and CO2 exchange with the atmosphere were the main processes affecting inorganic carbon dynamics, while the dissolution of ikaite was the main process affecting inorganic carbon dynamics in the underlying seawater. Based on the total alkalinity (TA) and total dissolved inorganic carbon (TCO2) within sea ice and seawater, we estimated ikaite precipitated up to 167 ± 3 µmol kg-1 within sea ice; up to 57 % of the ikaite precipitated within sea ice was exported to the underlying seawater where it was dissolved. Ikaite export from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased sea ice vertical connectivity due to the upward percolation of seawater, and meltwater flushing during sea ice melt. The dissolution of the ikaite crystals in the water column kept the seawater pCO2 undersaturated compared to the atmosphere in spite of increased salinity, TA, and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying seawater can potentially hamper the effect of oceanic acidification on the aragonite saturation state (Ωaragonite) in fall and winter in ice-covered areas, at the time when Ωaragonite is smallest.

scholarly journals Importance of open-water ice growth and ice concentration evolution: a study based on FESOM-ECHAM6

2015 ◽  
Vol 6 (2) ◽  
pp. 2137-2179
Author(s):  
X. Shi ◽  
G. Lohmann
Keyword(s):  
Sea Ice ◽  
Surface Albedo ◽  
Global Climate Model ◽  
Open Water ◽  
Arctic Sea Ice ◽  
Meridional Overturning Circulation ◽  
The Arctic ◽  
Water Ice ◽  
Ice Growth ◽  
Ice Concentration

Abstract. A newly developed global climate model FESOM-ECHAM6 with an unstructured mesh and high resolution is applied to investigate to what degree the area-thickness distribution of new ice formed in open water affects the ice and ocean properties. A sensitivity experiment is performed which reduces the horizontal-to-vertical aspect ratio of open-water ice growth. The resulting decrease in the Arctic winter sea-ice concentration strongly reduces the surface albedo, enhances the ocean heat release to the atmosphere, and increases the sea-ice production. Furthermore, our simulations show a positive feedback mechanism among the Arctic sea ice, the Atlantic Meridional Overturning Circulation (AMOC), and the surface air temperature in the Arctic, as the sea ice transport affects the freshwater budget in regions of deep water formation. A warming over Europe, Asia and North America, associated with a negative anomaly of Sea Level Pressure (SLP) over the Arctic (positive phase of the Arctic Oscillation (AO)), is also simulated by the model. For the Southern Ocean, the most pronounced change is a warming along the Antarctic Circumpolar Current (ACC), especially for the Pacific sector. Additionally, a series of sensitivity tests are performed using an idealized 1-D thermodynamic model to further investigate the influence of the open-water ice growth, which reveals similar results in terms of the change of sea ice and ocean temperature. In reality, the distribution of new ice on open water relies on many uncertain parameters, for example, surface albedo, wind speed and ocean currents. Knowledge of the detailed processes is currently too crude for those processes to be implemented realistically into models. Our sensitivity experiments indicate a pronounced uncertainty related to open-water sea ice growth which could significantly affect the climate system.

scholarly journals Radiocarbon isotopic evidence for assimilation of atmospheric CO<sub>2</sub> by the seagrass <i>Zostera marina</i>

2015 ◽  
Vol 12 (20) ◽  
pp. 6251-6258 ◽  
Author(s):  
K. Watanabe ◽  
T. Kuwae
Keyword(s):  
Carbon Source ◽  
Zostera Marina ◽  
Inorganic Carbon ◽  
Aquatic Vegetation ◽  
Dissolved Inorganic Carbon ◽  
Isotope Analysis ◽  
Co2 Exchange ◽  
Atmospheric Co2 ◽  
Isotopic Signatures ◽  
Seagrass Meadows

Abstract. Submerged aquatic vegetation takes up water-column dissolved inorganic carbon (DIC) as a carbon source across its thin cuticle layer. It is expected that marine macrophytes also use atmospheric CO2 when exposed to air during low tide, although assimilation of atmospheric CO2 has never been quantitatively evaluated. Using the radiocarbon isotopic signatures (Δ14C) of the seagrass Zostera marina, DIC and particulate organic carbon (POC), we show quantitatively that Z. marina takes up and assimilates atmospheric modern CO2 in a shallow coastal ecosystem. The Δ14C values of the seagrass (−40 to −10 ‰) were significantly higher than those of aquatic DIC (−46 to −18 ‰), indicating that the seagrass uses a 14C-rich carbon source (atmospheric CO2, +17 ‰). A carbon-source mixing model indicated that the seagrass assimilated 0–40 % (mean, 17 %) of its inorganic carbon as atmospheric CO2. CO2 exchange between the air and the seagrass might be enhanced by the presence of a very thin film of water over the air-exposed leaves during low tide. Our radiocarbon isotope analysis, showing assimilation of atmospheric modern CO2 as an inorganic carbon source, improves our understanding of the role of seagrass meadows in coastal carbon dynamics.

scholarly journals Amplified Inception of European Little Ice Age by Sea Ice–Ocean–Atmosphere Feedbacks

2013 ◽  
Vol 26 (19) ◽  
pp. 7586-7602 ◽  
Author(s):  
Flavio Lehner ◽  
Andreas Born ◽  
Christoph C. Raible ◽  
Thomas F. Stocker
Keyword(s):  
Sea Ice ◽  
North Atlantic ◽  
Little Ice Age ◽  
Barents Sea ◽  
Feedback Mechanism ◽  
Ice Age ◽  
The Arctic ◽  
Nordic Seas ◽  
Ice Growth ◽  
Ocean Atmosphere

Abstract The inception of the Little Ice Age (~1400–1700 AD) is believed to have been driven by an interplay of external forcing and climate system internal variability. While the hemispheric signal seems to have been dominated by solar irradiance and volcanic eruptions, the understanding of mechanisms shaping the climate on a continental scale is less robust. In an ensemble of transient model simulations and a new type of sensitivity experiments with artificial sea ice growth, the authors identify a sea ice–ocean–atmosphere feedback mechanism that amplifies the Little Ice Age cooling in the North Atlantic–European region and produces the temperature pattern suggested by paleoclimatic reconstructions. Initiated by increasing negative forcing, the Arctic sea ice substantially expands at the beginning of the Little Ice Age. The excess of sea ice is exported to the subpolar North Atlantic, where it melts, thereby weakening convection of the ocean. Consequently, northward ocean heat transport is reduced, reinforcing the expansion of the sea ice and the cooling of the Northern Hemisphere. In the Nordic Seas, sea surface height anomalies cause the oceanic recirculation to strengthen at the expense of the warm Barents Sea inflow, thereby further reinforcing sea ice growth. The absent ocean–atmosphere heat flux in the Barents Sea results in an amplified cooling over Northern Europe. The positive nature of this feedback mechanism enables sea ice to remain in an expanded state for decades up to a century, favoring sustained cold periods over Europe such as the Little Ice Age. Support for the feedback mechanism comes from recent proxy reconstructions around the Nordic Seas.

Sign in / Sign up

Export Citation Format

Share Document