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

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.

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Inorganic carbon fluxes on the Mackenzie Shelf of the Beaufort Sea

10.5194/bg-2017-318 ◽

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.

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

The Cryosphere ◽

10.5194/tc-10-2173-2016 ◽

2016 ◽

Vol 10 (5) ◽

pp. 2173-2189 ◽

Cited By ~ 10

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.

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Measurements of the dissolved inorganic carbon system and associated biogeochemical parameters in the Canadian Arctic, 1974–2009

Earth System Science Data ◽

10.5194/essd-6-91-2014 ◽

2014 ◽

Vol 6 (1) ◽

pp. 91-104 ◽

Cited By ~ 5

Author(s):

K. E. Giesbrecht ◽

L. A. Miller ◽

M. Davelaar ◽

S. Zimmermann ◽

E. Carmack ◽

...

Keyword(s):

Quality Control ◽

Inorganic Carbon ◽

Dissolved Inorganic Carbon ◽

Canadian Arctic ◽

The Arctic ◽

Data Set ◽

The North ◽

Western Side ◽

Biogeochemical Parameters ◽

Carbon System

Abstract. We have assembled and conducted primary quality control on previously publicly unavailable water column measurements of the dissolved inorganic carbon system and associated biogeochemical parameters (oxygen, nutrients, etc.) made on 26 cruises in the subarctic and Arctic regions dating back to 1974. The measurements are primarily from the western side of the Canadian Arctic, but also include data that cover an area ranging from the North Pacific to the Gulf of St. Lawrence. The data were subjected to primary quality control (QC) to identify outliers and obvious errors. This data set incorporates over four thousand individual measurements of total inorganic carbon (TIC), alkalinity, and pH from the Canadian Arctic over a period of more than 30 years and provides an opportunity to increase our understanding of temporal changes in the inorganic carbon system in northern waters and the Arctic Ocean. The data set is available for download on the CDIAC (Carbon Dioxide Information Analysis Center) website: http://cdiac.ornl.gov/ftp/oceans/IOS_Arctic_Database/ (doi:10.3334/CDIAC/OTG.IOS_ARCT_CARBN).

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

Elem Sci Anth ◽

10.12952/journal.elementa.000112 ◽

2016 ◽

Vol 4 ◽

Cited By ~ 5

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.

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

10.5194/tc-2016-14 ◽

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.

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Implications of sea-ice biogeochemistry for oceanic production and emissions of dimethyl sulfide in the Arctic

Biogeosciences ◽

10.5194/bg-14-3129-2017 ◽

2017 ◽

Vol 14 (12) ◽

pp. 3129-3155 ◽

Cited By ~ 17

Author(s):

Hakase Hayashida ◽

Nadja Steiner ◽

Adam Monahan ◽

Virginie Galindo ◽

Martine Lizotte ◽

...

Keyword(s):

Sea Ice ◽

Water Column ◽

Dimethyl Sulfide ◽

Phytoplankton Bloom ◽

Model Simulation ◽

Field Measurements ◽

Sulfur Cycle ◽

The Arctic ◽

Model Parameters ◽

Ocean Ecosystem

Abstract. Sea ice represents an additional oceanic source of the climatically active gas dimethyl sulfide (DMS) for the Arctic atmosphere. To what extent this source contributes to the dynamics of summertime Arctic clouds is, however, not known due to scarcity of field measurements. In this study, we developed a coupled sea ice–ocean ecosystem–sulfur cycle model to investigate the potential impact of bottom-ice DMS and its precursor dimethylsulfoniopropionate (DMSP) on the oceanic production and emissions of DMS in the Arctic. The results of the 1-D model simulation were compared with field data collected during May and June of 2010 in Resolute Passage. Our results reproduced the accumulation of DMS and DMSP in the bottom ice during the development of an ice algal bloom. The release of these sulfur species took place predominantly during the earlier phase of the melt period, resulting in an increase of DMS and DMSP in the underlying water column prior to the onset of an under-ice phytoplankton bloom. Production and removal rates of processes considered in the model are analyzed to identify the processes dominating the budgets of DMS and DMSP both in the bottom ice and the underlying water column. When openings in the ice were taken into account, the simulated sea–air DMS flux during the melt period was dominated by episodic spikes of up to 8.1 µmol m−2 d−1. Further model simulations were conducted to assess the effects of the incorporation of sea-ice biogeochemistry on DMS production and emissions, as well as the sensitivity of our results to changes of uncertain model parameters of the sea-ice sulfur cycle. The results highlight the importance of taking into account both the sea-ice sulfur cycle and ecosystem in the flux estimates of oceanic DMS near the ice margins and identify key uncertainties in processes and rates that should be better constrained by new observations.

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Export of calcium carbonate corrosive waters from the East Siberian Sea

10.5194/bg-2016-478 ◽

2016 ◽

Author(s):

Leif G. Anderson ◽

Jörgen Ek ◽

Ylva Ericson ◽

Christoph Humborg ◽

Igor Semiletov ◽

...

Keyword(s):

Calcium Carbonate ◽

Sea Ice ◽

North Atlantic Ocean ◽

The Arctic ◽

High Pco2 ◽

Low Oxygen ◽

Saturation State ◽

Ice Melt ◽

The North ◽

Transformation Of Organic Matter

Abstract. The Siberian Shelf Seas are areas of extensive biogeochemical transformation of organic matter, both of marine and terrestrial origin. This in combination with brine production from sea ice formation results in a cold bottom water of relative high salinity and partial pressure of carbon dioxide (pCO2). Data from the SWERUS-C3 expedition compiled on the icebreaker Oden in July to September 2014 show the distribution of such waters at the outer shelf, as well as their export into the deep central Arctic basins. Very high pCO2 water, up to close to 1000 µatm, was observed associated with high nutrients and low oxygen concentrations. Consequently the saturation state of calcium carbonate was low, down to less than 0.8 for calcite and 0.5 for aragonite. Waters undersaturated in aragonite were also observed in the surface in waters at equilibrium with atmospheric CO2, however, at these conditions the cause of under-saturation was low salinity from river runoff and/or sea ice melt. The calcium carbonate corrosive water was observed all along the continental margin and well out into the deep Makarov and Canada Basins at a depth from about 50 m depth in the west to about 150 m in the east. These waters of low aragonite saturation state are traced in historic data to the Canada Basin and in the waters flowing out of the Arctic Ocean north of Greenland and in the western Fram Strait, thus potentially impacting the marine life in the North Atlantic Ocean.

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

Earth System Dynamics Discussions ◽

10.5194/esdd-6-2137-2015 ◽

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.

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Ozone and carbon monoxide observations over open oceans on R/V <i>Mirai</i> from 67° S to 75° N during 2012 to 2017: Testing global chemical reanalysis in terms of Arctic processes, low ozone levels at low latitudes, and pollution transport

10.5194/acp-2018-1354 ◽

2019 ◽

Cited By ~ 1

Author(s):

Yugo Kanaya ◽

Kazuyuki Miyazaki ◽

Fumikazu Taketani ◽

Takuma Miyakawa ◽

Hisahiro Takashima ◽

...

Keyword(s):

Carbon Monoxide ◽

Atmospheric Chemistry ◽

Critical Evaluation ◽

Chemical Transport ◽

Tropospheric Chemistry ◽

Set Covering ◽

The Arctic ◽

Pollution Transport ◽

Data Set ◽

Air Masses

Abstract. Constraints from ozone (O3) observations over oceans are needed in addition to those from terrestrial regions to fully understand global tropospheric chemistry and its impact on the climate. Here, we provide a large data set of ozone and carbon monoxide (CO) levels observed (for 11 666 and 10 681 h, respectively) over oceans. The data set is derived from observations made during 24 research cruise legs of R/V Mirai during 2012 to 2017, in the Southern, Indian, Pacific, and Arctic Oceans, covering the region from 67° S to 75° N. The data are suitable for critical evaluation of the over-ocean distribution of ozone derived from chemical transport models. We first give an overview of the statistics in the data set and highlight key features in terms of geographical distribution and air mass type. We then use the data set to evaluate ozone concentration fields from Tropospheric Chemistry Reanalysis version 2 (TCR-2), produced by assimilating a suite of satellite observations of multiple species into a chemical transport model, namely CHASER. For long-range transport of polluted air masses from continents to the oceans, during which the effects of forest fires and fossil fuel combustion were recognized, TCR-2 gave an excellent performance in reproducing the observed temporal variations and photochemical buildup of O3 when assessed from ΔO3 / ΔCO ratios. For clean marine conditions with low and stable CO concentrations, two focused analyses were performed. The first was in the Arctic (> 70° N) in September every year from 2013 to 2016; TCR-2 underpredicted O3 levels by 6.7 ppb (21 %) on average. The observed vertical profiles from O3 soundings from R/V Mirai during September 2014 had less steep vertical gradients at low altitudes (> 850 hPa) than those obtained TCR-2. This suggests the possibilities of more efficient descent of the O3-rich air from above or less efficient dry deposition on the surface than were assumed in the model. In the second analysis, over the western Pacific equatorial region (125–165° E, 10° S to 25° N), the observed O3 level frequently decreased to less than 10 ppb in comparison to that obtained with TCR-2, and also those obtained in most of the Atmospheric Chemistry Climate Model Intercomparison Project (ACCMIP) model runs for the decade from 2000. These results imply loss processes that are unaccounted for in the models. We found that the model’s positive bias positively correlated with the daytime residence times of air masses over a particular grid, namely 165–180° E and 15–30° N; an additional loss rate of 0.25 ppb h−1 in the grid best explained the gap. Halogen chemistry, which is commonly omitted from currently used models, might be active in this region and could have contributed to additional losses. Our open data set covering wide ocean regions is complementary to the Tropospheric Ozone Assessment Report data set, which basically comprises ground-based observations, and enables a fully global study of the behavior of O3.

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Satellite-based sea ice thickness changes in the Laptev Sea from 2002 to 2017: comparison to mooring observations

The Cryosphere ◽

10.5194/tc-14-2189-2020 ◽

2020 ◽

Vol 14 (7) ◽

pp. 2189-2203

Author(s):

H. Jakob Belter ◽

Thomas Krumpen ◽

Stefan Hendricks ◽

Jens Hoelemann ◽

Markus A. Janout ◽

...

Keyword(s):

Sea Ice ◽

Source Region ◽

European Space Agency ◽

The Arctic ◽

Ice Thickness ◽

Laptev Sea ◽

Validation Data ◽

Data Set ◽

Sea Ice Thickness ◽

The Laptev Sea

Abstract. The gridded sea ice thickness (SIT) climate data record (CDR) produced by the European Space Agency (ESA) Sea Ice Climate Change Initiative Phase 2 (CCI-2) is the longest available, Arctic-wide SIT record covering the period from 2002 to 2017. SIT data are based on radar altimetry measurements of sea ice freeboard from the Environmental Satellite (ENVISAT) and CryoSat-2 (CS2). The CCI-2 SIT has previously been validated with in situ observations from drilling, airborne remote sensing, electromagnetic (EM) measurements and upward-looking sonars (ULSs) from multiple ice-covered regions of the Arctic. Here we present the Laptev Sea CCI-2 SIT record from 2002 to 2017 and use newly acquired ULS and upward-looking acoustic Doppler current profiler (ADCP) sea ice draft (VAL) data for validation of the gridded CCI-2 and additional satellite SIT products. The ULS and ADCP time series provide the first long-term satellite SIT validation data set from this important source region of sea ice in the Transpolar Drift. The comparison of VAL sea ice draft data with gridded monthly mean and orbit trajectory CCI-2 data, as well as merged CryoSat-2–SMOS (CS2SMOS) sea ice draft, shows that the agreement between the satellite and VAL draft data strongly depends on the thickness of the sampled ice. Rather than providing mean sea ice draft, the considered satellite products provide modal sea ice draft in the Laptev Sea. Ice drafts thinner than 0.7 m are overestimated, while drafts thicker than approximately 1.3 m are increasingly underestimated by all satellite products investigated for this study. The tendency of the satellite SIT products to better agree with modal sea ice draft and underestimate thicker ice needs to be considered for all past and future investigations into SIT changes in this important region. The performance of the CCI-2 SIT CDR is considered stable over time; however, observed trends in gridded CCI-2 SIT are strongly influenced by the uncertainties of ENVISAT and CS2 and the comparably short investigation period.

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