scholarly journals Planktic Foraminiferal and Pteropod Contributions to Carbon Dynamics in the Arctic Ocean (North Svalbard Margin)

2021 ◽  
Vol 8 ◽  
Author(s):  
Griselda Anglada-Ortiz ◽  
Katarzyna Zamelczyk ◽  
Julie Meilland ◽  
Patrizia Ziveri ◽  
Melissa Chierici ◽  
...  

Planktic foraminifera and shelled pteropods are some of the major producers of calcium carbonate (CaCO3) in the ocean. Their calcitic (foraminifera) and aragonitic (pteropods) shells are particularly sensitive to changes in the carbonate chemistry and play an important role for the inorganic and organic carbon pump of the ocean. Here, we have studied the abundance distribution of planktic foraminifera and pteropods (individuals m–3) and their contribution to the inorganic and organic carbon standing stocks (μg m–3) and export production (mg m–2 day–1) along a longitudinal transect north of Svalbard at 81° N, 22–32° E, in the Arctic Ocean. This transect, sampled in September 2018 consists of seven stations covering different oceanographic regimes, from the shelf to the slope and into the deep Nansen Basin. The sea surface temperature ranged between 1 and 5°C in the upper 300 m. Conditions were supersaturated with respect to CaCO3 (Ω > 1 for both calcite and aragonite). The abundance of planktic foraminifera ranged from 2.3 to 52.6 ind m–3 and pteropods from 0.1 to 21.3 ind m–3. The planktic foraminiferal population was composed mainly of the polar species Neogloboquadrina pachyderma (55.9%) and the subpolar species Turborotalita quinqueloba (21.7%), Neogloboquadrina incompta (13.5%) and Globigerina bulloides (5.2%). The pteropod population was dominated by the polar species Limacina helicina (99.6%). The rather high abundance of subpolar foraminiferal species is likely connected to the West Spitsbergen Current bringing warm Atlantic water to the study area. Pteropods dominated at the surface and subsurface. Below 100 m water depth, foraminifera predominated. Pteropods contribute 66–96% to the inorganic carbon standing stocks compared to 4–34% by the planktic foraminifera. The inorganic export production of planktic foraminifera and pteropods together exceeds their organic contribution by a factor of 3. The overall predominance of pteropods over foraminifera in this high Arctic region during the sampling period suggest that inorganic standing stocks and export production of biogenic carbonate would be reduced under the effects of ocean acidification.

2017 ◽  
Vol 17 (13) ◽  
pp. 8101-8128 ◽  
Author(s):  
Eyal Freud ◽  
Radovan Krejci ◽  
Peter Tunved ◽  
Richard Leaitch ◽  
Quynh T. Nguyen ◽  
...  

Abstract. The Arctic environment has an amplified response to global climatic change. It is sensitive to human activities that mostly take place elsewhere. For this study, a multi-year set of observed aerosol number size distributions in the diameter range of 10 to 500 nm from five sites around the Arctic Ocean (Alert, Villum Research Station – Station Nord, Zeppelin, Tiksi and Barrow) was assembled and analysed.A cluster analysis of the aerosol number size distributions revealed four distinct distributions. Together with Lagrangian air parcel back-trajectories, they were used to link the observed aerosol number size distributions with a variety of transport regimes. This analysis yields insight into aerosol dynamics, transport and removal processes, on both an intra- and an inter-monthly scale. For instance, the relative occurrence of aerosol number size distributions that indicate new particle formation (NPF) event is near zero during the dark months, increases gradually to  ∼ 40 % from spring to summer, and then collapses in autumn. Also, the likelihood of Arctic haze aerosols is minimal in summer and peaks in April at all sites.The residence time of accumulation-mode particles in the Arctic troposphere is typically long enough to allow tracking them back to their source regions. Air flow that passes at low altitude over central Siberia and western Russia is associated with relatively high concentrations of accumulation-mode particles (Nacc) at all five sites – often above 150 cm−3. There are also indications of air descending into the Arctic boundary layer after transport from lower latitudes.The analysis of the back-trajectories together with the meteorological fields along them indicates that the main driver of the Arctic annual cycle of Nacc, on the larger scale, is when atmospheric transport covers the source regions for these particles in the 10-day period preceding the observations in the Arctic. The scavenging of these particles by precipitation is shown to be important on a regional scale and it is most active in summer. Cloud processing is an additional factor that enhances the Nacc annual cycle.There are some consistent differences between the sites that are beyond the year-to-year variability. They are the result of differences in the proximity to the aerosol source regions and to the Arctic Ocean sea-ice edge, as well as in the exposure to free-tropospheric air and in precipitation patterns – to mention a few. Hence, for most purposes, aerosol observations from a single Arctic site cannot represent the entire Arctic region. Therefore, the results presented here are a powerful observational benchmark for evaluation of detailed climate and air chemistry modelling studies of aerosols throughout the vast Arctic region.


2019 ◽  
Vol 59 (4) ◽  
pp. 544-552
Author(s):  
A. A. Vetrov ◽  
E. A. Romankevich

Particulate organic carbon (POC) is one of main component of carbon cycle in the Ocean. In this study an attempt to construct a picture of the distribution and fluxes of POC in the Arctic Ocean adjusting for interchange with the Pacific and Atlantic Oceans has been made. The specificity of this construction is associated with an irregular distribution of POC measurements and complicated structure and hydrodynamics of the waters masses. To overcome these difficulties, Multiple Linear Regression technic (MLR) was performed to test the significant relation between POC, temperature, salinity, as well depth, horizon, latitude and offshore distance. The mapping of POC distribution and its fluxes was carrying out at 38 horizons from 5 to 4150 m (resolution 1°×1°). Data on temperature, salinity, meridional and zonal components of current velocities were obtained from ORA S4 database (Integrated Climate Data Center, http://icdc.cen.uni-hamburg.de/las). The import-export of POC between the Arctic, Atlantic and Pacific Oceans as well as between Arctic Seas was precomputed by summer fluxes. The import of POC in the Arctic Ocean is estimated to be 38±8Tg Cyr-1, and the export is -9.5±4.4Tg Cyr-1.


2019 ◽  
Vol 1 ◽  
pp. 1-1
Author(s):  
Haiyan Liu ◽  
Xiaoping Pang

<p><strong>Abstract.</strong> In recent years, Arctic glaciers have gradually melted due to the global warming, which makes the exploitation of Arctic and its seabed resources possible. Though numerous disagreements and potentials over Arctic maritime jurisdiction still exist, the surround-Arctic nations have agreed the United Nations' Convention on the Law of the Sea to divide the Arctic Ocean into zones that can be regulated and exploited. The IBRU of Durham University has mapped the known claims, agreed boundaries and potential claims of the surround-Arctic nations in the Arctic to clear the maritime jurisdiction in the region. However, different countries may have different requirements within their jurisdictional areas. Clarifying these requirements is essential for Arctic Navigation of investigation ships and merchant ships for their route planning.</p><p>In this paper, based on the map of maritime jurisdiction and boundaries in Arctic region (IBRU), we analysed the international conventions and relevant laws of the surround-Arctic nations to find out the rights and obligations of ships in different zones. The limitations on activities and recommendations on navigation planning are marked for different zones according to different purposes, i.e. science or commerce. The map could not only provide navigational guidance for the activities in the Arctic Ocean, but offer references for the countries not surrounding the Arctic in the formulation of the Arctic strategies.</p>


2011 ◽  
Vol 8 (2) ◽  
pp. 2093-2143 ◽  
Author(s):  
I. P. Semiletov ◽  
I. I. Pipko ◽  
N. E. Shakhova ◽  
O. V. Dudarev ◽  
S. P. Pugach ◽  
...  

Abstract. The Lena River integrates biogeochemical signals from its vast drainage basin and its signal reaches far out over the Arctic Ocean. Transformation of riverine organic carbon into mineral carbon, and mineral carbon into the organic form in the Lena River watershed, can be considered a quasi-equilibrated processes. Increasing the Lena discharge causes opposite effects on total organic (TOC) and inorganic (TCO2) carbon: TOC concentration increases, while TCO2 concentration decreases. Significant inter-annual variability in mean values of TCO2, TOC, and their sum (TC) has been found. This variability is determined by changes in land hydrology which cause differences in the Lena River discharge, because a negative correlation may be found between TC in September and mean discharge in August (a time shift of about one month is required for water to travel from Yakutsk to the Laptev Sea). Total carbon entering the sea with the Lena discharge is estimated to be almost 10 Tg C y−1. The annual Lena River discharge of particulate organic carbon (POC) may be equal to 0.38 Tg (moderate to high estimate). If we instead accept Lisytsin's (1994) statement concerning the precipitation of 85–95% of total particulate matter (PM) (and POC) on the marginal "filter", then only about 0.03–0.04 Tg of POC reaches the Laptev Sea from the Lena River. The Lena's POC export would then be two orders of magnitude less than the annual input of eroded terrestrial carbon onto the shelf of the Laptev and East Siberian seas, which is about 4 Tg. The Lena River is characterized by relatively high concentrations of primary greenhouse gases: CO2 and dissolved CH4. During all seasons the river is supersaturated in CO2 compared to the atmosphere: up to 1.5–2 fold in summer, and 4–5 fold in winter. This results in a narrow zone of significant CO2 supersaturation in the adjacent coastal sea. Spots of dissolved CH4 in the Lena delta channels may reach 100 nM, but the CH4 concentration decreases to 5–20 nM towards the sea, which suggests only a minor role of riverborne export of CH4 for the East Siberian Arctic Shelf (ESAS) CH4 budget in coastal waters. Instead, the seabed appears to be the source that provides most of the CH4 to the Arctic Ocean.


2015 ◽  
Vol 12 (11) ◽  
pp. 3551-3565 ◽  
Author(s):  
D. Doxaran ◽  
E. Devred ◽  
M. Babin

Abstract. Global warming has a significant impact on the regional scale on the Arctic Ocean and surrounding coastal zones (i.e., Alaska, Canada, Greenland, Norway and Russia). The recent increase in air temperature has resulted in increased precipitation along the drainage basins of Arctic rivers. It has also directly impacted land and seawater temperatures with the consequence of melting permafrost and sea ice. An increase in freshwater discharge by main Arctic rivers has been clearly identified in time series of field observations. The freshwater discharge of the Mackenzie River has increased by 25% since 2003. This may have increased the mobilization and transport of various dissolved and particulate substances, including organic carbon, as well as their export to the ocean. The release from land to the ocean of such organic material, which has been sequestered in a frozen state since the Last Glacial Maximum, may significantly impact the Arctic Ocean carbon cycle as well as marine ecosystems. In this study we use 11 years of ocean color satellite data and field observations collected in 2009 to estimate the mass of terrestrial suspended solids and particulate organic carbon delivered by the Mackenzie River into the Beaufort Sea (Arctic Ocean). Our results show that during the summer period, the concentration of suspended solids at the river mouth, in the delta zone and in the river plume has increased by 46, 71 and 33%, respectively, since 2003. Combined with the variations observed in the freshwater discharge, this corresponds to a more than 50% increase in the particulate (terrestrial suspended particles and organic carbon) export from the Mackenzie River into the Beaufort Sea.


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