scholarly journals Interannual variability of air-sea CO<sub>2</sub> fluxes and carbonate system parameters in the East Siberian Sea

2011 ◽  
Vol 8 (1) ◽  
pp. 1227-1273 ◽  
Author(s):  
I. I. Pipko ◽  
I. P. Semiletov ◽  
S. P. Pugach ◽  
I. Wåhlström ◽  
L. G. Anderson
Keyword(s):  
Organic Matter ◽  
Primary Production ◽  
Coastal Erosion ◽  
Atmospheric Co2 ◽  
The Arctic ◽  
Co2 Fluxes ◽  
Carbonate System ◽  
System Parameters ◽  
East Siberian Sea ◽  
Air Exchange

Abstract. Over the past couple of decades it has become apparent that air-land-sea interactions in the Arctic have a substantial impact on the composition of the overlying atmosphere (ACIA, 2004). The Arctic Ocean is small (only ~4% of the total World Ocean), but it is surrounded by offshore and onshore permafrost which thaws at increasing rates under warming conditions releasing carbon dioxide (CO2) into the water and atmosphere. This work summarizes data collected from three expeditions in the coastal-shelf zone of the East Siberian Sea (ESS) in September 2003, 2004 and late August–September 2008. It is proposed that the western part of the ESS represents a river- and coastal erosion-dominated ocean margin that is a source for atmospheric CO2. It receives substantial river discharge that also adds organic matter, both dissolved and particulate. This in combination with significant input of organic matter from coastal erosion makes this region being of dominantly heterotrophic character. The eastern part of the ESS is a Pacific water-dominated autotrophic area. It's a high-productive zone, which acts as a sink for atmospheric CO2. The year to year dynamics of partial pressure of CO2 in the surface water as well as the sea-air flux of CO2 varied substantially. In some years the ESS shelf can be mainly heterotrophic and serve as strong source of CO2 (year 2004). Another year significant part of the ESS, where gross primary production exceeds community respiration, acts as a sink for the atmospheric CO2 and the net CO2 flux into the atmosphere is weak (year 2008). High variability of carbon system parameters observed in the ESS shelf is determined by many factors such as riverine runoff, advection of waters from adjacent seas, coastal erosion, primary production/respiration etc. The dynamics of the CO2 sea-air exchange is determined by ocean processes but also by atmospheric circulation which hence has a significant impact on the CO2 sea-air exchange. In this contribution the sea-air CO2 fluxes were evaluated in the ESS based on measured carbonate system (CS) parameters data and annual sea-to-air CO2 fluxes were estimated. It was shown that the total ESS shelf is a net source of CO2 for the atmosphere at a range from 0.5×1012 to 3.3×1012 g C.

scholarly journals Interannual variability of air-sea CO<sub>2</sub> fluxes and carbon system in the East Siberian Sea

2011 ◽  
Vol 8 (7) ◽  
pp. 1987-2007 ◽  
Author(s):  
I. I. Pipko ◽  
I. P. Semiletov ◽  
S. P. Pugach ◽  
I. Wåhlström ◽  
L. G. Anderson
Keyword(s):  
Primary Production ◽  
Arctic Ocean ◽  
Coastal Erosion ◽  
Co2 Flux ◽  
Atmospheric Co2 ◽  
The Arctic ◽  
Flux Dynamics ◽  
East Siberian Sea ◽  
The Arctic Ocean ◽  
Carbon System

Abstract. Over the past couple of decades it has become apparent that air-land-sea interactions in the Arctic have a substantial impact on the composition of the overlying atmosphere (ACIA, 2004). The Arctic Ocean is small (only ~4 % of the total World Ocean), but it is surrounded by offshore and onshore permafrost which is thawing at increasing rates under warming conditions, releasing carbon dioxide (CO2) into the water and atmosphere. The Arctic Ocean shelf where the most intensive biogeochemical processes have occurred occupies 1/3 of the ocean. The East Siberian Sea (ESS) shelf is the shallowest and widest shelf among the Arctic seas, and the least studied. The objective of this study was to highlight the importance of different factors that impact the carbon system (CS) as well as the CO2 flux dynamics in the ESS. CS variables were measured in the ESS in September 2003 and, 2004 and in late August–September 2008. It was shown that the western part of the ESS represents a river- and coastal-erosion-dominated heterotrophic ocean margin that is a source for atmospheric CO2. The eastern part of the ESS is a Pacific-water-dominated autotrophic area, which acts as a sink for atmospheric CO2. Our results indicate that the year-to-year dynamics of the partial pressure of CO2 in the surface water as well as the air-sea flux of CO2 varies substantially. In one year the ESS shelf was mainly heterotrophic and served as a moderate summertime source of CO2 (year 2004). In another year gross primary production exceeded community respiration in a relatively large part of the ESS and the ESS shelf was only a weak source of CO2 into the atmosphere (year 2008). It was shown that many factors impact the CS and CO2 flux dynamics (such as river runoff, coastal erosion, primary production/respiration, etc.), but they were mainly determined by the interplay and distribution of water masses that are basically influenced by the atmospheric circulation. In this contribution the air-sea CO2 fluxes were evaluated in the ESS based on measured CS characteristics, and summertime fluxes were estimated. It was shown that the total ESS shelf is a net source of CO2 for the atmosphere in a range of 0.4 × 1012 to 2.3 × 1012 g C.

Multi-proxy evaluation of terrestrial organic matter degradation across the East Siberian Arctic Seas

2021 ◽  
Author(s):  
Felipe Matsubara ◽  
Birgit Wild ◽  
Jannik Martens ◽  
Rickard Wennström ◽  
Oleg Dudarev ◽  
...  
Keyword(s):  
Organic Matter ◽  
Coastal Erosion ◽  
River Discharge ◽  
The Arctic ◽  
Laptev Sea ◽  
Terrestrial Organic Matter ◽  
Arctic Seas ◽  
Transport Pathway ◽  
East Siberian Sea ◽  
Siberian Arctic

&lt;p&gt;&amp;#160; &amp;#160; Ongoing global warming is expected to accelerate the thaw of permafrost on land and to increase the input of terrigenous organic matter (terrOM) into the Arctic Ocean through coastal erosion and river discharge. Large remobilization of terrOM into the East Siberian Arctic Shelf (ESAS) dominates the organic matter in surface sediments over large parts of the shelf and its degradation contributes to ocean acidification. Previous studies have focused on the source apportionment of terrOM and the releases of CO&lt;sub&gt;2&lt;/sub&gt; and CH&lt;sub&gt;4&lt;/sub&gt; to the atmosphere from terrOM degradation; this study focuses on its diagenetic state during cross-shelf transport, since degradation is the link between permafrost thawing and greenhouse gases emissions. This study probes the degradation status of different terrOM components across the ESAS using various molecular and isotopic proxies and hence evaluates their differences to infer degradation.&lt;/p&gt;&lt;p&gt;&amp;#160; &amp;#160; High-molecular weight (HMW) lipid compounds and lignin phenols are exclusively produced by terrestrial plants, providing protection, strength and rigidity to the plant structure. Owing to diagenesis, microbial degradation leads to &lt;strong&gt;1)&lt;/strong&gt; &lt;strong&gt;loss of functional groups&lt;/strong&gt;, thus the ratios of HMW n-alkanoic acids, HMW n-alkanols and sterols relative to HMW n-alkanes decrease; &lt;strong&gt;2)&lt;/strong&gt; &lt;strong&gt;reduction of unsaturated to saturated carbons&lt;/strong&gt;, so ratios of stanols relative to stenols increase; &lt;strong&gt;3) a higher formation of carboxylic acids in the lignin polymer&lt;/strong&gt; and hence&lt;strong&gt; &lt;/strong&gt;ratios of acids to aldehydes of vanillyl (Vd and Vl) and syringyl (Sd and Sl) increase.&lt;/p&gt;&lt;p&gt;&amp;#160; &amp;#160; The concentrations of lipid- and lignin-derived products per sediment specific surface area decreased with offshore distance of the samples. During cross-shelf transport, the biomarker degradation proxies showed an increasing degradation for Sd/Sl, Vd/Vl, the &amp;#8220;tannin-like&amp;#8221; compound 3,5-dihydrobenzoic acid to vanillyl (3,5-Bd/V), &amp;#946;-sitostanol/ &amp;#946;-sitostenol and Carbon Preference Index (CPI) of HMW n-alkanes. Some other proxies showed no clear trend from inner to outer shelf and such inconsistent patterns are currently being investigated to better understand both the usefulness/response of different proxies and of the lability of terrOM in the ESAS. While &amp;#946;-sitostanol/&amp;#946;-sitostenol and CPI HMW n-alkane did not show strong differences between the East Siberian Sea and the Laptev Sea, Vd/Vl and Sd/Sl ratios indicated stronger degradation on the outer Laptev Sea and 3,5-Bd/V ratios indicated stronger degradation in the outer eastern East Siberian Sea. Such differences could reflect source properties of terrOM entering the ESAS, such as differences in source vegetation or transport pathway, i.e. coastal erosion or river discharge.&lt;/p&gt;

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 Complex Microbial Communities Drive Iron and Sulfur Cycling in Arctic Fjord Sediments

2019 ◽  
Vol 85 (14) ◽  
Author(s):  
J. Buongiorno ◽  
L. C. Herbert ◽  
L. M. Wehrmann ◽  
A. B. Michaud ◽  
K. Laufer ◽  
...  
Keyword(s):  
Organic Matter ◽  
Primary Production ◽  
Sulfate Reduction ◽  
The Arctic ◽  
Sulfur Cycling ◽  
Glacial Retreat ◽  
Sulfate Reducing ◽  
Glacial Runoff ◽  
Sulfate Reduction Rates ◽  
Fjord Sediments

ABSTRACTGlacial retreat is changing biogeochemical cycling in the Arctic, where glacial runoff contributes iron for oceanic shelf primary production. We hypothesize that in Svalbard fjords, microbes catalyze intense iron and sulfur cycling in low-organic-matter sediments. This is because low organic matter limits sulfide generation, allowing iron mobility to the water column instead of precipitation as iron monosulfides. In this study, we tested this with high-depth-resolution 16S rRNA gene libraries in the upper 20 cm at two sites in Van Keulenfjorden, Svalbard. At the site closer to the glaciers, iron-reducingDesulfuromonadales, iron-oxidizingGallionellaandMariprofundus, and sulfur-oxidizingThiotrichalesandEpsilonproteobacteriawere abundant above a 12-cm depth. Below this depth, the relative abundances of sequences for sulfate-reducingDesulfobacteraceaeandDesulfobulbaceaeincreased. At the outer station, the switch from iron-cycling clades to sulfate reducers occurred at shallower depths (∼5 cm), corresponding to higher sulfate reduction rates. Relatively labile organic matter (shown by δ13C and C/N ratios) was more abundant at this outer site, and ordination analysis suggested that this affected microbial community structure in surface sediments. Network analysis revealed more correlations between predicted iron- and sulfur-cycling taxa and with uncultured clades proximal to the glacier. Together, these results suggest that complex microbial communities catalyze redox cycling of iron and sulfur, especially closer to the glacier, where sulfate reduction is limited due to low availability of organic matter. Diminished sulfate reduction in upper sediments enables iron to flux into the overlying water, where it may be transported to the shelf.IMPORTANCEGlacial runoff is a key source of iron for primary production in the Arctic. In the fjords of the Svalbard archipelago, glacial retreat is predicted to stimulate phytoplankton blooms that were previously restricted to outer margins. Decreased sediment delivery and enhanced primary production have been hypothesized to alter sediment biogeochemistry, wherein any free reduced iron that could potentially be delivered to the shelf will instead become buried with sulfide generated through microbial sulfate reduction. We support this hypothesis with sequencing data that showed increases in the relative abundance of sulfate reducing taxa and sulfate reduction rates with increasing distance from the glaciers in Van Keulenfjorden, Svalbard. Community structure was driven by organic geochemistry, suggesting that enhanced input of organic material will stimulate sulfate reduction in interior fjord sediments as glaciers continue to recede.

scholarly journals Macromolecular composition of terrestrial and marine organic matter in sediments across the East Siberian Arctic Shelf

2016 ◽  
Vol 10 (5) ◽  
pp. 2485-2500 ◽  
Author(s):  
Robert B. Sparkes ◽  
Ayça Doğrul Selver ◽  
Örjan Gustafsson ◽  
Igor P. Semiletov ◽  
Negar Haghipour ◽  
...  
Keyword(s):  
Organic Matter ◽  
Coastal Erosion ◽  
Principal Component ◽  
Arctic Shelf ◽  
The Arctic ◽  
Gas Chromatography Mass Spectrometry ◽  
Terrestrial Organic Matter ◽  
Pyrolysis Gas ◽  
Siberian Arctic ◽  
Extractable Organic Matter

Abstract. Mobilisation of terrestrial organic carbon (terrOC) from permafrost environments in eastern Siberia has the potential to deliver significant amounts of carbon to the Arctic Ocean, via both fluvial and coastal erosion. Eroded terrOC can be degraded during offshore transport or deposited across the wide East Siberian Arctic Shelf (ESAS). Most studies of terrOC on the ESAS have concentrated on solvent-extractable organic matter, but this represents only a small proportion of the total terrOC load. In this study we have used pyrolysis–gas chromatography–mass spectrometry (py-GCMS) to study all major groups of macromolecular components of the terrOC; this is the first time that this technique has been applied to the ESAS. This has shown that there is a strong offshore trend from terrestrial phenols, aromatics and cyclopentenones to marine pyridines. There is good agreement between proportion phenols measured using py-GCMS and independent quantification of lignin phenol concentrations (r2 = 0.67, p < 0.01, n = 24). Furfurals, thought to represent carbohydrates, show no offshore trend and are likely found in both marine and terrestrial organic matter. We have also collected new radiocarbon data for bulk OC (14COC) which, when coupled with previous measurements, allows us to produce the most comprehensive 14COC map of the ESAS to date. Combining the 14COC and py-GCMS data suggests that the aromatics group of compounds is likely sourced from old, aged terrOC, in contrast to the phenols group, which is likely sourced from modern woody material. We propose that an index of the relative proportions of phenols and pyridines can be used as a novel terrestrial vs. marine proxy measurement for macromolecular organic matter. Principal component analysis found that various terrestrial vs. marine proxies show different patterns across the ESAS, and it shows that multiple river–ocean transects of surface sediments transition from river-dominated to coastal-erosion-dominated to marine-dominated signatures.

scholarly journals Geochemistry of Coastal Permafrost and Erosion-Driven Organic Matter Fluxes to the Beaufort Sea Near Drew Point, Alaska

2021 ◽  
Vol 8 ◽  
Author(s):  
Emily M. Bristol ◽  
Craig T. Connolly ◽  
Thomas D. Lorenson ◽  
Bruce M. Richmond ◽  
Anastasia G. Ilgen ◽  
...  
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Late Pleistocene ◽  
21St Century ◽  
Marine Sediments ◽  
Coastal Erosion ◽  
Beaufort Sea ◽  
The Arctic ◽  
The Holocene ◽  
Kuparuk River

Accelerating erosion of the Alaska Beaufort Sea coast is increasing inputs of organic matter from land to the Arctic Ocean, and improved estimates of organic matter stocks in eroding coastal permafrost are needed to assess their mobilization rates under contemporary conditions. We collected three permafrost cores (4.5–7.5 m long) along a geomorphic gradient near Drew Point, Alaska, where recent erosion rates average 17.2 m year−1. Down-core patterns indicate that organic-rich soils and lacustrine sediments (12–45% total organic carbon; TOC) in the active layer and upper permafrost accumulated during the Holocene. Deeper permafrost (below 3 m elevation) mainly consists of Late Pleistocene marine sediments with lower organic matter content (∼1% TOC), lower C:N ratios, and higher δ13C values. Radiocarbon-based estimates of organic carbon accumulation rates were 11.3 ± 3.6 g TOC m−2 year−1 during the Holocene and 0.5 ± 0.1 g TOC m−2 year−1 during the Late Pleistocene (12–38 kyr BP). Within relict marine sediments, porewater salinities increased with depth. Elevated salinity near sea level (∼20–37 in thawed samples) inhibited freezing despite year-round temperatures below 0°C. We used organic matter stock estimates from the cores in combination with remote sensing time-series data to estimate carbon fluxes for a 9 km stretch of coastline near Drew Point. Erosional fluxes of TOC averaged 1,369 kg C m−1 year−1 during the 21st century (2002–2018), nearly doubling the average flux of the previous half-century (1955–2002). Our estimate of the 21st century erosional TOC flux year−1 from this 9 km coastline (12,318 metric tons C year−1) is similar to the annual TOC flux from the Kuparuk River, which drains a 8,107 km2 area east of Drew Point and ranks as the third largest river on the North Slope of Alaska. Total nitrogen fluxes via coastal erosion at Drew Point were also quantified, and were similar to those from the Kuparuk River. This study emphasizes that coastal erosion represents a significant pathway for carbon and nitrogen trapped in permafrost to enter modern biogeochemical cycles, where it may fuel food webs and greenhouse gas emissions in the marine environment.

scholarly journals Permafrost Carbon and CO2 Pathways Differ at Contrasting Coastal Erosion Sites in the Canadian Arctic

2021 ◽  
Vol 9 ◽  
Author(s):  
George Tanski ◽  
Lisa Bröder ◽  
Dirk Wagner ◽  
Christian Knoblauch ◽  
Hugues Lantuit ◽  
...  
Keyword(s):  
Organic Matter ◽  
Coastal Erosion ◽  
Canadian Arctic ◽  
Warm Season ◽  
Open Water ◽  
The Arctic ◽  
Comprehensive Understanding ◽  
Erosion Process ◽  
Fresh Organic Matter ◽  
Transit Times

Warming air and sea temperatures, longer open-water seasons and sea-level rise collectively promote the erosion of permafrost coasts in the Arctic, which profoundly impacts organic matter pathways. Although estimates on organic carbon (OC) fluxes from erosion exist for some parts of the Arctic, little is known about how much OC is transformed into greenhouse gases (GHGs). In this study we investigated two different coastal erosion scenarios on Qikiqtaruk – Herschel Island (Canada) and estimate the potential for GHG formation. We distinguished between a delayed release represented by mud debris draining a coastal thermoerosional feature and a direct release represented by cliff debris at a low collapsing bluff. Carbon dioxide (CO2) production was measured during incubations at 4°C under aerobic conditions for two months and were modeled for four months and a full year. Our incubation results show that mud debris and cliff debris lost a considerable amount of OC as CO2 (2.5 ± 0.2 and 1.6 ± 0.3% of OC, respectively). Although relative OC losses were highest in mineral mud debris, higher initial OC content and fresh organic matter in cliff debris resulted in a ∼three times higher cumulative CO2 release (4.0 ± 0.9 compared to 1.4 ± 0.1 mg CO2 gdw–1), which was further increased by the addition of seawater. After four months, modeled OC losses were 4.9 ± 0.1 and 3.2 ± 0.3% in set-ups without seawater and 14.3 ± 0.1 and 7.3 ± 0.8% in set-ups with seawater. The results indicate that a delayed release may support substantial cycling of OC at relatively low CO2 production rates during long transit times onshore during the Arctic warm season. By contrast, direct erosion may result in a single CO2 pulse and less substantial OC cycling onshore as transfer times are short. Once eroded sediments are deposited in the nearshore, highest OC losses can be expected. We conclude that the release of CO2 from eroding permafrost coasts varies considerably between erosion types and residence time onshore. We emphasize the importance of a more comprehensive understanding of OC degradation during the coastal erosion process to improve thawed carbon trajectories and models.

scholarly journals Synoptic evaluation of carbon cycling in Beaufort Sea during summer: contrasting river inputs, ecosystem metabolism and air–sea CO<sub>2</sub> fluxes

2013 ◽  
Vol 10 (10) ◽  
pp. 15641-15710
Author(s):  
A. Forest ◽  
P. Coupel ◽  
B. Else ◽  
S. Nahavandian ◽  
B. Lansard ◽  
...  
Keyword(s):  
Surface Layer ◽  
Organic Carbon ◽  
Sea Ice ◽  
Primary Production ◽  
Arctic Ocean ◽  
Carbon Cycling ◽  
Shelf Break ◽  
The Arctic ◽  
Community Respiration ◽  
Co2 Fluxes

Abstract. The accelerated decline in Arctic sea ice combined with an ongoing trend toward a more dynamic atmosphere is modifying carbon cycling in the Arctic Ocean. A critical issue is to understand how net community production (NCP; the balance between gross primary production and community respiration) responds to changes and modulates air–sea CO2 fluxes. Using data collected as part of the ArcticNet-Malina 2009 expedition in southeastern Beaufort Sea (Arctic Ocean), we synthesize information on sea ice, wind, river, water column properties, metabolism of the planktonic food web, organic carbon fluxes and pools, as well as air–sea CO2 exchange, with the aim of identifying indices of ecosystem response to environmental changes. Data were analyzed to develop a non-steady-state carbon budget and an assessment of NCP against air–sea CO2 fluxes. The mean atmospheric forcing was a mild upwelling-favorable wind (~5 km h−1) blowing from the N-E and a decaying ice cover (<80% concentration) was observed beyond the shelf, the latter being fully exposed to the atmosphere. We detected some areas where the surface mixed layer was net autotrophic owing to high rates of primary production (PP), but the ecosystem was overall net heterotrophic. The region acted nonetheless as a sink for atmospheric CO2 with a mean uptake rate of −2.0 ± 3.3 mmol C m−2d−1. We attribute this discrepancy to: (1) elevated PP rates (>600 mg C m−2d−1) over the shelf prior to our survey, (2) freshwater dilution by river runoff and ice melt, and (3) the presence of cold surface waters offshore. Only the Mackenzie River delta and localized shelf areas directly affected by upwelling were identified as substantial sources of CO2 to the atmosphere (>10mmol C m−2d−1). Although generally <100 mg C m−2d−1, daily PP rates cumulated to a total PP of ~437.6 × 103 t C, which was roughly twice higher than the organic carbon delivery by river inputs (~241.2 × 103 t C). Subsurface PP represented 37.4% of total PP for the whole area and as much as ~72.0% seaward of the shelf break. In the upper 100 m, bacteria dominated (54%) total community respiration (~250 mg C m−2d−1), whereas protozoans, metazoans, and benthos, contributed to 24%, 10%, and 12%, respectively. The range of production-to-biomass ratios of bacteria was wide (1–27% d−1), while we estimated a narrower range for protozoans (6–11% d−1) and metazoans (1–3 % d−1). Over the shelf, benthic biomass was twice higher (~5.9 g C m−2) than the biomass of pelagic heterotrophs (~2.4 g C m−2), in accord with high vertical carbon fluxes on the shelf (956 ± 129 mg C m−2d−1). Threshold PP (PP at which NCP becomes positive) in the surface layer oscillated from 20–152 mg C m−2d−1, with a pattern from low-to-high values as the distance from the Mackenzie River decreased. We conclude that: (1) climate change is exacerbating the already extreme biological gradient across the Arctic shelf-basin system; (2) the Mackenzie Shelf acts as a weak sink for atmospheric CO2, implying that PP exceeds the respiration of terrigenous and marine organic matter in the surface layer; and (3) shelf break upwelling can transfer CO2 to the atmosphere, but massive outgassing can be attenuated if nutrients brought also by upwelling support diatom production. Our study underscores that cross-shelf exchange of waters, nutrients and particles is a key mechanism that needs to be properly monitored as the Arctic transits to a new state.

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

2013 ◽  
Vol 10 (2) ◽  
pp. 2937-2965 ◽  
Author(s):  
E. E. Popova ◽  
A. Yool ◽  
A. C. Coward ◽  
T. R. Anderson
Keyword(s):  
Sea Ice ◽  
Primary Production ◽  
Arctic Ocean ◽  
Canadian Arctic ◽  
Atmospheric Co2 ◽  
The Arctic ◽  
Canadian Arctic Archipelago ◽  
Climate Feedbacks ◽  
Regional Variability ◽  
The Arctic Ocean

Abstract. The Arctic Ocean is a region that is particularly vulnerable to the impact of ocean acidification driven by rising atmospheric CO2, negatively impacting calcifying organisms such as coccolithophorids and foraminiferans. In this study, we use an ocean general circulation model, with embedded biogeochemistry and a full description of the carbon cycle, to study the response of pH and saturation states of calcite and aragonite to 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 RCP 8.5 (the highest IPCC AR5 CO2 emission scenario). The separate impacts of the direct increase in atmospheric CO2 and indirect effects via climate feedbacks (changing temperature, stratification, primary production and fresh water fluxes) were examined by undertaking two simulations, one with the full system and the other in which ocean-atmosphera exchange of CO2 was prevented from increasing beyond the flux calculated for year 2000. Results indicate that climate feedbacks, and spatial heterogeneity thereof, play 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 weakening stratification associated with diminishing ice cover led to greater mixing and primary production. As a consequence, the predicted onset of undersaturation 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, in order to make future projections of acidification and carbon saturation state in the Arctic, regional variability needs to be adequately resolved, with particular emphasis on reliable predictions of the rates of retreat of the sea-ice which are a major source of uncertainty.

Land-to-ocean fluxes and biolability of organic matter eroding along the Beaufort Sea coast near Drew Point, Alaska

2021 ◽  
Author(s):  
Emily Bristol ◽  
Craig Connolly ◽  
Thomas Lorenson ◽  
Bruce Richmond ◽  
Anastasia Ilgen ◽  
...  
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Active Layer ◽  
Late Pleistocene ◽  
Coastal Erosion ◽  
Organic Matter Content ◽  
Beaufort Sea ◽  
The Arctic ◽  
Series Data ◽  
Sea Coast

&lt;p&gt;Coastal erosion rates are increasing along the Alaskan Beaufort Sea coast due to increases in wave action, the increasing length of the ice-free season, and warming permafrost. These eroding permafrost coastlines transport organic matter and inorganic nutrients to the Arctic Ocean, likely fueling biological production and CO&lt;sub&gt;2&lt;/sub&gt; emissions. To assess the impacts of Arctic coastal erosion on nearshore carbon and nitrogen cycling, we examined geochemical profiles from eroding coastal bluffs and estimated annual organic matter fluxes from 1955 to 2018 for a 9 km stretch of coastline near Drew Point, Alaska. Additionally, we conducted a laboratory incubation experiment to examine dissolved organic carbon (DOC) leaching and biolability from coastal soils/sediments added to seawater.&lt;/p&gt;&lt;p&gt;Three permafrost cores (4.5 &amp;#8211; 7.5 m long) revealed that two distinct horizons compose eroding bluffs near Drew Point: Holocene age, organic-rich (~12-45% total organic carbon; TOC) terrestrial soils and lacustrine sediments, and below, Late Pleistocene age marine sediments with lower organic matter content (~1% TOC), lower carbon to nitrogen ratios, and higher &amp;#948;&lt;sup&gt;13&lt;/sup&gt;C-TOC values. Organic matter stock estimates from the cores, paired with remote sensing time-series data, show that erosional TOC fluxes from this study coastline averaged 1,369 kg C m&lt;sup&gt;&amp;#8722;1&lt;/sup&gt; yr&lt;sup&gt;&amp;#8722;1&lt;/sup&gt; during the 21&lt;sup&gt;st&lt;/sup&gt; century, nearly double the average flux of the previous half century. Annual TOC flux from this 9 km coastline is now similar to the annual TOC flux from the Kuparuk River, the third largest river draining the North Slope of Alaska.&lt;/p&gt;&lt;p&gt;Experimental work demonstrates that there are distinct differences in DOC leaching yields and the fraction of biodegradable DOC across soil/sediment horizons. When core samples were submerged in seawater for 24 hours, the Holocene age organic-rich permafrost leached the most DOC in seawater (~6.3 mg DOC g&lt;sup&gt;-1&lt;/sup&gt; TOC), compared to active layer soils and Late-Pleistocene marine-derived permafrost (~2.5 mg DOC g&lt;sup&gt;-1&lt;/sup&gt; TOC). Filtered leachates were then incubated aerobically in the dark for 26 and 90 days at 20&amp;#176;C to examine biodegradable DOC (i.e. the proportion of DOC lost due to microbial uptake or remineralization). Of this leached DOC, Late Pleistocene permafrost was the most biolabile over 90 days (31 &amp;#177; 7%), followed by DOC from active layer soils (24 &amp;#177; 5%) and Holocene-age permafrost (14% &amp;#177; 3%). If we scale these results to a typical 4 m tall eroding bluff at Drew Point, we expect that ~341 g DOC m&lt;sup&gt;-2 &lt;/sup&gt;will rapidly leach, of which ~25% is biodegradable. These results demonstrate that eroding permafrost bluffs are an increasingly important source of biolabile DOC, likely contributing to greenhouse gas emissions and marine production in the coastal environment.&lt;/p&gt;

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