Seasonal variation of inorganic carbon parameters and air-sea exchange of CO2 in Marian Cove, King George Island, Western Antarctic Peninsula.

Inorganic carbon parameters were observed in Marian Cove, King George Island, Western Antarctic Peninsula, to assess the impact of the Antarctic coastal regions on air-sea CO2 exchange. The variations in total alkalinity (TA) and dissolved inorganic carbon (DIC) were caused by ice melting, formation, and biological activities. The net annual air-sea CO2 flux (5.6 ± 11.8 mmol m-2 d-1) indicated that Marian Cove was a CO2 source in the atmosphere, suggesting the opposite role of the Antarctic coastal regions to the Southern Ocean in CO2 flux estimates. Finally, this study identified the controlling factors of the annual variation of TA and DIC for the first time through direct field observations in King George Island. This study indicated that Antarctic coastal regions can act as a CO2 source to the atmosphere. Thus, further investigations and continuous monitoring are required in the coastal areas to improve our understanding of global carbon cycles.

Factors affecting the subsurface aragonite undersaturation layer in the Pacific Arctic region.

This study evaluated interannual variation in the subsurface aragonite undersaturation zone (ΩAr<1 layer) in the Pacific Arctic Ocean, using data from the 2016-2019 period. The upper boundary (DEPΩ<1UB) of the ΩAr<1 layer generally formed at a depth where the contribution of corrosive Pacific water was approximately 98 %. The intensity of the Beaufort Gyre associated with freshwater accumulation mainly determined interannual variation in DEPΩ<1UB, but the direction of its effect was opposite west and east of ~166°W. The lower boundary (DEPΩ<1LB) of the ΩAr<1 layer was generally found at a depth range where equal contributions of Pacific and Atlantic water were expected. An Atlantic-origin cold saline water intrusion event in 2017 caused by an anomalous atmospheric circulation pattern significantly lifted the DEPΩ<1LB, thus the thickness of the ΩAr<1 layer decreased.

Constraining the effectiveness of inherent tracers of captured CO2 for tracing CO2 leakage: Demonstration in a controlled release site.

Geological storage of carbon dioxide (CO2) is an integral component of cost-effective greenhouse gas emissions reduction scenarios. However, a robust monitoring regime is necessary for public and regulatory assurance that any leakage from a storage site can be detected. Here, we present the results from a controlled CO2 release experiment undertaken at the K-COSEM test site (South Korea) with the aim of demonstrating the effectiveness of the inherent tracer fingerprints (noble gases, δ13C) in monitoring CO2 leakage. Following injection of 396 kg CO2(g) into a shallow aquifer, gas release was monitored for 2 months in gas/water phases in and above the injection zone. The injection event resulted in negative concentration changes of the dissolved gases, attributed to the stripping action of the depleted CO2. Measured fingerprints from inherent noble gases successfully identified solubility-trapping of the injected CO2 within the shallow aquifer. The δ13C within the shallow aquifer could not resolve the level of gas trapping, due to the interaction with heterogeneous carbonate sources in the shallow aquifer. The time-series monitoring of δ13CDIC and dissolved gases detected the stripping action of injected CO2(g), which can provide an early warning of CO2 arrival. This study highlights that inherent noble gases can effectively trace the upwardly migrating and fate of CO2 within a shallow aquifer.

Emerging investigator series: influence of marine emissions and atmospheric processing on individual particle composition of summertime Arctic aerosol over the Bering Strait and Chukchi Sea.

The Arctic is rapidly transforming due to sea ice loss, increasing shipping activity, and oil and gas development. Associated marine and combustion emissions influence atmospheric aerosol composition, impacting complex aerosol-cloud-climate feedbacks. To improve understanding of the sources and processes determining Arctic aerosol composition, atmospheric particles were collected aboard the Korean icebreaker R/V Araon cruising within the Bering Strait and Chukchi Sea during August 2016. Offline analyses of individual particles by microspectroscopic techniques, including scanning electron microscopy with energy dispersive X-ray spectroscopy and atomic force microscopy with infrared spectroscopy, provided information on particle size, morphology, and chemical composition. The most commonly observed particle types were sea spray aerosol (SSA), comprising ∼60-90%, by number, of supermicron particles, and organic aerosol (OA), comprising ∼50-90%, by number, of submicron particles. Sulfate and nitrate were internally mixed within both SSA and OA particles, consistent with particle multiphase reactions during atmospheric transport. Within the Bering Strait, SSA and OA particles were more aged, with greater number fractions of particles containing sulfate and/or nitrate, compared to particles collected over the Chukchi Sea. This is indicative of greater pollution influence within the Bering Strait from coastal and inland sources, while the Chukchi Sea is primarily influenced by marine sources.

Unexpectedly high dimethyl sulfide concentration in high-latitude Arctic sea ice melt ponds.

Dimethyl sulfide (DMS) production in the northern Arctic Ocean has been considered to be minimal because of high sea ice concentration and extremely low productivity. However, we found DMS concentration (1-33 nM) in melt ponds on sea ice at a very high latitude (78°N) in the central Arctic Ocean to be up to ten times that in the adjacent open ocean (<3 nM). We divided melt ponds into three categories: freshwater melt ponds, brackish melt ponds, and open saline melt ponds. Melt ponds from each category had different formation mechanisms and associated DMS contents. Closed brackish ponds (salinity of >20) had particularly high DMS concentration. Water in brackish ponds was mixed with open ocean water in the past via a hole at the bottom of the floe that kept the pond open to the ocean; therefore, unlike freshwater melt ponds, brackish ponds became sites of DMS accumulation. Our results suggest that continuous increase in melt pond coverage on Arctic sea ice could considerably impact future Arctic climate as well as enhancing DMS concentration in the Arctic atmosphere.

Zooplankton and micronekton respond to climate fluctuations in the Amundsen Sea polynya, Antarctica.

The vertical migration of zooplankton and micronekton (hereafter 'zooplankton') has ramifications throughout the food web. Here, we present the first evidence that climate fluctuations affect the vertical migration of zooplankton in the Southern Ocean, based on multi-year acoustic backscatter data from one of the deep troughs in the Amundsen Sea, Antarctica. High net primary productivity (NPP) and the annual variation in seasonal ice cover make the Amundsen Sea coastal polynya an ideal site in which to examine how zooplankton behavior responds to climate fluctuations. Our observations show that the timing of the seasonal vertical migration and abundance of zooplankton in the seasonally varying sea ice is correlated with the Southern Annular Mode (SAM) and El Niño Southern Oscillation (ENSO). Zooplankton in this region migrate seasonally and overwinter at depth, returning to the surface in spring. During +SAM/La Niña periods, the at-depth overwintering period is shorter compared to -SAM/El Niño periods, and return to the surface layers starts earlier in the year. These differences may result from the higher sea ice cover and decreased NPP during +SAM/La Niña periods. This observation points to a new link between global climate fluctuations and the polar marine food web.

Characteristics of the horizontal and vertical distributions of dimethyl sulfide throughout the Amundsen Sea Polynya.

We investigated horizontal and vertical distributions of DMS in the upper water column of the Amundsen Sea Polynya and Pine Island Polynya during the austral summer (January-February) of 2016 using a membrane inlet mass spectrometer (MIMS) onboard the Korean icebreaker R/V Araon. The surface water concentrations of DMS varied from <1 to 400nM. The highest DMS (up to 300nM) were observed in sea ice-polynya transition zones and near the Getz ice shelf, where both the first local ice melting and high plankton productivity were observed. In other regions, high DMS concentration was generally accompanied by higher chlorophyll and ΔO2/Ar. The large spatial variability of DMS and primary productivity in the surface water of the Amundsen Sea seems to be attributed to melting conditions of sea ice, relative dominance of Phaeocystis Antarctica as a DMS producer, and timing differences between bloom and subsequent DMS productions. The depth profiles of DMS and ΔO2/Ar were consistent with the horizontal surface data, showing noticeable spatial variability. However, despite the large spatial variability, in contrast to the previous results from 2009, DMS concentrations and ΔO2/Ar in the surface water were indistinct between the two major domains: the sea ice zone and polynya region. The discrepancy may be associated with inter-annual variations of phytoplankton assemblages superimposed on differences in sea-ice conditions, blooming period, and spatial coverage along the vast surface area of the Amundsen Sea.

Oceanic source strength of carbon monoxide on the basis of basin-wide observations in the Atlantic.

We measured the carbon monoxide (CO) concentrations in the marine boundary layer and the surface waters of the Atlantic Ocean from 50°N to 50°S during the UK Atlantic Meridional Transect expedition (AMT-7) in October 1998, covering the open ocean and coastal regions. Throughout the cruise track, atmospheric CO concentrations continually decreased southwards in the northern hemisphere with sporadic low and high concentrations encountered. South of the intertropical convergence zone (ITCZ) atmospheric CO was enhanced by ∼10 ppb compared to north of the ITCZ due likely to biomass burning emissions prevailing in the tropical continents. The remainder of the southern hemisphere remains nearly invariable except for the vicinity of Rio de la Plata. The surface seawater was supersaturated everywhere along the track and its saturation anomaly oscillated up to 90, exhibiting a typical diurnal cycle. The maximal dissolved CO concentration in the diurnal cycle appeared 2-5 hours behind the local maximum of solar insolation in the open ocean and the time lag further increased in the coastal region. The global ocean flux of CO to the atmosphere was estimated to be 14 Tg(CO) a(-1) within the range of 4-24 Tg(CO) a(-1). This is within uncertainty almost identical to what was estimated on the basis of the basin-wide observations in the Pacific and the Atlantic, but more than ∼4 times lower than the values appeared in the Intergovernmental Panel on Climate Change (IPCC) reports.