Autonomous Surface and Underwater Vehicles as Effective Ecosystem Monitoring and Research Platforms in the Arctic-The Glider Project.

Effective ocean management requires integrated and sustainable ocean observing systems enabling us to map and understand ecosystem properties and the effects of human activities. Autonomous subsurface and surface vehicles, here collectively referred to as "gliders", are part of such ocean observing systems providing high spatiotemporal resolution. In this paper, we present some of the results achieved through the project "Unmanned ocean vehicles, a flexible and cost-efficient offshore monitoring and data management approach-GLIDER". In this project, three autonomous surface and underwater vehicles were deployed along the Lofoten-Vesterålen (LoVe) shelf-slope-oceanic system, in Arctic Norway. The aim of this effort was to test whether gliders equipped with novel sensors could effectively perform ecosystem surveys by recording physical, biogeochemical, and biological data simultaneously. From March to September 2018, a period of high biological activity in the area, the gliders were able to record a set of environmental parameters, including temperature, salinity, and oxygen, map the spatiotemporal distribution of zooplankton, and record cetacean vocalizations and anthropogenic noise. A subset of these parameters was effectively employed in near-real-time data assimilative ocean circulation models, improving their local predictive skills. The results presented here demonstrate that autonomous gliders can be effective long-term, remote, noninvasive ecosystem monitoring and research platforms capable of operating in high-latitude marine ecosystems. Accordingly, these platforms can record high-quality baseline environmental data in areas where extractive activities are planned and provide much-needed information for operational and management purposes.

Polycyclic aromatic hydrocarbons (PAHs) and organochlorines (OCs) in bottom sediments of the Guba Pechenga, Barents Sea, Russia.

Surface sediment samples from the Guba Penchenga and adjacent areas: Varangerfjord, Guba Malaya Volokovaya and Guba Bol'shaya Volokovaya (south-western Barents Sea) collected in March-April 1997 were analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), chlorinated pesticides: p,p'-DDT, p,p'-DDE, p,p'-DDD, alpha- and gamma-HCH, and hexachlorobenzene (HCB). Mean summation operator PAH (sum of the two- to six-ring PAHs) concentration in sediments from the Guba Pechenga (1481 ng/g dry wt.) was significantly higher than in sediments from adjacent areas (252 ng/g dry wt.), where PAH contamination levels were similar to reported for unpolluted sediments of the northern Norway fjords and open parts of the Barents Sea. Differences between HCB levels as well as summation operator HCH (sum of alpha- and gamma-HCH) levels found in Guba Pechenga sediments and adjacent area sediments were not significant. Concentrations of these contaminants varied in ranges 0.28-1.76 and 0.05-0.68 ng/g dry wt., respectively, and were consistent with literature data on PAH levels in sediments from the northern Norway harbours, Kola Bay (Russia) and south-eastern part of the Barents Sea. Average total DDT concentration in Guba Pechenga sediments (10.5 ng/g dry wt.) was one and 2-3 orders higher than those found in sediments from the Pechora Sea and from the seas of eastern Arctic, respectively, however, it was comparable with DDT levels reported for harbours of northern Norway and Kola Bay. Significant difference between total DDT levels in Guba Pechenga and in the adjacent areas (mean 1.8 ng/g) was found. Among compounds of DDT family, p,p'-DDT isomer prevailed in all sediment samples indicating a possible local 'fresh' DDT source. Mean summation operator PCB (sum of PCB-28, 31, 52, 101, 118, 105, 153, 138, 156, 180, 209) concentration in the Guba Pechenga sediments (12.8 ng/g dry wt.) was significantly higher than in sediments of adjacent areas (2.1 ng/g dry wt.), but it was lower in comparison with summation operator PCB levels reported for the northern Norway harbours and Kola Bay sediments. The highest levels of contaminants were found in sediments collected close to the Liinakhamari harbour. The origin of both PAHs and OCs in the Guba Pechenga sediments is a combination of local sources and long-range transport from lower latitudes.

Polycyclic aromatic hydrocarbons (PAHs) in bottom sediments of the Kara Sea shelf, Gulf of Ob and Yenisei Bay.

PAH concentration and distribution has been examined in surface sediments samples from the Kara Sea, Russia. The study includes 13 samples from the South-eastern Kara Sea shelf, one sample from the south-western part of the sea, 4 samples from the Baydaratskaya Bay, 5 samples from the Gulf of Ob and 4 samples from the Yenisei Bay, collected in August-September 1993-1994. Cluster analysis and principal component analysis (PCA) were used to identify common patterns and possible sources of PAHs. The total PAH concentration (sum of two- to six-ring aromatic hydrocarbons) in the Kara Sea sediments was generally lower than in the Barents Sea sediments and comparable to the levels in the Pechora and White seas. Two- and three-ring aromatic hydrocarbons predominated in Kara Sea sediments, which indicate a relatively stronger petrogenic origin than that in the adjacent seas. The highest total PAH concentrations within the Kara Sea were found in sediments from the Yenisei Bay and in the South-western part of the Kara Sea in the Eastern Novaya Zemlya Trough. The PAHs of the Yenisei Bay sediments were dominated by perylene and PAHs of petrogenic origin, but had also a strong indication of PAHs of pyrogenic origin. The dominating PAH group in the South-western part of the Kara Sea were four- to six-ring aromatic hydrocarbons, indicating pyrogenic origin. Perylene levels were high in all the Kara Sea samples, and highest levels were found in areas of strong terrigenous influence. The most probable source is decaying peat products being transported to the Kara Sea by both large and small rivers.

Artificial radionuclides in sediments of the Don River Estuary and Azov Sea.

The Don River Estuary-Azov Sea system is an extension of the shallow continental shelf area of the Black Sea. A large data set of artificial radionuclides in bottom sediments of the Azov Sea has been compiled in order to examine the storage and migration of radionuclides within this highly restricted inland sea and to estimate the annual dose received by individuals in the local population who regularly consume fish. In recent years (1997-1999), the radionuclide content of surface sediments has been: 137Cs < or = 0.5-100 Bq/kg d.w. (mean = 33.8 +/- 25.9 Bq/kg d.w., n = 57), 90Sr = 0.2-5.7 Bq/kg d.w. (mean = 2.1 +/- 1.4 Bq/kg d.w., n = 34) and 239,240Pu = 0.31-0.51 Bq/kg d.w. (n = 2). In general, 137Cs activities increase with distance from the mouth of the Don River and correlate negatively with sediment grain size (r2 = 0.77, n = 21). The annual 137Cs-derived dose received by an individual through the trophic chain water-fish-humans (approximately 10(-6) Sv/yr) is well below regulatory recommended limits, indicating that current levels of radioactivity in the environment pose no threat to commercial fisheries operations for the bordering nations of Russia and Ukraine.

PCBs, PBDEs and pesticides released to the Arctic Ocean by the Russian rivers Ob and Yenisei.

The Ob and Yenisei Rivers contribute 37% of riverine freshwater inputs to the Arctic Basin and thus represent an important pathway for the land-Arctic ocean exchange of contaminants. Sampling was carried out in the Yenisei (2003) and Ob (2005) River estuaries and Kara Sea to address the general lack of reliable dissolved contaminant flux data for these major rivers. Contaminant analyses were performed by high resolution mass spectrometry on sample extracts taken from filtered large volume water samples (50-100 L) and concentrated in situ onto XAD-2 resin columns. Hexachlorocyclohexanes (HCHs), the polychlorinated biphenyl (PCB) mixtures Sovol and trichlorodiphenyl, dichlorodiphenyltrichloroethane (DDT), as well as "penta" brominated technical mixtures of polybrominated diphenyl ethers (PBDEs) are important contributors to persistent organohalogen contamination for these waterways. Dissolved fluxes to the Kara Sea were estimated at sigmaHCH 246 kg/yr, sigmaPCB 63 kg/yr, sigmaDDT 16 kg/yr, hexachlorobenzene 8 kg/yr, alpha-endosulfan 8 kg/ yr, dieldrin 5 kg/yr, sigmaPBDE 4 kg/yr, and chlordanes 4 kg/yr. Contaminant fluxes from these rivers are similar to those reported for major Canadian rivers, confirming expectations that the Ob and Yenisei are also major point sources for the Arctic basin.

Radioactivity near the sunken submarine "Kursk" in the Southern Barents Sea.

Radioactivity measurements were conducted on seawater, sediment, and biota samples collected in the vicinity of the Russian submarine "Kursk" in September, 2000, within 1 month of the vessel's sinking in the Barents Sea to determine whether leakage of radioactivity from the vessel's two nuclear reactors had occurred and to assess the impact on one of the most productive fishing areas in the world. Levels of radioactivity in surface sediments and biota are within the range of values previously measured in the Barents Sea and can be ascribed to inputs from global fallout, European nuclear fuel reprocessing facilities, and the Chernobyl accident. However, levels of 1291 in seawater in the Southern Barents Sea increased by 500% between 1992 and 2000, and the 129I/137Cs ratio increased by more than an order of magnitude during this time, owing to long-range transport of releases from reprocessing facilities at Sellafield (U.K.) and La Hague (France). Although these results indicate that, at the time of sampling, leakage from the Kursk had a negligible impact on the environment, they also show that regional background levels of artificial radioactivity are varying rapidly on annual timescales and that Europe's nuclear reprocessing facilities are the leading contributor of anthropogenic radioactivity to the region.