The rates of organic matter destruction in the central part of the Arctic Basin

The intensity of the processes of organic matter (OM) destruction in the deep-water part of the Arctic Basin is considered in terms of the activities of hydrolytic enzymes (alkaline phosphatase and proteases) and of redox enzymes of the electron transport system (ETS). High concentrations of mineral phosphorus are shown to cause low phosphatase activity (0.000–0.005 μM P/l h). The average time of the phosphate recycling amounted to about 240 h. The ranges of the total and specific activity of protease are 0.000–0.192 mg of azocasein/(l h) and 0.00–3.57 mg of azocasein/h mg of protein, respectively. It is found that the microplankton production of exo- and endopeptidase in the Arctic Basin is controlled by the concentration of nitrates in the water. The values of the total and the specific activities of the ETS enzymes vary within 0.27–8.96 μl O₂/(l h) and 8.4–583 μl O₂/mg of protein h, respectively. It is shown that the maximum values of the total activities of the hydrolytic and redox enzymes are characteristic for the photic layer. The vertical fluxes of organic carbon from the photic layer, being calculated by the activity of the ETS enzymes, amounted to 220–600 g of C_org/year m². The presence of ice intensifies the redox processes by factors of 2–15.     

Spatiotemporal variability of the organic matter and the rates of its transformation in the Ob Inlet

The data on the qualitative and quantitative variability of the organic matter (OM) and its transformation rates in the waters of the Ob Inlet during different seasons are considered. The OM distribution was quite nonuniform over the entire Ob Inlet aquatic area: the concentrations of C_org varied from 2.8 to 14.1 mg/L and from 0.32 to 4.59 mg/L for the dissolved and particulate forms, respectively. The maximum concentrations of dissolved OM were registered in the main flow of the Ob River water supplied to the bay, whereas the minimum concentrations were characteristic for the near-bottom layers formed by the Kara Sea waters of high salinity in the northern part of the bay. Both in the summer and in the autumn, the fraction of particulate matter within the total OM reached its maximum values in the mixing zone of the Taz and Ob riverine waters, as well as in the mixing zone of the Ob River and Kara Sea waters. These boundary zones were characterized by the widest variability of the elemental (C: N: P) and biochemical (proteins and carbohydrates) composition of the OM, as well as of its transformation rates measured by the activities of the enzymes (alkaline phosphatase and the electron transport system).     

Organic matter of the North Atlantic

The areas that we studied in the North Atlantic (53 and 60°N) and in the Labrador Sea in the summer were characterized by a wide variability of the concentrations of dissolved and particulate organic matter and its elemental composition both in the surface and in the deep waters. The concentrations of dissolved and particulate C_org varied within 69–360 μM and 0.7–25.6 μM, respectively; the N_org and P_org contents varied within 1.4–22.2 μM and 0.02–0.86 μM, respectively. The maximal concentrations were registered in the photic layer and in the zones of mixing between the waters of different genesis. The particulate matter contribution to the total organic matter (OM) content varied from 0.5 to 15.4%. The waters of the photic layer contained more particulate C_org than those of the near-bottom layer. The values of the C/N molar ratios from the surface to the bottom over the entire aquatic area surveyed varied 5-to 6-fold; at that, the values of the C/P molar ratios varied more than tenfold. In the most productive waters, the values of the C/N ratios were close to the Redfield ratios (6–10). The values of the C/P molar ratios varied from 160 in the photic layer to 4831 in the deep waters. The pronounced non-uniformity in the spatial distribution of the OM and its elemental composition is caused not only by the penetration of the waters of different origins but also by the changes in the microplankton metabolism under mixing of these waters.     

The organic carbon in the water,the particulate matter,and the upper layer of the bottom sediments of the west Kara Sea

In three sections in the Kara Sea, the contents of the dissolved and particulate organic carbon (the DOC and POC, respectively), as well as of the organic carbon of the bottom sediments (C_org) were determined. The contents of varied from 6.3 to 2400 μg/l for the DOC and from 0.84 to 12.2 mg of C/l for the POC. The average concentrations for all the samples tested amounted to 200 μg/l for the DOC (n = 78, σ = 368) and 2.7 mg/l for the POC (n = 92, σ = 2.7). The concentrations of Corg in the samples of the upper layer of the bottom sediments of the area treated varied from 0.13 to 2.10% of the dry substance at an average value of 0.9% (n = 21, σ= 0.49%). It is shown that the distribution of the different forms of organic matter (OM) is an indicator of the supply and spreading of the particulate matter in the Kara Sea and that the DOC and POC of the Kara Sea are formed under the impact of the runoff of the Ob and Yenisei river waters. It is found that the distribution of the OM of the bottom sediments in the surveyed area of the Kara Sea is closely related to their grain-size composition and to the structure of the currents in the area studied. The variations in the Corg content in the bottom sediment cores from the zone of riverine and marine water mixing represent the variability of the OM burial.     

Role of colloidal material in the removal of 234Th in the Canada basin of the Arctic Ocean

The phase partitioning of ²³⁴Th between dissolved (<10-kiloDalton, kD), colloidal (10 kD—0.4 μm), and particulate (⩾0.5 μm) matter across a horizontal transect, from a coastal station to the deep Canada Basin, and a vertical profile in the deep Canada Basin of the western Arctic Ocean was investigated. Concentrations of suspended particulate matter (SPM), dissolved, colloidal and particulate organic carbon, particulate organic nitrogen and nutrients (silicate, phosphate and nitrate) were also measured to assess transport and scavenging processes.Total ²³⁴Th (colloidal+particulate+dissolved) indicated deficiencies relative to secular equilibrium with its parent, ²³⁸U in the upper 100 m, which suggests active scavenging of ²³⁴Th onto particle surfaces. In contrast, at depths >200 m, general equilibrium existed between total ²³⁴Th and ²³⁸U. The inventory of SPM and the specific activity of particulate ²³⁴Th in the Canada Basin was about an order of magnitude higher than the profile reported for the Alpha Ridge ice camp station. This higher concentration of SPM in the southwestern Canada Basin is likely derived from ice-rafted sedimentary particles. Inventories of nutrients, and dissolved organic carbon and nitrogen in the upper 100 m of the Canada Basin are comparable to the other estimates for the central Arctic Ocean. Comparison of the mass concentrations of colloidal and filter-retained particulate matter as well as the activity of ²³⁴Th in these phases indicates that only a very small component of the colloidal material is actively involved in Th scavenging. Lower values of the conditional partition coefficient between the colloidal and dissolved phase indicate that the Arctic colloids are less reactive than colloidal material from other regions. The conditional partition coefficient between the filter-retained and dissolved phases (K_f) is generally higher than that for other regions, which is attributed to the higher complexation capacity of glacio-marine sedimentary particles in these waters. The ²³⁴Th-derived export of POC for the shelf and deep Canada Basin ranges between 5.6 and 6.5 mmol m⁻² d⁻¹, and is in agreement with other estimates reported for the central Arctic Ocean and Beaufort Sea.     

Transformation of suspended particulate matter into sediment in the Kara Sea in September of 2011

The biogeochemical processes participating in the transformation of the particulate matter into sediment along the Yenisei River-St. Anna Trough (Kara Sea) meridional profile were studied using hydrochemical, geochemical, microbiological, radioisotope, and isotope methods. The water-sediment contact zone consists of three subzones: the suprabottom water, the fluffy layer, and the surface sediment. The total number, biomass, and integral activity of the microorganisms (dark ¹⁴CO₂ assimilation) in the fluffy layer are usually higher than in the suprabottom water and sediment. The fluffy layer shows a decrease in the oxygen content and the growth of the dissolved biogenic elements. It was provided by the particulate organic matter supporting the vital activity of the heterotrophs from the overlying water column and by the flux of reduced compounds (NH₄, H₂S, CH₄, Fe²⁺, Mn²⁺, and others) from the underlying sediments. The C_org isotopic composition of the fluffy layer and the sediments is 2–4 ‰ heavier than that of the particulate matter and sediment due to the presence of the isotopically heavy biomass of microorganisms. A change in the isotopic composition of the C_org in the fluffy layer and surface sediment as compared to the C_org of the particulate matter is a widespread phenomenon in the Arctic shelf seas and proves the leading role of microorganisms in the transformation of the particulate matter into sediment.     

Studies of hydrocarbons in the waters and snow-ice cover of the southeast sector of the antarctic

Data are presented on the content of hydrocarbons (HC) relative to the concentrations of particulate matter, lipids, C_org, and chlorophyll a in the surface waters and snow-ice cover of the East Antarctic coastal areas. It was shown that the growth of the concentrations of aliphatic HC (AHC) to 30 μg/l in the surface waters takes place in the frontal zones and under the young ice formation. The AHC content in the snow increases with the growth of the aerosol content in the atmosphere. In the lower part of the ice at the boundary with the seawater, despite the low temperatures, the autochthonous processes may provide high AHC concentrations (up to 289 μg/l). Within the snow-ice cover on fast ice, synchronous content variations of all the compounds considered take place.     

An improved method for the hydrolysis and MBTH analysis of dissolved and particulate carbohydrates in seawater

An improved method for the bulk characterization of particulate and dissolved combined carbohydrates in seawater is presented. Seawater samples are dried under vacuum and the residue is hydrolyzed with 12 M H₂SO₄. Carbohydrates in the hydrolysate are subsequently quantified spectrophotometrically by MBTH (3-methyl-2-benzothiazolinone hydrazone hydrochloride) analysis. Sulfuric acid was more effective in hydrolyzing high-molecular-weight structural carbohydrates (cellulose, chitin, and alginic acid) than weak (0.09 N) hydrochloric acid. Sulfuric acid hydrolysis of dissolved and particulate samples yielded estimates of carbohydrates equal to or greater (two- to four-fold) than those resulting from dilute (0.09 N) HCl hydrolysis. In samples from the Gulf of Mexico, total dissolved carbohydrates determined after sulfuric acid hydrolysis varied from 20 to 56 μM C and from 10 to 28% of the dissolved organic carbon determined by high-temperature catalytic oxidation.     

Grain-size composition of the suspended particulate matter in the marginal filter of the Severnaya Dvina River

The quantitative distribution and grain-size composition of the suspended particulate matter (SPM) in the marginal filter of the Severnaya Dvina River during the summer low-water periods of 2001–2005 were first analyzed in seawater on board of the vessel immediately after its sampling (without preliminary treatment) using a Coulter counter. This analysis revealed the main regularities in the transformation of the grain-size spectra at successive salinity steps of the marginal filter as well as the boundaries between these steps based on the data obtained by direct complex studies of the SPM dispersion. It is established that the water salinity is the main factor that controls the changes in the grain-size distribution and the composition of the particulate matter in the marginal filter. The concentrations of the pelitic fraction and the salinity demonstrate negative correlations between each other. It is shown that the areas characterized by the mass development of phytoplankton are located along the outer boundary of the marginal filter (at the biological step), where the salinity amounts to 23–24 psu. The content of the suspended forms of some chemical (lithogenic) elements and the C_org indicating the SPM’s genetic composition and their relations with the grain-size composition of the latter and the environments are studied.     

Decrease in anthropogenic nutrients and its effect on the C/N/P molar ratio of suspended particulate matter in hypertrophic Dokai Bay (Japan) in summer

Biologically important nutrient concentrations in Dokai Bay have declined as a result of reductions in anthropogenic inputs of total nitrogen and total phosphorus. A decrease in nutrient concentrations affects phytoplankton growth, thereby changing the biochemical characteristics of autochthonous particulate matter. We therefore investigated changes in the C/N/P molar ratio of suspended particulate matter (SPM) in the summer, when phytoplankton growth is vigorous, before environmental quality standards (EQSs) were attained (1995–1998) and afterward (2006–2009). We found that the ratio of particulate organic nitrogen (PON) to particulate phosphorus (PP) changed in conjunction with changes in the ratio of dissolved inorganic nitrogen to dissolved inorganic phosphorus (DIP) that resulted from reductions in nutrient loading. Furthermore, we suggest that because the DIP concentration in seawater was high before EQSs were attained, inorganic phosphorus was possibly adsorbed onto SPM. After the attainment of EQSs, however, the DIP concentration fell, and PON/PP was high. Phosphorus limitation of phytoplankton growth in the mouth of the bay may explain the high PON/PP ratios after EQS attainment.     

Seasonal trends in the abundance, composition and bioavailability of particulate and dissolved organic matter in the Chukchi/Beaufort Seas and western Canada Basin

The objectives of this study were to investigate the seasonality, abundance, sources and bioreactivity of organic matter in the water column of the western Arctic Ocean. The concentrations of particulate and dissolved amino acids and amino sugars, as well as bulk properties of particulate and dissolved organic matter (DOM), were measured in shelf, slope and basin waters collected during the spring and summer of 2002. Particulate organic matter concentrations in shelf waters increased by a factor of 10 between spring and summer. Dissolved organic carbon (DOC) and nitrogen (DON) concentrations exhibited only minor seasonal variations, whereas dissolved amino acid concentrations doubled between spring and summer, and dissolved amino sugars increased by 31% in shelf waters of the Chukchi and Beaufort Seas. Concentrations of DOC did not exhibit a significant seasonal change in surface waters of the Canada Basin, but dissolved amino acid concentrations increased by 45% between spring and summer. No significant seasonal differences were detected in the concentration or composition of DOM in waters below 100 m in depth. Concentrations of particulate and dissolved amino acids and amino sugars were strongly correlated with chlorophyll-a, indicating a plankton source of freshly produced organic matter. The amino acid and amino sugar compositions of freshly produced DOM indicated that a large portion of this material is bioavailable. While freshly produced DOM was found to be relatively bioreactive, preformed DOM in the Arctic appears to be less bioreactive but similar in degradation state to average DOM in the Atlantic and Pacific. These data demonstrate substantial summer production of POM and DOM on the Chukchi and Beaufort shelves that is available for utilization in shelf waters and export to the Canada Basin.     

Distribution and burial of organic carbon in sediments from the Indian Ocean upwelling region off Java and Sumatra,Indonesia

Sediments were sampled and oxygen profiles of the water column were determined in the Indian Ocean off west and south Indonesia in order to obtain information on the production, transformation, and accumulation of organic matter (OM). The stable carbon isotope composition (δ¹³C_org) in combination with C/N ratios depicts the almost exclusively marine origin of sedimentary organic matter in the entire study area. Maximum concentrations of organic carbon (C_org) and nitrogen (N) of 3.0% and 0.31%, respectively, were observed in the northern Mentawai Basin and in the Savu and Lombok basins. Minimum δ¹⁵N values of 3.7‰ were measured in the northern Mentawai Basin, whereas they varied around 5.4‰ at stations outside this region. Minimum bottom water oxygen concentrations of 1.1 mL L^?1, corresponding to an oxygen saturation of 16.1%, indicate reduced ventilation of bottom water in the northern Mentawai Basin. This low bottom water oxygen reduces organic matter decomposition, which is demonstrated by the almost unaltered isotopic composition of nitrogen during early diagenesis. Maximum C_org accumulation rates (CARs) were measured in the Lombok (10.4 g C m^?2 yr^?1) and northern Mentawai basins (5.2 g C m^?2 yr^?1). Upwelling-induced high productivity is responsible for the high CAR off East Java, Lombok, and Savu Basins, while a better OM preservation caused by reduced ventilation contributes to the high CAR observed in the northern Mentawai Basin. The interplay between primary production, remineralisation, and organic carbon burial determines the regional heterogeneity. CAR in the Indian Ocean upwelling region off Indonesia is lower than in the Peru and Chile upwellings, but in the same order of magnitude as in the Arabian Sea, the Benguela, and Gulf of California upwellings, and corresponds to 0.1–7.1% of the global ocean carbon burial. This demonstrates the relevance of the Indian Ocean margin off Indonesia for the global OM burial.     

Oceanographic controls on the carbon isotopic compositions of sinking particles from the Cariaco Basin

This study examined the relationship between carbon isotopic composition of sinking organic matter (OM) and the biological, physical and chemical properties of the surface ocean in the Cariaco Basin. The ¹³C/¹²C ratio of OM (δ¹³C_org) in sinking particles was determined on sediment trap samples from four depths collected from 1996 to 1999 as part of the CArbon Retention In A Colored Ocean time series. Water column properties, including temperature, productivity, chlorophyll and concentration of dissolved CO₂, were concurrently measured on monthly cruises. The δ¹³C_org varied from a high of –17.7‰ to a low of –22.6‰ during the study period. The variation of the δ¹³C_org throughout seasonal cycles was directly proportional to the strength of upwelling and was negatively correlated with temperature (r²=0.64). During the 1996–1997 upwelling event, the strongest during the study period, the δ¹³C_org increased by 4.4‰ whereas during the 1998–1999 upwelling event, the weakest during the study period, the δ¹³C_org only increased by 3.3‰. Contrary to most previous studies, we observed a negative relationship (r²=0.53) between [CO_2 aq] and the estimated isotopic fractionation factor (ε_p). However, there was no correlation between ε_p and the calculated growth rates indicating that there was non-diffusive uptake of carbon into phytoplankton cells. It thus appears that [CO_2 aq] does not control the δ¹³C_org in the water column of the study site. The best explanation for the isotopic enrichment observed is a carbon concentrating mechanism (CCM) in phytoplankton. The existence of a CCM in phytoplankton has major implications for the interpretation of the δ¹³C_org in the Cariaco Basin.     

The concentration and composition of hydrocarbons in water,particulate matter,and bottom sediments of the Kara Sea

Data are presented on the content of aliphatic and polycyclic aromatic hydrocarbons (AHC and PAH, respectively) in the interstitial waters and bottom sediments of the Kara Sea compared to the distribution of the particulate matter and organic carbon. It was found that the AHC concentrations within the water mass (16 μg/l on average) are mainly formed by natural processes. The AHC distribution represents the variability of the hydrological and sedimentation processes in different regions of the sea. The widest ranges of the concentrations were registered in the Ob Bay-Kara Sea section: in the water (10–310 μg/l for the AHC and 0.4–7.2 ng/l for the PAH) and in the surface layer of the bottom sediments (8–42 μg/l for the AHC and 9–94 ng/g for the PAH). The differentiation of the hydrocarbons (HC) in the different media follows the marginal filter’s regularities; therefore, no oil and pyrogenic compounds are supplied to the open parts of the sea. In the sediment mass, the HC content is determined by the variations in the oxidative conditions in the sediment and its material’s composition.     

The saturation of calcite and aragonite in the Arctic Ocean

We report on the chemical saturation of CaCO₃ in the waters of the Arctic Ocean calculated from total alkalinity (A_T) and total dissolved inorganic carbon (C_T). Data based on four different expeditions are presented: International Arctic Ocean Expedition (IAOE-91), Arctic Ocean Section 94 (AOS94), Polarstern Arctic '96 expedition (ACSYS 96), and Joint Ocean Ice Study 97 (JOIS 97). The results show a lysocline at around 3500 m for aragonite and that most of the Arctic Ocean sea floor lies above the lysocline for calcite. The only anomaly is the low degree of saturation at the shelf break depth in the Canadian Basin seen in the sections of the AOS94 and JOIS 97 cruises, correlated with nutrient maxima and very low O₂ concentration, suggesting decomposition of organic matter. The insignificant variability in degree of saturation between the deep waters of the different basins in the Arctic Ocean indicates a very low sedimentation/remineralisation of organic soft matter.     

The geochemistry of deepwater particulate matter over the hydrothermal field at 9°d50′ N (the East Pacific Rise)

The results of geochemical studies of particulate matter in the water mass over the hydrothermal field at 9°50′ N on the East Pacific Rise are presented. The particulate matter was tested in background waters, in the buoyant plume, and in the near-bottom waters. The contents of Si, Al, P, C_org, Fe, Mn, Cu, Zn, Ni, Co, As, Cr, Cd, Pb, Ag, and Hg were determined. No definite correlations were found between the ele-ments in the background waters. Many of the chemical elements correlated with Fe and associated with its oxyhydroxides in the buoyant plume. In the near-bottom waters, microelements are associated with Fe, Zn, and Cu (probably, to their sulfides formed under fluid mixing with seawater). The matter precipitated in a sed-imentation trap was similar to the near-bottom particulate matter in the elemental composition.     

Seasonal and spatial distribution of particulate organic matter (POM) in the Chukchi and Beaufort Seas

As part of the Western Arctic Shelf–Basin Interactions (SBI) project, the production and fate of organic carbon and nitrogen from the Chukchi and Beaufort Sea shelves were investigated during spring (5 May–15 June) and summer (15 July–25 August) cruises in 2002. Seasonal observations of suspended particulate organic carbon (POC) and nitrogen (PON) and large-particle (>53 μm) size class suggest that there was a large accumulation of carbon (C) and nitrogen (N) between spring and summer in the surface mixed layer due to high phytoplankton productivity. Considerable organic matter appeared to be transported from the shelf into the Arctic Ocean basin in an elevated POC and PON layer at the top of the upper halocline. Seasonal changes in the molar carbon:nitrogen (C:N) ratio of the suspended particulate organic matter (POM) pool reflect a change in the quality of the organic material that was present and presumably being exported to the sediment and to Arctic Ocean waters adjacent to the Chukchi and Beaufort Sea shelves. In spring, low particulate C:N ratios (<6; i.e., N rich) were observed in nitrate-replete surface waters. By the summer, localized high particulate C:N ratios (>9; i.e., N-poor) were observed in nitrate-depleted surface waters. Low POC and inorganic nutrient concentrations observed in the surface layer suggest that rates of primary, new and export production are low in the Canada Basin region of the Arctic Ocean.     

Contents and stable isotopic compositions of organic carbon and total nitrogen in the surface sediment of two coastal bays in Korea

Surface sediment from the coastal bays of Gwangyang and Masan in South Korea were analyzed for their contents and isotopic values of organic carbon and total nitrogen. The sources and diagenetic alteration of organic matter were also assessed. Total organic carbon varied from 0.22% to 3.48% (average = 1.40%, n = 75), and C/N ratios varied from 2.4 to 15.2 (average = 8.79, n = 75). δ¹³C_org ranged from −19.92‰ to −25.86‰ (average = −21.21‰, n = 75), and δ¹⁵N_TN ranged from 8.57‰ to 3.93‰ (average = 6.49‰, n = 75). Total organic carbon in both areas was associated with grain-size, with higher contents in finer grained sediment. The high carbon content observed in Masan Bay sediment correlated with its higher C/N ratio. δ¹³C_org and δ¹⁵N_TN varied widely, attributable to various influences such as the input of terrestrial organic matter and diagenetic alteration. The depleted δ¹³C_org and higher δ¹⁵N_TN observed in the sediment of Gwangyang Bay reflected terrestrial supply, implying that biogeochemical processes, i.e. bacterial degradation, were more active in Masan Bay sediment, which showed less depleted δ¹³C_org and higher δ¹⁵N_TN than Gwangyang Bay sediment. δ¹⁵N_TN was the more useful indicator of biogeochemical processes in the highly anoxic sediment. These results indicate that the δ¹³C_org and δ¹⁵N_TN of sedimentary organic matter in coastal bays can indicate the source and degree of diagenetic alteration of sedimentary organic matter.     

Nitrogen and carbon isotopic composition of marine and terrestrial organic matter in Arctic Ocean sediments:: implications for nutrient utilization and organic matter composition

Relationships between organic carbon, total nitrogen and organic nitrogen concentrations and variations in δ¹³C_org and δ¹⁵N_org are examined in surface sediments from the eastern central Arctic Ocean and the Yermak Plateau. Removing the organic matter from samples with KOBr/KOH and determining residual as well as total N shows that there is a significant amount of bound inorganic N in the samples, which causes TOC/N_total ratios to be low (4–10 depending on the organic content). TOC/N_org ratios are significantly higher (8–16). This correction of organic TOC/N ratios for the presence of soil-derived bound ammonium is especially important in samples with high illite concentrations, the clay mineral mainly responsible for ammonium adsorption. The isotopic composition of the organic N fraction was estimated by determining the isotopic composition of the total and inorganic nitrogen fractions and assuming mass-balance. A strong correlation between δ¹⁵N_org values of the sediments and the nitrate concentration of surface waters indicates different relative nitrate utilization rates of the phytoplankton in various regions of the Arctic Ocean. On the Yermak Plateau, low δ¹⁵N_org values correspond to high nitrate concentrations, whereas in the central Arctic Ocean high δ¹⁵N_org values are found beneath low nitrate waters. Sediment δ¹³C_org values are close to −23.0‰ in the Yermak Plateau region and approximately −21.4‰ in the central Arctic Ocean. Particulate organic matter collected from meltwater ponds and ice-cores are relatively enriched in ¹³C (δ¹³C_org=−15.3 to −20.6‰) most likely due to low CO₂(aq) concentrations in these environments. A maximum terrestrial contribution of 30% of the organic matter to sediments in the central Arctic Ocean is derived, based on the carbon isotope data and various assumptions about the isotopic composition of the potential endmembers.     

Microbial processes of the carbon and sulfur cycles in the Kara Sea

The results of microbiological, biogeochemical, and isotope geochemical studies in the Kara Sea are described. The samples for these studies were obtained during the 54th voyage of the research vessel Akademik Mstislav Keldysh in September 2007. The studied area covered the northern, central, and southwestern parts of the Kara Sea and the Gulf of Ob. The quantitative characteristics of the total bacterial population and the activity of the microbial processes in the water column and bottom sediments were obtained. The total population of the bacterioplankton (BP) varied from 250000 cells/ml in the northern water area to 3000000 cells/ml in the Gulf of Ob. The BP population depended on the content of the water suspension. The net BP production was minimal in the central water area, amounting to 0.15–0.2 μg C/(l day), and maximal (0.5–0.75 μg C/(l day)) in the Gulf of Ob. The organic material at the majority of the stations in the Ob transect predominantly contained light carbon isotopes (−28.0 to −30.18‰) of terrigenous origin. The methane content in the surface water layer varied from 0.18 to 2.0 μl CH₄/l, and the methane oxidation rate changed in the range of 0.1–100 nl CH₄/(l day). The methane concentration in the upper sediment layer varied from 30 to 300 μl CH₄/dm³; the rate of the methanogenesis was 44 to 500 nl CH₄/(dm³ day) and that of the methane oxidation, 30 to 2000 nl CH₄/(dm³ day). The rate of the sulfate reduction varied from 4 to 184 μg S/(dm³ day).