Characteristics of the Ecosystems of Water Bodies Separating from Kandalaksha Bay of the White Sea

The coastal water bodies that separate from White Sea water area due to Kandalaksha coast rise are examined. The hydrological and hydrochemical characteristics of these water bodies are found to notably differ from these in the bays and straits connected with them. Extreme values of water temperature and salinity were recorded. High concentrations of oxygen (>20 mg/l) were recorded in the near-surface water layers and high concentrations of hydrogen sulfide (>90 mg/l) in bottom waters. The species composition of phyto- and zooplankton was found to be poor. The characteristics of enzymatic destruction in subsurface waters of lakes are an order of magnitude greater than those in White Sea open areas.     

HYDROGEOCHEMISTRY OF GROUNDWATER IN CENTRAL ISRAEL

ABSTRACT

The regional groundwater groups of central Israel include:

1. bicarbonate waters representing the replenishment areas;

2. chloride waters representing the confined and the base-level zones;

3. sulfate waters of the intermediate zones (fig. 2).

These water types were found to fit broadly into five hydrogeographical groups.

The chemical evolution of the ground waters is a function of: a) lithology and solubility of the aquifer components and of the surrounding strata; b) mixing between groundwater bodies of different composition. The first factor is important mainly within the confined zones while the latter is conspicuous in the Rift Valley and adjacent areas.

Groundwater mixing within the Dead Sea basin produces waters with Mg > Na > Ca, and Cl ? SO > HCO₃. Other brines show the order: Ca > Na > Mg. All these brines show compositions different from ocean water.     

Changes in the dynamics/energetics of surface and internal tides in the White Sea on the coexistence of shore-fast and drifting ice covers

The results of modeling for _M2${\mathrm{M}}_2$ surface and internal tides in the White Sea are discussed. These results are obtained for the case when shore-fast and drifting ice covers are present concurrently. It is assumed that the interface between ice covers is of non-tidal origin (i.e., it is pre-assigned) and that ice rheology is viscous-elastic, representative of the low temperatures typical of winter conditions. Emphasis is placed on tidal energetics and, in particular, on the averaged (over a tidal cycle) values of the density and the dissipation rate of barotropic/baroclinic tidal energy. It is shown that in the White Sea, unlike in other marginal seas, the averaged (over a tidal cycle) and depth-integrated density of baroclinic tidal energy for the combined ice cover is much less than the same defined density of barotropic tidal energy. Similarly, the averaged and integrated (over the volume of the White Sea) rate of baroclinic tidal energy dissipation is much less than the same defined rate of barotropic tidal energy dissipation. The latter, in turn, is greater than for the shore-fast ice cover, but is smaller than for the drifting ice cover.     

Geothermal resources in the imperial valley of california

The Imperial Valley is a major rift valley characterized by unusually high heat flow and large quantities of water in storage in the thick fill of alluvium provided by the sediments of the delta of the Colorado River. The inventory of hot water appears to be sufliciently large that if used for water desalination it might add several million acreleet of new water to the resources of the lower Colorado River basin. This distilled water would serve to lower river salinity and provide extra water to help meet the U. S. — Mexico treaty commitments. A major fraction of water desalination costs lie in the cost of energy and are related to desalination technology which is directly related to water chemistry. The discovery of low salinity geothermal waters in the Imperial Valley opened th possibility for a major breakthrough in lowered water desalination costs. We have tried to develop a broad understanding of the origins of the waters of the Imperial Valley and how natural recharge occurs. The chemical composition of the waters of the central portion of Imperial Valley basin waters, while not that of present surface flow of the rivers, nevertheless does have a close affinity to Colorado River water. No sea water seems to be present in the valley although marine sediments appear to occur on basement on West Mesa and on basement to the east in Arizona south of Yuma. Low salinity waters dominate the basin hydrology and waters as saline or more saline than sea water appear to be restricted to the immediate area of the Salton Sea. The isotope work of T. Coplen makes it possible to determine the relative contribution of precipitation runoff from California watersheds and from Colorado River water. Both sources are significant. The Colorado River water in aquifers from 100–400 m appears to have been entrapped from a relatively homogeneous basin which was subject to substantial evaporation. Its original source was snow melt water from the Colorado River. Five types of waters, none of them sea water, were recognized by their salt geochemistry. Bromide/chloride data are particularly effective in resolving different types of water masses. The bromide/chloride data agree with the isotope data and identify rainfall and precipitation runoff from the high mountains to the west. Modern Colorado River water is easily recognized by its salts and two types of ancient Colorado River waters from previous lake stage are proposed on the basis of the bromide/chloride data. One old lake occurring during the pluvial stage associated with the last Ice Age is proposed to account for much of the water in artesian aquifers. Another younger lake stage, possibly with Lake Cahuilla affinities is also suggested. Mountain runoff waters can be distinguished in the subsurface by their relatively lower salinity and high bicarbonate concentration, and their heavy isotopic composition. Revised fluid reserve calculations based on additional porosity data continue to show that the low salinity water resources of the Imperial Valley may exceed two billion acre-feet. The oceanic plate tectonic model is modified in the Imperial Valley by the evidence of a series of complex blocks with the generation of both tensional and compressional features in the valley. Major strike slip faults dominate the tectonic fabric but conjugate features increase complexity by a large degree and a major amount of work will be needed before any geologically sound structural models can be generated. Xenoliths within the obsidians at the volcanoes at the south end of the Salton Sea provide samples of the basement under the Imperial Valley. These xenoliths include partially remelted granitic rocks, fragments of basalt, greenschist, and baked shale and sandstone. This is taken as evidence that the basement in the valley consists in part of partially remelted granite. This would render basement plastic and readily deformed. The source of the heat is suggested to be derived from basalt that comes into the basement and deeper sediments from below. This upward movement of basalt along a spreading zone is the continental equivalent to a sea floor spreading area. In the continental case the insulating blanket of wet sediment retains the heat and appears to produce a major geothermal resource. The geothermal resources of the Imperial Valley are the aggregate of the thermal energy of the large inventory of subsurface water heated by the complex mix of intrusive phenomena. The net result is to generate a polygenetic geothermal resource of very large dimensions.     

Addition of magmatic volatiles into the hot spring waters of loowit canyon,Mount St. Helens,Washington, USA

Geochemical studies on cold meteoric waters, post-1980 hot spring waters, fumarole emissions from the dacite dome, and volcanic rocks at Mount St. Helens (MSH) from 1985 to 1989 show that magmatic volatiles are involved in the formation of a new hydrothermal system. Hot spring waters are enriched in ¹⁸O by as much as 2 and display enrichments in D relative to cold waters. A well-defined isotopic trend is displayed by the isotopic composition of a>400°C fumarole condensate collected from the central crater in 1980 (-33 D, +6 ¹⁸O), of condensate samples collected on the dome, and of cold meteoric and hot spring waters. The trend indicates that mixing occurs between local meteoric water and magmatic water degassing from the dacite dome. Between 30 and 70% magmatic water is present in the dome fumarole discharges and 10% magnatic water has been added to the waters of the hydrothermal system. Relations between Cl, SO₄ and HCO₃ indicate that the hot spring waters are immature volcanic waters formed by reaction of rocks with waters generated by absorption of acidic volcanic fluids. In addition, the B/Cl ratios of the spring waters are similar to the B/Cl ratios of the fumarole condensates (0.02), values of ¹³C in the HCO₃ of the hot springs (-9.5 to-13.5) are similar to the magmatic value at MSH (-10.5), and the ³He/⁴He ratio, relative to air, in a hot spring water is 5.7, suggesting a magmatic origin for this component.managed by Martin Marietta Energy Systems, Inc., under contract DE-AC05-84OR21400 with the US Department of Energy     

Geochemical characterization of the organic matter, pore water constituents and shallow methane gas in the eastern part of the Ulleung Basin, East Sea (Japan Sea)

Abstract Geochemical analyses of sediments, pore water and headspace gas of the piston cores taken from the eastern part of Ulleung Basin of the East Sea (Japan Sea) were carried out to assess the origin of the sedimentary organic matter and interstitial fluid. Several tephra layers within the core are identified as the Ulleung‐Oki (10.1 ka), the Aira‐Tanzawa (23 ka) and the Ulleung‐Yamato (30.9 ka) tephras. With the exception of these volcanic layers, the cores consist predominantly of muddy sediments that contain >0.5% total organic carbon. Atomic C/N ratios and δ¹³C_org values suggest that the organic matter originated from marine algae rather than from land vascular plants, whereas Rock‐Eval pyrolysis suggests that the organic matter is thermally immature and comes from a land vascular plant (Type III). These conflicting results seem to be caused by the heavy oxidization of the marine organic matter. Sulphate concentration profiles of pore waters show strongly linear depletion (r² > 0.97) with sediment depth. The estimated sulphate–methane interface (SMI) depth using the sulphate concentration gradient was nearly 3.5 m below seafloor (mbsf) in the southern part of the study area, and deeper than 6 mbsf in the northern part of the area. The difference in SMI depths is likely associated with the amount of the methane flux. The methane concentration below the SMI in the two southern cores increases rapidly, implying the occurrence of methanogenesis and anaerobic methane oxidation (AMO). In contrast, the two northern cores have a low methane concentration below the SMI. values measured from all cores were in the range of −83.5 to −69.5‰, which suggests that the methane derives from a methanogenic microbe. values become decreased toward SMI, but increased below SMI; therefore, has eventually the minimum value near the SMI. The values are also decreased when the methane concentration is increased. These phenomena support the typical occurrence of AMO in the study area.     

An Estimation of the Mercury Content in the Waters of the Pomeranian Baltic-Shore-Area

In the catchment area of the Pomeranian Bay an average mercury concentration of 178 ng/l in precipitation was determined. Eight different flowing waters showed mean concentrations between 105 ng/l (?upawa) and 500 ng/l (Odra), a pronounced annual cycle having been demonstrated for the concentrations and for the freights with the minimum in February/March and the maximum in August/September. The total freight of the eight rivers amounts to 19.5 t/a, the share of the Wisla being 11 t/a. The ratio between the mercury precipitation of 335 to 410 μg/m²a Hg and the run-off varies of 30 … 75 μg/m²a Hg for the individual river basins between 0.08 and 0.21. In the Baltic Sea, the mercury concentrations are 40 ng/l in the open sea, 50 ng/l in the coastal region and 290 … 390 ng/l near the estuaries. Trough the eight investigated rivers about 48 km³/a water run off into the Baltic Sea with about 20 t/a Hg. The total introduction of Hg into the Baltic Sea is estimated at 100 t/a with the river water, 35 t/a with precipitation and 35 t/a with dust.     

Spatial differences in persistent organochlorine pollutant concentrations between the Bering and Chukchi Seas (1993)

During August-September 1993, a joint Russian-United States expedition to the Bering and Chukchi Seas took place. Surface water samples were collected from 21 sites and separated into dissolved (duplicates) and suspended solids; 19 sediment and 6 air samples were also collected. These samples were analysed for 19 organochlorine pesticides, 11 chlorobenzenes and 113 PCB congeners. The report provides data on selected compounds which occured in > or = 75% of the water samples. Highest water concentrations were observed for HCH in open waters north and south of the Bering Strait, both regions being similar (alpha-HCH; 2.2 ng/L and lindane: 0.35 ng/L). Air levels observed were also constant (alpha-HCH; 0.041 ng/m3, lindane: 0.0093 ng/m3). Suspended solids and air particulares contributed little to the concentrations in their respective media, an observation common to all analytes except for the PCBs and the DDT residues. The sum of PCB concentrations in water were higher in the Bering Sea area compared to the Chukchi Sea (1.0 vrs 0.67 ng/L) and lower for air (0.46 vrs 0.23 ng/m3). Sum of DDT in water was higher in the Bering Sea than in the Chukchi Sea (0.23 vrs 0.15 ng/L) while in sediments and air, the Bering Sea concentrations were lower (0.95 vrs 1.6 ng/g and 36 vrs 56 pg/m3, respectively). Other organochlorine compounds for which data are presented include: pp'-DDE, pp'-DDT, dieldrin, HCB, 3 chlorobenzenes and 3 PCB congeners. Fluxes of all these chemicals through the Berin Strait are estimated; they ranged from 57 t/a (alpha-HCH) through 26 t/a (for sum of PCBs) to 0.2 t/a (pp'-DDE, dieldrin and 1,2,3-trichlorobenzene). Fugacity ratios for the HCHs and PCBs indicate the alpha-HCH is degassing in both the Bering and Chukchi Seas and that the gamma-isomer is degassing in the Bering Sea and is close to equilibrium (weakly absorbing) in the Chuchi Sea; the sum of PCBs are strongly absorbing in both areas.     

A Point-process Analysis of the Matsushiro Earthquake Swarm Sequence: The Effect of Water on Earthquake Occurrence

Temporal characteristics of the famous Matsushiro earthquake swarm were investigated quantitatively using point-process analysis. Analysis of the earthquake occurrence rate revealed not only the precise and interesting process of the swarm, but also the relation between pore water pressure and the strength of the epidemic effect, and the modified Omori-type temporal decay of earthquake activity. The occurrence rate function (t) for this swarm is represented well aswhere f(t) represents the contribution of the swarm driver, which was the erupting water from the deep in this case, and the second term represents an epidemic effect of the modified Omori type. Based on changes in the form of f(t), this two-year long swarm was divided into six periods and one short transitional epoch. The form of f(t) in each period revealed the detail of the water erupting process. In the final stage, f (t) decayed according to the modified Omori-formula form, while it decayed exponentially in the brief respite of the water eruption in the fourth period. When an exponential decay of swarm activity is observed, we have to be cautious of a sudden restart of the violent activity. The epidemic effect is stronger when the pressure of the pore water is higher. Even when the pressure is not high, the p value in the epidemic effect is small, when there is plenty of pore water. However, the epidemic effect produced about a quarter of the earthquakes even though there was not much pore water in the rocks.     

Chemical and Isotopic Composition of Waters and Dissolved Gases in Some Thermal Springs of Sicily and Adjacent Volcanic Islands, Italy

Hydrochemical (major and some minor constituents), stable isotope ( and , δ13C_TDIC total dissolved inorganic carbon) and dissolved gas composition have been determined on 33 thermal discharges located throughout Sicily (Italy) and its adjacent islands. On the basis of major ion contents, four main water types have been distinguished: (1) a Na-Cl type; (2) a Ca-Mg > Na-SO₄-Cl type; (3) a Ca-Mg-HCO₃ type and (4) a Na-HCO₃ type water. Most waters are meteoric in origin or resulting from mixing between meteoric water and heavy-isotope end members. In some samples, δ¹⁸O values reflect the effects of equilibrium processes between thermal waters and rocks (positive ¹⁸O-shift) or thermal waters and CO₂ (negative ¹⁸O-shift). Dissolved gas composition indicates the occurrence of gas/water interaction processes in thermal aquifers. N₂/O₂ ratios higher than air-saturated water (ASW), suggest the presence of geochemical processes responsible for dissolved oxygen consumption. High CO₂ contents (more than 3000 cc/litre STP) dissolved in the thermal waters indicate the presence of an external source of carbon dioxide-rich gas. TDIC content and δ¹³C_TDIC show very large ranges from 4.6 to 145.3 mmol/Kg and from –10.0‰ and 2.8‰, respectively. Calculated values indicate the significant contribution from a deep source of carbon dioxide inorganic in origin. Interaction with Mediterranean magmatic CO₂ characterized by heavier carbon isotope ratios ( value from -3 to 0‰ vs V-PDB (CAPASSO et al., 1997, GIAMMANCO et al., 1998; INGUAGGIATO et al., 2000) with respect to MORB value and/or input of CO₂-derived from thermal decomposition of marine carbonates have been inferred.     

The distribution of several organochlorine compounds in the Baltic Sea

Summary On a cruise, covering the whole Baltic Sea area, in May/June 1983, from the Kattegat through the Belt Sea, the Baltic Proper, and the Gulfs of Finland and Bothnia, investigations concerning the distribution of several organochlorine compounds were made. In accordance with the water exchange in the Kattegat and Belt Sea, a vertical stratification can be seen for -, -, -HCH and DDT — with higher concentrations in the outflowing surface water with low salinity and lower values in the inflowing bottom water with high salinity. The bottom water concentrations in the Kattegat and Belt Sea are increasing from North to South by mixture with surface water. East of the Darss Sill, the distribution pattern becomes more homogeneous with only slight differences in the average mean concentrations between the various basins forming the Baltic Sea.

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Über die Verteilung einiger Organochlorverbindungen in der Ostsee

Zusammenfassung Im Wasser des Kattegats, der Beltsee, der zentralen Ostsee, des Finnischen Meerbusens und der Bottensee wurden im Mai und Juni 1983 Untersuchungen auf Organochlorverbindungen vorgenommen. In Übereinstimmung mit den Verhältnissen des Wasseraustausches im Kattegat und der Beltsee kann man für -, -, -HCH und DDT eine vertikale Schichtung erkennen — mit höheren Konzentrationen im abfließenden Oberflächenwasser mit niedrigem Salzgehalt und niedrigeren Werten im einströmenden Bodenwasser mit hohem Salzgehalt. Durch Vermischung mit dem Oberflächenwasser steigen die Konzentrationen im Bodenwasser im Kattegat und der Beltsee von Norden nach Süden hin an. Östlich der Darsser Schwelle ergibt sich eine gleichmäßigere Verteilung mit nur geringen Unterschieden in den mittleren Konzentrationen innerhalb der einzelnen Becken, die die Ostsee bilden.

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De la distribution de quelques composants organochlorés dans la mer Baltique

Résumé En mai et juin 1983 des recherches sur la distribution de plusieurs composants organochlorés furent effectuées durant une campagne couvrant le Kattegat, les Belts, la mer Baltique centrale, les Golfes de Finlande et de Bothnie. En accord avec les échanges des eaux dans le Kattegat et les Belts, une stratification verticale de l'-, -, -HCH et DDT fut mise en évidence, avec une concentration plus forte dans les eaux superficielles sortantes et des valeurs plus faibles dans les eaux de fond entrantes. A l'Est du seuil de Drss, la répartition des échantillons devient plus homogène avec seulement de légères différences des concentrations moyennes entre les différents bassins qui forment la mer Baltique.

     

First- and higher-order dynamical controls on water exchanges between tidal basins and the open ocean. A case study for the East Frisian Wadden Sea

Observational data, high-resolution numerical modelling results and a simple analytical theory are combined in this paper to demonstrate the dependence of the volume transports through tidal inlets on topographical or morphological parameters of a Wadden Sea system. The area of interest covers the East Frisian Wadden Sea and consists of seven weakly connected tidal basins. The observations include time series of tidal gauge data and surface currents measured at a pile station in the backbarrier basin of the island Langeoog, as well as several ADCP transects in the Accumer Ee tidal inlet. The numerical simulations are based on the 3-D primitive equation General Estuarine Transport Model (GETM) with a horizontal resolution of 200 m and terrain following vertical coordinates. The model is forced at its open boundaries with sea-level data from an operational model for the German Bight (German Hydrographic Office). The simple theoretical concepts presented illustrate the effect of topography (hypsometry) in the tidal basins on the temporal variability of the exchange of water. This topographic control is effectuated through the bottom slope in the areas prone to drying and flooding. For our study area it takes about twice as long from slack water to maximum flood current than from slack water to maximum ebb current. The underlying physics of this signal modulation from a more or less harmonic forcing at the open-sea boundary and the quantification of the contributing physical processes are the major results of this paper. Estimates based simply on volume conservation are consistent with observations and results from numerical modelling, but they do not completely capture the actual non-linear tidal response. Our analysis shows that at least during part of the tidal cycle characteristic topographic parameters of the inlet/bay system have a major impact on the rate of exchange of waters between the Wadden Sea and the open ocean. This impact is especially strong during the transition between flood and ebb conditions. The possible morphodynamic responses are also addressed focusing on some common (universal) topographic features in seven tidal basins.Responsible Editor: Hans Burchard     

Occurrence of perfluorinated compounds in water, sediment and mussels from the Cantabrian Sea (North Spain)

Perfluorinated compounds (PFCs) have emerged as significant global environmental pollutants with persistent, bioaccumulative and toxic properties. The aim of this study was to determine the occurrence of PFCs in water (wastewater, submarine emissaries and port-waters), sediment and transplanted mussels in estuarine areas of high urban and industrial impact from Northern Spain. Five PFCs of industrial use were studied: perfluorooctanesulfonate, perfluorohexanesulfonate, perfluorobutanesulfonate, perfluorooctanoate acid and perfluorononanoate acid. After selective extraction, samples were analyzed by Ultra Performance Liquid Chromatography coupled to tandem mass spectrometry. ΣPFCs ranged from 0.06 to 10.9 ng/L in water, with higher levels in wastewater treatment plants effluents and port waters than in submarine emissaries. Little accumulation was observed in sediments and mussels with ΣPFCs ranging from 0.01-0.13 ng/g dw and 0.01-0.06 ng/g ww, respectively. Most ubiquitous compounds were PFOS and PFOA. Mass fluxes of PFCs to the Cantabrian Sea are estimated and the impact to the coastal ecosystem is discussed.     

Role of cold water and beta-effect in the formation of the East Korean Warm Current in the East/Japan Sea: a numerical experiment

The contributions of bottom cold water and planetary β-effect to the formation of the East Korean Warm Current (EKWC), the western boundary current in the East/Japan Sea (EJS), were evaluated using an idealized three-dimensional numerical model. The model results suggest that the bottom cold water and, to a lesser extent, the planetary β-effect both contribute to the formation of the EKWC. The cold water functions as the bottom of the upper layer, to control the EKWC via conservation of potential vorticity. It is known that cold waters, such as the North Korean Cold Water and Korea Strait Bottom Cold Water often observed during summer along the southwestern coast of the EJS, originate from the winter convection in the northern area. Observational studies consistently show that the EKWC strengthens in summer when the cold water extends further south along the western boundary.     

A global survey of perfluorinated acids in oceans

Perfluorinated acids and their salts have emerged as an important class of global environmental contaminants. Biological monitoring surveys conducted using tissues of marine organisms reported the occurrence of perfluorooctanesulfonate (PFOS) and related perfluorinated compounds in biota from various seas and oceans, including the Arctic and the Antarctic Oceans. Occurrence of perfluorinated compounds in remote marine locations is of concern and indicates the need for studies to trace sources and pathways of these compounds to the oceans. Determination of sub-parts-per-trillion (ng/L) or parts-per-quadrillion (pg/L) concentrations of aqueous media has been impeded by relatively high background levels arising from procedural or instrumental blanks. Our research group has developed a reliable and highly sensitive analytical method by which to monitor perfluorinated compounds in oceanic waters. The method developed is capable of detecting PFOS, perfluorohexanesulfonate (PFHS), perfluorobutanesulfonate (PFBS), perfluorooctanoate (PFOA), perfluorononanoate (PFNA), and perfluorooctanesulfonamide (PFOSA) at a few pg/L in oceanic waters. The method was applied to seawater samples collected during several international research cruises undertaken during 2002–2004 in the central to eastern Pacific Ocean (19 locations), South China Sea and Sulu Seas (five), north and mid Atlantic Ocean (12), and the Labrador Sea (20). An additional 50 samples of coastal seawater from several Asian countries (Japan, China, Korea) were analyzed. PFOA was found at levels ranging from several thousands of pg/L in water samples collected from coastal areas in Japan to a few tens of pg/L in the central Pacific Ocean. PFOA was the major contaminant detected in oceanic waters, followed by PFOS. Further studies are being conducted to elucidate the distribution and fate of perfluorinated acids in oceans.     

The role of sediments in the phosphorus cycle in Lake Lugano. II. Seasonal and spatial variability of microbiological processes at the sediment-water interface

P, Fe, Mn, and S species were analyzed in water samples from the sediment-water interface collected at four seasonally different times during the course of a year at two sampling sites in the southern basin of Lake Lugano (Lago di Lugano). The results reveal the strong influence of the biogeochemical processes in the sediment on the chemical composition of the lake water above. Consumption of oxygen and nitrate under oxic to microoxic conditions in the water column as well as sequential release of reduced manganese and iron under anoxic conditions was observed as a direct or indirect consequence of microbially mediated degradation of organic matter. The seasonal pattern observed for the release and the retainment of dissolved reduced iron and manganese correlates well with the one for dissolved phosphate. Iron, manganese and phosphorus cycling are coupled tightly in these sediments. Both sediment types act as sinks for hydrogen sulfide and sulfate. An inner-sedimentary sulfur cycle is proposed to couple iron, manganese and phosphorus cycling with the degradation of organic matter. Nutrient cycling at the sediment-water interface might thus be driven by a microbially regulated electron pumping mechanism. The results contribute to a better understanding of the role of sediment processes in the lake's internal phosphorus cycle and its seasonal dynamics.     

Hydrocarbons in the White Sea: Their inflow and transformation in the marine environment in different regions

Literary data have been used to assess the inflow of petroleum hydrocarbons (with river runoff, precipitation, wastewaters, sea transport, and at ice thawing) into different regions of the White Sea. The hydroecological CNPSi-model was used as an instrument to reproduce the annual dynamics of hydrocarbon concentrations at their parallel inflow and subsequent transformation in the waters of the nine White Sea regions (the bays of Kandalaksha, Onega, Dvina, and Mezen; the Solovetskie Islands; the deep-water part: Bassein, Gorlo, Voronka, and Chupa Bay). The calculations were based on normal annual values of monthly variations of water temperature, light intensity, and transparency, the morphometric parameters of the regions (water areas, mean depths, and water volumes) and water exchange between the regions and with the Barents Sea (calculated by a hydrodynamic model). The calculated concentrations of hydrocarbons, the biomasses and activity characteristics of hydrocarbon-oxidizing bacteria have been analyzed (their values were estimated for the 2-m surface water layer). The results of calculations were used to evaluate hydrocarbon balances for regions and the sea as a whole. The calculations demonstrate the balanced character of hydrocarbon fluxes, the balance discrepancy for the regions being <0.1–16.1%.