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.     

The dependence of organohalogen compound concentrations on herring age and size in the Bothnian Sea, northern Baltic

The concentrations and composition profiles of polychlorinated dibenzo-p-dioxins and dibenzofurans, polychlorinated biphenyls, polybrominated diphenyl ethers and polychlorinated naphthalenes were determined in herring individuals collected from the commercial catches of the Bothnian Sea, northern Baltic. The median age of herring was 5.0 years and in the muscle the median toxic equivalent concentration of PCDD/Fs was 5.6 WHO(PCDD/F)-TEQ pg/g fresh weight (fw) and that of PCBs 2.7 WHO(PCB)-TEQ pg/g fw. The median sum concentration of PBDEs was 1.4 ng/g fw and that of PCNs 0.1 ng/g fw. Differences in age-dependent accumulation between the organohalogen groups and individual congeners were major. In the Bothnian Sea the content of organohalogen compounds in herring is obviously elevated due to the availability and large proportion of Mysis crustaceans in their diet. More intensive fishing could reduce the concentrations of organohalogens, including the abundant, accumulative and toxic 2,3,4,7,8-PeCDF congener in the Baltic herring catch.     

Iodine-129 concentrations in marginal seas of the north Pacific and Pacific-influenced waters of the Arctic Ocean

Water sampling during the 1993 IV Russian–US Joint Expedition to the Bering and Chukchi Seas (BERPAC) indicates that Pacific Ocean burdens of the long-lived radionuclide ¹²⁹I are relatively low in the Pacific-influenced Arctic, particularly compared to high latitude waters influenced by the North Atlantic. These low concentrations occur despite the presence of potential submerged anthropogenic sources in the East Sea (Sea of Japan), and in the northwest Pacific Ocean, east of the Kamchatka Peninsula. The concentration of ¹²⁹I entering the Arctic Ocean through Bering Strait, 0.7×10⁸ atoms kg⁻¹, is only slightly higher than observed in deep Pacific waters. Similar concentrations (0.44–0.76×10⁸ atoms kg⁻¹) measured in Long Strait indicate no significant transfer of ¹²⁹I eastward into the Chukchi Sea in the Siberian Coastal Current from the Siberian marginal seas to the west. However, the concentrations reported here are more than an order of magnitude higher than the Bering Strait input concentration estimated (1.0×10⁶ atoms kg⁻¹) from bomb fallout mass balances, which supports other existing evidence for a significant atmospheric deposition term for this radionuclide in surface ocean waters. Near-bottom water samples collected in productive waters of the Bering and Chukchi Seas also suggest that sediment regeneration may locally elevate ¹²⁹I concentrations, and impact its utility as a water mass tracer. As part of this study, two deep ¹²⁹I profiles were also measured in the East Sea in 1993–1994. The near-surface concentration of ¹²⁹I ranged from 0.12 to 0.31×10⁸ atoms kg⁻¹. The ¹²⁹I concentration showed a steady decrease with depth, although because of active deep water ventilation, the entire 3000 m water column exceeded natural concentrations of the radionuclide. Atom ratios of ¹²⁹I/¹³⁷Cs in the East Sea also suggest an excess of ¹²⁹I above bomb fallout estimates, also possibly resulting from atmospheric deposition ultimately originating from nuclear facilities.     

Sources of polyfluoroalkyl compounds in the North Sea, Baltic Sea and Norwegian Sea: Evidence from their spatial distribution in surface water

The spatial distribution of 15 polyfluoroalkyl compounds (PFCs) in surface water was investigated in the North Sea, Baltic Sea and Norwegian Sea. In addition, an interlaboratory comparison of the sampling techniques and analysis was conducted. Highest concentration in the North Sea was found near the coast, whereas the ∑PFC concentration decreased rapidly from 18.4 to 0.07 ng l⁻¹ towards the open North Sea. The river Elbe could identify as a local input source for PFCs into the North Sea, whereas perfluorobutanoic acid (PFBA) was transported into the sampling area with the easterly current. In contrast to the North Sea, the distribution of PFCs in the Baltic Sea was relatively homogenous, where diffuse sources dominated. In general, the composition profile was influenced from local sources caused by human activities, whereas atmospheric depositions of here analysed PFCs were negligible, but it could have possibly an influence on low contaminated sites like the open North Sea or Norwegian Sea.     

Measurement of soluble reactive phosphorus concentration profiles and fluxes in river-bed sediments using DET gel probes

DET (diffusive equilibrium in thin films) gel probes were used for sampling river-bed sediment porewaters, to characterise in situ soluble reactive phosphorus (SRP) concentration profiles and fluxes. DET probes were deployed in three contrasting rural streams: (1) a headwater ‘pristine’ stream, with minimal P inputs from low intensity grassland and no point sources, (2) an intensively cultivated arable catchment, and (3) a stream subject to high P loadings from sewage effluent and intensive arable farming. The DET results showed highly enriched porewater SRP concentrations of between ca. 400 and 5000 μg-P l⁻¹ in the sewage-impacted stream. In contrast, the arable and pristine streams had porewater SRP concentrations <70 μg-P l⁻¹ and <20 μg-P l⁻¹, respectively. Porewater SRP concentration profiles in both the sewage-impacted and arable-impacted streams showed well-defined vertical structure, indicating internal sources and sinks of SRP within the sediment. However, there was little variability in porewater SRP concentrations in the pristine stream. The DET porewater profiles indicated net diffusion of SRP (a) from the overlying river water into the surface sediment and (b) from subsurface sediment upwards towards the sediment–water interface. A mass balance for the sewage-impacted site showed that the influx of SRP into the surface sediments from the overlying river water was small (ca. 1% of the daily river SRP load). The DET results indicated that, in the arable and sewage-impacted streams, the surface ‘cap’ of fine sediment may play an important role in inhibiting upward movement of SRP from subsurface porewaters into the overlying river water, under steady-state, low-flow conditions.     

Pesticides in Sediments From Queensland Irrigation Channels and Drains

Pesticide concentration in sediment from irrigation areas can provide information required to assess exposure and fate of these chemicals in freshwater ecosystems and their likely impacts to the marine environment. In this study, 103 sediment samples collected from irrigation channels and drains in 11 agricultural areas of Queensland were analysed for a series of past and presently used pesticides including various organochlorines, synthetic pyrethroids, benzoyl ureas, triazines and organophosphates. The most often detected compounds were endosulphans (, β and/or endosulphan sulphate) which were detectable in 78 of the 103 samples and levels ranged from below the limit of quantification (0.1 ng g⁻¹ dw) up to 840 ng g⁻¹ dw. DDT and its metabolites were the second most often detected pesticide investigated (74 of the 103 samples) with concentrations up to 240 ng g⁻¹ dw of ∑DDTs. Mean ∑endosulphan and ∑DDT concentrations were 1–2 orders of magnitude higher in sediments from the irrigation areas which are dominated by cotton cultivation compared to those which are dominated by sugarcane cultivation. In contrast to these insecticides, the herbicides diuron, atrazine and ametryn were the compounds which were most often detected in sediments from irrigation drains in sugarcane areas with maximum concentrations in areas of 120, 70 and 130 ng g⁻¹ dw, respectively. In particular during flood events, when light is limiting, transport of these photosynthesis inhibiting herbicides from the sugarcane cultivation areas to the marine environment may result in additional stress of marine plants.     

Distribution of Cs and Pu in the surface waters of the East Sea (Sea of Japan)

Surface and subsurface water samples for ¹³⁷Cs and ^239,240Pu analysis were collected in the East Sea (Sea of Japan) during August 1993. The ¹³⁷Cs levels of the surface waters are quite homogeneous in the East Sea (average = 3.1±0.2 mBq kg⁻¹). The ^239,240Pu levels vary from 6 to 10 μBq kg⁻¹ in the surface. ^239,240Pu to ¹³⁷Cs ratios in the surface water are within 0.002 to 0.003. The East Sea may be regarded as a part of the North Pacific Ocean in terms of ¹³⁷Cs dispersal in the surface, where the ¹³⁷Cs contents of the surface seawater seem to be controlled primarily by the atmospheric input. However, since our sampling was made just two months prior to the widely publicized Russian dumping incident on the 17th October 1993, our measurements may provide background data to assess the immediate impact of the Russian dumping on the levels of ¹³⁷Cs and ^239,240Pu in the East Sea.     

Hydrogen peroxide production rates in clean and polluted coastal marine waters of the Mediterranean, Red and Baltic Seas

The main aim of this study was to assess the hydrogen peroxide (HP) production rates (HPPR) related to anthropogenic pollution in coastal waters by laboratory and field experiments. HPPR's were assessed by simultaneous measurements of HP concentrations, cumulative solar UV irradiation and dissolved organic matter (DOM) fluorescence in the seawater samples at clean and polluted sites in the Mediterranean, Red and the Baltic Seas. The natural HP concentrations at all sites (8–100 nM) fall within the normal range recorded elsewhere, and follows a diurnal pattern. The polluted stations in the Mediterranean and Baltic Seas showed higher HPPR (3.2–16.6 nM m² W⁻¹ h⁻¹) than the clean stations, while in the Red Sea no significant differences were found because the station that was considered a priori polluted was actually rather clean (2–3 nM m² W⁻¹ h⁻¹). Laboratory experiments demonstrated that HPPR was positively linearly correlated to DOM fluorescence, however, this relationship was not found in the natural seawater samples examined in the field. The lack of relationship between HPPR and DOM in the field was attributed to enzymatic breakdown of HP as observed in dark decay experiments. HP dark decay rates were highest in polluted stations, probably due to larger bacterioplankton populations in these samples. Moreover, the HP dark decay rates were much lower in filtered than in non-filtered samples. Sun incubation of filtered (0.2 μm) seawater samples were performed to assess whether elimination of particles would yield higher HPPRs than in non-filtered samples. In the Baltic Sea (low UV irradiation) HPPR was higher in the filtered samples, while at sites with relatively high UV irradiation (Mediterranean and Red Seas), filtration of seawater did not stimulate HPPRs, probably due to UV-damage to planktonic microorganisms.     

Levels and patterns of polychlorinated dibenzo-p-dioxins, dibenzofurans and biphenyls in surface sediments from the western Baltic Sea (Arkona Basin) and the Oder River estuarine system

Surface sediment samples were collected from the western Baltic Sea (Arkona Basin) and the Oder River estuarine system in May and August 1995 and analysed for polychlorinated dibenzo-p-dioxins, dibenzofurans and biphenyls. Contents of PCDF (sum) and PCDD (sum) varied from 2.5 to 820.0 pg g⁻¹ dw and from 12.7 to 2991.0 pg g⁻¹ dw, respectively. PCB contents (sum of 23 congeners) ranged between < 130.0 and 16267.0 pg g⁻¹ dw. Only slight variations in PCDF/D and PCB contents on dry weight basis were found between the Oder River estuarine system and the open Baltic Sea. TOC-normalization of the data showed an approximately homogen PCDF/D distribution in the study area. The distribution pattern for PCDF/D and PCB may be attributed to high sediment dynamics combined with transport processes from the temporary sedimentation basin (Oderhaff) to the deeper parts of the Baltic Sea.     

Estrogen equivalent concentration of individual isomer-specific 4-nonylphenol in Ariake sea water, Japan

Concentrations of 4-nonylphenol (NP) were determined by isomer-specific quantification of individual NP isomers based on relative response factor (RRF) quantification with GC–MS in combination with steam distillation extraction. Concentrations of NP in the Ariake Sea decreased with distance from the river mouth (St.A; 49 ng NP/l) to offshore areas (St.C; 11 ng NP/l). Even the least concentration in water from St.C in Ariake Sea was sufficient to have adverse effects on barnacles. The isomers, NP1–NP14 were separated by GC–PFC and identified structurally with NMR. The isomers varied in estrogenic activity with NP7 exhibiting the greatest estrogenic activity with a potency that was approximately 1.9 × 10⁻³ that of 17β-estradiol (E2) in recombinant yeast screen system. The coefficient of variation (CV) of NP isomer’s concentrations among three samples at St.A, B and C were 4–75%. This suggests that NP isomers might be independently degraded in aquatic environmental samples. The predicted estrogenic activity of measured concentrations of NP in Ariake Sea was 2.7–3.0-fold greater than the measured estrogen agonist activity.     

Distribution and Fate of Organochlorine Pollutants in the Pearl River Estuary

Samples of surface sediment and suspended particulate matter (SPM) were collected from the Pearl River estuary, China, and the distribution and concentration of hexachlorocyclohexanes (HCHs), DDTs and polychlorinated biphenyls (PCBs) were extensively studied. The concentration ranges of HCHs, DDTs and PCBs in the sediments were 0.28–1.23 ng g⁻¹, 1.36–8.99 ng g⁻¹ and 0.18–1.82 ng g⁻¹, respectively. The concentrations of HCHs, DDTs and PCBs in the SPM varied both with the sampling locations and the season of collection. Higher concentrations were recorded in the SPM as compared with sediments. The distribution pattern of such organochlorine compounds (OCs), in the Pearl River estuary, showed that sources were some major river mouths and input from Shenzhen Bay. The concentrations of OCs were, however, low as compared with other estuaries and seas. The environmental fate of the OCs during estuarine mixing was determined, in part, by physicochemical and biochemical properties. The absorption and sedimentation of SPM were also considered important factors. Marine sediments may, therefore, be regarded as an important reservoir of hydrophobic and persistent OCs.     

基于镭同位素分布的黄海和东海垂直混合速率计算

在黄海和东海采样测定了水体中的镭同位素分布,用平流扩散模型描述镭同位素分布,最小二乘方法计算了垂直涡动扩散系数和上升流或下降流流速.结果给出北黄海中部、南黄海中部、浙江沿岸和台湾北部海域存在上升流,流速分别为0.46×10^-3cm·s^-1、0.17×10^-3~1.39×10^-3cm·s^-1、2.02×10^-3~3.04×10^-3 cm·s^-1和1.06×10^-3~2.51×10^-3 cm·s^-1.北黄海中部和东海东北部存在下降流.流速分别为-2.30×10^-3 cm·s^-1和-0.61×10^-3~-2.10×10^-3 cm·s^-1.计算同时给出的垂直涡动扩散系数为5.84~48.2 cm²·s^-1,平均值为22.3 cm²·s^-1.北黄海和浙江沿岸上升流流速与文献的结果一致;北黄海中部存在下降流与文献的结论一致.本研究结果与文献结果一致是对所建立的方法的肯定,也是对文献研究结果的支持.     

Vertical concentration profiles of lead in the Central Pacific at 15°N and 20°S

Concentrations of lead were measured in a surface transect and at two vertical profile stations (15°N and 20°S) in the Central Pacific. These measurements complement similar measurements made earlier in the North Pacific at 33°N and in the Northwest Atlantic at 34°N [1,2], as well as recent measurements of eolian lead input fluxes near each of these locations [3]. The new transect of surface water concentrations of lead corroborates previous measurements, which decrease from 13 ng/kg at 30°N to 4 ng/kg at 17°S in the Central Pacific [4]. This transect gradient is shown to overlie a similar geographic gradient of subsurface maximum concentrations of lead in the three Pacific vertical profile stations, decreasing from 14 ng/kg at 33°N to 11 ng/kg at 14°N to 2.5 ng/kg at 20°S. Lead concentrations at each of those locations exhibit maxima at 400 m, decreasing concentrations to 2500 m and approximately concentrations of 0.8–1.1 ng/kg below that depth. The subsurface maximum at the northwest Atlantic profile station (36 ng/kg at 34°N) is also congruent with surface water lead concentrations which decrease from 806 ng/kg to 32 ng/kg in an offshore transect from Rhode Island to 34°N, 66°W [5], and the shape of the Atlantic profile is congruent with those in the Pacific. There is a positive correlation between the magnitudes of eolian lead input fluxes and the magnitudes of the upper water maxima in lead concentration profiles at corresponding locations as follows: South Pacific easterlies 3 ng/cm² yr vs. 2.5 ng/kg; North Pacific easterlies 6 ng/cm² yr vs. 11 ng/kg; North Pacific westerlies 50 ng/cm² yr vs. 14 ng/kg; and North Atlantic westerlies 170 ng/cm² yr vs. 36 ng/kg.This relationship enables one to view the anthropogenic perturbations of the marine lead cycle on a global scale, since the industrial origin of eolian and seawater lead has been established by correlations between geographic patterns of industrial lead emissions to the atmosphere and isotopic ratios of industrial leads [3] and by geographic patterns of Pb/silicate-dust ratios and lead isotopic ratios in ocean surface waters [3–5]. These new data coupled with earlier biogeochemical data indicate that surface water concentrations of lead in the North Pacific and North Atlantic are now conservatively estimated to be 8 to 20-fold greater and those in the South Pacific are 2-fold greater than natural concentrations because of industrial emissions of lead to the atmosphere.     

The exceptional Oder flood in summer 1997 — distribution patterns of the oder discharge in the Pomeranian Bight

The exceptional Oder flood in summer 1997 was a unique event in order to investigate the impacts on and the consequences for the ecosystem of the Baltic Sea of about 6.5 km³ additional water loaded with nutrients and contaminants and discharged within only 5 weeks. About 15 institutions participated in this investigation in both the Szczecin Lagoon and the Pomeranian Bight. The Baltic Sea Research Institute Warnemünde studied the water and nutrient inflow, the spreading of the Oder discharge, and the impact of the discharge on the ecosystem. The main topic of the presented investigations is a detailed study of the spatial and temporal spreading of the extreme river discharge in the Pomeranian Bight and the southern Baltic Sea by satellite data, ship observations and continuous buoy measurements as well as numerical modelling. The meteorological conditions were characterized by mainly easterly winds which guided the outflowing riverine water along the German coast into the Arkona Sea. The spatial and temporal development of the distribution patterns of the Oder discharge was monitored by about 80 Sea Surface Temperature (SST) images of NOAA satellites. Shipborne measurements showed that the vertical extent of the Oder plume ranged between 5 and 7 metres. The concentrations of inorganic nutrients, except higher silicate, were comparable to typical winter/early spring values (seasonal maximum) in this region. The high dilution effect of the flood water reduced the concentration of contaminants and thus, prevented a direct negative impact of trace metals and chlorinated organic compounds on the marine environment. Coupled physical-biochemical modelling in combination with SST-images demonstrated the temporal development and satellite data in the visible spectral range delivered the maximum extent of discharged river water into the southern Arkona Sea where a further western transport was limited by the upwelling region off Hiddensee. Thus, all detected effects of the Oder flood were confined to the Pomeranian Bight and the southern Arkona Sea, without long-term consequences for the ecosystem.     

Monitoring of organic pollutants in coastal waters of the Gulf of Gdańsk, Southern Baltic

This paper presents an overview of changes in organic pollution of coastal waters of the Gulf of Gdańsk (Baltic Sea). Toxic pollutants including volatile organic compounds (VOC), volatile organohalogen compounds (VOX), chlorophenols, phenoxyacids, polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) were determined in seawater from the Gulf of Gdańsk coastal waters in the period 1996-2001. In the case of the Gulf of Gdańsk, non-conservative behaviour of VOC was observed due to random temporal and spatial of inputs along the Vistula estuary and to the dilution of VOC-enriched river water with seawater. The concentrations of VOX in seawater decreased throughout the period and the concentrations of VOX were in the range of few ng dm(-3) up to 250 ng dm(-3), similar to estuaries elsewhere. The average concentrations of chlorophenols and phenoxyacids were between 0.1 and 6.0 and 0.05 and 2.2 microg dm(-3), respectively. However, remarkably high concentrations of 2,4-dichlorophenol (6 microg dm(-3)) were obtained in samples collected from the Vistula River. Generally concentrations of PCBs did not exceed few ng dm(-3) with the exception of 1999, when all samples exhibited elevated concentrations of PCBs. In addition, higher concentrations of PCBs in the open sea compared to river waters suggested localised inputs. Due to the ability of most organic pollutants to bioaccumulate and biomagnify, especially the persistent organic pollutants, continued monitoring is of crucial importance for the health of marine life in the Gulf of Gdańsk.     

Heavy metals in Baltic herring and cod

The monitoring programme of harmful substances in selected species in the Baltic Sea was started in 1979. In the present study, three-year averages of Zn, Cu, Cd and Pb in cod liver (Hg in cod muscle) and herring muscle are reported. The concentrations of heavy metals in cod show areal differences roughly in accordance with the concentrations of heavy metals in sea water. No significant differences between heavy metal concentrations in North Atlantic and Baltic Sea species were found, except for mercury, for which values in the Baltic Sea species are lower than in those from the North Atlantic.     

Hydrocarbons in surface sediments from the Changjiang (Yangtze River) Estuary, East China Sea

Sedimentary aliphatic (AH) and polycyclic aromatic hydrocarbons (PAHs) were studied in the Changjiang Estuary and the adjacent East China Sea. Total AH ranged from 2.20 to 11.82 μg g⁻¹ and consisted of n-alkanes and a dominant petroleum-related unresolved complex mixture (UCM). Within the n-alkanes, terrestrial plant wax compounds prevailed at nearly all stations. Of the PAHs, biogenic perylene dominated at stations receiving riverine inputs. Anthropogenic PAHs originating from combustion/pyrolysis processes varied from 17 to 157 ng g⁻¹, while fossil PAH concentrations ranged from 42 to 187 ng g⁻¹. Both biogenic and anthropogenic hydrocarbons are primarily derived from riverine discharges and accumulate at shallow-water stations. Distinct phase associations lead, nevertheless, to different sedimentation patterns. Fossil PAHs are enhanced at offshore stations where they are introduced directly by shipping activities. Biomarker fingerprints ascribe their source to Chinese crude oils. The overall levels of anthropogenic hydrocarbons are low compared to relevant areas worldwide and reveal a low/moderate level of hydrocarbon pollution.     

Organochlorine micropollutants in the Jiulong River Estuary and Western Xiamen Sea, China

Organochlorine contaminants including 12 polychlorinated biphenyl (PCB) congeners and 18 insecticides were determined in water, pore water and sediments of the Jiulong River Estuary and Western Xiamen Sea, China. The results showed that the levels of the total PCBs ranged from non-detectable to 1500 ng l⁻¹ in water, from 209 to 3870 ng l⁻¹ in pore water, and from 2.78 to 14.8 ng g⁻¹ dry weight in sediments. Total organochlorine insecticide concentrations were from below the limit of detection to 2480 ng l⁻¹ in water, from 267 to 33400 ng l⁻¹ in pore water, and from 4.22 to 46.3 ng g⁻¹ dry weight in sediments. Concentrations of PCBs and insecticides in pore water were significantly higher than those in surface water, due to the high affinity of these hydrophobic compounds for sediment phase. The PCB congeners with the highest concentrations were CB153, CB180 and CB194, which together accounted for 68–87% of total PCBs in water, pore water and sediment. Among the hexachlorocyclohexane (HCH) compounds, beta-HCH was found to be a major isomer. Analysis of 1,1,1-trichloro-2,2-bis-chlorophenyl-ethane (DDT) and its metabolites showed that 1,1-dichloro-2[o-chlorophenyl]-2[p-chlorophenyl]-ethylene (DDE) was dominant in the group. In comparison to a 1998 study in the Western Xiamen Sea, levels of organochlorines were enhanced due probably to recent inputs and changes in sediments.     

Comparison of particulate matter distribution, in relation to hydrography, in the mesotrophic Skagerrak and the oligotrophic northeastern Aegean Sea

The seasonal vertical distribution of particulate matter (PM) was studied in two contrasting areas: (a) the mesotrophic Skagerrak (in the North Sea); and (b) the oligotrophic northeastern Aegean Sea (eastern Mediterranean). Similarities and differences of the PM distribution in the two areas are assessed with respect to the prevailing hydrographic conditions and the PM composition. Hydrographic conditions in both of the areas are characterised by strong density gradients, resulting from the inflow of low-salinity water, i.e. Baltic Sea water and Black Sea water for the Skagerrak and the northeastern Aegean Sea, respectively.Enhanced primary production and particles mainly of biogenic origin characterise the mesotrophic Skagerrak, whereas five-fold lower particle concentrations appeared in the oligotrophic Aegean Sea. The input of riverine particulates was limited in both of the areas. In the Skagerrak, the strong stratification resulted in particle accumulation on/above the pycnocline and the development of pronounced intermediate nepheloid layers (INLs). The pycnocline-related INLs were formed entirely by dinoflagellates. The pycnocline hindered the vertical movement and sinking rates of particles, thus favouring primary production. Particle horizontal advection along the density discontinuities was probably enhanced. This pattern was not observed in the stratified waters of the northeastern Aegean Sea, probably due to the very low particle concentrations and/or the fact that phytoplankton maxima appeared in deeper waters. Pronounced INLs were identified in the Skagerrak below the pycnocline; these are attributed to accumulated or advected dinoflagellate skeletal remains mixed with clay mineral particles. This was revealed only by means of SEM observations. X-ray diffraction analysis could not provide information on the type of phytoplankton present, because dinoflagellates form their skeletons from organic material. Frontal stations in the northeastern Aegean Sea exhibited pronounced vertical movement of particles towards the deeper waters. Benthic nepheloid layers (BNL) were observed in the Skagerrak; these were related to the resuspended fine-grained surface sediments. In the northeastern Aegean Sea, although near-bottom current velocities were sufficient to resuspend surface sediments, resuspension occurred only episodically. The BNLs here are related mostly to near-bottom phytoplankton growth.     

The impact of freshwater discharges on the ocean circulation in the Skagerrak/northern North Sea area Part I: model validation

We assess the performance of an eddy-recognizing numerical ocean model in simulating the pattern and variability of the hydrography in the Skagerrak/northern North Sea area. The model we use is a version of the widely used Princeton ocean model employing a terrain-following vertical coordinate. Results from a series of five multi-year simulations of the mesoscale response are described. The simulations differ in their representation of the lateral freshwater supply to the model ocean of which the first is a reference simulation. The next four are variations in which the river discharges and/or the Baltic outflow are given more realistic representations. For validation, we have used in situ hydrographic data. A novelty is that we use the concepts of freshwater height and potential energy anomaly as objective validation tools. We find that, in general, the model faithfully reproduces many of the observed hydrographic features including their mean patterns and their variance. Not surprisingly, we find that the Baltic outflow is by far the most significant freshwater source in terms of its influence on the hydrography in the area, a result corroborating earlier findings. The best validation is obtained when all freshwater supply is made as realistic as possible, in particular the Baltic outflow. We also find that the large scale cyclonic circulation and the location of fronts are robust characteristics of the Skagerrak/northern North Sea circulation given the impact changes in the freshwater input has on the hydrography. Finally, we find that a further exploration of the impact of the lateral open boundary forcing, e.g., the input of Atlantic water, is needed.