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1.
Announcement     
Cadmium, lead and copper have been determined in both dissolved and particulate phases for 130 surface-water samples from the coastal zone of Scotland and England in the western North Sea. The concentrations reported are, in general, lower than those published previously for the same area.The distribution of total metal concentration between the dissolved and particulate phases varies for the three elements. The lead distribution is dominated by its associations with particulate material while cadmium shows the reverse behaviour, existing almost totally in the dissolved phase. Copper is intermediate in behaviour, with the dissolved phase generally being dominant.An inverse relationship between salinity and dissolved copper concentration suggests a freshwater origin for this element. It is suggested that sedimentary and/or anthropogenic sources affect dissolved copper concentrations in coastal waters. The dissolved lead distribution reveals plumes of contaminated coastal water. The lead distribution is, however, dominated by associations with particulate material and sediments which produce a sharp concentration gradient close to the coast. The Humber estuary is identified as a significant source of cadmium to the North Sea.  相似文献   

2.
Dissolved electroactive concentrations of zinc, cadmium, lead and copper in river Rhine and North Sea samples have been measured at natural and lower pH values by differential pulsed anodic stripping voltammetry using a Kemula-type hanging mercury drop electrode. Average concentrations detected in North Sea samples at salinities ? 32‰ S and their range are (in μgl?1): 3.9 (2.0–7.5) for zinc, 0.23 (0.13–0.31) for cadmium, 0.3 (0.1–0.6) for lead and 0.3 (0.25–0.60) for copper (pH 8.1). The APDC-MIBK extracting/concentrating method, followed by AAS measurement applied to the same samples, resulted in 3.9 (2.0–7.5) for zinc, 0.11 (0.01–0.27) for cadmium, 0.5 (0.2–0.9) for lead and 1.6 (0.7–3.2) for copper. A fraction of the electroactive concentrations at pH 2.7 (6.1 for Zn) is electroactive at pH 8.1. The fractions are 100% for Cd, 20% for Cu, 13% for Pb and 40% for Zn. The remaining fractions are partly composed of organically bound species in solution. The low value for lead may be caused by the presence of particulate lead that is dissolved at low pH.Ionic copper and lead species, added separately to seawater at pH 8.1 are removed from the electroactive form, and taken up in (organic) complexes in the same ratio (at least for copper) as the species already present. Added ionic zinc is not removed within the time scale of the measurements (30 min). North Sea water at the natural pH has a complexing capacity, probably due to the presence of dissolved organic compounds, in a concentration equivalent to 3.10?7M copper. The complexing capacity is zero at pH 2.7. The usual method of standard addition for the determination of electroactive copper and lead concentrations may lead to erroneous results in samples where complexation of this type occurs.  相似文献   

3.
We analyse the distribution of the dissolved forms of cadmium, lead, cobalt, copper, and manganese in the near-Danube part of the Black Sea and in a section made at 45° 10′N in the autumn of 1997. It is shown that the discharge of rivers results in the appearance of significant amounts of cadmium, lead, cobalt, copper, and manganese in the near-Danube region. Copper is the most labile element in this collection of metals. Its behaviour is correlated with the vital activity of diatomic algae. The distribution of dissolved manganese in the near-bottom region is correlated with the distribution of O2. Indeed, the elevated concentrations of manganese are observed in the regions with low concentrations of oxygen. Translated by Peter V. Malyshev and Dmitry V. Malyshev  相似文献   

4.
Copper complexing ligand concentrations in the Daya Bay, Qingdao coast, Jiaozhou Bay, South China Sea and Huanghe Estuary waters were determined by the anodic stripping voltammetry technique. The distribution regularity and the relationship with other parameters were discussed. The results were as follows： Copper complexing ligand concentrations of the South China Sea were a little higher than those of other sea areas, and they were apparently higher than those of the ocean. Compared with the subsurface layer （SSL） in the sea surface microlayer copper complexing ligand concentrations showed an enrichment phenomenon, of which the mechanism is similar to dissolved organic matter. The metal complexing ligand concentration profiles of the South China Sea showed that the value in the sea surface was the highest, then it decreased with depth accruing, and a higher value appeared at the bottom. Copper complex- ing ligand concentrations were higher than those of cadmium and lead. Ligands in each sea area exhibited a complicated property. In short, the distribution regularity of copper complexing ligand concentrations in China＇s coastal waters was consistent with that of other regions in the world. Meanwhile, the positive relationship between the copper complexing ligand concentrations and biological oxygen demand, chemical oxygen demand, dissolved organic carbon, and viscosity were found clearly.  相似文献   

5.
Copper complexing ligand concentrations in the Daya Bay, Qingdao coast, Jiaozhou Bay, South China Sea and Huanghe Estuary waters were determined by the anodic stripping voltammetry technique. The distribution regularity and the relationship with other parameters were discussed. The results were as follows: Copper complexing ligand concentrations of the South China Sea were a little higher than those of other sea areas, and they were apparently higher than those of the ocean. Compared with the subsurface layer (SSL) in the sea surface microlayer copper complexing ligand concentrations showed an enrichment phenomenon, of which the mechanism is similar to dissolved organic matter. The metal complexing ligand concentration profiles of the South China Sea showed that the value in the sea surface was the highest, then it decreased with depth accruing, and a higher value appeared at the bottom. Copper complexing ligand concentrations were higher than those of cadmium and lead. Ligands in each sea area exhibited a complicated property. In short, the distribution regularity of copper complexing ligand concentrations in China' s coastal waters was consistent with that of other regions in the world. Meanwhile, the positive relationship between the copper complexing ligand concentrations and biological oxygen demand, chemical oxygen demand, dissolved organic carbon, and viscosity were found clearly.  相似文献   

6.
A detailed study of particulate and dissolved cadmium distributions on 83 seawater samples from six profiles in the open North Atlantic Ocean showed a relatively homogenous distribution. The mean concentration of cadmium was 60 ± 27 ng/kg and the median concentration of particulate cadmium was 0.2 ng/kg. Although there are regional differences in dissolved cadmium concentrations among stations, it is suggested that cadmium behaves essentially as an inert element in sea water.Particulate cadmium is enriched by about a factor of four in samples from less than 400 m compared to samples from deeper than 1000 m. The high concentrations in surface waters are suggested to be due to aeolian transport of anthropogenically derived cadmium.Additional analyses of cadmium in the Gulf of Maine show a mean value of 230 ng/kg. The higher values in the Gulf of Maine are ascribed to the influence of continental runoff. Twelve sediment samples from the open North Atlantic show a relatively homogenous distribution, ranging from 0.13 to 0.21 ppm on a dry-weight basis.  相似文献   

7.
Mar Chiquita Coastal Lagoon is located on the Atlantic coast of Argentina, and it has been declared a Biosphere Reserve under the UNESCO Man and Biosphere Programme (MAB). This coastal lagoon constitutes an estuarine environment with a very particular behaviour and it is ecologically important due to its biological diversity. The aim of the present study was to evaluate the distribution and geochemical behaviour of several heavy metals in this coastal system, focusing on their distribution in both the dissolved phase (<0.45 μm) and the suspended particulate matter. Therefore, the general hydrochemical parameters (salinity, temperature, turbidity, pH and dissolved oxygen) and concentration of total particulate and dissolved metals (Cd, Cu, Ni, Zn, Fe, Pb, Cr and Mn) were measured along 2 years (2004–2006) at two different sites. As regards their distribution, hydrological parameters did not present any evidence of deviation with respect to historical values. Suspended particulate matter showed no seasonal variation or any relationship with the tide, thus indicating that in this shallow coastal lagoon neither tides nor freshwater sources regulate the particulate matter input. Heavy metals behaviour, both in dissolved and particulate phases did not reveal any relationship with tide or seasons. Mar Chiquita Coastal Lagoon showed a large input of dissolved and particulate metals, which is probably due to intensive agriculture within the drainage basin of this system.  相似文献   

8.
中国近岸部分海域海水中金属络合配位体浓度的研究   总被引：7，自引：0，他引：7  
采用阳极溶出伏安法对黄河口、青岛近海、大亚湾和南海海域海水中的金属络合配位体的浓度进行了测定,同时探讨了其分布规律与相关参量的关系.结果发现:南海海域海水中的金属络合配体的浓度稍高于其他3个海域,且都明显高于大洋水的浓度;在微表层存在富集现象;在垂直分布上表层最大,然后随深度增加而降低,在底层有较大值;各海域配位体的性质呈复杂性;铜的络合配位体浓度大于镉和铅;总的来说与世界其他海域的分布规律是一致的.同时发现铜络合配位体浓度与BOD(生化需氧量)、COD(化学需氧量)、DOC(溶解有机碳)及黏度存在显著的正相关性.  相似文献   

9.
近年来由于环渤海经济圈的快速发展,渤海接受了来自周边河流、沿岸排污及海上油气开采所产生的大量的重金属等污染物质,使得渤海的生态环境系统面临前所未有的压力。本文采用电感耦合等离子质谱仪（ICP-MS）对采自渤海中部的25个表层沉积物样品中的Cu、Co、Ni、Zn、Pb、Cr、Cd等重金属元素的含量和赋存相态进行了分析,探讨了重金属分布规律、污染状况及来源。研究结果表明,Cu、Co、Ni、Zn、Cr在渤海湾的近岸区域和渤海中部泥质区有较高的含量,而Pb和Cd则在整个研究区的含量都较高;表层沉积物中Cu、Co、Ni、Zn、Cr主要以残渣态形式存在,而Pb和Cd则具有较高的非残渣态含量;生态风险评价结果表明该区表层沉积物未受到Co、Ni、Cr的污染,Cu、Zn、Pb和Cd则为未污染-中等程度污染。重金属元素Co、Ni、Cr以自然来源为主,在沉积物中的分布主要受沉积物物质组成的影响,而Cu、Zn、Pb,尤其是Cd,则受到了人类活动的显著影响。黄河沉积物是研究区表层沉积物中重金属的主要来源,影响范围涵盖了本区大部分区域,但在研究区的北端受到滦河来源物质的影响,渤海湾和研究区中部则受到海河物质和大气沉降来源重金属的一定影响。  相似文献   

10.
During the first year of the Northeast Pacific GLOBEC program we examined the spatial distributions of dissolved and particulate organic carbon and nitrogen in the surface waters off the Oregon and Washington coasts of North America. Eleven east–west transects were sampled from nearshore waters to 190 km offshore. Hydrographic data and the distribution of inorganic nutrients were used to characterize three distinct water sources: oligotrophic offshore water, the Columbia River plume, and the coastal upwelling region inshore of the California Current. Warm, high salinity offshore water had very low levels of inorganic nutrients, particulate organic carbon (POC) and dissolved organic carbon (DOC). Warm, low salinity water in the Columbia River plume was relatively low in nitrate, but showed a strong negative correlation between salinity and silicate. The river plume water had the highest levels of total organic carbon (TOC) (up to 180 μM) and DOC (up to 150 μM) observed anywhere in the sampling area. Cold, high salinity coastal waters had high nutrient levels, moderate to high levels of POC and particulate organic nitrogen (PON), and low to moderate levels of DOC and dissolved organic nitrogen (DON). Each of these regions has characteristic C:N ratios for particulate and dissolved organic material. The results are compared to concentrations and partitioning of particulate and dissolved organic carbon and nitrogen in other regions of the North Pacific and North Atlantic Oceans.  相似文献   

11.
Dissolved and particulate Mn concentrations were investigated on a seasonal scale in surface waters of the NW German Wadden Sea (Spiekeroog Island) in 2002 and 2003. As the Wadden Sea forms the transition zone between the terrestrial and marine realms, Mn was analysed in coastal freshwater tributaries and in the adjoining German Bight as well. Additionally, sediments and porewaters of the tidal flat sediments were analysed for Mn partitioning and microbial activity.Dissolved Mn concentrations show strong tidal and seasonal variation with elevated concentrations during summer at low tide. Summer values in the Wadden Sea (av. 0.7 μM) are distinctly higher than in the central areas of the German Bight (av. 0.02 μM), suggesting a possible impact of the Wadden Sea environment on the Mn budget of the North Sea. Seasonality is also observed for particulate Mn in the Wadden Sea (winter av. 800 mg kg− 1; summer av. 1360 mg kg− 1). Although particles are relatively Mn-poor during winter, the high SPM load during this season causes elevated excess concentrations of particulate Mn, which in part exceed those of the dissolved phase. Therefore, winter values cannot be ignored in balance calculations for the Wadden Sea system.Porewater Mn concentrations differ depending on sediment type and season. Maximum concentrations are found in surface sediments at a mixed flat site (190 μM) during summer, while winter values are distinctly lower. This indicates that enhanced microbial activity owing to higher temperature during summer leads to increased reduction of Mn-oxides in surface sediments and enhances the corresponding diffusive and advective Mn flux across the sediment-water interface. Draining of Mn-rich porewaters from sediments is also documented by analyses of tidal creek waters, which are highly enriched in Mn during summer.Furthermore, an important Mn source is freshwater discharged into the Wadden Sea via a flood-gate. The concentration of dissolved Mn in freshwater was highly variable during the sampling campaigns in 2002 and 2003, averaging 4 μM. In contrast, particulate Mn displayed a seasonal behaviour with increasing contents during summer. On the basis of salinity variations in the Wadden Sea, the total amount of Mn contributed to the Wadden Sea via freshwater was estimated. This balance shows the importance of the freshwater environment for the Mn inventory of the Wadden Sea. During winter the total Mn inventory of the Wadden Sea water column may be explained almost completely by freshwater discharge, whereas in summer the porewater system forms the dominating source.  相似文献   

12.
Heavy metal concentrations were measured in the Changjiang Estuary and its adjacent waters. Results from a systematic survey in April 2002 to March 2003 indicate that the ranges of the concentrations of dissolved copper, lead, zinc and cadmium in the study waters are 1.01 - 6.86, 0. 10 - 0.39,3.17 - 9.12 and 0.011 - 0. 049 μg/dm^3 , respectively. Similar to zinc, the behavior of dissolved copper was essentially conservative, but high scatter has been observed for high salinity samples, which can be attributed to the decomposition or mineralization of organic matter by bacteria. Dissolved lead may have active behavior with an addition at high salinity. Overall concentrations of dissolved cadmium increase with salinity. The mean values of these dissolved metals calculated for the surface waters were higher than those for the middle and bottom ones. External inputs of dissolved heavy metals to the surface waters were the likely explanation for these higher values. The maximum seasonal average values of dissolved copper and zinc were found in summer, reflecting higher amounts of riverine input in this season. In contrast, the maximum seasonal average values of dissolved lead and copper were found in winter and the lowest ones in summer, respectively, which might be asso- ciated with a combination of low concentration with heterogeneous scavenging. Concentrations of these dissolved metals found for the Changjiang Estuary fall in the range observed for the other estuaries but are noticeably higher than those from uncontaminated rivers, except for cadmium. Compared with observations for the Changjiang Estuary in the last two decades, it is clear that the Changjiang estuarine waters has been contaminated with copper, lead, zinc and cadmium during China＇ s industrialization, but concentrations of them have decreased in the last few years.  相似文献   

13.
In the spring of 1995, short-term variations in the concentration of particulate and dissolved dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) were monitored in the western Wadden Sea, a shallow coastal region in open connection with the North Sea. Significant correlations were found between abundance of Phaeocystis globosa and particulate DMSP; concentrations increased rapidly from 100 to 1650 nM in the middle of April. Highest DMS concentrations were found during the initial phase of the exponential growth of the bloom. DMS production and loss rates of DMSP and DMS were estimated experimentally during various phases of the bloom. DMS production and consumption were roughly in balance, with production only slightly exceeding consumption at the start of the bloom. Rates of production and consumption were highest during the exponential growth phase of Phaeocystis and declined in the course of the bloom (from 300–375 to less than 5 nmol dm−3 d−1). Demethylation of DMSP increased during the bloom (from 11 to 1300 nmol dm−3 d−1); it accounted for up to 100% of the DMSP loss at the end of the bloom. The shift from DMSP cleavage to demethylation in the course of a Phaeocystis bloom implies that DMS concentrations are not necessarily highest at the peak or towards the end of blooms.  相似文献   

14.
During a cruise on the North Sea and the North East Atlantic, about 90 samples were obtained from various depths. Concentrations of cadmium, copper, lead, nickel and zinc were determined by atomic absorption spectroscopy after separation/concentration using two different extraction methods. One, using APDC and MIBK, was applied directly on board while the other, using a mixture of dithiocarbamates and freon, was applied after storage under acid conditions. About half of the samples were also analysed for cadmium, copper and lead using ASV. The results of these determinations are intercompared. Consistent results were obtained for cadmium with the two extraction methods and for lead with the freon extraction method and ASV. In the other cases discrepancies were found.  相似文献   

15.
Weakly and strongly bound copper, lead and cadmium have been determined in the dissolved and particulate fractions of water samples from Oslofjord. The differentiation was made possible by using different sequences of filtration, acidification and digestion. The quantitative measurements were done by differential pulse anodic stripping voltammetry. Lead was found to be associated mostly with particulate matter, while cadmium was present only in the dissolved fraction. A strong digestion was needed for the determination of total metal. The advantage of pretreating sample bottles and filters with a conditioning solution is illustrated.  相似文献   

16.
Field sampling of the dissolved and particulate material field downstream of a large volume bucket dredge operating in the lower Thames River estuary near New London, Connecticut, was conducted in order to examine the magnitude and character of the dredge-induced resuspension. These data indicate that large amounts of dissolved phosphate, ammonia, silica, manganese, copper and particulate materials are released into the water column, whereas cadmium concentrations were unaffected. Concentrations in the vicinity of the dredge exceed background levels by two to nine times for the dissolved materials and by two orders of magnitude for particulates. During the ebb cycle, downstream material concentrations decrease rapidly to background within approximately 180 m for dissolved materials and 700 m for particulates.Two mechanisms were found to control the distribution of materials downstream of the dredge: (a) physical transport, including advection, turbulent mixing and diffusion, and (b) geochemical processes (i.e. adsorption, desorption, precipitation, dissolution, etc.). The concentration of dissolved materials downstream of the dredge decrease at a first order exponential rate. The downstream distribution of the dissolved ammonia and silica was found to be consistent with the reactivity experiments (Figure 8) which predicted that PO4 would undergo a decay in concentration in the presence of suspended sediments. Absorption of phosphate onto suspended sediments and gravitational settling of the suspended particulates were the processes. Manganese and copper underwent a dual transformation which involved an initial dissolution, followed by flocculation and possible coprecipitation as MnO2. Cadmium concentrations in the water column were unaffected by the dredging process due to low pore water concentrations.The observed spatial distribution indicates that dredge-induced injection of dissolved and particulate materials is primarily a near field phenomenon producing relatively minor variations as compared to those caused by naturally occurring storm events. These latter systems have been shown (Tramontano, 1978; Bohlen et al., 1979) to produce estuary-wide variations in suspended materials, PO4 and NH4 concentrations increasing the mass of materials in suspension by at least a factor of two. This increase in total suspended load, PO4 and NH4, is nearly an order of magnitude larger than that produced by the dredge.  相似文献   

17.
The geochemistry of dissolved copper-organic complexes was investigated in the estuarine waters of Narragansett Bay. A transect survey was conducted in August 1980, while one mid-bay station was monitored from March through August of that year. The transect data indicated that most of the copper-organic complexes enter the bay via sewage effluent which is discharged into the Providence River at the head of the bay. Organic copper concentrations in the estuary ranged from 0.12 to 2.30 μg kg?1 and comprised from 14 to 70% of the total dissolved copper. The concentration of copper-organic complexes was not directly related to the amount of dissolved organic matter; and recently generated organic material from phytoplankton production within the bay had a negligible influence on the fraction of dissolved copper which was organically bound.The major source of total copper to the bay is anthropogenic inputs from sewage effluents. Particulate and dissolved copper concentrations ranged from 0.06 to 2.42 and 0.23 to 16.4 μg kg?1, respectively, giving average values of about 40% particulate and 60% dissolved copper. Particulate copper concentrations decreased rapidly from the upper to the lower bay as a result of both removal and dilution. About 75% of the dissolved copper entering the bay is rapidly removed in the Providence River and upper bay, and the remaining portion (which is largely organic copper) follows conservative mixing in the mid to lower bay. The data suggest that copper binding by dissolved organic matter may be an important control on the riverine flux of dissolved copper through estuaries into coastal and oceanic waters.  相似文献   

18.
Dissolved copper concentrations in surface waters of the Bering Sea ranged from 106 to 882 ngl–1. Higher concentrations were found in continental shelf waters. In the northwestern North Pacific dissolved copper ranged from 54 to 140 ngl–1. Particulate copper concentrations varied regionally and seasonally from 6 to 79 ngl–1. Regionally averaged particulate copper concentrations decreased from 175 to 33g g–1 against an increase in suspended materials because of the dilution effects of biological fractions. Apparent sporadic increases in copper concentrations were found in the mixing area of the Kuroshio and the Oyashio waters. The feature is attributed to the lateral distribution of different water types rather than to the upwelling of deeper waters by eddies. In the same area west of 160E, waters with high concentrations of dissolved copper (96±9 ngl–1) were found. Their origin appears to be the continental shelf of the Bering Sea. In spite of intensive biological activity, a considerable fraction of copper added to shelf waters was transported to the area off Japan via the circulation in the Bering Sea and the Oyashio current.  相似文献   

19.
This paper gives the results of determination of cadmium, lead and copper in interstitial water of the coastal sediment, Seto Inland Sea, Japan by using anodic stripping voltammetry. An aliquot of 4–5 ml interstitial water separated from 30–70 ml of sediment is used for the simultaneous determination of ionic cadmium, lead and copper. No significant differences were observed on the content of trace metals between surface water and interstitial water of the top of the sediment.  相似文献   

20.
黄、东海海域溶解无解机砷分布特征与化学形态   总被引：2，自引：1，他引：1  
Distribution and chemical speciation of dissolved inorganic arsenic were examined in Yellow Sea and East China Sea. Results demonstrated that: (1) both As(III) and As(V) were detected, with As(V) domin...  相似文献   

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