首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
In 1984, on a transect covering the whole Baltic Sea and parts of the adjacent North Sea, 160 water samples were taken and analysed for their concentrations of particulate and dissolved metals. In addition, the suspended materials were investigated for their elemental bulk composition.The particulate fractions represented from about 5% (Cd, Cu and Ni) to 50% (Fe and Pb) of the total (particulate plus dissolved) concentrations. For some elements (Ba, Cd, Cu, Pb and Zn), the particulate matter from the surface microlayer was enriched with respect to those suspended materials taken from 0.2 m depth. This could reflect the atmospheric input of metal-rich aerosols. In anoxic deep waters, maximum contents of Zn (6400 μg g−1), Cu (1330 μg g−1) and Cd (12 μg g−1) were observed in the particulate matter, indicating sulphidic forms. On the other hand, under oxic conditions the distribution coefficients (Kd) decreased with the water depth (Cd, Fe and Pb).Relative to global background levels, the particulate matter contained metal “excesses” amounting to more than 90% of the total contents (Cd, Mn, Pb and Zn). Automated electron probe X-ray microanalysis (EPXMA) revealed that the elemental composition of sediments is mainly governed by post-depositional processes of early diagenesis and is only weakly related to the composition of suspended matter in the overlying water body. For instance, in relation to surface mud sediments of the central Baltic net-sedimentation basins, Zn, Cd, Cu and Mn had 30–100% higher levels in the suspended materials. The general pattern of metal contents of particulate matter taken from 10 m depth on a transect between the Bothnian Bay and the North Sea were—possibly as a result of anthropogenic inputs—rather similar for Pb, Zn and Cu. For Fe and Mn, the distribution patterns along the transect were probably governed by the natural loading characteristics and by the biogeochemistry of those elements.  相似文献   

2.
Anoxic sulfidic waters provide important media for studying the effect of reducing conditions on the cycling of trace metals. In 1987–1988, dissolved and particulate trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) concentrations were determined in the water column of the anoxic Drammensfjord basins, southeastern Norway. The iminodiacetic acid type chelating resin (Chelex 100) was used for the preconcentration of trace metals. The trace metal concentrations were determined using atomic absorption spectrophotometry (AAS), differential pulse polarography (DPP), and differential pulse-anodic stripping voltammetry (DP-ASV).It was observed that the trace metals Mn and Fe were actively involved in the processes of redox cycling (oxidationreduction and precipitation-dissolution) at the O2/H2S interface. The dissolved concentrations of Mn, Fe and Co showed maxima just below the O2/H2S interface. The seasonal enhancement in the maxima of both dissolved and particulate Mn and Fe at the redox cline is mainly governed by the downward movement of water which carries oxygen. An association of Co with the Mn cycle was observed, while the total dissolved Ni was decreased by only 10–35% in the anoxic waters. The dissolved concentrations of Cu, Zn, Pb and, to a lesser extent, Cd decreased in the anoxic zone.  相似文献   

3.
The biogeochemical behavior of the group of heavy metals and metalloids in the water (including their dissolved and suspended particulate forms), bottom sediments, and zoobenthos was studied in the Ob River estuary-Kara Sea section on the basis of the data obtained during cruise 54 of the R/V Akademik Mstislav Keldysh in September–October 2007. The changes in the ratios of the dissolved and suspended particulate forms of Fe, Mn, Zn, Cu, Pb, Cd, and As were shown, as well as the growth of the fraction of adsorbed forms in the near-bottom suspended particulate matter under the mixing of the riverine and marine waters. The features of the metals’ accumulation in the typical benthic organisms of the Ob River estuary and the Kara Sea were revealed, and their concentrating factors were calculated based on the specific conditions of the environment. It was shown that the shells of the bivalves possessing a higher biomass compared to the other groups of organisms in the Ob River estuary play an important role in the deposition of heavy metals. The mollusks of the Ob River estuary accumulate Cd and Pb at the background level, whereas the Cu and Zn contents appear to be over the background level.  相似文献   

4.
Between 1980 and 1984 extensive studies were carried out in the Baltic Sea on trace metals (Cd, Co, Cu, Fe, Hg, Mn, Ni, Pb and Zn) in water, suspended matter and sediments. The results enabled the influence of different factors on metal distribution patterns to be considered. The vertical profiles of dissolved and particulate metals in waters of the central deep basins reflect influences caused by oxygen deficiency and anoxic conditions in near-bottom water layers. Peculiarities at Station BY15 in the Gotland Deep included high dissolved Fe, Mn and Co concentrations and remarkable enrichment of Zn (0.64%), Cd (51 μg g−1) and Cu (0.15%) in particulate matter from the anoxic zone. Manganese-rich particles were accumulated above this layer.In fine-grained soft sediments below anoxic deep waters, maximum contents of Cd, Cu and Zn were observed, relative to other coring sites, between Bothnian Bay and Lübeck Bight. The Hg content in sediments probably reflects the joint flocculation with organic matter. Land-based sources seem to play the leading part for maximum lead contents.  相似文献   

5.
The concentrations of the trace metals Cd, Cu, Fe, Ni, Pb and Zn in the Göta River estuary have been investigated. The following metal fractions have been determined: acid-leachable, dissolved, labile and particulate.The estuary represents a salt wedge type estuary and is situated in a densely populated region of Sweden. The metal concentrations found for the dissolved fraction is in the range of what can be considered as background levels for freshwater. It is difficult to evaluate any estuarine processes other than conservative mixing for Cd, Cu, Ni and Zn. The dissolved levels in the freshwater end member are Cd, 9–25 ngl?1; Cu, 1·1–1·4 μgl?1; Fe, 20–75 μg l?1: Ni, 0·7–0·9 μg l?1: Pb 0·09–0·2 μg l?1; and Zn, 6–7 μg l?1:The results from the acid-leachable fraction show that at high suspended load the particles sediment in the river mouth. The trace metal levels in this fraction are subject to large variations.  相似文献   

6.
Radionuclides (i.e., 7Be and 210Pb) can be used to trace particle and sediment dynamics and to quantify coastal oceanic processes with time scales ranging from a few days to a hundred years. Here, we study the settling dynamics of suspended particles and the implication by sedimentary heavy metals in the Wenjiao/Wenchang River and Wanquan River estuaries through the measurement of the particulate 7Be and 210Pb nuclides. Activity in the particulate phase had a range of 2.1–54.5 and 4.6–67.9 Bq kg−1 for 7Be and excess 210Pb (210Pbxs), respectively, in the Wenjiao/Wenchang River estuary. In the Wanquan River estuary, activity is in the range of 1.2–43.5 Bq kg−1 for 7Be and 6.2–194.5 Bq kg−1 for 210Pbxs. At the same time, activity in the dissolved phase had a range of 0.46–1.26 and 0.30–1.17 Bq m−3 for 7Be and 210Pb, respectively, in the Wenjiao/Wenchang River estuary; ranges of 0.10–2.31 and 0.09–1.87 Bq m−3 for 7Be and 210Pb, respectively, were observed in the Wanquan River estuary. The distribution coefficients (Kd) for the two nuclides decreased within increased in suspended particle matters (SPM) concentration and/or salinity in Wanquan River estuary. The residence times of particulate 7Be and 210Pbxs had ranges of 0.4–1.6 and 1.65–5.15 days, respectively, in the Wenjiao/Wenchang River estuary; and ranges of 0.02–3.2 and 0.61–4.44 days, respectively in the Wanquan River estuary. All residence times for the two nuclides increased in the seaward direction. In the Wenjiao/Wenchang River estuary, we found that 11.8–21.0% of Cu, 3.0–9.0% of Zn and 43.2–69.9% for Cd is removed from the water column and deposited into the estuary, and 24.2–34.8% for Cu, 7.2–23.8% for Zn, and 70.0–82.5% for Cd in the Wanquan River estuary, respectively.  相似文献   

7.
The distribution, partitioning and concentrations of trace metals (Cd, Cr, Cu, Fe, Mn, Pb and Zn) in seawater, including dissolved and particulate phases, and in copepods in the ocean outfall area off the northern coast of Taiwan were investigated. Normalization of metal concentrations to the background metal concentration to yield relative enrichment factors (EF), which were used to evaluate the contamination of dissolved and particulate trace metals in seawater around the ocean outfall. The EF results indicated that the outfall area was significantly contaminated by dissolved Fe and Zn, and by particulate Fe, Cr, Cu, Pb and Zn. In addition, most trace metals were chiefly in the particulate phase. The average percentage of total metal concentrations (dissolved plus particulate phases) bound by suspended particulate matter followed the sequence Al(95%) = Mn(95%) > Pb(88%) > Cu(86%) > Fe(72%) > Zn(32%) > Cr(17.5%) > Cd(3.4%). Therefore, metal contamination is better evaluated in solid phase than in the dissolved phase. The concentration ranges of trace metals in the copepods, Temora turbinata, Oncaea venusta and Euchaeta rimana, near the outfall were: Cd, 0.23-1.81 microg g(-1); Cr, 16.5-195 microg g(-1); Cu, 14-160 microg g(-1); Fe, 256-7255 microg g(-1); Mn, 5.5-80.8 microg g(-1); Pb, 2.6-56.2 microg g(-1); Zn, 132-3891 microg g(-1); and Al, 0.21-1.13%. Aluminum, and probably Fe, seemed to be the major elements in copepods. The concentrations of trace metals in copepods, especially Temora turbinata, near the outfall were generally higher than those obtained in the background station. The mean increase in bioconcentration factor of metals in copepods ranged from 4 to 7 and followed the sequence Al(6.4) > Cu(6.2) > Fe(6.0) > Zn(5.7) > Pb(5.6) > Cr(5.5) > Cd(5.1) > Mn(4.7). Therefore, marine copepods in the waters of northern Taiwan can accumulate trace metals over background concentrations and act as contamination indicators.  相似文献   

8.
用原子吸收光谱法(AAS)和原子荧光光度法(AFS)测定了采集于北海银滩镇、厦门海门岛、宁德漳湾镇、乐清西门岛、温岭坞根镇、三门花桥镇等地区自然滩涂以及温岭坞根镇养殖区的可口革囊星虫(Phascolosoma esculentas)及其栖息地的底泥样品中Zn、Cu、Mn、Fe、Cd、Pb、Hg 和As 等8 种重金属含量, 并对检测结果进行了含量特征、生物体与栖息地底泥中重金属含量相关性分析、生物体重金属富集系数分析。结果表明: 不同栖息地可口革囊星虫间的重金属含量差异性显著(P<0.05), 各群体中Pb 含量均超过标准, 厦门海门岛群体中Cd 含量超标; 厦门海门岛、乐清西门岛自然滩涂栖息地和温岭坞根镇养殖区等底泥中重金属含量相对较高, 所有采样点底泥中Cu 含量以及乐清西门岛自然滩涂底泥中Cd 含量达到沉积物质量标准Ⅱ类; 可口革囊星虫对Zn、Cu、Fe 的富集系数均小于1, 对Mn、Cd、Pb、Hg 和As 的富集系数均大于1。Zn、Cu、Fe、Pb 和As 的富集系数在大部分群体间差异性较小; 可口革囊星虫中的Fe 和As 含量与底泥中的Fe 和As 含量高度正相关, Zn 和Hg 含量的相关性次之, 其余重金属元素含量的相关性较差。  相似文献   

9.
The concentration changes of 12 metals (As, Hg, Cd, Cr, Co, Cu, Pb, Mn, Ni, V, Zn, Fe, and Hg) in the soft tissues of Tapes philippinarum during growth were investigated. Clams were seeded in two contaminated areas of the Venice lagoon (San Giuliano and Fusina) and in an area of the Marano lagoon (Lignano Sabbiadoro) close to the clam-farm where the seed was produced. Metal trends were very different according to the considered element, the study site and the growth period.Arsenic was always higher in clam tissues than in surface sediments and suspended particles in all the three stations. Mercury, Cd and Cu were higher in the clams from Marano and Fusina but not in those from San Giuliano. Zinc and Co in clams exceeded the concentrations in the sediment and suspended particles only at Marano. The other elements (Cr, Pb, Mn, Ni, and Fe) were always higher in SPM and sediments. In general metal concentrations in clams were more highly correlated to concentrations in the suspended particles rather than in the surface sediments and in suspended clams rather than in bottom clams, nevertheless significant differences between stations and contaminants were found. Metal concentrations in clams were always lower than the European regulatory limits.  相似文献   

10.
Cadmium and copper in the dissolved and particulate phase and in zooplankton were determined in the Bahía Blanca estuary during six surveys from March to December 2005. Temperature, pH, salinity, dissolved oxygen, suspended particulate matter, particulate organic matter and chlorophyll-a were also considered. Dissolved Cd was below the detection limit (0.2 μg L−1) for almost the entire study period whereas Cu concentrations (0.5–2.4 μg L−1) indicated a continuous dissolved Cu input. Particulate Cd concentrations ranged from below the detection limit (<0.01) to 28.6 μg g−1 d.w. while particulate Cu ranged from below the detection limit (<0.04) to 53.5 μg g−1 d.w. Cd in mesozooplankton ranged from below the detection limit (<0.01) to 37.4 μg g−1 d.w. Some of the Cd levels were higher than those reported for other aquatic ecosystems. Cu in the mesozooplankton ranged from 1.3 to 89.3 μg g−1 d.w., values which were within the reported values or higher than other studies. The log of the partition coefficients (log (Kd)) of Cd was 0.04, while log (Kd) for Cu ranged from −0.39 to 2.79. These values were lower than both those calculated for other estuaries and the typical coefficients for marine environments. The log of the bioconcentration factor (log BCF) of Cd was 1.78, indicating that Cd concentration was higher in the zooplankton than in the dissolved phase. Log BCF of Cu ranged from 1.15 to 3. The logs of the biomagnification factors (log BMF) of Cd were low, with a range between −3.45 and 2.21 and those for Cu ranged from −0.1 to 3.35. Positive values indicate biomagnification while negative values indicate biodiminution. In general, no significant dissolved Cd concentration appeared to be present in the Bahía Blanca estuary and Cu values did not indicate a critical environmental status. The particulate phase seemed to be the major carrier for Cd and Cu and TPCu values were within the normal values for an anthropogenically stressed estuary but not for a strongly polluted system. This fraction was the most important metal source for the mesozooplankton. Moreover, the highest metal concentrations were in the mesozooplankton since most of the bioconcentration and biomagnification factors were positive, especially for Cu.  相似文献   

11.
A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn2+ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl?1, indicating that the oxidation of Fe2+ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.  相似文献   

12.
We report a simplified synthesis, and some performance characteristics, for 8-hydroxyquinoline (8-HOQ) covalently bonded to a chemically resistant TosoHaas TSK vinyl polymer resin. The resin was used to concentrate trace metals from stored, acidified seawater samples collected from Jellyfish Lake, an anoxic marine lake in the Palau Islands. The Mn, Fe, and Zn profiles determined from the 8-HOQ resin extraction were similar to those determined using Chelex-100 resin. The Zn and Cd profiles did not exhibit removal by sulfide “stripping” in contrast to other anoxic marine basins. The profiles of Co and Ni also exhibited elevated concentrations in the anoxic hypolimnion. The solution speciation and saturation states for the metals were calculated using revised metal-bisulfide stability constants. The calculations suggest that the MS(HS)− species dominates the solution speciation for Mn, Co, Ni, Zn, Cd, and Pb. Cu(I) is modeled as the CuS− or Cu(HS)2− species, while Fe(II) behaves as the free Fe2+ cation. The Mn, Co, Ni, Cu and Cd concentrations appeared to be at least 10-fold undersaturated, while the Fe(II), Zn, and Pb concentrations were close to saturation with respect to their metal sulfides.  相似文献   

13.
Concentrations of P and of heavy metals (Zn, Cd, Pb, Cu) were determined in sediment cores from the Peel-Harvey Estuary in Western Australia. Two cores were extracted, each representing one of the two basins of the estuary. Sediments were dated by surplus210Pb, by137Cs and by changes in the Fe/S ratio. Increasing exports of P from the mainly agricultural catchments have resulted in more than a doubling of both total P and acid extractable inorganic P in sediments of the estuary. Accumulation of P in the estuary is less than expected for complete retention of inputs of P from the major tributaries. Historical data show that since 1950 average concentrations of dissolved inorganic P have approximately doubled in the Peel Inlet and increased by times seven in the Harvey Estuary. Increases in concentrations in surface sediments of acid extractable Zn, Cd, Pb and Cu are noticeable in the Peel Inlet, and of Zn and Cd in the Harvey Estuary. The greatest increase, relative to background, is shown by Zn. Concentrations of extractable Zn and Cd in surface sediments are similar to those estimated from average concentrations in the water column for equilibrium adsorption to organic matter in sediments. Extractable Pb is greater than estimated for equilibrium adsorption to sediments. Extractable Cu is of the order of what can be expected for equilibrium adsorption to sediments in the Peel Inlet, but is less than expected in the Harvey Estuary.  相似文献   

14.
The behavior and budget of Mn, Cd and Cu in the Gironde estuary were investigated through data from both the water column (WC) and sediment depth profiles. In the estuarine freshwater reaches, Mn and Cd removal from and Cu addition to the dissolved phase occurs with a magnitude equivalent to 10%, 30% and 25% of their respective annual fluvial gross dissolved input, respectively. In the saline estuary, diffusive benthic outflow is the main source of dissolved Mn (74% of the total gross dissolved input within the estuary) to the WC. In contrast, Cd (96%) and Cu (89%) are mainly released into the dissolved phase of the WC from fluvial, estuarine and dredging-related particles through complexation (Cd) and organic carbon mineralization (Cu). Anthropogenic activities (sediment dredging) induce pore water inputs, particulate sulfide oxidation and sediment resuspension, significantly contributing to the metal budget of the WC. The related amounts of metals released could be equivalent to 20–50% (Cd) and up to 70% (Cu) of their respective net dissolved addition. Mass balances suggest that a large part of the metals previously released into the dissolved phase from processes within the estuary are removed by suspended particles due to (co-)precipitation of Fe/Mn (oxy)hydroxides and scavenging on autochthonous organic matter. On an annual basis, the Gironde estuary acts as a net sink of dissolved Mn, removing 60% of the dissolved fluvial inputs, and as a net source of dissolved Cd and Cu, contributing ∼ 85% and 20–45% to the dissolved Cd and Cu fluxes to the ocean.  相似文献   

15.
In the estuary of the river Scheldt, where an oxygen gradient exists in addition to the salinity gradient, redox processes will be of major importance for trace metal mobilisation. In this study, the influence of salinity and pH on the redox processes of dissolved Zn and Cd sulphides is investigated together with the effects on the ratio of the dissolved Zn and Cd concentrations. The speciation of these metals is calculated with the chemical equilibrium programme +. Zn sulphides are oxidised at lower oxygen concentrations than Cd sulphides, due to lower stability constants, causing a sudden increase or peak in the dissolved Zn/Cd ratio. The formation of dissolved Cd chloride complexes when oxidation occurs at high salinities (S=15) increases the mobility of Cd, causing a decrease in the Zn/Cd peak of the total dissolved concentrations. The peak is three to four times smaller at S=15 than when oxidation occurs at S=2. The simple model calculations compare very well with field data. The Scheldt estuary is suitable to illustrate these calculations. In the 1970s, the anoxic part of the estuary reached S=15–20, but since the early 1980s it has dropped to S=2–10. Historic data on metals in the estuary from 1978, 1987 and the 1990s were used to compare with the equilibrium calculations. The increase of the dissolved Zn/Cd peak at low salinity as a consequence, of the decreasing anoxic region is confirmed well by the data. The good agreement between model calculations and field data is a proof of the extreme importance of redox processes for the solubility of Zn and Cd sulphides in the estuary.  相似文献   

16.
The ratio of marine to fluvial suspended matter in the Scheldt Estuary was calculated by applying factor analysis to a data set of elemental concentrations. The data set consisted of 98 samples collected under various river discharge conditions. Each sample was analysed for the concentration of Cr, Pb, Fe, Mn, Ni, Co, Ba, Zn, Cu, Cd, S, Ca, Sr, Ag, Sn and Na. Five linearly independent processes were found to describe the variability of the elemental concentrations: (1) the supply of fluvial material to the mixing zone; (2) manganese oxidation in the transition area between the anoxic upper estuary and the oxic lower estuary; (3) the supply of marine material to the mixing zone; (4) a phytoplankton bloom in the lower estuary; and (5) the formation of insoluble metal sulphides in the anoxic high-turbidity zone. Scores of the first and third factor were used to calculate the ratio of marine to fluvial suspended matter in the mixing zone. Information on the origin of both the inorganic and organic fraction of suspended matter was obtained in this way.  相似文献   

17.
In June 1981, dissolved Zn, Cd, Cu, Ni, Co, Fe, and Mn were determined from two detailed profiles in anoxic Baltic waters (with extra data for Fe and Mn from August 1979). Dramatic changes across the O2H2S interface occur in the abundances of Cu, Co, Fe, and Mn (by factors of ?100). The concentrations of Zn, Cd, and Ni at the redox front decrease by factors between 3 to 5.Equilibrium calculations are presented for varying concentrations of hydrogen sulfide and compared with the field data. The study strongly supports the assumption that the solubility of Zn, Cd, Cu, and Ni is greatly enhanced and controlled by the formation of bisulfide and(or) polysulfide complexes. Differences between predicted and measured concentrations of these elements are mainly evident at lower ΣH2S concentrations.Cobalt proved to be very mobile in anoxic regions, and the results indicate that the concentrations are limited by CoS precipitation. The iron (Fe2+) and manganese (Mn2+) distribution in sulfide-containing waters is controlled by total flux from sediment-water interfaces rather than by equilibrium concentrations of their solid phases (FeS and MnCO3). The concentrations of these metals are therefore expected to increase with prolonged stagnation periods in the basin.  相似文献   

18.
陈水土  杨慧辉 《台湾海峡》1993,12(4):376-384
根据１９８７年３月至１９８８年１２月九龙江口，厦门西港海域的调查资料，初步探讨该海域Ｆｅ，Ｍｎ，Ｃｕ，Ｚｎ，Ｎｉ，Ｃｏ，Ｐｂ，Ｃｄ等重金属元素的生物地球化学特性，及其与磷的生物地球化学的关系。结果表明该海域重金属元素的分布主要受九龙江径流的影响。在河水与海水混合过程中，悬浮颗粒态重金属元素发生明显转移，Ｆｅ，Ｍｎ，Ｃｏ，Ｚｎ等元素自悬浮颗粒物上解吸，Ｃｕ可能被吸附，颗粒态重金属元素与颗粒态磷呈良好  相似文献   

19.
Water column samples have been collected in the outer channel of the Ferrol Ria (NW Spain) during four occasions over a tidal cycle. The objective was to study the exchange of dissolved and particulate Cd, Cu, Pb and Zn and particulate Al, Fe and Si between the ria and the adjacent coastal waters. This study provides the first extensive dataset on dissolved and particulate metal concentrations in the water column of a Galician ria. Typical concentrations of dissolved Cd (96 ± 31 pM), Cu (8 ± 4 nM), Pb (270 ± 170 pM) and Zn (21 ± 10 nM) were similar than in other European Atlantic shelf and coastal waters. The fraction of metals in the particulate phase followed the trend: Pb > Cu Zn > Cd. The outgoing water from the ria was enriched in dissolved and particulate Cu, Pb and Zn compared with incoming waters, whereas Cd concentrations were similar for both waters. The suspended particulate matter was composed of a mixture of marine and continental material. The latter end-member was found to arise from the metal-rich ria bed sediments, which is diluted by the dominant metal-poor marine end-member. The net output flux of Cu from the channel is balanced by the freshwater inputs to the ria, and the net Zn flux gave a positive output to coastal waters. For Pb, the net flux to the coastal waters is less than that input from the rivers, as a result of its particle reactivity and deposition in sediments. On the contrary, a net input flux of dissolved Cd from coastal waters was observed, highlighting the oceanic source of this metal in the Galician rias. Results from the budget calculations are in agreement with the differential geochemical behavior of these elements in coastal waters.  相似文献   

20.
Concentration and distribution of Fe, Zn, Cu, Cd, Mn, Pb, Ni among subcellular fractions (cellular membrane structures and cytosol) and Zn, Cu, Cd among cytoplasmic proteins in the kidney and digestive gland of musselModiolus modiolus living along a polymetallic concentration gradient were studied. It was found in the kidney ofM. modiolus from contaminated sites that the Fe percent increased in the “membrane” fraction, whereas Zn, Pb, Ni and Mn percent increased in the cytosol compared to the kidney of the control mussel. Note kidney cytosol ofM. modiolus from clean and contaminated sites sequestered major parts of Cu and Cd. In the digestive gland ofM. modiolus from contaminated sites Fe, Zn, Cd, Mn, Ni percent increased in the “membrane” fraction, whereas Cu, Pb percent increased in the cytosol compared to digestive gland of control mussel. Gel-filtration chromatography shows kidney ofM. modiolus contains increased metallothionein-like protein levels irrespective of ambient dissolved metal concentrations. It was shown that the metal detoxification system in the kidney and digestive gland ofM. modiolus was efficient under extremely high ambient metal levels. However, under complex environmental contamination in the kidney ofM. modiolus, the metal detoxification capacity of metallothionein-like proteins was damaged.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号