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1.
Cathodic stripping voltammetry (CSV) is used to determine total (after UV-irradiation) and labile dissolved metal concentrations as well as complexing ligand concentrations in samples from the river Scheldt estuary. It was found that even at high added concentrations of catechol (1 m for copper and 0·4 m for iron) and of APDC (1 m for zinc) only part of the dissolved metal was labile (5–58% for copper, 34–69% for zinc, 10–38% for iron); this discrepancy could be explained by the low solubility of iron which is largely present as colloidal material, and by competition for dissolved copper and zinc by organic complexing ligands. Ligand concentrations varied between 28 and 206 n for copper and between 22 and 220 n for zinc; part of the copper complexing ligands could be sub-divided into strong complexing sites with concentrations between 23 and 121 n and weaker sites with concentrations between 44 and 131 n . Values for conditional stability constants varied between (logK′ values) 13·0 and 14·8 for strong and between 11·5 and 12·1 for weaker copper complexing ligands, whereas for zinc the values were between 8·6 and 10·6. The average products of ligand concentrations and conditional stability constants (a-coefficients) were 6 × 102 for zinc and 6 × 106 for copper.The dissolved zinc concentration was found to co-vary with the zinc complexing ligand concentration throughout the estuary. It is argued that the zinc concentration is regulated, in this estuary at least, by interactions with dissolved organic complexing ligands. A similar relationship was apparent between the dissolved copper and the strong copper complexing ligand concentration. The total copper complexing ligand concentrations were much greater than the dissolved copper concentrations, suggesting that only strongly complexed copper is kept in solution.These results provide evidence for the first time that interactions of copper and zinc with dissolved organic complexing ligands determine the geochemical pathway of these metals.  相似文献   

2.
The purpose of this study was to determine the long-term accumulation of either silver or copper from low concentrations in seawater by blue mussels, Mytilus edulis. Mussels raised from eggs in the laboratory to the age of 2·5 months (approximately 4·5 mm in length) were continuously exposed to 0, 1, 5 and 10μg/liter of either silver (nitrate) or copper (chloride) and sampled at 12, 18 and 21 months for growth studies, measurements of metal accumulation and histopathological examination.Whole-body soft tissues were analyzed for the presence of both silver and copper, as background levels of copper in the incoming seawater averaged 2–4 μg/liter. Mussels exposed to silver had accumulated significant amounts of silver only at the highest test concentration (10 μg/liter Ag) after 12 months, but at 18 and 21 months significant levels were accumulated at all three test concentrations. Mussels exposed to copper accumulated significant amounts of copper at 5 and 10 μg/liter Cu after all three sampling periods, but not at 1μg/liter. Silver-exposed animals also accumulated significantly greater amounts of copper than control animals.In a comparative study, field-collected juvenile mussels (approximately 16·1 mm in shell length) and adult mussels (approximately 53·4 mm in shell length) were exposed for 12 months to 0, 5, 25 and 50 μg/liter silver only and subsequently sampled for metal-accumulation analyses and growth measurements. Juvenile mussels accumulated significant amounts of silver at all test concentrations, with the exception of mussels exposed to 5 μg/liter Ag for 6 months. Copper accumulation in the silver-exposed juveniles was significant only at 50 μg/liter Ag after 6 months, but at all test concentrations after 12 months. Adult mussels exposed to silver accumulated significant levels of both silver and copper, but at somewhat lower levels than juveniles.In the growth study, silver had no effect on laboratory reared mussels at the highest concentration of 10 μg/liter tested, whereas copper at 10 μg/liter did appear to affect growth as early as 4 months after the start of experimental exposure. Field-collected juvenile mussels did show inhibition in growth after 6 months' exposure to 25 and 50 μg/liter Ag, with some growth occurring after 12 months. Adults also showed inhibition in growth after 6 months but not at 12 months.Histopathological examination of mussels exposed to either 5 or 10 μg/liter of copper for 18 months showed changes in the digestive diverticula, gastrointestinal tract, reproductive tract and muscle tissues. These changes were more noticeable in mussels exposed to 5 μg/liter Cu than in those exposed to 10 μg/liter. Mussels exposed to silver for 21 months showed yellowish to black particulate deposition in the basement membrane and connective tissue of the various organs and tissues. Silver deposition increased with increasing test concentration.  相似文献   

3.
Microcosms were used to assess the impact of copper mine tailings disposal on the littoral meiofaunal assemblages of the Atacama region of northern Chile. The specific purpose was to establish a cause and effect relationship between the elevated copper concentrations and altered meiofaunal assemblages observed at the study sites. Meiofaunal assemblages were exposed to a series of copper concentrations to assess general toxicity, both densities and taxa diversities decreased with increasing copper. Natural coarse sediments were mixed with a tailings substitute to assess the physical impact of the tailings dumping on meiofaunal assemblages. Meiofaunal assemblage densities increased with increasing amounts of tailings substitute, entirely due to an increase in surface utilising foraminiferans. However, taxa diversities decreased as the interstitial spaces became blocked. Finally, the microcosms were used to conduct bioassays of sediments and seawaters from the impacted sites. The sediments from the impacted sites proved to be toxic resulting in reduced meiofaunal densities and taxa diversities. Seawater samples did not prove to be significantly toxic. The use of microcosms has allowed the effects of the physical and chemical components of tailings to be assessed individually, which was not possible in the field. Additionally, it allowed a cause and effect relationship to be established between elevated concentrations of porewater copper observed in the field and the reduced densities and taxa diversities of the meiofaunal assemblages observed at the same sites.  相似文献   

4.
The concentrations of cadmium, copper, lead and zinc were measured at two locations in surface waters of the western North Atlantic. Samples were collected upstream of the research vessel in 1-1 teflon bottles, and in a 30-1 teflon-coated Go-flo bottle. Surface mixed-layer samples were also collected at each location by ship cast using this same Go-flo sampler. A comparison of the three sampling modes shows that all the samples taken with the Go-flo sampler possessed much higher concentrations of zinc (7–10-fold) and lead (2–3-fold) than those collected directly in teflon bottles. No apparent differences were noted at each station in the concentrations of either copper or cadmium among the samples collected by the three different procedures. The measured values for copper and cadmium in these waters are in good agreement with recent reports for the western North Atlantic.  相似文献   

5.
Pacific oyster, Crassostrea gigas Thunberg, embryos were exposed to copper and silver salts, alone and in combination, through the completion of embryogenesis and metal effects upon normal embryonic development were monitored. Copper concentrations throughout the test period ranged from 0·0 to 12·0 μg litre?1 while silver concentrations were between 0·0 and 18·0 μg litre?1.Administered individually, silver and copper yielded decreasing per cent normal embryonic development with increasing metal concentration. However, both metals exhibited ‘plateaus’ wherein per cent normal embryonic development did not decrease with increasing metal concentration until a particular concentration was attained. A rapid decrease in per cent normal embryonic development occurred with increasing metal concentrations greater than 6·0 μg litre?1 copper and 11·0 μg litre?1 silver.The dose-response patterns of copper and silver appear to be similar with copper exhibiting somewhat greater toxicity. At a copper concentration of 10 μg litre?1 only 50% of the embryos could be considered normally developed, whereas silver concentrations between 16·0 and 18·0 μg litre?1 yielded 50% normal embryonic development.Response surface methodology indicated that copper and silver interacted additively, with embryonic development affected to a much greater degree by copper than by silver. Optimum development of Crassostrea gigas embryos was greatly influenced by copper concentrations and occurred at all silver concentrations wherein the corresponding copper concentrations were 6·0 μg litre?1 or less. Above 6·0 μg litre?1 copper, per cent normal embryonic development was significantly reduced, even at the lowest tested silver concentrations.Abnormal embryos exhibited retarded shell growth, reduced size and extremely erratic swimming behaviour. These sublethal effects probably have a biochemical origin and would limit the organism's capacity to feed properly, escape predation and develop normally, thereby reducing the chances of successful metamorphosis and recruitment into the adult population.  相似文献   

6.
Determinations of copper consumption capacity (CuCs.C) and labile copper concentrations in surface coastal seawater, using a copper ion selective electrode (Cu-ISE) potentiometric method under predominantly diffusive conditions, are reported. For evaluation of the copper concentrations, the points of the endpoint contiguity zone of the CuCs.C titration curve were treated by an ISE multiple standard addition technique. The results were compared with those obtained by means of a Chelex-100 (calcic form) ‘batch’ procedure-potentiometric stripping analysis.The labile copper of the sample was determined at concentrations down to 10.70 nM with an average RSD of 12%, independent of the Cu-ISE employed. For adjacent subsamples, the mean CuCs.C values obtained for El Way seawater were equivalent to 81.05 and 48.00 nM copper, with an RSD of 4 and 7%, and for Isla Santa Maria seawater the value was equivalent to 70.27 nM copper, with an RSD of 7%. The theoretical approach of the electrode diffusive mechanism proposed, which would depend, fundamentally, on the adsorptive, complexing and reducing properties of the dissolved organic matter in the seawater sample, allows simultaneous analytical determination of CuCs.C and labile copper concentration in seawater.  相似文献   

7.
Benthic fluxes of copper, copper complexing ligands and thiol compounds in the shallow waters of Venice Lagoon (Italy) were determined using benthic chambers and compared to porewater concentrations to confirm their origin. Benthic copper fluxes were small due to small concentration differences between the porewaters and the overlying water, and the equilibrium concentration was the same at both sites, suggesting that the sediments acted to buffer the copper concentration. Thiol fluxes were ~10 × greater at 50–60 pmol cm?2 h?1, at the two sites. Porewater measurements demonstrated that the sediments were an important source of the thiols to the overlying waters. The overlying waters were found to contain at least two ligands, a strong one, L1 (log K′CuL1 = 14.2) and a weaker one, L2 (log K′CuL2 = 12.5). The concentration of L1 remained relatively constant during the incubation and similar to that of copper, whereas that of L2 was in great excess of copper, its concentration balanced by porewater releases and breakdown, probably due to uptake by microorganisms, similar to that of the thiol compounds. Similarity of the thiol and L2 concentrations and similar complex stability with copper suggest that L2 was dominated by the thiols. The free copper concentration ([Cu´]) in the Lagoon waters was lowered by a factor of 105 as a result of the organic complexation.  相似文献   

8.
亚致死剂量铜对文昌鱼和玫瑰无须钯的组织病理学影响   总被引:1,自引:0,他引:1  
采用半静水实验法测试研究了重金属Cu^2+对文昌鱼(Branchiostoma belcher)和玫瑰无须喜巴(Puntius conchonius)的急性致死毒性和亚急性毒性。实验结果表明,Cu^2+对文昌鱼和玫瑰无须喜巴24,48,72,96h的半致死浓度分别为0.561,0.373,0.261,0.211mg/L及0.976,0.783,0.562,0.473mg/L,其安全质量浓度分别为0.021和0.047mg/L。亚急性毒性实验中,文昌鱼和玫瑰无须喜巴分别用浓度为20%和30%的96h LC50的Cu^2+处理。不同器官的组织病理学观察结果表明,过量Cu^2+对玫瑰无须喜巴的鳃、肝脏、肾脏等器官产生毒害,对文昌鱼鳃和肝盲囊细胞也产生了严重的毒害,表现为细胞空泡化等明显的结构破坏。实验结果显示文昌鱼的肝盲囊和脊椎动物的肝脏一样,也是受过量铜显著毒害的主要靶器官器官。因此,文昌鱼的肝盲囊至少在经受过量Cu^2+毒害方面与脊椎动物肝脏具有相似性,从生理功能方面为类文昌鱼祖先的盲囊(digestive caecum)是脊椎动物肝脏的前体这一假说提供了资料。  相似文献   

9.
Metals are natural components in ecosystems; however, if these elements are in excess, they can have adverse effects on living organisms. This study analyzes the interference of copper, lead, iron and cadmium in acetylcholinesterase (AChE) and carboxylesterase (CbE) activities in zebrafish. AChE was significantly inhibited in vitro by copper, iron, lead and cadmium at higher concentrations (10 and 20 mmol/L), whereas CbE was inhibited only at a concentration of 20 mmol/L. In vivo, only lead and cadmium were able to cause AChE inhibition at higher concentrations, while iron didn't cause any changes, and copper promoted an increase in AChE activity at a concentration of 0.06 mg/L. CbE activity did not change at any of the times (two and seven days) and concentrations tested, except in the case of copper exposure, which resulted in a decrease in CbE activity. Indeed, iodoacetamide treatment didn't changed AChE neither CbE activities, results which indicate that the metal inhibiting effect is probably not due to its biding to thiol groups close the active site of the enzyme. This outcome reveals that metals are important esterase inhibitors in zebrafish, and should be considered in environmental monitoring studies that use esterase inhibition as exposure biomarkers of organophosphate and carbamate pesticides.  相似文献   

10.

Heavy metal pollution is an environmental issue globally and the aim of this study was to isolate endophytic fungi from mangrove wetlands of Sarawak to assess and test their ability to grow in the presence of various heavy metals (copper (Cu), zinc (Zn), lead (Pb), and chromium (Cr)). Samples of Nypa fruticans were collected from Kuching Wetland National Park (KWNP) for subsequent endophyte isolation. Ninety-three (93) isolates were obtained and assessed and the most resistant isolates (growing at concentrations up to 1000 ppm) were identified using fungal primers ITS 1 and ITS 4. All of the endophytic fungi were identified to be closely related to Pestalotiopsis sp. and this is to our knowledge the first study reporting the ability of Pestalotiopsis sp. to grow at high concentrations of copper, lead, zinc and chromium. Our results highlight the potential of using endophytic fungi for the treatment of heavy metal pollution, for example as biosorbents.

  相似文献   

11.
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   

12.
渤海中部表层沉积物中重金属赋存相态及来源   总被引:1,自引:1,他引:0  
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   

13.
The concentrations of a number of trace metals (Co, Ni, Cu, Zn, Ag, Cd and Hg) have been determined in sediments from cores collected in the Southampton Water region. Measurements of total hydrocarbons were also made on several of the cores. Markedly elevated concentrations of copper, up to 362 μg/g dry wt, were found in sediments which were collected close to the discharge points of oil refinery outfalls and which also showed concentrations of total hydrocarbons considerably greater than the background levels for the estuary. The results of selective chemical extractions showed that much of the copper was present in the non-lattice fraction of the sediment. Although the concentrations of Co, Ni, Zn and Cd were significantly correlated with those of copper in the core showing the highest concentrations of this element, these metals were not enhanced in comparison with the levels found in several other parts of the estuary. Variations in concentrations of metals in sediments throughout the estuary were not correlated with differences in organic carbon content.  相似文献   

14.
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   

15.
16.
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   

17.
Common dab were fed a casein based diet containing copper at a concentration of 1·4 mg copper kg−1 (dry weight) or a similar diet supplemented with 200 mg copper kg−1. Fish were sampled after 10 weeks and 20 weeks and hepatic and renal copper, zinc and metallothionein concentrations were measured. All hepatic cytosolic copper in test and control fish co-eluted from Sephadex G-75 with metallothionein, as did some of the cytosolic zinc. After 20 weeks there was three times as much of this metallothionein-bound copper in the livers of the test fish compared to the control fish, although metallothionein concentration was little elevated. On the basis of these results it is proposed that cytosolic liver copper concentration or heat stable liver copper concentration can be used as an indication of excess dietary copper in the dab Limanda limanda.  相似文献   

18.
The response of embryos of the American oyster, Crassostrea virginica, to various combinations of two or three metals (copper, mercury and zinc as the nitrates and chlorides) was studied in the laboratory at the optimal temperature and salinity regime for their development. The experimental design was a 3 × 3 × 3 factorial experiment using copper concentrations of 0,8 and 16 ppb; zinc concentrations of 0, 100 and 200 ppb and mercury concentrations of 0, 6 and 10 ppb. Highly significant toxic synergism was observed in the copper-zinc mixtures and three-metal mixtures of both salts, particularly at high concentrations. Although the chloride salt appeared to be slightly more toxic than the nitrate salt, the overall difference was not significant.  相似文献   

19.
We investigated the concentrations of cadmium, chromium, copper, iron, nickel, lead and zinc among feather tissues in sexes of Black-browed Albatross Thalassarche melanophrys killed in longliners off Argentina in 2005. We found no different metal concentration with sex for cadmium, copper, iron, lead and zinc in feathers of adult birds, though there were significant body-size differences between sexes. However, the concentrations of trace metals differed significantly among the type of feather within individual bird. The mean concentrations of copper, iron, and zinc in breast feathers of T.?melanophrys were lower than those reported for the species from Georgias del Sur/South Georgia, the southern Indian Ocean and for other seabirds' worldwide. While cadmium fall within the known range of concentrations for bird feathers lead were not. Our results may be indicating that level of pollution in Patagonia may not be as negligible as previously thought at least for some trace metals.  相似文献   

20.
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   

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