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1.
Dissolved and particulate trace metals (Cu, Cd, Pb, Zn, Ni, Fe and Mn) measured at six stations along the Scheldt estuary in October/November 1978 are compared with more recent data. Based on Ca content in the suspended matter, three distinct geochemical regions could be distinguished: the upper estuary (salinity 1–7) dominated by fluvial mud, mid-estuary (salinity 7–17) where the composition of the suspended matter remained relatively constant, and the lower estuary where marine mud prevailed. Re-suspension of sediments is the major factor controlling the composition of the particles in the upstream region. Anoxic conditions prevailed in the upper part of the estuary extending to a salinity of 15 in 1978, while at present the seaward boundary of the anoxic water body is located at less saline waters. Furthermore, the present-day metal load is much lower than in 1978. As a consequence of the changed situation, maxima in dissolved concentrations of redox-sensitive metals in the mid/lower estuary have moved as well, which affects the trace metal re-distribution pattern. In the anoxic zone, exchange processes between dissolved and particulate metal fractions were strongly redox regulated, with Fe and Mn as excellent examples. Iron was removed from the dissolved phase in the early stages of mixing resulting in an increase in the suspended particulate matter of the leachable ‘non-residual' Fe fraction from 2 to 3.5%. Due to its slower kinetics, removal of Mn from solution occurred in mid-estuary where oxygen concentrations increased. Cu, Cd and Zn on the contrary were mobilised from the suspended particles during estuarine mixing. External inputs of Pb, and to a lesser extent of Cu, in the lower estuary resulted in the increase of their particulate and the dissolved concentrations. Calculated Kd (distribution coefficient) values were used to assess the redistribution between the dissolved and particulate phase of the investigated metals. Due to the existence of the anoxic water body in the upper estuary, the importance of redox processes in determining the Kd values could be demonstrated. The sequence of Kd values in the upper estuary (Fe, Cd, Zn, Pb > Cu > Ni, Mn) is significantly different from that in the lower estuary (Fe > Mn > Pb, Ni, Zn, Cu, Cd). Thus, in such a dynamic estuary single metal-specific Kd values cannot be used to describe redistribution processes.  相似文献   

2.
The adsorption of trace metals (Pb, Zn, Cu, Cd and Hg) on calcite, kaolinite and bentonite has been studied in Krka river water of various salinities (S = 3, 20 and 38‰).Model experiments were performed at pH 8 in natural water and in UV-irradiated water samples to determine the importance of natural soluble organic matter. Cold vapour atomic absorption spectrometry was used for the Hg determination, and a differential pulse anodic stripping voltammetry (DPASV) method for determination of other trace metals, using either a hanging mercury drop electrode or a mercury-coated glassy carbon working electrode. The following results have been obtained on calcite:
1. (1) a powerful absorption of Pb and Zn was observed for both natural and UV-irradiated waters at S=20‰;
2. (2) a strong adsorption of Hg was observed in natural water, and significantly lower adsorption in UV-irradiated water at all three salinities, particularly at low salinity;
3. (3) Cd adsorption was of medium intensity in both waters at S=20‰;
4. (4) Cu was practically not adsorbable in both waters at S=20‰ if the total Cu ion concentration was lower than the copper complexing capacity value;
5. (5) Cu adsorption was of a medium intensity at S=38‰. It has not influenced by the EDTA model ligand.
Trace metals Pb, Zn and Cu are adsorbable on kaolinite and bentonite at S=38‰, whereas Cd is practically not adsorbed. The Krka River is a calcareous river, which supplies the sea with calcite and aluminosilicates. In the light of our model experiments, we suggest that the self-purification of the Krka River is remarkable in respect to Pb, Zn and Hg; this occurs to a lesser extent for Cu, and is negligible in the case of Cd.  相似文献   

3.
朱明  刘峰  陈璐  刘兆普 《海洋与湖沼》2018,49(5):975-982
我国黄海出现的绿潮发源于黄海南部苏北辐射沙洲紫菜养殖区,苏北沙洲区濒临的沿岸河网众多,来自沿岸径流的淡水携带大量氮磷等营养盐间歇性入海,导致海水的富营养化并伴随着盐度的周期性波动。本研究通过模拟实验研究低盐度(15和5)对浒苔吸收氮盐(NO_3~–-N和NH_4~+-N)和磷盐(PO_4~(3–)-P)的影响,主要发现:与盐度30相比,在低盐度(15和5)时,浒苔对NO_3~–-N的1h最大吸收速率(V_(max))和亲和力(V_(max)/Ks)分别提高280%和350%左右,半饱和常数(Ks)下降15%左右,并能够维持对NO_3~–-N的高效吸收(24h);盐度15和5时,浒苔对NH_4~+-N的1h最大吸收速率(V_(max))分别提高40%和200%,亲和力(V_(max)/Ks)分别提高20%和180%, Ks分别提高15%和30%,但是盐度降低对NH_4~+-N的长效吸收产生负面影响,甚至在盐度5条件下出现吸收高浓度NH_4~+-N后再释放的现象;与盐度30相似,盐度15条件下浒苔能够快速吸收PO_4~(3–)-P,而盐度5则导致藻细胞内的PO_4~(3–)-P在早期阶段快速流失,并在后期不能有效吸收PO_4~(3–)-P。本实验的结果表明,降低盐度有利于浒苔对氮源的快速吸收,在盐度15下浒苔能够实现对硝酸盐和磷盐的高效吸收。  相似文献   

4.
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   

5.
Laboratory radiotracer experiments were conducted to determine assimilation efficiencies (AE) from ingested algal food and oxic sediment particles, uptake rates from the dissolved phase, and the efflux rates of Cd, Cr and Zn in the Asiatic clamCorbicula fluminea. Among three elements, AE from both algal and sediment food was greatest for Cd, followed by Zn and Cr. The AEs of tested elements from algal food(Phaeodactylum tricornutum) were consistently higher than those from sediments at a given salinity and temperature. The influence of salinity (0, 4 and 8 psu) and temperature (5, 13 and 21¼) on the metal AEs was not evident for most tested elements, except Cd AEs from sediment. The rate constant of metal uptake from the dissolved phase (k u was greatest for Cd, followed by Zn and Cr in freshwater media. However, in saline water, thek u of Zn were greater than those of Cd. The influx rate of all tested metals increased with temperature. The efflux rate constant was greatest for Cr (0.02 d-1), followed by Zn (0.010~0.017 d-1) and Cd (0.006 d-1). The efflux rate constant for Zn in clam tissues depurated in 0 psu (0.017 d-1) was faster than that in 8 psu (0.010 d-1). Overall results showed that the variation of salinity and temperature in estuarine systems can considerably influence the metal bioaccumulation potential in the estuarine clamC. fluminea. The relatively high Cd accumulation capacity ofC. fluminea characterized by the high AE, high dissolved influx rate and low efflux rate, suggested that this clam species can be used as an efficient biomonitor for the Cd contamination in freshwater and estuarine environments.  相似文献   

6.
The pathway and fate of heavy metals were studied in 10m3 enclosures at Xiamen Bay in 1985. The dissolved metals added are removed rather quickly during the first days, and their half-removal times ( t1/2) (d) are as follows: Pb 5. 4-5. 8, Hg 6. 7-14, Zn 11-22, Cu 16 - 29, and Cd 30-89. Zinc is transferred biologically to particles during phytoplankton bloom. The main Fate of added metals after 27 days is as follows; over 80% Cd and 60% Cu remain in dissolved phase, more than 60% Pb and 50% Hg transfer to settling settlement, while Zn is equally distributed in dissolved phase and settling settlement. The wall uptake is less than 2% of the total metals added. Organic materials play an essential role in the partition and the transfer of heavy metals in water column. Terrigenous and autochthonous particles show different affinities to different metals. Most heavy metals associate weakly with zooplankton. The Binding of Cd, Pb, Zn and Cu to the particles shows distinctive features related to the diagenetic  相似文献   

7.
《Marine Chemistry》2001,75(3):229-248
Dissolved and particulate mercury and methylmercury concentrations were determined in the Southern Bight of the North Sea and the Scheldt estuary in the period 1991–1999. Mercury and methylmercury concentrations are higher before 1995 than after 1995, especially in the fluvial part.The North Sea: In the offshore stations, dissolved Hg concentrations are generally higher in winter than in summer while the reverse is true for particulate Hg KD values (KD=the concentration of particulate Hg (HgP in pmol kg−1) divided by the concentration of dissolved Hg (HgD in pmol l−1)) range from 100,000 to 1000,000 l kg−1. Dissolved methylmercury concentrations vary from 0.05 to 0.25 pmol l−1 in summer and from d.l. to 0.23 pmol l−1 in winter and particulate methylmercury concentrations from 1.8 to 36 pmol g−1 in summer and from 0.9 to 21 pmol g−1 in winter. The KD ranges from 9,000 to 219,000 l kg−1.The Scheldt estuary: In winter, dissolved Hg concentrations are elevated in the upper estuary, decrease exponentially in the low salinity range followed by a very slow decrease towards the mouth. In summer, they are low in the fluvial part, increase in the low salinity range or in the mid-estuary and sometimes show an increase in the lower estuary. Particulate Hg concentrations do not show any seasonal trend.Dissolved MMHg concentrations are much lower in winter, when maximum concentrations are found in the upper estuary, than in summer. In summer, the MMHg concentrations are low at low salinity, they show a first increase in the salinity range from 3 to 12, a decrease in the mid-estuary and a second increase in the lower estuary.The highest particulate MMHg concentrations are found in the upper estuary, while in the lower estuary generally lower and more constant values are observed. The ratio of dissolved MMHg to dissolved Hg (cruise averages between 1.3% and 20%), is higher than the ratio of particulate MMHg to particulate Hg (cruise averages of 0.27–0.90%). The KD values for MMHg are lower in the summer (30,000–65,000) than in autumn and winter (77,000–114,000).The Scheldt river: In the fluvial part of the Scheldt, dissolved increases in the most upstream stations, while particulate Hg shows no particular pattern. Dissolved MMHg ranges from 0.1 to 0.39 pmol l−1 and particulate MMHg from 3.1 to 43.5 pmol g−1. The MMHg concentrations are comparable to those found in the estuary and no seasonal variations could be observed.  相似文献   

8.
The natural human female hormones oestrone and 17β-oestradiol have been implicated in the disruption of endocrine systems in some wildlife adjacent to sewage effluents. The sorption behaviour of these two compounds under estuarine conditions was studied by spiking either 2.55 μg of oestrone or 2.65 μg of 17β-oestradiol in kinetic experiments. In equilibrium experiments, 3 ng of oestrone or 3.2 ng of 17β-oestradiol was added in each of the centrifuge tubes. Sorption onto sediment particles was relatively slow, with sorption equilibrium being reached in about 70 and 170 h for oestrone and 17β-oestradiol, respectively. The effects of a variety of environmental parameters on sorption were studied including salinity, sediment concentration (SC), the presence of a third phase, particle size and, also, surfactant concentrations. Results show that although salinity did not induce any statistically significant effect on the sorption of 17β-oestradiol, it did statistically enhance the sorption of oestrone, and a salting constant of 0.3 l mol−1 was derived. The partition coefficient for both compounds decreased with increasing sediment concentration, a phenomenon that has been widely reported and attributed to the presence of colloids (which could enhance dissolved concentrations). In this paper, the true partition coefficients for sediment particles (Kptrue) and colloidal particles (Kctrue) have been calculated, and a Kptrue value of 141 and 102 ml g−1 was obtained for oestrone and 17β-oestradiol, respectively. In addition, Kctrue values for oestrone (222×102 ml g−1) and 17β-oestradiol (135×102 ml g−1) were two orders of magnitude higher than their respective Kptrue values, suggesting that the colloidal particles are significantly stronger sorbents for natural oestrogens than sediment particles. Particles of different sizes were found to have different partition coefficients due to the strong relationships between partition coefficients for the two compounds and particulate organic carbon (POC) contents and specific surface areas (SSAs). The presence of a surfactant was shown to reduce the partition coefficients for the two compounds, although its concentrations being used were higher than those normally found in the natural environment.  相似文献   

9.
Suspended Particles: Their Role in Estuarine Biogeochemical Cycles   总被引：11，自引：0，他引：11  
Suspended particles are instrumental in controlling the reactivity, transport and biological impacts of substances in aquatic environments, and provide a crucial link for chemical constituents between the water column, bed sediment and food chain. This article reviews the role of suspended particles in the chemical and biological cycling of trace constituents (trace metals, organo-metallic compounds and hydrophobic organic micropollutants; HOMs) in estuaries, with particular emphasis on the effects of and changes to particle reactivity and composition.The partitioning (or distribution coefficient,KD ) and bioavailability of chemical constituents, and assimilation efficiency (AE) of such by bivalve suspension feeders, are identified as key parameters requiring definition for accurate biogeochemical modelling, and the discussion centres around the determination of and controls on these parameters. Particle-water interactions encompass a variety of physical, biological, electrostatic and hydrophobic effects, and are largely dependent on the character and concentration of suspended particles and salinity. The salinity-dependence results from the competing and complexing effects of seawater ions for trace metals, and the compression of water in the presence of dissolved seawater ions and consequent salting out of neutral solute (HOMs, organo-metallic compounds and some trace metal complexes). The extent of biological solubilization of chemical constituents from suspended particles is dependent on the nature of chemical components of the gastro-intestinal environment and their interactions with ingested particles, and the physiological (e.g. gut passage time) and chemical (e.g. redox conditions and pH) constraints imposed on these interactions. Generally, chemicals that associate with fine, organic-rich particles (or, for some HOMs, fine inorganic particles), and desorb at pH 5–6 and/or complex with digestive enzymes or surfactants are most readily solubilized in the gut. The extent of assimilation of solubilized chemical is then determined by its ability to pass the gut lining and partition into cytosolic material.In practice, KD and AE are determined experimentally by means of radiotracers added to contained suspensions or mesocosms, while operational measurement of bioavailability relies on in vitro chemical or biological (enzymatic) extraction of particles. What is lacking, however, and is identified as an ultimate goal of future research, is the ability to predict these parameters from theoretical principles and thermodynamic constants. Since many of the inherent interactions and mechanisms are controlled by particle composition and reactivity, a more immediate objective would be better characterization of the biogeochemical properties of suspended particles themselves. This includes chemical resolution of the bulk organic matter, definition of the abundance and synergistic effects of component sorbent phases, and determination of the effects of particle-seawater ion interactions on the reactivity of the particle surface.  相似文献   

10.
The effect of the flood water salinity on the mobility of heavy metals was studied for intertidal sediments of the Scheldt estuary (Belgium). Soils and sediments of 4 sampling sites were flooded with water of different salinities (0.5, 2.5, and 5 g NaCl L−1). Metal concentrations were monitored in pore water and surface water. To study the potential effects of flood water salinity on metal bioavailability, duckweed (Lemna minor) was grown in the surface water. The salinity was found to primarily enhance the mobility of Cd and its uptake by duckweed. Cadmium concentrations in pore water of soils and sediments and surrounding surface waters significantly exceeded sanitation thresholds and quality standards during flooding of initially oxidized sediments. Moreover, the effect was observed already at lower salinities of 0.5 g NaCl L−1. This implies that risks related to Cd uptake by organisms and Cd leaching to ground water are relevant when constructing flooding areas in the brackish zones of estuaries. These risks can be reduced by inducing sulphide precipitation because Cd is then immobilised as sulphide and its mobility becomes independent of flood water salinity. This could be achieved by permanently flooding the polluted sediments, because sulphates are sufficiently available in the river water of the brackish part of the estuary.  相似文献   

11.
The influence of salinity on growth and Cu uptake in the green macroalga Ulva reticulata collected from the intertidal area in the Western Indian Ocean was studied under controlled laboratory conditions. Exposure concentrations ranged from 5 to 500 μg Cu l−1 at five salinities (ranging 20–40). The accumulation of Cu increased with decreasing salinity, so that the uptake at 500 μg Cu l−1 was approximately 2.7, 2.4 and 2.0 times higher at salinities of 20, 25, and 30 respectively, than uptake at salinity of 35, and with uptake being lowest at salinity of 40. Ulva maintained a positive growth rate over the whole salinity range (20–40), with highest rates at salinity of 35. When exposing to Cu at low salinities (20 and 25), the growth rate of Ulva was strongly inhibited suggesting an increase in toxicity of Cu with decreasing salinity. EC50 and NOEC increased with increase in salinity, implying a reduced Cu toxicity at high salinities. It was concluded that salinity needs to be considered when using macroalgae, such as U. reticulata, as a bioindicator of heavy metals in areas with heavy rainfall, underground fresh water intrusion or in estuaries, as they might accumulate more metals and be more negatively affected.  相似文献   

12.
Experiments on the uptake of Zn and Cd by synthetic hydrous Mn oxides were carried out in an ionic medium at pH 3.5 and at pH 4. A slight preference for uptake of Cd2+ over Zn2+ was observed with both birnessite and nsutite, the Cd/Zn ratio being different for each mineral. Subsequently, the desorption of Zn and Cd from the obtained products in artificial seawater was studied. In this medium Cd is desorbed from the Mn oxides to a much higher extent than is Zn. The latter observations can be satisfactorily explained by the large difference of complex formation for the two metals in seawater, slightly counteracted by the preferential uptake of Cd2+ over Zn2+. The order of magnitude of the Zn/Cd ratio in natural manganese nodules is compatible with the ratio calculated on the basis of experimental results, taking fair estimates of the actual inorganic Zn/Cd ratio in seawater and of the pH of deep ocean water.  相似文献   

13.
The conditional acid dissociation constants (pKa′) of two sulfonephthalein dyes, thymol blue (TB) and m-cresol purple (mCP), were assessed throughout the estuarine salinity range (0<S<40) using a tris/tris–HCl buffer and spectrophotometric measurement. The salinity dependence of the pKa′ of both dyes was fitted to the equations (25 °C, total proton pH scale, mol kg soln−1):
The estimated accuracy of pH measurements using these calculated pKa′ values is considered to be comparable to that possible with careful use of a glass electrode (±0.01 pH unit) but spectrophotometric measurements in an estuary have the significant advantage that it is not necessary to calibrate an electrode at different salinities. pH was measured in an estuary over a tidal cycle with a precision of ±0.0005 pH unit at high (S>30) salinity, and ±0.002 pH unit at low (S<5) salinity. The pH increased rapidly in the lower salinity ranges (0<S<15) but less rapidly at higher salinities.  相似文献   

14.
Kinetics and the extent of metal partitioning between colloidal and dissolved phases and coagulation of metals associated with colloids were examined to determine their effects on the bioavailability of selected metals (Cd, Co, Hg, Ag, Fe, and Zn) to American oysters (Crassostrea virginica) using radiotracer and short term exposure experiments. After dispersion of radiolabeled colloids into low molecular weight (LMW, < 1 kDa) seawater, metal partitioning between dissolved (<1 kDa) and colloidal (1 kDa-0.2 microm) phases resulted in a consistent pattern, with a relatively constant percentage in the colloidal phase for each metal. On average, about 90% of Hg and Fe, approximately 60% of Ag and approximately 40% of Zn, Co, and Cd were measured in the colloidal fraction during a short term exposure experiment, consistent with their partitioning in natural waters. Controlled laboratory experiments carried out in parallel using radioactively tagged colloids showed that coagulation of colloidal species, quantified as the fraction retained by a 0.2 microm filter, was insignificant for most metals under the conditions and time periods of the uptake experiments. The bioavailability of colloidally complexed metals, measured in terms of dry weight concentration factor (DCF, ml g(-1)) and uptake rate constant (ml g(-1) h(-1)), was somewhat depressed compared with their counterpart in the LMW treatment, but could be well predicted from the results of the LMW treatment and metal partitioning. Both DCF values and uptake rate constants were higher in the LMW treatment than in the colloidal treatment. In addition, B-type metals, such as Ag, Hg, and Zn, all had higher values of DCF and uptake rate constants, regardless of treatments, except for Cd which had a lower DCF and uptake rate constant. In contrast, Co and Fe had significantly lower DCF values and uptake rate constants. Most of Hg and Ag (60-80%) were measured in the soft tissue of oysters in both LMW and colloidal treatments. In contrast, 80% of Fe, 75% of Co, and approximately 60% of Cd were observed on the shell, while Zn was found evenly distributed between shell and soft tissue of oysters. These results agree well with the variation pattern of both DCF value and uptake rate constant for these two groups of metals.  相似文献   

15.
Methylmercury (MeHg) concentration and production rates were studied in bottom sediments along the mainstem of Chesapeake Bay and on the adjoining continental shelf and slope. Our objectives were to 1) observe spatial and temporal changes in total mercury (HgT) and MeHg concentrations in the mid-Atlantic coastal region, 2) investigate biogeochemical factors that affect MeHg production, and 3) examine the potential of these sediments as sources of MeHg to coastal and open waters. Estuarine, shelf and slope sediments contained on average 0.5 to 1.5% Hg as MeHg (% MeHg), which increased significantly with salinity across our study site, with weak seasonal trends. Methylation rate constants (kmeth), estimated using enriched stable mercury isotope spikes to intact cores, showed a similar, but weaker, salinity trend, but strong seasonality, and was highly correlated with % MeHg. Together, these patterns suggest that some fraction of MeHg is preserved thru seasons, as found by others [Orihel, D.M., Paterson, M.J., Blanchfield, P.J., Bodaly, R.A., Gilmour, C.C., Hintelmann, H., 2008. Temporal changes in the distribution, methylation, and bioaccumulation of newly deposited mercury in an aquatic ecosystem. Environmental Pollution 154, 77] Similar to other ecosystems, methylation was most favored in sediment depth horizons where sulfate was available, but sulfide concentrations were low (between 0.1 and 10 μM). MeHg production was maximal at the sediment surface in the organic sediments of the upper and mid Bay where oxygen penetration was small, but was found at increasingly deeper depths, and across a wider vertical range, as salinity increased, where oxygen penetration was deeper. Vertical trends in MeHg production mirrored the deeper, vertically expanded redox boundary layers in these offshore sediments. The organic content of the sediments had a strong impact on the sediment:water partitioning of Hg, and therefore, on methylation rates. However, the HgT distribution coefficient (KD) normalized to organic matter varied by more than an order of magnitude across the study area, suggesting an important role of organic matter quality in Hg sequestration. We hypothesize that the lower sulfur content organic matter of shelf and slope sediments has a lower binding capacity for Hg resulting in higher MeHg production, relative to sediments in the estuary. Substantially higher MeHg concentrations in pore water relative to the water column indicate all sites are sources of MeHg to the water column throughout the seasons studied. Calculated diffusional fluxes for MeHg averaged  1 pmol m− 2 day− 1. It is likely that the total MeHg flux in sediments of the lower Bay and continental margin are significantly higher than their estimated diffusive fluxes due to enhanced MeHg mobilization by biological and/or physical processes. Our flux estimates across the full salinity gradient of Chesapeake Bay and its adjacent slope and shelf strongly suggest that the flux from coastal sediments is of the same order as other sources and contributes substantially to the coastal MeHg budget.  相似文献   

16.
于1990年10月 - 1992年7月在室内条件下测定黄河中游乌拉特前旗、包头黄河大桥及清水河地段水体中天然配体与铜、铅、锌、镉反应的络会容量（C?C），计算总条件稳定常数（K）和络合容量指数（I）。实验证明：乌拉特前旗水体中络合客量最大，包头和清水河相近。络合容量顺序为：Cu＞Zn＞Cd＞Pb，和可溶性有机碳及碳酸盐分析结果一致。总条件稳定常数为：KPbL最大，KCuL，KZnL，KCdL相近。和长江水做了比较。络合容量指数在IgK相近情况下，随络合容量增大而增大。  相似文献   

17.
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   

18.
The ability of the oyster to accumulate trace metals, particularly the transition metals (Cd, Cu, Zn, and Hg), from food and water has been well documented. There is little information, however, on how these metals interact to affect whole animal retention, partitioning, and binding to metallothionein (Mt). In this study oysters were exposed to Cd and Cu, both alone and in combination, and significant effects have been demonstrated on subcellular partitioning. These studies showed that Cu can displace Cd from Mt, but the Cd is not lost from the animal. Two metal-binding protein peaks have been separated by gel chromatography (<10 K and 24 K daltons). The lower molecular weight protein peak has been characterized as Mt, consisting of two isoproteins, but the higher molecular weight protein peak appears to be an aggregation of metal-binding proteins, some of which may be Mt or a Mt dimer. In environments that are contaminated with trace metals, Mt binds primarily Hg, Cu, and/or Cd and Zn, but in noncontaminated areas Mt binds primarily Zn on one of the two isoMts.  相似文献   

19.
Crangon crangon (L.) (Crustacea: Decapoda) were subjected to three metals (Cd, Cu and Zn) at respective concentrations (0·35, 1·6 and 14·4mg/litre) that would induce 50% mortality in 5–6 days. Significantly different (P < 0·05) rates of mortality occurred in the three groups, although their ET50's were almost identical. No moultstage-dependent mortality was observed for Cd, but in Cu and Zn the post-moult stages (A and B) were more susceptible than either the intermoult (Ca and Cb) or premoult (D0–D4) stages.No significant (P> 0·05) sex- or size-dependent mortality was evident at the tested concentrations of these metals.Feeding and ecdysis were inhibited in all metals after day 3 and development from one moult-stage to the next was greatly reduced in Cd.Possible modes of toxicity have been discussed in terms of the physiological condition inferred from the moult-stage at the time of death.  相似文献   

20.
The chemical speciation of Cu and Zn was investigated by voltammetric titration methods in the surface waters (10 m) of the western Black Sea during an Istanbul–Sevastopol cruise conducted in November 1998. Supporting parameters (temperature (T), salinity (S), pH, alkalinity (Alk), suspended particulate matter (SPM) and dissolved and particulate 234Th) were obtained in order to distinguish hydrographic features against involvement of the metals in biogeochemical processes. In the Turkish continental slope region, the cruise track intersected a narrow vein of colder water originating on the western shelf. The core of this cold water vein was characterised by a relatively low salinity, higher specific alkalinity and higher metal (especially Cu) and metal-binding ligand concentrations.A very large portion of Cu (93–99.8%) and Zn (82–97%) was organically complexed. The degree of complexation was highest in shelf waters and lowest in the central gyre. Titration data for Cu were modelled by two classes of organic binding ligands characterised by (CL1=3–12 nM, log K1′=13.1–13.9) and (CL2=20–70 nM, log K2′=9.4–11.2). These ligands occurred mainly in the ‘dissolved’ phase, as defined by 0.4-μm filtration. The stronger Cu-binding ligand seemed to be produced in situ in response to Cu concentration, whereas the weaker Cu-binding ligand appeared to be derived from terrestrial sources and/or reducing shelf sediments. Titration results for Zn were generally represented by one class of ligands (CL1=8–23 nM, log K1′=9.4–10.2), which were almost uniformly distributed between the ‘dissolved’ (78±8%) and the particulate phase (22±8%). The concentration of these strong Zn-binding ligands showed a very good correlation with SPM (r2=0.64), which improved when the dissolved ligands alone were considered (r2=0.78). It is hypothesised that these ligands were produced in situ by the bacterial breakdown of particulate organic matter.  相似文献   

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