Trace metals: Cd, Cu, Pb and Zn in gelatinous macroplankton from the Northwestern Mediterranean

Gelatinous macroplankton organisms were collected in May 1984 in Villefranche-sur-Mer Bay and analysed for cadmium, copper, lead and zinc. Analyses were carried out by polarography for Cd, Cu and Pb and by flame atomic absorption for Zn. Phosphorus was also measured in the samples as a biomass parameter due to difficulties inherent in measuring dry weight of gelatinous organisms. The samples belong to the Tunicates, the Cnidarians (Hydromedusae, Siphonophores and Scyphomedusae), the Ctenophores and the Molluscs. Crustaceans living on some Tunicates were also sampled.As regards cadmium, copper and lead, mean concentrations did not show significant differences among the phyla studied: especially for Tunicates with mean values of 0.1 ng Cd μg P⁻¹, 2.0 ng Cu μg P⁻¹ and 0.9 ng Pb μg P⁻¹ and for Cnidarians with mean values of 0.5 ng Cd μg P⁻¹, 2.0 ng Cu μg P⁻¹ and 0.9 ng Pb μg P⁻¹ and for Cnidarians with mean values of 0.5 ng Cd μg P⁻¹, 2.0 ng Cu μg P⁻¹, 1.0 ng Pb μg P⁻¹. On the other hand, mean zinc concentrations were significantly lower in Tunicates (7.9 ng Zn μg P⁻¹) than in Cnidarians (36.8 ng Zn μg P⁻¹).Zinc seems to be preferentially concentrated in organisms which are rich in collagen, constituting the mesoglea, such as the Cnidarians, the Ctenophore and the gelatinous Mollusc studied, rather than in organisms rich in tunicin such as the Tunicates.     

Accumulation de quelques metaux lourds (Cd, Cu, Pb et Zn) chez l'eperlan (Osmerus mordax) preleve sur la rive Nord de l'Estuaire du Saint-Laurent

Heavy metals in trace amounts are normal constituents of marine organisms. At sufficiently high concentrations, heavy metals are toxic to living organisms and so it is important to know by how much their concentration may be increased before effects on marine or estuarine populations can be detected or commercial species become unsuitable as food. A method of removing metals is by storage in a particular tissue. Several different sites for storing metals were investigated and concentrations of Cd, Cu, Pb and Zn were examined in muscle, liver and gonads of the smelt (Osmerus mordax) from the North shore of the St Lawrence estuary. Copper and zinc are constituents of several enzymes and are absolutely essential for normal growth and development, while cadmium and lead are not known to have necessary physiological function. A modified wet digestion procedure was used to prepare biological samples for the determination of trace elements by flameless atomic absorption spectrophotometry procedure, using calibration standards made up in a matrix of similar acidity (Table 1). NBS reference material bovine liver was analyzed along with the samples and the results were within the specified tolerance (Table 2). Analyses were reported on a dry weight basis (Table 3) and the correlations with total body weight were determined by regression analysis. Copper (range 0.3–3.3 μg g⁻¹) and zinc (range 19–38 μg g⁻¹) in muscle fillets were found to be negatively correlated with total body weight (Fig. 1). Apparent decreasing concentrations in these two metal levels in muscle sample with increasing body weight were possibly due to factor such as dilution with growth. Growth may dilute metal concentrations in an organism if tissue is added faster than metal. Livers and gonads contained greater levels of the four metals than somatic muscle. Liver metal concentrations of Zn (range 29–108 μg g⁻¹) and Cd (range 0.06–0.37 μg g⁻¹) increased with total body weight. All equations fit data at P < 0.01 (Fig. 2). Positive correlations between size and metal concentrations suggest that net uptake may occur. Inessential, slowly exchanging metals such as Cd appear to reflect an uptake which tend to become a cumulative process (age dependence of concentrations). The occurrence of insignificant correlation between liver concentrations of Cu (mean value: 4 μg g⁻¹) and environmental concentrations of this metal was consistent with equilibration. Since fish are known to possess the metal binding protein metallothionein, a sequestering agent, detoxification of these metals in fish liver may be by sequestration rather than elimination. Increasing metal concentrations in liver may represent storage of sequestered products in that organ. In the gonads, no significant relationship exists between total body weight and trace metal contents. Results of t-test indicated that females had significantly greater Cu and Zn concentrations, but no significant difference existed between males and females for Cd concentrations (Figs 3 and 4). Thus, the relation between concentration and total body weight appears to be specific as to the species, tissues analyzed and environmental conditions. The comparison of metal concentrations in fish to assess variations in contamination levels requires understanding the relationship between metal concentration and body size within each population.     

Concentrations of heavy metals in small Norwegian lakes

As part of regional surveys of lakes in Norway the concentrations of Zn, Pb, Cu and Cd were measured in surface- and bottom-water samples collected from representative, small, pristine lakes (136 in southern Norway sampled in October 1974, 58 resampled in March 1975, and 77 in northern Norway sampled in March 1975). The lakes, a statistically representative sample of small lakes in Norway, were chosen such that their watersheds are undisturbed. Heavy-metal concentrations in these lakes thus reflect only natural inputs and anthropogenic inputs via the atmosphere.The generally low concentrations (Zn 0.5–12.0 μg l⁻¹; Pb 0–2.0 μg l⁻¹; Cu 0–2.0 μg l⁻¹; Cd 0.1-0.5 μg l⁻¹) measured in lakes in central and northern Norway provide estimates of natural “background” levels. These estimates may be too high because they include the global-scale deposition of heavy metals from the atmosphere which has increased as a result of industrial activities.Concentrations of Zn and Pb in lakes in southernmost and southeastern Norway lie above these “background” levels, apparently because of atmospheric deposition associated with the acidic precipitation that falls over southern Scandinavia. Increased heavy-metal concentrations in acid lakes may also be due to increased mobilization of metals due to acidification of soil- and surface-waters.     

Behavior of Mn, Fe, Cu, Zn, Cd and Pb discharged from a wastewater treatment plant into an estuarine environment

To obtain information on the fate of trace metals discharged to an estuarine environment, analyses have been made on water and sediment samples from Back River, MD., and on effluent from the large wastewater treatment plant that discharges there. Within 2–3 km of the outfall, the concentration (in μg 1⁻¹) of all metals decreases as follows: Mn, > 120-90; Fe, > 570-300; Cu, 53-7; Zn, 280-9; Cd, 3.5-0.5 and Pb, 31-<4. Except possibly for Mn and Fe, these decreases are much greater than can be ascribed to simple dilution, so physical, chemical or biological processes must be removing metals to the sediments. Correspondingly, sediment concentrations of Cu, Zn, Cd and Pb are approximately one order of magnitude higher than normally found in uncontaminated areas. After the initial decrease, concentrations of Mn and Cd in the water begin to rise again, suggesting remobilization from the sediments. Comparison of the estimated annual discharge of 8 trace metals to the Chesapeake Bay from wastewater treatment plants and from rivers suggests that the wastewater input may be within one order of magnitude of the fluvial input for Cr, Cu, Zn, Cd and Pb. Of the metals studied, Cd presents the greatest potential for serious pollution because its input from wastewater probably exceeds fluvial input, it appears to be readily remobilized from sediments, and it is known to be toxic to many organisms.     

Particulate and dissolved trace metals in Lake Ontario

Particulate metal concentrations in the nearshore waters of Lake Ontario have been determined to be 690 ng l⁻¹ for Cu; 40 ng l⁻¹ for Cd; 180 ng l⁻¹ for Ni; 1690 ng l⁻¹ for Zn; 2100 ng l⁻¹ for Mn; and 700 μg l⁻¹ for Fe. These values are considerably higher than the particulate metal concentrations in the offshore waters: 130, 8, 34, 230, 110, 260 and 9000 ng l⁻¹ for Cu, Cd, Ni, Zn, Pb, Mn and Fe respectively. In general, 50–80% of the Cu, 10–40% of the Ni, 20–60% of the Cd and >60% of the Pb in the lake water were bound to the suspended particulates. From the standing crop of the particulate metals and the estimated rates of their deposition on the lake bottom, the residence times of the particulate metals in the lake water column have been estimated to be about 0.5 yr. on the average. The suggestion is made that particulate organic matter may be an important vehicle for metal transport to the Lake Ontario sediments.     

Distribution of species of Cu, Pb, Zn and Cd in a water profile of the Yarra river estuary

The behaviour of Cu, Pb, Zn and Cd in a highly stratified estuary was examined. The distribution of ionic and ‘organically bound” forms of the metals was determined by differential pulse anodic stripping voltammetry (dpasv) before and after u.v. irradiation. The two forms of the metals were compared with the water characteristics of salinity, temperature, turbidity, flow, and inorganic and organic carbon.Irradiation increased the concentration of all four elements detectable by dpasv. The greatest increase was for Cu in the 1 m depth river water which yielded 7.5 μg l⁻¹ before irradiation and 29 μg l⁻¹ after irradiation. Cu and Cd showed minimum concentrations in the seawater layer at 4 m depth, corresponding to the fresh seawater flowing upstream below the halocline. The concentrations of Cu and Cd were higher in the river water than in the underlying seawater. Zn concentration in the river water was lower than in the seawater. Relationships between the trace metal concentrations and the characteristics of the water column are not clear, but the direction of water movement is a major influence.     

Restoration of heavily polluted branches of the Shatt Al-Arab river, Iraq

In view of the desire to improve the water quality of the heavily polluted branches of the Shatt al-Arab River at the City of Basrah, it was proposed to maintain effective flushing as well as contracting sewerage system. The present study was conducted in order to examine the water quality of these branches in an attempt to evaluate the effectiveness of the proposed flushing system. It has been found that their waters contained very low levels of dissolved oxygen and relatively high amounts of both COD and BOD₅. The annual average water quality parameters for Basrah Branches were: dissolved oxygen 3.4 ppm; pH 7.67; hydrogen sulphide 1.4 ppm; ammonia 97 μg-at. N l⁻¹; COD 15.9 mg l⁻¹; BOD₅ 12.7 mg l⁻¹; dissolved silicates 202 μg-at. Si l⁻¹; dissolved reactive phosphate 13.4 μg-at. P-PO₄³⁻ l⁻¹; nitrate 10.4 μg-at. N-NO₃⁻ l⁻¹; nitrite 2.1 μg-at. N-NO₂⁻ l⁻¹ and chlorophyll-α 14.3 mg m⁻³. Based on our calculations, it has been concluded that the proposed system is effective, thus within a flushing cycle all of the above mentioned parameters will become within the acceptable values of the Shatt al-Arab water quality. Moreover, this system has no appreciable effect upon the water quality characteristics of the Shatt al-Arab River due to the fact that it discharges a high volume of water annually. However, It has been recommended to dredge the deposited sludge to a minimum depth of 50 cm.     

Speciation (including adsorbed species) of copper, lead, nickel and zinc in the Meuse River: Observed results compared to values calculated with a chemical equilibrium computer program

The adsorption of trace metals on sediments of the Meuse River was interpreted in terms of competition between metals and protons for surface sites. Surface constants (^*β₁^surf) were determined for Cu, Zn and Cd (10^−1.8, 10^−3.6 and 10^−3.7). The constants for Pb, Ni, Ca and Mg (10^−1.7, 10^−3.8, 10^−6.5 and 10^−5.2) were estimated using a correlation between hydrolysis and surface constants. A chemical equilibrium computer program in which surface sites (for adsorption reactions) are treated as conventional ligands was used to calculate the speciation of Cu, Pb, Ni and Zn in the Meuse River. Calculated values of the adsorbed/dissolved distribution agreed well with observed values, after some realistic data manipulation. This work indicates that dissolved trace metal concentrations in the Meuse River are controlled by adsorption and not by precipitation mechanisms. The relationship between organic matter and suspended matter greatly influences the adsorption of metals like Cu and Pb.     

Comparative bioaccumulation of mercury in two adjacent freshwater ecosystems

Mercury levels were determined in sediments, clams and representative fish species in two adjacent uncontaminated waterbodies situated on the Ontario Precambrian Shield. Food chain biomagnification of mercury occurred within both ecosystems. Significantly higher mercury levels were observed in most species resident in Tadenac Lake than in Tadenac Bay. For example, mean length adjusted fish mercury levels in Tadenac Lake and Tadenac Bay, respectively, were: smelt, 0.26 and 0.12 μg g⁻¹; rockbass, 0.34 and 0.18 μg g⁻¹; yellow perch, 0.29 and 0.12 μg g⁻¹; smallmouth bass, 0.55 and 0.25 μg g⁻¹ and northern pike 0.86 and 0.38 μg g⁻¹. The observed differences in fish mercury levels between the two sites cannot be explained in terms of differences in fish growth rates, lake trophic status or fish selenium levels, but appeared to be related to sediment mercury levels and ambient water quality.     

Submersible integrating water sampler for heavy metals

A simple submersible apparatus for the collection of a continuous composite water sample, suitable for heavy metal determination, is described. A comparison between results obtained for Cd, Pb, Cu, Zn and Hg using this sampler and a series of hand collected samples showed a satisfactory level of agreement. The apparatus is suitable for pollution monitoring purposes in relatively shallow (<20 m) waters where the concentrations of Cd, Pb, Cu, Zn and Hg are expected to exceed 0.05, 0.2, 0.2, 0.4 and 0.02 μg l⁻¹ respectively.     

Total metal concentrations and partitioning of Cd, Cr, Cu, Fe, Ni and Zn in sewage sludge

Application of the BCR three-step sequential extraction procedure to sewage sludge samples collected at an urban wastewater treatment plant (Dom ale, Slovenia) is reported. The total concentrations of Cd, Cr, Cu, Fe, Ni and Zn and their concentrations in fractions after extraction were determined by flame or electrothermal atomic absorption spectrometry (FAAS, ETAAS) under optimised measurement conditions. Total acid digestion including hydrofluoric acid (HF) treatment and aqua regia extraction were compared in order to estimate the efficiency of aqua regia extraction for determination of total metal concentrations in sewage sludge. It was found experimentally that aqua regia quantitatively leached these heavy metals from the sewage sludge and could therefore be applied in analysis of total heavy metal concentrations. The total concentrations of 856 mg kg⁻¹ Cr, 621 mg kg⁻¹ Ni and 2032 mg kg⁻¹ Zn were higher than those set by Slovenian legislation for sludge to be used in agriculture. Total concentrations of 2.78 mg kg⁻¹ Cd, 433 mg kg⁻¹ Cu and 126 mg kg⁻¹ Pb were below those permitted in the relevant legislation. CRM 146R reference material was used to follow the quality of the analytical process. The results of the BCR three-step sequential extraction procedure indicate high Ni and Zn mobility in the sludge analysed. The other heavy metals were primarily in sparingly soluble fractions and hence poorly mobile. Due to the high total Ni concentration and its high mobility the investigated sewage sludge could not be used in agriculture.     

Trace metals in the marine bivalve Macoma balthica in the westerschelde estuary, The Nertherlands. Part 3: Variability of the role of cytosol in metal uptake by the clams

Tellinid clams Macoma balthica were sampled every 2 months for 2.5 years at two locations from the Westerschelde estuary (The Netherlands) and submitted to in vitro short-term exposure to Cd, Cu and Zn. Total and heat-stable cytosolic metal concentrations have been measured before and after exposure to study the effects of the sampling season on metal uptake by the bivalve. We observed much higher uptakes of Cd and, to a lesser extent, Cu in winter than in summer, while Zn appears to be constantly regulated. These phenomena are amplified in the cytosol, especially for Cd, a non-essential element, for which the concentrations after exposure can reach 35–45 μg·g⁻¹ (dry wt.) in winter, but only a maximum of 0.5 μg·g⁻¹ in summer, all natural values being between 0.01 and 0.1 μg·g⁻¹ on average. The contents (μg) of the various elements, either at the total or at the cytosolic level, are not constant, hence showing that the seasonal body weight fluctuation of the clams (dilution or concentration effect) is not the only parameter responsible for the metal uptake variability. Furthermore, we have shown that the proportion of cytosolic metal is not constant, but increases with the absolute cytosolic concentration up to 35–40. Therefore, the cytosolic phase of the cells plays a growing role in Cd, Cu and Zn storage as long as their total concentration increases.     

Mercury concentrations in fish inhabiting two polluted lakes in Northern Canada

The concentrations of total mercury in the sediments, water and fish of Giauque Lake and Thompson Lake in northern Canada were determined during 1977 and 1978. Both lakes had formerly received mercury-laden industrial discharges, which were terminated in 1968 (Giauque Lake) and 1949 (Thompson Lake). In Giaque Lake, lake trout (Salvelinus namaycusy) contained an average of 3.79 mg kg⁻¹ in their muscle while the average concentrations in northern pike (Esox lucius) and round whitefish (Prosopium cylindraceum) were 1.75 and 1.22 mg kg⁻¹ respectively. About 7% of the lake's bottom contained mercury levels of > 500 μg kg⁻¹ (dry weight) but, in the water, concentrations were always below detectable limits (0.2 μg l⁻¹). In Thompson Lake, mercury levels in northern pike averaged 1.69 mg kg⁻¹, whereas in lake whitefish (Coregonus clupeaformis), the highest recorded value was 0.6 mg kg⁻¹. Although mercury was usually not detectable in the water column, there was heavy contamination of the sediments, with values reaching 1300 μg kg⁻¹. In addition, approximately 15% of the lake bottom contained mercury in excess of 500 μg kg⁻¹. Based on these data, it is concluded that: (1) northern pike are still accumulating mercury from exposed tailings which were deposited in Thompson Lake 30 years ago, and (2) contamination of only a small part of a lake may result in high levels in fish throughout the lake: this is probably due to the movement of fish from contaminated to noncontaminated areas.     

Preliminary studies on the leaching of some trace metals from kitchen faucets

Preliminary studies were carried out on the leaching of copper, zinc, chromium, cadmium and lead from eight kitchen faucets by samples of raw, filtered and distributed Ottawa water, a sample of well water and deionized water containing 2 mg l⁻¹ aqueous fulvic acid. Leaching was effected by allowing the test solutions to stand in the inverted faucets for two successive 24-h periods. Concentrations of the metals found in the leachates were copper: first leaching, 0.12–28.0 mg l⁻¹, second leaching, 0.08-3.54 mg l⁻¹; zinc: first leaching, 0.13-10.25 mg l⁻¹, second leaching, 0.06-2.85 mg l⁻¹; chromium: first leaching, < 1.0 × 10⁻³ − 0.395 mg l⁻¹, second leaching, < 1.0 × 10⁻³−0.032 mg l⁻¹; cadmium: first leaching, < 0.05 × 10⁻³−0.01 mg l⁻¹, second leaching, < 0.05 × 10⁻³−4 × 10⁻³ mg l⁻¹; and lead: first leaching, < 0.2−110.0 mg l⁻¹, second leaching, < 0.2−82.0 mg l⁻¹. The faucets containing lead-soldered copper joints released high concentrations of lead, particularly in the case of leaching with the aqueous fulvic acid solution. Under the conditions of the present investigations it is indicated that in some cases the concentrations of metals leached could lead to intakes in excess of the maximum permissible limits for these metals. However, further investigations will be required to determine the possible contribution of these faucets to metal intake under normal usage.     

Heavy metals in animals of Lake Balaton

Hg, Cd, Cu, Pb, Zn, Fe and Mn concentrations were measured in Chironomidae larvae, Crustacea plankton, as well as in various organs of mussels and fishes collected from the open water area of Lake Balaton. The values were comparatively low. However, there were significant differences in the metal concentrations of species and tissue.Most Cd was found in the gill of Unio pictorum L., most Pb, Zn and Mn in the gill of Anodonta cygnea L., most Cu in Crustacea plankton and in the liver of Abramis brama L., and most Hg and Fe in Chironomidae larvae. Low concentrations occurred in fishes, the lowest in the flesh of Stizostedion lucioperca L.Accumulation of metals in organs as compared with their concentration in the lake water was in the range of 3.4 × 10²−2.6 × 10³ for Hg; 7.0 × 10²−6.8 × 10³ for Cd; 3.3 × 10²−9.7 × 10³ for Cu; 6.9 × 10²−8.1 × 10³ for Zn; 1.5 × 10³−2.4 × 10⁴ for Pb; 3.5 × 10²−3.1 × 10⁴ for Fe; and 5.0 × 10¹−3.5 × 10⁵ for Mn.     

Uptake and release of zinc by aquatic bryophytes (Fontinalis antipyretica L. ex. Hedw.)

The zinc uptake and posterior release by an aquatic bryophyte—Fontinalis antipyretica L. Ex Hedw.—was experimentally studied in laboratory exposing the plants to different zinc concentrations in the range, 1.0–5.0 mg l⁻¹, for a 144 h contamination period, and then exposed to metal-free water for a 120 h decontamination period. The experiments were carried out in perfectly mixed contactors at controlled illumination, using mosses picked out in February 1997, with a background initial zinc concentration of 263 mg g⁻¹ (dry wt.). A first-order mass transfer kinetic model was fitted to the experimental data to determine the uptake and release constants, k₁ and k₂, the zinc concentration in mosses at the end of the uptake period, C_mu, and at the equilibrium, for the contamination and decontamination stages, C_me and C_mr, respectively. A bioconcentration factor, BCF=k₁/k₂ (zinc concentration in the plant, dry wt./zinc concentration in the water) was determined. A biological elimination factor defined as BEF=1−C_mr/C_mu was also calculated. BCF decreases from about 4500 to 2950 as Zn concentration in water increases from 1.05 to 3.80 mg l⁻¹. BEF is approximately constant and equal to 0.80. Comparing Zn and Cu accumulation by Fontinalis antipyretica, it was concluded that the uptake rate for Zn (145 h⁻¹) is much lower than for Cu (628 h⁻¹) and the amount retained by the plant decreased by a factor of about seven.     

The crayfish as a “biological indicator” of aquatic contamination by heavy metals

Cu, Cd. Mg, Mn and Ni concentrations in whole Cambarus bartoni, trapped from Nepahwin Lake, Joe Lake and Wizard Lake, lying at distances of 10, 30 and 150 km, respectively, from the Sudbury smelters in Northeastern Ontario, showed an inverse relationship with the distance of the habitat from the emission site. Highest concentrations of Cu were observed in the hepatopancreas, Cd in the hepatopancreas and the gut, Fe and Mn in the gut, and Mg in the exoskeleton. Tissue concentrations of Ni and Zn were highly variable. Differences between males and females at each sampling site were not significant at the 5% level. The general relationship between crayfish tissue metal concentrations at the three sites was Cu > Mg > Mn > Zn > Ni > Cd. This observed relationship, except for Mg and Mn, agreed with the concentration relationship of these metals in the water and the sediments (top 10–20 cm) in the three lakes. In laboratory studies, Cu concentrations in the hepatopancreas, gills, exoskeleton and the viscera increased significantly over the control during the 4-weeks exposure to 125,250 and 500 μg Cu 1⁻¹. Hepatopancreas, in general, had the highest Cu concentration, and the exoskeleton, the lowest. Relationship between Ni exposure and the tissue Ni concentrations in the four treatments was 800 μg Ni l⁻¹ > 400 μg Ni l⁻¹ = 200 μg Ni l⁻¹ > control, while between the exposure periods and the tissue Ni concentrations was week 4 > week 1 > week 3 = week 2. Highest Ni concentrations at the end of the 4-week exposure to Ni were observed in the gut, gills and the hepatopancreas, and the lowest in the viscera. The present study suggests that Cambarus bartoni is a reliable indicator of the presence of class B and borderline elements with specific gravity > 5 in the aquatic environment. However, their value as biomonitors of variations in Cu and Ni concentrations in freshwater ecosystems is debatable.     

Removal of heavy metals from electroplating rinsewaters by precipitation, flocculation and ultrafiltration

Chromium, nickel, copper and zinc can be effectively removed from electroplating rinsewaters by hydroxide precipitation, flocculation and ultrafiltration. Prior to precipitation, chromium is reduced from the hexavalent to the trivalent form by ferrous sulfate and cyanide in copper and zinc rinsewaters are oxidized by sodium hypochlorite. Minimum metal concentrations in the permeate from separate batches of chromium, nickel, copper and zinc rinsewaters were found to be, respectively, 0.17 mg 1⁻¹ Cr (T), 0.26 mg 1⁻¹ Ni, 0.30 mg 1⁻¹ Cu and 1.84 mg 1⁻¹ Zn. These solubilities are in good agreement with the theoretical solubility curves, except for copper where the formation of stable copper cyanide complexes appears to increase the solubilities at least two orders of magnitude relative to those predicted on the basis of the equilibrium constants for copper hydroxides and oxides. A simple mass balance model, assuming concentrate recycle and constant metal concentration in the permeate, is adequate for the prediction of feed and permeate concentrations as a function of the volume filtered up to a relative volume of about 0.3. Above this value, the feed concentrations are lower than predicted, apparently because of entrapment of metal precipitate in the strainer. Water recoveries are strongly dependent on the specific metal removed and are found to be 24% for Ni with a 0.20 μm membrane, 10% for Cr with a 0.80 μm membrane, 6.5% for Cu and 3.7% for Zn, both with a 0.45 μm membrane.     

Effects of copper, zinc and cadmium on Selanastrum Capricornutum

The algicidal and algistatic effects of copper, zinc and cadmium on Selanastrum capricornutum, a unicellular green algae were analyzed by using a modification of the Algal Assay Procedures Bottle Test.Algicidal concentrations of copper, zinc and cadmium were 0.30, 0.70, and 0.65 mg 1⁻¹. Treatment of Selanastrum with various concentrations of the metals resulted in similar growth rates characterized by extended lag growth phases.Combinations of copper, zinc and cadmium were similar in toxicity to equal concentrations of zinc. Combinations of copper and cadmium resulted in a greater growth rate than equal concentrations of copper suggesting that cadmium inhibits copper toxicity.Selanastrum was able to exist in waters from the upper South Fork and North Fork of the Coeur d'Alene River where zinc and other metals were in low concentration. However, the algae was not able to tolerate zinc concentrations greater than 0·5 mg 1⁻¹ from waters of other parts of the drainage. These observations were consistent with laboratory findings where 0.7 mg 1⁻¹ zinc was algicidal and 0.1 mg 1⁻¹ inhibited the growth of Selanastrum.     

Aspects of the aquatic chemistry of cadmium and zinc in a heavy metal contaminated lake

Concentrations of the heavy metals cadmium (Cd) and zinc (Zn) were determined at several sites in Palestine Lake, Indiana, and in the stream (Williamson Ditch) which transports metal-bearing wastes to the lake. Average dissolved Cd and Zn concentrations in the lake were as high as 17.3 μg 1^-1 and 293 μg 1^-1, respectively, while corresponding suspended levels were 30.3 μg Cd 1^-1 and 270 μg Zn 1^-1. Average levels of both Cd and Zn in the dissolved fraction exceeded those in the suspended fraction, except at one site in the lake where suspended Cd was higher. During anaerobic conditions occurring in lake's hypolimnion, a marked decrease in the dissolved fraction and concomitant increase in the suspended fraction of both Cd and Zn were noted. A cadmium-specific ion electrode was used to determine the chemical forms of dissolved Cd present in the lake. Free Cd²⁺ was the dominant form; however, Cd-organic complexes sometimes comprised a significant portion of the total dissolved Cd.