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.     

Cadmium in the Rhône river

The distribution of cadmium in the Rhône river was studied using differential pulse anodic stripping voltametry with a static mercury drop electrode. For 11 potentially contaminated river stations, the Cd in true solution averaged 39 ± 23 ng kg⁻¹, adsorbed on suspended matter was 19 ± 22 ng kg⁻¹ (liquid phase) and suspended matter content was 2.4 ± 1.5 mg kg⁻¹ (solid phase), equivalent to 40 ± 24, 22 ± 24 and 38 ± 31%, respectively, of the total carried under these conditions. For sediments the mean Cd content was 0.9 ± 0.6 mg kg⁻¹. The water values are low by world standards, even though sampling was biased towards sites potentially contaminated. This could be partially due to the unusual water pH of 7.8–8.5.     

Zinc, cadmium and lead in water, sediments and submerged plants of the Derwent Reservoir, Northern England

A partial budget is presented of the zinc, cadmium and lead entering the Derwent Reservoir. The mean levels in the water column upstream of the site of inflow are: Zn, 0.216 mg 1⁻¹ ; Cd, 0.003 mg 1⁻¹; Pb, 0.065 mg 1⁻¹; the levels after passage through the 4.1 km² reservoir fall by: Zn, 70.3%; Cd, 98.3%; Pb, 89.2%. Most of these metals are deposited in sediments, the mean values for which are: Zn, 1035 μg⁻¹; Cd, 13μg⁻¹; Pb, 827μg⁻¹. Lead, a higher percentage of which occurs as particulate material, is deposited more rapidly than zinc; this effect is especially obvious when streaming of colder water along the bottom of the reservoir takes place at the time of floods. Macroscopic plants are only occasional in this reservoir, due perhaps in part to heavy metal toxicity. Of the two most common submerged species, Nitella flexilis probably accumulates almost all of its metal content directly from the water, but the data suggest that sediments are a source of some of the heavy metals accumulated by Glyceria fluitans.     

Application de la spectrometrie d'absorption atomique zeeman aux dosages de huit elements traces (Ag, Cd, Cr, Cu, Mn, Ni, Pb et Se) dans des matrices biologiques solides

The use of biological indicators in studies of aquatic pollution (in fresh, estuarine or sea waters), as well as research about the metal transfers in food chains, need a great accuracy of the trace element determination. Therefore, as shown by the results of international intercalibration exercises, the mastery of analytical techniques is far from being perfect in all the laboratories.One of the main sources of error in atomic absorption results from non-specific absorptions due to the presence of important organic and mineral matrixes in biological materials and especially in aquatic and marine organisms. In this case, the correction of unspecific absorption by using deuterium lamp was insufficient and the determination of trace elements had to be preceded by a pre-instrumental stage which allowed the elimination of the organic matter by mineralization and of a large part of the mineral matrix by extraction. The previous separation was long and induced contamination risks. The use of the Zeeman effect background correction allows the transfer of most processes from the pre-instrumental to the instrumental stage. Moreover, the Zeeman effect has three advantages: (1) the background correction is effective up to 2 units of absorbance; (2) the correction is effective from 190 to 900 nm; (3) the method of the double beam is optimalized.The aim of this study was to apply the Zeeman effect to the determination of eight trace elements (Ag, Cd, Cr, Cu, Mn, Ni, Pb, Se) in three different biological solid samples, two originated from the marine environment (lobster hepatopancreas TORT-1, standard reference material from the National Research Council Canada; oyster tissues SRM 1566 from the US National Bureau of Standards) and one from the vegetable kingdom (tomato leaves, SRM 1573 from the US NBS).The experimental procedure is reduced to a minimum since it consists in the digestion of an aliquot of 100 mg of the powdered sample with 1 ml of concentrated nitric acid at 95°C for 1 h. Then the volume is adjusted to 4 ml with deionized water. The metal analysis is carried out using a graphite furnace coated with tantalum carbide.This analysis is achieved according to the method of standard addition. The three added concentrations used for each element are listed in Table 1. The analytical conditions and graphite atomizer program are indicated in Table 2. The temperature program has to be modified according to the type of equipment.The internal quality control of the suggested method related to four criteria: sensitivity, repeatability, accuracy, practicability. The results are shown in Table 3. The threshold of sensitivity (3 times the SD of a series of eight results obtained for a blank of digestion) are low: < 1 μg kg⁻¹ for Ag, Cd and Mn; 1 μg kg⁻¹ for Cr and Pb; 5 μg kg⁻¹ for Cu and Ni and 15 μg kg⁻¹ for Se. The variation coefficients, calculated for both two series of six determinations each, are generally included between 5 and 10%. The trace element concentrations determined by using this method are in perfect agreement with the certified values of the US NBS and NRC Canada (Table 3.)The quality of the results establishes the possibility of using a very easy and fast method to determine the level of eight trace elements in materials with high mineral and organic matter content.     

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.     

Growth responses of selected freshwater algae to trace elements and scrubber ash slurry generated by coal-fired power plants

In laboratory studies, the freshwater algae Ankistrodesmus falcatus, Scenedesmus obliquus, Selenastrum capricornutum, and Microcoleus vaginatus were exposed to potential pollutants from coal-fired power plants, and their growth responses were evaluated. Using a modification of the EPA Algal Assay Procedure Bottle Test, algae were incubated in media containing As(V) as Na₂HAsO₄ · 7H₂O, Cd(II) as CdSO₄, Hg(II) as HgSO₄, Se(VI) as Na₂SeO₄, in solution, and scrubber ash slurry generated at a western U.S. coal-fired power plant complex. First significant inhibition levels as well as algistatic-algicidal levels are reported. The median effective concentration (EC50) values for the potential pollutants ranged from 0.048–30.761 mg l⁻¹ (0.00064–0.41058 M) As(V), 0.005–0.019 mg l⁻¹ (0.00004–0.00017 M) Cd(II), 0.033–0.253 mg l⁻¹ (0.00016–0.00126 M) Hg(II), 0.033–8.511 mg l⁻¹ (0.00042–0.10779 M) Se(VI), and 3.048–15.417% scrubber ash slurry extract (SASE).     

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.     

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.     

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.     

Distribution of total mercury in the fishes of Lake Oahe

In 1971, a joint Federal-State survey was conducted to investigate the total mercury content of fish and sediment in Lake Oahe, South Dakota. Average total mercury concentration of 225 fish flesh samples was 0.27 mg kg⁻¹; game fish samples averaged 0.31 mg kg⁻¹ and nongame fish samples averaged 0.22 mg kg⁻¹. Frequency distributions of total mercury concentrations in the fish are presented by fish species and sampling location. Data include total mercury analyses of 43 sediment samples.     

Toxic effects of hexavalent chromium on brook trout (Salvelinus fontinalis) and rainbow trout (Salmo gairdneri)

Exposing brook trout to various concentrations of chromium [Cr(VI)] for up to 22 months (including reproduction) significantly increased alevin mortality at 0.35 mg Cr l⁻¹ and retarded growth of young brook trout at the lowest concentration tested (0.01 mg Cr l⁻¹). Eight month exposures of rainbow trout significantly increased alevin mortality at 0.34 mg Cr l⁻¹ and also retarded growth at the lowest concentration tested (0.10 mg Cr l⁻¹). Exposures of brook trout lasting 22 months showed, however, that growth was only temporarily affected, and therefore, it was not used as an end point to measure the affects of chromium on either species. Reproduction, and embryo hatchability of brook trout were unaffected at Cr(VI) concentrations that affected survival of newly hatched alevins. The maximum acceptable toxicant concentration (MATC) for brook and rainbow trout exposed to Cr(VI) in water with a hardness of 45 mg l⁻¹ (as CaCO₃) and a pH range of 7–8 lies between 0.20 and 0.35 mg Cr l⁻¹. The 96-h lc₅₀ for brook and rainbow trout was 59 and 69 mg Cr l⁻¹, respectively: therefore, the application factor (MATC/96-h lc₅₀) for both species lies between 0.003 and 0.006.     

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.     

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.     

Health risk from heavy metals via consumption of food crops in the vicinity of Dabaoshan mine, South China

Heavy metal contamination of soils resulting from mining and smelting is causing major concern due to the potential risk involved. This study was designed to investigate the heavy metal (Cu, Zn, Pb and Cd) concentrations in soils and food crops and estimate the potential health risks of metals to humans via consumption of polluted food crops grown at four villages around the Dabaoshan mine, South China. The heavy metal concentrations in paddy and garden soils exceeded the maximum allowable concentrations for Chinese agricultural soil. The paddy soil at Fandong village was heavily contaminated with Cu (703 mg kg^− 1), Zn (1100 mg kg^− 1), Pb (386 mg kg^− 1) and Cd (5.5 mg kg^− 1). Rice tended to accumulated higher Cd and Pb concentration in grain parts. The concentrations of Cd, Pb and Zn in vegetables exceeded the maximum permissible concentration in China. Taro grown at the four sampled villages accumulated high concentrations of Zn, Pb and Cd. Bio-accumulation factors for heavy metals in different vegetables showed a trend in the order: Cd > Zn > Cu > Pb. Bio-accumulation factors of heavy metals were significantly higher for leafy than for non-leafy vegetable. The target hazard quotient (THQ) of rice at four sites varied from 0.66-0.89 for Cu, 0.48-0.60 for Zn, 1.43-1.99 for Pb, and 2.61-6.25 for Cd. Estimated daily intake (EDI) and THQs for Cd and Pb of rice and vegetables exceeded the FAO/WHO permissible limit. Heavy metal contamination of food crops grown around the mine posed a great health risk to the local population through consumption of rice and vegetables.     

Trace element concentrations in hair of healthy Chinese centenarians

Trace element concentrations, as indicators of micronutrient status of healthy centenarians, have not been widely analyzed. This study aimed to assess trace element concentrations in the hair of healthy centenarians. The effects of gender and age on element concentrations were also investigated. Eleven trace elements (Al, Ba, Cd, Cr, Cu, Fe, Mo, Pb, Se, Sr and Zn) in the scalp hair of 107 healthy Chinese centenarians were examined. The overall reference values (RVs) in mg/kg for the hair concentrations of trace elements in centenarians were as follows: Al, 14.95; Ba, 2.68; Cd, 0.06; Cr, 0.59; Cu, 6.21); Fe, 19.37; Mo, 0.50; Pb, 4.64; Se, 0.37; Sr, 4.84; and Zn, 154.37. Data analysis found that only Cu and Zn concentrations show a normal distribution, and there is no significant difference between males and females in any element except Zn. However, the levels of Al, Cd, Cr, Fe, Mo, Pb decrease and the levels of Ba, Cu, Se, Sr, Zn increase with age in the centenarian cohort. Results also revealed that sufficient Zn and Se concentrations as well as low exposure to heavy metals pollution contribute to the longevity of centenarians. The results imply the possibility of manipulating trace element concentrations, especially Zn and Se concentrations in tissues, as a means for therapeutic modality in geriatric disease.     

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.     

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.     

Recovery of chromium(VI) from wastewaters with iron(III) hydroxide—I: Adsorption mechanism of chromium(VI) on iron(III) hydroxide

Chromium(VI) [Cr(VI)] is adsorbed as HCrO⁻₄ on iron(III) hydroxide at pH below 8.5. The Cr(VI) adsorption is suppressed by the presence of other anions such as SO²⁻₄ and SCN⁻, and enhanced by the presence of metal ions such as Cd(II) and Pb(II). The suppression is due to the competitive adsorption of other anions, depending upon the stability of their iron complexes. The enhancement is probably due to the increase in adsorption sites as a result of coprecipitation of metal ion with iron(III) hydroxide.     

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.     

Environmental chemistry of copper in Lake Monona, Wisconsin

Lake Monona, located at Madison, Wisconsin, received over 1.5 × 10⁶ pounds of copper sulfate in the past 50 yr to control excessive algal growth. Dissolved copper on Lake Monona epilimnion is inversely related to pH which indicates possible control of dissolved copper by basic copper carbonate. Concentrations as high as about 4 μg Cu l⁻¹ were found in Lake Monona epilimnion, which also contains 3.3 me l⁻¹ (milliequivalents per liter) of alkalinity, mostly bicarbonate. Concentrations of dissolved copper were consistently lower (0.3 μg Cu l⁻¹) in the hypolimnion. Sulfide probably controls dissolved copper in the hypolimnion during anoxic conditions because of sulfide insolubility. Particulate copper concentrations of about 3 μg l⁻¹ increased slightly with depth. The highest concentrations of copper in Lake Monona sediments (650 mg kg⁻¹) were found approximately 60 cm below the current sediment surface. Surface sediments of Lake Monona contained approximately 250 mg Cu kg⁻¹ sediment dry weight.