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.     

Role of bacterial extracellular polymers in metal uptake in pure bacterial culture and activated sludge—II Effects of mean cell retention time

A gel filtration technique afforded a good separation between metal complexed with bacterial extracellular polymers and free metal ions. The complexation of polymers extracted from cultures of Klehsiella aerogenes and activated sludge with cadmium, nickel, manganese and cobalt was demonstrated. The extraction of extracellular polymers from cultures of K. aerogenes and activated sludge reduced the capacity of the cells and flocs to adsorb metal. Adsorption and complexation of metals by cells of K. aerogenes and extracellular polymers extracted from activated sludge were fitted to Freundlich equilibrium isotherms. Saturation of activated sludge polymer binding sites occurred at 10 mg 1⁻¹ metal additions for all the metals studied except manganese which was complexed to a very limited extent. Cells of K. aerogenes exhibited no saturation effects in the range of metal concentrations studied.Precipitation of metals below a concentration of 1 mg 1⁻¹ was minimal, with the exception of cadmium precipitation. At a concentration of 10 mg 1⁻¹, precipitation of cadmium, cobalt and manganese may have been the major mechanism of metal removal. The more soluble metals generally displayed the lowest removals. Concentrations of extracellular polymers and soluble chelating agents may be important in controlling removals of metals which are largely soluble in activated sludge.     

Removing metals from waste solutions with low rank coals and related materials

Ion exchange media were produced by contacting brown coal, peat or wood sawdust with a solution of calcium hydroxide, preferably as an aqueous slurry of lime. The resultant calcium loading on the media, which ranged up to 8% for sawdust, 12% for peat and to 19% for brown coal, was exchanged for many metals in solution.Preliminary work showed the method to be amenable to extraction of copper, nickel, chromium, cadmium, lead, zinc, mercury, cobalt, silver, iron, manganese, vanadium, germanium, gallium, aluminium, antimony and uranium. For most of the metals more than 99% was removed from I g 1⁻¹ solutions.In more detailed work, confined to calcium loaded brown coal and solutions having metal concentrations more typical of industrial operations, minimum residual metal concentrations of 0.0005 mg l⁻¹ mercury; 0.02 mg 1⁻¹ copper; 0.02 mg 1⁻¹ zinc; <0.05 mg l⁻¹ cadmium; 0.1 mg 1⁻¹ lead and 0.2 mg l⁻¹ manganese were obtained. These results compare favourably with those reported for other relevant processes and there might be operational advantages in the method.The method can be applied either by agitating the calcium loaded media in the solution and then filtering, or by passing the solution through packed beds of the media. Where appropriate, dilute solutions can be up-graded for re-use by stripping the metals from the media which can also be re-used. Alternatively, the loaded media can be combusted and the metals recovered from the residues.The method might be applicable to mine drainage and to effluents from metallurgical processing and electroplating, but more work is required to assess costs.It is suggested that the method is environmentally preferable to other common effluent treatment procedures because it enables collection and recycling of heavy metal pollutants.     

The effect of surfactants on the extraction-atomic absorption spectrophotometric determination of copper, iron, manganese, lead, nickel, zinc cadmium and cobalt

Nine surfactants representing pure cationic, anionic and non-ionic detergents, three industrially prepared detergents. sodium pyrophosphate. sodium tripolyphosphate, and a soap were investigated for their effect on the extraction-atomic absorption spectrophotometric determination of copper. iron, manganese and lead. Some results are also given for nickel, zinc, cadmium and cobalt. Cations were extracted into 10 ml of MIBK as APDC chelates. To Avoid emulsion formation, maximum concentration of LAS was 1 mg 1⁻¹, and for formulated and non-ionic detergents and washing powders it was 5 mg 1⁻¹.A standard addition procedure was used to obtain correct results for copper and nickel. Two extractions of iron, cobalt and lead, and one extraction of manganese, zinc and cadmium gave a recovery of 100 ± 5%. Soap gave high recoveries for iron and copper. NTA in concentrations up to 25 mg l⁻¹ did not interfere. EDTA in concentrations up to 25 mg l⁻¹ interfered with iron and nickel determinations, but the addition of 3 mg of aluminium removed the EDTA interference in the determination of copper, manganese, lead, zinc, cadmium and cobalt.For the determination of trace metals in polluted natural waters the amount of 4% APDC was increased to 10 ml and for manganese to 25 ml. An addition of 3 mg aluminium as nitrate after the addition of buffer with subsequent 20 min reaction time is required for the determination of all eight metals by the recommended procedures. The effect of humic acid was also investigated.     

Accumulation of zinc, cadmium and lead by field populations of Lemanea

A study has been made of the concentrations of zinc, cadmium and lead in populations of the red alga Lemanea growing in fast-flowing rivers in Britain, France. Germany, Ireland and Sardinia (Italy). The sites were selected to provide a wide range of aqueous concentrations of these metals. Many of the sites are influenced by past or present mining activities and Lemanea was found at aqueous concentrations of zinc up to 1.16 mg 1⁻¹. In contrast to previous studies with filamentous green algae, no evidence could be found to support the hypothesis that populations differ genetically in their ability to tolerate these heavy metals. Samples of alga consisted of pooled 2 cm long terminal tips of filaments detached from approx. 1 cm² rock surface. Significant positive correlations were found between the logarithm of the mean concentration of zinc, cadmium and lead in four such samples collected from within 10 m reaches at 59 sites and the logarithm of the concentration of each metal in both unfiltered and filtered water. The enrichment ratios for each metal decreased with increasing aqueous metal concentrations. Although the aqueous concentrations of the three metals were strongly intercorrelated, differences in the ratio of metal concentrations were reflected in the composition of Lemanea filaments. The results suggest that high levels of calcium (and/or magnesium) result in decreased uptake of zinc. Intensive sampling from a single population showed that part of the zinc content of filaments is sensitive to short-term fluctuations in concentrations in the surrounding water. In the particular population studied this was about 20%; a similar percentage could be eluted in the laboratory with EDTA. Transplants of Lemanea were made between reaches with different aqueous concentrations of zinc and in all cases the zinc concentration in filament tips increased or decreased to stabilise at a concentration similar to that in filaments native to the reach. It is suggested that chemical analyses of natural or transplanted populations of Lemanea could provide a valuable aid in monitoring contamination of rivers by zinc, cadmium or lead.     

The influence of substrate, pH, diet and temperature upon cadmium accumulation in the asiatic clam (Corbicula fluminea) in laboratory artificial streams

The influence of substrate, pH, diet and temperature upon the accumulation of cadmium (0.05 mg l⁻¹ dose < 0.001 mg l⁻¹ control) in the visceral mass of the Asiatic clam Corbicula fluminea was studied in laboratory artificial stream systems at intervals of 0, 3, 5, 7, 10 and 14-day exposures. Four substrate conditions, sand; sand, silt and clay (SSC); sand, clay and organic matter (SCO); and no substrate (NoS), were considered. The greatest tissue accumulation of cadmium in C. fluminea occurred at 0.05 mg l⁻¹ Cd in NoS and the lowest in clams occupying SCO. Complexation of available metals, lower clam filtering rates and physical protection by the substrate were attributed to the depressed cadmium accumulation of clams exposed in the SCO substrate. Lower pH exposures (5.0 vs 7.8) significantly (P 0.05 level) reduced cadmium uptake at 21°C but had little effect at 9°C. Uptake was higher in clams fed with cadmium-exposed Chlamydomonas reinhardt at 21°C but not at 9°C. In temperature exposures alone at 0.05 mg l⁻¹ Cd, accumulation was significantly higher in C. fluminea exposed at 21°C than at 9°C. The results are discussed relative to the importance of standardized laboratory protocol and the use of C. fluminea as a bioindicator of heavy metal stress.     

Chronic toxicity of a copper, cadmium and zinc mixture to the fathead minnow (Pimephales promelas rafinesque)

Fathead minnows were exposed to a series or concentrations of a copper, cadmium and zinc mixture during a 12.5 month chronic test in water of 200 mg 1⁻¹ total hardness. The metal concentrations in the mixture were selected on the basis of results obtained during previous chronic exposures to each of the metals individually in the same water. Strict summation of the chronic toxicities of the metals was not indicated when they were tested in combination. Toxic effects of the mixture attributable to copper appeared to be increased, but that attributable to cadmium was reduced. The effects thought to be due to zinc were similar in degree to those observed in the single chronic exposure. Summation of effects resulting from a mixture containing about the same proportions of copper, cadmium and zinc occurred at a much higher, acutely lethal concentration. A lethal threshold was attained in the mixture when each metal was present at a concentration of 0.4 or less of its individual lethal threshold.     

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.     

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.     

Scavenging cadmium,copper, lead,nickel and zinc ions from aqueous solution by modified cellulosic sorbent

The adsorption of cadmium, copper, lead, nickel and zinc ions on maize Zea mays stalk meal was examined by equilibrium studies at 29°C. The amounts of the metal ions removed from solution depended on the metal ion type, the ionic size of the metals and were enhanced by EDTA (% N = 12.05) modification of the cellulosic sorbent. The sorption coefficient, K_d, of the metal ions between the adsorbent phase and the bulk aqueous phase was found. The sorption on the unmodified sorbent of lead ions from solutions containing zinc ions shows that lead ions are preferentially removed from solution.     

Use of moss-bags for monitoring heavy metals in rivers

Methods were developed for the use of aquatic mosses in mesh bags to monitor heavy metal pollution by measuring concentrations in 2-cm tips of the widespread species, Rhynchostegium riparioides and (in one experiment) Fontinalis antipyretica. Intermittent pollution events were simulated by transporting moss from streams with low concentrations to ones with high concentrations of zinc, cadmium and lead and also in one case back from high to a low concentration. Factors affecting accumulation were also studied; these included position inside bag, density of packing, mesh size and differences between moss on boulders and in bags. In general these factors influenced accumulation only slightly over a wide range of treatments. The influence of time period for which the moss was exposed to pollution on subsequent loss was tested for zinc: a greater proportion was lost over the first 2 h in moss exposed for 1 h than 24 h. The potential for using the moss-bag technique is discussed: it is robust and convenient to handle and is recommended for monitoring heavy metals in stretches of rivers where there are no natural moss populations.     

Electrodeposition of six heavy metals on reticulated vitreous carbon electrode

Six heavy metals, copper, cadmium, chromium, lead, uranium and zinc were deposited on cathodes made of a newly developed form of carbon, Reticulated Vitreous Carbon, in a laboratory scale electrochemical reactor. Different metals varied in the extent of their removal with copper depositing 100% at a flow rate of 0.24 cm min⁻¹ in a single pass while it would require a maximum of 20 passes for 100% chromium deposition at a flow rate of 1.8 cm min⁻¹, initial concentrations for both metals being 50 μmol 1⁻¹.Experiments conducted using 0.5 × 10⁻³ M CuSO₄ in 0.5 M Na₂SO₄ supporting electrolyte resulted in a mass transfer coefficient of the order of 10⁻³ cm s⁻¹ and a current efficiency of 64% for the electrodeposition of copper at a cell voltage of 4.0V. Because of very high porosity, 97%, high specific surface area, up to 66 cm² cm⁻³ for RVC grade 100, and useful electrochemical characteristics, RVC can be advantageously used as electrode material for heavy metal removal from dilute industrial effluents.     

Role of bacterial extracellular polymers in metal uptake in pure bacterial culture and activated sludge—I. Effects of metal concentration

A gel filtration technique afforded a good separation between metal complexed with bacterial extracellular polymers and free metal ions. The complexation of polymers extracted from cultures of Klehsiella aerogenes and activated sludge with cadmium, nickel, manganese and cobalt was demonstrated. The extraction of extracellular polymers from cultures of K. aerogenes and activated sludge reduced the capacity of the cells and flocs to adsorb metal. Adsorption and complexation of metals by cells of K. aerogenes and extracellular polymers extracted from activated sludge were fitted to Freundlich equilibrium isotherms. Saturation of activated sludge polymer binding sites occurred at 10 mg 1^?1 metal additions for all the metals studied except manganese which was complexed to a very limited extent. Cells of K. aerogenes exhibited no saturation effects in the range of metal concentrations studied.Precipitation of metals below a concentration of 1 mg 1^?1 was minimal, with the exception of cadmium precipitation. At a concentration of 10 mg 1^?1, precipitation of cadmium, cobalt and manganese may have been the major mechanism of metal removal. The more soluble metals generally displayed the lowest removals. Concentrations of extracellular polymers and soluble chelating agents may be important in controlling removals of metals which are largely soluble in activated sludge.     

The effect of surfactants on the mixed chelate extraction-atomic absorption spectrophotometric determination of copper, nickel, iron, cobalt, cadmium, zinc and lead

Twelve surfactants representing pure cationic, anionic and non-ionic detergents, three commercial detergents, sodium pyrophosphate, sodium tripolyphosphate, a soap, nitrilotriacetic acid (NTA), EDTA, and humic acid were investigated for their effect on the extraction-atomic absorption spectrophotometric determination of copper, nickel, iron, cobalt, cadmium, zinc and lead. Cations were extracted into 10 ml of a solution containing diphenylthiocarbazone, 8-quinolinol and acetyl acetone in ethyl propionate. To avoid emulsion formation, the maximum concentration of linear alkylate sulphonate (LAS) was 10 mg l⁻¹ and for solid industrial LAS-type detergent was 50 mg l⁻¹, but washing powder did not interfere at 100 mg l⁻¹. Cationic and non-ionic detergents gave low recoveries for cobalt. Condensed phosphates at a concentration of 20 mg l⁻¹ did not cause significant interference. NTA interfered with nickel extraction and EDTA with all metals. Humic acid, however, gave no interference. A standard addition procedure can be used to correct the results.A comparison is made between the APDC-MIBK and the mixed chelate-ethyl propionate methods for the determination of trace metals in the presence of various surfactants in natural waters; the latter is preferable.     

On the potential of combining neutron activation analysis and particle induced X-ray emission (PIXE) for micro- and microdistribution analysis of hard metals in human tissues

Tungsten carbide and cobalt are the main components of hard metal alloy while other metals such as chromium, niobium, tantalum, titanium and vanadium are sometimes added in smaller amounts. Exposure to hard metal dusts can induce a lung fibrosis with cobalt playing a major role. In order to provide information on the role that each metal may have in causing this disease, determination of the total content and the distribution of inhaled metals in lung tissue of hard metal workers is of paramount importance. However, samples such as transbronchial biopsy and bronchoalveolar lavage (BAL), often used in the medical diagnosis of pneumoconiosis, only allow for a small amount of material. This calls for sensitive and accurate analytical procedures for microdetermination and distribution of metals in pulmonary tissue and cellular material, such as macrophages. This work proposes a combination of sophisticated analytical techniques such as neutron activation analysis (NAA), currently applied to the determination of the total concentration of more than 30 elements in biological specimens, and PIXE analysis, particularly microPIXE, which has a great potential for microdistribution analysis in small biological samples. Principles and perspectives for the combined use of these techniques for the analysis of human tissue are outlined and discussed. NAA: determination of hard metals in lung tissue are carried out by neutron irradiation (2 × 10¹⁴ neutrons cm⁻² s⁻¹) in the HFR reactor of Petten. After neutron activation, radiochemical separations of ⁶⁰Co, ¹⁸⁷W, ¹⁸²Ta, ⁵¹Cr followed by computer-based high resolution gamma ray spectrometry allow the measurement of these elements in pulmonary tissues with sensitivities ranging from 10⁻⁴ μg (Cr) to 10⁻⁶ μg (W). PIXE: this technique is multielemental and of relatively high sensitivity (μg/g) even in small total sample masses of from 10 to 100 μg, thus allowing the analysis of parts of needle biopsies. Whereas PIXE has been successfully applied to many medical problems, its usefulness is limited in the total samples analysis for cobalt-related hard metal disease, due to the low levels of cobalt in tissue combined with severe element interferences from the generally more abundant metal, iron. Nevertheless, microPIXE, a special variety of the method scanning over the sample with a focussed ion beam of about 2 × 2 μm², could complement the NAA findings in total samples in the sense of achieving a microdistribution analysis of hard metals (including cobalt) in suitable thin tissue sections.The availability of specialized facilities at the JRC such as the powerful HFR reactor (Petten), the NAA laboratories (Ispra) and the microPIXE facility (Geel) could represent a European ‘reference pole’ for the study of metals in tissues of hard metal diseased subjects.     

Determination of no effect levels of heavy metals for rainbow trout using hepatic metallothionein

Rainbow trout (Salmo gairdneri) were exposed to various sublethal concentrations of a mixture of zinc, copper and cadmium for periods of time ranging from 4 to 16 weeks and the concentration of metallothionein (MT) in the livers was determined. The data were described by linear regressions of hepatic MT (with 95% confidence limits) against concentration of metal. From these data could be determined a “no observable effect” concentration for each metal at which the concentration of hepatic MT in exposed fish was not distinguishable from that in unexposed fish. The value thus determined was in close agreement with estimates of the “no observable effect” concentrations of zinc, copper and cadmium calculated for soft water by other authors. The elevation of hepatic MT in rainbow trout therefore appears to provide a useful biological response for the estimation of “no observable effects” of zinc, copper and cadmium in mixture in the natural environment.     

Experiments with haliscomenobacter hydrossis in continuous culture without and with zoogloea ramigera

A study has been made of the sheath-forming bacterium Haliscomenobacter hydrossis, by growing the organism in continuous culture. Glucose together with components from trypticase soy broth/yeast extract were used as the energy source. At low dilution rates glucose was a more important energy source than components from trypticase soy broth/yeast extract. H. hydrossis was unable to produce large amounts of reserve material even in the presence of an excess of glucose. The minimum doubling time was approximately 13 h in the complex medium. The uptake sequence of amino acids derived from the trypticase soy broth yeast extract was found to be as follows: glutamic acid, glycine, methionine, tryptophan, lysine and arginine were easily consumed by the micro-organism, whereas the other amino acids were taken up mainly at low dilution rates.Competition experiments were carried out with H. hydrossis and Z. ramigera at two different dilution rates (0.016 and 0.005 h^-t). At both dilution rates Z. ramigera was dominantly present in the cultures.Finally the glucose respiration and glucose uptake of a washed cell suspension of H. hydrossis was studied. The oxygen uptake rate increased only very slightly upon addition of glucose. The difference between endogenous respiration and oxygen uptake rate in the presence of glucose was increased when the washed cells had been aerated a period of time.     

The determination of cadmium. lead, copper and zinc in ground water, estuarine water, sewage and sewage effluent by anodic stripping voltammetry

Anodic stripping voltammetry (ASV) using the thin-film mercury electrode was shown to be a successful technique for the determination of total (free plus complexed) trace metal concentrations in various types of aqueous sample. The method developed involved the minimum of sample treatment and required only simple and inexpensive equipment. The practical limit of sensitivity was about 0·1 μg I⁻¹ for cadmium, lead and copper. The determination of zinc was found to be complicated by the formation of an intermetallic compound with copper. Interference by other trace metals and by complexing agents was investigated. Photochemical oxidation for the decomposition of complexes of the metals with organic ligands in filtered sewage and sewage effluent was found to be successful, although the process is slower for cadmium than for the other metals. Good agreement with atomic absorption spectroscopy was obtained for all the types of aqueous sample investigated. Possible improvements of the ASV technique are discussed.     

Heavy metal accumulation by aquatic fungi and reduction in viability of Gammarus pulex fed Cd contaminated mycelium

The addition of Pb²⁺ (1.0 and 2.5 μg ml⁻¹) and Cd²⁺ (2.5 and 5.0 μg ml⁻¹) to growth medium decreased the growth of aquatic fungi, while Zn²⁺ even at a concentration of 10 μg ml⁻¹ had no inhibitory effect. Low concentrations of Cd²⁺ and Zn²⁺ on the other hand stimulated mycelial growth. The fungi accumulated considerable amounts of metal from the growth medium, generally in the order Zn²⁺ > Pb²⁺ > Cd²⁺ · Cd²⁺ was also accumulated by fungi from successive changes of medium containing low concentrations of the metal. Application of Langmuir and Freundlich isotherms to the results showed that the metals were accumulated largely by adsorption to the surface of the mycelium.Three species of aquatic fungi supported the growth of the freshwater shrimp. Gammarus pulex when provided as sole food source, sustaining from 30 to 60% of shrimps fed for a period of 21 days. A marked reduction in shrimp viability occurred however, when G. pulex was fed Pythium sp. containing Cd²⁺ (150–170 μg g⁻¹), with none of the shrimps surviving beyond 13 days, compared with a survival rate of 60% after 21 days for shrimps fed uncontaminated mycelium. Bodies of poisoned shrimps sampled on day 13 were found to contain Cd²⁺ (22.03 μg g⁻¹) showing that the metal can be transferred from aquatic fungi to G. pulex, the first step in a food chain involving freshwater fish and higher organisms.     

Uptake of cadmium, zinc, copper, lead and chromium in the pacific oyster. Crassostrea gigas. Grown in the tamar river. Tasmania

Hundreds of oysters and mud samples from 15 sites along the Tamar River were analysed for cadmium, copper, zinc, lead and chromium. The widely accepted concept of enrichment factors of up to several hundred thousand, describing accumulation by oysters of cadmium, zinc and copper from seawater has been found to be grossly misleading. Concentrations found for these three metals in oysters were only 10–40 times the concentrations in inhabited muds. Concentrations of metals in muds may be used to indicate whether a potential oyster bed would produce oysters that were grossly contaminated. Approximately 1 ppm cadmium in mud could result in oysters containing at least 25 ppm, i.e. 4–5 ppm wet wt. Similarly. 100 ppm zinc in mud could produce oysters containing at least 4000 ppm. i.e. 800–1000 ppm wet wt. Three heavy metal accumulation processes were discernible. Copper and chromium appeared to be absorbed up to a maximum weight that was limited by the size of the oyster and was independent of the amount of metal in the mud. Lead was not absorbed through any physiological demand, but was randomly incorporated at sites containing high concentrations in the mud. Zinc and cadmium were accumulated by a process that depended primarily on the concentrations of these metals in the mud at each site. Mean dry wt concentrations of metals in oysters and mud samples ranged from: 4.2–134 ppm and 0·4 to 5·7 ppm cadmium; 200–1700 ppm and 3–224 ppm copper: 0 135 ppm and 4–1500 ppm lead: 1–37 ppm and 2–88 ppm chromium; 1700 14.000 ppm and 20–500 ppm zinc. respectively.