Concentrations of heavy metals and plant nutrients in water, sediments and aquatic macrophytes of anthropogenic lakes (former open cut brown coal mines) differing in stage of acidification.

Concentration of heavy metals (Al, Ba, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sr, V and Zn) as well as macronutrients (N, P, K, Ca, Mg, S) were measured in water, bottom sediments and plants from anthropogenic lakes in West Poland. The collected plants were: Phragmites australis, Potamogeton natans, Iris pseudoacorus, Juncus effusus, Drepanocladus aduncus, Juncus bulbosus, Phalaris arundinacea, Carex remota and Calamagrostis epigeios. Two reference lakes were sampled for Nymphaea alba, Phragmites australis, Schoenoplectus lacustris, Typha angustifolia and Polygonum hydropiper. These plants contained elevated levels of Cd, Co, Cr, Cu and Mn, and part of the plants contained in addition elevated levels of Mn, Fe, Pb, Ni and Zn. Analyses of water indicated pollution with sulfates, Cd, Co, Ni. Zn, Pb and Cu, and bottom sediments indicated that some of the examined lakes were polluted with Cd, Co and Cr. Strong positive correlations were found between concentrations of Co in water and in plants and between Zn in sediments and plants, indicating the potential of plants for pollution monitoring for this metal. Heavy metal accumulation seemed to be directly associated with the exclusion of Ca and Mg.     

A comparison of native and transplanted Fontinalis antipyretica Hedw. as biomonitors of water polluted with heavy metals

Native and transplanted mosses of the species Fontinalis antipyretica were studied to assess their capacity as biomonitors of heavy metals. Assays were carried out with transplanted mosses (sampled from an unpolluted control stream) exposed for 60 days to five streams polluted with heavy metals. At the same time, native mosses were collected from the exposure sites. Concentrations of N, P, K, Ca, Mg, S, Fe, Al, Ba, Cd, Co, Cr, Cu, Mn, Ni, Pb, V, and Zn were determined in the mosses (native and transplants), stream waters, and sediments of both exposure and control sites. The results showed that the transplanted mosses accumulated significantly more Al, Cr, Cu, Pb, V, and Zn than the native mosses. The concentrations of Co and Mn in all streams were significantly higher in the native mosses.     

Trace metals and water chemistry of forest lakes in northern Sweden

To study the influence of airborne pollutants on water quality, water samples were taken from 59 forest lakes in northern Sweden along a section of about 1000 km in length. Determinations were made of pH, water colour, conductivity, major ions, nitrogen and phosphorus, as well as the metals Fe, Mn, Al, Zn, Cu, Pb, Cd, Ni, Cr, Co, As and V.The lake waters were generally soft, with low levels of electrolytes. The pH values increased and the sulphate concentrations decreased from south to north. The lakes in the southern parts of the area showed evidence of increased deposition of acidifying substances, shown by higher Ca + Mg/alkalinity ratio.A geographical distribution pattern was observed from Zn and to some extent also for Pb and Cd, with the highest concentrations in the south. However, pH and water colour were of major importance for the distribution of trace metals. Mn, Al and Zn were negatively correlated to pH and Fe, Mn, Al, Pb and As were positively correlated to water colour. A multiple regression analysis showed that the distribution of Fe was influenced mainly by water colour, Zn mainly by pH, while Mn and Al were influenced both by pH and colour. Some of the lakes were sampled both in winter and summer and the concentration of metals was found to be around two-fold higher in winter than in summer.     

Assessment of metal mobility in dredged harbour sediments from Barcelona, Spain

In order to assess heavy metal mobility in dredged harbour sediments, six superficial sediment samples covering a range of pollution levels and environments were collected in Barcelona Harbour. Samples were characterised in terms of major compounds (Al, Ca, Fe, Mn, Si, Ti, Mg, K and Na); total C, N and S contents; organic matter; and water content. Pseudo-total trace metal contents were assessed after aqua regia digestion (ISO 11466:1995). The modified BCR three-step sequential extraction procedure (BCR-SEP) was applied, and both major compounds (Al, Ca, Fe and Mn) and trace metals (Cd, Cr, Cu, Ni, Pb and Zn) were determined in the different extracts. Both the pseudo-total digestion method and the BCR-SEP were validated using two sediment certified materials from lakes (BCR CRM 701 and BCR CRM 601). The highest metal concentrations were observed in one of the sampling points which receives an urban discharge. The observed mobility order (percentage of metal extracted in the first step) of the six trace metals studied was Cd>Zn>Pb>Cu>Ni>Cr. The good agreement observed with the results obtained as the sum of the four steps (extractable+residue) and the pseudo-total content shows that laboratory working conditions were under control.     

Metal concentrations in a shallow groundwater aquifer underneath petrochemical complex

Duplicate groundwater samples were collected from 104 monitoring wells (piezometers) from shallow aquifers underneath an industrial city in the Eastern Province of Saudi Arabia. Concentrations of Al, As, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Ti, V, Zn, Ca, Mg, K, Na, Cl, SO₄, alkalinity, salinity, total dissolved salts, and pH were determined in these samples. Analysis of variance showed significantly (p < 0.05) wide variations in the concentrations of the above parameters. The contour maps of metal concentrations indicated that these variations were related to important landmarks in the study area. The results of correlation analyses suggest that geographical as well as chemical factors may influence metal distribution in the groundwater samples. To investigate the geographical effects, the analytical data were normalized (element/Cl ratios were calculated) for chemical variability. As expected, contour mapping of the ratio data of element/Cl of Na, Ca, Mg, K, SO₄, alkalinity, salinity, total dissolved salts, and Sr vary in a relatively small range and did not show a particular geographical trend. The groundwater sample from the industrial-dust area contained higher ratios between concentrations of Cl and Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, and Zn. These observations clearly suggest an extraneous contamination source, probably industrial dust, in the area. Another geographical area where metal (As, Cd, Cu, Mo, Ni, Ti,and V)/Cl ratios were found to be large was in the vicinity of an oil-refinery. Groundwater samples collected from the vicinity of a fertilizer plant and green-belt area contained relatively higher ratios of Al, Cd, Cr, Co, and Ni. The results of this study suggest that leachate from the industrial dust, leakage from the oil refinery and fertilizer plant, and drainage of irrigation water are some of the important pollution sources in the industrial city.     

The efficiency of oxidation ponds at the Kraft pulp and paper mill at Webuye in Kenya

Two streams of wastewater from the Kraft Pulp and Paper Mills at Webuye are released from the pulping, bleaching and paper pressing departments. One stream is made up of clear wastewater and the second is made up of turbid wastewater. The wastewaters from the mills are treated using oxidation ponds, after which the treated wastewater is discharged into the River Nzoia. The wastewater was analysed for Cd, Cr, Cu, Ni, Pb. Zn, Ca, K, Mg and Na. The results are that the concentrations of Ca and Na significantly increased in the treated wastewater. The concentrations of Cd, Pb, Zn, K and Mg also increased in the treated wastewater, though not significantly. The concentrations of Cr, Cu and Ni decreased in the treated wastewater but not significantly. Mass loadings of the metals discharged into River Nzoia were calculated. It was found that the mean mass loading of two metals (Ca and Na) significantly increased in the treated wastewater. Five metals (Cd, Pb, Zn, K and Mg) increased in the treated wastewater although not significantly. Three metals (Cr, Cu and Ni) decreased in the treated wastewater but the decrease was not significant. The concentrations of Cd, Cu, Ni, Pb and Zn were all above the limits set by EC for drinking water. These findings pose serious questions of the effectiveness of oxidation ponds system to safeguard the receptor against pollutants from the pulp and paper industry at Webuye.     

Use of numerical taxonomy for comparison of metal pollution in the environment

Numerical taxonomy has been applied to explain the behaviour of macroconstituents (Na, K, Ca, Mg) and heavy metals (Cr, Mn, Fe, Co, Ni, Pb, Cu, Zn, Cd) in different ecological sections (mollucs, plants, rain, drv deposition, soils, airborne dust, lixiviates through soils, springs) in the industrialized area near Bilbao (Spain). Distances based on correlation coefficients and mean Euclidean distances have been used for drawing dendrograms of metals and sections. Three types of effects may be distinguished, due to potassium, other macrocomponents (Na, Ca, Mg) and heavy metals as a result of the accumulation of these constituents in specific sections of the environment.     

Dietary intake of metals by Mumbai adult population

Daily intake of 12 metals (Na, K, Ca, Cu, Zn, Fe, Mn, Mg, Pb, Cd, Co and Ni) by Mumbai adult population were assessed by analysing duplicate diet samples. These metals were determined by flame atomic absorption spectrophotometry (AAS) and stripping voltammetric techniques. A total of 250 diet samples containing 170 vegetarian diet and 80 non-vegetarian diet collected during April 2003 to March 2004 were analysed during this study. Daily dietary intakes of 2.4 g Na and 1.2 g K were observed for Mumbai adults. Daily dietary intakes of Ca, Cu, Zn, Fe, Mn and Mg were 367, 1.0, 6.3, 6.7, 2.0 and 304 mg, respectively. Pb, Cd, Co and Ni intakes by Mumbai adults were 32.3, 2.2, 2.2 and 108 microg/day, respectively. From this study it has been observed that the intake of toxic metals such as Pb, Cd and Ni is much lower than the tolerable daily intake derived from PTWI given by FAO/WHO and could not be considered harmful in this group of subjects. Daily intake of the studied 12 metals was found to be higher in non-vegetarian diet compared to the vegetarian diet (P<0.02, 0.01).     

Sex- and age-related variation in elemental concentrations of contemporary Japanese ribs

Twenty elements (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, Sr, Ti, V, Zn, C and N) in 42 Japanese ribs (forensic medical autopsy cases) were determined using inductively coupled plasma atomic emission spectrometry (ICP-AES), atomic absorption spectrometry (AAS) and carbon and nitrogen analysis to examine sex- and age-related variation in the concentrations of these elements. Bone Fe and Pb concentrations were significantly higher, while P concentrations were lower in males. Elements which showed age-related variation were Ca, P, Al, Fe, Mg, Na, Pb and Zn. Of these, Al, Fe, Pb and Zn linearly accumulate in bone with advancing age. The elements Na and Mg showed the lowest and highest concentrations in the youngest age group (0-19 years), respectively, and reached plateau levels in older age groups. The Ca and P concentrations were highest in the 20-39-year age group, gradually decreasing throughout older age groups, indicating that osteoporotic bone loss occurs in the older subjects. In addition, the results of correlation analysis indicated that the organic matter content of the bone, represented by C or N concentration, was a factor which contributed to the elemental variation of the bone.     

Elemental composition of ancient Japanese bones

Excavated bones (rib) obtained from 50 sites in Japan were measured by ICP atomic emission spectrometry and atomic absorption spectrometry for concentration of 19 elements, including Al, B, Ca, Cd, Cr, Co, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, Sr, Ti, V and Zn. One hundred and forty-one specimens were classified into five groups according to Japanese prehistoric and historic eras (Jomon, Yayoi, Kofun, Kamakura and Muromachi, and Edo). The elements, with concentrations which showed no significant change with era were Al, B and Cr. Average concentrations of Ca were in the range 2-2.5 X 10(-1) g g-1 and those of P ranged from 1.1 to 1.3 X 10(-1) g g-1, indicating a well-preserved bone mineral matrix. The Ca/P ratio (mol/mol) was lowest in the Edo group--1.48 as compared with 1.54-1.66 in the other groups. Among the elements which showed changes with era were Pb, Fe, Co and Mn, all of which showed remarkably elevated concentrations in the Edo group. In addition to this unique elemental composition of Edo bones, samples from the Kofun era showed a completely different composition from those of other periods, i.e. they had the highest concentrations of Cd, Zn and Mg, and the lowest concentrations of Cu, K, Ni and Sr. The cause of the elevated Pb concentration in Edo bones is discussed in relation to human activities which may have led to environmental Pb pollution.     

Marine trace metal pollution assessment by fish as indicator species

Levels of eleven trace metals (Ag, As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn and Hg) and four macronutrients (Na, K, Ca and Mg) were estimated in the edible muscle of six commercially exploited fish species using the atomic absorption spectrophotometric method. The fish included in the study were: Argyrops spinifer, Fistularia petimba, Bramnoplaties suppositus, Lepidotriqla omaneaisis, Pampus argentus and Sphyraena obtusata harvested from the south‐west coast of the Arabian Sea along the Karachi coast, Pakistan. All metals have shown substantial increase in their average levels over the past few years. Pampus argentus was found undesirable for human consumption as it contained elevated levels of five metals (As, Cr, Pb, Zn and Hg). This species could be used to monitor marine trace metal pollution since it was found to contain consistently enhanced levels of the industrial metals.     

Concentrations and leachability of chemical elements in estuarine sulfur-rich sediments, W. Finland

Concentrations, distributions and mobility of chemical elements were investigated in reduced sulfur-rich estuarine sediments located in western Finland. The main objective was to determine the possible extent of metal leaching when dredged masses of these sulfur-rich sediments are dumped on the land and thus exposed to air. When dredged, the reduced sulfur in the sediments oxidises resulting in a lowering of pH, which in turn is expected to leach metals. The study area is an artificial lake claimed from the Botnian sea in 1962. In this lake, several mass-kills of fish have occurred, believed partly to be due to dredging. Two sediment samples (0-50 and 50-100 cm) were taken from 39 sampling points in the lake. These samples were leached in aqua regia (2:2:2 HNO3/HCl/H2O1) and analysed for Fe, Al, Mg, Ca, K, P, Na, Mn, Zn, Ba, V, Sr, Cr, Ni, Cu, Co, As, Pb, B, Mo and Cd with ICP-AES. Sulfur and organic carbon were analysed with Leco. In a controlled laboratory experiment, the sediments were allowed to oxidise for 1 year while moisturised with deionised water every month. The pH and conductivity were determined in the beginning of the experiment (reduced state) and in the end (oxidised state). In the supernatants in the oxidised states the amount of leached metals (Na, Al, Mn, Zn, Sr, Co, Ni, Cu, Cd, Cr, Pb, U, Li, Rb and As) were determined with ICP-MS. The sediments were found to contain low levels of toxic metals but, as expected, high concentrations of sulfur. In the experiment, pH was lowered (down to 3.0) and the conductivity increased in all samples due to oxidation and release of metal ions. The extent of leaching varied between 0.03% for As and 12.3% for Na. Critical pH values, at which high amounts of metals begin to leach, were obtained graphically. These values varied between 4.8 (Ni) and 3.3 (Cr). Not all elements were controlled by pH, e.g. Mn correlated well with its aqua regia leachable concentration. In a planned dredging operation in the area some 23,300 t (10,500 m3) (dry wt.) of sediments will be dredged. The amounts of metals likely to be leached, according to the results from this study, are as follows (kg): Al (1710), Mn (1230), Zn (59), Sr (39), Co (13), Ni (12), Cu (2) and less than 1 kg of Cd-Cr-As-Pb.     

Concentrations of selected metals in honey consumed in Nigeria

The concentration of metals, cadmium (Cd), lead (Pb), nickel (Ni), chromium (Cr), copper (Cu), cobalt (Co), iron (Fe), manganese (Mn), and zinc (Zn) was measured in selected samples of honey in Nigeria with a view to providing information on the regional concentration profile of metals in these honeys. The honey samples were digested with a mixture of acids and analysed for metal concentrations using atomic absorption spectrophotometry. The concentrations of metals (mg kg^?1) in these honeys ranged from < 0.3 for Cd,<0.50–39.75 for Pb,<0.25–6.98 for Ni,<0.25–55.25 for Cr,<0.25–71.25 for Cu,<0.25–3.50 for Co,<5.0–163.15 for Fe,<11.0–31.75 for Mn and 1.0–31.0 for Zn. The concentrations of metals were relatively high but lower than their respective permissible limits in food except for Pb and Cu in some samples. The regional distribution patterns of metals indicated that honey samples from the Niger Delta region of Nigeria had higher mean concentrations of Ni, Cr, Co, Fe and Zn than honey samples from other regions. The honey samples from the northern region had higher mean concentrations of Pb and Cu.     

Partitioning of trace metals before and after biological removal of metals from sediments

Metal removal by biological solubilization in three strongly contaminated sediments was carried out in a two-liter stirred bioreactor. Biological treatment yielded metal removal efficiencies in the range of 11-30%, 43-57%, 60-79%, 61-90%, 18-21%, 0-10% for Pb, Cu, Zn, Cd, Ni and Cr, respectively. The treated sediments were then rinsed with a NaCl solution (0.5 M), resulting in an increase by nearly 47% in Pb removal for the three sediments, while for other metals (Cu, Zn, Cd, Ni, Cr), the NaCl rinse did not seem to allow any significant increase in metal solubilization. A standard procedure of sequential selective extraction (SSE) was applied to the sediments before and after each treatment. With regard to Pb, Zn and Cd, the carbonate bound fractions (2/3 sediments) represented 18-42% of metals prior to treatment, while the iron and manganese oxides bound fraction constituted 39-60% of metals for the three sediments. Between 90 and 100% of Pb, Zn and Cd removed by the process came from the fractions bound to carbonates and from those bound to Fe and Mn oxides. The organic matter and sulfide bound fractions contained 65-72% of total Cu present before treatment and the process removed, on average, 63% Cu present in this fraction. In contrast, Ni and Cr were found mainly in the residual fractions (50-80%). Finally, this biological treatment did not solubilize Cr appreciably, while removal of Ni mostly originated from the carbonate and Fe/Mn oxides fractions (70-80%).     

Kidney and liver levels of some major, minor and trace elements in two Ontario communities

The contents of Ag, As, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Mo, Na, Ni, P, Pb, Se, Sr, Th, Ti and Zn in 143 autopsied liver and kidney specimens from two Ontario communities (Kingston and Ottawa) were determined using the techniques of inductively-coupled plasma--atomic emission spectrometry, and electrothermal atomization--atomic absorption spectrometry coupled with hydride evolution (As, Se), reduction--aeration (Hg), or solvent extraction (Pb). The majority of samples came from individuals older than 50 y. In general, the data for the various elements were independent of age or sex but showed some dependence on location for elements such as Cu, Fe, K, Mg, Mn, Na, P, Se and Zn. Despite these differences the elemental values of the liver and kidney samples from both the communities were within the normal range.     

Heavy metal behaviour during the activated sludge process I. Extent of soluble and insoluble metal removal

The extent of removal of Ag, Bi, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Tl and Zn and their distribution between the soluble and insoluble phases in the influent, and effluent of the activated sludge process has been studied using a pilot-scale plant operated at sludge ages of 3, 6, 9 and 12 days. Molybdenum, Tl, Co, Mn and Ni were >50% soluble in the influent settled sewage. The mean removals of the former two metals were <3% and the latter three were 35 and 50%. Silver, Bi, Cd, Cr, Cu, Pb and Zn were all <35% soluble in the influent and had substantial removals of >75%. Solubilities were greater in the effluent than the influent with the exception of Mn. The observed overall removals of Ag, Bi, Co, Ni, Pb, Tl and Zn were almost entirely due to insoluble metal removal; Cd, Cr and Cu removals had a significant contribution from soluble metal removal. Overall Mn removal appeared to be solely due to soluble metal removal.     

Element levels in birch and spruce wood ashes: green energy?

Production of wood ash has increased strongly in the last ten years due to the increasing popularity of renewable and CO(2)-neutral heat and energy production via wood burning. Wood ashes are rich in many essential plant nutrients. In addition they are alkaline. The idea of using the waste ash as fertiliser in forests is appealing. However, wood is also known for its ability to strongly enrich certain heavy metals from the underlying soils, e.g. Cd, without any anthropogenic input. Concentrations of 26 chemical elements (Ag, As, Au, B, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, La, Mg, Mn, Mo, Na, Ni, P, Pb, S, Sb, Sr, Ti, and Zn) in 40 samples each of birch and spruce wood ashes collected along a 120 km long transect in southern Norway are reported. The observed maximum concentrations are 1.3 wt.% Pb, 4.4 wt.% Zn and 203 mg/kg Cd in birch wood ashes. Wood ashes can thus contain very high heavy metal concentrations. Spreading wood ashes in a forest is a major anthropogenic interference with the natural biogeochemical cycles. As with the use of sewage sludge in agriculture the use of wood ashes in forests clearly needs regulation.     

Trace metals in Shatt al-Arab River,Iraq

The distribution of 10 trace metals Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, V and Zn have been determined along the northern section of the Shatt al-Arab River, Iraq. Analyses were carried out, employing a flameless AAS instrument. The mean concentrations of the dissolved species were as follows (expressed in μg l^?1): 0.25 Cd, 0.9 Cu, 716 Fe, 1.3 Mn, 0.3 Pb, 0.2 V and 1.8 Zn. Mean concentrations of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, V and Zn in the particulate matter were 55.2, 6.0, 188, 77, 31 472, 1731, 3807, 93, 207 and 77 μg g^?1 respectively. In the exchangeable fraction of the sediment were 0.15, 5.5, 11.1, 11.9, 1625, 482, 42, 30.5, 25.7 and 6 μg g^?1, whereas in the residual were 0.025, 11.5, 96.1, 22, 5176, 258, 613, 3.9, 162 and 56.8 μg g^?1 respectively. Thus, the exchangeable trace metals represent the following mean percentage of the total; 75% Cd, 33% Co, 10% Cr, 34% Cu, 24% Fe, 63% Mn, 7% Ni, 74% Pb, 14% V and 23% Zn. The concentration of Ni and V were relatively high, this was attributed to the petroleum-rich deposits of the region. The concentrations observed for other metals were lower or equal to those reported for control sites except for Pb which was slightly higher. The data obtained were subjected to simple linear regression analysis and expressed in the form of correlation coefficients. It was found that the inter-elemental relationships are rather complex.     

Transformation of metals speciation in a combined landfill leachate treatment

Landfill leachate was treated by a combined sequential batch reactor (SBR), coagulation, Fenton oxidation and biological aerated filter (BAF) technology. The metals in treatment process were fractionated into three fractions: particulate and colloidal (size charge filtration), free ion/labile (cation exchange) and non-labile fractions. Fifty percent to 66% Cu, Ni, Zn, Mn, Pb and Cd were present as particulate/colloidal matter in raw leachate, whereas Cr was present 94.9% as non-labile complexes. The free ion/labile fractions of Ni, Zn, Mg, Mn, Pb and Cd increased significantly after treatment except Cr. Fifty-nine percent to 100% of Al was present mainly as particulate/colloidal matter > 0.45 μm and the remaining portions were predicted as non-labile complexes except in coagulation effluent. The speciation of Fe varied significantly in various individual processes. Visual MINTEQ simulation showed that 95-100% colloidal species for Cu, Cd and Pb were present as metal-humic complexes even with the lower dissolved organic carbon. Optimum agreements for the free ion/labile species were within acidic solution, whereas under-estimated in alkaline effluents. Overestimated particulate/colloidal fraction consisted with the hypothesis that a portion of colloids in fraction < 0.45 μm were considered as dissolved.     

Application of high Cu compost to Swiss chard and basil

A greenhouse container experiment was conducted to evaluate the effect of high Cu compost on basil and Swiss chard productivity, and the accumulation of As, Ca, Fe, Hg, K, Mg, Na, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, S and Se in growth medium and plant tissue. The Cu content of the compost was over 1200 mg/kg, much higher than Canadian standards for type B compost quality. The treatments consisted of control soil (0% compost), and 20, 40 and 60% (by volume) of high Cu compost added to soil. All compost application treatments (20, 40 and 60%) resulted in increased dry matter yields in Swiss chard and basil. Addition of high Cu compost influenced basil plant development. Plants from the 20 and 40% treatments had higher numbers of buds and flowers. There were no differences between the control and 60% compost treatments with respect to flower initiation. Addition of 20, 40 and 60% compost to the soil resulted in increased EXCH fractions of Cu, but not of Mn and Zn. Compost additions resulted in increase in the HNO(3) extractable, CARB, FeMnOX, and in OM fractions of Cu, Mn and Zn in soils. Compost application increased soil pH and EC, soil HNO(3) extractable Ca, K, Mg, P, Na, B and Pb, but did not alter soil HNO(3) extractable Cd, Co, Cr, Mo, Ni, Se. Increased rates of compost application decreased tissue Ca in basil, tissue Na in both plants, increased tissue K, Mg in both plants, but, did not alter tissue P, Co, Cr, Mo, Ni of either plants, and B in basil. Tissue As, Hg, Pb, and Se from all treatments were under the detection limits of VGA-AAS (for As, Hg, Se) and ICP (for Pb). Compost additions altered basil oil chemical composition. Copper in the essential oil of basil was below 0.25 mg/l. In conclusion, the addition of high rates of relatively immature high Cu compost may not always increase Cu concentration in plants and in plant oils.