Heavy metal content and distribution in surface sediments of the Seyhan River, Turkey

Chemical fractionation of seven heavy metals (Cd, Cr, Cu, Mn, Ni, Pb and Zn) was studied using a modified three-step sequential procedure to assess their impacts in the sediments of the Seyhan River, Turkey. Samples were collected from six representative stations in two campaigns in October 2009 and June 2010, which correspond to the wet and dry seasons, respectively. The total metal concentrations in the sediments demonstrated different distribution patterns at the various stations. Cadmium was the only metal that was below detection at all stations during both sampling periods. Metal fractionation showed that, except for Mn and Pb, the majority of metals were found in the residual fraction regardless of sampling time, indicating that these metals were strongly bound to the sediments. The potential mobility of the metals (non-residual fractions) is reflected in the following ranking: Pb > Mn > Zn > Cu > Ni > Cr in October 2009 and Mn > Pb > Zn > Cu > Ni > Cr in June 2010. The second highest proportion of metals was bound to organic matter/sulfides, originating primarily from anthropogenic activities. Non-residual metal fractions for all stations were highest in June 2010, which may be linked to higher organic matter concentrations in the sediment samples with 1.40% and 15.1% in October 2009 and June 2010, respectively. Potential sediment toxicity was evaluated using the Risk Assessment Code (RAC). Based on RAC classification, Cd and Cr pose no risk, Cu and Ni pose low risk, Pb and Zn were classified as medium risk metals, while the environmental risk from Mn was high. In addition, based on the sediment quality guidelines (SQG), the Seyhan River can be classified as a river with no, to moderate, toxicological risks, based on total metal concentrations.     

Characteristics of heavy metals and Pb isotopic signatures in sediment cores collected from typical urban shallow lakes in Nanjing, China

To investigate the contamination levels and sources for heavy metals that have occurred during the development of cities, sediment cores collected from typical urban shallow lakes (Xuanwu Lake and Mochou Lake) in Nanjing, China were analyzed for Cu, Pb, Zn, Cd, Cr, Ni, and for Pb stable isotopic ratios. No significant differences were found in the concentrations of Cu, Ni and Cd among sediment layers from Xuanwu or in the levels of Cr and Ni among sediment layers from Mochou. However, there were significant differences among the layers in the concentrations of Cr, Zn and Pb in Xuanwu and Cu, Zn, Cd and Pb in Mochou. Based on geoaccumulation indexes and enrichment factors, Cd was the primary pollutant at all depths in the sediment cores. The ratios of (206)Pb/(207)Pb and (208)Pb/(206)Pb differ significantly among sediment layers in Xuanwu. No significant differences were found on the ratios of (208)Pb/(206)Pb in Mochou, but the ratios of (206)Pb/(207)Pb differ significantly among some of the sediment layers in Mochou. The range of (208)Pb/(206)Pb and (206)Pb/(207)Pb ratios was found to be 2.098-2.106 and 1.170-1.176, respectively, for sediment cores from Mochou Lake and 2.091-2.104 and 1.168-1.183, respectively, for cores from Xuanwu Lake. The differences in heavy metal concentrations and the Pb isotopic ratios with depth for the cores from Xuanwu and Mochou confirmed that the contamination sources changed during the formation of the different sediment layers. Furthermore, the ratios of (206)Pb/(207)Pb demonstrated that gasoline and vehicular Pb were not the primary sources of Pb contamination at different depths in the sediment cores in Xuanwu Lake and Mochou Lake.     

Assessment of the Effectiveness of Environmental Dredging in South Lake,China

Environmental dredging is a primary remedial option for removal of the contaminated material from aquatic environment. Of primary concern in environmental dredging is the effectiveness of the intended sediment removal. A 5-year field monitoring study was conducted to assess the effectiveness of the environmental dredging in South Lake, China. The concentrations of total nitrogen (TN), total phosphors, and heavy metals (Zn, Pb, Cd, Cu, Cr, Ni, Hg, and As) before and after dredging in sediment were determined and compared. Multiple ecological risk indices were employed to assess the contamination of heavy metals before and after dredging. Our results showed that the total phosphorus levels reduced 42% after dredging. Similar changes for Hg, Zn, As Pb, Cd, Cu, Cr, and Ni were observed, with reduction percentages of 97.0, 93.1, 82.6, 63.9, 52.7, 50.1, 32.0, and 23.6, respectively, and the quality of sediment improved based on the criterion of Sediment Quality Guidelines by USEPA and contamination degree values (C_d) decreased significantly (paired t-test, p < 0.05). Unexpectedly, the TN increased 49% after dredging compared to before dredging. Findings from the study demonstrated that the environmental dredging was an effective mechanism for removal of total phosphorus and heavy metals from South Lake. Nevertheless, the dredging was ineffective to remove total nitrogen from sediment. We conclude that the reason for the observed increase in TN after dredging was likely ammonia release from the sediment impairing the dredging effectiveness.     

Characteristic levels of heavy metals in soil profiles of automobile mechanic waste dumps in Nigeria

The characteristic levels of heavy metals (Cd, Cr, Cu, Pb, Ni and Zn) of soil profiles of automobile mechanic waste dumps were studied. The concentration of heavy metals decreased with the depth of the profile and lateral distance from the dumpsites. The levels found in this study exceeded background concentrations and limits for agricultural and residential purposes. The distribution pattern of heavy metals in the soil profiles were in the following order Pb > Zn > Cu > Cd > Ni > Cr. The mechanic waste dumps represent potential sources of heavy metal pollution to environment. The elevated levels of heavy metals in these soil profiles constitute a serious threat to both surface and groundwater.     

Solubility of phosphorus and heavy metals in potting media amended with yard waste-biosolids compost

The potential risk of surface and ground water contamination by phosphorus (P) and heavy metals leached from compost-based containerized media has become an environmental concern. Solubility and fractionation of P and heavy metals were evaluated in media containing 0, 25, 50, 75, or 100% compost derived from biosolids and yard trimmings for potential impacts on the environment. As compost proportion in peat-based media increased from 0 to 100%, concentrations of total P, Cd, Cu, Ni, Pb, Zn, and Mn in the media increased whereas concentrations of total Co and Cr decreased. Except for Cu, all heavy metals in the water-soluble fraction decreased with increasing compost proportion in the media, because of higher Fe, Al, and Ca concentrations and pH values of the composts than the peat. When the media pH is controlled and maintained at normal range of plant growth (5.5-6.5), leaching of the heavy metals is minimal. Incorporation of compost to the peat-based media also decreased the proportion of total P that was water-soluble. However, concentrations of bioavailable inorganic phosphorus (NaHCO3-IP), readily mineralizable organic phosphorus (NaHCO3-OP), potentially bioavailable inorganic phosphorus (NaOH-IP), and potentially bioavailable organic phosphorus (NaOH-OP) were still higher in the media amended with compost because of higher total P concentration in the compost. Further study is needed to verify if less or no topdressing of chemical P fertilizer should be applied to the compost-amended media to minimize P effect on the environment when compost-amended potting media are used for nursery or greenhouse crop production systems.     

Granulometric and Metal Distributions for Post‐Katrina Surficial Particulate Matter Recovered From New Orleans1

Bhadha, Jehangir H., Casey Schmidt, Robert Rooney, Paul Indeglia, Ruben Kertesz, Elizabeth Bevc, and John Sansalone, 2009. Granulometric and Metal Distributions for Post‐Katrina Surficial Particulate Matter Recovered From New Orleans. Journal of the American Water Resources Association (JAWRA) 45(6):1434‐1447. Abstract: Hurricane Katrina and the resulting failure of the levees that surrounded and protected New Orleans generated a significant detained volume of stormwater within the urban area of New Orleans. Between the inundation resulting from levee failure and eventual pumped evacuation of stormwater from the urban area of New Orleans, a large mass of storm‐entrained particulate matter (PM) was deposited in the inundated areas. This study examined the granulometry and granulometric distribution of metals for post‐Katrina surficial PM deposits recovered from 15 sites (10 inundated and 5 non‐inundated) in New Orleans. Results of this examination were compared to pre‐Katrina data from New Orleans. While post‐Katrina analysis of PM indicates that Pb, Zn, and Cu concentrations for PM are reduced for all sites, inundated sites had higher Cu, Pb, and Zn concentrations for the settleable (～25‐75 μm) and sediment (>75 μm) size fractions. A comparison between total metal concentration and the bioavailable (leachable) fraction for PM reveals that inundated sites had up to 19% higher leachable metal concentration compared to non‐inundated sites. The reduction in PM‐bound total metal concentrations for recovered PM can be explained through a combination of scouring (and therefore change in granulometry from pre‐Katrina) that resulted from transport of suspended PM by storm flows and pumped evacuation; as well as leaching and PM‐based redistribution from extended contact with rainfall and during stormwater detention. New Orleans has been exposed to elevated levels of metals through decades of activities that include vehicular transportation, chemical, industrial, and oil production facilities resulting in higher metal concentrations for urban soil‐residual complexes. As a result, the influent storm flows associated with Katrina as an episodic event cannot solely explain the distribution and fate of PM‐associated metal concentrations.     

Phytoextraction of heavy metals by willows growing in biosolids under field conditions

Biosolids produced by sewage treatment facilities can exceed guideline thresholds for contaminant elements. Phytoextraction is one technique with the potential to reduce these elements allowing reuse of the biosolids as a soil amendment. In this field trial, cuttings of seven species/cultivars of Salix(willows) were planted directly into soil and into biosolids to identify their suitability for decontaminating biosolids. Trees were irrigated and harvested each year for three consecutive years. Harvested biomass was weighed and analyzed for the contaminant elements: As, Cd, Cu, Cr, Hg, Pb, Ni, and Zn. All Salix cultivars, except S. chilensis, growing in soils produced 10 to 20 t ha(-1) of biomass, whereas most Salix cultivars growing in biosolids produced significantly less biomass (<6 t ha(-1)). Salix matsudana (30 t ha(-1)) and S. × reichardtii A. Kerner (18 t ha(-1)) had similar aboveground biomass production in both soil and biosolids. These were also the most successful cultivars in extracting metals from biosolids, driven by superior biomass increases and not high tissue concentrations. The willows were effectual in extracting the most soluble/exchangeable metals (Cd, 0.18; Ni, 0.40; and Zn, 11.66 kg ha(-1)), whereas Cr and Cu were extracted to a lesser degree (0.02 and 0.11 kg ha(-1)). Low bioavailable elements, As, Hg, and Pb, were not detectable in any of the aboveground biomass of the willows.     

Total Contents and Sequential Extraction of Heavy Metals in Soils Irrigated with Wastewater,Akaki, Ethiopia

The Akaki River, laden with untreated wastes from domestic, industrial, and commercial sources, serves as a source of water for irrigating vegetable farms. The purpose of this study is to identify the impact of waste-water irrigation on the level of heavy metals and to predict their potential mobility and bioavailability. Zn and V had the highest, whereas Hg the lowest, concentrations observed in the soils. The average contents of As, Co, Cr, Cu, Ni, Zn, V, and Hg of both soils; and Pb and Se from Fluvisol surpassed the mean + 2 SD of the corresponding levels reported for their uncontaminated counterparts. Apparently, irrigation with waste water for the last few decades has contributed to the observed higher concentrations of the above elements in the study soils (Vertisol and Fluvisol) when compared to uncontaminated Vertisol and Fluvisol. On the other hand, Vertisol accommodated comparatively higher average levels of Cr, Cu, Ni, Zn, etc V, and Cd, whereas high contents of Pb and Se were observed in Fluvisol. Alternatively, comparable levels of Co and Hg were found in either soil. Except for Ni, Cr, and Cd in contaminated Vertisol, heavy metals in the soils were not significantly affected by the depth (0–20 and 30–50 cm). When the same element from the two soils was compared, the levels of Cr, Cu, Ni, Pb, Se, Zn, V, Cd at 0–20 cm; and Cr, Ni, Cu, Cd, and Zn at 30–50 cm were significantly different. Organic carbon (in both soils), CEC (Fluvisol), and clay (Vertisol) exhibited significant positive correspondences with the total heavy metal levels. Conversely, Se and Hg contents revealed perceptible associations with carbonate and pH. The exchangeable fraction was dominated by Hg and Cd, whereas the carbonate fraction was abounded with Cd, Pb, and Co. conversely, V and Pb displayed strong affinity to reducible fraction, where as Cr, Cu, Zn, and Ni dominated the oxidizable fraction. Cr, Hg, Se, and Zn (in both soils) showed preference to the residual fraction. Generally, a considerable proportion of the total levels of many of the heavy metals resided in non residual fractions. The enhanced lability is generally expected to follow the order: Cd > Co > Pb > Cu > Ni > Se > V and Pb > Cd > Co > Cu > Ni > Zn in Vertisol and Fluvisol, respectively. For the similar wastewater application, the soil variables influence the status and the distribution of the associated heavy metals among the different soil fractions in the study soils. Among heavy metals that presented relatively elevated levels and with potential mobility, Co, Cu, Ni (either soil), V (Vertisol), Pb, and Zn (Fluvisol) could pose health threat through their introduction into the food chain in the wastewater irrigated soils.     

Metal contamination in sediments of the western Bohai Bay and adjacent estuaries, China

Twelve sediment cores were collected in July 2007 in open waters of western Bohai Bay, the Port of Tianjin, and the adjacent estuaries of the Haihe and Yongding Rivers. While overall concentrations of trace metals at incremental depths in these cores met the Marine Sediment Quality (GB18668-2002) criteria of China, the magnitude of both metal enrichment factors (EF) and geoaccumulation indices (I(geo)) suggested that pollution with Ag, Cd, Cr, Cu and Zn was occurring in the estuaries and Port. Risk analysis also suggested that Ag and Ni concentrations were sufficiently elevated as to cause adverse biological effects in the study area. Although metal concentrations in western Bohai Bay were of less concern, a positive relationship between EF values and excess (210)Pb activity for several metals suggested that their concentrations were increasing over time.     

Sorption of hazardous metals from single and multi-element solutions by saltbush biomass in batch and continuous mode: interference of calcium and magnesium in batch mode

Batch studies were performed to determine the interference of calcium (Ca) and magnesium (Mg) on the sorption of Cu(II), Cd(II), Cr(III), Cr(VI), Pb(II), and Zn(II) [from CuSO(4), K(2)Cr(2)O(7), Pb(NO(3))(2), Cr(NO(3))(3), ZnCl(2), and Cd(NO(3))(2)] by saltbush (Atriplex canescens) biomass. The results demonstrated that Ca and Mg at concentrations of at least 20 times higher than the concentration of most of the target metals did not interfere with the metal binding. The data show that the batch binding capacity from a multimetal solution at pH 5.0 was (micromol/g) about 260 for Cr(III) and Pb, and about 117, 54, and 49 for Cu, Zn, and Cd, respectively. The use of 0.1M HCl allowed the recovery of 85-100% of the bound Cu, Cr(III), and Pb, and more than 37% of the bound Cd and Zn. The column binding capacity for Pb was about 49 micromol/g from both the single and multimetal solutions, while it was, respectively about 35 and 23 micromol/g for Cr(III). The binding capacity for Cu and Zn from the single and multimetal column experiments was 35 micromol/g and less than 10 micromol/g, respectively. The stripping data from the single column experiment showed that 0.1M HCl allowed the recovery of all the bound Cu and Zn, 90% and 74% of the bound Pb and Cr(VI), respectively, and less than 25% of the bound Cd and Cr(III), while the stripping from the multimetal experiment showed that 0.1M HCl allowed the recovery of all the bound Cu and about 74%, 54%, 43%, and 40% of the bound Pb, Zn, Cd, and Cr(III), respectively.     

Changes in Extractable Metal Concentrations During Storage of Surface Water Samples Containing Sediments1

ABSTRACT: Changes in metal concentrations during storage of acidified water samples were studied. Water samples with high concentrations of suspended sediment were collected from the Fraser River, British Columbia. These samples were analyzed for “extractable” metals, which are defined to be the dissolved metals plus those metals extracted from suspended sediment by dilute mineral acid. Concentrations of extractable Cu, Fe, Pb, Zn, Ni, Co, Mn, and Cd were determined over time. Metal concentrations in these water samples were not stable and showed significant increases throughout the storage period. These results suggest that the extractable metal technique is inappropriate for the analysis of water samples containing suspended sediment.     

Recovery and distribution of biosolids-derived trace metals in a clay loam soil

The long-term mobility of trace metals has been cited as a potential hazard by critics of EPA 503 rule governing the land application of biosolids. The objectives of this study were to assess the accumulation of Cu, Ni, Cd, and Zn within the soil profile; the distribution of exchangeable, specifically adsorbed, organic, and oxide fractions of each metal; and mass balance of Cu, Ni, and Zn 17 yr after a single biosolids application. Biosolids were applied to 1.5- x 2.3-m confined plots of a Davidson clay loam (fine, kaolinitic, thermic Rhodic Kandiudult) in 1984 at 0, 42, 84, 126, 168, and 210 Mg ha(-1). The highest biosolids application supplied 4.5, 750, 43, and 600 kg ha(-1) of Cd, Cu, Ni, and Zn, respectively. Soils were sampled to a depth of 0.9 m and sectioned into 5-cm increments after separating the Ap horizon. Total (EPA-3050B), bioavailable (Mehlich-I), sequential extraction, and dispersible clay analyses were performed on samples from the control, 126 Mg ha(-1), and 210 Mg ha(-1) treatments. Trace metals are still concentrated in the top 0.2 m with slight enrichment down to 0.3 m. More than 85% of applied Cu, Ni, and Zn are still found in the topsoil where biosolids was incorporated and 95% or more of the applied metals were accounted for with mass balance calculations. Mehlich-I results showed a slight increase in metal concentration down to 0.35 m. Biosolids application increased the concentrations of trace metals in all the extracted fractions. The major portions of Cu, Zn, and Ni are associated with the metal-oxides fraction. Dispersible clay content and water-soluble metal contents were low and except for water-soluble Zn they were not affected by biosolids application. Results from this study showed that 17 yr after biosolids application there was negligible movement of trace metals through the soil profile and consequently there is little risk of contamination of ground water at this site.     

柴窝堡湖表层底泥重金属污染评价

研究了乌鲁木齐市柴窝堡湖表层底泥的重金属含量,并采用Hakanson潜在生态危害指数法对底泥中的重金属潜在生态风险进行评价。结果表明:底泥中Cu、Zn、Pb、Cd含量均超出乌鲁木齐市土壤背景值。除湖心区外,Cd在5个监测区域中的潜在生态危害均为中等;其它重金属在5个采样点的潜在生态危害均为轻微。各重金属间的相关性分析表明,Zn与Cu,Pb与Cd、Cu呈显著正相关,说明这4种元素污染源可能相同。柴窝堡湖表层底泥受到Cu、Zn、Pb、Cd污染,需采取相应措施防止重金属由底泥进入水相。     

Characteristic levels of heavy metals in sediments and dredged sediments of a municipal creek in the Niger delta, Nigeria

Characteristic levels of metal ions in post dredged sediment and dredged sediments materials of a municipal creek in the Niger Delta show that significant concentrations of heavy metals are found to be accumulated more on the surface (0–15cm depth) of the dredged material as compared to the sub surface (15–30cm) and post dredged sediments. The distribution patterns were in the following order Fe > Mn > Zn > Cu > Pb > Ni > Cd and Fe > Mn > Zn > Pb > Cu > Ni > Cd for the post dredged sediment and dredged sediment materials respectively. The levels of the various metals were far below the EPA screening levels for open water disposal, consequently total levels of heavy metal found in these sediments pose no problem by open-water or upland disposal     

Metal distribution and stability in constructed wetland sediment

The A-01 wetland treatment system (WTS) is a surface flow wetland planted with giant bulrush [Schoenoplectus californicus (C.A. Mey.) Palla] that is designed to remove Cu and other metals from the A-01 National Pollution Discharge Elimination System (NPDES) effluent at the Savannah River Site near Aiken, SC. Copper, Zn, and Pb concentrations in water were usually reduced 60 to 80% by passage through the treatment system. The Cu concentrations in the wetland sediments increased from about 4 to 205 and 796 mg kg(-1), respectively, in the organic and floc sediment layers in cell 4A over a 5-yr period. Metal concentrations were higher in the two top layers of sediment (i.e., the floc and organic layers) than in the deeper inorganic layers. Sequential extraction was used to evaluate remobilization and retention of Cu, Pb, Zn, Mn, and Fe in the wetland sediment. Metal remobilization was determined by the potentially mobile fraction (PMF) and metal retention by the recalcitrant factor (RF). The PMF values were high in the floc layer but comparatively low in the organic and inorganic layers. High RF values for Cu, Zn, and Pb in the organic and inorganic layers indicated that these metals were strongly bound in the sediment. The RF values for Mn were lower than for the other elements especially in the floc layer, indicating low retention or binding capacity. Retention of contaminants was also evaluated by distribution coefficient (Kd) values. Distribution coefficient (Kd) values were lower for Cu and Zn than for Pb, indicating a smaller exchangeable fraction for Pb.     

杭州城区河道底泥重金属污染及潜在生态风险评价

对杭州城区34条河道45个点位河道底泥进行采样,分析了pH及汞、砷、铅、铬、镉、铜、锌、镍等重金属含量,并进行污染及潜在生态风险评价。结果表明,监测点位的底泥为中性偏碱性,重金属含量分布不均,且范围波动很大,部分河道底泥重金属中汞、铅、镉、铬、锌、镍等有不同程度的超标,少数河道镉、铬、锌污染严重;按《农用污泥中污染物控...     

Metal pollution in sediments of Jamaica Bay,New York,USA—An urban estuary

Calculations of the annual input of heavy metals to Jamaica Bay, New York, USA, reveal that sewage effluent carries the largest quantities of Ni, Zn, Cu, and Cd to the bay. Storm sewers and atmospheric fallout are the main sources of Pb. Atmospheric fallout of Zn, Cu, and Cd, although smaller than the combined input from sewers, contributes a significant fraction of these metals. The metal input from landfill leachate is far smaller than that from other sources. Analysis of available data shows that metal concentrations in the sediment of the bay correlate with each other and with percent total organic carbon (%TOC). This is consistent with the observation that the input of metals is predominantly associated with sewage. It is demonstrated that metal-TOC ratios, rather than metal concentrations, must be used in efforts to detect local intensive sources of metals in solution; metal-TOC ratios in intertidal sediment adjacent to these landfills are elevated by the adsorption of leachate metals, while metal concentrations are not. Subtidal sediment within a few hundred meters from two landfills shows no evidence of the addition of metals from that source, which is consistent with the small input of metals estimated for these landfills. The evidence cited in this study sharply contradicts the implication made in a widely publicized report issued by an environmental advocacy group that a significant link exists between metals found in subtidal sediment of Jamaica Bay and landfill leachate.     

不同酸消解方法在土壤重金属测定中的比较研究

分别用三种不同的酸消解方法进行土壤标准样品的前处理,用原子吸收分光光度法测定其中铜、铅、锌、镉、镍、锰、总铬元素的含量。结果表明,电热板/硝酸-过氧化氢-氢氟酸消解方法耗酸量少,消解时间短,适用于土壤中铜、铅、锌、镉、镍、锰元素的前处理,相对标准偏差为1.0%～5.0%;而使用电热板/硝酸-硫酸-氢氟酸方法针对土壤中总铬元素进行消解前处理,准确度更高,相对标准偏差为2.7%～5.1%。     

Trace elements in sediments in a city with agricultural development

The objective of this study was to determine the concentrations of trace elements in sediment samples taken from impermeable urban areas of a city with predominantly agroindustrial development characteristics. For this, samples were taken every month from paved streets in the city of Toledo, Paraná State (PR), Brazil. Thus, trace element levels were obtained through analysis performed by optical emission spectrometry with inductively coupled plasma. Levels of total organic carbon were also obtained through the dry combustion method. When compared to local background levels, the trace element levels were shown to be enriched in the following percentage proportions: barium (Ba) (45.4%), copper (Cu) (48.6%), chromium (Cr) (37.2%), manganese (Mn) (81.6%), nickel (Ni) (0%), lead (Pb) (40%), zinc (Zn) (283.7%), magnesium (Mg) (34.3%), and sodium (Na) (250.2%), whereas the carbon (C) percentages were around 1%. The most significant enrichment factors occurred for Ba, Cr, Pb, Zn, Mg, and Na. The highest rates occurred in geoaccumulation where the sediments were enriched by zinc. According to the principal guidelines, the concentrations obtained for cadmium (Cd), Cr, Cu, Ni, and Zn can cause adverse environmental impacts.     

Overexpression of ATP sulfurylase in Indian mustard: effects on tolerance and accumulation of twelve metals

Indian mustard [Brassica juncea (L.) Czern.] transgenics overexpressing ATP sulfurylase (APS plants) were shown previously to have higher levels of total thiols, S, and Se. The present study explores the effect of ATP sulfurylase overexpression on tolerance and accumulation of other metals, both oxyanions and cations, reasoning that some anions may react directly with ATP sulfurylase, while other ions may be bound by its thiol end products. The APS transgenics were compared with wild-type plants with respect to tolerance and accumulation of As, Cd, Cr, Cu, Hg, Mn, Mo, Ni, Pb, V, W, and Zn, supplied individually in agar medium (seedlings) or in hydroponics (mature plants). At the seedling stage, APS transgenics were more tolerant than wild type to As(III), As(V), Cd, Cu, Hg, and Zn, but less tolerant to Mo and V. The APS seedlings had up to 2.5-fold higher shoot concentrations of As(III), As(V), Hg, Mo, Pb, and V, and somewhat lower Cr levels. Mature APS plants contained up to 2.5-fold higher shoot concentrations of Cd, Cr, Cu, Mo, V, and W than wild type. They also contained 1.5- to 2-fold higher levels of the essential elements Fe, Mo, and S in most of the treatments. Mature APS plants showed no differences in metal tolerance compared with the wild type. Overexpression of ATP sulfurylase may be a promising approach to create plants with enhanced phytoextraction capacity for mixtures of metals.