This is a study of trace metal competition in the complexation of Pb(II) by well-characterized humic substances, namely Suwannee River Fulvic Acid (SRFA) in model solutions. It was found that Cu(II) seems to compete with Pb(II) for strong binding sites of SRFA when present at the same concentration as Pb(II). However, Cd(II) and Zn(II) did not seem to compete with Pb(II) for strong binding sites of SRFA. These two metals did compete with Pb(II) for the weaker binding sites of SRFA. Heterogeneity of SRFA was found to play a crucial role in metal-SRFA interactions. The environmental significance of this research for freshwater is that even at relatively low Pb(II) loadings, the metals associated with lead in minerals, e.g. Cu(II), may successfully compete with Pb(II) for the same binding sites of the naturally occurring organic complexants, with the result that some of the Pb(II) may exist as free Pb²⁺ ions, which has been reported to be one of the toxic forms of Pb in aquatic environment.

The immobilization of lead by the reaction with phosphate bearing materials is a promising remediation method for contaminated soils. Low soluble neo-formed lead-phosphate phases similar to chloropyromorphite [Pb₅(PO₄)₃Cl], can control availability and mobility of lead in the environment, and consequently reduce human exposure, if soils are the main contamination pathway. We used three phosphate source materials [NaH₂(PO₄)₃, commercial superphosphate and phosphate rock] to study lead immobilization in soil and mining waste samples. Products were examined after 1, 3 and 6 months of contact. The samples are from a contaminated area by former Pb mining and smelting activities, in southeastern Brazil, where epidemiological studies showed high lead blood levels in local population. The PBET (physiological based extraction test) bioaccessibility test was used to measure changes in the amount of soluble lead after sample treatment. Results show that the most efficient phosphate source was NaH₂(PO₄)₃, which reduced lead solubility to 92% in acidic gastric conditions after the first month of contact. Superphosphate and phosphate rock also diminished Pb solubility, but the effect was more time dependent. None specific Pb-phosphate phases could be identified by XRD in whole treated samples, but the Pb-Ca-P elemental associations, observed on SEM images and EDS spectra of portions of the samples, combined with the reduced solubility, indicate that more insoluble lead phases were formed after the treatment. Based in these results, the in site phosphate application on soils to induce lead immobilization should be considered as a possible alternative to reduce human exposure at the area.

The distribution of nonylphenol ethoxylates (NPEOn) and their derivatives of nonylphenol (NP) and nonylphenoxy ethoxy acetic acids (NPEnC) in the sediments of a relatively closed freshwater reservoir was investigated using sediment layers sliced from undisturbed sediment cores collected with a gravity core sampler at three sampling sites (St. 1, St. 2 and St. 3) along the water flow direction. The relationships between the bound content of these compounds and the sediment organic matter as well as the likely transformation pathways were evaluated. The total content of NPEOn (n = 1-15) fell in 84.6-336.5, 59.9-135.5 and 77.0-623.4 μg/kg-dry for all sliced layers at St.1, St.2 and St.3, respectively, with the content of individual NPEOn species showing a general decreasing trend with the attached molar number of the ethoxy (EO) chain. Compared to each detected NPEOn species, the bound content of NP was much higher, falling in 73.2-248.4, 79.9-358.2 and 25.5-1,988.4 μg/kg-dry at St. 1, St. 2 and St. 3, respectively. A general increasing trend of the NP content along the water flow direction of the reservoir was revealed. NPEnC (n = 1-10) varied in 1.93-4.12, 2.85-9.84 and 1.05-19.1 μg/kg-dry for sediment at the respective site of St. 1, St. 2 and St. 3, with the averaged values at these sites (2.91, 4.71 and 6.72 μg/kg-dry) showing an increasing trend from the upstream to the downstream. For NPEnC, a parametric trend of increases in the content of NPE₁C, NPE₂C and NPE₃C with the bound sediment organic matter (9.06-11.8%) seemed to be existent. Furthermore, the computed magnitudes of NPEO₁-₂/NPEO₁-₁₅, NP/NPEO₁-₁₅ and NPEC₁-₁₀/NPEO₁-₁₅ suggested that non-oxidative hydrolytic transformation was probably prevailing within the sedimented mud phase of the reservoir, with the oxidative hydrolytic transformation pathway being less involved.

The content of Pb, Cd, Mn, K, Ca, Mg and ²⁰⁶Pb/²⁰⁷Pb isotope ratios in spruce tree rings (Picea abies) and peat cores from the Brdy Hills area (10 km W of the Pb smelter) were compared with those in spruce tree rings in the vicinity of the Pb smelter. Maximum Pb content in tree rings (up to 60 mg kg-¹ Pb) corresponds to a peak of metallurgical production in the mid 1970s and highest smelter emissions in the early 1970s. The Pb concentration curves obtained from peat deposit profiles closely correlate with the Pb concentrations in tree rings at both sampling sites. The small differences between the individual tree cores, with the identical general trend, may be attributed to the difference in distance from the smelter and the altitude of each sampling site. Similar behaviour to Pb can be observed for Cd and Ca. Lead isotope composition in tree rings (²⁰⁶Pb/²⁰⁷Pb ~1.143-1.174) is controlled mainly by the smelter emissions (²⁰⁶Pb/²⁰⁷Pb ~1.16-1.17), with the exception of the youngest segments from the more distant locality from the smelter, which yield isotopic signatures corresponding to car-emission Pb (²⁰⁶Pb/²⁰⁷Pb ~1.143-1.150). Higher content of Mn, Mg and Ca in tree rings corresponding to the 1970s and 1980s may be related to soil chemistry changes caused by acid deposition. In addition, an increase in K, Mg (and in some cases also Mn) in the youngest part of wood cores corresponds to the physiological processes in sapwood, and may be influenced by a decrease in Pb in organic soil horizons, which limited the cycling of basic inorganic nutrients.

In order to estimate acute-to-chronic toxicity ratios (ACRs) relevant to a coldwater stream community, we exposed rainbow trout (Oncorhynchus mykiss) to cadmium (Cd), lead (Pb), and zinc (Zn) in 96-h acute and 60+ day early-life stage (ELS) exposures. We also tested the acute and sublethal responses of a mayfly (Baetis tricaudatus) and a midge (Chironomus dilutus, formerly C. tentans) with Pb. We examine the statistical interpretation of test endpoints and the acute-to-chronic ratio concept. Increasing the number of control replicates by 2 to 3x decreased the minimum detectable differences by almost half. Pb ACR estimates mostly increased with increasing acute resistance of the organisms (rainbow trout ACRs <[almost equal to] mayfly < Chironomus). The choice of test endpoint and statistical analysis influenced ACR estimates by up to a factor of four. When calculated using the geometric means of the no- and lowest-observed effect concentrations, ACRs with rainbow trout and Cd were 0.6 and 0.95; Zn about 1.0; and for Pb 3.3 and 11. The comparable Pb ACRs for the mayfly and Chironomus were 5.2 and 51 respectively. Our rainbow trout ACRs with Pb were about 5-20x lower than earlier reports with salmonids. We suggest discounting previous ACR results that used larger and older fish in their acute tests.

A novel silicate mesoporous material, SBA-15 supported Fe₂O₃, was synthesized by post-synthesis method via ultrasonic-assisted route. The desulfurization test from a gas mixture containing 0.1 vol% H₂S was carried out over SBA-15 supported Fe₂O₃ in a fixed-bed system at atmospheric pressure and room temperature. The effects of the chemical nature of Fe₂O₃ and the textural properties of the material on desulfurization capacity were studied. Materials before and after the desulfurization test were characterized using nitrogen adsorption, XRD, TEM, FTIR, XPS, ICP and other standard methods. The characterization results suggest that modification process does not change the two-dimensional hexagonal mesostructure of SBA-15. Iron species disperses inside channels and the outside surface in the crystalline phase of iron oxide. The material with iron content of 31.3 wt% presented highest H₂S uptake capacity. Structural properties of the material also play important roles in desulfurization performance besides the catalytic effects of iron oxide. The basic feature of material and enough oxygen supply are benefit for the reaction. SBA-15 supported Fe₂O₃ can be an effective alternative to capture H₂S from gas streams.

In the present study, during a period of 16 months Colilert 3000 was validated in laboratory and field tests and compared to standard laboratory methods for monitoring of coliforms and E. coli. No false positive/negative results for coliforms/E. coli were found in 80 potable well water samples monitored with the Colilert 3000 and compared to standard methods. Although usage of Colilert 3000 to monitor raw water is not recommended by the manufacturer, the E. coli results of 100 samples were 100% positive by membrane filtration, Colilert 18 and MPN and only 80% positive by the Colilert 3000. In addition, in all positive samples, Colilert 3000 and Colilert 18 showed higher results of two to three orders of magnitude compared to MF and MPN. This significant difference was probably due to the presence of Aeromonas spp. and Vibrio spp. (natural inhabitants of the raw surface water) known to interfere with the Colilert test. Treated surface water was monitored by Colilert 3000 for the presence of coliforms and E. coli. Among the 100 samples tested in parallel by membrane filtration all were negative, while with Colilert 3000 only 76% were negative. Post-test identification of the positive samples did not reveal the presence of E. coli but interfering microorganisms. The last application was to evaluate Colilert 3000 to monitor accidental or deliberate pollution of drinking water with sewage sources. Among 20 samples spiked with raw sewage (0.1 and 1%) all results were positive for both coliforms and E. coli. The time span required for Colilert 3000 to detect positive samples was 6-10 h compared to 24 h with the standard membrane filtration.

The relationships between heavy metal concentrations and physico-chemical properties of natural lake waters and also with chemical fractions of these metals in lake sediments were investigated in seven natural lakes of Kumaun region of Uttarakhand Province of India during 2003-2004 and 2004-2005. The concentrations of Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb in waters of different lakes ranged from 0.29-2.39, 10.3-38.3, 431-1407, 1.0-6.6, 5.3-12.1, 12.6-166.3, 0.7-2.7 and 3.9-27.1 μg l-¹ and in sediments 14.3-21.5, 90.1-197.5, 5,265-6,428, 17.7-45.9, 13.4-32.0, 40.0-149.2, 11.1-14.6 and 88.9-167.4 μg g-¹, respectively. The concentrations of all metals except Fe in waters were found well below the notified toxic limits. The concentrations of Cr, Mn, Ni, Cu, Zn, Cd and Pb were positively correlated with pH, electrical conductivity, biological oxygen demand, chemical oxygen demand and alkalinity of waters, but negatively correlated with dissolved oxygen. The concentrations of Cr, Ni, Zn, Cd and Pb in waters were positively correlated with water soluble + exchangeable fraction of these metals in lake sediments. The concentrations of Zn, Cd and Pb in waters were positively correlated with carbonate bound fraction of these metals in lake sediments. Except for Ni, Zn and Cd, the concentrations of rest of the heavy metals in waters were positively correlated with organically bound fraction of these metals in lake sediments. The concentrations of Cr, Mn, Ni, Cu and Zn in waters were positively correlated with reducible fraction of these metals in lake sediments. Except for Cd, the concentrations of rest of the metals in waters were positively correlated with residual fraction and total content of these heavy metals in lake sediments.

A biological source treatment (BST) technique using remote sensing and biogeochemistry has been developed to address acid mine drainage (AMD) at its source. The BST technique utilizes down-hole injections of microbial inoculum and substrate amendments to establish a biofilm on the surface of metal sulfides (AMD source material). The treatment results in an elevated groundwater pH (from acidic to circum-neutral levels) and prevents further oxidation of AMD source material. The first 2 years of an ongoing field study of the BST technique at a reclaimed coal mine in central Tennessee (USA) has produced successful results. For instance, the water chemistry in a monitoring well down-gradient from injection wells has improved substantially as follows: the pH increased 1.3 units from 5.7 to 7.3, the dissolved (0.45 μm-filtered) iron concentration decreased by 84% from 93 to 15 mg/l, the conductivity decreased by 379 μS/cm, and sulfate decreased by 78 mg/l. Electromagnetic induction surveys were conducted to identify AMD source material and monitor BST performance by measuring changes in subsurface resistivity throughout the site. These surveys revealed a treatment zone created between injection wells where the resistance of contaminated groundwater from up-gradient AMD sources increased as it flowed past injection wells, thus, suggesting this technique could be used to treat AMD sources directly or to intercept and neutralize sub-surface AMD.