The phytoremediation potential for Pb of Buddleja asiatica (a wild species) and a closely related cultivated species, B. paniculata, was investigated by means of field survey, hydroponic and pot experiments, and field trial experiments. Field surveys showed that B. asiatica had an extraordinary accumulation capacity and tolerance for Pb. Plants grown in soil with 2,369.8-206,152 mg kg⁻¹ total Pb accumulated 1,835.5-4,335.8 mg kg⁻¹ Pb in their shoots. Under hydroponic conditions (10, 20 mg l⁻¹ Pb), both B. asiatica and B. paniculata showed unusually high concentrations of Pb in their roots (12,133-21,667 mg kg⁻¹) and increased biomass production. A pot experiment in a greenhouse without any soil amendments was conducted on three different soils with various Pb contents (10,652, 31,304, 89,083 mg kg⁻¹) for 3 months. The results showed that both species of Buddleja had an increase in the biomass similar to the control plants. There was a slight decrease in survival rates of plants grown in soil with 89,083 mg kg⁻¹ Pb content. A field trial experiment was conducted for 6 months at three sites around the Pb mine area in which plants were provided with Osmocote fertilizer. Both Buddleja species showed 100% survival, increased biomass production and phytoextraction capacity (TF 1.1-2.3) when grown in soil with Pb content of 94,584-101,405 mg kg⁻¹. Plants accumulated 2,273-3,675 mg kg⁻¹ Pb in their shoots. The results suggest these Buddleja plants are suitable for use in the phytoremediation of Pb-contaminated soil.

A column of soil, excavated from a contaminated landscape was evaluated by means of X-ray fluorescence analysis. The measurements were intended to assess the vertical distribution of heavy metals and toxic elements in the depth profile. To judge fitness for purpose of the analytical method used the element specific power functions were derived yielding the minimum detectable variations of analyte concentrations refer to the investigated soil profile. The required measurement uncertainty components caused by both the sampling procedure and chemical analysis were empirically estimated using a nested sampling design (duplicate method). For this purpose the full length of the soil core was divided into horizontal layers. From each selected layer (sampling target) two composite samples were taken by simple random sampling to represent the typical composition of the sampling target. The pool of measurement results, obtained for the nested sampling design finally was subjected to variance analysis. The evaluation of the estimated variance components in terms of the percentage of total variance confirmed fitness for purpose for the method used.

In 1997, total petroleum hydrocarbon (TPH) remediation started at a former Air Force Base, which operated from 1940 to 1991. TPH had been released to soil and groundwater at the site by military activities. The TPH was 70% jet fuel and the affected area covered 28 ha. Remediation involved a combination of technologies, including removal of volatile organic compounds using soil vapor extraction and air sparging, free product vacuum recovery and aerobic biodegradation of organics with oxygen supplied by the air sparging system, along with nutrient addition. The primary remedial method was found to be biodegradation, which has removed 93% of the contaminants from the site to date. A significant aspect of the remedial action was performance monitoring, including documentation of remediation efficiency. The goal of the research was to assess the relative accuracy of methods commonly used for monitoring in situ TPH remediation. Two such methods were selected for the research: monitoring change in soil TPH concentration (specified as non-polar extractable substances) and monitoring respiration activity in soil with a subsequent stoichiometric mass balance to estimate the mass of TPH destroyed. The study demonstrated that both of the methods provided comparable results regarding the effectiveness of in situ TPH remediation, despite the fact that their methodologies are very different.

The presence of pharmaceuticals and personal care products (PPCPs) and endocrine disrupting chemicals (EDCs) in treated wastewater is gaining attention due to their potential environmental impact. An analytical method was developed to quantify estrogen compounds in samples from a concentrated wastewater matrix typical of water recycling systems used in space. The method employed conventional HPLC with UV detection. Solid phase extraction (SPE) was used to isolate the compounds of interest from wastewater. Spike-recovery tests in clean and wastewater matrices were used to test the extraction process. The results of these experiments suggest that deconjugation is the most predominant reaction occurring in the systems, as effluent concentrations of free estrogens typically exceeded influent concentrations. Despite the long retention times of the system or the near infinite solids retention time, free estrogens were not removed from graywater representative of space waste streams. For a closed-loop wastewater treatment system, these compounds may accumulate to levels requiring other removal mechanisms (i.e., reverse osmosis).

The major objective of this paper is to provide insights to sources and sinks of nitrous acid in urban areas, and their seasonal dependency on meteorology, photochemistry and long range transport. With this aim, nitrous acid (HONO) mixing ratios and other compounds were measured in Ashdod (south of Tel Aviv, Israel), a typical Mediterranean urban area. Statistical data analysis revealed the expected correlation between HONO and nitrogen oxides during the autumn campaign when HONO sources appeared to be traffic-, harbor-, and industry-related. Conversely, during summer HONO and NO₂ were no longer correlated: NO₂ at nighttime was probably deposited onto surfaces, soil and plants, whereas HONO at daytime was likely destroyed photolytically contributing to the OH concentration. Photolysis was expected to be the dominant HONO sink at daytime, especially during the summer period. Using modeled photolytical HONO lifetimes we estimate the magnitude of heterogeneous and/or organic electron transfer source reactions of HONO as 6-8 ppbv/h.

To increase the phytoextraction efficiency of heavy metals and to reduce the potential negative effects of mobilized metals on the surrounding environment are the two major objectives in a chemically enhanced phytoextraction process. In the present study, a biodegradable chelating agent, NTA, was added in a hot solution at 90°C to soil in which beans (Phaseolus vulgaris L., white bean) were growing. The concentrations of Cu, Zn and Cd, and the total phytoextraction of metals by the shoots of the plant from a 1 mmol kg-¹ hot NTA application exceeded those in the shoots of plants treated with 5 mmol kg-¹ normal NTA and EDTA solutions (without heating treatment). A significant correlation was found between the concentrations of metals in the shoots of beans and the relative electrolyte leakage rate of root cells, indicating that the root damage resulting from the application of a hot solution might play an important role in the process of chelate-enhanced metal uptake in plants. The application of hot NTA solutions did not significantly increase metal solubilization in soil in comparison with a normal application of solution of the same dosage. Therefore, the application of a hot NTA solution may provide a more efficient alternative in chemical-enhanced phytoextraction, although further studies of techniques of application in fields are sill required.

A mesocosm system was designed to study evaporation kinetics and transport of TCE in flowing surface water. The airtight unit, with a total internal volume of 52.01 x 10⁻² m³, was fabricated with glass and Teflon material, and was provided with 8.53 m long channel to simulate water flow in an open channel. The peristaltic pumps, connected to the inlet and the outlet of the mesocosm, provided a constant water flow through the channels. The experimental studies were conducted at two different velocities, 9.42 x 10⁻³ and 4.71 x 10⁻³ m/s, respectively. For both the velocities, a tracer (NaBr) test confirmed uniform water flow in the channels. The total length and the length between the sampling ports were found sufficient to record gradual decrease in TCE concentrations along the direction of the flow in the channels. The volatilization coefficient for TCE was found to be 0.49 and 1.07 h⁻¹ for the experiments conducted at lower and higher water velocities, respectively. The TCE evaporation half life (t 1/2) and the corresponding evaporation half distance (d 1/2) were 1.41 h and 23.98 m for lower velocity, and 0.65 h and 21.96 m for higher velocity, respectively.

Total Suspended particulate matter (TSP) in urban atmosphere of Islamabad was collected using a high volume sampling technique for a period of one year. The nitric acid-perchloric acid extraction method was used and the metal contents were estimated by atomic absorption spectrophotometer. The highest mean concentration was found for Ca at 4.531 μg/m³, followed by Na (3.905 μg/m³), Fe (2.464 μg/m³), Zn (2.311 μg/m³), K (2.086 μg/m³), Mg (0.962 μg/m³), Cu (0.306 μg/m³), Sb (0.157 μg/m³), Pb (0.144 μg/m³) and Sr (0.101 μg/m³). On an average basis, the decreasing metal concentration trend was: Ca > Na > Fe > Zn > K > Mg > Cu > Sb > Pb > Sr > Mn > Co > Ni > Cr > Li > Cd [almost equal to] Ag. The TSP levels varied from a minimum of 41.8 to a maximum of 977 μg/m³, with a mean value of 164 μg/m³, which was found to be higher than WHO primary and secondary standards. The correlation study revealed very strong correlations (r > 0.71) between Fe-Mn, Sb-Co, Na-K, Mn-Mg, Pb-Cd and Sb-Sr. Among the meteorological parameters, temperature, wind speed and pan evaporation were found to be positively correlated with TSP, Ca, Fe, K, Mg, Mn and Ag, whereas, they exhibited negative relationships with relative humidity. On the other hand, Pb, Sb, Zn, Co, Cd and Li revealed significant positive correlations with relative humidity and negative with temperature, wind speed and pan evaporation. The major sources of airborne trace metals identified with the help of principle component analysis and cluster analysis were industrial emissions, automobile exhaust, biomass burning, oil combustion, fugitive emissions, resuspended soil dust and earth crust. The TSP and selected metals were also studied for seasonal variations, which showed that Na, K, Zn, Cu, Pb, Sb, Sr, Co and Cd peaked during the winter and remained lowest during the summer, while Ca, Fe, Mg and Mn were recorded highest during the spring.

Eight soils from the Gulf of Kalloni in Lesvos Island, Greece, most of which were of low clay and low organic matter content, were used in a series of leaching experiments. The aim was to investigate the role of sewage sludge on Zn leaching and determine the soil properties that affect it. It was found that sludge addition at a low application rate (10 t ha⁻¹) decreased Zn leaching significantly by 30%. From a regression analysis it was found that eluted Zn was reduced with increasing Fe oxides content, probably due to Zn adsorption onto them, and that Zn transport increased with clay content. This indicates that Zn leaching was facilitated by the downward movement of clay particles, which was also suggested by the erratic Zn breakthrough observed in many soils. This was further confirmed by the fact that colloid concentrations increased with clay content in the soils (R = 0.85, P < 0.05). The results show that the addition of sewage sludge to low organic matter and clay content soils at moderate application rates enhances soil organic carbon and increases metal retention capacity.

In recent years, arsenic (As) has received increased attention as humans may be exposed to it through occupational and environmental exposure. Tobacco (Nicotiana tabacum L.) like other crops can uptake this element from the soil, which may lead to human exposure. Here, we report on a survey on arsenic in cured or processed tobacco leaves obtained from Africa, Asia, Europe, South and North America. A total of 1,431 leaf samples of flue-cured, burley, and Oriental tobaccos were obtained from various sampling locations during 2002 to 2004. Arsenic concentration in the samples averaged 0.4 ± 0.6 μg g⁻¹ as determined by inductively coupled plasma-mass spectrometry. Recorded values from most samples showed that concentrations of arsenic were usually found at the lower end of the distribution. Significant differences were found among tobacco types, sampling locations, and crop years. Arsenic concentrations were rather low in the majority of regions investigated, which is compatible with data from the literature. However, sample size was small and sampling geographically restricted. Our results would need to be validated with a larger dataset.