Near-infrared diffuse reflectance sensing (NIRS) of soils has been the object of considerable interest and research in the last few years. This has been motivated by the prospect that this method seems to provide a cheap, convenient alternative to conventional, time-consuming methods for the measurement of a wide range of soil parameters. In particular, various authors have advocated that NIRS could be used to measure rapidly and non-destructively the concentration of trace metals in surface soils. Correlation analyses between NIRS spectra and trace metal concentration have yielded inconclusive results to date, suggesting that trace metal concentration may belong to a class of “tertiary” soil parameters, linked to NIRS spectra through “surrogate”, or indirect, correlations, involving some other primary or secondary parameter like clay or organic matter content, to which NIRS spectra are very sensitive. To assess the validity of this surrogate correlation hypothesis in the case of trace metals, experiments were carried out with soil samples varying only in the amount of trace metals they contain. Field-aged Hudson and Arkport soil pots spiked with Cu and Zn, freshly spiked samples of the same soils, and samples of a metalliferous peat soil from Western New York naturally rich in Cd and Zn were subjected to NIRS under laboratory conditions. Detailed analysis indicates that the NIR spectrum is sensitive to sample handling, including the orientation of the samples in the NIRS instrument, but that, at the same time, there is no discernable effect of the presence of trace metals on any part of the NIR spectrum. These results provide strong experimental support to the hypothesis of “surrogate” correlation for trace metals, and indicate that trace metals, even in severely contaminated soils, should not interfere with the NIR sensing of primary or secondary parameters, like organic matter content. Further work is needed to determine if this feature of NIR spectra extends to other soil chemical parameters.

Water retention and transport in soils is dependent upon the surface tension of the aqueous phase. Surfactants present in aqueous solution reduce the surface tension of aqueous phase. In soil-water systems, this can result in water drainage and reductions in field capacity and hydraulic conductivity. In this investigation, the surface tension of surfactant solutions mixed with soil—in a constant fixed ratio—was measured as a function of surfactant concentration. Two anionic surfactants were used: sodium dodecyl sulphate and sodium bis (2-ethylhexyl) sulfosuccinate. Two soils were also used—a clay soil and a sandy soil. The key observation made by this investigation was that the addition of soil to the surfactant solution provided a further component of surface tension reduction. Neither soil sample reduced the surface tension of water when surfactant was absent from the aqueous phase, though both soils released soil organic matter at low surfactant concentrations as shown by measurement of the chemical oxygen demand of the supernatant solutions. Furthermore, both surfactants were shown to be weakly adsorbed by soil as shown by the use of a methylene blue assay. It is therefore proposed that the additional reduction in surface tension arises from synergistic interactions between the surfactants and dissolved soil organic matter.

The evolution of microbial communities with increasing carbon tetrachloride concentrations was studied in two anaerobic columns containing sand and two different clay soils, one of which contained high levels of iron. Microbial communities were characterized through analysis of column effluents with denaturing gradient gel electrophoresis and quantitative polymerase chain reaction for archaea and eubacteria as inlet carbon tetrachloride concentrations were increased from 0.8 to 29 μM. Inhibition of microbial activity was observed in both columns, and was associated with the accumulation of chloroform at concentrations of 0.2 to 0.4 μM as inlet CT concentrations were increased to 2.4-3.0 μM in the low-iron clay column and approximately 16 μM in the iron rich clay column. Inhibition was indicated by decreasing rates of methanol and carbon tetrachloride degradation, decreases in effluent levels of DNA, and shifts in microbial communities of the columns. Even with the inhibition observed, in the iron-rich clay column CT degradation continued to the end of the study with inlet CT concentrations of 29 μM, in contrast to the low-iron clay column in which minimal CT degradation occurred once CT inlet concentrations exceeded 3 μM. The greater capacity for CT degradation in the column containing the iron-rich clay was hypothesized to be the result of reaction with biogenic ferrous iron produced by biological dissimilatory iron reduction.

Phytoextraction is a soil remediation technique involving plants that concentrate heavy metals in their shoots, which may be removed from the area by harvest. The application of synthetic chelants to soil increases metal solubility, and therefore enhances phytoextraction. However, synthetic chelants degrade poorly in soil, and metal leaching poses a threat to human and animal health. The aim of this study is to assess the use of two biodegradable chelants (citric acid and nitrilotriacetic acid (NTA)) for Pb phytoextraction by maize from a soil contaminated by battery-casing disposal. In order to assess the behavior of a non-degradable chelant, ethylenediaminetetraacetic acid (EDTA) was also included in the experiment. The chelants NTA and EDTA were applied to soil pots at rates of 0, 3, 5, 7, and 10 mmol kg⁻¹ of soil. The rates used to citric acid were 0, 5, 10, 15, and 30 mmol kg⁻¹. Maize plants were grown for 72 days and chelants were applied 9 days before harvest. Soil samples were extracted with CaCl₂ to assess the Pb solubility after chelants application. The results showed that NTA was more efficient than citric acid to solubilize Pb from soil; however, citric acid promoted higher net removal of Pb (120 mg pot⁻¹) than NTA (57 mg pot⁻¹). Thus, the use of citric acid, a biodegradable organic acid, could be feasible for enhancing the phytoextraction of Pb from the site studied with no environmental constraints.

The chemical dynamics at Meio Stream Basin, São Paulo State, Brazil were evaluated using major elements as natural tracers. The surface water samples from Meio Stream were collected near the mouth of Meio Stream at the confluence with the Mogi-Guaçu River on February 25, 2005, April 20, 2005, and July 8, 2005. Rainwater samples were collected (using a “bulk” collector) for 1 year at one sampling point located about 4 km from downtown Leme city and other possible sources of contamination. The analyses were performed by pH, temperature, dissolved oxygen, electrical conductivity, total solids, sulfate, nitrate, phosphate, alkalinity, chloride, sodium, calcium, potassium, and magnesium. This basin has serious environmental problems in terms of rainwater and surface water quality, which result in the negative annual flux of cations and anions at Meio Stream Basin, with the exception of chlorine. The Meio Stream, downstream from Leme city, receives several elements/compounds through anthropogenic activities, mainly related to the discharge of domestic effluents. Anthropogenic inputs (mining, fossil fuel burning, and agricultural activities) are responsible for the higher concentrations of cations and anions in the rainwater from this basin.

Atmospheric and sea sediment concentrations were measured for eight nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) and three unsubstituted PAHs in a suburban area and sea sediments in the Hiroshima Bay watershed area, Japan, from July to December, 2006 (atmospheric particulate matter) and in September and November, 2004 (sea sediments). Atmospheric concentration was higher in winter than summer for both nitro-PAHs and PAHs. Concentrations in sea sediments were less than 10%, and pattern was similar to those of atmospheric particles. Several combustion emission sources were also measured, and the 1-NP/Pyr ratio was compared to environmental values. The ratio of atmospheric and sea sediments were significantly lower than diesel particulate matters. Further, the vehicle emission loading and sea sedimentation loading was evaluated in this watershed area, and from the comparison, the existence of other important sources PAHs were suggested.

Lake Vela (Littoral Centre of Portugal) is considered a natural habitat with community interest and consequently was included in the Natura 2000 Network. However, this freshwater ecosystem has been potentially exposed to diffuse pollution generated by agricultural and livestock activities, which seriously compromise its ecological balance. As part of the Ecological Risk Assessment (ERA) proposed for Lake Vela, this study aimed to evaluate the occurrence of pesticides in different compartments: surface water, groundwater, sediments, and fish tissues. Moreover, to assess potential concerning effects on ecosystem and human health, the measured concentrations of pesticides were compared with regulatory and toxicological benchmarks. The results confirmed the presence of high concentrations of pesticides, including organochloride pesticides banned decades ago, in surface water, groundwater, and sediment. The measured concentrations of pesticides, compared with toxicological benchmarks, indicated that harmful effects are likely for aquatic species due to the presence of alachlor, aldrin, and dieldrin. Additionally, the concentrations of pesticides detected in groundwater were also above the recommended safety levels for drinking water, which constitutes a concern for the local population's health. Results also showed an accumulation of alachlor in predator and benthic fish species which could represent a risk to human consumers and particularly to the regular fish predators (e.g., otters and birds). This study, as the first exposure characterization performed on the Lake Vela system, constitutes valuable and useful information for the ERA process. Although this preliminary assessment of risks should be continued and confirmed through a weight-of-evidence approach, it had already unraveled how concerning are the problems in this ecosystem and the urgency of implementing restoration measures to guaranty its sustainability. Furthermore, this study reinforces the importance of evaluating similar freshwater ecosystems that are also highly threatened by diffuse pollution.

Phosphorus (P) loss from agricultural soils to water is a major contributor to eutrophication. In an incubation experiment with five contrasting soils, lime and gypsum showed potential as source measures to decrease P loss risk, as assessed by water extractions. Soils were incubated with lime to achieve a target pH of 6.5 and with gypsum at equivalent Ca rates for 108 days. P was added (17 kg P ha⁻¹) as KH₂PO₄ in solution. Gypsum appears to have greater potential as a source measure, decreasing molybdate-reactive P (RP) solubility by 14-56% and organic P (OP) by 10-53% across all soils. RP and Ca may have precipitated or co-sorbed, and OP may have been stabilised in organic matter complexes due to the bridging effect of Ca and the flocculating effect of increased ionic strength. Greater effectiveness of gypsum may be due to its higher solubility and the fact that it increases Ca concentrations without increasing pH. Lime decreased RP solubility in two soils (by 4% and 20%) but increased solubility in two and had no effect in a third. The overall effect of lime may depend on several competing effects of raised pH and Ca concentration that may vary in importance depending on soil characteristics such as base cation and P status. For the highest P status soil, both lime and gypsum were effective, decreasing RP solubility by 4% and 15%, respectively. Targeted treatment of high P soils may be an effective and economical strategy to minimise P losses.

The present study determines the source of dust particles and investigates their impact on the chemical compositions of plants and soils around a cement factory in Oman within a radius of 10 km of this disturbed ecosystem. A total number of nine samples of the species of plants (Rhazya stricta), nine samples of soils, and nine samples of dust were collected and analyzed for major ions and trace elements including rare earth elements (REEs). Principal component analysis applied to the major and trace element concentrations in the dust indicated the input of at least two sources to the dust in the study area: ophiolites and cement. The REE distribution in the plants and soils revealed that the most available elements to plants originated dominantly from ophiolites rather than from cement. The contribution of cement industry is significant only in the zone located at about 0.500 to 2 km around the cement factory, whereas the contribution of ophiolites increases with distance from the cement factory.