Evidence of ecological impacts from pesticide runoff has prompted installation of vegetated treatment systems (VTS) along the central coast of California, USA. During five surveys of two on-farm VTS ponds, 88% of inlet and outlet water samples were toxic to Ceriodaphnia dubia. Toxicity identification evaluations (TIEs) indicated water toxicity was caused by diazinon at VTS-1, and chlorpyrifos at VTS-2. Diazinon levels in VTS-1 were variable, but high pulse inflow concentrations were reduced through dilution. At VTS-2, chlorpyrifos concentrations averaged 52% lower at the VTS outlet than at the inlet. Water concentrations of most other pesticides averaged 20–90% lower at VTS outlets. All VTS sediment samples were toxic to amphipods (Hyalella azteca). Sediment TIEs indicated toxicity was caused by cypermethrin and lambda-cyhalothrin at VTS-1, and chlorpyrifos and permethrin at VTS-2. As with water, sediment concentrations were lower at VTS outlets, indicating substantial reductions in farm runoff pesticide concentrations. Toxicity identification evaluations identified key pesticides in agricultural runoff, and their concentrations were reduced by farmer-installed vegetated treatment systems.

Advanced oxidation processes (AOPs) are among the most efficient methods for wastewater treatment. To achieve the degradation of persistent organic pollutants (POPs), AOPs have been developed that employ Fenton reactions promoted by ultrasound (US) or microwaves (MW). Integrated methods combining AOPs with biological treatments are also of great interest. The present paper describes such an integrated approach for the decontamination of water from nonylphenol (NP), a common pollutant that accumulates in aquatic organisms and is quite resistant to biodegradation. Polluted water (containing 1,000 ppm of NP) was sequentially subjected to a sonochemical Fenton reaction and biosorption by the filamentous fungus Paecilomyces lilacinus. Although these methods can be used separately, the sequential approach proved more advantageous. In 1 h the sonochemical oxidation, carried out in a 300 kHz US-reactor equipped with a cooling system, halved NP content in polluted water, as determined by GC-MS analysis. The water was then inoculated with pure cultures of the fungus, whose mycelial biomass further reduced NP content in 7 days. Thus an initial NP concentration of 1,000 ppm was reduced approximately by 90%.

This paper reports a laboratory-scale investigation concerning the use of sulphate-reducing bacteria (SRB) in a semi-continuous process, where column packed-bed type bioreactors were used for the treatment of acid mine drainage (AMD). The use of different materials as solid matrices was tested and the performance of the bioremediation processes was discussed in terms of sulphate and metals removal and acid neutralization. The behaviour of a reactor filled with acidic soil from a mining area and organic wastes was compared with other three reactors where coarse sand, glass spheres and cereal straw were used as packaging materials. Batch experiments showed the presence and growth of SRB from the acidic soil in different pH conditions and the effect of the absence or presence of several added carbon sources: lactate, ethanol and lactose. The data showed that it is possible to grow SRB using the acidic soil as source of inocula, in the absence and in the presence of the carbon sources tested, since the pH of the media was previously increased to values of 5 or higher. When acidic soil from the mining area and organic wastes were utilised as column matrices, it is possible to remove the metals and to neutralise the acidity of AMD, although an inefficient sulphate removal was observed. When coarse sand or glass spheres were utilised, efficient metals sulphate removal were achieved. However, the incapacity of both systems to generate enough alkalinity does not allow maintaining their good performances in terms of iron removal and sulphate reduction. As a result, the incorporation of materials with neutralizing and buffer capacity to the matrix is recommended. Due to its low density, cereal straw was not suitable to obtain an anaerobic environment inside the column for SRB activity.

A conceptual model of solute transport with bioremediation processes using sawdust as a matrix to improve the efficiency of bioremediation in porous media is presented. The transport part of the model solves the advection dispersion differential equations and the reaction part describes the heterotrophic metabolisms of several groups of bacteria. The bacterial growth is formulated using the double Monod kinetic equation. The model depicts the utilization of oxygen, nitrate, manganese, iron oxides and sulfate as electron acceptors for oxidation of organic carbon in porous media. Exchange between the different phases (mobile pore water phase, bio phase and matrix phase) is also considered in this model. Model parameters were adopted from literature on bioremediation processes. Feasibility and applicability of parameters were assessed by conducting a laboratory soil-sawdust columns experiments and comparing the simulated results with the experimental data. The results indicate that sawdust could be employed as low-cost materials to enhance the bioremediation processes in porous media. While the availability of organic carbon is one of the most important factors that affect bacterial activity in porous media, this study demonstrates that using sawdust as a carbon source can improve the bacterial activity and increase the column permeability.

This paper presents transformations of saturated hydrocarbons of petroleum type pollutants during ex situ bioremediation of soil on the pilot heap (halde), during a period of 6 months, within the grounds of Petroleum Refinery Pančevo (Serbia). Samples for analysis were taken in time intervals of 2 weeks (P₁-P₁₂ samples). Organic substance was extracted by Soxhlet's method and quantified. Isoprenoid aliphatics, in particular pristane and phytane, and polycyclic aliphatics of sterane and triterpane types in saturated hydrocarbon fractions were analysed by GC-MS (SIM method). Significant amounts of n-alkanes have not been detected. The MS-chromatogram revealed only marginal amounts of pristane and phytane in sample P₁. Pristane and phytane occurred in sample P₈, and in even higher quantities in the final sample P₁₂. The proceeding bioremediation process was accompanied by the decrease of the relative amounts of pentacyclic terpanes of hopane type, compared to tri- and tetracyclic terpanes. In the initial sample P₁ the distribution of steranes and hopanes follows a pattern, which is characteristic for crude oils. However, their identification by SIM method was not possible in samples P₈ and P₁₂ because of the reduced concentration. The observed changes in the alkane fractions' compositions may be considered as atypical, referring to the fact that during oil biodegradation under natural conditions, decomposition of isoprenoids occurs much easier and faster than decomposition of polycyclic alkanes of tri-, tetra- and pentacyclic terpane, sterane and diasterane types, after the decomposition of n-alkanes has been almost completed.

A fungal strain possibly capable of removing hexavalent chromium was to be isolated from industrial effluent from a leather factory located in the city of Guadalajara, state of Jalisco, Mexico. The strain was identified as Trichoderma inhamatum by the D1/D2 domain sequence of the 28S rDNA gene. Batch cultures of T. inhamatum in media containing initial Cr(VI) concentrations from 0.83 to 2.43 mM Cr(VI) were prepared. Experimental results suggest that the fungus is capable of transforming hexavalent chromium to trivalent chromium; a transformation of a highly toxic contaminant to a low toxic form. The specific and volumetric rates of Cr(VI) reduction by T. inhamatum cultures decreased as the initial Cr(VI) concentration increased. The fungus exhibited a remarkable capacity to tolerate and completely reduce Cr(VI) concentrations up to 2.43 mM. These results indicate that the T. inhamatum fungal strain may have potential applications in bioremediation of Cr(VI)-contaminated wastewaters.

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.

Although microbially-mediated redox environments can alter the characteristics of soil/sediment organic matter (SOM) and its interactions with persistent hydrophobic organic contaminants (HOCs) bound to soils and sediments, the nature of their effects has not been adequately addressed. In this study, a field soil collected from a manufacturer gas plant site and contaminated historically with creosotes was incubated under aerobic and anoxic/anaerobic conditions along with various amendments (extra carbon and enrichment minerals) for stimulating microbial activities. Anaerobic conditions stimulated significant fractions of bound polycyclic aromatic hydrocarbons (PAHs) encompassing naphthalene through benzo[g,h,i]perylene to be mobilized to the aqueous phase, leaving their aqueous phase concentrations far in excess of solubility (increases in their apparent aqueous phase concentrations by factors as high as 62.8 relative to their initial aqueous phase concentrations). Such effects became more evident for high molecular weight PAHs. Dissolved organic matter exhibiting a high affinity for PAHs was liberated from soils during the anaerobic soil incubations. Feasibility of this concept for field applications was evaluated with a lab-scale continuous flow system composed of an anaerobic soil column followed by an aerobic bioreactor inoculated with PAH-degrading microbes. High quantities of PAHs exceeding their aqueous solubilities were eluted from the anaerobic soil column and those mobilized PAHs were readily bioavailable in the secondary aerobic bioreactor. This study may offer a potential method for cost-effective and performance-efficient ex situ remediation technologies (or in situ if appropriate hydrological control available in the contaminated field site) and risk assessment for the HOC-contaminated soils/sediments.

The bioremediation of petroleum contaminated soil was investigated using a laboratory scale aerated reactor. The Indigenous bacteria, Stenotrophomonas multophilia, were isolated from the contaminated sites near to Jordan Petroleum Refinery and used further in the bioremediation experiments. First order kinetic equation has been proven to satisfactorily describe the biodegradation of petroleum contained in soil in the presence of the isolated bacteria. The results also showed that the first order kinetic constants for the different bioreactors vary between 0.041 and 0.0071/day. The overall kinetic constant k' was determined based on food-to-microorganisms ratio and found to be 0.02/day.