This paper compares lake chemistry in the Adirondack region of New York measured by the Temporally Integrated Monitoring of Ecosystems (TIME) and Adirondack Long-Term Monitoring (ALTM) programs by examining the data from six lakes common to both programs. Both programs were initiated in the early 1990s to track the efficacy of emission reduction policies and to assess the full impacts of acid deposition on surface water chemistry. They now serve to inform on the emerging chemical recovery of these waters. The Adirondack TIME program utilizes a probability-based approach to assess chronic acidification in a population of lakes using one summer sample per year. The ALTM attempts to track changes in both chronic and episodic acidification across a gradient of lake types using monthly samples. The ALTM project has two important attributes that contrast with the TIME program in the Adirondacks: higher temporal resolution (monthly versus once during the summer or fall) and speciation of aluminum. In particular, the ALTM program provides inorganic monomeric aluminum (AlIM), the fraction of Al that is most toxic. The monthly sampling of the ALTM program includes the spring snowmelt period when acid-neutralizing capacity and pH are near their lowest and Al levels are near their highest. We compare chemistry trends (1992–2008) for sulfate, nitrate, base cations, dissolved organic carbon, hydrogen ion, acid neutralizing capacity, and Al for the six lakes common to both programs. We also compare relatively high springtime AlIM concentrations from the ALTM with relatively low summertime total Al concentrations from the TIME, showing that the ALTM program provides a more biologically relevant indicator of the effects of acid deposition, illustrating the value of the complementary monitoring efforts in the Adirondack region.

The degradation of diesel and phenanthrene in waste water was studied in a column combining a submerged trickling-flow with a fixed-film at a determined biofilm thickness with recirculation. Degradation efficiencies were found to be high with the production of a biofilm thickness of 789 μm structured in a package material with proper adsorption and physicochemical properties necessary to reach a stable state condition for the degradation of recalcitrant components in 78% at a retention time of 3 h. Improved degradation rates were reached with a biofilm built from an adapted inoculum that showed the presence of Pseudomonas sp., Klebsiella sp. Enterobacter in a concentration of 6.45 × 109 CFU mL−1. Moreover, the biodegradation rate of the inoculumn was quantified. The diesel kinetic experimental data were well described by Gompertz model which provides a specific grow rate (Kb) of 0.76 ±â€‰0.36 h−1 and a correlation of R 2 = 0.93. The integral approach study of the variables of a complex degradation process lead to improve the complete operation of the reactor in comparison with other more specific component-based approaches.

The present investigation was carried out to evaluate the detoxification potential of Pseudomonas fluorescens SM1 strain immobilized in calcium alginate beads for some major toxicants of Indian water bodies. The toxicants selected in this study were benzene hexachloride, mancozeb, 2,4-dichloro-phenoxyacetic acid (pesticides); phenol, catechol, cresol (phenolics); and Cd++, Cr(VI), Cu++ and Ni++ (heavy metals), which were taken as mixtures up to a concentration of roughly twice that usually found in highly polluted sites. Allium cepa phytotoxicity test, Ames fluctuation test and plasmid nicking assay were employed to estimate the phytotoxicity and genotoxicity of the model water containing the test toxicants under different combinations before and after exposure to our bioremediation-cum-detoxification system. The IC50 of the model water containing all the test toxicants, treated with the immobilized SM1 cells, was recorded to be 0.7× compared to 0.06× for the same but untreated water sample, enhancing the IC50 value by 12-fold. The IC25 of the test heavy metal mixture only could enhance from 0.07 to 1.30× (18-fold). The IC25 of the test pesticide mixture alone was increased from 0.07 to 1.71× (24-fold). The IC25 values for the mixture of test phenolics were 0.07× and 2.18× under the pre- and post-treatment conditions, respectively, exhibiting a 31-fold increase. A mutational induction (Mi) corresponding to the 0.5 value in the Ames fluctuation test was used to evaluate the mutagenicity of the test model water containing all the toxicants before and after exposure to the immobilized SM1 cell system. The Mi (0.5) value with the TA98 tester strain was estimated to be 0.08× for the untreated and 0.6× for the treated model water, whereas the same index was calculated to be 0.48× and 1.8×, respectively, for the TA100 strain. A remarkable improvement in the quality of the test water as a result of exposure to this bioremediating system was observed in terms of the absence of the linear form of the plasmid contrary to the visible linearization with the untreated model water. In view of the above findings, it is quite clear that the test of P. fluorescens SM1 strain immobilized in the calcium alginate beads could be used as an efficient system of bioremediation and for water decontamination strategies owing to its remarkable detoxification potential.

Granular bentonite has been assessed regarding its capacity to remove Hg(II), Cd(II) and Pb(II) from aqueous solutions. Sorption capacities, kinetics and the dependence of the sorption process on pH were determined. Fractional power, pseudo-first-order, pseudo-second-order and intra-particle diffusion equations were used to model the kinetics of metal adsorption. The pseudo-second-order model showed the best fit to experimental data. Different two-parameter sorption isotherm models (Langmuir, Freundlich, Temkin and Dubinin–Radushkevich) were used to fit the equilibrium data. Freundlich's isotherm model gave the best fit to experimental data. The selectivity of granular bentonite towards these metals is Pb(II) > Cd(II) > Hg(II). The adsorption capacities of granular bentonite towards the metals expressed in milligramme metal per gramme granular bentonite are 19.45, 13.05 and 1.7 for Pb(II), Cd(II) and Hg(II), respectively (for an initial concentration of 100 mg metal/L).

Achieving high productivity in agriculture is increasingly needed and requested; however, this activity should be performed in a sustainable and rational way. The use of micronutrients in the fertilization of the most diverse cultures is becoming a common practice on farms, but it is important to conduct studies in relation to fertilizers used for this supplement, including raw materials with which they are produced. Therefore, this study aimed to evaluate the phytoavailability of nutrients and toxic heavy metals Cd, Pb, and Cr; productivity; and yield components in wheat sown in soil with residue of N/P2O5/K2O + Zn-based fertilizer applied in previous crop. Treatments consisted of residual fertilization of five forms arranged in two doses (D1 = 300 kg ha−1 and D2 = 600 kg ha−1). The five types of fertilization were composed of formulated N/P2O5/K2O and the variation of different Zn sources. In the assessment of phytoavailability were determined levels of K, Ca, Mg, Cu, Mn, Zn, Fe, Cd, Pb, and Cr in wheat leaves. The results show that the residual effect of fertilization was not enough for there being difference between treatments at both doses used; however, it was found that the fertilizers used to Zn supply provided residual effect, providing significant levels of Pb and Cr for wheat plants.

In this work, the sorption of strontium on a Ca-bentonite (CGA) from Almería (Spain) in column experiments was studied, and the results obtained were compared with the sorption onto the Na-bentonite (MX-80). The code CTXFIT (two site non-equilibrium sorption model) was used in order to fit the experimental data and to determine sorption and transport parameters. The effect of inlet Sr(II) initial concentration and the ionic strength were evaluated. The results obtained showed that the sorption capacities as well as the transport and sorption parameters of both bentonites were affected by the initial metal concentration. In experiments with higher inlet concentrations, columns were saturated faster, leading to shorter breakthrough and exhaustion times. On the other hand, a decrease of sorption and transport parameters was observed at higher ionic strengths, which would confirm ion exchange as the main mechanism of Sr(II) sorption onto both bentonites. The sorption parameters (sorption capacity and retardation factor) obtained indicated that the Ca-bentonite from Almería (Spain) presented better sorption performance than the Na-bentonite, which was related to the physical properties of the Ca-bentonite.

We investigated the potential of soil moisture and nutrient amendments to enhance the biodegradation of oil in the soils from an ecologically unique semi-arid island. This was achieved using a series of controlled laboratory incubations where moisture or nutrient levels were experimentally manipulated. Respired CO2 increased sharply with moisture amendment reflecting the severe moisture limitation of these porous and semi-arid soils. The greatest levels of CO2 respiration were generally obtained with a soil pore water saturation of 50–70%. Biodegradation in these nutrient poor soils was also promoted by the moderate addition of a nitrogen fertiliser. Increased biodegradation was greater at the lowest amendment rate (100 mg N kg−1 soil) than the higher levels (500 or 1,000 mg N kg−1 soil), suggesting the higher application rates may introduce N toxicity. Addition of phosphorous alone had little effect, but a combined 500 mg N and 200 mg P kg−1 soil amendment led to a synergistic increase in CO2 respiration (3.0×), suggesting P can limit the biodegradation of hydrocarbons following exogenous N amendment.

Pine needles were selected as cost-effective and easy collectable matrices suitable for long-term monitoring of the lower troposphere pollution with polycyclic aromatic hydrocarbons (PAHs). Overall, 27 sampling sites around the island of Crete were selected, and upon availability, second- and third-year needles from two pine species (Pinus brutia Ten. and Pinus pinea L.) were collected. In general, the results for both pine species showed that sites belonging in the urban group yielded the highest contamination levels when compared to the rural and the remote ones and that third-year needles had higher PAH contamination than the second-year ones. Phenanthrene was the prevailing PAH, representing 39% and 46% of the total contamination for second- and third-year needles, respectively. Fluoranthene, pyrene, chrysene and fluorene followed, with individual concentrations between 6% and 12%. The dominance of three-ringed PAHs was evidenced for the vast majority of the sites. An urban, rural and remote fingerprint was determined over a more general uniform contamination pattern, and the diagnostic PAH ratios pointed towards mixed petrogenic and pyrogenic sources. Overall, the present findings showed that the presence of PAHs is not negligible throughout the Cretan atmosphere and can be even considered quite high in some areas, especially when comparing the results to the ones found for more densely populated or industry-related areas.

The majority of oil from oceanic oil spills (e.g. the recent accident in the Gulf of Mexico) converges on coastal ecosystems such as mangroves. Microorganisms are directly involved in biogeochemical cycles as key drivers of the degradation of many carbon sources, including petroleum hydrocarbons. When properly understood and managed, microorganisms provide a wide range of ecosystem services, such as bioremediation, and are a promising alternative for the recovery of impacted environments. Previous studies have been conducted with emphasis on developing and selecting strategies for bioremediation of mangroves, mostly in vitro, with few field applications described in the literature. Many factors can affect the success of bioremediation of oil in mangroves, including the presence and activity of the oil-degrading microorganisms in the sediment, availability and concentration of oil and nutrients, salinity, temperature and oil toxicity. More studies are needed to provide efficient bioremediation strategies to be applicable in large areas of mangroves impacted with oil. A major challenge to mangrove bioremediation is defining pollution levels and measuring recuperation of a mangrove. Typically, chemical parameters of pollution levels, such as polycyclic aromatic hydrocarbons (PAHs), are used but are extremely variable in field measurements. Therefore, meaningful mangrove monitoring strategies must be developed. This review will present the state of the art of bioremediation in oil-contaminated mangroves, new data about the use of different mangrove microcosms with and without tide simulation, the main factors that influence the success of bioremediation in mangroves and new prospects for the use of molecular tools to monitor the bioremediation process. We believe that in some environments, such as mangroves, bioremediation may be the most appropriate approach for cleanup. Because of the peculiarities and heterogeneity of these environments, which hinder the use of other physical and chemical analyses, we suggest that measuring plant recuperation should be considered with reduction in polycyclic aromatic hydrocarbons (PAHs). This is a crucial discussion because these key marine environments are threatened with worldwide disappearance. We highlight the need for and suggest new ways to conserve, protect and restore these environments.

The variability of hydrogeochemical conditions can affect groundwater microbial communities and the natural attenuation of organic chemicals in contaminated aquifers. It is suspected that in situ biodegradation in anoxic plumes of chloroethenes depends on the spatial location of the contaminants and the electron donors and acceptors, as well as the patchiness of bacterial populations capable of reductive dechlorination. However, knowledge about the spatial variability of bacterial communities and in situ biodegradation of chloroethenes in aquifers is limited. Here, we show that changes of the bacterial communities, the distribution of putative dechlorinating bacteria and in situ biodegradation at the border of a chloroethenes plume (Bitterfeld, Germany) are related to local hydrogeochemical conditions. Biotic reductive dechlorination occurred along a 50 m vertical gradient, although significant changes of the hydrogeochemistry and contaminant concentrations, bacterial communities and distribution of putative dechlorinating bacteria (Dehalobacter spp., Desulfitobacterium spp., Dehalococcoides spp., and Geobacter spp.) were observed. The occurrence and variability of in situ biodegradation of chloroethenes were revealed by shifts in the isotope compositions of the chloroethenes along the vertical gradient (δ13C ranging from −14.4‰ to −4.4‰). Our results indicate that habitat characteristics were compartmentalized along the vertical gradient and in situ biodegradation occurred with specific reaction conditions at discrete depth. The polyphasic approach that combined geochemical and biomolecular methods with compound-specific analysis enabled to characterize the spatial variability of hydrochemistry, bacterial communities and in situ biodegradation of chloroethenes in a heterogeneous aquifer.