The use of multiwall carbon nanotubes (MWCNT) as an efficient solid extractor in preconcentration/cleanup studies for tin determination in water samples by electrothermal atomic absorption spectrometry (ETAAS) is proposed. In the proposed method, tin adsorption onto MWCNT was carried out by percolating the solution previously buffered (pH 4.79 with 0.24 mol L−1 acetic acid/acetate buffer) at 4.0-mL min−1 flow rate, followed by elution with 1.0 mL of 2.7 mol L−1 HNO3. Factors such as sample pH, preconcentration/cleanup flow rate, type and concentration of eluent, and buffer concentration were appraised and optimized from chemometric tools based on fractional factorial design and Doehlert design. A limit of detection of 0.73 μg L−1 and precision (n = 8) assessed as relative standard deviation of 8.6% and 7.0% for tin concentration of 8.0 and 43.0 μg L−1, respectively, were achieved. Foreign metallic ions (Ni2+, Pb2+, Co2+, Zn2+, Cd2+, Mn2+, and Fe3+) were checked as potential interferents, and no interference was observed up to an analyte/interference ratio of 1:10 (m/v). Direct tin determination by ETAAS in water samples containing high salt amount is drastically affected by background signal. However, previous cleanup of sample by MWCNT has promoted a significant improvement and makes the method useful for tin monitoring in water samples (mineral, lake, mine, and natural waters) by ETAAS. Quantitative recovery values ranging from 91.5% to 103.0% attested the applicability of the proposed preconcentration/cleanup for tin determination in water samples.

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.

We report the isolation of a new bacterium species (named as DN-06) that degrades pyridine, a model compound containing both carbon and nitrogen, from the aerobic activated sludge in a coking wastewater treatment plant. DN-06 was identified as Achromobacter sp. using 16S rDNA sequence analysis. In batch culture, more than 95% of pyridine (500 mg/L) was degraded within 18 h by DN-06 grown at 35°C and pH 8 with agitation at 170 rpm. Degradation experiments of pyridine at different initial concentrations (50–4,300 mg/L) revealed that pyridine was an inhibitory substrate, and that neither yield coefficient Y nor endogenous decay coefficient K d was a constant. The values of Y and K d were 0.55–0.74 and 0.0032–0.0057 h−1, respectively. Five kinetic models (Haldane, Yano, Aiba, Webb, and Monod) were fitted to the experimental growth kinetic data. Models of Haldane and Yano (correlation coefficient R 2 = 0.929) were the most suitable models. For Haldane kinetic model, the values of μ max, K s, and K i were 0.161 h−1, 142.6 mg/L, and 4234.8 mg/L, respectively. The large values of Y and K i indicated that DN-06 had good tolerance against high pyridine concentrations. These results indicated possible future applications of Achromobacter sp. DN-06 in removing pyridine from industrial wastewaters, as well as in destroying pyridine in concentrated solutions during further treatment of trial water coupling with adsorption technology.

The biofilter system containing tire-derived rubber particle (TDRP) filter media was utilized to treat the odorous gas contaminant, hydrogen sulfide, in consideration of the economic advantage of reusing discarded tire materials and the high potential of TDRP media for biofilm attachment. The pilot-scale system having 0.38 m3 of bed volume operated with synthetic hydrogen sulfide gas on continuous basis from a range of 0.34 to 1.15 m3/min. This bioreactor system achieved over 94% removal efficiency at 20–90 ppm of inlet H2S concentration while operating in 20–67 s of empty bed retention time, indicating that overall effective operation was performed at mass loading rates of H2S ranging from 19.6 to 28.5 g H2S/(m3 h). It was apparent by the effectiveness of the system’s performance that this system had the capability to effectively remove hydrogen sulfide with high efficiency over a range of concentrations. A maximum elimination capacity was not found for the biofilter during this study, which tested loading rates between 0 and 30 g H2S/(m3 h).

Fly ash is one of the residues produced during combustion of coal, and its disposal is a major environmental concern throughout coal-based power-generated counties. Deficiencies of essential nutrients, low soil microbial activity, and high-soluble salt concentrations of trace elements are some of the concerns for reclamation of fly ash ponds. The effect of fly-ash-adapted arbuscular mycorrhizal (AM) fungi and phosphate solubilizing fungus Aspergillus tubingensis was studied on the growth, nutrient, and metal uptake of bamboo (Dendrocalamus strictus) plants grown in fly ash. Co-inoculation of these fungi significantly increased the P (150%), K (67%), Ca (106%), and Mg (180%) in shoot tissues compared control plants. The Al and Fe content were significantly reduced (50% and 60%, respectively) due to the presence of AM fungi and A. tubingensis. The physicochemical and biochemical properties of fly ash were improved compared to those of individual inoculation and control. The results showed that combination of AM fungi and A. tubingensis elicited a synergetic effect by increasing plant growth and uptake of nutrients with reducing metal translocation.

This study evaluated the toxic effects of arsenic (As) on the growth, total antioxidant activity, total content of phenolic compounds, and content of photosynthetic pigments of Azolla filiculoides. The aquatic fern was propagated and exposed to Yoshida nutrient solution contaminated with sodium arsenate (Na2HAsO4·7H2O) at six concentrations (5, 10, 20, 30, 60, and 120 μg As mL−1), including the control without As contamination. Azolla cultures were kept under environmental chamber conditions 26°C, 12 h photoperiod and 80% HR for 96 h. Increased As concentrations (>30 μg mL−1) significantly diminished growth of A. filiculoides and the total content of chlorophyll and total phenolic compounds, but significantly enhanced of total carotenoid + xanthophylls content. The concentrations of 5 and 10 μg As mL−1 significantly stimulated the growth of A. filiculoides. This aquatic fern tolerates As concentrations lower than 30 μg mL−1, and its maximum As accumulation (28 μg g−1 dry weight) was achieved when exposed to 60 μg As mL−1, but showing clear symptoms of As toxicity.

The concentrations of selected metals—Cr, Ni, Cu, Zn, Cd, and Pb—were determined in the samples of Hypogymnia physodes lichen and Pleurozium schreberi moss collected in Polish and Czech Euroregions Praded and Glacensis. More specifically, the samples were collected in Bory Stobrawskie, Bory Niemodlińskie, and Kotlina Kłodzka (Poland) and in Jeseniki (Czech Republic). The concentration of metals in the samples was measured using the atomic absorption spectrometry (flame AAS technique and electrothermal atomization AAS technique). The results were used to calculate the comparison factor (CF) that quantifies the difference in concentration of a given bioavailable analyte × accumulated in lichens and mosses: CF = 2 (c x,lichen − c x,moss) (c x,lichen + c x,moss)−1. The values of CF greater than 0.62 indicate the most probable location of heavy metals deposited in the considered area. In this work, the method was used to show a significant contribution of urban emissions to the deposition of heavy metals in the area of Bory Stobrawskie and in the vicinity of Kłodzko City.

This study assessed the foliar uptake of 15N-labelled nitrogen (N) originating from wet deposition along with leaf surface conditions, measured by wettability and water storage capacity. Foliar 15N uptake was measured on saplings of silver birch, European beech, pedunculate oak and Scots pine and the effect of nitrogen form (NH4 + or NO3 −), NH4 + to NO3 − ratio and leaf phenology on this N uptake was assessed. Next to this, leaf wettability and water storage capacity were determined for each tree species and phenological stage, and the relationship with 15NH4 + and 15NO3 − uptake was examined. Uptake rates were on average five times higher (p < 0.05) for NH4 + than for NO3 − and four times higher for deciduous species than for Scots pine. Developing leaves showed lower uptake than fully developed and senescent leaves, but this effect was tree species dependent. The applied NH4 + to NO3 − ratio did only affect the amount of N uptake by senescent leaves. The negative correlation between measured leaf contact angles and foliar N uptake demonstrates that the observed effects of tree species and phenological stage are related to differences in leaf wettability and not to water storage capacity.

The toxicities of three synthetic surfactants to the marine macroalga, Ulva lactuca, have been examined by monitoring chlorophyll a fluorescence quenching. The anionic surfactant, sodium dodecyl sulphate (SDS), exerted no measurable toxicity over the concentration range 0–10 mg L−1, while presence of the non-ionic surfactant, Triton X-100 (TX), elicited a small reduction in photochemical efficiency that was independent of concentration. The cationic surfactant, hexadecyltrimethylammonium bromide (HDTMA), incurred a dose-dependent response to ∼3 mg L−1 (EC50 = 2.4 mg L−1), but a reduction in toxicity thereafter. Presence of TX had little effect on the toxicity of HDTMA but an equimolar concentration of SDS directly offset the impact of HDTMA on photochemical efficiency. Relative toxicities of the surfactants are attributed to differences in affinity for the algal surface and tendencies to disrupt cell membranes and interact with intracellular macromolecules. Non-linear dose responses and antagonistic effects are attributed to non-specific interactions between molecules of the same surfactant and electrostatic interactions between molecules of different amphiphilic character.

The influence of the operational variables on the Anammox process has been generally researched considering each variable separately. However, the optimization of the process also requires the identification of the more significant variables and their possible interactions. Response surface models were successfully applied to evaluate the performance of the Anammox process in a deammonification system (i.e., one-stage biofilm Anammox process) taking into account the combined effects caused by two sets of three variables. Specific Anammox activity was measured by a manometric method and used as the response variable. The obtained models pointed out that the significant variables were the temperature, the value of pH, and the ratio between the unionized species of the substrates (free ammonia and free nitrous acid (FA/FNA)). There were interactions among them caused by chemical equilibriums. Total nitrogen concentration and ammonium concentration were found to be not significant in the tested range. According to the models, the optimum values of temperature, pH, and free ammonia to free nitrous acid ratio within the test ranges were, respectively, 30°C, 7.0, and 0.3. Further research at higher temperatures and lower values of pH and FA/FNA ratios would be necessary in order to find the absolute optimum conditions for the process. The obtained model can be also useful in order to develop control strategies that take into account the significant variables and their optimum ranges. A strategy to control deammonification reactors has been proposed, according to the results of the modeling.