A method that utilizes solid-phase microextraction (SPME) coupled with gas chromatography (GC) and chemical ionization tandem mass spectrometry (MS/MS) was developed for analyzing a group of emerging pollutants, N-nitrosamines, in water. The developed analytical method requires a water sample of less than 5 ml and only 1.5 h for complete analysis. The method detection limits for N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine, and N-nitrosodi-n-propylamine were in the range of 3.2 to 3.5 ng/l; for N-nitrosomorpholine, it was 15.2 ng/l. The method was successfully employed to measure the N-nitrosamine concentration at trace levels of nanogram per liter in four water treatment plants (WTPs) and one water distribution system. In the WTPs, only NDMA was detected in the treatment processes. Within the treatment train, NDMA was observed after chlorination. The level of NDMA significantly declined after slow sand filtration due presumably to microbial degradation. The NDMA concentration collected from consumer tap water was about 40% higher on average than that in the finished water. The excellent performance of the SPME/GC/MS/MS method in various water matrices as well as the shorter analysis time and smaller sample volume compared to currently used extraction techniques makes it an alternative means for the analysis of N-nitrosamine in drinking water, wastewater, and laboratory research with small reactors.

The adsorption and photocatalytic degradation of methyl orange (MO) aqueous solution under visible light illumination by polythiophene/titanium dioxide (PTh/TiO₂) composite particles were studied. The experimental observations from UV-vis spectrophotometer indicate that MO molecules were degraded in a different degree during the visible light-induced photocatalysis reaction. We propose a new degradation mechanism of MO during the photocatalytic reaction, based on blue shift of UV-vis absorption spectra of MO solution and other researches. The data from total organic carbon analyzer definitely prove that MO can be mineralized to CO₂ and H₂O, and some intermediate products are generated during the photocatalysis degradation of MO.

Amine-functionalized SiO₂/TiO₂ photocatalytic films have been synthesized using the peroxo titanic acid (PTA) approach coupled with the sol-gel dip-coating method. The 3-aminopropyl-trimethoxysilane (APTMS) and methyltrimethoxysilane (MTMOS) were employed as the amine functional groups and silica precursor. The effects of the ratio of APTMS/MTMOS, PTA refluxed time, and pH of prepared sol on the characteristics and the formaldehyde degradation efficiency were investigated. Physicochemical properties of prepared photocatalysts were characterized with nitrogen adsorption-desorption isotherm measurement, SEM, X-ray diffraction (XRD), UV-vis spectrophotometer, and Fourier transform infrared (FTIR) spectroscopy. The XRD and FTIR results indicated that the obtained photocatalysts consisted of -NH₂ groups, SiO₂, and anatase TiO₂. The photocatalytic films showed high transmittance of 80-90% in the visible light region. The obtained film prepared with the APTMS/MTMOS ratio of 0.03, pH of 1.8, and 10 h of refluxed time possessed high specific surface area (604.0 m² g⁻¹) and 85% formaldehyde degradation efficiency. The enhancement of formaldehyde degradation efficiency was observed when increasing the PTA refluxed time. The repeatability of photocatalytic film was also tested, and the degradation efficiency was 92.0% of initial efficiency after seven cycles.

Dissolved organic nitrogen (DON) plays an important ecological role in forest ecosystems, and its concentration is related to that of dissolved organic carbon (DOC). We investigated DON concentrations and ratios of DOC to DON in throughfall and soil waters in 16 Norway spruce and two Scots pine forest stands sampled at weekly intervals between 1996 and 2006. The stands are all included in the ICP Forests Level II monitoring program and are located throughout Norway. DON concentrations were significantly and positively related to DOC concentrations in throughfall (r ² = 0.72, p < 0.0001) and soil water at 5, 15, and 40 cm (r ² = 0.86, 0.32, and 0.84 and p < 0.0001, 0.04, and <0.0001, respectively). At most sites, the annual median DOC/DON ratio in throughfall ranged from 20.3 to 55.5, which is lower than values in soil water, which ranged from 24.5 to 81.3, gradually decreasing with soil depth. DON concentrations varied seasonally in throughfall at many plots and in soil water at 5-cm depth at one plot only, with higher values in the growing season, but there was no noticeable seasonality at greater depth. The ratios of DOC/DON in soil water were significantly positively related to the C/N ratio in soil at the same depth. Above-ground litter input was the main factor having a significant, negative relationship to DOC/DON in soil water at all depths studied. This might reflect the effect of site conditions on both DOC/DON ratios and litter quantity.

Distribution of ¹³⁷Cs and ²³⁹,²⁴⁰Pu in the forest soils horizons of the Opole Anomaly was established. Gamma and alpha spectrometry was used for determination of these isotopes. It was found that the ¹³⁷Cs activity was approx. 1,000 times higher than that of ²³⁹,²⁴⁰Pu. The highest activities of both radioisotopes were found close to the boundary region in soil profile where the organic horizon turns into the inorganic one. Cluster analysis did not clearly indicate the group's existence in data in respect to ¹³⁷Cs and ²³⁹,²⁴⁰Pu activities and organic matter content. Distributions of ¹³⁷Cs and ²³⁹,²⁴⁰Pu in soil horizons were non-normal but similar to each other. These distributions were substantially different from that one for organic matter content. The data were separated into two groups, for organic and inorganic soil horizons, respectively. Data transformation using Box-Cox formula was performed following by standardization. Mutual relationships between variables were investigated using ordinary and robust regression methods. Good correlation between ¹³⁷Cs and ²³⁹,²⁴⁰Pu was found. No significant relationship between organic matter content and radioisotopes activity was asserted.

Although the climate change effects on plants have been a focus for more than two decades, such effects on aquatic species remain largely unknown. To evaluate the potential effects of elevated CO₂ on growth and nutrient uptake of Eichhornia crassipe Solms (commonly known as water hyacinth, the world's most significant invasive aquatic weed), plants were grown at two CO₂ concentrations (380 and 800 ppm) combined with four nutrient levels (oligo-, meso-, eu-, and hypertrophic) for 2 months. Overall, elevated CO₂ consistently enhanced plant growth at all nutrient levels, indicating more infestations of water hyacinth in future natural eutrophic waters. Moreover, the enhancement extent varied among nutrient availabilities, being more in eu- and hypertrophic levels and less in meso- and oligotrophic levels. Furthermore, the CO₂ enrichment-deduced assimilation was allocated more to plant roots than shoots which would improve the nutrient absorption capacity and mostly transferred to offspring ramets rather than maintained at the mother ramet which would benefit the vegetative reproduction. Finally, under elevated CO₂, although the nitrogen (N) and phosphorus (P) contents of E. crassipe slightly decreased which might mean increased difficulties in preventing its infestation by reducing N and/or P in eutrophic waters, the total N and P accumulation increased suggesting higher bioremediation efficiency of using water hyacinth for water eutrophication.

Mercury concentrations in largemouth bass and mercury accumulation rates in age-dated sediment cores were examined at Lake Ozette and Lake Dickey in Washington State. Goals of the study were to compare concentrations in fish tissues at the two lakes with a larger statewide dataset and examine mercury pathways to the lakes. After accounting for fish length, tissue concentrations at the lakes were significantly higher than other Washington State lakes. Wet deposition and historical atmospheric monitoring from the area show no indication of enhanced local or regional deposition. Sediment core records from the lakes indicate rising sedimentation rates coinciding with logging in the lakes' drainages has greatly increased the net flux of mercury to the waterbodies.

Side effects related to liming have been studied in four dimictic lakes (553-642 m a.s.l.; 59°57′N) in Finnemarka, a forested area in Southern Norway with poor catchment buffer capacity. Data series from lake profiles have been sampled two decades apart; 10 years prior to liming and after 10 years of liming. Water samples were collected during spring after ice breakup and during summer after the development of thermal stratification. Before liming, there were very low concentrations of bicarbonate (HCO ₃ ⁻ ; or alkalinity) in the lakes. After 10 years of liming, up to 90% of the ions in hypolimnion originate from lime products. Hence, liming strengthened the chemical stratification and increased the vertical stability. Differences in chemocline developments between lakes were explained by differences in physical properties, i.e. their depth/surface area ratio. The chemocline developments lead to increased concentrations of organic matter in the hypolimnion with a subsequent reduction in oxygen concentrations. Lime additions during late spring, as an alternative to early autumn, lead to pronounced anoxic conditions in the hypolimnion.

The contamination of soils and waters by dye-containing effluents is of environmental concern. Due to the increasing awareness and concern of the global community over the discharge of synthetic dyes into the environment and their persistence there, much attention has been focused on the remediation of these pollutants. Among the current pollution control technologies, biodegradation of synthetic dyes by different microbes is emerging as an effective and promising approach. The bioremediation potentials of many microbes for synthetic dyes have been demonstrated and those of others to be explored in future. The biodegradation of synthetic dyes is an economic, effective, biofriendly, and environmentally benign process. Bioremediation of xenobiotics including synthetic dyes by different microbes will hopefully prove a green solution to the problem of environmental soil and water pollution in future. This review paper discusses comprehensively the science and arts of biodegradation of synthetic dyes.

Recent studies have shown that the lower basin of the Salado River is highly polluted with copper and chromium. In order to evaluate the effect of those metals on Notodiaptomus conifer, a representative calanoid copepod, we carried out two (acute and chronic) experimental assays. In the first one, the 24- and 48-h EC₅₀ values were determined in nauplii and adults. Chronic assays were conducted to evaluate the time of development for nauplii, time of development for each copepodite stage, total development time, growth, number of ovigerous females, fecundity, and time required to produce the first egg sac. Additionally, the effect of those metals on the equiproportional model proposed for copepods was evaluated. Acute experiments reveled that juveniles were more sensible than adults. Although growth was not seriously affected by metal exposition, development time was delayed and reproductive variables were altered with the increase of metal concentrations. The deviation from the equiproportional model proposed for copepods proved to be a useful parameter to provide relevant information on toxicity of both metals along development time. In comparison with other zooplanktonic species, the highest sensitivity of N. conifer to copper and chromium makes it a suitable bioindicator in ecotoxicological tests.