Pilot-scale experiments were performed to investigate the role of equalization basins used with constructed wetland systems for treatment of flue gas desulfurization (FGD) waters. Analysis of FGD water samples indicated that aqueous concentrations of Hg, As, and Se remained constant or changed very slightly in a pilot-scale equalization basin during a 24-h hydraulic retention time (HRT). No change in toxicity of FGD water occurred after one HRT. FGD particles were predominantly silt size, and approximately 99% of particles suspended in FGD water settled to the bottom of a 2.5-m-deep equalization basin during the first 4 h of the 24-h HRT. Approximately 90% of the total As, and smaller percentages of Hg and Se, in FGD water and particles were removed by particle settling in the equalization basin. Results of this investigation lend support to the use of equalization basins for treating FGD waters in constructed wetland treatment systems.

The fate and transport of tricyclazole and imidacloprid in paddy plots after nursery-box application was monitored. Water and surface soil samples were collected over a period of 35 days. Rates of dissipation from paddy waters and soils were also measured. Dissipation of the two pesticides from paddy water can be described by first-order kinetics. In the soil, only the dissipation of imidacloprid fitted to the simple first-order kinetics, whereas tricyclazole concentrations fluctuated until the end of the monitoring period. Mean half-life (DT₅₀) values for tricyclazole were 11.8 and 305 days, respectively, in paddy water and surface soil. The corresponding values of imidacloprid were 2.0 and 12.5 days, respectively, in water and in surface soil. Less than 0.9% of tricyclazole and 0.1% of imidacloprid were lost through runoff during the monitoring period even under 6.3 cm of rainfall. The pesticide formulation seemed to affect the environmental fate of these pesticides when these results were compared to those of other studies.

An experiment was set up to assess the factors affecting metal mobility in five wetland soils of the Scheldt estuary at different sampling depths when subjecting the soils to various water table levels. Pore water metal concentrations were monitored for 10 months at four sampling depths (10, 30, 60 and 90 cm) upon adjusting the water table level to 0, 40 and 80 cm below the surface of the soils. Nickel (Ni) release is facilitated by reductive conditions. These reductive conditions mainly occur below the water table. The fate of chromium (Cr) under reductive conditions seems to be promoted by the presence of dissolved organic matter. However, Cr fate seems to be inconsistent between the soils, as it is affected by a series of counteracting mechanisms. Copper (Cu), zinc (Zn) and especially cadmium (Cd) are all primarily released above the water table under high salinity conditions. These elements are also released below or just above the water table when organic matter is being decomposed, resulting in calcium (Ca), manganese (Mn), Ni and/or iron (Fe) release upon CO₂ accumulation and Fe/Mn oxide reduction, without being accompanied by sulphide production. Their mobility is low under reducing conditions, i.e. in the presence of sulphides, whereas the complexation by soluble organic matter especially seems to promote Cu mobility.

Flooded post-harvest rice paddies were examined as systems for reducing diazinon (organophosphate insecticide) concentrations in stormwater runoff. Two paddies were cultivated in Oryza sativa L. and amended with a 3-h simulated stormwater diazinon runoff event. Initial diazinon adsorption peaked at 347 and 571 μg kg⁻¹ (3% mass load reduction) for mean above-ground plant tissue concentrations in each pond, respectively. Subsequent senescence of above-ground tissue showed significant decreases in tissue mass (r ² = 0.985) and adsorbed diazinon mass (90 ± 4% and 82 ± 1%) within 1 month of amendment. There were no corollary increases in water column diazinon concentrations. Furthermore, control O. sativa tissue placed within the treatment ponds had below-detectable levels of diazinon throughout the decomposition phase, suggesting a lack of within pond transference of dissipated diazinon. This study shows the relative effectiveness of diazinon adsorption by post-harvest rice plants and a potential mitigation strategy of senescence and pesticide degradation for contaminated tailwater.

The effects of bentazon and molinate, two selective herbicides recommended for integrated weed management in rice, were studied in Anabaena cylindrica, an abundant cyanobacterium isolated from a Portuguese rice field agro-ecosystem. Comparative effects of both herbicides on A. cylindrica were estimated under laboratory conditions by measuring its dry weight yield, photopigments, and carbohydrate and protein contents in a time- and dose-dependent exposure throughout 72 h. Photosynthesis and respiration were also monitored. The results revealed that both herbicides exerted a pleiotropic effect on the cyanobacterium at the range of concentrations tested (0.75-2 mM). Growth, chlorophyll a, carotenoids and phycobiliproteins were more adversely affected by molinate than by bentazon. Cyanobacterial growth inhibitions of over 50% were observed after 48 h when 1.5-2 mM of molinate were applied. Bentazon concentrations ranging from 0.75 to 2 mM did not significantly modified chlorophyll a content with time, however, considerable reductions in chlorophyll a, carotenoids and specially phycobiliproteins were observed with molinate. Protein content increased with both herbicides although the effect was particularly noticeable with the highest concentration of molinate. Herbicide effects on carbohydrate content were contrasting: molinate increased this organic fraction whereas bentazon decrease it. Photosynthesis and respiration were inhibited by both herbicides and higher molinate concentrations (1.5-2 mM) completely ceased O₂ evolution after 48 h. Since A. cylindrica is abundant in Portuguese rice fields and could be used as an inoculum source in rice biofertilization programs, their protection from potential residual effects of herbicides is fundamental for a correct management of local soil fertility.

The effect of exogenously added sodium dodecylbenzenesulphonate (SDBS) surfactant on biodegradation of a mixture of straight-chain aliphatic hydrocarbons (dodecane and hexadecane) and resulting cell surface hydrophobicity changes of Candida maltosa EH 15 were investigated. Results indicated that up to 75 mg/L SDBS improves the biodegradation potential of examined yeast. A decrease in hydrophobicity was observed when SDBS was supplemented in higher concentrations, having strong impact on biodegradation rates. Phase distribution of surfactant molecules was investigated using methylene blue active substances method (MBAS), accompanied by surface and interfacial tension measurements. Studies showed that portion of SDBS molecules adsorbed on cell surface may play significant role in interaction between anionic surfactant and yeast cells, having influence on biodegradation rates.

The present study aimed to elucidate the atmosphere-forest exchange of ammoniacal nitrogen (NHX-N) at a young larch ecosystem. NHX-N exchanges were measured at a remote site in northernmost Japan where 4-year-old larches were growing after a pristine forest had been clear-cut and subsequent dense dwarf bamboo (Sasa) had been strip-cut. The site was a clean area for atmospheric ammonia with mean concentrations of 0.38 and 0.11 μg N m⁻³ in snowless and snow seasons, respectively. However, there was a general net emission of NHX-N. The annual estimated emission of NHX-N of 4.8 kg N ha⁻¹ year⁻¹ exceeded the annual wet deposition of 2.4 kg N ha⁻¹ year⁻¹, but the weekly exchange fluxes may have been underestimated by 28-60%. The main cause of the ammonia loss from the young larch ecosystem was probably enhanced nitrogen supply stimulated by the cutting of the pristine forest and Sasa, in particular, the Sasa.

The goal of this study is to clarify the surface-chemical and microphysical variables that influence bacterial spore transport through soil, thereby defining the factors that may affect spore transport velocity. Bacillus cereus spores were continuously monitored in a soil column under saturated conditions with experimental variations in soil grain size (0.359 and 0.718 mm), pH (7.2 and 8.5), and water flow rate (1.3 and 3.0 mL/min). Increasing soil grain size, flow rate, and pH resulted in enhanced spore movement. Spore transport increased 82% when soil grain size was doubled. An increase in effluent flow rate from 1.3 to 3.0 mL/min increased spore movement by 71%. An increase in pH increased spore transport by 53%. The increase in hydrodynamic forces resulting from the larger grain size soil and higher flow rate functioned to overcome the hydrophobic nature of the spore's coat, and the interparticle bonding forces between the spore and soil particles.

The chemical characteristics of the Urauchi River water in Iriomote Island National park, Okinawa, Japan have been studied. Concentrations of PO₄ ³⁻, NO₂ ⁻, and NH₄ ⁺ were barely detectable. We compared the concentration ratios of Mg²⁺/Na⁺, HCO₃ ⁻/Na⁺, and Ca²⁺/Na⁺ in the Urauchi River to those of 60 large rivers in the world and indicated that the chemical composition of the river is most likely formed by the binary mixing of sea salt components and silicate rock weathering components. Although rock weathering in the catchments area is driven by both H₂CO₃ and H₂SO₄, the role of H₂CO₃ is dominant. The percentages of the concentration of each cation in the river water are almost the same as those of other rivers with drainage areas consisting of silicate rock and sandstone. Thus, the Urauchi River shows the typical chemical characteristics of a river in a silicate rock area that includes sandstone.

In order to recover and reuse water in the Kraft mill process, evaluation of separate streams is required to identify toxic compounds or microcontaminants. The stage E1 Kraft effluent, corresponding to the first extraction step of the bleaching Kraft mill process, provides the main toxic compounds found in the final process effluent. This paper uses the toxicity identification evaluation (TIE) procedure for the physicochemical and ecotoxicological characterization of the E1 Kraft effluent. To distinguish the most important toxic compounds, a physicochemical characterization and Phase I of the TIE procedure were performed. The acute toxic effect of the E1 Kraft effluent and treated fraction was performed on Daphnia magna. Results show that untreated E1 Kraft effluent exerts an acute toxic effect on D. magna (24 h LC₅₀ = 27.6%), where the E1 Kraft effluent is characterized by pH 10.5, chemical organic demand (COD) 1,348.8 mg/l, and biological organic demand (BOD₅) 397.5 mg/l, while total phenolic compounds and color are 853.7 mg/l and 0.204 1 x 1 cm, respectively. Additionally, Cu⁺² (0.51 mg/l) and Fe⁺² (0.64 mg/l) were detected. With respect to different treatments, our results indicate that activated carbon, anionic and cationic exchange treatments were able to reduce more that 45% of E1 Kraft effluent's acute toxicity and that the ethylenediaminetetraacetic acid treatment was able to reduce the E1 Kraft effluent's acute toxicity to around 75% and the Cu⁺² concentration to 0.019 mg/l. Moreover, specific analysis of heavy metals and organic compounds by GC-MS show that the main compound responsible for the toxicity was Cu⁺², whose tolerance level on D. magna of the 0.12 mg/l.