A novel system for organic waste stabilization and reuse, combined with production of nitrate-rich liquid fertilizer was developed by manure digestion followed by volatilization of ammonia-rich gas (originating in manure extract) and its nitrification and recovery. This approach has several advantages, including biowaste stabilization and high recovery (over 60%) of manure N mainly as nitrate which is a better N form for many plants as compared to ammonium as the sole fertilizer N. Moreover, the potential utilization of different wastes as N sources in organic horticulture is possible as well as removal of suspended particles and microorganisms (including pathogens) that might otherwise clog the irrigation system and pose health risks, respectively. In a pilot-scale study, the system yielded several hundred liters of nitrate-rich (ca. 11 g N L−1) liquid fertilizer using guano as substrate. In a fertilization experiment, lettuce fertigated with the nitrate-rich extract exhibited better growth and quality compared to the common organic practice of fertigation with guano extract. The resulting stabilized biowaste was estimated as “low-risk” according to current guidelines and may be used for liming or land application.

Metal contamination of freshwater bodies resulting from mining activities or deactivated mines is a common problem worldwide such as in Portugal. Braçal (galena ore) and Palhal (pyrrhotite, chalcopyrite, galena, sphalerite, and pyrite ore), located in a riverside position, are both examples of deactivated mining areas lacking implemented recovery plans since their shutdown in the early mid-1900s. In both mining areas, effluents still flow into two rivers. The purpose of this work was to evaluate the potential hazard posed by the mining effluents to freshwater communities. Therefore, short- and long-term ecotoxicological tests were performed on elutriates from river sediments collected at each site using standard test organisms that cover different functional levels (Vibrio fischeri, Pseudokirchneriella subcapitata, Lemna minor, and Daphnia sp.). The results show that elutriates from the sediments of Palhal were very toxic to all tested species, while in contrast, elutriates from Braçal showed generally no toxicity for the tested species. Our study highlights the usefulness of using an ecotoxicological approach to help in the prioritization/scoring of the most critical areas impacted by deactivated mines. This ecotoxicological test battery can provide important information about the ecological status of each concerning site before investing in the application of time-consuming and costly methods defined by the Water Framework Directive or can stand as a meaningful complementary analysis.

In this experiment, the effects of the Hungarian red mud disaster were studied in a soil column experiment focusing on element solubility. The effect of flooding with the highly alkaline red mud suspension and the effect of the percolation of precipitation water through the 10 cm thick red mud layer were modelled separately. Both scenarios affected the soil pH up to a depth of 80 cm. An increase in the total element concentration was only observed for Na and Mo, probably due to the leaching of red mud particles measuring 0.05–0.02 and <0.002 mm in the column. At the same time, the water-soluble concentrations of the potentially toxic elements As, Co, Cr, Cu, Ni, Pb, and Zn rose, at least in the top soil layer, but the concentration values remained below the limit values laid down by quality standards. Over a longer period of time, the main environmental risk raised by the disaster is the secondary salinization of the area.

We assessed the suitability of two nonnative poeciliid fishes—western mosquitofish (Gambusia affinis) and sailfin mollies (Poecilia latipinna)—for monitoring selenium exposure in desert pupfish (Cyprinodon macularius). Our investigation was prompted by a need to avoid lethal take of an endangered species (pupfish) when sampling fish for chemical analysis. Total selenium (SeTot) concentrations in both poeciliids were highly correlated with SeTot concentrations in pupfish. However, mean SeTot concentrations varied among fish species, with higher concentrations measured in mosquitofish than in mollies and pupfish from one of three sampled agricultural drains. Moreover, regression equations describing the relationship of selenomethionine to SeTot differed between mosquitofish and pupfish, but not between mollies and pupfish. Because selenium accumulates in animals primarily through dietary exposure, we examined fish trophic relationships by measuring stable isotopes (δ 13C and δ 15N) and gut contents. According to δ 13C measurements, the trophic pathway leading to mosquitofish was more carbon-depleted than trophic pathways leading to mollies and pupfish, suggesting that energy flow to mosquitofish originated from allochthonous sources (terrestrial vegetation, emergent macrophytes, or both), whereas energy flow to mollies and pupfish originated from autochthonous sources (filamentous algae, submerged macrophytes, or both). The δ 15N measurements indicated that mosquitofish and mollies occupied similar trophic levels, whereas pupfish occupied a slightly higher trophic level. Analysis of gut contents showed that mosquitofish consumed mostly winged insects (an indication of terrestrial taxa), whereas mollies and pupfish consumed mostly organic detritus. Judging from our results, only mollies (not mosquitofish) are suitable for monitoring selenium exposure in pupfish.

A new sampling system has been developed for the measurement of time-averaged concentrations (TWA) and diffusion coefficients of organic micropollutants in aquatic environments. The system is based on the diffusion of targeted organic compounds through a rate-limiting membrane and the subsequent accumulation of these species in a bound, hydrophobic solid-phase material. Two separate prototype systems are described. One is suitable for the sampling of carbamates such as carbaryl, carbofuran, 3-hydroxycarbofuran, baygon, propham, clorpropham, and the other one for s-triazines such as atrazine, prometryn, propazine, simazine, terbuthylazine, terbutryn, metribuzin, cyanazine, and metamitron pesticides. The systems use solid-phase material (47-mm C₁₈ Empore disk) as the receiving phase but are fitted with rate-limiting membranes of either polysulfone or polycarbonate. For the two designs investigated, the cumulative uptake of all target analytes was considered over exposure periods of 7 days. The determined sampling rates ranged from 0.1323 to 0.0465 L day⁻¹ with both membranes. The best system was the one with the polysulfone membrane allowing a better cumulative uptake.

The occurrence of fluoride in groundwater has been reported in many countries, mainly because the excess fluoride in drinking water can lead to dental or skeletal fluorosis. Fluoride removal by coagulation with Moringa oleifera seeds, followed by separation with membranes, was investigated in this work. Artificially fluoridated water, at a starting fluoride concentration of 10 mg L⁻¹, was submitted to a coagulation process with aqueous extracts of M. oleifera seeds. The coagulation process was followed by ultrafiltration with membranes at different pressures. The coagulation process with 2.5 g L⁻¹ of M. oleifera promoted a reduction of 90.90 % in the fluoride content of the treated water, making it possible for poor communities to consume this water. It is noteworthy that the combined coagulation/filtration process using raw coagulant showed the highest values of colour and turbidity, which, however, were still below the limits set for drinking water by Brazilian legislation. The advantage of proposing a sequential process using membrane separation is that it removes colour and turbidity, caused by the use of M. oleifera as a coagulant, resulting in water that meets potability standards.

Following the Deepwater Horizon explosion and crude oil contamination of a marsh ecosystem in AL in June 2010, hydrocarbon-degrader microbial abundances of aerobic alkane, total hydrocarbon, and polycyclic aromatic hydrocarbon (PAH) degraders were enumerated seasonally. Surface sediment samples were collected in October and December of 2010 and in April and July of 2011 along 40–70-m transects from the high tide to the intertidal zone including Spartina alterniflora-vegetated marsh, seagrass (Ruppia maritima)-dominated sediments, and nonvegetated sediments. Alkane and total hydrocarbon degraders in the sediment were detected, while PAH degraders were below detection limit at all locations examined during the sampling periods. The highest counts for microbial alkane degraders were observed at the high tide line in April and averaged to 8.65 × 105 of cells/g dry weight (dw) sediment. The abundance of alkane degraders during other months ranged from 9.49 × 103 to 3.87 × 104, while for total hydrocarbon degraders, it ranged between 5.62 × 103 and 1.14 × 105 of cells/g dw sediment. Pore water nutrient concentrations (NH 4 + , NO 3 − , NO 2 − , and PO 4 3− ) showed seasonal changes with minimum values observed in December and April and maximum values in October and July. Concentrations of total petroleum hydrocarbons in sediments averaged 100.4 ± 52.4 and 141.9 ± 57.5 mg/kg in January and July, 2011, respectively. The presence of aerobic microbial communities during all seasons in these nearshore ecosystems suggests that an active and resident microbial community is capable of mineralizing a fraction of petroleum hydrocarbons.

A laboratory study was conducted to assess the feasibility of remediating diesel-contaminated soils using sodium persulfate (SPS) oxidation under an alkaline pH. Lime (CaO) and sodium hydroxide (NaOH) were used as the alkaline sources, and various factors, including temperature, reaction time and concentration level, were investigated. Moreover, the combined usage of hydrogen peroxide (HP) and SPS in the presence or absence of NaOH was also studied. It was found that lime hydration resulted in rapid increases in pH (>12) and temperature (75 °C maximum) at a CaO/H₂O mass ratio of 3/20. In the NaOH or CaO/SPS system, the maximum diesel degradation achieved was approximately 30 %. It was observed that using a larger amount of alkaline increased SPS decomposition and had almost no effect on diesel degradation. Limited solubilization of contaminants may have inhibited the effectiveness of alkaline-activated persulfate oxidation during the aqueous phase and hence resulted in incomplete diesel degradation. The highest rate of diesel degradation (i.e., 56 % in 7 days) was achieved using the dual oxidation system, in which a HP/SPS molar ratio of 3.3/0.5 was used. An aggressive oxidation process, coupled with HP, may enhance desorption of diesel from soils and allow oxidation to occur during the aqueous phase.

Photocatalytic methods were applied to remove the recalcitrant or toxic pollutants from the water. The two models of wastewater containing either non-ionic surfactant Triton X-100 or commercially available wash-up liquid were tested in a self-constructed band reactor during the laboratory studies. The photocatalyst, being typed TiO₂, was supported by porous Al₂O₃ and modified by the addition of Cu, Fe, Zn, Ni, Mo or Co. The photocatalysts were characterised by N₂ adsorption–desorption, XRF, XRD, SEM-EDX, Raman and UV–Vis spectroscopy. All catalysts were efficient in the photocatalytic oxidation of surfactants, and they enabled at least 85 % COD reduction. TiO₂/Al₂O₃ photocatalysts modified by the transition metals were efficient only for more complicated compositions of surfactants. The effect of H₂O₂ (0.01 vol.%) addition was also examined and compared with a type of compound and catalyst used—in this case a positive effect for Triton X-100 was only observed over the photocatalyst modified by Ni. When it comes to the wash-up liquid photoremoval, all studied photocatalysts seem to be slightly influenced by H₂O₂ addition. It was also observed that it is not economically justified to conduct such treatment for more than 2 h.

Black rice husk ash (BRHA) was obtained by means of thermal degradation of raw rice husks (RRH) on a pilot plant fluidized bed reactor. BRHA was characterized using chemical analyses, scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy and thermal analysis. The kinetics was studied using batch adsorption technique and on the basis of prior characterization by X-ray diffraction patterns and scanning electron microscopy. The adsorption capacities of diesel fuel at 288, 293 and 298 K onto BRHA were determined. Results showed that the material studied has very high adsorption capacity and low cost and may successfully be used as an effective adsorbent to clean up spills of oil products in water basins. The adsorption of diesel fuel onto BRHA proceeds rapidly to reach adsorption equilibrium in about 10 min. The saturated BRHA can be burnt in incinerators, industrial ovens or steam generators, and through this way ecological and economic benefits are attained.