Anthropogenic disturbances change the trophic structure of streams, ultimately affecting ecosystem functioning. We investigated the effects of human disturbances, mainly organic pollution, on ciliate functional feeding groups (FFG) in 10 tropical streams near agricultural and urban habitats, in the dry and rainy seasons. We hypothesised that the organic pollution would affect the ciliate composition and that the richness and abundance of ciliate FFG would be associated with different disturbances, such that an increase in the load of organic matter would result in an increase in the percentage of bacterivores ciliates, while streams with low organic matter concentration and wide canopy openness will determine a higher contribution of algivorous ciliates. Our results corroborate our hypothesis of an increased development of bacterivorous ciliates with increasing organic pollution, but only in the abundance of this FFG. Also, algivorous ciliates were found to be related to riparian vegetation clearing. Thus, ciliate FFG accurately reflected different anthropogenic disturbances, revealing a change in the trophic structure of the streams. In addition, we found that organic pollution can lead to both taxonomic and functional homogenization of the ciliate community, which implies serious consequences for ecosystem functioning.

Creatinine-corrected urinary analyte concentration is usually computed as the ratio of the observed level of analyte concentration divided by the observed level of the urinary creatinine concentration (UCR). This ratio-based method is flawed since it implicitly assumes that hydration is the only factor that affects urinary creatinine concentrations. On the contrary, it has been shown in the literature, that age, gender, race/ethnicity, and other factors also affect UCR. Consequently, an optimal method to correct for UCR should correct for hydration as well as other factors like age, gender, and race/ethnicity that affect UCR. Model-based creatinine correction in which observed UCRs are used as an independent variable in regression models has been proposed. This study was conducted to evaluate the performance of ratio-based and model-based creatinine correction methods when the effects of gender, age, and race/ethnicity are evaluated one factor at a time for selected urinary analytes and metabolites. It was observed that ratio-based method leads to statistically significant pairwise differences, for example, between males and females or between non-Hispanic whites (NHW) and non-Hispanic blacks (NHB), more often than the model-based method. However, depending upon the analyte of interest, the reverse is also possible. The estimated ratios of geometric means (GM), for example, male to female or NHW to NHB, were also compared for the two methods. When estimated UCRs were higher for the group (for example, males) in the numerator of this ratio, these ratios were higher for the model-based method, for example, male to female ratio of GMs. When estimated UCR were lower for the group (for example, NHW) in the numerator of this ratio, these ratios were higher for the ratio-based method, for example, NHW to NHB ratio of GMs. Model-based method is the method of choice if all factors that affect UCR are to be accounted for.

A simple method based on dispersive solid-phase extraction (DSPE) and dispersive liquid–liquid microextraction method based on solidification of floating organic droplets (DLLME-SFO) was developed for the extraction of chlorpyrifos (CP), chlorpyrifos-methyl (CPM), and their main degradation product 3,5,6-trichloro-2-pyridinol (TCP) in tomato and cucumber samples. The determination was carried out by high performance liquid chromatography with ultraviolet detection (HPLC-UV). In the DSPE-DLLME-SFO, the analytes were first extracted with acetone. The clean-up of the extract by DSPE was carried out by directly adding activated carbon sorbent into the extract solution, followed by shaking and filtration. Under the optimum conditions, the proposed method was sensitive and showed a good linearity within a range of 2–500 ng/g, with the correlation coefficients (r) varying from 0.9991 to 0.9996. The enrichment factors ranged from 127 to 138. The limit of detections (LODs) were in the range of 0.12–0.68 ng/g, and the relative standard deviations (RSDs) for 50 ng/g of each analytes in tomato samples were in the range of 3.25–6.26 % (n = 5). The proposed method was successfully applied for the extraction and determination of the mentioned analytes residues in tomato and cucumber samples, and satisfactory results were obtained.

In the present study, we investigated structural effects of various ionic liquids (ILs) on microalgal growth inhibition and microbial biodegradability. For this, we tested pyridinium- and pyrrolidinium-based ILs with various alkyl chain lengths and bromide anion, and compared the toxicological effects with log EC₅₀ values of imidazolium-based IL with the same alkyl chains and anion from literature. Comparing determined EC₅₀ values of cationic moieties with the same alkyl chain length, pyridinium-based ILs were found to be slightly more toxic towards the freshwater green alga, Pseudokirchneriella subcapitata, than a series of pyrrolidinium and imidazolium except to 1-octyl-3-methylimidazolium bromide. Concerning the biodegradation study of 12 ILs using the activated sludge microorganisms, the results showed that the pyridinium derivatives except to 1-propyl-3-methylpyridinium cation were degraded. Whereas in case of imidazolium- and pyrrolidinium-based compounds, only n-hexyl and n-octyl substituted cations were fully degraded but no significant biodegradation was observed for the short chains (three and four alkyl chains).

The effects of supplemental ultraviolet-B (s-UV-B; 3.6 kJ m⁻² day⁻¹ above ambient) radiation were investigated on plant metabolite profile, essential oil content and composition, and free radical scavenging capacities of methanolic extracts of Coleus forskohlii (an indigenous medicinal plant) grown under field conditions. Essential oil was isolated using hydrodistillation technique while alterations in metabolite profile and oil composition were determined via gas chromatography-mass spectroscopy (GC-MS). Leaf and root methanolic extracts were investigated via various in vitro assays for their DPPH radical-, superoxide radical-, hydrogen peroxide-, hydroxyl radical-, and nitric oxide radical scavenging activities, ferrous ion chelating activity, and reducing power. Phytochemical analysis revealed the presence of alkaloids, anthocyanins, coumarins, flavonoids, glycosides, phenols, saponins, steroids, tannins, and terpenoids. Oil content was found to be reduced (by ∼7 %) in supplemental UV-B (s-UV-B) treated plants; the composition of the plant extracts as well as essential oil was also considerably altered. Methanolic extracts from treated plant organs showed more potency as free radical scavengers (their EC₅₀ values being lower than their respective controls). Anomalies were observed in Fe²⁺ chelating activity for both leaves and roots. The present study concludes that s-UV-B adversely affects oil content in C. forskohlii and also alters the composition and contents of metabolites in both plant extracts and oil. The results also denote that s-UV-B treated plant organs might be more effective in safeguarding against oxidative stress, though further studies are required to authenticate these findings.

Separation between primary and secondary sludge treatment could be a valuable solution for sludge management. According to this approach, secondary sludge can be conveniently used in agriculture while primary sludge could be easily dried and incinerated. It follows that some concern may arise from incinerating primary sludge with respect to the current practice to incinerate mixed digested sludge. Incineration of primary and mixed digested municipal sludge was investigated with a lab-scale equipment in terms of emissions of products of incomplete combustion (PICs) during incineration failure modes. PICs can be grouped in three sub-categories, namely aliphatic hydrocarbons (alkanes and alkenes), compounds with a single aromatic ring, and polycyclic aromatic hydrocarbons (PAHs). After-burning temperature was the most important parameter to be controlled in order to minimize emissions of alkanes and alkenes. As for mono-aromatic compounds, benzene and toluene are the most thermally resistant compounds, and in some cases, an after-burning temperature of 1100 °C was not enough to get the complete destruction of benzene leading to a residual emission of 18 mg/kgₛₗᵤdgₑ. PAHs showed an opposite trend with respect to aliphatic and mono-aromatic hydrocarbons being the thermal failure mode the main responsible of PIC emissions. A proper oxygen concentration is more important than elevated temperature thus reflecting the high thermal stability of PAHs. Overall, obtained results, even though obtained under flameless conditions that are different from those of the industrial plants, demonstrated that separation of primary and secondary sludge does not pose any drawbacks or concern regarding primary sludge being disposed of by incineration even though it is more contaminated than mixed digested sludge in terms of organic pollutants.

The present study focused on the influence of temperature variation on the aging mechanisms of arsenic in soils. The results showed that higher temperature aggravated the decrease of more mobilizable fractions and the increase of less mobilizable or immobilizable fractions in soils over time. During the aging process, the redistribution of both carbonate-bound fraction and specifically sorbed and organic-bound fraction in soils occurred at various temperatures, and the higher temperature accelerated the redistribution of specifically sorbed and organic-bound fraction. The aging processes of arsenic in soils at different temperatures were characterized by several stages, and the aging processes were not complete within 180 days. Arsenic bioaccessibility in soils decreased significantly by the aging, and the decrease was intensified by the higher temperature. In terms of arsenic bioaccessibility, higher temperature accelerated the aging process of arsenic in soils remarkably.

Biogeochemical cycling of sulfur and selenium (Se) could play an important role in methylmercury (MeHg) dynamics in soil, while their potential effects on MeHg production in rice paddy soil are less understood. The main objective of this study was to explore the effects of sulfate and selenite on net MeHg production in contaminated rice paddy soil, characterized with massive MeHg production and thus MeHg accumulation in rice. A series of microcosm incubation experiments were conducted using a contaminated paddy soil amended with sulfate and/or selenite, in which sulfate-reducing bacteria were mainly responsible for MeHg production. Our results demonstrated that sulfate addition reduced solid and dissolved MeHg levels in soils by ≤18 and ≤25 %, respectively. Compared to sulfate, selenite was more effective in inhibiting net MeHg production, and the inhibitory effect depended largely on amended selenite doses. Moreover, sulfate input played a dual role in affecting Hg-Se interactions in soil, which could be explained by the dynamics of sulfate under anoxic conditions. Therefore, the effects of sulfate and selenium input should be carefully considered when assessing risk of Hg in anoxic environments (e.g., rice paddy field and wetland).

The dynamics of arsenic (As) and antimony (Sb) in wetland soil periodically submitted to agricultural pressure as well as the impact of soil enrichment with NO₃ ⁻ (50 mg L⁻¹) and PO₄ ³⁻ (20 mg L⁻¹) on As and Sb release were evaluated at both field and laboratory scales. The results showed that As and Sb exhibited different temporal behaviors, depending on the study scale. At field scale, As release (up to 93 μg L⁻¹) occurred under Fe-reducing conditions, whereas Sb release was favored under oxidizing conditions (up to 5 μg L⁻¹) and particularity when dissolved organic carbon (DOC) increased in soil pore water (up to 92.8 mg L⁻¹). At laboratory scale, As and Sb release was much higher under reducing conditions (up to 138 and 1 μg L⁻¹, respectively) compared to oxic conditions (up to 6 and 0.5 μg L⁻¹, respectively) and was enhanced by NO₃ ⁻ and PO₄ ³⁻ addition (increased by a factor of 2.3 for As and 1.6 for Sb). The higher release of As and Sb in the enriched reduced soil compared to the non-enriched soil was probably induced by the combined effect of PO₄ ³⁻ and HCO₃ ⁻ which compete for the same binding sites of soil surfaces. Modeling results using Visual Minteq were in accordance with experimental results regarding As but failed in simulating the effects of PO₄ ³⁻ and HCO₃ ⁻ on Sb release.