We studied the effects of N deposition (0, 10, 20 and 50 kg N ha⁻¹ year⁻¹) on cover and physiology of Pleurochaete squarrosa, a terricolous moss from semiarid Mediterranean ecosystems. We also investigated the effects of N fertilization under competition with vascular plants or under water stress. Under greenhouse conditions, vascular plant competition reduced moss cover, and there was a significant interaction between N and competition. Water stress reduced moss cover under high and low competition conditions. Nitrogen fertilization increased moss cover irrespectively of the N dose supplied at low competition conditions. Under field conditions, N deposition affected moss physiology but not cover. Most of the physiological variables analyzed responded to N deposition, although the response of some of them was saturated with only 10 kg N ha⁻¹ year⁻¹ over the background (nitrate reductase; phosphomonoesterase; tissue N and K⁺). The response of indicators such as chlorophyll a and lutein contents did not show any evidence of saturation, which probably makes them the best candidates in monitoring programs. Based on the data provided, the applicability of the phosphomonoesterase can also be considered. In addition, the importance of taking into account the existence of superimposed environmental gradients (such as those in soil mineral N content) interacting with the response of P. squarrosa to predict impacts of N deposition has been demonstrated. Therefore, detailed soil surveys and integrative physiological evaluations will be required to produce a significantly better picture of the effects of N deposition on Mediterranean ecosystems along extant N deposition gradients.

The connection between hydrocarbon biodegradation and surface-active substance production has attracted great interest in recent years. Pseudomonas fluorescens PT, isolated from a biotrickling filter, was not only able to degrade α-pinene but also to use it as a carbon source to produce a surface-active substance. Response surface methodology analysis showed that the optimal medium composition was K⁺, 69.8; Mn²⁺, 65.1; and NH₄ ⁺, 482.5 mg L⁻¹, at which the surface tension of the medium was reduced to 40.7 mN m⁻¹ after 36 h. Based on compositional analysis and information on α-pinene metabolism, the purified compound was identified as perilla acid. The surface-active properties of the purified compound were more stable than those of a synthetic surfactant, and it had lower ecological toxicity to Chlorella vulgaris. The naphthalene solubility and mass transfer of α-pinene were enhanced almost twofold by the surface-active substance (at its critical micelle concentration). The results suggested that the PT strain may be promising for generating surface-active substances with improved physiochemical properties for a wide range of applications in environmental remediation.

A titanium mesostructure was synthesized, and its surface was subsequently modified by adsorbing phosphate. The modified structure was later investigated for photocatalytic activity against the organic contaminant 2,4,6-trichlorophenol with UV irradiation. This research found that the effects of calcination temperature, phosphate concentration for surface modification, amine grafting as a function, and initial pH condition contributed to the enhanced degradation rate of the chlorinated phenol. The results of this study demonstrated an increased photocatalytic degradation rate for 2,4,6-trichlorophenol under the following conditions: (1) titanium mesostructure calcined at 600 °C; (2) adsorption from a 100 mg/L as PO₄-P solution; (3) an amine-functionalized titanium mesostructure synthesized with the molar ration of 1:0.5 (titanium mesostructure: amine group); and (4) acidic condition (pH 4) to promote efficient adsorption of phosphate. This research indicates that phosphate removal and enhanced degradation of organic contaminants could be carried out simultaneously in sewage treatment.

There are growing concerns about the increasing trends of emerging micropollutants in the environment due to their potential negative impacts on natural ecosystems and humans. This has attracted attention from both governmental and non-governmental organisations worldwide. Pharmaceuticals, personal care products, and endocrine disruptors are continuously being released consciously or unconsciously into water sources due to poor regulatory frameworks especially in the developing countries. The effects of these contaminants are poorly known. They are not easily biodegradable and have become an environmental nuisance and public health issue. This has heightened the risk of exposure to their deleterious effects in such countries where the majority of the population are still struggling to have access to good quality drinking water supplies and better sanitation. With the rising fear of short- and long-term impacts of the ever-increasing number of persistent recalcitrant organic compounds accumulating in the environment, their removal is gradually becoming an issue to the water treatment industry. Hence, there is a need to develop functional techniques for the management of water contaminated by these emerging contaminants so as to increase the availability and access to safe and good-quality drinking water. We conducted a narrative review on these emerging micropollutants and examined their various documented sources, effects, as well as recent techniques for their effective removal. This becomes necessary due to the increasing occurrence of these pollutants in the aquatic and terrestrial environment. These levels are expected to further increase in the coming years as a consequence of the ever-increasing population density which undoubtedly characterizes developing economies. Our findings show that the present reported treatment techniques in the literature such as biological oxidation/biodegradation, coagulation/flocculation, ozonation, electrodialysis, reverse osmosis, sedimentation, filtration, and activated carbon were not designed for removal of these newly identified contaminants, and as such, the techniques are not sufficient and unable to completely degrade the compounds. We therefore recommended the need for concerted efforts to develop better techniques, especially combined advanced oxidative methods to address the shortcomings of and growing challenge to current practices.

Sediment cores were collected from ten eutrophic lakes in South Dakota to determine the lateral extent of sediment-bound mercury (Hg) concentrations and to assess the relationship between watershed and land use characteristics with lake Hg fish tissue consumption advisory (>1.0 mg Hg/kg fish tissue) status. Advisory lakes were characterized as having higher sediment Hg and organic matter and lower total sulfur content compared to non-advisory lakes, and results highlight the importance of sulfide and organic carbon availability associated with potential Hg methylation biogeochemical processes. Advisory lakes generally had higher percentage of areal development and grasslands, higher catchment to lake area, and lower percentage of wetlands compared to non-advisory lakes. These results signify the importance of minimizing watershed sediment transport and associated organic carbon loading as effective Hg fish tissue lake management strategies.

The performance of the Purolite A847 weak basic anion exchanger in the simultaneous removal of the azo dye Lanasyn Navy M-DNL (LNCr) and the phthalocyanine dye Acid Blue 249 (CuPc) from acidic aqueous solutions was studied under dynamic conditions. The comparison of FTIR spectra of unloaded and dye-loaded anion exchangers made it possible to consider suitable sorption mechanisms. The results of dynamic experiments revealed that anion exchanger had a greater dynamic sorption capacity with a longer breakthrough time and a shorter length of mass transfer zone when both dyes LNCr and CuPc were removed from the one-component solution as compared to those of their mixture. Models of Wolborska and Juang were found to be suitable to predict the character of breakthrough curves and to determine the characteristic parameters of the Purolite A847 column useful for process design: the mass transfer coefficient β (1/min) and time at the break point τ (minutes). The result would be useful in the design of wastewater treatment plants for removal of azo and phthalocyanine dyes from aqueous solutions and water recycling.

Tobacco (Nicotiana tabacum L.) stem ash (TSA) was evaluated as an adsorbent for removal of methylene blue (MB) from aqueous solution by batch adsorption method. MB adsorption increased with increase in contact time, initial solution pH, and adsorbent dose. Contact time for adsorption equilibrium was 180 min. The MB adsorption per unit mass of adsorbent (in milligram per gram) increased with the increasing initial dye concentration. Adsorption of MB onto TSA followed the pseudo-second-order kinetic model with a rate constant (k ₂) of 0.017 g mg⁻¹ min⁻¹. The mechanism of adsorption was described with intra-particle diffusion model. It was found that the intra-particle diffusion was not a sole rate-controlling step. Equilibrium adsorption was investigated by the Freundlich, Langmuir, Temkin, and Jovanoic isotherms. On the basis of coefficient of determination, the order of isotherm fit was Langmuir (R ² = 0.974) > Freundlich (R ² = 0.957) = Temkin (R ² = 0.957) > Jovanoic (R ² = 0.764) isotherm. The maximum monolayer adsorption capacity of TSA was 35.7 mg g⁻¹. The dimensionless separation factor (R L) was low (0.137), indicating favorable adsorption of MB onto TSA. The results clearly demonstrate the potential of TSA as a low-cost and an easily available adsorbent for sequestering MB from wastewater.

The effects of irrigation with meat processing factory effluent (MPE) in combination with additions of paunch to three arable sites and one pasture site on soil chemical and microbial properties were investigated in fields surrounding a beef meat processing factory. A pasture site that had only received MPE was also sampled along with adjoining arable and pasture control fields that had never received MPE or paunch. Additions of MPE/paunch caused increases in electrical conductivity, exchangeable Na and K, exchangeable sodium percentage (ESP), extractable P, organic C, total N, microbial biomass C, and metabolic quotient and decreases in exchangeable Ca and Mg, pH, and the proportion of organic C present as microbial biomass. The structure and diversity of bacterial and fungal communities was measured by polymerase chain reaction–denaturing gradient gel electrophoresis of 16S rDNA and internal transcribed spacer-RNA amplicons respectively and catabolic diversity by analysis of catabolic response profiles to 25 substrates. Principal component analysis of catabolic response profiles clearly separated control from MPE/paunch-treated sites, and this was associated with greater catabolic responses to the carboxylic acids α-ketoglutaric, α-ketobutyric, L-ascorbic, and citric acid in the control. At the arable sites, application of MPE and paunch caused increases in bacterial, fungal, and catabolic diversity. Canonical correspondence analysis of the relationship between catabolic, bacterial, and fungal fingerprints and soil properties indicated that the main soil variables separating MPE/paunch treatments from controls were the higher organic C, ESP, and extractable P and a lower pH, exchangeable Ca, and Mg. It was concluded that, although long-term MPE/paunch additions induce soil salinity, sodicity, and acidity, in general, they cause an increase in the size, activity, and structural and functional diversity of in the soil microbial community.

It was found that some of the medicinal plants accumulate increased amounts of toxic elements like Cd or Pb. Less is known about the accumulation of other hazardous elements like arsenic (As) and antimony (Sb) in these species. The present paper investigated selected medicinal plants naturally growing on old mining sites in Slovakia, Central Europe, contaminated by As and Sb. Both these elements are nonessential for plants and, in higher level, might be phytotoxic. The soil concentration of As and Sb at three different localities extensively used for mining of Sb ores in former times highly exceed values characteristic for noncontaminated substrates and ranged between 146 and 540 mg kg⁻¹ for As and 525 and 4,463 mg kg⁻¹ for Sb. Extraction experiments of soils show differences between As and Sb leaching, as the highest amount of mobile As was released in acetic acid while Sb was predominantly released in distilled water. In total, seven different plant species were investigated (Fragaria vesca, Taraxacum officinale, Tussilago farfara, Plantago major, Veronica officinalis, Plantago media, and Primula elatior), and the concentration of investigated elements in shoot ranged between 1 and 519 mg kg⁻¹ for As and 10 and 920 mg kg⁻¹ for Sb. Differences in the bioaccumulation of As and Sb as well as in the translocation of these elements from root to shoot within the same species growing on different localities have been found. This indicate that efficiency of As and Sb uptake might vary between individual plants of the same species on different sites. Increased bioaccumulation of As and Sb in biomass of investigated plants might be dangerous for human when used for traditional medicinal purposes.

The present study consisted of an in vitro experiment based on columns to restore a soil affected by the tsunami of 27 February 2010 that struck the Coliumo District, Bio-Bio region, Chile. The agricultural productivity of many coastal lands was severely affected, rendering them unfit for crop production. Composite soil samples were taken at 0 to 20 cm soil depth in Coliumo, Bio-Bio region. The initial physical and chemical analysis showed textural changes, low pH, high levels of electrical conductivity (EC), sodium (Na⁺), and sulfate (SO₄²⁻), whereas bioassay tests showed severe toxicity for lettuce (Lactuca sativa L.) seeds. Germination index (GI), length of hypocotyl (LH), and length of radicle (LR) were used as indicators in the bioassay tests. Two different treatments were used: T1 = soil amended with 7.7 t ha⁻¹ of limestone (CaCO₃) and T2 = soil amended with 7.7 t ha⁻¹ of gypsum (CaSO₄). A control treatment (T0) with unamended soil was included. Each treatment received a total of 1,100 mm of clean water (4 water loads, 275 mm each), which was equivalent to the mean annual precipitation of the area studied. The T2 treatment produced a significant decrease in the concentration of Na⁺ (8.27 to 0.16 meq L⁻¹), decreased EC (1.58 to 0.03 dS m⁻¹), and increased pH from 4.83 to 6.27 in the soil under study. Leaching of Na⁺ and SO₄²⁻ with successive water loads was effective in the soil. The bioindicators as GI, LH and LR revealed that T2 was more effective than T1 and control in removing Na and SO₄ analytes from the soil matrix. The CaSO₄ amendment showed good potential for seed development, but further research on plant growth to maturity is required to determine yield parameters in the affected area.