Eduarda Pereira

Silica coated magnetite particles for magnetic removal of Hg2+ from water

The magnetic removal of Hg(2+) from water has been assessed using silica coated magnetite particles. The magnetite particles were first prepared by hydrolysis of FeSO(4) and their surfaces were modified with amorphous silica shells that were then functionalized with organic moieties containing terminal dithiocarbamate groups. Under the experimental conditions used, the materials reported here displayed high efficiency for Hg(2+) uptake (74%) even at contaminant levels as low as 50 μg l(-1). Therefore these eco-nanomagnets show great potential for the removal of heavy metal ions of polluted water, via magnetic separation.

Structural and optical properties of InGaN/GaN layers close to the critical layer thickness

In this work, we investigate structural and optical properties of metalorganic chemical vapor deposition grown wurtzite InxGa1−xN/GaN epitaxial layers with thicknesses that are close to the critical layer thickness (CLT) for strain relaxation. CLT for InxGa1−xN/GaN structures was calculated as a function of the InN content, x, using the energy balance model proposed by People and Bean [Appl. Phys. Lett. 47, 322 (1985)]. Experimentally determined CLT are in good agreement with these calculations. The occurrence of discontinuous strain relaxation (DSR), when the CLT is exceeded, is revealed in the case of a 120 nm thick In0.19Ga0.89N layer by x-ray reciprocal space mapping of an asymmetrical reflection. The effect of DSR on the luminescence of this layer is clear: The luminescence spectrum shows two peaks centered at ∼2.50 and ∼2.67 eV, respectively. These two components of the luminescence of the sample originate in regions of different strain, as discriminated by depth-resolving cathodoluminescence spectr...

Accumulation of Mercury in Sea Bass from a Contaminated Lagoon (Ria de Aveiro, Portugal)

This work reports the distribution of total mercury (Hg) in Dicentrarchus labrax (sea bass) and in material collected in plankton nets from an inner basin contaminated with the effluent from a chlor-alkali plant, and in other locations of a coastal lagoon (Ria de Aveiro, Portugal). Mercury concentrations were higher in material collected in 200 than in 63 μm mesh net. Mercury in seston decreased pronouncedly with the distance to the industrial source (1.3–0.015 μg g−1 on a wet weight basis), and was higher at low tide than at high tide. This indicates that mercury is exported from the contaminated basin through the first levels of the estuarine chain. Mercury was analysed in muscle, liver, gills and stomach content of sea bass. Specimens captured in the contaminated basin showed higher accumulation of mercury: levels in muscle and liver of young specimens exceeded 1 μg g−1 and 2 μg g−1, respectively; gills and stomach content also presented higher concentrations. Mercury increased more drastically in liver than in muscle of specimens exposed to high contamination, changing the liver/muscle Hg ratio. Although juveniles exhibited higher concentrations in the contaminated basin than in other areas, there is an age effect on the accumulation of mercury in sea bass at the contaminated basin. Occasionally, intermediate concentrations were found in specimens captured in other areas of the lagoon.

Nanoscale materials and their use in water contaminants removal—a review

Water scarcity is being recognized as a present and future threat to human activity and as a consequence water purification technologies are gaining major attention worldwide. Nanotechnology has many successful applications in different fields but recently its application for water and wastewater treatment has emerged as a fast-developing, promising area. This review highlights the recent advances on the development of nanoscale materials and processes for treatment of surface water, groundwater and industrial wastewater that are contaminated by toxic metals, organic and inorganic compounds, bacteria and viruses. In addition, the toxic potential of engineered nanomaterials for human health and the environment will also be discussed.

Mercury contamination in the vicinity of a chlor-alkali plant and potential risks to local population.

A mercury-cell chlor-alkali plant operated in Estarreja (North-western Portugal) for 50 years causing widespread environmental contamination. Although production by this process ceased in 2002, mercury contamination from the plant remains significant. The main objective of this study was to investigate mercury impact on the nearby environment and potential risks to local population. To assess the level of contamination soil samples were collected from agricultural fields in the vicinity of the plant, extending the study by taking samples of the predominant vegetation suitable for animal and human consumption, water samples, and fish species from a nearby coastal lagoon, to gain a preliminary insight into the potential for contamination of the terrestrial and aquatic food web. To determine population exposure to mercury, hair samples were collected from local residents. Total mercury concentration in the 0-15 cm layer of soil was found to be highly variable, ranging between 0.010 and 91 mg kg(-1), although mercury contamination of soils was found to be restricted to a confined area. Lolium perenne roots contained between 0.0070 and 2.0 mg kg(-1), and there is evidence that root systems uptake mercury from the soil. Levels of mercury in the aerial parts of plants ranged between 0.018 and 0.98 mg kg(-1). It appears that plants with higher mercury concentration in soils and roots also display higher mercury concentration in leaves. Total mercury concentration in water samples ranged between 12 and 846 ng L(-1), all samples presenting concentrations below the maximum level allowable for drinking water defined in the Portuguese law (1.0 microg L(-1)). Mercury levels in fish samples were below the maximum limit defined in the Portuguese law (0.5 mg kg(-1)), ranging from 0.0040 to 0.24 mg kg(-1). Vegetables collected presented maximum mercury concentration of 0.17 mg kg(-1). In general, food is not contaminated and should not be responsible for major human exposure to the metal. Mercury determined in human hair samples (0.090-4.2 mg kg(-1); mean 1.5 mg kg(-1)) can be considered within normal limits, according to WHO guidelines suggesting that it is not affecting the local population. Despite being subject to decades of mercury emissions, nowadays this pollutant is only found in limited small areas and must not constitute a risk for human health, should these areas be restricted and monitored. Considering the present data, it appears that the population from Estarreja is currently not being affected by mercury levels that still remain in the environment.

Silver nanoparticles in soil–plant systems

Silver nanoparticles (AgNPs) have broad spectrum antimicrobial/biocidal properties against all classes of microorganisms and possess numerous distinctive physico-chemical properties compared to bulk Ag. Hence, AgNPs are among the most widely used engineered NPs in a wide range of consumer products and are expected to enter natural ecosystems including soil via diverse pathways. However, despite: (i) soil has been considered as a critical pathway for NPs environmental fate, (ii) plants (essential base component of all ecosystems) have been strongly recommended to be included for the development of a comprehensive toxicity profile for rapidly mounting NPs in varied environmental compartments, and (iii) the occurrence of an intricate relationship between “soil–plant systems” where any change in soil chemical/biological properties is bound to have impact on plant system, the knowledge about AgNPs in soils and investigations on AgNPs–plants interaction is still rare and in its rudimentary stage. To this end, the current paper: (a) overviews sources, status, fate, and chemistry of AgNPs in soils, AgNPs-impact on soil biota, (b) critically discusses terrestrial plant responses to AgNPs exposure, and (c) illustrates the knowledge-gaps in the current perspective. Based on the available literature critically appraised herein, a multidisciplinary integrated approach is strongly recommended for future research in the current direction aimed at unveiling the rapidly mounting AgNPs-fate, transformation, accumulation, and toxicity potential in “soil–plant systems,” and their cumulative impact on environmental and human health.

Lipids and proteins—major targets of oxidative modifications in abiotic stressed plants

Stress factors provoke enhanced production of reactive oxygen species (ROS) in plants. ROS that escape antioxidant-mediated scavenging/detoxification react with biomolecules such as cellular lipids and proteins and cause irreversible damage to the structure of these molecules, initiate their oxidation, and subsequently inactivate key cellular functions. The lipid- and protein-oxidation products are considered as the significant oxidative stress biomarkers in stressed plants. Also, there exists an abundance of information on the abiotic stress-mediated elevations in the generation of ROS, and the modulation of lipid and protein oxidation in abiotic stressed plants. However, the available literature reflects a wide information gap on the mechanisms underlying lipid- and protein-oxidation processes, major techniques for the determination of lipid- and protein-oxidation products, and on critical cross-talks among these aspects. Based on recent reports, this article (a) introduces ROS and highlights their relationship with abiotic stress-caused consequences in crop plants, (b) examines critically the various physiological/biochemical aspects of oxidative damage to lipids (membrane lipids) and proteins in stressed crop plants, (c) summarizes the principles of current technologies used to evaluate the extent of lipid and protein oxidation, (d) synthesizes major outcomes of studies on lipid and protein oxidation in plants under abiotic stress, and finally, (e) considers a brief cross-talk on the ROS-accrued lipid and protein oxidation, pointing to the aspects unexplored so far.

Extractability and mobility of mercury from agricultural soils surrounding industrial and mining contaminated areas

This study focussed on a comparison of the extractability of mercury in soils with two different contamination sources (a chlor-alkali plant and mining activities) and on the evaluation of the influence of specific soil properties on the behaviour of the contaminant. The method applied here did not target the identification of individual species, but instead provided information concerning the mobility of mercury species in soil. Mercury fractions were classified as mobile, semi-mobile and non-mobile. The fractionation study revealed that in all samples mercury was mainly present in the semi-mobile phase (between 63% and 97%). The highest mercury mobility (2.7 mg kg(-1)) was found in soils from the industrial area. Mining soils exhibited higher percentage of non-mobile mercury, up to 35%, due to their elevated sulfur content. Results of factor analysis indicate that the presence of mercury in the mobile phase could be related to manganese and aluminium soil contents. A positive relation between mercury in the semi-mobile fraction and the aluminium content was also observed. By contrary, organic matter and sulfur contents contributed to mercury retention in the soil matrix reducing the mobility of the metal. Despite known limitations of sequential extraction procedures, the methodology applied in this study for the fractionation of mercury in contaminated soil samples provided relevant information on mercurys relative mobility.

Accumulation, distribution and cellular partitioning of mercury in several halophytes of a contaminated salt marsh

This work evaluates the role of a plant community in mercury (Hg) stabilization and mobility in a contaminated Portuguese salt marsh. With this aim, the distribution of Hg in below and aboveground tissues, as well as the metal partitioning between cellular fractions (soluble and insoluble) in four different species (Triglochin maritima L., Juncus maritimus Lam, Sarcocornia perennis (Miller) A.J. Scott, and Halimione portulacoides (L.) Aellen) was assessed. Mercury accumulation, translocation and compartmentation between organs and cellular fractions were related to the plant species. Results showed that the degree of Hg absorption and retention was influenced both by environmental parameters and metal translocation/partitioning strategies. Different plant species presented different allocation patterns, with marked differences between monocots (T. maritima and J. maritimus) and dicots (S. perennis, H. portulacoides). Overall, the two monocots, in particular T. maritima showed higher Hg retention in the belowground organs whereas the dicots, particularly S. perennis presented a more pronounced translocation to the aboveground tissues. Considering cellular Hg partitioning, all species showed a higher Hg binding to cell walls and membranes rather than in the soluble fractions. This strategy can be related to the high degree of tolerance observed in the studied species. These results indicate that the composition of salt marsh plant communities can be very important in dictating the Hg mobility within the marsh ecosystem and in the rest of the aquatic system as well as providing important insights to future phytoremediation approaches in Hg contaminated salt marshes.

Glutathione and proline can coordinately make plants withstand the joint attack of metal(loid) and salinity stresses

Agricultural soils in the vicinity of extensive anthropogenic activities may exhibit salinity together with high levels of metals/metalloids (hereafter termed as “metal/s”) as co-stressors. Elevated concentrations of metals (such as As, Cd, Cr, Hg, Ni, and Pb) may affect photosynthetic apparatus, electron transport chain and chlorophyll biosynthesis, induce cellular damage, impair cellular redox homeostasis, and finally cause cellular metabolic arrest (Anjum et al., 2010, 2012a; Gill and Tuteja, 2010; Talukdar, 2012; Talukdar and Talukdar, 2014). Saline soil conditions, on the other hand, can cause osmotic stress that in turn can inhibit cell expansion and cell division, impact stomatal closure, induce cell turgor via lowering water potential, and alter the normal homeostasis of cells (Miller et al., 2010). However, the generation of osmotic stress through impaired plant water relations, and oxidative stress caused by uncontrolled generation of varied reactive oxygen species (ROS; such as such as -OH, H2O2, O−2) are common in plants exposed to high levels of salinity and/or metals (Benavides et al., 2005; Anjum et al., 2010, 2012a). Diverse plant taxa have been reported to adapt metabolically to salinity and exposure to metals by enhancing synthesis of sulfur (S)-rich peptides (such as glutathione, GSH) and low-molecular-weight nitrogenous and proteogenic amino acids/osmolytes (such as proline, Pro) (Khan et al., 2009; Anjum et al., 2010, 2012a; Talukdar, 2012; Kishor and Sreenivasulu, 2014; Talukdar and Talukdar, 2014). Nevertheless, both GSH and Pro share L-glutamate as a common biosynthesis precursor (Moat et al., 2003) (Figure ​(Figure1).1). However, very little or no effort has been made so far to dissect the intricacies of potential metabolic interrelationships between the GSH and Pro induction either under salinity/osmotic or metal stress conditions. Figure 1 Schematic representation of the points of interrelationships in the major metabolic pathway of sulfur-rich peptide—glutathione (GSH) and nitrogenous and proteogenic amino acid—proline (Pro). Therefore, we discuss and interpret through this note the facts related with the mainstays (chemistry, biosynthesis, compartmentalization, significance) commonly and potentially shared by these two enigmatic compounds (GSH and Pro) in plants. The outcome of the present endeavor can be useful in designing future research aimed at sustainably alleviating isolated and/or joint impact of metal and salinity stresses in crop plants through exploiting the GSH and Pro metabolism.