Nickel tolerance and toxicity mechanisms in the halophyte Sesuvium portulacastrum L. as revealed by Ni localization and ligand environment studies.

Halophytes are able to tolerate relatively high concentrations of hazardous metals in a growing substrate, what makes them suitable candidates for phytoremediation of metal-contaminated soils. In this work, we aimed to study the physiological responses of the halophyte Sesuvium portulacastrum L. to Ni, with main focus on Ni localization, compartmentation and ligand environment, to decipher Ni tolerance and toxicity mechanisms. Seedlings were grown in hydroponic nutrient solution containing 0, 25, 50 and 100 µM Ni as NiCl2 for 3 weeks. Ni localization in leaves was assessed by micro-proton-induced X-ray emission (micro-PIXE). Ni ligand environment was studied by Ni K-edge X-ray absorption near edge structure (XANES). In addition, Ni-soluble, weakly bound/exchangeable and insoluble leaf tissue fractions were determined by sequential extraction. Results show that S. portulacastrum is able to tolerate up to ~ 500 µg g-1 dry weight (DW) of Ni in the shoots without significant growth reduction. At higher Ni concentrations (> 50 µM Ni in nutrient solution), chloroses were observed due to the accumulation of Ni in photosynthetically active chlorenchyma as revealed by micro-PIXE. Water storage tissue represented the main pool for Ni storage. Incorporation of Ni into Ca-oxalate crystals was also observed in some specimens, conferring tolerance to high leaf Ni concentrations. The majority of Ni (> 70%) was found in soluble tissue fraction. Ni K XANES revealed Ni bound mainly to O- (55%) and N-ligands (45%). Ni toxicity at higher Ni levels was associated with Ni binding to amino groups of proteins in cytosol of chlorenchyma and increased level of lipid peroxidation. Proline levels also increased at high Ni exposures and were associated with Ni-induced oxidative stress and alteration of water regime.

Uptake, translocation and ligand of silver in Lactuca sativa exposed to silver nanoparticles of different size, coatings and concentration.

The broad use of silver nanoparticles (AgNPs) in daily life products enhances their possibilities to reach the environment. Therefore, it is important to understand the uptake, translocation and biotransformation in plants and the toxicological impacts derived from these biological processes. In this work, Lactuca sativa (lettuce) was exposed during 9 days to different coated (citrate, polyvinylpyrrolidone, polyethylene glycol) and sized (60, 75, 100 nm) AgNPs at different concentrations (1, 3, 5, 7, 10, 15 mg L-1). Total silver measurements in lettuce roots indicated that accumulation of AgNPs is influenced by size and concentration, but not by nanoparticle coating. On the other hand, nanosilver translocation to shoots was more pronounced for neutral charged and large sized NPs at higher NP concentrations. Single particle inductively coupled plasma mass spectrometry analysis, after an enzymatic digestion of lettuce tissues indicated the dissolution of some NPs. Ag K-edge X-ray absorption spectroscopy analysis corroborated the AgNPs dissolution due to the presence of less Ag-Ag bonds and appearance of Ag-O and/or Ag-S bonds in lettuce roots. Toxicological effects on lettuces were observed after exposure to nanosilver, especially for transpiration and stomatal conductance. These findings indicated that AgNPs can enter to edible plants, exerting toxicological effects on them.

Localization, ligand environment, bioavailability and toxicity of mercury in Boletus spp. and Scutiger pes-caprae mushrooms.

This study provides information on mercury (Hg) localization, speciation and ligand environment in edible mushrooms: Boletus edulis, B. aereus and Scutiger pes-caprae collected at non-polluted and Hg polluted sites, by LA-ICP-MS, SR-µ-XRF and Hg L3-edge XANES and EXAFS. Mushrooms (especially young ones) collected at Hg polluted sites can contain more than 100 µg Hg g-1 of dry mass. Imaging of the element distribution shows that Hg accumulates mainly in the spore-forming part (hymenium) of the cap. Removal of hymenium before consumption can eliminate more than 50% of accumulated Hg. Mercury is mainly coordinated to di-thiols (43-82%), followed by di-selenols (13-35%) and tetra-thiols (12-20%). Mercury bioavailability, as determined by feeding the mushrooms to Spanish slugs (known metal bioindicators owing to accumulation of metals in their digestive gland), ranged from 4% (S. pes-caprae) to 30% (B. aereus), and decreased with increasing selenium (Se) levels in the mushrooms. Elevated Hg levels in mushrooms fed to the slugs induced toxic effects, but these effects were counteracted with increasing Se concentrations in the mushrooms, pointing to a protective role of Se against Hg toxicity through HgSe complexation. Nevertheless, consumption of the studied mushroom species from Hg polluted sites should be avoided.

An extracellular polymeric substance quickly chelates mercury(II) with N-heterocyclic groups.

A strain of Klebsiella oxytoca DSM 29614 is grown on sodium citrate in the presence of 50 mg l-1 of Hg as Hg(NO3)2. During growth, the strain produces an extracellular polymeric substance (EPS), constituted by a mixture of proteins and a specific exopolysaccharide. The protein components, derived from the outer membrane of cells, are co-extracted with the extracellular exopolysaccharide using ethanol. The extracted EPS contains 7.5% of Hg (total amount). This indicates that EPS is an excellent material for the biosorption of Hg2+, through chemical complexation with the EPS components. The binding capacity of these species towards Hg2+ is studied by cyclic voltammetry, and Hg L3-edge XANES and EXAFS spectroscopy. The results found indicate that Hg2+ is mainly bound to the nitrogen of the imidazole ring or other N-heterocycle compounds. The hydroxyl moities of sugars and/or the carboxyl groups of two glucuronic acids in the polysaccharide can also play an important role in sequestring Hg2+ ions. However, N-heterocyclic groups of proteins bind Hg2+ faster than hydroxyl and carboxyl groups of the polysaccharide.

Atomic absorption background of Ba in EXAFS analysis of BaFe(12)O(19) nanoparticles.

The approximate barium X-ray atomic absorption in the energy region of L-edges is reconstructed from the absorption spectrum of an aqueous solution of BaCl(2). The result is corroborated by comparison with pure atomic absorption spectra of neighbour elements Xe and Cs. The application of the atomic absorption signal as a proper EXAFS background is demonstrated and discussed in the analysis of Ba hexaferrite nanoparticles with a very weak structural signal. The essential gain is found in the decrease of uncertainty intervals of structural parameters and their correlations. A simple analytical model of the absorption background for the practical EXAFS analysis is demonstrated.

One-dimensional simulation of thin liquid-film-edge retraction.

The phenomenon of liquid film retraction, occurring in bursting bubbles, is investigated in the simplest case of a semi-infinite sheet of inviscid liquid. Discretized equations of motion are solved on a staggered grid, with the boundary condition adapted to handle movement and breakup of liquid domain. Two independent approaches show a perfect agreement. The calculation shows a periodic pinchoff of small droplets, in contrast to the published results on viscid fluids where the liquid accumulates at the rim. A quantitative analysis of simulated liquid profiles shows that the characteristic parameters are very close to the theoretical predictions obtained from energy conservation and laws of motion.

Metal-ion environment in solid Mn(II), Co(II) and Ni(II) hyaluronates.

Amorphous powders and films of some metal hyaluronate complexes of general composition (C14H20O11N)2 x xH2O (M = Mn2+, Ni2+ and Co2+) have been prepared at pH 5.5-6.0. The coordination geometry around the metal ions has been analyzed by EXAFS (extended X-ray absorption fine structure) and FTIR spectroscopy. Mn2+, Ni2+, and Co2+ ions are coordinated to carboxylate oxygen atoms and water molecules. The process of local geometry formation round the metal ions is sensitive to sample preparation.

Compressed octahedral coordination in chain compounds containing divalent copper: structure and magnetic properties of CuFAsF6 and CsCuAlF6.

Crystal structures and magnetic investigations of CuFAsF6 and CsCuAlF6 are reported. Together with KCuAlF6, these appear to be the only examples of Jahn-Teller pure Cu(II) compounds containing only one type of ligand that exhibits a compressed octahedral coordination geometry. The Rietveld method has been used for refining the CsCuAlF6 structure based on neutron powder diffraction data at 4 K. The compound crystallizes in space group Pnma (no. 62) with a=7.055(1), b=7.112(1), c=10.153(1) A and Z=4 at 4 K. The structure is built from infinite [CuF5]n(3n-) chains of [CuF6]4- octahedra running along the [1 0 0] direction and (AlF6)3- octahedra connected by corners in the trans position, thus giving rise to chains oriented along the [0 1 0] direction. Single crystals of CuFAsF6 were prepared under solvothermal conditions in AsF5 above its critical temperature. The structure was determined from single-crystal data. CuFAsF6 crystallises in the orthorhombic space group Imma (No. 74) with a=10.732(5), b=6.941(3), c=6.814(3) A and Z=4 at 200 K. The structure can also be described in terms of one-dimensional infinite [CuF5]n(3n-) chains of tilted [CuF6](4-) octahedra linked by trans-vertices running along the b axis. The [CuF5]n(3n-) chains are connected through [AsF6]- units sharing joint vertices. The compressed octahedral coordination of CuII atoms in CuFAsF6 and CsCuAlF6 compounds at room temperature is confirmed by Cu K-edge EXAFS (extended x-ray absorption fine structure) analysis. For both compounds strong antiferromagnetic interactions within the [CuF5]n(3n-) chains were observed (theta(p)=-290+/-10 K and theta(p)=-390+/-10 K for CuFAsF6 and CsCuAlF6, respectively). The peculiar magnetic behaviour of chain compounds containing divalent copper at low temperature could be related to uncompensated magnetic moments in the one-dimensional network.