The high consumption of crabs (Ucides cordatus) stimulated interest in the present study on the northern coast of Brazil, which encompasses a preserved area of mangrove forest. The objective was to describe and quantify the transfer of metals from the muddy sediments to the leaves of the Rhizophora mangle, and thence the crabs and humans. The samples were collected along two transects, while samples of hair were obtained from local habitants. The pH, interstitial salinity, Eh (mV) were measured, the granulometry and mineralogical and multi-element chemical analyses were run, and the organic material determined. The sediments are silty-clayey, composed of quartz, kaolinite, iron oxides, and illite, as well as smaller portions of smectite, pyrite, halite, and high levels of SiO2 (56.5 %), Al2O3 (18.5 %), and Fe2O3 (7 %). The elements Zn, Sr, As, and Zr are concentrated in the leaves, while the bioaccumulation of Zn, Se, Sr, and As was recorded in the crabs, of which, Se is the most concentrated in the tissue of the muscles and the hepatopancreas. The concentrations of nutrient and toxic elements were similar in all age groups (hair samples), with only Hg presenting an increasing concentration between infants and adults. The highest rates of transfer were recorded for the elements Zn and Se in the crabs and Hg in leaves and hair. The accumulation of metals in the leaves and crabs reflects the chemical composition of the sediments and low rates of sediment-vegetation-crab transfer, with the exception of Hg, which accumulated in the hair.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10653-013-9509-zDOI Listing

Publication Analysis

Top Keywords

transfer metals
8
crabs
5
accumulation transfer
4
metals sediment-vegetation-crab-human
4
sediment-vegetation-crab-human food
4
food chain
4
chain coastal
4
coastal zone
4
zone northern
4
northern brazilian
4

Similar Publications

Two π-radical complexes containing bisazo-aromatic-centered radical anion (1•-) were synthesized through in-situ electron transfer from metal-to-ligand using [IrI] and 2-(2-Pyridylazo)azobenzene (1) in inert hydrocarbon solvent. These are characterized as diradical [IrIII(1•-)2]+[2]+ and monoradical [IrIII(1•-)Cl2(PPh3)] 3. In contrast, a rare metal-mediated hydrolytic cleavage of the C(sp2)-N bond occurred in protic solvent resulting in quaternary radical complex [IrIII(1•-)(1')(PPh3)]+(4)+.

View Article and Find Full Text PDF

The prominence of binuclear catalysts underlines the need for the design and development of diverse bifunctional ligand frameworks that exhibit tunable electronic and structural properties. Such strategies enable metal-metal and ligand-metal cooperation towards catalytic applications, improve catalytic activity, and are essential for advancing multi-electron transfers for catalytic application. Hereby, we present the synthesis, crystal structure, and photocatalytic properties of a binuclear Ni(II) complex, [Ni2(1,10-phenanthroline)2(2-sulfidophenolate)2] (1), which crystallizes in the centrosymmetric triclinic system (P-1) showing extensive intra- and inter- non-coordinated interactions.

View Article and Find Full Text PDF

Direct photochemical conversion of CO2 into a single carbon-based product currently represents one of the major issues in the catalysis of the CO2 reduction reaction (CO2RR). In this work, we demonstrate that the combination of an organic photosensitizer with a heptacoordinated iron(II) complex allows to attain a noble-metal-free photochemical system capable of efficient and selective conversion of CO2 into CO upon light irradiation in the presence of N,N-diisopropylethylamine (DIPEA) and 2,2,2-trifluoroethanol (TFE) as the electron and proton donor, respectively, with unprecedented performances (ΦCO up to 36%, TONCO > 1000, selectivity > 99%). As shown by transient absorption spectroscopy studies, this can be achieved thanks to the fast rates associated with the electron transfer from the photogenerated reduced dye to the catalyst, which protect the dye from parallel degradation pathways ensuring its stability along the photochemical reaction.

View Article and Find Full Text PDF

While synthesizing circular polymers with telechelic polyolefin building blocks recently emerged as a promising strategy for addressing conventional polyethylenes' sustainability challenges, the lack of telechelic PP (PP) with sufficient difunctional purity for polycondensation has been limiting the development of circular polypropylenes with PP-like structures and properties. Here we described a combined approach of coordinative chain transfer polymerization and transition-metal-catalyzed quenching reaction with various acyl chlorides, affording PPs with a high difunctional ratio (up to ∼99%) and broad end functional group scope. The steric effect of polymeryl-Zn species and the role of Pd catalyst were revealed by DFT.

View Article and Find Full Text PDF

[FeFe] hydrogenases make up a structurally diverse family of metalloenzymes that catalyze proton/dihydrogen interconversion. They can be classified into phylogenetically distinct groups denoted A-G, which differ in structure and reactivity. Prototypical Group A hydrogenases have high turnover rates and remarkable energy efficiency.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!