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A fast and cost-effective procedure based on Inductively Coupled Plasma - Mass Spectrometry (ICP-MS) for the selective determination of methylmercury (MeHg) is proposed and validated for fish tissue analysis. Selectivity for MeHg is achieved by simply inserting a strong anion exchange resin to block inorganic mercury as negatively charged chloride species, leaving MeHg unretained. The procedure features a 15 min extraction time followed by a 100 s analysis time achieving a limit of detection of 1.6 μg kg -1 on solid samples. The effect of the solution composition and inorganic mercury concentration were extensively studied to fully assess the selectivity of the procedure: Hg(II):MeHg ratios up to 50 are tolerated and cause systematic errors lower than 15%. The entire procedure was successfully validated by standard reference material from the marine food web, namely fish muscle and liver plus zooplankton. The method was finally applied to the detection of MeHg in the marine trophic web of Djibouti (Gulf of Aden): a trophic magnification factor of 13.5 proved the high risk associated with the biomagnification of methylmercury., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Thiols are compounds of paramount importance in the cellular metabolism due to their double detoxifying role as radical scavengers and trace metal ligands. However, we have scarce information about their extracellular cycling as limited data are available about their concentration, stability and speciation in the aquatic medium. In natural waters, they form part of the pool of reduced sulfur substance (RSS) whose presence has been documented by voltammetric and chromatographic methods. Traditional use of cathodic stripping voltammetry (CSV) for the analysis of RSS could only give an overall concentration due to the coalescence of their CSV peaks. Recently, it has been shown that the use of multiple deposition potentials could take voltammetry of RSS to a higher level, permitting the identification and quantification of the mixtures of RSS despite showing as a single coalescent peak. Here, due to its similarity with classical pseudopolarography, we propose to rename this analytical strategy as cathodic pseudopolarography (CP) and we present for the first time its use for the analysis of mixes of low molecular weight thiols (LMWT) at the nanomolar level. Despite limitations caused by the identical behavior of some LMWT, the CP allowed to isolate the contribution of cysteine and cystine from a coalescent signal in LMWT mixtures. Sample handling with clean protocols allowed the direct determination of the cystine:cysteine ratio without sample modification. Finally, we show the application of CP to identify LMWT in seawater samples extracted from benthic chambers and suggest future applications in other areas of environmental electroanalysis., (Copyright © 2014 Elsevier B.V. All rights reserved.)

The analytical performances of Competitive Ligand Equilibration with Cathodic Stripping Voltammetric detection of the labile fraction (CLE-CSV) were assessed. This speciation method enables the concentration of natural ligand(s) and their conditional stability constants for the complexation of the investigated metal to be determined through thermodynamic considerations. Literature data were discussed and general trends in the precision of the determined parameters identified: ligand concentrations were affected, on average, by a 10% relative percentage standard deviation (RSD%), whereas conditional stability constants showed much lower precision, with an average RSD% of 50%. New experimental data were collected to obtain a complete assessment of accuracy and precision attainable for the determination of strong ligands at the ultra trace level, enabling the whole protocol to be evaluated. Firstly, the side reaction coefficient alpha for the formation of the complex between the added ligand and the investigated metal (alpha(CuL)) was determined. The method was subsequently applied to the analysis of solution containing ligand at trace levels (5-50 nM) with known complexing characteristics. Copper was used as the model metal ion and ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA) as the model ligands. Results evidenced that the CLE-CSV protocol is not affected by systematic errors in the determination of both ligand concentration and the conditional stability constants. Good precision is obtained for ligand concentrations, with an average relative standard deviation (RSD%) of 5%; an average RSD% of 23% was calculated for the conditional stability constants. Including the contribution of the uncertainty in the value of alpha(CuL) in the evaluation of the uncertainty in the latter parameter increased the RSD% up to 40%. The CLE-CSV protocol was subsequently applied to the detection of strong ligands in water samples collected in Antarctica: precision was shown to be comparable with literature data., (2010 Elsevier B.V. All rights reserved.)

Cultural heritage represents a bridge between the contemporary society and the past populations, and a strong collaboration between archaeologists, art historians and analysts may lead to the decryption of the information hidden in an ancient object. Quantitative elemental compositional data play a key role in solving questions concerning dating, provenance, technology, use and the relationship of ancient cultures with the environment. Nevertheless, the scientific investigation of an artifact should be carried out complying with some important constraints: above all the analyses should be as little destructive as possible and performed directly on the object to preserve its integrity. Laser ablation sampling coupled to inductively coupled plasma-mass spectrometry (LA-ICP-MS) fulfils these requirements exhibiting comparably strong analytical performance in trace element determination. This review intends to show through the applications found in the literature how valuable is the contribution of LA-ICP-MS in the investigation of ancient materials such as obsidian, glass, pottery, human remains, written heritage, metal objects and miscellaneous stone materials. The main issues related to cultural heritage investigation are introduced, followed by a brief description of the features of this technique. An overview of the exploitation of LA-ICP-MS is then presented. Finally, advantages and drawbacks of this technique are critically discussed: the fit for purpose and prospects of the use of LA-ICP-MS are presented.