Mireia Irazola

Comprehensive two-dimensional gas chromatography to characterize hydrocarbon mixtures in lithic materials

The analysis of organic biomarkers in chert samples offers key information about the environmental conditions in which these samples were formed, and this information can be used to track the lithic materials of many archaeological artifacts. Since the content of the organic fraction is very low and the complexity of the organic extracts is quite high, we have optimized the GC×GC separation of these mixtures. Making use of mixture of C(16)H(34)-C(44)H(90)n-alkane standards, a central composite design was carried out taking into account the carrier flow in the first and second columns, the modulation period and the discharge time. Regarding the measured responses, though the initially considered one was the peak volume, we have also evaluated the effects on the number of modulated peaks per analyte, the symmetry of the modulated peaks and the number of detected compounds. The final optimum conditions were defined as follows: a hydrogen flow of 1.2 mL/min in the first column and 18 mL/min in the second one, a modulation period of 1.4 s and a discharge time of 0.1 s and under these conditions all the response variables showed optimum values. Based on this optimized method several chert samples obtained from different stratigraphic levels in an ancient quarry were studied and we were able to distinguish them on the basis of the different constituents of organic biomarkers, such as mono-methylated alkanes, cyclic n-alkanes, branched alkanes, steranes and hopanes.

Optimisation of focused ultrasound extraction (FUSE) and microwave-assisted extraction (MAE) of hydrocarbons in geological chert samples

The analysis of hydrocarbons in chert rocks provides a worthwhile source of information regarding the geochemical features of a depositional setting. Since the typical analytical procedure requires long Soxhlet extractions and the use of large quantities of sample (30-50 g), in this work we have optimised the focused ultrasound extraction (FUSE) and the microwave-assisted extraction (MAE) to make available a less severe procedure. In both cases a full experimental design including solvent mixture composition (Dichloromethane/Hexane/Acetone) and process variables (sonication time and cycles, and extraction temperature and time) by means of D-optimal designs. In the extracted fractions hydrocarbons (C(16)-C(40)) were analysed by gas-chromatography-mass spectrometry. In the case of FUSE the process variables were the most sensitive variables and the optimum conditions were defined at 60:40 DCM/Hex mixture and a sonication time of 30 min and 9 cycles. In the case of MAE all the variables shown a significant effect on the extraction yield and the most adequate conditions (60:30:10 DCM/Hex/Ace mixture and an irradiation time of 15 min at 110 °C) were established from the analysis of the response surface. Both methods were systematically applied with different chert samples collected in Cucho (Trebiño County, Burgos, Spain) and we were able to assure quantitative extractions (>85%) in the first extraction. Additionally, from the distribution patterns of n-alkanes obtained in the different chert samples (nodular chert, laminar chert and massive-brechoid chert) collected in Cucho, we were able to distinguish different origins and diagenetic history.

Finnish wallpaper pigments in the 18th-19th century: presence of KFe3(CrO4)2(OH)6 and odd pigment mixtures.

Several Finish wallpapers from the 18th and 19th century were analysed by using Raman spectroscopy assisted with EDXRF instrumentation, in an attempt of determine the pigments used in their manufacture process as well as of trying to date some of the samples through pigment composition. All pigments present in samples were determined and surprisingly the unusual and strange iron (III) chromate yellow pigment was found. Besides, unusual mixtures were found to obtain fashionable colours, especially in blue and green areas, where more than one blue pigments were mixed with green and yellow pigments. Blue verditer, ultramarine blue, Prussian blue, chrome yellow, calcite, lead white, red and yellow iron oxide, gypsum and carbon black were identified. The presence of the risky and poisonous emerald green must be highlighted. The results were compared with those found in other wallpapers from Spain and France.

Applicability of polydimethylsiloxane (PDMS) and polyethersulfone (PES) as passive samplers of more hydrophobic organic compounds in intertidal estuarine environments

The uptake calibration of three passive samplers, stir-bars, MESCO/stir-bars and polyethersulfone tubes (PESt), was assessed in seawater at different salinities for 17 organic compounds including organochlorine compounds, pesticides, phthalates, musk fragrances and triclosan. The calibration procedure was accomplished by exposing the samplers to a continuous flow of fortified seawater for up to 14days under laboratory conditions. Prior to the exposure, stir-bars and MESCO/stir-bars were loaded with a known amount of deuterated PAH mixture as performance reference compounds (PRC). For most of the studied compounds, the sampling rates (Rs, mL·day-1) were determined for each sampler at two salinities (15 and 30‰) and two nominal concentrations (25 and 50ng·L-1). Among the tested devices, though PES can be an outstanding cheap alternative to other passive samplers, naked or free stir-bars provided the best results in terms of uptake rates (i.e., the Rs values ranged from 30 to 350mL·day-1). Regarding the variation of the salinity, the Rs values obtained with naked stir-bars were statistically comparable in the full range of salinities (0-30‰) but the values obtained with MESCO/stir-bars and PESt were salinity dependent. Consequently, only stir-bars assured the required robustness to be used as passive samplers in intertidal estuarine environments. Finally, the stir-bars were applied to estimate the time-weighted average concentration of some of those contaminants in the feeding seawater of the experimental aquaria at the Plentzia Marine Station (Basque Country) and low levels of musks fragrances (0.1-0.2ng·L-1) were estimated.

Non-destructive crystal size determination in geological samples of archaeological use by means of infrared spectroscopy.

The determination of crystal size of chert samples can provide suitable information about the raw material used for the manufacture of archeological items. X-ray diffraction (XRD) has been widely used for this purpose in several scientific areas. However, the historical value of archeological pieces makes this procedure sometimes unfeasible and thus, non-invasive new analytical approaches are required. In this sense, a new method was developed relating the crystal size obtained by means of XRD and infrared spectroscopy (IR) using partial least squares regression. The IR spectra collected from a large amount of different geological chert samples of archeological use were pre-processed following different treatments (i.e., derivatization or sample-wise normalization) to obtain the best regression model. The full cross-validation was satisfactorily validated using real samples and the experimental root mean standard error of precision value was 165 Å whereas the average precision of the estimated size value was 3%. The features of infrared bands were also evaluated in order to know the background of the prediction ability. In the studied case, the variance in the model was associated to the differences in the characteristic stretching and bending infrared bands of SiO(2). Based on this fact, it would be feasible to estimate the crystal size if it is built beforehand a chemometric model relating the size measured by standard methods and the IR spectra.

Ciprofloxacin by-products in seawater environment in the presence and absence of gilt-head bream

The widespread use of pharmaceuticals has caused a growing concern on the presence of pharmaceuticals such as the antibiotic ciprofloxacin (CIPRO) in the aquatic environment, since they may exert adverse effects on non-target organisms, including fish. In order to study the uptake, distribution in different tissues (liver, muscle, brain and gill) and biofluids (plasma and bile), metabolism and elimination of CIPRO in gilt-head bream (Sparus aurata), controlled dosing experiments for 8 days at 200 μg/L concentration were carried out. CIPRO was only observed in bile at concentration up to 315 ± 4 ng/mL, probably due to its low octanol-water partition coefficient (log P = -2.4 at pH 7.4) and the zwitterionic behavior (pKa1 = 5.76 and pKa2 = 8.68). CIPRO by-products (BPs) were also identified in seawater environment, both in presence and absence of fish. The analysis done by means of liquid chromatography-high resolution mass spectrometry (hybrid quadrupole-Orbitrap) permitted the annotation of up to 35 BPs of CIPRO in seawater and bile, from which 30 structures were reported for the first time. These results confirm that CIPRO is very susceptible to photolysis, and that it goes through various phase I and phase II metabolisms in the fish. All these results suggested that, for a complete characterization of CIPRO exposure, BPs should also be included in the biomonitoring campaigns since they might also be toxicologically relevant.

Non-targeted metabolomics reveals alterations in liver and plasma of gilt-head bream exposed to oxybenzone

The extensive use of the organic UV filter oxybenzone has led to its ubiquitous occurrence in the aquatic environment, causing an ecotoxicological risk to biota. Although some studies reported adverse effects, such as reproductive toxicity, further research needs to be done in order to assess its molecular effects and mechanism of action. Therefore, in the present work, we investigated metabolic perturbations in juvenile gilt-head bream (Sparus aurata) exposed over 14 days via the water to oxybenzone (50 mg/L). The non-targeted analysis of brain, liver and plasma extracts was performed by means of UHPLC-qOrbitrap MS in positive and negative modes with both C18 and HILIC separation. Although there was no mortality or alterations in general physiological parameters during the experiment, and the metabolic profile of brain was not affected, the results of this study showed that oxybenzone could perturb both liver and plasma metabolome. The pathway enrichment suggested that different pathways in lipid metabolism (fatty acid elongation, α-linolenic acid metabolism, biosynthesis of unsaturated fatty acids and fatty acid metabolism) were significantly altered, as well as metabolites involved in phenylalanine and tyrosine metabolism. Overall, these changes are signs of possible oxidative stress and energy metabolism modification. Therefore, this research indicates that oxybenzone has adverse effects beyond the commonly studied hormonal activity, and demonstrates the sensitivity of metabolomics to assess molecular-level effects of emerging contaminants.