Fanny Claverie

Simultaneous use of strontium:calcium and barium:calcium ratios in otoliths as markers of habitat: Application to the European eel (Anguilla anguilla) in the Adour basin, South West France

Sr:Ca and Ba:Ca ratios in water from the Adour estuary show a clear relationship with the salinity of the surrounding water for salinities <20, while ratios are almost constant above this level of salinity. A positive relationship was observed for the Sr:Ca ratio, whereas it was inverse for the Ba:Ca ratio. These two elemental ratios were measured in the otoliths of the European eels (Anguilla anguilla L.) using femtosecond laser ablation linked to an ICP-MS (fs-LA-ICP-MS). There was a direct relationship between the elemental ratios recorded in eel otoliths and those found in water from fresh and marine areas, suggesting that Sr:Ca and Ba:Ca ratios in eel otoliths can be used as markers of habitat in this estuary. Continuous profiling allowed the determination of three behaviour patterns in terms of habitat: freshwater, estuary and migratory individuals. Finally, the above results support the simultaneous use of both ratios for a better understanding of the migratory contingents and also as a relevant method to avoid a misidentification of environmental migratory history due to the presence of vaterite crystal in the otolith matrix.

Elemental fractionation effects in high repetition rate IR femtosecond laser ablation ICP-MS analysis of glasses

An IR-femtosecond laser ablation ICPMS coupling was used to investigate the influence of the high repetition rate on elemental fractionation effects for the analysis of silicate glass SRM NIST 610. First, elemental fractionation inherent to the ICP was minimised by working on wet plasma conditions which had greater tolerance to mass loading and demonstrated a higher robustness compared to dry plasma conditions. Because of the use of a narrow laser beam producing small craters (17 µm in diameter), a special arrangement of pulses was used to perform resulting craters of 100 µm diameter. The ablation strategy developed in this work consisted in a series of concentric circle trajectories ablated at high repetition rates by moving the laser beam rapidly thanks to a scanning beam device. Two scanner speeds (0.25 mm s−1 and 1.5 mm s−1), five laser repetition rates (from 0.1 kHz to 10 kHz) and three fluence values (5 J cm−2, 14 J cm−2, and 25 J cm−2) were investigated in detail. For this purpose, critical elemental ratios (namely 238U/232Th, 208Pb/238U, and 66Zn/65Cu) of aerosols produced by fs-LA of silicate glass were studied to evaluate the impact of the different laser parameters on elemental fractionation. No heating zones or preferential evaporation of elements were found depending on the repetition rate employed. However, particle-size-fractionation was measured during the ablation of the sample surface, and this effect was reduced by using a high repetition rate as well as a high scanner speed which allow the dilution of the large particles coming from the surface layer with finer particles coming to deeper levels. Additionally, the ablation rate induced by the selected ablation strategy had a low influence on fractionation effects due to the high robustness of the ICP plasma and, on the other hand, fractionation indices were not particularly affected by the laser repetition rate although they could be improved by the use of high fluence values. Finally, it could be stressed that no differences on the structure of the aerosol particles collected on membrane filters were found depending on the ablation parameters.

Solid-spiking isotope dilution laser ablation ICP-MS for the direct and simultaneous determination of trace elements in soils and sediments

The direct and simultaneous determination of Cu, Zn, Sn and Pb in soil and sediment samples by femtosecond laser ablation inductively coupled plasma isotope dilution mass spectrometry (fs-LA-ICP-IDMS) has been accomplished in this work with the development of a solid-spiking sample preparation procedure. The total analysis time, in comparison with previous approaches, has been significantly reduced by developing a solid-spiking procedure based on the synthesis of a unique isotopically-enriched solid spike and the preparation of isotope-diluted blend pellets for each sample. The laser repetition rate and the ablation mode were carefully selected (10 kHz and the 2D scanning sampling mode, respectively) in order to reduce the effect of possible local inhomogeneities of the powdered samples on the precision of isotope ratio measurements. Special attention was focused on the heterogeneous distribution of trace elements in the isotopically-enriched solid spike and the isotope-diluted blend samples in order to assure that the measured isotope ratios remained constant (precisions lower than 10% RSD; n = 8). The proposed methodology was tested for the analysis of two soil (CRM 142R, GBW-07405) and two sediment (PACS-2, IAEA-405) reference materials. The concentrations obtained by solid-spiking fs-LA-ICP-IDMS were in agreement not only with the certified values but also with those obtained by ICP-IDMS after the microwave-assisted digestion of the solid samples, demonstrating therefore the validity of the proposed solid-spiking procedure for a rapid and accurate analysis of solid samples.

Direct determination of trace elements in powdered samples by in-cell isotope dilution femtosecond laser ablation ICPMS

A method has been developed for the direct and simultaneous multielement determination of Cu, Zn, Sn, and Pb in soil and sediment samples using femtosecond laser ablation inductively coupled plasma mass spectrometry (fs-LA-ICPMS) in combination with isotope dilution mass spectrometry (IDMS). The in-cell isotope dilution fs-LA-ICPMS method proposed in this work was based on the quasi-simultaneous ablation of the natural abundance sample and the isotopically enriched solid spike, which was performed using a high repetition rate laser and a fast scanning beam device in a combined manner. Both the sample preparation procedure and the total analysis time have been drastically reduced, in comparison with previous approaches, since a unique multielement isotopically enriched solid spike was employed to analyze different powdered samples. Numerous experimental parameters were carefully selected (e.g., carrier gas flow rate, inlet diameter of the ablation cell, sample translation speed, scanner speed, etc.) in order to ensure the complete mixing between the sample and the solid spike aerosols. The proposed in-cell fs-LA-ICP-IDMS method was tested for the analysis of two soil (CRM 142R, GBW-07405) and two sediment (PACS-2, IAEA-405) reference materials, and the analysis of Cu, Zn, Sn, and Pb yielded good agreement of usually not more than 10% deviation from the certified values and precisions of less than 15% relative standard deviation. Furthermore, the concentrations were in agreement not only with the certified values but also with those obtained by ICP-IDMS after the microwave-assisted digestion of the solid samples, demonstrating therefore that in-cell fs-LA-ICP-IDMS opens the possibility for accurate and precise determinations of trace elements in powdered samples reducing the total sample preparation time to less than 5 min. Additionally, scanning electron microscope measurements showed that the aerosol generated by in-cell fs-LA-ICP-IDMS predominantly consisted of linear agglomerates of small particles (in the order of few tens of nanometers) and a few large spherical particles with diameters below 225 nm.

Toward chromium speciation in solids using wavelength dispersive X-ray fluorescence spectrometry Cr Kβ lines

The determination of chromium speciation in solid samples is critical for environmental and industrial purposes. Several analytical methods exist to perform such a determination either directly in solid state or liquid state after an extraction step, each of them having some limitations. In this study, the use of a high-resolution wavelength-dispersive X-ray fluorescence spectrometer to determine and quantify chromium species is investigated by looking at the differences in the Kβ transition profiles between Cr(0), Cr(III) and Cr(VI) compounds. Three different approaches were tested and compared to determine the Cr(VI) fraction of known mixtures: relative height and peak fitting using calibration mixtures, partial least square regression (PLS) of pure compounds, and principal component regression (PCR) of pure compounds. The accuracy of these methods was found to be about the same with an average relative error in the range of 15%. However, PLS and PCR can be easily implemented in an automated way contrary to peak fitting which can be sometimes perceived as analyst-dependant. Another advantage of using PLS and PCR is that information concerning the other oxidation states present in the sample can be retrieved. Finally, PLS and the peak height approach can be used up to 0.5% total chromium which make the XRF an alternative technique to X-ray induced photoelectron spectroscopy (XPS) for chromium speciation in solid state.

Femtosecond laser ablation ICP-MS measurement of otolith Sr:Ca and Ba:Ca composition reveal differential use of freshwater habitats for three amphidromous Sicyopterus (Teleostei: Gobioidei: Sicydiinae) species

The use of freshwater habitats was examined in three amphidromous goby species of the genus Sicyopterus using otolith microchemistry. Two species were endemic to either New Caledonia or Vanuatu whilst the other was widely distributed. Depositional patterns of strontium (Sr) and barium (Ba) in the otolith of adults were analysed with femtosecond laser ablation inductively coupled plasma mass spectrometry (ICP-MS). The Sr:Ca and Ba:Ca results uncovered three different adult behaviours within the freshwater habitat. Some fishes stayed in elevated locations (square profile); others undertook back-and-forth migrations between higher and lower reaches (up-and-down profile), and finally, others stayed in the lower reaches (constant profile). The consequences of these movements to larval survival or competition for food and territory are discussed. This work brings new knowledge on amphidromous behaviour, and it highlights the necessity of multi-elemental analysis to study amphidromy in freshwater systems.

Standard addition method for laser ablation ICPMS using a spinning platform.

A method has been developed for the fast and easy determination of Pb, Sr, Ba, Ni, Cu, and Zn, which are of geological and environmental interest, in solid samples by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) using a spinning sample platform. The platform, containing a sample and a standard, is spun during the ablation, allowing the quasi-simultaneous ablation of both materials. The aerosols resulting from the ablation of sample and standard were mixed in the ablation cell allowing quantification of analytes by standard additions. The proportion of standard versus sample of the mixing can be increased by performing the ablation further from the axis of rotation. The ablated masses have been determined using a new strategy based on isotope dilution analysis. This spinning laser ablation method has been applied to the Allende meteorite and four powdered standard reference materials (SRMs) fused in lithium borate glasses: two sediments as well as a soil and a rock material. SRM 612 (Trace Elements in Glass) was also analyzed despite having a matrix slightly different from the glass standard obtained by lithium borate fusion. The deviation from the certified values was found to be less than 15% for most of the mass fractions for all the elements and samples studied, with an average precision of 10%. These results demonstrate the validity of the proposed method for the direct and fast analysis of solid samples of different matrixes by standard additions, using a single standard sample.

Elemental analyses of soil and sediment fused with lithium borate using isotope dilution laser ablation-inductively coupled plasma-mass spectrometry

Quantitative analysis using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) remains challenging primarily due to the lack of appropriate reference materials available for the wide variety of samples of interest and to elemental fractionation effects. Isotopic dilution mass spectrometry (IDMS) is becoming the methodology of choice to address these issues because the different isotopes of an element represent near-perfect internal standards. In this work, we investigated the lithium borate fusion of powdered solid samples, including soils, sediments, rock mine waste and a meteorite, as a strategy to homogenously distribute, i.e. equilibrate the elements and the added isotopically enriched standards. A comparison of this methodology using two pulsed laser ablation systems (ArF* excimer and Nd:YAG) with different wavelengths as well as two ICP-MS instruments (quadrupole and double-focusing sector field) was performed. Emphasis was put on using standard equipment to show the potential of the proposed strategy for its application in routine laboratories. Cr, Zn, Ba, Sr and Pb were successfully determined by LA-ICP-IDMS in six Standard Reference Materials (SRMs) representing different matrices of environmental interest. Experimental results showed the SRM fused glasses exhibited a low level of heterogeneity (intra- and inter-sample) for both natural abundance and isotopically enriched samples (RSD <3%, n=3, 1σ). A good agreement between experimental results and the certified values was also observed.

Improving Precision and Accuracy of Isotope Ratios from Short Transient Laser Ablation-Multicollector-Inductively Coupled Plasma Mass Spectrometry Signals: Application to Micrometer-Size Uranium Particles.

The isotope drift encountered on short transient signals measured by multicollector inductively coupled plasma mass spectrometry (MC-ICPMS) is related to differences in detector time responses. Faraday to Faraday and Faraday to ion counter time lags were determined and corrected using VBA data processing based on the synchronization of the isotope signals. The coefficient of determination of the linear fit between the two isotopes was selected as the best criterion to obtain accurate detector time lag. The procedure was applied to the analysis by laser ablation-MC-ICPMS of micrometer sized uranium particles (1-3.5 μm). Linear regression slope (LRS) (one isotope plotted over the other), point-by-point, and integration methods were tested to calculate the (235)U/(238)U and (234)U/(238)U ratios. Relative internal precisions of 0.86 to 1.7% and 1.2 to 2.4% were obtained for (235)U/(238)U and (234)U/(238)U, respectively, using LRS calculation, time lag, and mass bias corrections. A relative external precision of 2.1% was obtained for (235)U/(238)U ratios with good accuracy (relative difference with respect to the reference value below 1%).

Isotope dilution mass spectrometry for quantitative elemental analysis of powdered samples by radiofrequency pulsed glow discharge time of flight mass spectrometry

In recent years particular effort is being devoted to the development of pulsed glow discharges (PGDs) for mass spectrometry because this powering operation mode could offer important ionization analytical advantages. However, the capabilities of radiofrequency (RF) PGD coupled to a time of flight mass spectrometry (ToFMS) for accurate isotope ratio measurements have not been demonstrated yet. This work is focused on investigating different time positions along the pulse profile for the accurate measurement of isotope ratios. As a result, a method has been developed for the direct and simultaneous multielement determination of trace elements in powdered geological samples by RF-PGD-ToFMS in combination with isotope dilution mass spectrometry (IDMS) as an absolute measurement method directly traceable to the International System of Units. Optimized operating conditions were 70 W of applied radiofrequency power, 250 Pa of pressure, 2 ms of pulse width and 4 ms of pulse period, being argon the plasma gas used. To homogeneously distribute the added isotopically-enriched standards, lithium borate fusion of powdered solid samples was used as sample preparation approach. In this way, Cu, Zn, Ba and Pb were successfully determined by RF-PGD-ToF(IDMS) in two NIST Standard Reference Materials (SRM 2586 and SRM 2780) representing two different matrices of geological interest (soil and rock samples). Cu, Zn, Ba and Pb concentrations determined by RF-PGD-ToF(IDMS) were well in agreement with the certified values at 95% confidence interval and precisions below 12% relative standard deviation were observed for three independent analyses. Elemental concentrations investigated were in the range of 81-5770 mg/kg, demonstrating the potential of RF-PGD-ToF(IDMS) for a sensitive, accurate and robust analysis of powdered samples.