RISK-ASSESSMENT; PLANT MATERIALS; LIBS; PELLETS

In seeking a novel method with the ability of green analysis in monitoring toxic heavy metals residue in fresh leafy vegetables, laser-induced breakdownspectroscopy (LIBS) was applied to prove its capability in performing this work. The spectra of fresh vegetable samples polluted in the lab were collected by optimized LIBS experimental setup, and the reference concentrations of cadmium (Cd) from samples were obtained by conventional atomic absorption spectroscopy after wet digestion. The direct calibration employing intensity of single Cd line and Cd concentration exposed the weakness of this calibration method. Furthermore, the accuracy of linear calibration can be improved a little by triple Cd lines as characteristic variables, especially after the spectra were pretreated. However, it is not enough in predicting Cd in samples. Therefore, partial least-squares regression (PLSR) was utilized to enhance the robustness of quantitative analysis. The results of the PLSR model showed that the prediction accuracy of the Cd target can meet the requirement of determination in food safety. This investigation presented that LIBS is a promising and emerging method in analyzing toxic compositions in agricultural products, especially combined with suitable chemometrics. (C) 2017 Optical Society of America

SOILS; AGE; LIBS

Laser-induced breakdown spectroscopy (LIBS) is showing to be a promising, quick, accurate, and practical technique to detect and measure metal contaminants and nutrients in urban wastes and landfill leachates. Although conventional LIBS presents some limitations, such as low sensitivity, when used in the single pulse configuration if compared to other spectroscopic techniques, the use of the double-pulse (DP) configuration represents an adequate alternative. In this work DP LIBS has been applied to the qualitative and quantitative analysis of mercury (Hg) in landfill leachates. The correlation analysis performed between each intensified charge-coupled device pixel and the Hg concentration allowed us to choose the most appropriate Hg emission line to be used for its measure. The normalization process applied to LIBS spectra to correct physical matrix effects and small fluctuations increased from 0.82 to 0.98 the linear correlation of the calibration curve between LIBS and the reference data. The limit of detection for Hg estimated using DP LIBS was 76 mg Kg(-1). The cross validation (leave-one-out) analysis yielded an absolute average error of about 21%. These values showed that the calibration models were close to the optimization limit and satisfactory for Hg quantification in landfill leachate. (C) 2017 Optical Society of America

INDUCED PLASMA; LIGHT-BEAMS; AIR; WATER; PARTICLES; VAPORIZATION; CONSTITUENTS; SPECTROMETRY; CLOUDS

Nanosecond laser-induced breakdown spectroscopy has been examined for the analysis of suspended matter in a free stream of air. The real-time monitoring of this scenario poses major challenges for an accurate categorization due to its changing characteristics such as composition, size, and density of particles. The effects of particle size and matrix in the optical emission responses registered from such scenarios have been evaluated. Distant (10 m) plasmas of saline solutions, containing either NaCl or Na2SO4 at different concentrations, have been induced by nanosecond laser pulses at a wavelength of 1064 nm. The effects of the droplet size and its concentration on differences in the laser-induced breakdown probability, the intensity of the characteristic lines, and the plasma emission continuum have been discussed. The quantification of sodium in distant water droplets has been proved. However, an initial knowledge on the average droplet size is required. The average droplet size could be determined from the slope of H I and O I lines versus the continuum plasma emission, which is only weakly influenced by the salt content in the droplets. (C) 2017 Optical Society of America.

INDUCED BREAKDOWN SPECTROSCOPY; SATURATION VAPOR-PRESSURE; INDUCED INCANDESCENCE; SI-I; NANOSECOND; RADIATION; SURFACE

The temporal luminescence behavior of silicon atoms during and after laser-heating of gas-borne silicon nanoparticles was investigated. Silicon nanoparticles were formed in the exhaust stream of a microwave plasma reactor at 100 mbar. The observed prompt atomic line intensities correspond with thermal excitation of the evaporated species. A prompt signal at 251.61 and 288.15 nm originating from the 3s(2)3p(2) -> 3s(2)3p4s transitions showed a lifetime of 16 ns that matches the documented excited-state lifetime for the respective transitions. A secondary delayed signal contribution with similar peak intensities was observed commencing approximately 100-300 ns after the laser pulse and persisting for hundreds of nanoseconds. This signal contribution is attributed to electron impact excitation or recombination after electron impact ionization of the silicon evaporated as a consequence of the laser heating of the plasma leading to non-thermal population of electronically excited silicon. The observations support a nanoparticle evaporation model that can be used to recover nanoparticle sizes from timeresolved LII data. (C) 2017 Optical Society of America

MINERALS; ELEMENTS; SAMPLES; WATER; PB

On-stream analysis of the element content in ore slurry has important significance in the control of the flotation process and full use of raw materials. Therefore, techniques that can monitor the chemistry in slurries online are required. Laser-induced breakdown spectroscopy (LIBS) is one of the potential approaches to online measurements due to its capability of in situ and real-time analysis. However, using LIBS for on-stream analysis of slurries is challenging due to the issues such as surface ripples, sample splashing, sedimentation, etc. To address these problems, we developed a slurry circulation system. The effects of slurry flow rate on LIBS spectra were investigated to achieve the optimal detecting surface for better repeatability of LIBS. The coefficient of determination R-2 of the calibration curve for Fe element is 0.982, and the limit of detection of Fe element was estimated to be 0.075 wt. % under the optimized experimental parameters. The results show that this slurry circulation system is applicable to the on-stream slurry analysis. (C) 2017 Optical Society of America

PLASMA-MASS SPECTROMETRY; ICP-MS; EMISSION-SPECTROMETRY; PRECONCENTRATION; SAMPLES; ROCKS; SOIL; CHROMATOGRAPHY; SEPARATION; THORIUM

Univariate and multivariate analyses of six rare earth elements [cerium (Ce), europium (Eu), gadolinium (Gd), neodymium (Nd), samarium (Sm), and yttrium (Y)] have been performed using data from laser-induced breakdown spectroscopy (LIBS). Binary mixtures of oxide forms of each rare earth element in an Al2O3 matrix with their concentrations varying from 1% to 10% by weight in powder form were used as working samples for univariate analysis. For multivariate analysis, complex mixtures of oxides of all these six rare earth elements and Al2O3 in powder form, where the concentration of each element oxide was varied from 1% to 50% by weight one by one, were used to record LIBS spectra. Optimum values of gate delay, gate width, and laser energy were used to get spectra from these samples and spectra were used to develop calibration models. The limits of detection for Ce, Eu, Gd, Nd, Sm, and Y were calculated to be 0.098%, 0.052%, 0.077%, 0.047%, 0.250%, and 0.036%, respectively, from the calibration curves. (C) 2017 Optical Society of America

ELECTRON NUMBER DENSITY; TEMPORAL EVOLUTION; ABEL-INVERSION; AIR; BREAKDOWN

Microplasma is generated in an ultra-high-pure H-2 and N-2 gas mixture with a Nd:YAG laser device that is operated at the fundamental wavelength of 1064 nm. The gas mixture ratio of H-2 and N-2 is 9 to 1 at a pressure of 1.21 +/- 0.03 10(5) Pa inside a chamber. A Czerny-Turner-type spectrometer and an intensified charge-coupled device are utilized for the recording of plasma emission spectra. The line-of-sight measurements are Abel inverted to determine the radial distributions of electron number density and temperature. Recently derived empirical formulas are utilized for the extraction of values for electron density. The Boltzmann plot and line-to-continuum methods are implemented for the diagnostic of electron excitation temperature. The expansion speed of the plasma kernel maximum electron temperature amounts to 1 km/s at a time delay of 300 ns. The microplasma, initiated by focusing 14 ns, 140 mJ pulses, can be described by an isentropic expansion model. (C) 2017 Optical Society of America

DATA NORMALIZATION; DOMINANT FACTOR; CLASSIFICATION; MODEL; LIBS; REGRESSION; SAMPLES; STEEL; RAMAN; NIR

Laser-induced breakdown spectroscopy (LIBS) as a rapid and green method was used to detect heavy metals Cr and Pb in pork contaminated in the lab. The laser-induced plasma was generated by a Q-switched Nd:YAG laser, and the LIBS signal was collected by a spectrometer with a charge-coupled device detector. The traditional calibration curves (CC) and multivariate partial least squares (PLS) algorithm were applied and compared to validate the accuracy in predicting the content of heavy metals in samples. The results demonstrated that the correlation coefficient of CC is poor by the classical univariate calibration method, so the univariate calibration analysis cannot effectively serve the quantitative purpose in analyzing heavy metals' residue in pork with a complex matrix. The analysis accuracy was improved effectively by the PLS method, and the correlation coefficient is 0.9894 for Cr and 0.9908 for Pb. The concentration of Cr and Pb in samples from a prediction set was obtained using the PLS calibration method, and the average relative errors for the 21 samples in the prediction set are lower than 6.53% and 7.82% for Cr and Pb, respectively. The investigated results display that the matrix effect would be reduced effectively during the quantitative analysis of pork by a LIBS-combined PLS model, and the predictive accuracy would be improved greatly compared to traditional univariate analysis. (C) 2017 Optical Society of America

CHEMICAL-ANALYSIS; PULSE; PLASMA; PRESSURES; SEAWATER; WATER

The exploitation and research of deep-sea hydrothermal vent has been an issue of great interest in ocean research in recent years. Laser-induced breakdownspectroscopy (LIBS) has great potential for ocean application due to the capabilities of stand-off, multiphase, and multielement analysis. In this work, a newly developed compact 4000 m rated LIBS system (LIBSea) is introduced with preliminary results of sea trials. The underwater system consists of an Nd:YAG single-pulsed laser operating at 1064 nm, an optical fiber spectrometer, an optics module, and an electronic controller module. The whole system is housed in an L800 mm x Phi 258 mm pressure housing with an optical window on the end cap. It was deployed on the remote operated vehicle Faxian on the research vessel Kexue, and in June 2015 was successfully applied for hydrothermal field measurements at the Manus area. The obtained results are shown that the LIBS system is capable of detecting elements Li, Na, K, Ca, and Mg in the hydrothermal area. Profiles of LIBS signals of elements K and Ca have also been obtained during the sea trial. The results show that the K emission line is gradually broadened with depth from sea surface to sea floor (1800 m or so); the K intensity shows a hump shape with maximum value at about 1050 m. The Ca emission line is rapidly broadened below 400 m and slowly narrowed to the sea floor; the Ca intensity shows no obvious change below 400 m and increases continuously to sea floor. A very interesting finding is that the small fluctuations of intensity profile curve of Ca show a degree of correlation with seawater temperature change. The sea trial results prove the performance of LIBSea. After further optimization, it is hoped to apply the LIBS system to the in situ mineral deposits and hydrothermal vent fluid detection in deep sea. (C) 2017 Optical Society of America

RARE-EARTH-ELEMENTS; SPACE EXPLORATION; IRON OBJECTS; STEEL WORKS; ICP-MS; LIBS; SPECTROMETRY; UNIVARIATE; SAMPLES; CURVES

Laser-induced breakdown spectroscopy (LIBS) was used for the analysis of charcoal blast furnace slags. Plasma was generated by an application of a 1064 nm wavelength Nd:YAG laser beam to the surface of pellets created from the slags. The presence of Al, Ca, Fe, K, Mg, Mn, and Si was determined by identifying their characteristic spectral signatures. Multivariate analysis was performed for the quantification of these elements. The predicted LIBS results were found in agreement with the inductively coupled plasma optical emission spectrometry analysis. The limit of detection for Al, Ca, Fe, K, Mg, Mn, and Si was calculated to be 0.10%, 0.22%, 0.02%, 0.01%, 0.01%, 0.005%, and 0.18%, respectively. (C) 2017 Optical Society of America

IMPROVEMENT; CHEMOMETRICS; SPECTROMETRY; CONFINEMENT; CALIBRATION; SELECTION; PLASMA; LIBS; SOIL

In this work, a genetic algorithm (GA) was employed to select the intensity ratios of the spectral lines belonging to the target and domain matrix elements, then these selected line-intensity ratios were taken as inputs to construct an analysis model based on an artificial neural network (ANN) to analyze the elements copper (Cu) and vanadium (V) in steel samples. The results revealed that the root mean square errors of prediction (RMSEPs) for the elements Cu and V can reach 0.0040 wt. % and 0.0039 wt. %, respectively. Compared to 0.0190 wt. % and 0.0201 wt. % of the conventional internal calibration approach, the reduction rates of the RMSEP values reached 78.9% and 80.6%, respectively. These results indicate that the GA combining ANN can excellently execute the quantitative analysis in laser-induced breakdown spectroscopy for steel samples and further improve analytical accuracy. (C) 2017 Optical Society of America

POLISHING-INDUCED CONTAMINATION; INDUCED DAMAGE THRESHOLD; X-RAY REFLECTION; REFRACTIVE-INDEX; ROUGHNESS; OPTICS; GLASS; MITIGATION; CRACKS; ELLIPSOMETRY

We report on investigations of the spatial variations of contamination, roughness, and index of refraction of classically manufactured polished fused silica surfaces. Therefore, laser-induced breakdown spectroscopy was used to probe surface and subsurface impurities via the detection of aluminum. Measurements at different positions on the surface of the cylindrical fused silica windows evidenced an almost contamination-free center region, whereas a relatively large contamination area was found close to the edge. In-depth measurements verify the presence of aluminum atoms in the bulk until a depth of several tens of microns for the edge region. In addition, atomic force microscopic measurements show that the surface roughness is larger in the center region compared to the edge. Further, the index of refraction increases from the center region towards the edge as measured via ellipsometry. The results indicate a nonuniform impact of the grinding, lapping, and polishing tools on the surface. The findings turn out to be of specific interest for different applications, particularly for the realization of large-scale high-performance coatings. (C) 2017 Optical Society of America

INDUCED BREAKDOWN SPECTROSCOPY; MULTIELEMENT; SAMPLES; CARBON; LINES

The laser induced breakdown spectroscopy (LIBS) technique is an effective method to detect material composition by obtaining the plasma emission spectrum. The overlapping peaks in the spectrum are a fundamental problem in the qualitative and quantitative analysis of LIBS. Based on a curve fitting method, this paper studies an error compensation method to achieve the decomposition and correction of overlapping peaks. The vital step is that the fitting residual is fed back to the overlapping peaks and performs multiple curve fitting processes to obtain a lower residual result. For the quantitative experiments of Cu, the Cu-Fe overlapping peaks in the range of 321-327 nm obtained from the LIBS spectrum of five different concentrations of CuSO4 . 5H(2)O solution were decomposed and corrected using curve fitting and error compensation methods. Compared with the curve fitting method, the error compensation reduced the fitting residual about 18.12-32.64% and improved the correlation about 0.86-1.82%. Then, the calibration curve between the intensity and concentration of the Cu was established. It can be seen that the error compensation method exhibits a higher linear correlation between the intensity and concentration of Cu, which can be applied to the decomposition and correction of overlapping peaks in the LIBS spectrum. (c) 2017 Optical Society of America

URANIUM; LIBS; FLUORESCENCE; SPECTROMETRY; MATRICES; SAMPLES; SYSTEM; PULSE; UF6

A hand-held device for laser-induced breakdown spectroscopy has been investigated for the determination of uranyl fluoride surface contamination. This research demonstrates the ability to successfully detect uranium on surfaces when using a low resolving power (lambda/Delta lambda = 4000) spectrograph, with a 5 mJ energy per 1 ns pulsed laser radiation, available as a commercially packaged hand-held system. Sand/uranyl fluoride mixtures are prepared to simulate residue likely encountered during decontamination efforts at facilities that handle uranium hexafluoride. Detection limits are described for four uranium lines with one revealing the capability to detect uranium at a level of 250 parts per million. Advantages of the studied compact device include that location specific information can be obtained on-site to augment contamination identification. (c) 2017 Optical Society of America

INDUCED BREAKDOWN SPECTROSCOPY; YAG LASER; EMISSION SPECTROSCOPY; PLANT MATERIALS; HYDROGEN; DEUTERIUM; RESIDUES; ABLATION; NITROGEN

We report the experimental evidence of shock wave plasma generation by direct observation of the plasma propagation using 68 mJ 1064 nm Nd-doped yttrium aluminum garnet laser irradiation on a relatively soft organic sample in He ambient gas at 2 kPa. The density jump associated with the arrival of the plasma front at a certain position is detected by means of the highly sensitive interferometric technique, in conjunction with the observation of the first appearance of the plasma emission at the same position and time of the plasma front arrival. The result shows that the plasma front moves at the Sedov speed, which is typical of shock wave propagation, yielding an excellent emission spectrum for the harder sample. The shock front speed is further found to decrease in the case of a softer sample, resulting in lesser spectroscopic performance, as demonstrated by the emission spectra measured from mochi samples of different hardnesses. The result of this study is promising for paving the way to extending the laser-induced breakdown spectroscopy application to the much needed spectrochemical analysis of agricultural and food products. (c) 2017 Optical Society of America

QUANTITATIVE-ANALYSIS; PARAMETERS; SAMPLES; LIBS

A calibration method based on homogeneous material for correcting laser-induced breakdown spectroscopy (LIBS) measurement-error bias in the case of dust pollution under laboratory conditions is proposed. The measured plasma spectra of the sample can be corrected by measuring the spectral integral of the homogeneous material. Thus, we can effectively minimize the dust pollution effect on LIBS and guarantee its precision. Results show that the mean absolute errors of CaO, MgO, Fe2O3, Al2O3, and SiO2 in cement samples are decreased notably from 1.02%, 0.06%, 0.15%, 0.57%, and 0.80% to 0.41%, 0.02%, 0.04%, 0.35%, and 0.39%, respectively. Combination of this calibration method with the traditional optical dustproof methods will significantly extend the LIBS equipment maintenance cycle and make preliminary preparations for the next practical industrial application. (C) 2017 Optical Society of America

HIGH-SPATIAL-RESOLUTION; STEEL-INDUSTRY; CHEMICAL MAPS; SPECTROMETRY; PLASMA; IDENTIFICATION; LIBS; MICROANALYSIS; CONVERTERS; SAMPLES

Three-dimensional multi-elemental mapping of composite wear-resistant coatings by laser-induced breakdown spectroscopy has been demonstrated for the first time, to the best of our knowledge. Individual clads of 1560 nickel alloy reinforced with tungsten carbide were synthesized by a co-axial laser cladding technique. Electron energy dispersive x-ray spectroscopy revealed elemental maps for major elements (W, Ni, Co, Cr, Fe) but failed to measure silicon and carbon. Laser-induced breakdown spectroscopy was utilized for elemental mapping of carbon and all other elements of interest. It was demonstrated that three-dimensional elemental profiling for a few tens of micrometers requires substantial laser spot overlapping during the scanning procedure in order to achieve good accuracy of depth measurements. Elemental maps for nickel, iron, chromium, silicon, tungsten, and carbon were quantified for 900 mu m x 900 mu m x 45 mu m volume with 30 mu m lateral and 4 mu m depth resolution in the case of tungsten carbide particles in nickel alloy. (C) 2017 Optical Society of America

MEAT; PLANT

Meat can be polluted by heavy metals during the feeding of livestock and processing of meat. It is necessary to monitor the concentration of toxic metals in meat. The element chromium (Cr) in pork was selected as a determination target for this work. Fresh pork was polluted in a Cr solution to create a different content level, then dried and pressed into pellets to eliminate the effect of water and improve the stability and sensitivity of laser-induced breakdownspectroscopy (LIBS). The spectra of pressed pellets were collected at optimized LIBS experimental parameters. After that, the real content of samples was obtained by atomic absorption spectroscopy. Characteristic lines Cr I 425.43, Cr I 427.48, and Cr I 428.97 were verified, and a model comparing the LIBS intensity of the line peak and the actual concentration of Cr was constructed. The results showed that the model has better predicted precision and accuracy, especially applying the line Cr I 425.43 for calibration. This work makes it obvious that LIBS has food safety potential for detecting residue of heavy metals in meat. (C) 2016 Optical Society of America

LIBS; POLLUTION; CHINA

In this work, a mobile laser-induced breakdown spectroscopy (LIBS) system has been successfully applied to in situ analysis of heavy metals in soil samples. The LIBS system had two working methods, which were a fixed measuring method and a handheld method. For the fixed measuring method, a simple sample pretreatment was needed to reduce the soilmatrix effect generated by moisture and porosity. Experiments proved that this method could be used to semi-quantitatively detect heavy metals when combined with the traditional calibration curve method. The limits of detection for copper, lead, and zinc were all below 10 mg/kg, which satisfied the need of heavy metal detection in soil. Principal component analysis was used for soil classification, which helped to build appropriate calibration curves. On the basis of soil classification, accurate and rapid detection of heavy metals in soil is feasible. For the handheld method, spectrum intensity and stability decreased significantly compared with the fixed measuring method. However, by using the internal standard method, the stability of LIBS data was improved significantly to 6%. For soil samples with serious heavy-metal pollution, the measurement errors were less than 12%, which indicated that handheld LIBS was effective to monitor heavy-metal pollution in soil. The research results provide application support for rapid and on-site monitoring of heavy metals in soil. (C) 2017 Optical Society of America

ECHELLE SPECTROGRAPH; SPECTROMETER

High-resolution spectrographs extract detailed spectral information of a sample and are frequently used in astronomy, laser-induced breakdown spectroscopy, and Raman spectroscopy. These instruments employ dispersive elements such as prisms and diffraction gratings to spatially separate different wavelengths of light, which are then detected by a charge-coupled device (CCD) or complementary metal-oxide-semiconductor (CMOS) detector array. Precise alignment along the optical axis (focus position) of the detector array is critical to maximize the instrumental resolution; however, traditional approaches of scanning the detector through focus lack a quantitative measure of precision, limiting the repeatability and relying on one's experience. Here we propose a method to evaluate the focus alignment of spectrograph detector arrays by establishing confidence intervals to measure the alignment precision. We show that propagation of uncertainty can be used to estimate the variance in an alignment, thus providing a quantitative and repeatable means to evaluate the precision and confidence of an alignment. We test the approach by aligning the detector array of a prototype miniature echelle spectrograph. The results indicate that the procedure effectively quantifies alignment precision, enabling one to objectively determine when an alignment has reached an acceptable level. This quantitative approach also provides a foundation for further optimization, including automated alignment. Furthermore, the procedure introduced here can be extended to other alignment techniques that rely on numerically fitting data to a model, providing a general framework for evaluating the precision of alignment methods. (C) 2017 Optical Society of America

TRACE-METAL ANALYSIS; AQUEOUS-SOLUTION; MATRIX CONVERSION; HEAVY-METALS; LIBS; MEMBRANE; WATER; SPECTROMETRY; DEPOSITION; ADSORBENT

A highly concentrated, ring-shaped phase conversion (RSPC) method was developed for liquid sample analysis using the laser-induced breakdownspectroscopy (LIBS) technique. In this work, test samples were prepared by mixing the metal particles with polyvinyl alcohol (PVA) supporter in liquid phase. With heat, the PVA solution solidified inside a modified glass petri dish, forming a metal-enriched polymer ring film. Distinguished from other traditional liquid-to-solid conversing methods, the proposed new method takes advantage of enhanced homogeneity for the target elements inside the ring film. The modified glass petri dish was used to control the ring-shaped concentration. Due to the specially designed circular groove at the bottom of this dish, where the PVA solution and liquid sample mixture accumulated, the target elements were concentrated in this small ring, which is beneficial for enhancing and stabilizing the plasma signals compared to the direct liquid sample analysis using LIBS. The limits of detection for Ag, Cu, Cr, and Ba obtained with the RSPC-LIBS technology were 0.098 mu g . mL(-1), 0.18 mu g . mL(-1), 0.83 mu g . mL(-1), and 0.046 mu g . mL(-1), respectively, which provided greater improvement than the direct bulk liquid analysis using LIBS. (C) 2017 Optical Society of America

Laser-induced breakdown spectroscopy (LIBS) and laser ablation (LA) inductively coupled plasma (ICP) mass spectrometry (MS) were utilized for microspatial analyses of a prehistoric bear (Ursus arctos) tooth dentine. The distribution of selected trace elements (Sr, Ba, Fe) was measured on a 26 mm×15 mm26 mm×15 mm large and 3 mm3 mm thick transverse cross section of a canine tooth. The Na and Mg content together with the distribution of matrix elements (Ca, P) was also monitored within this area. The depth of the LIBS craters was measured with an optical profilometer. As shown, both LIBS and LA-ICP-MS can be successfully used for the fast, spatially resolved analysis of prehistoric teeth samples. In addition to micro chemical analysis, the sample hardness was calculated using LIBS plasma ionic-to-atomic line intensity ratios of Mg (or Ca). To validate the sample hardness calculations, the hardness was also measured with a Vickers microhardness tester.

The development of a remote laser-induced breakdown spectroscopy (LIBS) setup with an off-axis Newtonian collection optics, Galilean-based focusing telescope, and a 532 nm532 nm flattop laser beam source is presented. The device was tested at a 6 m6 m distance on a slice of bone to simulate its possible use in the field, e.g., during archaeological excavations. It is shown that this setup is sufficiently sensitive to both major (P, Mg) and minor elements (Na, Zn, Sr). The measured quantities of Mg, Zn, and Sr correspond to the values obtained by reference laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) measurements within an approximately 20% range of uncertainty. A single point calibration was performed by use of a bone meal standard . The radial element distribution is almost invariable by use of LA-ICP-MS, whereas the LIBS measurement showed a strong dependence on the sample porosity. Based on these results, this remote LIBS setup with a relatively large (350 mm350 mm) collecting mirror is capable of semiquantitative analysis at the level of units of mg kg-1.