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This chapter (Laser‐Induced Breakdown Spectroscopy (LIBS)) is a contribution to the Geostandards and Geoanalytical Research Handbook of Rock and Mineral Analysis – an online textbook that is a fully revised and updated edition of A Handbook of Silicate Rock Analysis (P. J. Potts, 1987, Blackie, Glasgow). Chapter 13 (from Section 3 of the handbook dealing with microbeam techniques) provides first a history of the development of laser‐induced breakdown spectroscopy, and of the LIBS process, followed by an examination of the fundamental principles of LIBS and its instrumentation. Discussion is then provided on the preparation of sample material, LIBS matrix effects and signal processing. Different modes of compositional analysis that can be tackled by LIBS are described, including quantitative measurement (covering isotope measurements), compositional mapping, depth profiling and the determination of physical properties of geological materials. The recent tandem coupling of LIBS with laser ablation ICP‐MS instrumentation is explored. Finally, a suite of examples of LIBS analyses of silicate rocks and minerals is provided, demonstrating the utility of this measurement principle in rapid compositional assessment, detailed petrological studies and microgeochemical mapping. [ABSTRACT FROM AUTHOR]

Laser-induced breakdown spectroscopy (LIBS) is a type of optical emission spectroscopy capable of rapid, simultaneous multi-element analysis. LIBS is effective for the analysis of atmospheric gases, geological fluids, and a broad spectrum of minerals, rocks, sediments, and soils both in and outside the traditional laboratory setting. With the recent introduction of commercial laboratory systems and handheld analyzers for use outside the laboratory for real-time in situ analysis in the field, LIBS is finding increasing application across the geosciences. This article first overviews the LIBS technique and then reviews its application in the domain of mineral exploration and ore processing, where LIBS offers some unique capabilities. [ABSTRACT FROM AUTHOR]

Numerous ephemeral streams flow within the McMurdo Dry Valley Region of Antarctica that transport glacial meltwater to perennially ice-covered, closed-basin lakes during the austral summer. The diurnal behavior for two Taylor Valley streams of different character was examined during the summer of 2010-11. Andersen Creek is a short, 1st-order proglacial stream, whereas Von Guerard Stream is a long, high-order stream with an extensive hyporheic zone that has a substantial cyanobacterial algal mat community in its middle reaches. Both streams display strong daily cycles for temperature, electrical conductivity, dissolved oxygen, and pH. Conductivity varies in concert with flow, with solute dilution occurring during the daily high-flow pulse. Dissolved oxygen co-varies strongly with pH at Andersen Creek but not for Von Guerard Stream. Each stream has a distinct geochemical character that for Andersen Creek is a direct reflection of its glacial source, unmodified by secondary effects, whereas that for Von Guerard Stream is modulated by its resident algal mat community and through extensive hyporheic zone interaction and exchange.

The McMurdo Dry Valley region is the largest ice-free area of Antarctica. Ephemeral streams flow here during the austral summer, transporting glacial meltwater to perennially ice-covered, closed basin lakes. The chemistry of 24 Taylor Valley streams was examined over the two-decade period of monitoring from 1993 to 2014, and the geochemical behavior of two streams of contrasting physical and biological character was monitored across the seven weeks of the 2010-2011 flow season. Four species dominate stream solute budgets: HCO3-, Ca2+, Na+, and Cl-, with SO42-, Mg2+, and K+ present in significantly lesser proportions. All streams contain dissolved silica at low concentrations. Across Taylor Valley, streams are characterized by their consistent anionic geochemical fingerprint of HCO3 > Cl > SO4, but there is a split in cation composition between 14 streams with Ca > Na > Mg > K and 10 streams with Na > Ca > Mg > K. Andersen Creek is a first-order proglacial stream representative of the 13 short streams that flow <1.5 km from source to gage. Von Guerard is representative of 11 long streams 2-7 km in length characterized by extensive hyporheic zones. Both streams exhibit a strong daily cycle for solute load, temperature, dissolved oxygen, and pH, which vary in proportion to discharge. A well-expressed diurnal co-variation of pH with dissolved oxygen is observed for both streams that reflects different types of biological control. The relative consistency of Von Guerard composition over the summer flow season reflects chemostatic regulation, where water in transient storage introduced during times of high streamflow has an extended opportunity for water-sediment interaction, silicate mineral dissolution, and pore-water exchange. [ABSTRACT FROM AUTHOR]

As calculated from data archived in the IAEA-WMO Global Network of Isotopes in Precipitation programme, the amount-weighted local meteoric water line for the Pacific coast of central Panama is:δ2H = 7.63(±0.08) × δ18O + 6.51(±0.49). Amount-weighted mean isotopic values were regressed against the sea surface temperature (SST) fields of the adjacent tropical oceans. A negative correlation of precipitation isotope composition with Caribbean SSTs is observed only for the early wet season (May–June), whilst the mid-summer dry period is characterized by positive correlation with eastern Pacific SSTs, similar to the late wet season (October–November). The negative response of May–June rainfall isotopic composition to Caribbean SSTs is explained by a SST-mediated change in stratiform rain fraction from organized convective systems proximal to the Inter Tropical Convergence Zone (ITCZ). The positive correlation for the rest of the wet season, when the organized convective zone of ITCZ and its attached stratiform belt are distant from the Pacific coast of Panama, is interpreted as simple evaporative temperature effect on isotopic fractionation. [ABSTRACT FROM AUTHOR]

The mineral exploration industry requires new methods and tools to address the challenges of declining mineral reserves and increasing discovery costs. Laser-induced breakdown spectroscopy (LIBS) represents an emerging geochemical tool for mineral exploration that can provide rapid, in situ, compositional analysis and high-resolution imaging in both laboratory and field and settings. We demonstrate through a review of previously published research and our new results how LIBS can be applied to qualitative element detection for geochemical fingerprinting, sample classification, and discrimination, as well as quantitative geochemical analysis, rock characterization by grain size analysis, and in situ geochemical imaging. LIBS can detect elements with low atomic number (i.e., light elements), some of which are important pathfinder elements for mineral exploration and/or are classified as critical commodities for emerging green technologies. LIBS data can be acquired in situ, facilitating the interpretation of geochemical data in a mineralogical context, which is important for unraveling the complex geological history of most ore systems. LIBS technology is available as a handheld analyzer, thus providing a field capability to acquire low-cost geochemical analyses in real time. As a consequence, LIBS has wide potential to be utilized in mineral exploration, prospect evaluation, and deposit exploitation quality control. LIBS is ideally suited for field exploration programs that would benefit from rapid chemical analysis under ambient environmental conditions. [ABSTRACT FROM AUTHOR]