Nanosecond and femtosecond laser pulses were combined in an orthogonal preablation spark dual-pulse laser-induced breakdown spectroscopy (LIBS) configuration. Even without full optimization of interpulse alignment, ablation focus, large signal, signal-to-noise ratio, and signal-to-background ratio enhancements were observed for both copper and aluminum targets. Despite the preliminary nature of this study, these results have significant implications in the attempt to explain the sources of dual-pulse LIBS enhancements.

The predominant data used in ecological risk assessment today are individual-based rather than population-based; yet environmental policies are usually designed to protect populations of threatened species or communities. Most current methods in ecotoxicology are limited by largely logistic/ technology-driven requirements that yield data for a relatively small number of test species and end points that focus on acute lethality or sublethal nonproduction-based parameters (e.g., biomarkers, mutagenesis, genetic change, physiological condition). A contrasting example is presented here showing the predictive ability of meiobenthos-based full life cycle toxicity testing to extrapolate multi-generational effects of chemicals on variables of import to population growth and maintenance. Less than 24-h-old larvae of a meiobenthic copepod were reared individually in 96-well microplate exposures to parent and degradates of the phenylpyrazole insecticide fipronil. Survival, development rates, sex ratio change, fertility, fecundity, and hatching success were tracked daily for 32 d through mating and production of three broods in spiked seawater. These data were then inserted in a Leslie (Lefkovitch) matrix stage-based population growth model to predict relative rates of population increase (lambda) and changes in net population growth with time and toxicant concentration. Field-reported test concentrations produced strong reproductive (52-88%) and net production (40-80%) depressions for parent (at 0.25 and 0.5 microg/L), desthionyl (0.25 and 0.5 microg/L), and sulfide (0.15 microg/L) moieties as compared to controls. Spiked sediment exposures of 65-300 ng of fipronil/g of dry sediment yielded significantly reduced production rates per female that were 67-50% of control production. The consistent reproductively linked impacts of fipronil and its degradation products at the population maintenance levels suggest risks to sediment-dwelling crustaceans at concentrations well below noneffects for most aquatic test species based on risk assessment data from primarily acute and sub-life cycle toxicity tests.

A new method for the speciation of ng/mL concentrations of Cr(III) and Cr(VI) solutions with analysis by laser-induced breakdown spectroscopy (LIBS) is reported. Speciation is achieved by pre-concentration of the chromium onto commercially available cation exchange polymer membranes. Chromium(III) is removed directly by cation exchange; chromium(VI) in the filtrate is reduced to Cr(III) and concentrated onto a second cation exchange membrane, affording independent measurement of both species. Large volumes of waters containing Cr(III) and Cr(VI) can be concentrated onto the membranes and directly analyzed by laser-induced breakdown spectroscopy. The estimated limit of detection corresponds to 500 ng of Cr on the membrane: if a solution volume of 1 L is used, then the detection limit corresponds to a solution concentration of 0.5 ng/mL. Excellent separation of the chromium species is attained. Results show that overall method efficiencies range from 94-116% and are independent of the matrix. The influence of pH has been measured, and although Cr(VI) converts to Cr(III) in acidic solutions, the total Cr recoveries are not appreciably influenced by pH over the range of natural waters (4 to 9). In addition, speciation was performed in the presence of a number of different cations and showed that the method is robust in many different and complex matrices.

Resonance-enhanced multiphoton ionization ͑REMPI͒ is investigated as a potential technique for realtime monitoring of selected volatile organochloride compounds ͑VOCs͒. In a proof-of-concept experiment, the progress of the reductive-degradation of tetrachloroethylene ͑PCE͒ to trichloroethylene ͑TCE͒ by zero-valent zinc was monitored by REMPI measurements performed in the headspace above the PCE solution. Two-photon resonant REMPI spectra of TCE and PCE were recorded over the wavelength range 305-320 nm. The concentrations of PCE and TCE in the headspace were monitored by measurement of the ionization signal with 315.64-and 310.48-nm excitation for PCE and TCE, respectively. Calibration curves yielded a linear range of more than 2 orders of magnitude for both compounds. The REMPI headspace results agreed well with the solution-phase results from gas chromatography analysis, which was used for independent verification of the progress of the reaction.

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Signal enhncement, limits of detection, and relevance to environmental concentrations for metals and metal ions in aqueous solution using combined 1064 nm nanosecond and 800 nm femtosecond pulses in dual-pulse LIBS will be presented.