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Natural samples of the rare earth element (REE)-bearing silicate minerals cerite, mosandrite, kainosite, zircon, and eudialyte were studied using reflectance spectroscopy in the visible to short-wave infrared regions (500 to 2500 nm) and further characterized by scanning electron microscopy and electron microprobe analysis. Spectral features of these minerals are driven primarily by 4f-4f intraconfigurational electronic transitions of trivalent lanthanides, as well as 5f-5f electronic transitions of uranium and vibrational overtones and combinations of H2O and OH–. Spectra of eudialyte are also impacted by relative amounts of IVFe2+ and VFe2+. Respective spectra of these REE-bearing silicate minerals are sufficiently distinct to enable spectral classification. Spectral variability (e.g., band depths and locations) of some specific REE-related absorptions, such as an Er3+- and Yb3+-related absorption near 978 nm and Nd3+-related absorptions near 746, 803, and 875 nm, are interpreted to be driven by cation site differences in the crystal structures. This work adds to the growing understanding of REE-bearing mineral reflectance spectroscopy, which facilitates detection, identification, and quantification of REE-bearing silicate minerals in remote sensing applications. This is especially relevant for hyperspectral imaging spectroscopy with high spatial resolutions where the spectral response of a pixel becomes increasingly dominated by mineralogy rather than lithology. [ABSTRACT FROM AUTHOR]

Reflectance spectroscopy in the visible to short-wave infrared regions (500 to 2500 nm) was carried out using natural samples of the rare earth element (REE) phosphate minerals monazite, xenotime, and britholite. Samples were characterized by scanning electron microscopy and electron microprobe analysis. Absorption band positions were recorded with their probable origins, and spectral variability among the samples is discussed. Spectral features of these minerals are driven primarily by 4f-4f intraconfigurational electronic transitions of trivalent lanthanides. The distinct REE distributions of monazite, xenotime, and britholite drive their bulk spectral patterns, which in turn are sufficiently distinct to enable spectral classification. Spectral variability of some specific REE-related absorptions are interpreted to be driven by differences of the coordination polyhedra for the lanthanide cations between the crystal structures. Spectra of these minerals were also compared against carbonatitehosted REE bearing fluorapatite. The work presented here strengthens the growing foundation for the interpretation of reflectance spectra of these REE phosphate minerals and enables exploitation of the observed features by the remote sensing community for detection, identification, and quantification of REE phosphate minerals. This is especially relevant for hyperspectral imaging spectroscopy with high spatial resolution, where the spectral response of a pixel becomes increasingly dominated by mineralogy. [ABSTRACT FROM AUTHOR]

Abstract: After leaves are clipped their reflectance properties change over time at variable rates. Spectral change can in part be attributed to the changing water content of the leaf, which affects absorption in the VIS, NIR and the SWIR. Maintaining water volume within samples has been the motivation behind many leaf handling techniques. This study has assessed the time constraints between leaf collection and spectral measurement. Specifically the relationship between leaf water content and foliar spectra (350–2500 nm) was examined over time for five tropical trees (common guava (Psidium guajava), purple guava (Psidium littorale), weeping fig (Ficus benjamina), floss silk (Chorisia speciosa), and coffee (Coffea arabica)). This investigation was carried for leaves wrapped with moist gauze around their petiole (treatment leaves) and leaves with no treatment. Spectral measurements and mass measurements were repeated for each leaf once every hour for the first 12 h, then every 4–6 h for 18 h, followed by one measurement after 12 h, and finally once a day until the control samples became air-dry. Foliar reflectance in the visible spectrum was not immediately responsive to water content changes and did not change until wilting of the leaf was observed. The NIR and SWIR wavelength regions were affected immediately by small changes in water content. Thus, by the time wilting was first observed the NIR and SWIR foliar reflectance differed considerably from corresponding fresh leaf reflectance. No common time limit could be observed for leaf clipping and reflectance measurement. Leaves have a variety of water contents and dehydration rates hence measurement time constraints are dependent on the properties of the leaf or species. Rather than using a time limit it is recommended that leaf handling techniques be based upon managing leaf water content and leaf structure. The results of this study indicate that leaves with petioles wrapped in moist paper towel and placed within plastic bags will maintain leaf reflectance longer than equivalent leaves without treatment; samples tested here lasted a minimum of 7 days. θ and D indices (“angle difference” and “root mean square difference”, respectively) revealed a stronger relationship between leaf water content and spectral shape than between leaf water and raw reflectance magnitude. The ratio of 1187/1096 nm, when compared with θ and D indices and individual reflectance bands, showed the highest coefficient of determination with leaf water content (r 2 =0.952). [Copyright &y& Elsevier]