ALBERT

Description: High-resolution laboratory-based thermal infrared spectroscopy is an up-and-coming tool in the field of geological remote sensing. Its spatial resolution allows for detailed analyses at centimeter to sub-millimeter scales. However, this increase in resolution creates challenges with sample characteristics, such as grain size, surface roughness, and porosity, which can influence the spectral signature. This research explores the effect of rock sample surface preparation on the thermal infrared spectral signatures. We applied three surface preparation methods (split, saw, and polish) to determine how the resulting differences in surface roughness affects both the spectral shape as well as the spectral contrast. The selected samples are a pure quartz sandstone, a quartz sandstone containing a small percentage of kaolinite, and an intermediate-grained gabbro. To avoid instrument or measurement type biases we conducted measurements on three TIR instruments, resulting in directional hemispherical reflectance spectra, emissivity spectra and bi-directional reflectance images. Surface imaging and analyses were performed with scanning electron microscopy and profilometer measurements. We demonstrate that surface preparation affects the TIR spectral signatures influencing both the spectral contrast, as well as the spectral shape. The results show that polished surfaces predominantly display a high spectral contrast while the sawed and split surfaces display up to 25% lower reflectance values. Furthermore, the sawed and split surfaces display spectral signature shape differences at specific wavelengths, which we link to mineral transmission features, surface orientation effects, and multiple reflections in fine-grained minerals. Hence, the influence of rock surface preparation should be taken in consideration to avoid an inaccurate geological interpretation.

Description: Minerals, Vol. 8, Pages 259: Near-Infrared Spectroscopy of Hydrothermal versus Low-Grade Metamorphic Chlorites Minerals doi: 10.3390/min8060259 Authors: Oscar M. Kamps Frank J.A. van Ruitenbeek Paul R.D. Mason Freek D. van der Meer Although the composition of chlorite group minerals represents a known proxy for conditions in various geological environments, few comparative studies of chlorites from different geological environments have been carried out. In this study, we compare chlorites from a hydrothermal system with those formed under low-grade metamorphic conditions. Both sets of samples were collected from the Pilbara Craton, Western Australia. Near-infrared (NIR) spectroscopy was used to determine if spectral differences record compositional differences between chlorites from the two geological environments. The spectra showed a significant difference in the Mg-OH absorption wavelength, near 2350 nm, with the hydrothermal group showing longer absorption wavelengths than the metamorphic one. A comparison of the spectral data with geochemical analyses showed a relation between the absorption wavelength and the magnesium-to-iron ratio (magnesium number) of chlorite, as well as the bulk rock composition. Metamorphic rocks have a higher magnesium-to-iron ratio than the hydrothermal ones, predominantly explained by differences in the degree of metasomatism. In the hydrothermal system, mass transfer changes the bulk rock composition while for the metamorphic samples the original bulk chemistry determines the current composition of the rock.

Description: Sentinel-2A MSI is the Landsat-like spatial resolution (10–60 m) super-spectral instrument of the European Space Agency (ESA), aimed at additional data continuity for global land surface monitoring with Landsat and Satellite Pour l’Observation de la Terre (SPOT) missions. Several simulation studies have been conducted in the last several years to show the potential of Sentinel-2A MSI (MultiSpectral Instrument). Now that real data are available, the first confirmations of this potential and comparisons with other operational systems are being made. This paper aims at evaluating Sentinel-2A MSI band ratio products that are relevant for geological remote sensing. A Sentinel-2A MSI and a Landsat 8 OLI (Operational Land Imager) scene were processed from their respective levels L1C and L1T to level L2A (bottom of atmosphere reflectance). Then, three band ratios originally defined for Landsat TM (Thematic Mapper) were used to map mineralogy associated with a hydrothermal alteration system in southeast Spain. The results obtained with Sentinel-2A MSI were compared with those obtained with Landsat 8 OLI and a simulated Sentinel-2A MSI dataset that was used before actual data were released. Results show that the images appear similar to the human eye having a correlation of approximately 0.8 and higher, but that the associated data ranges differ significantly. The resulting products are also compared to a published geologic map of the study area, and it is shown that the resulting maps correspond with the conceptual geologic model of the epithermal deposit.

Description: Shortwave infrared (SWIR) spectroscopy can be applied directly to analyze the mineral chemistry of raw or geologic materials. It provides diagnostic spectral characteristics of the chemical composition of minerals, information that is invaluable for the identification and quality control of such materials. The present study aims to investigate the potential of SWIR spectroscopy as an alternative quality control technique for the mineral chemistry analysis of Portland cement-grade limestone. We used the spectroscopic (wavelength position and depth of absorption feature) and geochemical characteristics of limestone samples to estimate the abundance and composition of carbonate and clay minerals on rock surfaces. The depth of the carbonate (CO3) and Al-OH absorption features are linearly correlated with the contents of CaO and Al2O3 in the samples, respectively, as determined by portable X-ray fluorescence (PXRF) measurements. Variations in the wavelength position of CO3 and Al-OH absorption features are related to changes in the chemical compositions of the samples. The results showed that the dark gray and light gray limestone samples are better suited for manufacturing Portland cement clinker than the dolomitic limestone samples. This finding is based on the CaO, MgO, Al2O3, and SiO2 concentrations and compositions. The results indicate that SWIR spectroscopy is an appropriate approach for the chemical quality control of cement raw materials.

Description: The soil minerals determine essential soil properties such as the cation exchange capacity, texture, structure, and their capacity to form bonds with organic matter. Any alteration of these organo-mineral interactions due to the soil moisture variations needs attention. Visible near-infrared imaging spectroscopy is capable of assessing spectral soil constituents that are responsible for the organo-mineral interactions. In this study, we hypothesized that the alterations of the surface soil mineralogy occur due to the moisture variations. For eight weeks, under laboratory conditions, imaging spectroscopy data were collected on a 72 h basis for three Silty Loam soils varying in the organic matter (no, low and high) placed at the drying-field capacity, field capacity and waterlogging-field capacity treatments. Using the Spectral Information Divergence image classifier, the image area occupied by the Mg-clinochlore, goethite, quartz coated 50% by goethite, hematite dimorphous with maghemite was detected and quantified (percentage). Our results showed these minerals behaved differently, depending on the soil type and soil treatment. While for the soils with organic matter, the mineralogical alterations were evident at the field capacity state, for the one with no organic matter, these changes were insignificant. Using imaging spectroscopy data on the Silty Loam soil, we showed that the surface mineralogy changes over time due to the moisture conditions.

Description: The soil minerals determine essential soil properties such as the cation exchange capacity, texture, structure, and their capacity to form bonds with organic matter. Any alteration of these organo-mineral interactions due to the soil moisture variations needs attention. Visible near-infrared imaging spectroscopy is capable of assessing spectral soil constituents that are responsible for the organo-mineral interactions. In this study, we hypothesized that the alterations of the surface soil mineralogy occur due to the moisture variations. For eight weeks, under laboratory conditions, imaging spectroscopy data were collected on a 72 h basis for three Silty Loam soils varying in the organic matter (no, low and high) placed at the drying-field capacity, field capacity and waterlogging-field capacity treatments. Using the Spectral Information Divergence image classifier, the image area occupied by the Mg-clinochlore, goethite, quartz coated 50% by goethite, hematite dimorphous with maghemite was detected and quantified (percentage). Our results showed these minerals behaved differently, depending on the soil type and soil treatment. While for the soils with organic matter, the mineralogical alterations were evident at the field capacity state, for the one with no organic matter, these changes were insignificant. Using imaging spectroscopy data on the Silty Loam soil, we showed that the surface mineralogy changes over time due to the moisture conditions.

Description: High-resolution laboratory-based thermal infrared spectroscopy is an up-and-coming tool in the field of geological remote sensing. Its spatial resolution allows for detailed analyses at centimeter to sub-millimeter scales. However, this increase in resolution creates challenges with sample characteristics, such as grain size, surface roughness, and porosity, which can influence the spectral signature. This research explores the effect of rock sample surface preparation on the thermal infrared spectral signatures. We applied three surface preparation methods (split, saw, and polish) to determine how the resulting differences in surface roughness affects both the spectral shape as well as the spectral contrast. The selected samples are a pure quartz sandstone, a quartz sandstone containing a small percentage of kaolinite, and an intermediate-grained gabbro. To avoid instrument or measurement type biases we conducted measurements on three TIR instruments, resulting in directional hemispherical reflectance spectra, emissivity spectra and bi-directional reflectance images. Surface imaging and analyses were performed with scanning electron microscopy and profilometer measurements. We demonstrate that surface preparation affects the TIR spectral signatures influencing both the spectral contrast, as well as the spectral shape. The results show that polished surfaces predominantly display a high spectral contrast while the sawed and split surfaces display up to 25% lower reflectance values. Furthermore, the sawed and split surfaces display spectral signature shape differences at specific wavelengths, which we link to mineral transmission features, surface orientation effects, and multiple reflections in fine-grained minerals. Hence, the influence of rock surface preparation should be taken in consideration to avoid an inaccurate geological interpretation.