ALBERT

Description: Reflectance spectra of carbonate minerals in the shortwave infrared (SWIR) and thermal infrared (TIR) wavelength regions contain a number of diagnostic absorption features. The shape of these features depends on various physical and chemical parameters. To accurately identify carbonate minerals or rocks in pure and mixed form, it is necessary to analyze the effects of the parameters on spectral characteristics. In this study, we analyzed spectral absorption feature characteristics of calcite and dolomite in the SWIR (features at 2.3 and 2.5 μm) and TIR (features at 11.5 and 14 μm) wavelength regions, as a function of grain size and carbonate mineral mixtures. Results showed that varying grain sizes and mineral contents in the sample, influence reflectance values and absorption feature characteristics. Absorption band positions of pure and mixed calcite and dolomite in the SWIR and TIR regions for both features were displaced slightly as observed in previous studies. The band positions of calcite and dolomite varied relative to grain size only in the TIR region. These positions shifted to longer wavelengths for the feature at 11.5 μm and to shorter wavelengths for the feature at 14 μm from fine to coarse grain size. The band positions of calcite-dolomite mixtures in the SWIR and TIR regions were determined by the quantity of calcite and dolomite in the sample. These results can be applied for the identification of pure and mixed calcite and dolomite, as well as estimating the relative abundance of both minerals with different grain size and mineral mixtures in a synthetic sample or rock. They can also be used as a preliminary proxy for assessing dolomitization patterns in carbonate rocks.

Description: In this article we describe a new instrumental setup at the University of Twente Faculty ITC with an optimized processing chain to measure absolute directional-hemispherical reflectance values of typical earth science samples in the 2.5 to 16 µm range. A Bruker Vertex 70 FTIR spectrometer was chosen as the base instrument. It was modified with an external integrating sphere with a 30 mm sampling port to allow measuring large, inhomogeneous samples and quantitatively compare the laboratory results to airborne and spaceborne remote sensing data. During the processing to directional-hemispherical reflectance values, a background radiation subtraction is performed, removing the effect of radiance not reflected from the sample itself on the detector. This provides more accurate reflectance values for low-reflecting samples. Repeat measurements taken over a 20 month period on a quartz sand standard show that the repeatability of the system is very high, with a standard deviation ranging between 0.001 and 0.006 reflectance units depending on wavelength. This high level of repeatability is achieved even after replacing optical components, re-aligning mirrors and placement of sample port reducers. Absolute reflectance values of measurements taken by the instrument here presented compare very favorably to measurements of other leading laboratories taken on identical sample standards.

Description: The development of advanced laboratory-based imaging hyperspectral sensors, such as SisuCHEMA, has created an opportunity to extract compositional information of mineral mixtures from spectral images. Determining proportions of minerals on rock surfaces based on spectral signature is a challenging approach due to naturally-occurring minerals that exist in the form of intimate mixtures, and grain size variations. This study demonstrates the application of SisuCHEMA hyperspectral data to determine mineral components in hand specimens of carbonate rocks. Here, we applied wavelength position, spectral angle mapper (SAM) and linear spectral unmixing (LSU) approaches to estimate the chemical composition and the relative abundance of carbonate minerals on the rock surfaces. The accuracy of these classification methods and correlation between mineral chemistry and mineral spectral characteristics in determining mineral constituents of rocks are also analyzed. Results showed that chemical composition (Ca-Mg ratio) of carbonate minerals at a pixel (e.g., sub-grain) level can be extracted from the image pixel spectra using these spectral analysis methods. The results also indicated that the spatial distribution and the proportions of calcite-dolomite mixtures on the rock surfaces vary between the spectral methods. For the image shortwave infrared (SWIR) spectra, the wavelength position approach was found to be sensitive to all compositional variations of carbonate mineral mixtures when compared to the SAM and LSU approaches. The correlation between geochemical elements and spectroscopic parameters also revealed the presence of these carbonate mixtures with various chemical compositions in the rock samples. This study concludes that the wavelength position approach is a stable and reproducible technique for estimating carbonate mineral chemistry on the rock surfaces using laboratory-based hyperspectral data.

Description: Hydrocarbon seeps cause chemical and mineralogical changes at the surface, which can be detected by remote sensing. This paper aims at the detection of mineral alteration induced by gas seeps in a marly limestone formation, SW Iran. For this purpose, the multispectral Advance Spaceborne Thermal Emission and Reflection Radiometer (ASTER) and the high spatial resolution WorldView-2 (WV-2) data were utilized for mapping surficial rock alteration. In addition, the potential of Visible Near Infrared (VNIR) bands of the WV-2 and its high spatial resolution for mapping alterations was determined. Band ratioing, principal component analysis (PCA), data fusion and the boosted regression trees (BRT) were applied to enhance and classify the altered and unaltered marly limestone formation. The alteration zones were identified and mapped by remote sensing analyses. Integrating the WV-2 into the ASTER data improved the spatial accuracy of the BRT classifications. The results showed that the BRT classification of the multiple band imagery (created from ASTER and WV-2) using regions of interest (ROIs) around field data provides the best discrimination between altered and unaltered areas. It is suggested that the WV-2 dataset can provide a potential tool along higher spectral resolution data for mapping alteration minerals related to hydrocarbon seeps in arid and semi-arid areas.

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: Reflectance spectra of carbonate minerals in the shortwave infrared (SWIR) and thermal infrared (TIR) wavelength regions contain a number of diagnostic absorption features. The shape of these features depends on various physical and chemical parameters. To accurately identify carbonate minerals or rocks in pure and mixed form, it is necessary to analyze the effects of the parameters on spectral characteristics. In this study, we analyzed spectral absorption feature characteristics of calcite and dolomite in the SWIR (features at 2.3 and 2.5 μm) and TIR (features at 11.5 and 14 μm) wavelength regions, as a function of grain size and carbonate mineral mixtures. Results showed that varying grain sizes and mineral contents in the sample, influence reflectance values and absorption feature characteristics. Absorption band positions of pure and mixed calcite and dolomite in the SWIR and TIR regions for both features were displaced slightly as observed in previous studies. The band positions of calcite and dolomite varied relative to grain size only in the TIR region. These positions shifted to longer wavelengths for the feature at 11.5 μm and to shorter wavelengths for the feature at 14 μm from fine to coarse grain size. The band positions of calcite-dolomite mixtures in the SWIR and TIR regions were determined by the quantity of calcite and dolomite in the sample. These results can be applied for the identification of pure and mixed calcite and dolomite, as well as estimating the relative abundance of both minerals with different grain size and mineral mixtures in a synthetic sample or rock. They can also be used as a preliminary proxy for assessing dolomitization patterns in carbonate rocks.

Description: IJERPH, Vol. 14, Pages 1059: Distribution of Non-Persistent Endocrine Disruptors in Two Different Regions of the Human Brain International Journal of Environmental Research and Public Health doi: 10.3390/ijerph14091059 Authors: Thomas P. van der Meer Francisco Artacho-Cordón Dick F. Swaab Dicky Struik Konstantinos C. Makris Bruce H. R. Wolffenbuttel Hanne Frederiksen Jana V. van Vliet-Ostaptchouk Non-persistent endocrine disrupting chemicals (npEDCs) can affect multiple organs and systems in the body. Whether npEDCs can accumulate in the human brain is largely unknown. The major aim of this pilot study was to examine the presence of environmental phenols and parabens in two distinct brain regions: the hypothalamus and white-matter tissue. In addition, a potential association between these npEDCs concentrations and obesity was investigated. Post-mortem brain material was obtained from 24 individuals, made up of 12 obese and 12 normal-weight subjects (defined as body mass index (BMI) > 30 and BMI < 25 kg/m2, respectively). Nine phenols and seven parabens were measured by isotope dilution TurboFlow-LC-MS/MS. In the hypothalamus, seven suspect npEDCs (bisphenol A, triclosan, triclocarban and methyl-, ethyl-, n-propyl-, and benzyl paraben) were detected, while five npEDCs (bisphenol A, benzophenone-3, triclocarban, methyl-, and n-propyl paraben) were found in the white-matter brain tissue. We observed higher levels of methylparaben (MeP) in the hypothalamic tissue of obese subjects as compared to controls (p = 0.008). Our findings indicate that some suspected npEDCs are able to cross the blood–brain barrier. Whether the presence of npEDCs can adversely affect brain function and to which extent the detected concentrations are physiologically relevant needs to be further investigated.

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: Remote sensing has shown its potential to assess soil properties and is a fast and non-destructive method for monitoring soil surface changes. In this paper, we monitor soil aggregate breakdown under natural conditions. From November 2014 to February 2015, images and weather data were collected on a daily basis from five soils susceptible to detachment (Silty Loam with various organic matter content, Loam and Sandy Loam). Three techniques that vary in image processing complexity and user interaction were tested for the ability of monitoring aggregate breakdown. Considering that the soil surface roughness causes shadow cast, the blue/red band ratio is utilized to observe the soil aggregate changes. Dealing with images with high spatial resolution, image texture entropy, which reflects the process of soil aggregate breakdown, is used. In addition, the Huang thresholding technique, which allows estimation of the image area occupied by soil aggregate, is performed. Our results show that all three techniques indicate soil aggregate breakdown over time. The shadow ratio shows a gradual change over time with no details related to weather conditions. Both the entropy and the Huang thresholding technique show variations of soil aggregate breakdown responding to weather conditions. Using data obtained with a regular camera, we found that freezing–thawing cycles are the cause of soil aggregate breakdown.

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.