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John Michael Meyer

Publications and source records attributed to John Michael Meyer.

8 recordsLinked to original sources

USGS addresses needs for lithium calibration and quality control materials for pLIBS analysis

Lithium (Li) is a globally important commodity used for energy storage, national defense, human health, and advanced technologies. Lithium resource development requires identifying deposits with elevated concentrations and optimal mineralogy, typically associated with select clays and pegmatites. Lithium is a light, highly reactive alkali metal with low atomic mass that is difficult to detect and quantify using conventional portable geochemical techniques such as X-ray fluorescence (XRF). However, portable laser-induced breakdown spectroscopy (pLIBS) is a powerful analytical technique for lithium exploration due to its ability to analyze solids quickly with minimal preparation. The expanded utility of pLIBS is hampered by the lack of matrix-matched calibration and quality control (QC) materials. The United States Geological Survey (USGS) has developed in-house lithium calibration and QC materials for lithium in clay and pegmatite matrices to address this limitation. We present the workflow and implementation of a custom-built matrix specific calibration on a SciAps Z-300 pLIBS, using proprietary Profile Builder software. The implementation of the custom calibration and quality control standards enables us to collect semiquantitative results directly from the pLIBS while in the field. Ultimately, this calibration has improved confidence in sample selection and collection in the field, providing more efficient site characterization.

Conference Paper↗

Hyperspectral mapping of magmatic-hydrothermal sericite, Battle Mountain mining district, Nevada

We demonstrate the utility of multi-scale imaging spectroscopy data (hyperspectral data) to differentiate magmatic-hydrothermal sericite from other white micas based on grain size, in a case study of the Battle Mountain mining district in Humboldt and Lander Counties, Nevada. The Battle Mountain mining district contains porphyry, skarn, and distal disseminated deposits that formed in magmatic-hydrothermal systems, as well as sedimentary-rock hosted gold deposits of less certain origin. We generated spectral-based mineral maps of the Battle Mountain mining district to examine the spatial distribution of spectrally dominant minerals such as kaolinite, montmorillonite , and white micas (muscovite, sericite, and illite). We then used spectral-based mineral mapping to characterize the grain size and composition of white micas, enabling us to differentiate igneous muscovite from magmatic-hydrothermal sericite. By integrating our spectral-based maps with geologic mapping, airborne aeromagnetic data, and prior studies on mines and deposits in Battle Mountain, we determined that finer grained, higher Al sericite spatially correlated with the footprints of known magmatic-hydrothermal systems and is interpreted as forming from magmatic-hydrothermal alteration. Larger grained, lower Al muscovites are distal from known magmatic-hydrothermal systems and are interpreted as being igneous derived siliciclastic sediments that became constituents of the host sedimentary rocks. Techniques described in this contribution can be applied to any appropriate hyperspectral data, regardless of sensor type used to collect the data.

Nevada↗

On-orbit calibration and performance of the EMIT imaging spectrometer

The Earth surface Mineral dust source InvesTigation (EMIT) is a remote visible to shortwave infrared (VSWIR) imaging spectrometer that has been operating onboard the International Space Station since July 2022. This article describes EMIT's on-orbit spectroradiometric calibration and validation. Accurate spectroscopy is vital to achieve consistent mapping results with orbital imaging spectrometers. EMIT takes a unique approach to this challenge, with just six optical elements, no shutter, and no onboard calibration systems. Its simple design focuses on uniformity and stability to enable vicarious spectroradiometric calibration. Our experiments demonstrate that this approach is successful, approaching the fidelity of manual field spectroscopy in some cases, and enabling new and more accurate products across diverse Earth science disciplines. EMIT achieves several notable firsts for an instrument of its class. It demonstrates successful on-orbit adjustments of Focal Plane Array (FPA) alignment with sub-micron precision. It offers spectral uniformity better than 98%. Optical artifacts in the measurement channels are at least three orders of magnitude below the primary solar-reflected surface signals. Its noise performance enables percent-level discrimination in the depths of mineral absorption features. In these aspects, EMIT satisfies the stringent performance needs for the next generation of VSWIR imaging spectrometers to observe the Earth's ecosystems, geology , and water resources.

Remote Sensing of Environment↗

An accuracy assessment of the surface reflectance product from the EMIT imaging spectrometer

The Earth surface Mineral dust source InvesTigation (EMIT) is an imaging spectrometer launched to the International Space Station in July 2022 to measure the mineral composition of Earth’s dust-producing regions. We present a systematic accuracy assessment of the EMIT surface reflectance product in two parts. First, we characterize the surface reflectance product’s overall performance using multiple independent vicarious calibration field experiments with hand-held and automated field spectrometers. We find that the EMIT surface reflectance product has a standard error of ±1.0 % in absolute reflectance units for temporally coincident observations. Discrepancies rise to ±2.7 % for spectra acquired at different dates and times of day, which we attribute mainly to changes in solar geometry. Second, we develop an error budget that explains the differences between EMIT and in-situ field spectrometer data. We find that uncertainties in spatial footprints, field spectroscopy, and the EMIT-reported measurement were sufficient to explain discrepancies in most cases. Our approach did not detect any systematic calibration or reflectance errors in the timespan considered. Together, these findings demonstrate that a space-based imaging spectrometer can acquire high-quality spectra across a wide range of observational and atmospheric conditions.

Nevada↗

Hyperspectral remote sensing of white mica: A review of imaging and point-based spectrometer studies for mineral resources, with spectrometer design considerations

Over the past ~30 years, hyperspectral remote sensing of chemical variations in white mica have proven to be useful for ore deposit studies in a range of deposit types. To better understand mineral deposits and to guide spectrometer design, this contribution reviews relevant papers from the fields of remote sensing, spectroscopy, and geology that have utilized spectral changes caused by chemical variation in white micas. This contribution reviews spectral studies conducted at the following types of mineral deposits: base metal sulfide, epithermal, porphyry, sedimentary rock hosted gold deposits, orogenic gold, iron oxide copper gold, and unconformity-related uranium. The structure, chemical composition, and spectral features of white micas, in this contribution defined as muscovite, paragonite, celadonite, phengite, illite, and sericite, are given. Reviewed laboratory spectral studies determined that shifts in the position of the white mica 2200 nm combination feature of 1 nm correspond to a change in Al oct content of approximately ±1.05%. Many of the reviewed spectral studies indicated that a shift in the position of the white mica 2200 nm combination feature of 1 nm was geologically significant. A sensitivity analysis of spectrometer characteristics; bandpass, sampling interval, and channel position, is conducted using spectra of 19 white micas with deep absorption features to determine minimum characteristics required to accurately measure a shift in the position of the white mica 2200 nm combination feature. It was determined that a sampling interval < 16.3 nm and bandpass <17.5 nm are needed to achieve a root mean square error (RMSE) of 2 nm, whereas a sampling interval < 8.8 nm and bandpass <9.8 nm are needed to achieve a RMSE of 1 nm. For comparison, commonly used imaging spectrometers HyMap, AVIRIS-Classic, SpecTIR®'s AisaFENIX 1K, and HySpex tm SWIR 384 have 2.1, 1.2, 0.96, and 0.95 nm RMSE in determining the position of the 2200 nm white mica combination feature, respectively. An additional sensitivity analysis is conducted to determine the effect of signal to noise ratio (SNR) on the RMSE of the position of the white mica 2200 nm combination feature, using spectra of 18 white micas with deep absorption features. For a spectrometer with sampling interval and bandpass of 1 nm, we estimate that RMSEs of 1 and 1.5 nm are achievable with spectra having a minimum SNR of approximately 246 and 64, respectively. For a spectrometer with sampling interval and bandpass of 5 nm, we estimate that RMSEs of 1 and 1.5 nm are attainable with spectra having a minimum SNR of approximately 431 and 84, respectively. When using a spectrometer with a sampling interval 8.8 nm and a bandpass of 9.8 nm, a RMSE of 1 is only achievable with convolved, noiseless reference spectra. For the 8.8_9.8 nm spectrometer, spectra with SNR of 250 and 100 result in RMSE of 1.1 and 1.3, respectively. Therefore, fine spectral resolution characteristics achieve RMSEs better than 1 nm for high SNR spectra while spectrometers with coarse spectral resolution have larger RMSE, perform well with noisy data, and are useful for white mica studies if RMSE of 1.1 to 1.5 nm is acceptable.

Remote Sensing of Environment↗

Mineral Mapping of the Battle Mountain District, Nevada, USA, Using AVIRIS-Classic and SpecTIR Inc. AisaFENIX 1K Imaging Spectrometer Datasets

Imaging spectroscopy (hyperspectral imaging) has been used to successfully map minerals at the outcrop, deposit, district, and regional scale. This contribution presents spectral-based mineral maps of the Battle Mountain mining district, Nevada, USA, generated using multi-scale airborne imaging and ground-based point spectrometers. Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) and AisaFENIX 1K imaging spectrometer data were processed using Atmospheric and Topographic Correction (ATCOR-4) software with an empirical correction multiplier derived from field data. Data were used to generate spectral-based mineral maps with spatial resolutions of 13.5 and 1.8 m. A comparison of the various radiative transfer models used to convert radiance data to reflectance indicated that the ATCOR4 rugged model performed best for these datasets. These mineral maps were then used to spectrally characterize two potential porphyry mineral targets in the district.

Nevada↗

Multiscale hyperspectral imaging of hydrothermal alteration in Yellowstone National Park, USA

Imaging spectroscopy (hyperspectral imaging) data have mainly been used to map surface materials covering relatively small areas from airborne sensors over the past 20+ years. As part of the U.S. Geological Survey Integrated hyperspectral, geophysical and geochemical studies of Yellowstone National Park hydrothermal systems project, we have collected multiscale imaging spectrometer data including borehole core, field, and airborne data. These data give us the unique opportunity to map subsurface and surface alteration of shallow epithermal systems at scales ranging from microns to meters per pixel. Airborne Visible and Infrared Imaging Spectrometer (AVIRIS), Corescan HCI-3, HySpex VNIR-1800 and SWIR-384 imaging spectrometers, and a Riegl VZ-2000i terrestrial lidar system were used in this study. Maps utilizing spectral analysis of multiscale hyperspectral data indicate the presence of mineral assemblages consistent with epithermal deposits. Minerals such as alunite, hydrated silica, and kaolinite typically form in steam-heated cap systems and can be found in core and AVIRIS data. At depth, higher temperature fluids that are less acidic produce mixed-layer kaolinite with clay/muscovite and then montmorillonite and muscovite towards the bottom of the borehole. This transition can be seen in AVIRIS and field data at the Grand Canyon of the Yellowstone and in borehole Corescan data at Y-12 Norris-Ii R874. Instrument specifications, collection parameters, and setup for data acquisition will be discussed as well as mapping software and preliminary results.

Idaho, Montana, Wyoming↗

Imaging spectroscopy applied to mineral mapping over large areas: Impact of residual atmospheric artefacts in reflectance spectra on mineral identification and mapping

Around the world, imaging spectroscopy (hyperspectral imaging) has been successfully applied to mapping surface minerals over small areas. In this paper, we examine one challenge to reliably mapping surface mineral composition over large areas: the impacts of atmospheric artefacts in reflectance spectra on mineral identification. To examine these impacts, we use a set of Airborne Visible and Infrared Imaging Spectrometer-Classic (AVIRISc) data collected over ~30,000 sq. km of southern California (SoCal) in 2018. The AVIRISc2018 SoCal reflectance data showed residual atmospheric contamination in wavelength regions at the edges of strong water vapor absorption features: 1.44-1.5 µm, 1.75-1.8 µm, and 2.35-2.5 µm. These three regions of atmospheric residuals affect identification and discrimination of mineral absorption features, especially when mineral abundances are low and spectral features are weak. Of these three regions, improving atmospheric correction of imaging spectrometer data in the 2.35-2.5 µm region will result in the most enhancement in mineral identification, discrimination, and mapping. An additional region near 2.2 µm affects phyllosilicate mineral identification. The cause of the distorted reflectance in this region is still being investigated.

Conference Paper↗