Geology topics

Roger N. Clark

Publications and source records attributed to Roger N. Clark.

At least 19 recordsLinked to original sources

USGS2024

Evidence for low-grade metamorphism, hydrothermal alteration, and diagenesis on Mars from phyllosilicate mineral assemblages

The enhanced spatial and spectral resolution provided by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) on the Mars Reconnaissance Orbiter (MRO) has led to the discovery of numerous hydrated silicate minerals on Mars, particularly in the ancient, cratered crust comprising the southern highlands. Phases recently identified using visible/near-infrared spectra include: smectite, chlorite, prehnite, high-charge phyllosilicates (illite or muscovite), the zeolite analcime, opaline silica, and serpentine. Some mineral assemblages represent the products of aqueous alteration at elevated temperatures. Geologic occurrences of these mineral assemblages are described using examples from west of the Isidis basin near the Nili Fossae and with reference to differences in implied temperature, fluid composition, and starting materials during alteration. The alteration minerals are not distributed homogeneously. Rather, certain craters host distinctive alteration assemblages: (1) prehnite-chlorite-silica, (2) analcime-silica-Fe,Mg-smectite-chlorite, (3) chlorite-illite (muscovite), and (4) serpentine, which furthermore has been found in bedrock units. These assemblages contrast with the prevalence of solely Fe,Mg-smectites in most phyllosilicate-bearing terrains on Mars, and they represent materials altered at depth then exposed by cratering. Of the minerals found to date, prehnite provides the clearest evidence for subsurface, hydrothermal/metamorphic alteration, as it forms only under highly restricted conditions ( T = 200–400ºC). Multiple mechanisms exist for forming the other individual minerals; however, the most likely formation mechanisms for the characteristic mineralogic assemblages observed are, for (1) and (2), low-grade metamorphism or hydrothermal (<400ºC) circulation of fluids in basalt; for (3), transformation of trioctahedral smectites to chlorite and dioctahedral smectites to illite during diagenesis; and for (4), low-grade metamorphism or hydrothermal (<400ºC) circulation of fluids in ultramafic rocks. Evidence for high-grade metamorphism at elevated pressures or temperatures >400ºC has not been found.

Clays and Clay Minerals↗

USGS2024

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↗

USGS2021

Maximizing the science and resource mapping potential of Orbital VSWIR Spectral measurements of Mars

The last 16 years witnessed a rapid growth in understanding the composition and aqueous alteration of Mars’ surface from orbital data from the Observatoire pour la Mineralogie, l’Eau, les Glaces et l’Activité (OMEGA) [1] and Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) [2]. Both are sensitive to water-, hydroxyl-, sulfate-, and carbonate-bearing and ferric phases that record past liquid water. As the spatial resolution of such data has improved, and supporting laboratory data have been acquired, the diversity of mineral phases that are recognized has likewise expanded. The same phases typically contain recoverable water, a resource for future human exploration, and are the only near-surface water reservoir in the >50% of Mars over which ice likely does not occur in the shallowest subsurface. Knowledge of the distribution and abundance of these water-bearing phases, and their geologic implications, is limited by spatial resolution of the available data. A revolutionary advance in understanding the inventory, diversity, and stratigraphy of these materials can be obtained from Mars orbit, using two complementary approaches: hyperspectral imaging at ~6 meters per pixel at 0.7–4 µm, and 1 meter-per-pixel imaging at selected VSWIR wavelengths from 0.4–1.7 µm.

Bulletin of the AAS↗

USGS2020

Quantifying uncertainty for remote spectroscopy of surface composition

Remote surface measurements by imaging spectrometers play an important role in planetary and Earth science. To make these measurements, investigators calibrate instrument data to absolute units, invert physical models to estimate atmospheric effects, and then determine surface properties from the spectral reflectance. This study quantifies the uncertainty in this process. Global missions demand predictive uncertainty models that can estimate future errors for varied environments and observing conditions. Here we validate uncertainty predictions with remote surface composition retrievals and in situ measurements in a field analogue of Earth and planetary exploration. We consider rover transects at Cuprite, Nevada, and remote observations by NASA's Next- Generation Airborne Visible Infrared Imaging Spectrometer (AVIRIS-NG). We show that accounting for input uncertainties can benefit mineral detection methods such as constrained spectrum fitting. This suggests that operational uncertainty estimates could improve future NASA missions like the Earth Mineral dust source InvesTigation (EMIT) and the Lunar Trailblazer mission, as well as NASA's Decadal Surface Biology and Geology (SBG) Investigation.

Remote Sensing of Environment↗

USGS2019

Imaging spectroscopy for the detection, assessment and monitoring of natural and anthropogenic hazards

Natural and anthropogenic hazards have the potential to impact all aspects of society including its economy and the environment. Diagnostic data to inform decision-making are critical for hazard management whether for emergency response, routine monitoring or assessments of potential risks. Imaging spectroscopy (IS) has unique contributions to make via the ability to provide some key quantitative diagnostic information. In this paper, we examine a selection of key case histories representing the state of the art to gain an insight into the achievements and perspectives in the use of visible to shortwave infrared IS for the detection, assessment and monitoring of a selection of significant natural and anthropogenic hazards. The selected key case studies examined provide compelling evidence for the use of the IS technology and its ability to contribute diagnostic information currently unattainable from operational spaceborne Earth observation systems. User requirements for the applications were also evaluated. The evaluation showed that the projected launch of spaceborne IS sensors in the near-, mid and long term future, together with the increasing availability, quality and moderate cost of off the shelf sensors, the possibilities to couple unmanned autonomous systems with miniaturized sensors, should be able to meet these requirements. The challenges and opportunities for the scientific community in the future when such data become available will then be ensuring consistency between data from different sensors, developing techniques to efficiently handle, process, integrate and deliver the large volumes of data, and most importantly translating the data to information that meets specific needs of the user community in a form that can be digested/understood by them. The latter is especially important to transforming the technology from a scientific to an operational tool. Additionally, the information must be independently validated using current trusted practices and uncertainties quantified before IS derived measurement can be integrated into operational monitoring services.

Colorado↗

USGS2019

Isotopic ratios of Saturn's rings and satellites: Implications for the origin of water and Phoebe

Isotopic ratios have long been used to learn about physical processes acting over a wide range of geological environments, and in constraining the origin and/or evolution of planetary bodies. We report the spectroscopic detection of deuterium in Saturn's rings and satellites, and use these measurements to determine the (D/H) ratios in their near-surface regions. Saturn's moons, Phoebe and Iapetus, show a strong signature of CO2 and the 13C component of this molecule is detected and quantified. Large averages of spectra obtained by the Cassini Visual and Infrared Mapping Spectrometer, VIMS, were computed for the rings and icy satellites. The observed intensities of the infrared absorptions in H2O and CO2 and their isotopes were calibrated using laboratory data and radiative transfer models to derive the D/H and 13C/12C ratios. We find that the D/H in Saturn's rings and satellites is close to the Vienna Standard Mean Ocean Water (VSMOW) and bulk Earth (4% lower than VSMOW) value except for Phoebe, which is 8.3 times the VSMOW value. This is the highest value for any Solar-System surface yet measured, and suggests that Phoebe formed from material with a different D/H ratio than the other satellites in the Saturn system. Phoebe’s 13C/12C ratio is also unusual: 4.7 times greater than terrestrial, and greater than values measured for the interstellar medium and the galactic center. The high 13C abundance in the CO2 suggests that Phoebe was never warm enough for the large D/H ratio in its surface to have originated by evaporative fractionation of its waterice (e.g., from heating in the inner Solar System before its eventual capture by Saturn). We also report the detection of a probable O-D stretch absorption due to OD in minerals on Phoebe at 3.62 μm. This absorption is not detected on other Saturnian satellites. Stronger signatures of bound water absorptions are found in the dark material of Iapetus and we report a new detection of bound water at 1.9 μm. The position of this absorption matches that seen in spectra of hydrated iron oxides but does not match absorptions seen in spectra of tholins. Despite the strong bound water signature in the Iapetus dark material, no 3.62-μm OD absorption is seen in the spectra, further indicating the high deuterium level on Phoebe is unusual. As such, it is likely that Phoebe originated in a colder part of the outer Solar System, relative to the prevailing temperatures at Saturn’s distance from the Sun.

Icarus↗

USGS2018

Characterizing the source of potentially asbestos-bearing commercial vermiculite insulation using in situ IR spectroscopy

Commercially produced vermiculite insulation from Libby, Montana, contains trace levels of asbestiform amphibole, which is known to cause asbestos-related diseases. When vermiculite insulation is found in a building, evaluation for its potential asbestos content traditionally involves collecting a sample from an attic or wall and submitting it for time-consuming analyses at an off-site laboratory. The goal of this study was to determine if in situ near-infrared reflectance measurements could be used to reliably identify the source of vermiculite ore and therefore its potential to contain asbestos. Spectra of 52 expanded ore samples, including attic insulation, commercial packing materials, and horticultural products from Libby, Montana; Louisa, Virginia; Enoree, South Carolina; Palabora, South Africa; and Jiangsu, China, were measured with a portable spectrometer. The mine sources for these vermiculite ores were identified based on collection location, when known, and on differences in elemental composition as measured by electron probe microanalysis. Reflectance spectra of the insulation samples show vibrational overtone and combination absorptions that vary in wavelength position and relative intensity depending on elemental composition and proportions of their constituent micas (i.e., vermiculite ore usually consists of a mixture of hydrobiotite and vermiculite mineral flakes). Band depth ratios of the 1.38/2.32, 1.40/1.42, and 2.24/2.38 μm absorptions allow determination of a vermiculite insulation's source and detection of its potential to contain amphibole, talc, and/or serpentine impurities. Spectroscopy cannot distinguish asbestiform vs. non-asbestiform amphiboles. However, if the spectrally determined mica composition and mineralogy of an insulation sample is consistent with ore from Libby, then it is likely that some portion of the sodic-calcic amphibole it contains is asbestiform, given that all of the nearly two dozen Libby vermiculite insulation samples examined with scanning electron microscopy in this study contain amphiboles. One sample of expanded vermiculite ore from multiple sources was recognized as a limitation of the spectral method, therefore an additional test (i.e., 2.24 μm absorption position vs. 2.24/2.38 μm band depth ratio) was incorporated into the spectral method to eliminate misclassification caused by such mixtures. With portable field spectrometers, the methodology developed can be used to determine vermiculite insulation's source and estimate its potential amphibole content, thereby providing low-cost analysis with onsite reporting to property owners.

American Mineralogist↗

USGS2017

USGS Spectral Library Version 7

We have assembled a library of spectra measured with laboratory, field, and airborne spectrometers. The instruments used cover wavelengths from the ultraviolet to the far infrared (0.2 to 200 microns [μm]). Laboratory samples of specific minerals, plants, chemical compounds, and manmade materials were measured. In many cases, samples were purified, so that unique spectral features of a material can be related to its chemical structure. These spectro-chemical links are important for interpreting remotely sensed data collected in the field or from an aircraft or spacecraft. This library also contains physically constructed as well as mathematically computed mixtures. Four different spectrometer types were used to measure spectra in the library: (1) Beckman™ 5270 covering the spectral range 0.2 to 3 µm, (2) standard, high resolution (hi-res), and high-resolution Next Generation (hi-resNG) models of Analytical Spectral Devices (ASD) field portable spectrometers covering the range from 0.35 to 2.5 µm, (3) Nicolet™ Fourier Transform Infra-Red (FTIR) interferometer spectrometers covering the range from about 1.12 to 216 µm, and (4) the NASA Airborne Visible/Infra-Red Imaging Spectrometer AVIRIS, covering the range 0.37 to 2.5 µm. Measurements of rocks, soils, and natural mixtures of minerals were made in laboratory and field settings. Spectra of plant components and vegetation plots, comprising many plant types and species with varying backgrounds, are also in this library. Measurements by airborne spectrometers are included for forested vegetation plots, in which the trees are too tall for measurement by a field spectrometer. This report describes the instruments used, the organization of materials into chapters, metadata descriptions of spectra and samples, and possible artifacts in the spectral measurements. To facilitate greater application of the spectra, the library has also been convolved to selected spectrometer and imaging spectrometers sampling and bandpasses, and resampled to selected broadband multispectral sensors. The native file format of the library is the SPECtrum Processing Routines (SPECPR) data format. This report describes how to access freely available software to read the SPECPR format. To facilitate broader access to the library, we produced generic formats of the spectra and metadata in text files. The library is provided on digital media and online at https://speclab.cr.usgs.gov/spectral-lib.html . A long-term archive of these data are stored on the USGS ScienceBase data server ( https://dx.doi.org/10.5066/F7RR1WDJ ).

Data Series↗

USGS2016

Discovery of alunite in Cross crater, Terra Sirenum, Mars: Evidence for acidic, sulfurous waters

Cross crater is a 65 km impact crater, located in the Noachian highlands of the Terra Sirenum region of Mars (30°S, 158°W), which hosts aluminum phyllosilicate deposits first detected by the Observatoire pour la Minéralogie, L’Eau, les Glaces et l’Activitié (OMEGA) imaging spectrometer on Mars Express. Using high-resolution data from the Mars Reconnaissance Orbiter, we examine Cross crater’s basin-filling sedimentary deposits. Visible/shortwave infrared (VSWIR) spectra from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) show absorptions diagnostic of alunite. Combining spectral data with high-resolution images, we map a large (10 km × 5 km) alunite-bearing deposit in southwest Cross crater, widespread kaolin-bearing sediments with variable amounts of alunite that are layered in <10 m scale beds, and silica- and/or montmorillonite-bearing deposits that occupy topographically lower, heavily fractured units. The secondary minerals are found at elevations ranging from 700 to 1550 m, forming a discontinuous ring along the crater wall beneath darker capping materials. The mineralogy inside Cross crater is different from that of the surrounding terrains and other martian basins, where Fe/Mg-phyllosilicates and Ca/Mg-sulfates are commonly found. Alunite in Cross crater indicates acidic, sulfurous waters at the time of its formation. Waters in Cross crater were likely supplied by regionally upwelling groundwaters as well as through an inlet valley from a small adjacent depression to the east, perhaps occasionally forming a lake or series of shallow playa lakes in the closed basin. Like nearby Columbus crater, Cross crater exhibits evidence for acid sulfate alteration, but the alteration in Cross is more extensive/complete. The large but localized occurrence of alunite suggests a localized, high-volume source of acidic waters or vapors, possibly supplied by sulfurous (H 2 S- and/or SO 2 -bearing) waters in contact with a magmatic source, upwelling steam or fluids through fracture zones. The unique, highly aluminous nature of the Cross crater deposits relative to other martian acid sulfate deposits indicates acid waters, high water throughput during alteration, atypically glassy and/or felsic materials, or a combination of these conditions.

American Mineralogist↗

USGS2014

Mapping advanced argillic alteration at Cuprite, Nevada, using imaging spectroscopy

Mineral maps based on Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data were used to study late Miocene advanced argillic alteration at Cuprite, Nevada. Distributions of Fe-bearing minerals, clays, micas, sulfates, and carbonates were mapped using the Tetracorder spectral-shape matching system. The Al content of white micas increases toward altered areas and near intrusive rocks. Alunite composition varies from pure K to intimate mixtures of Na-K endmembers with subpixel occurrences of huangite, the Ca analogue of alunite. Intimately mixed Na-K alunite marks areas of relatively lower alteration temperature, whereas co-occurring Na-alunite and dickite may delineate relict hydrothermal conduits. The presence of dickite, halloysite, and well-ordered kaolinite, but absence of disordered kaolinite, is consistent with acidic conditions during hydrothermal alteration. Partial lichen cover on opal spectrally mimics chalcedony, limiting its detection to lichen-free areas. Pods of buddingtonite are remnants of initial quartz-adularia-smectite alteration. Thus, spectral maps provide a synoptic view of the surface mineralogy, and define a previously unrecognized early steam-heated hydrothermal event. Faulting and episodes of hydrothermal alteration at Cuprite were intimately linked to upper plate movements above the Silver Peak-Lone Mountain detachment and growth, collapse, and resurgence of the nearby Stonewall Mountain volcanic complex between 8 and 5 Ma. Isotopic dating indicates that hydrothermal activity started at least by 7.61 Ma and ended by about 6.2 Ma. Spectral and stable isotope data suggest that Cuprite is a late Miocene low-sulfidation adularia-sericite type hot spring deposit overprinted by late-stage, steam-heated advanced argillic alteration formed along the margin of the Stonewall Mountain caldera.

Nevada↗

USGS2014

Spectroscopy from Space

This chapter reviews detection of materials on solid and liquid (lakes and ocean) surfaces in the solar system using ultraviolet to infrared spectroscopy from space, or near space (high altitude aircraft on the Earth), or in the case of remote objects, earth-based and earth-orbiting telescopes. Point spectrometers and imaging spectrometers have been probing the surfaces of our solar system for decades. Spacecraft carrying imaging spectrometers are currently in orbit around Mercury, Venus, Earth, Mars, and Saturn, and systems have recently visited Jupiter, comets, asteroids, and one spectrometer-carrying spacecraft is on its way to Pluto. Together these systems are providing a wealth of data that will enable a better understanding of the composition of condensed matter bodies in the solar system. Minerals, ices, liquids, and other materials have been detected and mapped on the Earth and all planets and/or their satellites where the surface can be observed from space, with the exception of Venus whose thick atmosphere limits surface observation. Basaltic minerals (e.g., pyroxene and olivine) have been detected with spectroscopy on the Earth, Moon, Mars and some asteroids. The greatest mineralogic diversity seen from space is observed on the Earth and Mars. The Earth, with oceans, active tectonic and hydrologic cycles, and biological processes, displays the greatest material diversity including the detection of amorphous and crystalline inorganic materials, organic compounds, water and water ice. Water ice is a very common mineral throughout the Solar System and has been unambiguously detected or inferred in every planet and/or their moon(s) where good spectroscopic data has been obtained. In addition to water ice, other molecular solids have been observed in the solar system using spectroscopic methods. Solid carbon dioxide is found on all systems beyond the Earth except Pluto, although CO 2 sometimes appears to be trapped in other solids rather than as an ice on some objects. The largest deposits of carbon dioxide ice are found on Mars. Sulfur dioxide ice is found in the Jupiter system. Nitrogen and methane ices are common beyond the Uranian system. Saturn’s moon Titan probably has the most complex active extra-terrestrial surface chemistry involving organic compounds. Some of the observed or inferred compounds include ices of benzene (C 6 H 6 ), cyanoacetylene (HC 3 N), toluene (C 7 H 8 ), cyanogen (C 2 N 2 ), acetonitrile (CH 3 CN), water (H 2 O), carbon dioxide (CO 2 ), and ammonia (NH 3 ). Confirming compounds on Titan is hampered by its thick smoggy atmosphere, where in relative terms the atmospheric interferences that hamper surface characterization lie between that of Venus and Earth. In this chapter we exclude discussion of the planets Jupiter, Saturn, Uranus, and Neptune because their thick atmospheres preclude observing the surface, even if surfaces exist. However, we do discuss spectroscopic observations on a number of the extra-terrestrial satellite bodies. Ammonia was predicted on many icy moons but is notably absent among the definitively detected ices with possible exceptions on Charon and possible trace amounts on some of the Saturnian satellites. Comets, storehouses of many compounds that could exist as ices in their nuclei, have only had small amounts of water ice definitively detected on their surfaces from spectroscopy. Only two asteroids have had a direct detection of surface water ice, although its presence can be inferred in others.

Reviews in Mineralogy and Geochemistry↗

USGS2014

The Tetracorder user guide: version 4.4

Imaging spectroscopy mapping software assists in the identification and mapping of materials based on their chemical properties as expressed in spectral measurements of a planet including the solid or liquid surface or atmosphere. Such software can be used to analyze field, aircraft, or spacecraft data; remote sensing datasets; or laboratory spectra. Tetracorder is a set of software algorithms commanded through an expert system to identify materials based on their spectra (Clark and others, 2003). Tetracorder also can be used in traditional remote sensing analyses, because some of the algorithms are a version of a matched filter. Thus, depending on the instructions fed to the Tetracorder system, results can range from simple matched filter output, to spectral feature fitting, to full identification of surface materials (within the limits of the spectral signatures of materials over the spectral range and resolution of the imaging spectroscopy data). A basic understanding of spectroscopy by the user is required for developing an optimum mapping strategy and assessing the results.

Open-File Report↗

USGS2012

Hydrous carbonates on Mars?: Evidence from Mariner 6/7 infrared spectrometer and ground‐based telescopic spectra

Absorption features at 2.28 and 5.4 μm identified in Mariner 6/7 infrared spectrometer and terrestrial telescopic spectra are consistent with the spectra of hydrous magnesium carbonates such as hydromagnesite and artinite. Spectral characteristics of these hydrous carbonates are different from those of the anhydrous carbonates, as the former do not have the strong spectral features typically associated with anhydrous carbonates such as calcite and siderite. Theoretical mixing indicates that, depending on the type of hydrous carbonate, 10–20 wt % can be incorporated into the regolith without contradicting the spectral observations or the Viking x ray fluorescence chemical analysis. Hydrous carbonates form as weathering products of mafic minerals in the presence of H 2 O and CO 2 , even in the Antarctic. Their formation as evaporite minerals from either original magmas or hydrothermally altered rocks is consistent with the Martian environment, provided liquid water is or has been at least transiently present. On Earth, formation of hydrous Mg carbonates is associated with the production of amorphous iron oxides, which is consistent with both the environment and the inferred surface mineralogy of Mars. These minerals are about 60 wt % H 2 O, CO 3 , and OH; if they are abundant everywhere at the 10% level, then about 6% of the surface weight could be volatiles bound in this type of mineral. Although the stability of hydrous carbonates in a Martian environment is uncertain, there may be kinetic factors inhibiting the dehydration of these minerals, which may persist metastably in the current environment. Although the spectroscopic evidence for anhydrous carbonates is scant, the possible presence of hydrous carbonates provides an appealing mechanism for the existence of carbonates on Mars.

Journal of Geophysical Research↗

USGS2012

Reflectance spectroscopy: Quantitative analysis techniques for remote sensing applications

Several methods for the analysis of remotely sensed reflectance data are compared, including empirical methods and scattering theories, both of which are important for solving remote sensing problems. The concept of the photon mean optical path length and the implications for use in modeling reflectance spectra are presented. It is shown that the mean optical path length in a particulate surface is in rough inverse proportion to the square root of the absorption coefficient. Thus, the stronger absorber a material is, the less photons will penetrate into the surface. The concept of apparent absorbance (‐In reflectance) is presented, and it is shown that absorption bands, which are Gaussian in shape when plotted as absorption coefficient (true absorbance) versus photon energy, are also Gaussians in apparent absorbance. However, the Gaussians in apparent absorbance have a smaller intensity and a width which is a factor of √2 larger. An apparent continuum in a reflectance spectrum is modeled as a mathematical function used to isolate a particular absorption feature for analysis. It is shown that a continuum should be removed by dividing it into the reflectance spectrum or subtracting it from the apparent absorbance and that the fitting of Gaussians to absorption features should be done using apparent absorbance versus photon energy. Kubelka‐Munk theory is only valid for materials with small total absorption and for bihemispherical reflectance, which are rarely encountered in geologic remote sensing. It is shown that the recently advocated bidirectional reflectance theories have the potential for use in deriving mineral abundance from a reflectance spectrum.

Journal of Geophysical Research↗

USGS2012

Spectral properties of ice‐particulate mixtures and implications for remote sensing: 1. Intimate mixtures

The spectral properties of water ice-particulate mixtures are studied for the purpose of deriving the ice and particulate abundances from remotely obtained spectra (particulates referring to nonicy materials in the form of grains). Reflectance levels and ice absorption band depths are a complex function of the single scattering albedo of the particulates embedded in the ice. The ice absorption band depths are related to the mean optical path length of photons in ice through Beers law, Fresnel reflection from the ice-crystal faces on the surface, and ice absorption coefficient as a function of wavelength. Laboratory spectra of many ice-particulate mixtures are studied with high-, medium-, and low-albedo particulates. From the laboratory spectra the band depth, the continuum reflectance, and the ratio of band depth to continuum reflectance are derived for each particulate albedo as a function of the logarithm of the particulate weight fraction in the sample. Ice band depths are dependent on the particulate albedo and increase with smaller weight fractions of particulates until the bands saturate and their depths decrease. The continuum reflectance is a complex function of the particulate albedo and wavelength of light, while the band depth to continuum reflectance ratio appear independent of particulate albedo such that, for a given grain size of particulate, a calibration curve to abundance of ice and particulates is derived. The derived abundance calibrations are accurate if the source of scattering is dominated by particulates and not ice-vacuum (air) interfaces. If ice-vacuum interfaces are dominant, then the derived particulate abundance is an upper limit. Theoretically produced frost spectra show similar curves of growth of band depth, continuum reflectance, and corresponding ratio versus the photon mean optical path length similar to that for intimate mixtures of ice and high-albedo particulates. In all scattering cases the ice absorption coefficients determine the path length needed to produce a given band depth; thus different absorptions are sensitive to different amounts of particulates, with the 3-μm fundamental being the most sensitive to the presence of ice (very low ice abundance) and the 1.04-μm overtone being the most sensitive to the presence of particulates (very high ice abundance).

Journal of Geophysical Research: Solid Earth↗

USGS2012

Spectral characteristics of chlorites and Mg‐serpentines using high‐resolution reflectance spectroscopy

The present laboratory study using high‐resolution reflectance spectroscopy (0.25–2.7 μm) focuses on two primary phyllosilicate groups, serpentines and chlorites. The results show that it is possible to spectrally distinguish between isochemical end‐members of the Mg‐rich serpentine group (chrysotile, antigorite, and lizardite) and to recognize spectral variations in chlorites as a function of Fe/Mg ratio (∼8–38 wt % Fe). The position and relative strength of the 1.4‐μm absorption feature in the trioctahedral chlorites appear to be correlated to the total iron content and/or the Mg/Si ratio and the loss on ignition values of the sample. Spectral differences in the 2.3‐μm wavelength region can be attributed to differences in lattice environments and are characteristic for specific trioctahedral chlorites. The 1.4‐μm feature in the isochemical Mg‐rich serpentines (total iron content ∼1.5–7.0 wt%) show marked spectral differences, apparently due to structural differences.

Journal of Geophysical Research: Solid Earth↗

USGS2012

High-resolution reflectance spectra of Mars in the 2.3-μm region: evidence for the mineral scapolite

patially resolved reflectance spectra of Mars in the 2.2- to 2.4-μm spectral region were obtained in August 1988 using the NASA 3-m Infrared Telescope Facility. The spectra show weak absorption features due to Martian atmospheric carbon monoxide and a surface mineral. Both CO and the mineral absorptions are composed of overlapping narrow features, but in many locations, such as Hellas, Chryse, Eden, and Moab, the mineral absorptions are quite strong, at least 3 times stronger than at the most absorbing wavelengths of CO near 2.33 μm. Therefore CO complicates the analysis of the surface mineral but does not always overwhelm its signature. Model removal of the Martian atmospheric CO has been performed, and the remaining absorption bands are identified as scapolite. Relatively strong absorptions that match bands in the spectrum of scapolite and have little or no CO absorption interference are seen near 2.41, 2.39, and 2.29 μm. Absorption also occurs at the scapolite bands at 2.36 and 2.33 μm, but the analysis is complicated by uncertainty in the atmospheric CO removal at these wavelengths. Weaker scapolite bands are seen at 2.44 and 2.23 μm where there is virtually no atmospheric interference. The scapolite bands observed on Mars are due to HCO 3 − and HSO 4 − ions in the scapolite structure. The bicarbonate and bisulfate contents appear to vary with location: the scapolite in Hellas is more bisulfate-rich relative to that in the Chryse/Moab/Eden area. Other locations contain little (Arabia, Syrtis Major, Hellespontica, and Isidis) or no scapolite (e.g., Margaritifer, Ausonia, and Erythraeum). The calculated abundances are unconstrained because the amounts of HCO 3 − and HSO 4 − in the Martian scapolites as well as their grain sizes are not known. If the scapolites contain about 3 wt % of each, near the maximum possible, the scapolite abundances probably range from about 5 wt % scapolite at Eden and Hellas; 3–5% at Chryse, Moab, and Oxia Palus; 2–3% at Arabia, Syrtis Major, and Isidis; to less than 2% at Hellespontica, Syrtis Minor, and Margaritifer, assuming a relatively large grain size of 50–100 μm. If the characteristic grain sizes are smaller or the HCO 3 − and HSO 4 − contents are lower, the scapolite abundances required to match the observed band depths would be higher. The mineral bands are apparent in many of the Mars spectra measured, so it appears to be widely but not uniformly distributed. The newly observed fine structure also varies greatly in both depth and spectral detail with location on Mars. Thus there appears to be regional variations in composition. The mineral phases appear to reflect local or regional geology and are not primarily contained in the homogeneous, globally redistributed aeolian dust. Higher spectral resolution Martian spectra in the 2.3-μm region as well as at 3.9 μm are needed to confirm the scapolite identification and to constrain its abundance.

Journal of Geophysical Research↗

USGS2012

Infrared spectra and crystal chemistry of scapolites: implications for Martian mineralogy

Near‐infrared and midinfrared spectra of a wide range of scapolite compositions were studied to determine the cause of the 2.36‐μm features that have been correlated with similar features in the near‐IR spectrum of Mars. We attribute the 2.36−μm features to vibrations caused by HCO 3 − and HSO 4 − in the anion sites of scapolite. The 2.36‐μm absorption complex consists of four overlapping bands with the following assignments: absorptions at 2.33 and 2.35 μm are attributed to combinations of hydroxyl stretches and a O‐H … O bend from HCO 3 − , absorptions at 2.39 and 2.41 μm are attributed to combinations of hydroxyl stretches and a O‐H ··· O bend from HSO 4 − . The relative intensities of all four bands vary according to the HCO 3 − /HSO 4 − ratio and disordered anion site occupancy. Oriented single‐crystal polarized spectra of a bicarbonate‐bisulfate bearing scapolite show that the 3.9‐μm hydrogen bond stretch, from HCO 3 − , is polarization controlled. This verifies that HCO 3 − is an intimate part of the scapolite crystal structure and that hydrogen in HCO 3 − is forming hydrogen bonds with T 1 framework oxygens. The association of yellow fluorescence, attributed to S 2 − in the anion site, with vibrational features of HCO 3 − and HSO 4 − in the rims and fractures of scapolite grains suggests that some common geochemical process is incorporating these ions into the crystal structure during later stage alteration of scapolite. The positional disorder of HCO 3 − and HSO 4 − in the low‐symmetry anion site of scapolite gives the 2.36‐μm band complex a unique spectral signature not likely to be duplicated in any other mineral.

Journal of Geophysical Research↗