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Diffuse spectral reflectance of optically thick cloud and powder layers composed of particles with strong IR resonance, noting effect of particle size
Diffuse spectral reflectance of optically thick cloud and powder layers composed of particles with strong IR resonance, noting effect of particle size
Near-infrared spectral reflectance data are presented for systematic variations in weight percent of two component mixtures of ferromagnesium and iron oxide minerals used to study the dark materials on Mars. Olivine spectral features are greatly reduced in contrast by admixture of other phases but remain distinctive even for low olivine contents. Clinopyroxene and orthopyroxene mixtures show resolved pyroxene absorptions near 2 microns. Limonite greatly modifies pyroxene and olivine reflectance, but does not fully eliminate distinctive spectral characteristics. Using only spectral data in the 1 micron region, it is difficult to differentiate orthopyroxene and limonite in a mixture. All composite mineral absorptions were either weaker than or intermediate in strength to the end-member absorptions and have bandwidths greater than or equal to those for the end members. In general, spectral properties in an intimate mixture combine in a complex, nonadditive manner, with features demonstrating a regular but usually nonlinear variation as a function of end-member phase proportions.
The effect is analyzed of variations in glass, end member abundance, and compositional variations on the reflectance spectra of glass and mafic silicate-bearing mineral mixtures chosen to reproduce spectral reflectance properties of lunar regoliths. The spectral properties of the glasses appear to be sensitive to parameters such as fusion techniques and initial composition. Variations in these parameters can yield classes which show spectral variations far in excess of those found for naturally occurring lunar impact-derived glasses and surface fines. The addition of glass to a mafic silicate-bearing assemblage results in a reduction in overall reflectance, band depths, and band area ratios, as well as a general decrease in band II minimum wavelength position and an increase in interband peak position.
Technique to measure spectral reflectances at low temperatures in IR and far IR
Relative IR spectral reflectivity of selected lunar surface areas measured using double beam photoelectric filter photometer
Lunar surface spectral reflectivity measured with ground based telescopes for remote mineralogical analysis
A collection of spectral reflectances of 156 natural targets is presented in a uniform format. For each target both a graphical plot and a digital tabulation of reflectance is given. The data were taken from the literature and include laboratory, field, and aircraft measurements. A discussion of the different measurements of reflectance is given, along with the changes in apparent reflectance when targets are viewed through the atmosphere. The salient features of the reflectance curves of common target types are presented and discussed.
Techniques and instruments used to collect spectral reflectance data on Vermont spruce and fir stands subjected to stress (due to acid rain and ozone) are described and illustrated. The healthy and stressed sites selected are characterized; the data-quality requirements are indicated; and particular attention is given to (1) a helicopter-mounted instrument package (radiometer, spectrometer, cameras, and video camera) for canopy-level remote sensing of reflectance and (2) a portable hemispherical light source for use in taking laboratory reflectance measurements from branches or needles. Typical data are presented in graphs and briefly discussed.
The basic spectral response related to the salt content of soils in the visible and reflective IR wavelengths is analyzed in order to explore remote sensing applications for monitoring processes of the earth system. The bidirectional reflectance factor (BRF) was determined at 10 nm of increments over the 520-2320-nm spectral range. The effect of salts on reflectance was analyzed on the basis of 162 spectral measurements. MSS and TM bands were simulated within the measured spectral region. A strong relationship was found in variations of reflectance and soil characteristics pertaining to salinization and desalinization. Although the individual MSS bands had high R-squared values and 75-79 percent of soil/treatment combinations were separable, there was a large number of soil/treatment combinations not distinguished by any of the four highly correlated MSS bands under consideration.
Visible and near-infrared field spectral reflectance measurements of plutonic rocks were acquired in the 0.45- to 2.45-micron region with a portable field reflectance spectrometer. These spectra were used to determine spectral signatures for the various rock types and to evaluate the separability of these rocks based on their spectral characteristics. A total of 135 samples were divided into 11 groups based on their mineralogy. These 11 groups approximately correspond to traditional rock classifications and include five granitic groups, three gabbroic groups, and three ultramafic groups. The positions, intensity, and presence of iron, CO3(-2), and Al-OH and Mg-OH absorption bands varied among the 11 groups. Each rock group also had a range of albedos characteristic of the group. Stepwise linear discriminant analysis was performed on the spectral data to determine the separability of the 11 groups. Classification accuracy for 30 equally spaced wavelength bands between 0.45 and 2.45 microns was 78% with 10% serious misclassifications. The same analysis was repeated, limiting the spectral data to the wavelength regions corresponding to the proposed Landsat D thematic mapper scanner.
Identification of hydrophytes will improve the delineation and classification of wetlands on remotely sensed imagery. Spectral reflectance measurements of 10 species of hydrophytes were made with an Exotech radiometer during three phenological stages, flowering and early seed, senescent, and early emergent. Reflectance data were analyzed to determine significant (P not greater than 0.5) differences between species in each of four spectral regions during each phenological stage. Eight species had significantly (P not greater than 0.05) different reflectances during the flower and early seed stage. Among the ten species only one could not be spectrally isolated during at least 1 phenological stage. The results indicate that films sensitive to both visible and infrared spectra (e.g., Ektachrome infrared) should enable recognition of different species of hydrophytes.
Spectral reflectances of Produra wheat were measured at 13 different times of the day at Phoenix, Arizona, during April 1979 using a nadir-oriented hand-held 4-band radiometer which had bandpass characteristics similar to those on LANDSAT satellites. Different Sun altitude and azimuth angles caused significant diurnal changes in radiant return in both visible and near-IR regions of the spectrum and in several vegetation indices derived from them. The magnitude of these changes were related to different canopy architecture, percent cover and green leaf area conditions. Spectral measurements taken at each time period were well correlated with green leaf area index but the nature of the relationship changed significantly with time of day. Thus, a significant bias in the estimation of the green leaf area index from remotely sensed spectral data could occur if sun angles are not properly accounted for.
Long-term Objective: - Enable on-orbit high-accuracy absolute calibration for the past, current, and future reflected solar sensors in LEO and GEO by providing lunar spectral irradiance as function of satellite viewing geometry and specified wavelength. IIP Objective (complete): - Design, build, and characterize a prototype instrument demonstrating form-fit-function for a 6U CubeSat. InVEST Objective: - Demonstrate high-accuracy measurements of lunar spectral reflectance, < 0.5% (k=1), via 6U CubeSat on-orbit in LEO for 6 months, with validation and data analysis
Solar absorptances and spectral reflectances of metals
The spectral reflectance properties of electroplated and chemically converted zinc were measured for both chromate and chloride conversion coatings. The reflectance properties were measured for various times of conversion and for conversion at various chromate concentrations. The values of absorptance, integrated over the solar spectrum, and of infrared emittance, integrated over black body radiation at 250 F were then calculated from the measured reflectance values. The interdependent variations of absorptance and infrared emittance were plotted. The results indicate that the optimum combination of the highest absorptance in the solar spectrum and the lowest emittance in the infrared of the converted electroplated zinc is produced by chromate conversion at 1/2 concentration of the standard NEOSTAR chromate black solution for 0.50 minute or by chloride conversion for 0.50 minute.
The spectral reflectance properties of electroplated and chemically converted zinc were measured for both chromate and chloride conversion coatings. The reflectance properties were measured for various times of conversion and for conversion at various chromate concentrations. The values of absorptance, alpha, integrated over the solar spectrum, and of infrared emittance, epsilon, integrated over black body radiation at 250 F were then calculated from the measured reflectance values. The interdependent variations of alpha and epsilon were plotted. The results indicate that the optimum combination of the highest absorptance in the solar spectrum and the lowest emittance in the infrared of the converted electroplated zinc is produced by chromate conversion at 1/2 concentration of the standard NEOSTAR chromate black solution for 0.50 minute or by chloride conversion for 0.50 minute.
A unit map of nearside basalt types has been prepared from all telescopic spectral reflectance data currently available for lunar soils. Four parameters were chosen (UV/VIS ratio, albedo, 1 micron band strength, 2 micron band strength) to distinguish and map each of 13 mare basalt types and three additional volcanic groups. Multispectral imagery and albedo maps were used to define unit boundaries while spectra were used to examine the 1 and 2 micron bands and calibrate and quantify the multispectral images. Although the volume of each basalt type is not known, it is clear from the unit map that only 1/3 to 1/2 of the surface basalt types are likely to be represented in the returned lunar samples. For mature lunar soils a single parameter alone does not provide chemical information, but when the four are used together, TiO2 and in some cases FeO can be estimated. Further study of the mineralogy of unsampled lunar basalts requires precise spectra to 2.5 microns with higher spectra and spatial resolution.