The optical effects of small iron particles that darken but do not redden: Evidence of intense space weathering on Mercury

Submicroscopic iron particles larger than about 50 nm, infused throughout mineral grains or glasses, are abundant in planetary materials altered by their environment such as shocked meteorites and lunar agglutinate glasses. Such particles darken their host material but do not redden their spectra but to date there has been no theoretical treatment of their optical effects. Using Mie theory, we modify the Hapke (2001) radiative transfer model of the effects of space weathering to include these effects. Comparison with laboratory measurements shows that the new treatment reproduces the relationship between submicroscopic iron size, abundance and reflectance. We apply this new model to near-IR spectra of Mercury recently obtained by the MESSENGER spacecraft and find that submicroscopic iron is much more abundant on Mercury than in lunar soils, with typical total submicroscopic iron abundances near 3.5 wt.% compared to about 0.5 wt.% for lunar soils We also find that the ratio of iron particles that darken but do not redden to the abundance of very small iron particles that impart the red slope to space weathered material is much larger than lunar (6 vs. 2). Both the total submicroscopic iron abundance and ratio of particle size fractions are consistent with the higher production of melt and vapor in micrometeorite impact on Mercury relative to the Moon (Cintala, 1992) that enables more accumulation of space weathering products before sequestration by regolith overturn. The radiative transfer model cannot directly constrain the abundance of opaque minerals on Mercury because of ambiguities between the darkening effects of opaques and submicroscopic iron particles larger than 50 nm, but assuming the opaques are the ultimate source of the submicroscopic iron, our results place a lower limit of 4-20 wt.% on opaque abundance on Mercury depending on the composition of the opaque phase and whether titanium metal also contributes to the space weathering effect.     

Mercury's albedo from Mariner 10: Implications for the presence of ferrous iron

Mariner 10 clear filter (490 nm) images of Mercury were recalibrated and photometrically normalized to produce a mosaic of nearly an entire hemisphere of the planet. Albedo contrasts are slightly larger than seen in the lunar highlands (excluding maria). Variegations indicative of compositional differences include diffuse low albedo units often overlain by smooth plains, the high albedo smooth plains of Borealis Planitia, and high-albedo enigmatic crater floor deposits. A higher level of contrast between immature crater ejecta and average mature material on Mercury compared to the Moon is consistent with a more intense space weathering environment on Mercury that results in a more mature regolith. Immature lunar highlands materials are ∼1.5 times higher in reflectance than analogous immature mercurian materials. Immature materials of the same composition would have the same reflectance on both bodies, thus this observation requires that Mercury's crust contains a significant darkening agent, either opaque minerals or ferrous iron bearing silicates, in abundances significantly higher than those of the lunar highlands. If the darkening agent is opaque minerals (e.g. ilmenite or ulvospinel) Mercury's crust may contain significant ferrous iron and yet not exhibit a 1-μm absorption band.     

Effects of space weathering on diagnostic spectral features: Results from He+ irradiation experiments

We performed ion irradiation of mineral samples with 50 keV He⁺, aimed to investigate ion irradiation effects on diagnostic spectral features. Reflectance spectra of samples in 0.375–2.5 μm are measured before and after ion irradiation. Silicates, including Luobusha olivine, plagioclase and basaltic glass, have shown reddening and darkening of reflectance spectra at the VIS–NIR range. Olivine is more sensitive to ion irradiation than plagioclase and basaltic glass. Irradiated Panzhihua ilmenite exhibits higher reflectance and stronger absorption features, which is totally different from lunar soil and analog silicate materials in other experiments. Using continuum removal and MGM fit, we extracted and compared absorption features of olivine spectra before and after irradiation. Ion irradiation can induce band strength decrease of olivine but negligible band centers shift. We estimate band centers shift caused by ion irradiation are quite limited, even less than variations due to chemical composition in silicates. It provides one possible explanation for no systematic shift in band positions in lunar soil. Irradiated Luobusha olivine spectrum matches spectra of olivine-dominated asteroids. Our results suggest space weathering should be new clues to explain the subtle difference between A-type asteroid spectra and laboratory spectra of olivine.     

Reflectance spectra of analog anorthosites: Implications for lunar highland mapping

Lunar highland region and associated craters are mostly composed of anorthosite. In the present study, we studied the reflectance spectra of terrestrial anorthosites collected from Sittampundi Anorthosites Complex, which is considered as equivalent (simulant) of lunar highland anorthosites. The objective of the study is to interpret diagnostic spectral features of analog anorthosite for remotely exploring lunar highland region. Reflectance spectra of anorthosites were measured under two different environments, such as controlled field and laboratory conditions. In these two procedures, the laboratory spectra give clear, diagnostic spectral information in the present study. Reflectance spectra captured under 350-2500 nm covering UV, Visible, NIR, and SWIR part of the electromagnetic spectrum. The spectral characteristics of anorthosites measured under various parts of electromagnetic spectrum have diagnostic absorption features at 380-387, 700-740, 930-1100, 1160-1200, 1415, 1920, 2200 and 2330 nm correspondingly due to plagioclase UV absorption, Fe³⁺ electron transition absorption, Fe²⁺ pyroxene and olivine absorption, OH/Mn³⁺ crystal transition absorption, pyroxene absorption, Al-OH absorption and Mg-OH absorption. Mineralogical and chemical analyses were carried out for four anorthosites and compared with the results of chemical component of lunar anorthosite. The percentage of plagioclase content, relative abundance of low and high calcium pyroxene and olivine in different anorthosite samples are correlated with the albedo range, absorption shape, absorption centers and band depth. The similarity in the diagnostic spectral features of the anolog anorthosite with lunar anorthosites could be effectively utilized for remotely mapping the lunar highland region.     

The oxidation state of nanophase Fe particles in lunar soil: Implications for space weathering

We report measurements of the oxidation state of Fe nanoparticles within lunar soils that experienced varied degrees of space weathering. We measured >100 particles from immature, submature, and mature lunar samples using electron energy‐loss spectroscopy (EELS) coupled to an aberration‐corrected transmission electron microscope. The EELS measurements show that the nanoparticles are composed of a mixture of Fe⁰, Fe²⁺, and Fe³⁺ oxidation states, and exhibit a trend of increasing oxidation state with higher maturity. We hypothesize that the oxidation is driven by the diffusion of O atoms to the surface of the Fe nanoparticles from the oxygen‐rich matrix that surrounds them. The oxidation state of Fe in the nanoparticles has an effect on modeled reflectance properties of lunar soil. These results are relevant to remote sensing data for the Moon and to the remote determination of relative soil maturities for various regions of the lunar surface.     

Constraints on Mercury’s surface composition from MESSENGER and ground-based spectroscopy

The composition and chemistry of Mercury’s regolith has been calculated from MESSENGER MASCS 0.3-1.3 μm spectra from the first flyby, using an implementation of Hapke’s radiative transfer-based photometric model for light scattering in semi-transparent porous media, and a linear spectral mixing algorithm. We combine this investigation with linear spectral fitting results from mid-infrared spectra and compare derived oxide abundances with mercurian formation models and lunar samples. Hapke modeling results indicate a regolith that is optically dominated by finely comminuted particles with average area weighted grain size near 20 μm. Mercury shows lunar-style space weathering, with maturation-produced microphase iron present at ∼0.065 wt.% abundance, with only small variations between mature and immature sites, the amount of which is unable to explain Mercury’s low brightness relative to the Moon. The average modal mineralogies for the flyby 1 spectra derived from Hapke modeling are 35-70% Na-rich plagioclase or orthoclase, up to 30% Mg-rich clinopyroxene, <5% Mg-rich orthopyroxene, minute olivine, ∼20-45% low-Fe, low-Ti agglutinitic glass, and <10% of one or more lunar-like opaque minerals. Mercurian average oxide abundances derived from Hapke models and mid-infrared linear fitting include 40-50 wt.% SiO₂, 10-35 wt.% Al₂O₃, 1-8 wt.% FeO, and <25 wt.% TiO₂; the inferred rock type is basalt. Lunar-like opaques or glasses with high Fe and/or Ti abundances cannot on their own, or in combination, explain Mercury’s low brightness. The linear mixing results indicate the presence of clinopyroxenes that contain up to 21 wt.% MnO and the presence of a Mn-rich hedenbergite. Mn in M1 crystalline lattice sites of hedenbergite suppresses the strong 1 and 2 μm crystal field absorption bands and may thus act as a strong darkening agent on Mercury. Also, one or more of thermally darkened silicates, Fe-poor opaques and matured glasses, or Mercury-unique Ostwald-ripened microphase iron nickel may lower the albedo. A major part of the total microphase iron present in Mercury’s regolith is likely derived from FeO that is not intrinsic to the crust but has been subsequently delivered by exogenic sources.     

The effects of space weathering on Apollo 17 mare soils: Petrographie and chemical characterization

Abstract— The lunar soil characterization consortium, a group of lunar‐sample and remote‐sensing scientists, has undertaken the extensive task of characterization of the finest fractions of lunar soils, with respect to their mineralogical and chemical makeup. These compositional data form the basis for integration and modeling with the reflectance spectra of these same soil fractions. This endeavor is aimed at deciphering the effects of space weathering of soils on airless bodies with quantification of the links between remotely sensed reflectance spectra and composition. A beneficial byproduct is an understanding of the complexities involved in the formation of lunar soil. Several significant findings have been documented in the study of the <45 μm size fractions of selected Apollo 17 mare soils. As grain size decreases, the abundance of agglutinitic glass increases, as does the plagioclase, whereas the other minerals decrease. The composition of the agglutinitic glass is relatively constant for all size fractions, being more feldspathic than any of the bulk compositions; notably, TiO₂ is substantially depleted in the agglutinitic glass. However, as grain size decreases, the bulk composition of each size fraction continuously changes, becoming more Al‐rich and Fe‐poor, and approaches the composition of the agglutinitic glasses. Between the smallest grain sizes (10–20 and < 10 μm), the I_S/FeO values (amount of total iron present as nanophase Fe⁰) increase by greater than 100% (>2x), whereas the abundance of agglutinitic glass increases by only 10–15%. This is evidence for a large contribution from surface‐correlated nanophase Fe⁰ to the I_S/FeO values, particularly in the <10 μm size fraction. The surface nanophase Fe⁰ is present largely as vapor‐deposited patinas on the surfaces of almost every particle of the mature soils, and to a lesser degree for the immature soils (Keller et al., 1999a). It is reasoned that the vapor‐deposited patinas may have far greater effects upon reflectance spectra of mare soils than the agglutinitic Fe⁰.     

Iron oxidation state in impact glass from the K/T boundary at Beloc,Haiti, by high‐resolution XANES spectroscopy

Abstract— We examined the local iron environment in nine impact glasses from the Cretaceous‐Tertiary (K/T) boundary section at Beloc, Haiti, which formed as the result of impact melting during the Chicxulub impact event. The samples have been analyzed by Fe K‐edge high‐resolution X‐ray absorption near edge structure (XANES) spectroscopy to obtain data on both the Fe oxidation state and the coordination number. The pre‐edge peak of our high‐resolution XANES spectra display noticeable variations indicative of significant changes in the Fe oxidation state spanning a wide range from about 20 to 75 mol% trivalent Fe. All data plot along the same trend, falling between two mixing lines joining a point calculated as the mean of a group of tektites studied so far (consisting of four‐ and five‐coordinated Fe²⁺) to ^[4]Fe³⁺ and ^[5]Fe³⁺, respectively. Thus, the XANES spectra can be interpreted as a mixture of ^[4]Fe²⁺, ^[5]Fe²⁺, ^[4]Fe³⁺, and ^[5]Fe³⁺. There is no evidence for six‐fold coordinated Fe; however, its presence in small amounts cannot be excluded from XANES data alone. Our observations can be explained by two possible scenarios: either these impact glasses formed under very reducing conditions and, because of their small size, were easily oxidized in air while still molten, or they formed under a variety of different oxygen fugacities resulting in different Fe oxidation states. In the first case, the oxidation state and coordination number would imply similar formation conditions as splash‐form tektites, followed by progressive oxidation.     

Polarized absorption spectra of single crystals of lunar pyroxenes and olivines

Measurements have been made of the polarized absorption spectra (360-2200 nm.) of compositionally zoned pyroxene minerals in rocks 10045, 10047 and 10058 and olivines in rocks 10020 and 10022. Specimens in the form of petrographic thin sections were mounted on polarizing microscopes equipped with three-axis universal stage attachments and inserted into a Cary 17 spectrophotometer. The Apollo 11 pyroxenes with relatively high Ti/Fe ratios were chosen initially to investigate the presence of crystal field spectra of Fe²⁺ and Ti³⁺ ions in the minerals.Broad intense bands at about 1000 and 2100 nm. arise from spin-allowed, polarization-dependent transitions in Fe²⁺ ions in pyroxenes. Several weak sharp peaks occur in the visible region. Peaks at 402, 425, 505, 550 and 585 nm. represent spin-forbidden transitions in Fe²⁺ ions, while broader bands at 460–470 nm. and 650–660 nm. are attributed to Ti³⁺ ions. Charge transfer bands, which in terrestrial pyroxenes often extend into the visible region, are displaced to shorter wavelengths in lunar pyroxenes. This feature correlates with the absence of Fe³⁺ ions in these minerals. The magnitudes of the intensity ratios: band 465 nm. (Ti³⁺) to band 1000 nm. (Fe²⁺) are similar to Ti/Fe ratios from lunar pyroxene bulk chemical analyses, suggesting that an appreciable amount of titanium occurs as Ti³⁺ ions in the lunar pyroxenes. The 505 nm. spin-forbidden peak in Fe²⁺, together with absorption at 465 nm. by Ti³⁺, contribute to the pink or pale reddish-brown colors of lunar pyroxenes in transmitted lights.The absorption spectral measurements not only provide information on the redox behavior and crystal chemistry of lunar pyroxenes, but also form a basis for interpreting spectral reflectivity properties of lunar rocks and the Moon's surface.     

Ultraviolet spectral reflectance properties of common planetary minerals

Ultraviolet spectral reflectance properties (200-400 nm) of a large number of minerals known or presumed to exist on the surfaces of Mars, the Moon, and asteroids, and in many meteorites, were investigated. Ultraviolet reflectance spectra (200-400 nm) of these minerals range from slightly blue-sloped (reflectance decreasing toward longer wavelengths) to strongly red-sloped (reflectance increasing toward longer wavelengths). Most exhibit one or two absorption features that are attributable to FeO charge transfers involving Fe³⁺ or Fe²⁺. The UV region is a very sensitive indicator of the presence of even trace amounts (<0.01 wt%) of Fe³⁺ and Fe²⁺. The major Fe³⁺O absorption band occurs at shorter wavelengths (∼210-230 nm), and is more intense than the major Fe²⁺O absorption band (∼250-270 nm). Ti-bearing minerals, such as ilmenite, rutile and anatase exhibit UV absorption bands attributable to Ti⁴⁺O charge transfers. While the positions of metal-O charge transfer bands sometimes differ for different minerals, the variation is often not diagnostic enough to permit unique mineral identification. However, iron oxides and oxyhydroxides can generally be distinguished from Fe-bearing silicates in the 200-400 nm region on the basis of absorption band positions. Within a given mineral group (e.g., low-calcium pyroxene, olivine, plagioclase feldspar), changes in Fe²⁺ or Fe³⁺ abundance do not appear to result in a measurable change in absorption band minima positions. Absorption band positions can vary as a function of grain size, however, and this variation is likely due to band saturation effects. The intensity of metal-O charge transfers means that some minerals will exhibit saturated UV absorption bands even for fine-grained (<45 μm) powders. In cases where absorption bands are not saturated (e.g., Fe²⁺O bands in some plagioclase feldspars and pyroxenes), changes in Fe²⁺ content do not appear to cause variations in band position. In other minerals (e.g., olivine), changes in band positions are correlated with compositional and/or grain size variations, but this is likely due to increasing band saturation rather than compositional variations. Overall, we find that the UV spectral region is sensitive to different mineral properties than longer wavelength regions, and thus offers the potential to provide complementary capabilities and unique opportunities for planetary remote sensing.     

The lunar geochemistry of chromium and vanadium

Crystal/liquid partition coefficients for Cr, V, Mn, and Fe have been determined experimentally between olivine, orthopyroxene, clinopyroxene and silicate melt possesing the composition of a primitive lunar green glass, at oxygen fugacities appropriate to the lunar interior. These species all behave essentially as compatible elements and possess crystal/liquid partition coefficients mostly between 0.3 and 0.9. Partition coefficients for Cr, V, and Mn are generally similar to those of Fe. This implies that crystal/liquid fractionation processes in the lunar interior which do not involve the participation of spinels would not have been effective in fractionating MnO, CrO, and VO from FeO. The well-known constancy of FeO/MnO ratios in nearly all lunar rocks is a reflection of this behaviour. It is shown that comparably strong correlations between CrO-;FeO and VO-;FeO exist for lunar highland breccias and soils from all sites and that these correlations extend to primitive lunar volcanic glasses associated with mare volcanism, strongly suggesting that the CrO/FeO and VO/FeO ratios so derived are of global importance. The observed ratios characterizing differentiated regions of the Moon can be combined with the corresponding ratios for residual refractory portions of the Moon, using measured partition coefficients for Fe, Mg, Cr, V, and Mn between olivine, orthopyroxene and liquid. Bulk Moon abundances for Cr and V have been calculated for a range of reasonable assumptions concerning the petrogenetic relationships between differentiated portions of the Moon and complementary refractory residua consisting of olivine and orthopyroxene mineralogies. Because of the small differences in crystal liquid partition coefficients between FeO, CrO, and VO, these estimates are insensitive to large variations in the models. The bulk Moon is accordingly estimated to contain 2190–2463 ppm Cr and 79–95 ppm V. These values are very similar to the Cr and V contents of the Earth's mantle, estimated as 3010 ppm Cr and 81 ppm V by Sun (1982). The geochemical implications of these similarities are discussed.     

Kaitianite,Ti3+2Ti4+O5, a new titanium oxide mineral from Allende

Kaitianite, Ti³⁺₂Ti⁴⁺O₅, is a new titanium oxide mineral discovered in the Allende CV3 carbonaceous chondrite. The type grain coexists with tistarite (Ti₂O₃) and rutile. Corundum, xifengite, mullite, osbornite, and a new Ti,Al,Zr‐oxide mineral are also present, although not in contact. The chemical composition of type kaitianite is (wt%) Ti₂O₃ 56.55, TiO₂ 39.29, Al₂O₃ 1.18, MgO 1.39, FeO 0.59, V₂O₃ 0.08 (sum 99.07), yielding an empirical formula of (Ti³⁺_1.75Al_0.05Ti⁴⁺_0.10Mg_0.08Fe_0.02)(Ti⁴⁺_1.00)O₅, with Ti³⁺ and Ti⁴⁺ partitioned, assuming a stoichiometry of three cations and five oxygen anions pfu. The end‐member formula is Ti³⁺₂Ti⁴⁺O₅. Kaitianite is the natural form of γ‐Ti₃O₅ with space group C2/c and cell parameters a = 10.115 Å, b = 5.074 Å, c = 7.182 Å, β = 112°, V = 341.77 Å³, and Z = 4. Both the type kaitianite and associated rutile likely formed as oxidation products of tistarite at temperatures below 1200 K, but this oxidation event could have been in a very reducing environment, even more reducing than a gas of solar composition. Based on experimental data on the solubility of Ti³⁺ in equilibrium with corundum from the literature, the absence of tistarite in or on Ti³⁺‐rich corundum (0.27–1.45 mol% Ti₂O₃) suggests that these grains formed at higher temperatures than the kaitianite (>1579–1696 K, depending on the Ti concentration). The absence of rutile or kaitianite in or on corundum suggests that any exposure to the oxidizing environment producing kaitianite in tistarite was too short to cause the precipitation of Ti‐oxides in or on associated corundum.     

Lunar meteorites from Oman

Abstract– Sixty named lunar meteorite stones representing about 24 falls have been found in Oman. In an area of 10.7 × 10³ km² in southern Oman, lunar meteorite areal densities average 1 g km^?2. All lunar meteorites from Oman are breccias, although two are dominated by large igneous clasts (a mare basalt and a crystalline impact‐melt breccia). Among the meteorites, the range of compositions is large: 9–32% Al₂O₃, 2.5–21.1% FeO, 0.3–38 μg g^?1 Sm, and <1 to 22.5 ng g^?1 Ir. The proportion of nonmare lunar meteorites is higher among those from Oman than those from Antarctica or Africa. Omani lunar meteorites extend the compositional range of lunar rocks as known from the Apollo collection and from lunar meteorites from other continents. Some of the feldspathic meteorites are highly magnesian (high MgO/[MgO + FeO]) compared with most similarly feldspathic Apollo rocks. Two have greater concentrations of incompatible trace elements than all but a few Apollo samples. A few have moderately high abundances of siderophile elements from impacts of iron meteorites on the Moon. All lunar meteorites from Oman are contaminated, to various degrees, with terrestrial Na, K, P, Zn, As, Se, Br, Sr, Sb, Ba, U, carbonates, or sulfates. The contamination is not so great, however, that it seriously compromises the scientific usefulness of the meteorites as samples from randomly distributed locations on the Moon.     

Yellow impact glass from the K/T boundary at Beloc (Haiti): XANES determination of the Fe oxidation state and implications for formation conditions

Abstract— We determined the iron oxidation state and coordination number in five samples of yellow impact glass from the Cretaceous‐Tertiary (K/T) boundary section at Beloc, Haiti, which formed as the result of impact melting during the Chicxulub impact event. The samples were analyzed by Fe K‐edge XANES spectroscopy and the results were compared with published data on eight black impact glasses and one high Si‐K impact spherule from the same impact layer. The pre‐edge peak of our high‐resolution XANES spectra displays evident variations indicative of significant changes in the Fe oxidation state, spanning a wide range from about 75 to 100 mole% Fe³⁺. Yellow K/T glasses have significantly higher Fe³⁺/(Fe²⁺ + Fe³⁺) ratios compared to black K/T impact glasses (from 20 to 75 mole% Fe³⁺) and high Si‐K glass (20 mole% Fe³⁺). In particular, all the pre‐edge peak data on these three types of impact glasses plot between two mixing lines joining a point calculated as the mean of a group of tektites studied so far (consisting of ^[4]Fe²⁺ and ^[5]Fe²⁺) to ^[4]Fe³⁺ and ^[5]Fe³⁺, respectively. Thus, the XANES spectra of the yellow K/T glasses can be interpreted as a mixture of ^[4]Fe^{2+, [5]}Fe^{2+, [4]}Fe³⁺, and ^[5]Fe³⁺. Our observations can be explained by a very large range of oxygen fugacity conditions during melt formation. Furthermore, there is a clear positive relationship between the Fe³⁺/(Fe²⁺ + Fe³⁺) ratio and the Ca content of these glasses, suggesting that the Fe oxidation state was influenced by the relative contribution of Ca‐sulfate‐ and Ca‐carbonate‐bearing sedimentary rocks at the impact site.     

Elastic collisions in ion irradiation experiments: A mechanism for space weathering of silicates

Ion irradiation experiments have been performed on silicates (bulk samples) rich of olivine, pyroxene, and serpentine to simulate the effects of space weathering induced on asteroids by solar wind ions. We have used different ions (H⁺, He⁺, Ar⁺, Ar²⁺) having different energies (from 60 to 400 keV) to weather the samples, probed by Raman spectroscopy and UV-vis-NIR reflectance spectroscopy. All the irradiated materials have shown reddening and darkening of reflectance spectra in the 0.25-2.7 μm spectral range. We have found that the increase of the spectral slope of the continuum across the 1-μm band is strongly related with the number of displacements caused by colliding ions because of elastic collisions with the target nuclei. The spectral slopes have been compared, at increasing ion fluence, with those from irradiated Epinal meteorite. We show that formation of nuclear displacements by solar wind ion irradiation is a physical mechanism that reddens the asteroidal surfaces on a time-scale lower than 10⁶ years.     

Lunar surface agglutinates: Mapping composition anomalies

From the Clementine UVVIS imagery of the lunar surface, the abundance of agglutinates in the lunar regolith and their composition in terms of FeO and Al₂O₃ oxides have been predicted. Data on the spectral, chemical, and mineralogic measurements of about 30 lunar soil samples from the Lunar Samples Characterization Consortium (LSCC) collection were used. The fulfilled prognosis confirms that the mare agglutinates are enriched in Al₂O₃ and depleted of FeO, while the highland agglutinates are depleted of Al₂O₃ and enriched in FeO. This behavior can be caused by the global transport of the lunar surface material induced by cosmogenic factors.     

Classification of lunar rocks and glasses by a new statistical technique

A new multivariate statistical technique have been developed for detection of populations groupings in data arrays. General characteristics of the method are described. Results obtained analyzing lunar rocks and glasses are discussed. Lunar rocks lie in a genetically related sequence: pyroxenitic mantle materials produce mare type basalts; anorthositic rocks are the most distant members of the differentiation; noritic, hi-Ti and high KREEP basalts materials appear to be intermediate products. Lunar glasses parallel the overall behaviour of rocks, with some peculiar local characteristics. Granitic materials are present only as glasses, suggesting an origin as residuals. Links between several identified classes are discussed in terms of the evolution of the lunar crust.     

The dependence of reflectance spectra of Mercury on surface terrain

Reflectance spectra of Mercury, covering the spectral range of ～0.3–1.1 μm obtained during 1963–1976, were examined for any correlations with surface terrain. Mercury's 6.1385°/day rotational rate, the phases of the planet around maximum elongations, and bidirectional reflectance spectroscopy theory were used to identify the surface area associated with each spectrum. Data from 1974–1975, re-reduced with improved standard star flux ratios, show a weak absorption band in the near infrared not see in earlier analyses. Older spectra suggest that the western longitudes of the unimaged side of Mercury are similar to the rest of the planet. Spectra of the intercrater plains in the 0–90° quadrant suggest a possible absorption band. Spectra of areas dominated by Caloris Basin with the encompassing smooth plains may show Fe²⁺ abundances in the soil comparable to lunar highlands soil. No striking differences between spectra of intercrater plains and spectra of smooth plains are found. The absorption features seen in spectra of Mercury are generally weaker than features seen in lunar spectra.     

An experimental approach to understanding the optical effects of space weathering

The creation and accumulation of nanophase iron (npFe⁰) is a principal mechanism by which spectra of materials exposed to the space environment incur systematic changes referred to as “space weathering.” Since there is no reason to assume that cumulative space weathering products throughout the Solar System will be the same as those found in lunar soils, these products are likely to be very dependent on the specific environmental conditions under which they were produced. We have prepared a suite of analog soils to explore the optical effects of npFe⁰. By varying the size and concentration of npFe⁰ in the analogs we found significant systematic changes in the Vis/NIR spectral properties of the materials. Smaller npFe⁰ (<10 nm in diameter) dramatically reddens spectra in the visible wavelengths while leaving the infrared region largely unaffected. Larger npFe⁰ (>40 nm in diameter) lowers the albedo across the Vis/NIR range with little change in the overall shape of the continuum. Intermediate npFe⁰ sizes impact the spectra in a distinct pattern that changes with concentration. The products of these controlled experiments have implications for space-weathered material throughout the inner Solar System. Our results indicate that the lunar soil continuum is best modeled by npFe⁰ particles with bulk properties in the 15–25 nm size range. Larger npFe⁰ grains result in spectra that are similar in shape to the Mercury continuum. The continuum of S-type asteroid spectra appear to be best represented by low abundances of npFe⁰. The size of asteroidal npFe⁰ is similar to that of lunar soils, but slightly smaller on average (10–15 nm).