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At least 73 records · Page 4
All sourcesNASA NTRSDOE OSTI
NASA NTRS2017

The Effect of Shock on the Amorphous Component in Altered Basalt

Investigation of the geochemical and mineralogical composition of the Martian surface provides insight into the geologic history of the predominantly basaltic crust. The Chemistry and Mineralogy (CheMin) instrument onboard the Curiosity rover has returned the first X-Ray diffraction data from the Martian surface. However, large proportions (27 +/- 14 with some estimates as high as 50 weight percentage) of an amorphous component have been reported. As a remedy to this problem, mass balance equations using geochemistry, volatile chemistry, and mineralogy have been employed to constrain the geochemistry of the amorphous component. However, "the nature and number of amorphous phases that constitute the amorphous component is not unequivocally known". Multiple hypotheses have been proposed to explain the origin of this amorphous component: Allophane (Al2O); Basaltic glass (Volcanic and impact); Palagonite (Altered basaltic glass); Hisingerite (Fe (sup 3 plus)-bearing phyllosilicate); S/Cl-rich component (sulfates and/or akaganeite); Nanophase ferric oxide component (npOx). Establishing a multi-phase amorphous component from a basaltic precursor that has undergone physical and chemical weathering within geochemical constraints is of paramount importance to better understand the composition of a large portion of the Martian surface (up to 50 weight percentage). Shocked basalts from Lonar Crater in India are valuable analogs for the Martian surface because it is a well-preserved impact crater in a basaltic target. Having undergone pre- and post-shock aqueous alteration, these rocks provide crucial data regarding the effect of shock on the amorphous component in altered basalt. By conducting mass balance equations similar to what has been performed for Gale crater materials, we attempt to calculate the geochemistry of the amorphous component in altered basalts ranging from unshocked to Class 5 (Table 1). This has the potential to reveal the nature and origin (i.e. primary igneous, shock metamorphic, and/or aqueous alteration occurring before or after the impact event) of the amorphous component in shocked basalt with the goal of unravelling the history of the Martian surface.

Eckley, S. A.↗
NASA NTRS1978

The lunar mare basalt suite

Recent studies have greatly expanded knowledge of lunar mare basalts. Since 1976 there has been a revision of the Apollo 12 low-Ti mare basalt suite and the discovery of a new very low-Ti (VLT: less than 1% TiO2) basalt suite at Apollo 17 and in the new Soviet samples from Mare Crisium (LUNA 24). Current studies suggest that the VLT basalts may be in some way related to the enigmatic 'green glasses' which are found in the soils from every lunar landing site. Telescopic studies of spectral reflectance and crater systematics show that basalts of varying Ti content were extruded throughout the history of mare volcanism. These new discoveries indicate that mare basalts can no longer be classified into the two simple groups of older high-Ti basalts and younger low-Ti basalts.

Papike, J. J.↗
NASA NTRS1977

Sr-isotopic constraints on the petrogenesis of Apollo 12 mare basalts

As part of a study of Apollo 12 basalts, crystallization ages and initial Sr-87/Sr-86 (I) were determined for pigeonite basalts 12039 and 12055 and ilmenite basalt 12051. Sr-86/Sr-87 measurements for a larger suite of whole rock and plagioclase samples were obtained, and it is found that I-values for olivine and pigeonite basalts are indistinguishable while I-values for ilmenite basalts are distinctly lower. A self-consistent model for the evolution of the Sr-isotopic composition and REE abundances suggests that basalt was formed by small (2-10%) degrees of melting of cumulate sources composed of varying proportions of olivine, orthopyroxene, and clinopyroxene. This model requires nonchondritic relative abundances of the REE in the parental liquid at the time of formation of the cumulate sources. The model also describes Sr-isotopic composition and REE abundances of Apollo 17 high-Ti basalts and Apollo 15 low-Ti basalts. A lunar 'scenario' involving open system crystallization of a magma ocean from the crust downward is proposed.

Nyquist, L. E.↗
NASA NTRS1978

Genesis of Apollo 15 olivine normative mare basalts - Trace element correlations

Chemical and petrographic studies of 21 Apollo 15 rake basalts are reported; one pyroxene-phyric basalt, four olivine-phyric basalts, 15 olivine microgabbros, and one brecciated basalt are distinguished. The olivine-normative basalts (i.e., all samples but the pyroxene-phyric basalt) show correlation trends of La/Sm vs. La and Sm/Eu vs. La that are within the observed dispersion ranges of La/Sm and Sm/Eu ratios for a single lava flow. Trace element fractionation trends in the sample could be due to mobilization (perhaps by filter pressing) of fractionated residual liquid during the crystallization of a lava flow. However, it is also possible that the suite of olivine-normative basalts represents several basalt flows produced by partial melting of cumulate layers having interstitial liquids with variable trace-element compositions.

Ma, M.-S.↗
NASA NTRS1980

Petrology of mare-type basalt clasts from consortium breccia 73255

Breccia 73255 contains sparse small clasts of basalts that have mare affinities; the basalts are members of a single differentiated suite. The clasts have been fractured throughout and locally granulated. Textural and compositional evidence indicates that the fracturing and granulation were produced by the 73255 breccia-forming event, and this event took place before the basalts had completely solidified. Thus, it appears that the eruption of the basalts took place at about the same time as the formation of the 73255 breccia, about 3.9 b.y. ago. The mineral assemblages and modes of the basalt clasts are those typical of mare basalts, but the clasts are not identical in detail with any basalts returned from the mare surfaces. They are instead most similar to the 14053-type basalts from the Apollo 14 site.

James, O. B.↗
NASA NTRS1987

On the connection between mare basalts and picritic volcanic glasses

The liquid lines of descent were calculated for low-pressure equilibrium and fractional crystallization of mare basaltic liquids in order to examine the postulated link between picritic volcanic glasses and mare basalts. The models of Longhi (1977, 1982) were modified by including expressions for the armalcolite/ilmenite surface boundary and the Cr-spinel liquidus surface, average molar partition coefficients for armalcolite/liquid pairs, and new experimental data of Longhi and Pan (1987). The results indicate that, with two exceptions, mare basalts and picritic volcanic glasses are not related by simple, linear-surface crystallization processes. However, the compositions of Luna 24 ferrobasalt and Apollo 11 high-K basalts could be closely matched with the lines of liquid descent of certain green and orange picritic glasses, respectively. The calculations also show that the picritic magmas would have fractionated to produce basalts with bulk and mineral compositions similar to those of mare basalts, supporting the hypothesis that mare basalts have fractionated compositions and that the small number of observed linkages between basalts and picritic parents is a consequence of limited sampling.

Longhi, John↗
NASA NTRS1989

High alumina (HA) and very high potassium (VHK) basalt clasts from Apollo 14 breccias. II - Whole rock geochemistry - Further evidence for combined assimilation and fractional crystallization within the lunar crust

The understanding of basalt petrogenesis at the Apollo 14 site has increased markedly due to the study of 'new' samples from breccia 'pull-apart' efforts. Whole-rock compositions of 26 new high alumina (HA) and 7 very high potassium (VHK) basalts emphasize the importance of combined assimilation and fractional crystallization in a lunar regime. Previously formulated models for HA and VHK basalt petrogenesis are modified in order to accomodate these new data, although modeling parameters are essentially the same. The required range in HA basalt compositions is generated by the assimilation of KREEP by a 'primitive' parental magma. The VHK basalts can be generated by three parental HA basalts assimilating granite. Results indicate that VHK basalt compositions are dominated by the parental magma, and only up to 8 percent granite assimilation is required. This modeling indicates that at least three VHK basalt flows must be present at the Apollo 14 site.

Neal, C. R.↗
NASA NTRS1992

Rb-Sr and Sm-Nd chronology of an Apollo 17 KREEP basalt

The paper determines Sm-Nd and Rb-Sr mineral isochrons for an Apollo 17 KREEP (pigeonite) basalt clast from breccia 72275 collected from Boulder 1, Station 2 in the Valley of Taurus-Littrow. Sm-Nd analyses of the basalt yield a precise mineral isochron age of 4.08 +/-0.07 Ga for lambda(Sm-147) = 0.00654/Ga. The concordancy of Sm-Nd and Rb-Sr ages for the basalt suggests that it crystallized about 4.08 Ga ago. Distinct ages and initial Sr isotopic ratios for Apollo 17 KREEP basalts and Apollo 14 and 15 KREEP suggest that these two types of KREEP basalts were not derived from the same source. Apollo 17 KREEP basalts are contemporaneous with some Apollo 14 aluminous mare basalts. The ages and Sr and Nd isotopic data suggest that these two different types of basalts were produced from sources having similar Rb/Sr ratios but different Sm/Nd ratios.

Shih, C.-Y.↗
NASA NTRS1993

Searching for neuKREEP: An EMP study of Apollo 11 Group A basalts

The Apollo 11 and 17 landing sites are characterized by the presence of high-Ti basalts (TiO2 greater than 6 percent). The Group A basalts of Apollo 11 have elevated K compositions (greater than 2000 ppm); and are enriched in incompatible trace elements relative to the other types of high-Ti basalt found in the region. These unique basalts also are the youngest of all high-Ti basalts, with an age of 3.56 +/- 0.02 Ga. Recent modelling of the Apollo 11 Group A basalts by Jerde et al. has demonstrated that this unique variety of high-Ti basalt may have formed through fractionation of a liquid with the composition of the Apollo 11 orange glass, coupled with assimilation of evolved material (dubbed neuKREEP and having similarities to lunar quartz monzodiorite). Assimilation of this material would impart its REE signature on the liquid, resulting in the elevated REE abundances observed. Minerals such as whitlockite which contain a large portion of the REE budget can be expected to reflect the REE characteristics of the assimilant. To this end, an examination of the whitlockite present in the Apollo 11 Group A basalts was undertaken to search for evidence of the neuKREEP material assimilated.

Jerde, Eric A.↗
NASA NTRS2005

Li, B - Behavior in Lunar Basalts During Shock and Thermal Metamorphism: Implications for H2O in Martian Magmas

Introduction: The water-content of Martian magmas is a topic of debate among researchers. Some Martian basalts are characterized with melt inclusions of biotite, apatite and amphibole; phases typically associated with hydration reactions on Earth [1-3]. However, the H-content of melt inclusions from these basalts is low, and bulk-rock H2O-contents range from a meager 0.013 to 0.035 wt. % in Shergotty [4]. Nonetheless, researchers note that low present-day water contents do not preclude a once hydrous past [5]. Since light lithophile elements (LLE), such as Li and B, partition into aqueous fluids at T > 350 C, workers proposed that Li-B depletions in pyroxene rims of Nakhlite and Shergottite basalts reflect the loss of several weight percent water from Martian magmas during crystallization [6]. Since similar depletions were observed in pyroxene rims from completely dry lunar basalts, it is likely that alternative mechanisms also contribute to the distribution of elements such as Li and B [7]. Given that many Martian basalts have experienced considerable shock pressures (15-45 GPa), it is possible that shock and subsequent thermal metamorphism may have influenced the volatile element records of these basalts [8]. In order to better understand the distribution of Li and B, we are studying the effects of crystal chemistry, shock pressure, and thermal metamorphism in pyroxenes from lunar basalts. Below, we discuss results from experimentally shocked and thermally metamorphosed Apollo 11, 10017 (A-11) and Apollo 17, 75035 (A-17) basalts.

Chaklader, Johny↗
NASA NTRS2007

Valence State Partitioning of Cr and V Between Pyroxene - Melt: Estimates of Oxygen Fugacity for Martian Basalt QUE 94201

Several studies, using different oxybarometers, have suggested that the variation of fO2 in martian basalts spans about 3 log units from approx. IW-1 to IW+2. The relatively oxidized basalts (e.g., pyroxene-phyric Shergotty) are enriched in incompatible elements, while the relatively reduced basalts (e.g., olivine-phyric Y980459) are depleted in incompatible elements. A popular interpretation of the above observations is that the martian mantle contains two reservoirs; 1) oxidized and enriched, and 2) reduced and depleted. The basalts are thus thought to represent mixing between these two reservoirs. Recently, Shearer et al. determined the fO2 of primitive olivine-phyric basalt Y980459 to be IW+0.9 using the partitioning of V between olivine and melt. In applying this technique to other basalts, Shearer et al. concluded that the martian mantle shergottite source was depleted and varied only slightly in fO2 (IW to IW+1). Thus the more oxidized, enriched basalts had assimilated a crustal component on their path to the martian surface. In this study we attempt to address the above debate on martian mantle fO2 using the partitioning of Cr and V into pyroxene in pyroxene-phyric basalt QUE 94201.

Karner, J. M.↗
NASA NTRS2022

The Zn, S, and Cl Isotope Compositions of Mare Basalts: Implications for the Effects of Eruption Style and Pressure on Volatile Element Stable Isotope Fractionation on the Moon

We compare the stable isotope compositions of Zn, S, and Cl for Apollo mare basalts to better constrain the sources and timescales of lunar volatile loss. Mare basalts have broadly elevated yet limited ranges in δ(66)Zn, δ(34)S, and δ(37)Cl_(SBC+WSC) values of 1.27 ± 0.71, 0.55 ± 0.18, and 4.1 ± 4.0‰, respectively, compared to the silicate Earth at 0.15, –1.28, and 0‰, respectively. We find that the Zn, S, and Cl isotope compositions are similar between the low- and high-Ti mare basalts, providing evidence of a geochemical signature in the mare basalt source region that is inherited from lunar formation and magma ocean crystallization. The uniformity of these compositions implies mixing following mantle overturn, as well as minimal changes associated with subsequent mare magmatism. Degassing of mare magmas and lavas did not contribute to the large variations in Zn, S, and Cl isotope compositions found in some lunar materials (i.e., 15‰ in δ(66)Zn, 60‰ in δ(34)S, and 30‰ in δ(37)Cl). This reflects magma sources that experienced minimal volatile loss due to high confining pressures that generally exceeded their equilibrium saturation pressures. Alternatively, these data indicate effective isotopic fractionation factors were near unity. Our observations of S isotope compositions in mare basalts contrast to those for picritic glasses (Saal and Hauri 2021), which vary widely in S isotope compositions from –14.0 to 1.3‰, explained by extensive degassing of picritic magmas under high-P/P_(Sat) values (>0.9) during pyroclastic eruptions. The difference in the isotope compositions of picritic glass beads and mare basalts may result from differences in effusive (mare) and explosive (picritic) eruption styles, wherein the high-gas contents necessary for magma fragmentation would result in large effective isotopic fractionation factors during degassing of picritic magmas. Additionally, in highly vesiculated basalts, the δ(34)S and δ(37)Cl values of apatite grains are higher and more variable than the corresponding bulk-rock values. The large isotopic range in the vesiculated samples is explained by late-stage low-pressure “vacuum” degassing (P/P-(Sat) ~ 0) of mare lavas wherein vesicle formation and apatite crystallization took place post-eruption. Bulk-rock mare basalts were seemingly unaffected by vacuum degassing. Degassing of mare lavas only became important in the final stages of crystallization recorded in apatite—potentially facilitated by cracks/fractures in the crystallizing flow. We conclude that samples with wide-ranging volatile element isotope compositions are likely explained by localized processes, which do not represent the bulk Moon.

Halogens↗
NASA NTRSDate not supplied

Phase Transitions and Melting in the Venusian Basaltic Crust: Implications for Crustal Recycling

Understanding phase transitions and melting in the Venusian crust and the associated changes in density are critical to constrain crustal thickness, recycling, and remelting processes. For example, average surface conditions on Venus of 92 bars and 460 °C correspond to low-grade metamorphic conditions on Earth equivalent to hornfels- and greenschist-facies. Further, the primary igneous mineralogy in the Venusian crust should be replaced by metamorphic minerals over time and potentially melt, as temperatures and pressures increase with depth along geothermal gradients. Here, we use Perple_X (Connolly, 2005), a Gibbs free energy minimization program to calculates table phase equilibria over a range of pressure and temperature conditions for whole-rock compositions of a dry basalt, alkali basalt, and peridotite. Further, we extract mineral abundancies along five geotherms of 5, 10, 15, 20 and 25 °C/km and calculate the rock density after the extraction of melt. On the coldest geotherm of 5 °C/km, melting would start at ~ 197 km and ~121 km in the basalt and alkali basalt, respectively, and therefore at depths that significantly exceed the estimated thickness of the Venusian crust (8-25 km). A density cross-over, where the crustal density would exceed that of the mantle could potentially induce delamination and is estimated to occur at ~ 40 km for both compositions. On the 10 °C/km geotherm, melting of the basalt starts at 65 km and melt extraction only causes a gradual densification due the formation of initially lower melt proportions. In contrast, the alkali basalt starts to melt at a depth of ~ 57 km and the subsequent densification of the residual composition could trigger delamination at ~ 60km depth. For hotter geotherms (i.e., 25 °C/km gradient), melting would occur at shallower depths of 21 – 23 km. However, the basalt will not get significantly denser than the mantle while the residuum of the alkali basalt would reach a density cross-over at 30 km. Hence, differences in Venusian crustal compositions can significantly influence the thickness of the crust on individual geotherms. Our results demonstrate that phase transitions and melting are strongly dependent on the assumed geotherm and could, combined with geodynamic models, further constrain crustal parameters.

Julia Semprich↗
DOE OSTI2023

New Insights from Legacy Seismic Data regarding Basalt Elevations and Variability on the Hanford Site

Migration of groundwater contaminants in the Gable Gap area of the Hanford Site in southeastern Washington State is strongly influenced by the distribution and permeability of basalts that lie beneath an unconfined aquifer. Locally, folding and faulting of the Columbia River Basalt associated with the Yakima fold and thrust belt followed by erosion due to the Lake Missoula floods resulted in a complex basalt surface that represents either an impermeable lower boundary to the unconfined aquifer system or localized regions of increased permeability that potentially promote communication between the unconfined aquifer system and deeper, confined aquifer systems. Paleo-channels carved into the basalt by floodwaters are thought to provide preferential flow paths for groundwater contaminants. In 2011, a seismic landstreamer campaign was carried out to image the basalt surface and produced pre-stack depth migrated p-wave reflection images. The reflection images identified two large troughs that may represent paleo-channels and several areas of possible faulting. Here, the streamer data are re-analyzed using refraction travel-time and Rayleigh wave dispersion analyses to obtain images of compressional and shear wave velocities within the suprabasalt sediment sections and the upper basalt surface. The combined interpretation of reflection and seismic velocity images shows complexity in the basalt velocity and elevation, which varies by 50 m or more within the study area. These results, along with other ongoing geophysical investigations, will be used to inform the site geologic model and potentially guide placement of future boreholes needed to quantify vertical flow between the confined and unconfined aquifers.

58 GEOSCIENCES↗
DOE OSTI2020

In silico assessment of the potential of basalt amendments to reduce N 2 O emissions from bioenergy crops

Abstract The potential of large‐scale deployment of basalt to reduce N 2 O emissions from cultivated soils may contribute to climate stabilization beyond the CO 2 ‐removal effect from enhanced weathering. We used 3 years of field observations from maize ( Zea mays ) and miscanthus ( Miscanthus × giganteus ) to improve the nitrogen (N) module of the DayCent model and evaluate the potential of basalt amendments to reduce N losses and increase yields from two bioenergy crops. We found 20%–60% improvement in our N 2 O flux estimates over previous model descriptions. Model results predict that the application of basalt would reduce N 2 O emissions by 16% in maize and 9% in miscanthus. Lower N 2 O emissions responded to increases in the N 2 :N 2 O ratio of denitrification with basalt‐induced increases in soil pH, with minor contributions from the impact of P additions (a minor component of some basalts) on N immobilization. The larger reduction of N 2 O emissions in maize than in miscanthus was likely explained by a synergistic effect between soil pH and N content, leading to a higher sensitivity of the N 2 :N 2 O ratio to changes in pH in heavily fertilized maize. Basalt amendments led to modest increases in modeled yields and the nitrogen use efficiency (i.e., fertilizer‐N recover in crop production) of maize but did not affect the productivity of miscanthus. However, enhanced soil P availability maintained the long‐term productivity of crops with high nutrient requirements. The alleviation of plant P limitation led to enhanced plant N uptake, thereby contributing to lower microbial N availability and N 2 O emissions from crops with high nutrient requirements. Our results from the improved model suggest that the large‐scale deployment of basalt, by reducing N 2 O fluxes of cropping systems, could contribute to the sustainable intensification of agriculture and enhance the climate mitigation potential of bioenergy with carbon capture and storage strategies.

59 BASIC BIOLOGICAL SCIENCES↗
NASA NTRS1977

Luna 24 - Opaque mineral chemistry of gabbroic and basaltic fragments from Mare Crisium

Spinels and ilmenites are relatively sparse in the Luna 24 gabbro and basalts. Spinel compositions show some affinities to those of spinels in Apollo 12, Apollo 14 and Luna 16 basalts; a characteristic feature is high Al2O3, reaching a maximum of 19.8 wt%. A comparison of spinels in the Luna 24 gabbro with those in other deep-seated lunar intrusive rocks shows a characteristic trend for Fe/Mg. This trend is systematic from gabbro to anorthosite to troctolite and is interpreted to be P-T dependent. Compositions of spinels in the gabbro fall within the Cr/Al trend defined by the spinels of the basalts, but form a Fe/Mg trend parallel to that of the basalts; this relationship suggests that both the gabbro and the basalts are derived from a closely similar source region, with the basalts originating at a slightly greater depth than the gabbro. The spinels in both rock types are considered to have formed at high crustal levels, at low pressures. The Luna 24 data suggest that the compositional discontinuities which exist between chromian spinels and titanian spinels in a large proportion of mare basalts are the result of nucleation of chromian spinels at high crustal levels prior to eruption, and of titanian spinels during melt crystallization at the lunar surface.

Haggerty, S. E.↗
NASA NTRS1978

Trace elements in ocean ridge basalts

A study is made of the trace elements found in ocean ridge basalts. General assumptions regarding melting behavior, trace element fractionation, and alteration effects are presented. Data on the trace elements are grouped according to refractory lithophile elements, refractory siderophile elements, and volatile metals. Variations in ocean ridge basalt chemistry are noted both for regional and temporal characteristics. Ocean ridge basalts are compared to other terrestrial basalts, such as those having La/Yb ratios greater than those of chondrites, and those having La/Yb ratios less than those of chondrites. It is found that (1) as compared to solar or chondrite ratios, ocean ridge basalts have low ratios of large, highly-charged elements to smaller less highly-charged elements, (2) ocean ridge basalts exhibit low ratios of volatile to nonvolatile elements, and (3) the transition metals Cr through Zn in ocean ridge basalts are not fractionated more than a factor of 2 or 3 from the chondritic abundance ratios.

Kay, R. W.↗
NASA NTRS1977

Chemistry of Apollo 12 mare basalts - Magma types and fractionation processes

Major and trace element data for a large suite of petrographically diverse Apollo 12 mare basalts are presented, and magma types sampled at the Apollo 12 site are characterized. The data confirm earlier classifications of the basalts into olivine, pigeonite, ilmenite, and feldspathic basalts. The olivine and pigeonite basalts are shown to be comagnetic and related by olivine fractionation. The other types, which differ in trace element and isotopic characteristics, are derived from different sources within the lunar interior. The spatial relations between the main basalt types are discussed in terms of local cratering events, and it is suggested that the younger ilmenite basalts overlie the olivine-pigeonite basalts. The role of olivine-dominated near-surface crystal fractionation in causing chemical variation is examined, and a relation between inferred cooling rate and the position of a sample in the fractionation sequence is determined.

Rhodes, J. M.↗