Emission spectrographic determination of trace elements in lunar samples from Apollo 11
Apollo 11 lunar rock trace elements, examining basalt, gabbroic igneous rocks, breccias and fines by DC arc emission spectroscopy
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Apollo 11 lunar rock trace elements, examining basalt, gabbroic igneous rocks, breccias and fines by DC arc emission spectroscopy
Photomicrographic study of 200 thin sections of Apollo 14 rock samples suggests that these monomineralic aggregates are recrystallized single-mineral grains. It is contended, therefore, that the source rocks are not properly characterized by igneous rock names, being more moderately coarse-grained gabbroic rather than ultramafic rocks.
Thin sections and polished electron probe mounts of Apollo 15 glasscoated breccias 15255, 15286, 15466, and 15505 were examined optically and analyzed by sem/microprobe. Sections from breccias 15465 and 15466 were examined in detail, and chemical and mineralogical analyses of several larger lithic clasts, green glass, and partly crystallized green glass spheres are presented. Area analyses of 33 clasts from the above breccias were also done using the SEM/EDS system. Mineralogical and bulk chemical analyses of clasts from the Apollo 15 glass-coated breccias reveal a diverse set of potential rock types, including plutonic and extrusive igneous rocks and impact melts. Examination of the chemistry of the clasts suggests that many of these clasts, like those found in 61175, are impact melts. Their variability suggests formation by several small local impacts rather than by a large basin-forming event.
Subtle color variations of martian surface materials were enhanced in eight Viking Lander (VL) color images. Well-defined soil units recognized at each site (six at VL-1 and four at VL-2), are identified on the basis of color, texture, morphology, and contact relations. The soil units at the Viking 2 site form a well-defined stratigraphic sequence, whereas the sequence at the Viking 1 site is only partially defined. The same relative soil colors occur at the two sites, suggesting that similar soil units are widespread on Mars. Several types of rock surface materials can be recognized at the two sites; dark, relatively 'blue' rock surfaces are probably minimally weathered igneous rock, whereas bright rock surfaces, with a green/(blue + red) ratio higher than that of any other surface material, are interpreted as a weathering product formed in situ on the rock. These rock surface types are common at both sites. Soil adhering to rocks is common at VL-2, but rare at VL-1. The mechanism that produces the weathering coating on rocks probably operates planet-wide.
Volatiles in planetary interiors play important roles in magma genesis, crust formation, eruption style, and even habitability of planetary surfaces. Allan Treiman’s career has touched on volatiles in the Moon, Mars, HED-parent body, the Earth, Venus, and other planetary bodies through studies of igneous rocks, volatile-bearing igneous minerals within these rocks, and the secondary alteration products produced from these rocks and minerals. His seminal work in many of these fields has inspired our careers and many others in our field. Here, we will build on and summarize what we know of the volatile content of basaltic rocks in the inner solar system. Specifically, this talk will focus on using volatile-bearing minerals (amphibole and apatite) along with bulk compositions to constrain the pre-eruptive, and potentially predegassed, volatile content of the magma and their source regions. We will then use these estimates to compare the volatile content of the Earth, Moon, Mars, Venus, and Mercury and what open questions there are for each planetary body.
Apollo 12 lunar soil, breccia and igneous rock samples, determining elemental abundances with spark source mass spectrometry and neutron activation analysis
Lunar rock 78235 is a coarse-grained igneous rock which was chipped from the top of a boulder about 1/2 m in size at Station 8 at the base of the Sculptured Hills, Taurus-Littrow Valley. The rock is a shocked coarse-grained norite with a relict subophitic texture; it is composed of about equal proportions of chromian bronzite and anorthite. Evidence is presented for the shock history of the rock. It is concluded that 78235 is a deep-seated norite of cumulate origin which has been intensely shocked. Although it may be possible to account for the observed shock-induced features by invoking a single shock event, the evidence is best explained by a history which includes at least two discrete shock events. In the first identifiable shock event much of the plagioclase was transformed to maskelynite and the associated bronzite was deformed and acquired a mosaic structure. In a later shock event, localized melting of both plagioclase pyroxene occurred.
A study of two clasts of coarse-grained anorthositic-noritic-troctolitic-suite norites from the fragment-laden melt rock 73255 is presented. Both clasts are igneous rocks crystallized from melts that were probably internally generated; clast 27,80 is a cumulate, and the parent magmas of both rocks probably crystallized below the lunar surface. Despite similar history, the parent rocks of the two clasts appear to be derived from distinct magma types: the 27,80 is characterized by plagioclase and orthopyroxene as the major constituents and by a high K, Nb, and Zr content, while the 27,45 type also contains augite and has a low content of K, Nb, and Zr.
Assemblages with titanite, pyroxene(s), olivine, ilmenite, magnetite, and quartz can be used to constrain the intensive and compositional variables that operate during crystallization. Such assemblages are relatively rare in metamorphic rocks, but they are more common in igneous rocks and more frequently reported in plutonic than volcanic rocks. We used the program QUILF, enhanced with thermodynamic data for titanite, to compute stable reactions among titanite (CaTiOSiO4), Fe-Mg-Ti ilmenite and magnetite (hereafter ilmenite and magnetite), Ca-Mg-Fe pyroxenes and olivine, and quartz, and to evaluate some of the factors that control titanite stability. Calculations at 1, 3, and 6 Kbar and 650, 850, 1100 0 C, in the system CaO - MgO - FeO Fe2O3 - TiO2 - SiO2, suggest that the reactions: Augitc + Ilmenite = Titanite + Magnetite + Quartz and Augite + Ilmenite + Quartz = Titanite + Orthopyroxene, impose well defined fugacity of O2, alpha(sub SiO2), , and compositional restrictions to the assemblages: (1) Titanite + Magnetite + Quartz, (2) Titanite + Orthopyroxene, (3) Augite + Ilmenite, and consequently titanite stability. From our calculations in this system we can draw the following general conclusions: (1) The assemblage Titanite + Magnetite + Quartz is always a good indicator of relatively high fugacity of O2, and it is likely more common in relatively iron-rich bulk compositions and for decreasing temperature and pressure conditions. (2) At high temperatures (>= 650 C) titanite is not stable in quartz-saturated rocks that contain the assemblage Orthopyroxene + Augite + Ilmenite + Magnetite. (3) In quartz-saturated rocks the coexistence of titanite and magnetite with either orthopyroxene or olivine requires a confluence of conditions relating bulk composition, fugacity of O2, and slow cooling. Thus, such assemblages must be rare. (4) Regardless of T and fugacity of O2 conditions, and bulk-composition, titanite is not stable in quartz-absent rocks that contain Olivine + Orthopyroxene + Augite + Ilmenite + Magnetite. Decreasing temperature and pressure conditions appear to favor titanite crystallization, thus, it is not unsurprising that titanite is frequently observed in slowly cooled rocks, albeit, in association with amphibole. We argue that the titanite + amphibole association is likely favored by high water activity, regardless of oxygen fugacity. Because water activity increases during crystallization of a pluton, the association titanite + amphibole, and consequently titanite, is likely to be more common in plutonic rocks than in volcanic rocks.
Part VI of the evolutionary system of mineralogy catalogs 262 kinds of minerals, formed by 18 different processes, that we suggest represent the earliest solid phases in Earth’s crust. All of these minerals likely formed during the first tens of millions of years following the global-scale disruption of the Moon-forming impact prior to ~4.4 Ga, though no samples of terrestrial minerals older than ~4.37 Ga are known to have survived on Earth today. Our catalog of the earliest Hadean species includes 80 primary phases associated with ultramafic and mafic igneous rocks, as well as more than 80 minerals deposited from immiscible S-rich fluids and late-stage Si-rich residual melts. Earth’s earliest crustal minerals also included more than 200 secondary phases of these primary minerals that were generated by thermal metamorphism, aqueous alteration, impacts, and other processes. In particular, secondary mineralization related to pervasive near-surface aqueous fluids may have included serpentinization of mafic and ultramafic rocks, hot springs and submarine volcanic vent mineralization, hydrothermal sulfide deposits, zeolite and associated mineral formation in basaltic cavities, marine authigenesis, and hydration of subaerial lithologies. Additional Hadean minerals may have formed by thermal metamorphism of lava xenoliths, sublimation at volcanic fumaroles, impact processes, and volcanic lightning. These minerals would have occurred along with more than 180 additional phases found in the variety of meteorites that continuously fell to Earth’s surface during the early Hadean Eon.
Comparative optical and high-voltage electron petrographic analyses of igneous rocks and several types of breccias the Fra Mauro and Apennine sites of Apollo 14 and 15 are reported and interpreted. The crystalline rocks are found to differ substantially from the Apollo 11 and 12 basalts. Substructures in the Apollo 14 breccias are complex. At least two bonding mechanisms can be discerned from the electron petrographic examination: (a) 'shock sintering' due to high pressures and temperatures associated with the shock waves of meteoritic impacts; and (b) lithification by glass bonding.
The abundances of indium in the cosmos, meteorites, and tektites, in rock-forming and ore minerals, and in common igneous rocks are tabulated, with brief comments. Indium's behavior in magmatogenic processes and during weathering and alteration of rocks is described. Attention is given to solubilities of compounds, adsorption processes, and valence states. Also tabulated are the abundances in common sediments and in sedimentary and metamorphic rocks.
Carbides and the surrounding metal of eight particles from Apollo 14, 16, and 17 soils were analyzed for C, Fe, Ni, and Co with the electron microprobe. In addition, carbide-containing metal particles in two Apollo 17 rocks were studied. Carbide-metal assemblages were found in anorthositic hornfels, melt rock, and agglutinate, but not in any primary igneous rocks. Carbon measurements show that cohenite is the carbide phase present in all the samples. Cohenite exsolves from the carbon-rich metal phase during cooling of the lunar metal particle in the host rocks or soil fragments. Measurements of two-phase interface compositions indicate equilibration for carbides and metal during cooling below 600 C and possibly below 500 C.
In our analyses, we utilize a microdrilling technique that removes 40 to 100 micron diameter cores from mineral grains in thin sections analyzed by microprobe. The cores are then analyzed by INAA using the technique of Lindstrom. Three eucrites were selected for application of this analytical technique: monomict breccias Pasamonte and Stannern and unbrecciated EET90020. Pasamonte is among the most unequilibrated of the eucrites on the basis of zoning in pyroxenes and is considered to be an igneous rock not significantly affected by metamorphism. Stannern has igneous texture but its pyroxenes indicate some re-equilibration, although little, if any, recrystallization. EET90020 has a granulite texture and has been substantially recrystallized. Our sample of Pasamonte contains several clasts of different grain sizes ranging from glass to fine grained with diabasic texture containing lathy plagioclase, unexsolved pigeonite, and mesostasis. Cores were taken of the glass and from minerals and mesostases in six lithic clasts which normally allowed sampling of more than one phase per clast. Our sample of Stannern is also a breccia but with little difference in grain size between clasts and matrix. The plagioclase and pigeonite are blocky, twinned, and exsolved and coexist with a bit of mesostasis. Cores were taken of plagioclase and pigeonite with no attempt to distinguish separate clasts. EET90020 is a granular mixture of twinned plagioclase and pigeonite having rather uniform size and many triple junctions. Several cores were taken of both phases. Both clear and cloudy grains of plagioclase and pyroxene were sampled in all three eucrites.
Element abundances in igneous rocks measured by instrumental neutron activation using high resolution lithium drifted germanium detectors
Apollo 11 lunar rock and fines chemistry, mineralogy and petrology, discussing composition, igneous rocks, microbreccias, glasses and pyroxene relations
Three fragments of holocrystalline igneous rocks of the gabbro type, weighing 30 to 50 mg each, were investigated. The density of the fragments was established with a mercury pycnometer and was found to be 3.05 to 3.12 g/cu cm, with a relative error not more than 2 percent. The porosity was found for the difference between the volumes determined with the mercury and with the gas techniques; for all three samples together it was 13 percent, and the error of determination was 70 percent owing to the small volumes. It can be anticipated that the porosity of the rock in bulk will be higher than the value obtained based on small fragments. The porosity of lunar rocks can markedly affect the isostatic distribution of rocks and must be taken into account when developing models of lunar structure.
Magnesian granulitic breccias have high Th/Sm ratios, they are not related to Mg-suite plutonic rocks in any straightforward manner, and they may have an igneous rock precursor that is not yet recognized among our samples of the Moon. Additional information is contained in the original extended abstract.