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At least 253 records · Page 14

Petrology, mineralogy and chemistry of KREEP basalt

KREEP basalt is an important lunar material that was formed in large quantities early in the evolutionary history of the moon. Fragments of KREEP basalt were returned from all landing sites and make up most of the material of the Apollo 14 collection. These fragments have a wide variety of textures caused by various secondary processes but they are all characterized by a large and distinctive trace-element content. They are also characterized by a general basaltic composition that is similar to the olivine-plagioclase-pyroxene peritectic in the system silica-anorthite-olivine (Fe/Fe + Mg = 0.3).

Meyer, C., Jr.↗

The crystallisation trends of spinels in tertiary basalts from Rhum and Muck and their petrogenetic significance

Spinels found in transitional olivine basalts from the Islands of Rhum and Muck in the British Tertiary Province are analyzed to determine their chemical variability and their relationship to silicate phases. Chemical zoning of the cores of spinels which spilled into the basaltic liquid may be due to a reaction between the spinel and the liquid resulting in more Fe- and Ti-rich spinels. In addition, a peritectic-type reaction seems to have occurred, causing the transformation of aluminum spinel to chrome spinel with precipitation of plagioclase. Changes in the basaltic liquid are reflected by these transformations in the spinel composition.

Ridley, W. I.↗

Evolution of mare basalts - The complexity of the U-Th-Pb system

An attempt has been made to gain more insight into mare-basalt evolution by performing a very detailed leaching and mineral-separation U-Th-Pb systematics study on mare basalt 15085. It is found that about 20-50% of the U, Th, and Pb reside on the grain boundaries or in the mesostasis and that the Pb-207/Pb-206 ratios of the grain boundaries and crystal interiors are distinctly different. These distinct trends appear to represent either continuous or episodic postcrystallizational disturbances to the U-Th-Pb system of this rock. Using U and Pb partition coefficients, it is concluded that existing two- and three-stage U-Pb evolution models do not accurately describe mare-basalt genesis. An alternative two-stage + KREEP mixing model is proposed as a simple approximation to U-Pb evolution in lunar rocks. Most Rb-Sr and Sm-Nd data are compatible with this model.

Unruh, D. M.↗

Shock compression and adiabatic release of a titaniferous mare basalt

A report is presented regarding the dynamic properties of a rock indigenous to the mare basins of the moon. The reported data were obtained in a study of sample 70215, a very titanium-rich basalt (58% pyroxene, 18% ilmenite, 15% plagioclase, 6% olivine, and 3% quartz by weight). This rock is probably representative of a class of the earliest mare-filling extrusive rocks which are exposed on the present lunar surface. Two series of experiments were performed. One set of experiments involved the measuring of Hugoniot and release adiabats to 15.7 GPa with a propellant gun apparatus. In the second set of experiments, a light-gas gun was employed to yield Hugoniot data at about 120 GPa and release states at about 90 GPa. Lunar basalt 70215 appears to be among the densest rocks in the present lunar sample collection, having a crystal density of 3.38 g/cu cm and a porosity of about 1.3%. The results of the experiments have important implications for both the degree of shock metamorphism expected for impact processes and the extent of ejecta transport on mare surfaces with high-titanium basalt composition.

Ahrens, T. J.↗

Experimentally reproduced textures and mineral chemistries of high-titanium mare basalts

Many of the textures, morphologies, and mineral chemistries of the high-titanium mare basalts have been experimentally duplicated using single-stage cooling histories. Lunar high-titanium mare basalts are modeled in a 1 m thick gravitationally differentiating flow based on cooling rates, thermal models, and modal olivine contents. The low-pressure equilibrium phase relations of a synthetic high-titanium basalt composition were investigated as a function of oxygen fugacity, and petrographic criteria are developed for the recognition of phenocrysts which were present in the liquid at the time of eruption.

Usselman, T. M.↗

Sulfur abundances and distributions in mare basalts and their source magmas

An inverse correlation between metallic iron content and total sulfur abundances was observed by Gibson and Moore (1974) for five Apollo 17 and six Apollo 15 basalts. An investigation was conducted with the objective to distinguish between two processes leading to the inverse metallic iron and total sulfur correlation. The investigation included analyses of ten Apollo 15 and five Apollo 17 basalts for their sulfur and metallic iron abundances along with carbon and hydrogen. The sulfur isotopic compositions were measured for a possible identification of the fractionation processes which might have occurred during volatilization of the basalts.

Gibson, E. K., Jr.↗

Comparative petrology and possible genetic relations among the Apollo 11 basalts

A comparative petrological study has been performed on 19 large Apollo-11 basalt fragments as well as two smaller vitrophyres in order to determine how many igneous bodies are presented by this suite of rocks. Detailed petrographic and mineral chemical studies have been performed on each sample along with an electron microprobe point count, which gives the mode, the range and distribution of all mineral zonation and the bulk composition. These data confirm the twofold division of the Apollo-11 basalts into high-K (type A) and low-K (type B) basalts.

Beaty, D. W.↗

Causes of compositional variations within mare basalt suites

The short-range unmixing model, which explains compositional variations produced during crystallization of a single undifferentiated basalt flow, has been applied to the variations found within each of the suites of mare basalts. Based on this modelling, the following suites of mare basalts could represent random samples from single, undifferentiated lava flows: Apollo 11 A (high K), Apollo 15 olivine, Apollo 17 A-U, Apollo 17 B, Apollo 17 C. The short range unmixing model fails to account for variations within the Apollo 12 olivine-pigeonite group and Apollo 12 ilmenite group, which are well explained by fractional crystallization. The fact that the compositional variations within a suite of samples of unknown affinity can be explained in terms of short-range unmixing of a single lava does not mean that they are necessarily related in that way. It does, however, mean that independent evidence (stratigraphic, petrographic, isotropic, or age) is required to support arguments for the variations being caused by fraction crystallization or different magma batches.

Lindstrom, M. M.↗

The consanguinity of the oldest Apollo 11 mare basalts

The textural, mineralogical, and chemical relationships between three of the oldest dates lunar mare basalt samples returned by Apollo 11 (10003, 10029 and 10062) were investigated. Very strong resemblances were noted between the modal minerologies of 10003 and 10029. Significantly more modal olivine and cristobalite was observed in 10062 than in the other basalt samples. A detailed examination of mineral-chemical relationships among the samples revealed similarities between 10003 and 10062 and differences between these two rocks and 10029, the most significant of which is the presence of akaganeite in 10029, implying that lawrencite was present in the pristine sample of 10029 but not in 10003 and 10062. Results of a Wright-Doherty mixing program used to test various fractional crystallization schemes show that 10062 can be derived from a liquid with the composition of either 10003 or 10029 by removing 2-5% ilmenite and 5% olivine. By removing about 6% plagioclase, 10003 can be derived from a liquid with the bulk composition of 10062. It is concluded that 10003 and 10029 may have come from different basaltic flows, whereas it is possible that 10003 and 10062 were derived from the same parental magma by near-surface fractionation of olivine plus ilmenite or of plagioclase plus or minus olivine.

Gamble, R. P.↗

Effects of kinetics on the crystallization of quartz normative basalt 15597 - An experimental study

Equilibrium experiments on a residual liquid composition from the dynamic crystallization study on quartz normative basalt (QNB) 15597 are used to evaluate the effects of kinetics on the crystallization of pyroxene-porphyritic basalts. The results indicate that the liquids coexisting with pyroxene phenocryst rims before the precipitation of groundmass plagioclase + pyroxene have left the equilibrium liquid line of descent and metastably penetrated the plagioclase primary phase volume. The precipitation of groundmass plagioclase + pyroxene brings the basalt system closer to equilibrium with respect to the residual liquid and crystals. At rapid cooling rates pyroxene phenocryst growth produces substantial compositional gradients in the residual silicate liquid at the pyroxene/liquid interface. The compositional gradients enhance the nucleation and growth of groundmass phases at the phenocryst interface, because effects related to constitutional supercooling for these phases (e.g., plagioclase, pyroxene, etc.) favor nucleation at the interface.

Grove, T. L.↗

Experimental partitioning of rare earth elements and scandium among armalcolite, ilmenite, olivine and mare basalt liquid

An experimental study was carried out to measure partition coefficients for two rare-earth elements (Sm and Tm) and Sc among armalcolite, ilmenite, olivine and liquid coexisting in a system modeled on high-Ti mare basalt 74275. This 'primitive' sample was chosen for study because its major and trace element chemistry as well as its equilibrium phase relations at atmospheric pressure are known from previous studies. Beta-track analytical techniques were used so that partition coefficients could be measured in an environment whose bulk trace element composition is similar to that of the natural basalt. Partition coefficients for Cr and Mn were determined in the same experiments by microprobe analysis. The only equilibrium partial melting model appears to be one in which ilmenite is initially present in the source region but is consumed by melting before segregation of the high-Ti mare basalt liquid from the residue.

Irving, A. J.↗

How thick are lunar mare basalts

It is argued that De Hon's estimates of the thickness of lunar mare basalts, made by analyzing 'ghost' craters on mare surfaces, were inflated as the result of the crater morphometric data of Pike (1977) to reconstruct rim heights of degraded craters. Crater rim heights of 82 randomly selected highland craters of various states of degradation were determined, and median rim height was compared to that of corresponding fresh impact structures. Results indicate that the thickness estimates of De Hon may be reduced by a factor of 2, and that the total volume of mare basalt produced throughout lunar history could be as little as 1-2 million cubic kilometers. A survey of geochemical and petrographic evidence indicates that lateral transport of regolith components over distances of much greater than 10 km is relatively inefficient; it is suggested that vertical mixing of a highland substrate underlying the basaltic fill may have had a primordial role in generating the observed mare width distributions and high concentrations of exotic components in intrabasin regoliths.

Hoerz, F.↗

Occurrence and mineral chemistry of high pressure phases, Portrillo basalt, southcentral New Mexico

Inclusions of clinopyroxenite, kaersutiteclinopyroxenite, kaersutite-rich inclusions, wehrlite and olivine-clinopyroxenite together with megacrysts of feldspar, kaersutite and spinel are found loose on the flanks of cinder cones, as inclusions within lava flows and within the cores of volcanic bombs in the Quaternary alkali-olivine basalt of the West Potrillo Mountains, southcentral New Mexico. Based on petrological and geochemical evidence the megacysts are interpreted to be phenocrysts which formed at great depth rather that xenocrysts of larger crystal aggregates. These large crystals are believed to have formed as stable phases at high temperature and pressure and have partially reacted with the basalt to produce subhedral to anhedral crystal boundaries. It can be demonstrated that the mafic and ultramafic crystal aggregates were derived from an alkali-basalt source rock generated in the mantle. The inclusions are believed to represent a cumulus body or bodies injected within the lower crust or upper mantle.

Hoffer, J. M.↗

The petrology and chemistry of basaltic fragments from the Apollo 11 soil - I

A study of basaltic fragments from the Apollo 11 bulk sample using instrumental neutron activation analysis, the petrographic microscope, and the electron microprobe is presented. The fragments include Group A, B2, and B3 basalts, of which two of the Group A samples are vitrophyres with bulk compositions similar to the crystalline high-K rocks which crystallized under different physical conditions and represent a second high-K cooling unit. The B2 samples relate to each other through ilmenite fractionation, and the B3 samples relate through olivine fractionation; it is concluded that the B2 samples have an anomalously high La/K ratio and may have generated in the same source region as the Group D basalts.

Beaty, D. W.↗

The Sr and Nd isotopic record of Apollo 12 basalts - Implications for lunar geochemical evolution

Alkali, alkaline earth, and rare earth element data are reported for several Apollo 12 basalts which are representative of the four Apollo 12 magma types. Results confirm the heterogeneity of the lunar mantle and show that the Sm/Nd ratio of at least the Apollo 12 ilmenite basalts was decreased by 13-24% during magma genesis. In addition, whole mare basalt Sm-Nd data are not collinear on an isochron diagram; thus it is no longer possible to explain these data via mixing of 'primitive material' and 'early differentiates' as in the hybridization and assimilation models.

Nyquist, L. E.↗

Apollo 17 high-Ti mare basalts - New bulk compositional data, magma types, and petrogenesis

Bulk compositional and mineral chemical data for 28 previously unanalyzed samples support the classification of Apollo-17 high-Ti mare basalts into three-types (A, B, and C), defined on the basis of analyses of fine-grained basalts. The most MgO- and TiO2-rich fine-grained basalts of these types appear to be the best choices for representing the compositions of the parent magmas.

Warner, R. D.↗

Are early magnesium-rich basalts widespread on the moon

Orbital X-ray data indicate that high-magnesium material systematically occurs along mare/terra boundaries in all the lunar nearside basins for which there is orbital X-ray coverage. These peripheral units appear to represent the earliest stages of volcanism within each of the basins, although they were not necessarily emplaced at the same time in lunar history. High-magnesium subsurface layers excavated by post-mare impact craters in central Mare Crisium and Mare Fecunditatis suggest that the peripheral units are the only visible edges of a basin-wide basalt layer, largely buried by younger less-magnesian flows. This evidence suggests that early magnesium-rich mare basalts are widespread on the moon and that their volumes may be greatly underestimated. Abundant early mare deposits of this type would place severe constraints on models of mare basalt petrogenesis.

Andre, C. G.↗

Regional chemical variations in lunar basaltic lavas

The higher Al2O3 concentrations in mare soils at Apollo landing sites, relative to mare basalts, have generally been attributed to the presence of 20-30% of terra material in the mare surface regolith. This viewpoint is shown to be erroneous when entire maria are studied; the amount of terra material in typical mare surface regoliths is only about 5%, or less. The bulk of the mare soils are the comminuted remains of aluminous mare basalt flows. On a regional scale, the sample and orbital data for maria define prominent chemical variations that are well beyond those expected from simple igneous processes and therefore indicate that gradations in one or more of the major parameters of planetary differentiation caused these variations. The increasingly abundant evidence for regional variations in the chemical compositions of lunar basalts requires that regional petrogenetic provinces must be considered in models of lunar evolution.

Hubbard, N.↗