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An evaluation has been made of the relative roles of fractional crystallization and crustal contamination in the genesis of basaltic magmas from the Black Rock Desert region in Utah. As a result, geochemical variations of these basalts have been defined as a function of their ages of eruption.
Sample 10071,33 is a thin section of Apollo 11 ferrobasalt showing an unusual dual texture. The major portion of the sample is very similar to other fine grained Apollo 11 basalts, but the thin section also includes materials with a distinct variolitic texture. The two areas are separated by a sharp boundary and the mineralogy and composition of the two textural types are quite distinct. The mineralogy and chemistry of the variolitic portion show it to be the product of rapid cooling of a liquid, intermediate between the typical Apollo 11 ferrobasalt and the associated Si and K-rich mesostasis. This liquid is the result of fractional crystallization of a magma of composition closely corresponding to the major portion of the 10071 system, followed by crystal-liquid separation. The sample provides strong and direct evidence for igneous differentiation on the lunar surface.
Results of melting experiments over the pressure range from 0 to 20 kb on Apollo 14 igneous rocks 14310 and 14072, and on comprehensive fines 14259. It is found that low-pressure crystallization of rocks 14310 and 14072 proceeds as predicted from the textural relationships displayed by thin sections of these rocks. The mineralogy and textures of these rocks are the result of near-surface crystallization. The chemical compositions of these lunar samples all show special relationships to multiply saturated liquids in the system anorthite-forsterite-fayalite-silica at low pressure. Partial melting of a lunar crust consisting largely of plagioclase, low-calcium pyroxene, and olivine, followed by crystal fractionation at the lunar surface, is a satisfactory mechanism for the production of the igneous rocks and soil glasses sampled by Apollo 14. The KREEP component of other lunar soils, may have a similar origin.
Melting experiments and petrographic studies of lunar feldspathic rocks reveal possible genetic relationships among several compositionally and mineralogically distinct groups of lunar rocks and soil fragments. Dry, low PO2 partial melting of crustal anorthositic norites of the anorthositic-noritic-troctolitic (ANT) suite produces liquids of the KREEP-Fra Mauro basalt type; dry, low PO2 partial melting of pink spinel troctolite (PST) produces liquids of the 'very high alumina basalt' or microtroctolite type. Both ANT and PST are probable components of the primitive terra crust. If crystal fractionation in a cooling basaltic liquid could have produced such a crust, it would also produce a mafic interior capable of yielding mare basalts by later remelting at depth.
There is now abundant geophysical and geochemical evidence suggesting that the moon has a thick plagioclase rich outer shell. This is most easily explained by early and extensive melting of a CaO and Al2O3 rich moon followed by fractional crystallization involving plagioclase flotation. Melilite is probably an important constituent of the interior. This model explains the seismic velocities, the mean density, and the moment of inertia of the moon. The moon is 73-88% high-temperature condensate.
Petrographic studies of Apollo 17 mare basalts indicate that 70215 and 71569 arrived at the lunar surface as liquids. Low-pressure melting experiments show that compositional variations within the Apollo 17 and Apollo 11 ophitic basalt suites may be generated by near-surface fractional crystallization of liquids with compositions similar to 70215 and 70017. High-pressure melting experiments show that liquids similar in composition to 70017 and 70215 can be generated by partial melting of an olivine+clinopyroxene+Fe-Ti-oxide source at depths of 100-150 km within the moon.
The paper describes one possible liquid line of descent produced for a high-titanium mare basalt composition through an arbitrarily chosen series of partial equilibrium and fractional crystallization experiments on basalt 70017. The liquid line of descent leading to immiscibility at 994 C is characterized by enrichment of FeO, K2O, SiO2, and MnO and depletion of MgO and TiO2 in the residual liquids. The composition of the residual liquid at the onset of immiscibility is ferrobasaltic, and the initial appearance of immiscible liquids in the form of silica-rich spherules is in the vicinity of plagioclase-liquid contacts. The integrated bulk composition of the areas of finely exsolved liquids indicates that the trend of the liquid line of descent is at a small angle to the tie lines joining the two liquids.
Delineation of low pressure phase equilibria in the composition space relevant to titaniferous lunar basalts demonstrates a significant degree of control by those equilibria on the compositions of the basalts. The existence of two distinct chemical groups of basalts (high and low K) which cannot be related one to the other by fractional crystallization at any pressure, suggests that melting is responsible for the two groups. Consideration of the pressure shift required to produce the differences between groups constrains magma segregation to have occurred in the outer 150 km of the moon. It is difficult to relate low-Ti and high-Ti basalts to the same source region. The preferred source region of high-Ti basalts, based on phase equilibrium considerations, is a late ilmenite-rich cumulate produced from the residual liquid of the primordial differentiation of the outer portions of the moon. This ilmenite-rich layer is sandwiched between the lunar feldspathic crust and a complementary mafic cumulate.
The nucleation frequency of Lunar Composition 70019, a lithified soil breccia from the center of a small crater in the Taurus-Littrow Valley, is determined using a relation that describes nucleation throughout the volume of a liquid together with measurements of the time required at temperatures of 780 to 930 C to obtain sensibly crystalline bodies. Curves indicating the time required at a given temperature to reach a particular fraction crystallized are shown to have the general form predicted by kinetic analysis. Nucleation frequencies are evaluated by applying such analysis to a curve representing the transition between glassy material and material with a sensible degree of crystallinity. The results obtained are found to be in excellent agreement with the values expected from the classical theory of homogeneous nucleation, indicating that such nucleation represents the dominant contribution to crystal formation, at least over the range of undercoolings covered (250 to 400 C).
Major- and trace-element data is presented for a large number of petrographically diverse Apollo 17 basalts, and an attempt is made to evaluate what proportion of the total compositional variance can be attributed to near-surface crystal fractionation and what proportion to magma-generating processes such as partial melting and source heterogeneity. Three well-defined and self-consistent basalt types were identified on the basis of data for fine-grained, rapidly-chilled samples.
Bulk compositions, petrology, and mineralogy of lithic fragments discovered in polished sections of Apollo 17 drill core samples 70007, 70008, and 70009 and Luna 24 soil 24077, 43 are described. The fragments have unambiguous affinities to mare basalts, but are exceptionally low in TiO2 (less than 1.0 wt.% TiO2). Apollo 17 rake sample 78526 is a green glassy rock of similar composition. Together the samples represent a distinct variety of mare basalts. Bulk compositional relationships suggest that they are related to Apollo 15 green glass, but the data do not permit one to discern the precise nature of the relationship. Both fractional crystallization and partial melting models can explain the observed compositional trends.
The metal and sulfide phases in the Luna 24 soil samples were studied with the optical microscope and the electron microprobe. The compositions of the metal particles fall into three groups based on their Ni and Co contents: (1) Samples of meteoritic composition which have undergone metamorphism on the lunar surface. (2) Samples of submeteoritic, low Ni and low Co contents, including most of the metal particles observed. These particles are contained in glass and agglutinate particles and were probably formed by the mixing of meteoritic metal with lunar metal produced by the reduction of silicates during shock-impact. (3) Samples of high-CO content probably formed by mixing of meteoritic material with high-Co metal from the mare basalt or by fractional crystallization from a metal silicate melt. The sulfide minerals were also studied. These are almost pure FeS, and crystallized from a late stage liquid in the mare basalt. Three high-Ni sulfides were also found in the glass phase of agglutinates.
Tungsten concentrations have been determined by instrumental neutron activation in 104 iron meteorites, and range from 0.07 to 5 microg/g. In individual groups, concentrations vary by factors of between 1.5 and 8, but there are negative W-Ni correlations in 8 groups: IAB, IC, IIAB, IID, IIE, IIIAB, IIICD, and IIIF. The lowest W concentrations are found in groups IAB and IIICD, which also have the smallest slopes on a W-Ni plot. Eighteen anomalous irons have W concentrations between 5 microg/g (Butler) and 0.11 microg/g (Rafrueti). The distribution of W in irons shows similarities to that of other refractory sideophilic elements (except Mo), but is closest to the distribution of Ru and Pt. Assuming that chemical trends in group IIIAB were produced by fractional crystallization, a value of 1.6 can be deduced for the distribution coefficient of W between solid and liquid metal, as compared with 0.89 for Mo. Experimental evidence in support of these values is tenuous.
Phaneritic fragments, vitrophyres, and glass beads of a new very low Ti (VLT) mare basalt are found in the Apollo 17 drill core. VLT lithic fragments are characterized by TiO2 content of approximately 0.5%, Mg/(Mg + Fe) of approximately 0.52, CaO/Al2O3 of approximately 0.9, and low alkali content. Although mineral systematics and modal composition of VLT basalt are similar to Apollo 12 and 15 low Ti basalts, VLT basalts cannot be related to these mare basalts by crystal fractionation. Since VLT basalt is isochemical with some of the less mafic green glasses, fractionation of VLT magma from a liquid of green-glass composition is a possibility. Spectral reflectance studies suggest that VLT-type basalts may be relatively common in mare basins.
An unusually high concentration of granitic fragments, with textures ranging from holocrystalline to glassy, occurs throughout Boulder 1, a complex breccia of highland rocks from Apollo 17, Station 2. Among the minerals included in the granites are enigmatic K-Ca-rich feldspars that fall in the forbidden region of the ternary diagram. The great variability in chemistry and texture is probably the result of impact degradation and melting of a granitic source-rock. Studies of the breccia matrix suggest that this original granitic source-rock may have contained more pyroxenes and phosphates than most of the present clasts contain. Petrographic observations on Apollo 15 KREEP basalts indicate that granitic liquids may be produced by differentiation without immiscibility, and the association of the granites with KREEP-rich fragments in the boulder suggests that the granites represent a residual liquid from the plutonic fractional crystallization of a KREEP-rich magma. Boulder 1 is unique among Apollo 17 samples in its silica-KREEP-rich composition. We conclude that the boulder represents a source-rock unlike the bedrock of South Massif.
Mass-balance calculations indicate that the molten layer originally covering the moon may have been several hundred kilometers deep. The solidification of this magma ocean involved some unusual effects resulting from the large-pressure differential in the thick magma layer. The sunken cumulates from this differentiation would be more iron-rich, less refractory, and would contain more incompatible elements than would be expected in simple isobaric fractional crystallization and crystal sinking models of magma differentiation. These lower cumulates can have the mineralogical and chemical properties of the source regions of the low-Ti mare basalts.
A model of lunar evolution is proposed. At 4.6 AE an outer shell 60-100 km thick of an initially homogeneous moon was totally molten following accretion. 'Highland basalt' represents remnants of the chilled crust of this molten layer and, therefore, the mean lunar composition. Melt from the partially molten region below the outer shell intruded into it, enriching it in FeO, SiO2, radiogenic, and trivalent trace LIL (large ion lithop) elements. Fractional crystallization of the outer shell produced toward its base a mafic cumulate zone less than 40 km thick, the upper 60 km being anorthosite. The radiogenic elements concentrated together with dense residual melt in the upper parts pf the mafic cumulate zone. Between 4.6 and 4.3 AE a second differentiation led to localized enrichment from below of radiogenic elements in the plagioclase-rich, high-Mg/Mg + Fe residuum below the outer 100-km-thick shell. Melting at these enriched sites at about 4.0 AE produced to KREEP basalts. Later melting at sites of radiogenic element enrichment in the outer 100-km-thick shell produced the mare basalts.
Analyses were conducted of sixteen Apollo 17 mare basalts for alkali, alkaline-earth, and rare-earth elements, Co, and Sc. The obtained data were utilized in a study concerning the nature of the igneous processes responsible for the chemical variations among the high-Ti, low-K basalts. Estimates were obtained regarding the abundances of the large-ion, lithophile elements in the source regions for the basalts. It is shown that the source regions could plausibly have been produced by processes believed to have occurred during the early history of the moon. Attention is given to chemical variations among the Apollo 17 mare basalts, near-surface (low-pressure) crystal fractionation, partial melting, limits on the extent of partial melting, and a summary of possible events leading to formation of high-Ti mare basalts.