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Basaltic Magmatism: The Dominant Factor in the Petrologic and Tectonic Evolution of the Earth

Silicate bodies such as the Moon, Mars, probably Mercury, and possibly Venus, appear to have evolved in three main stages: a first (felsic) differentiation, a late heavy bombardment, and a second (basaltic) differentiation. It has been proposed that the Earth underwent a similar sequence. This paper argues that the second differentiation, basaltic magmatism, has dominated the petrologic and tectonic evolution of the Earth for four billion years. A global andesitic crust, formed during and after accretion of the planet, was disrupted by major impacts that triggered mantle upwelling and sea-floor spreading about 4 billion years ago. The oceanic crust collectively has since been formed by basaltic volcanism, from spreading centers and mantle plumes. However, the continental crust has also been greatly affected. Basaltic underplating has promoted anatexis and diapiric intrusion of granitoids in granite-greenstone terrains, as well as providing heat for regional metamorphism. Basaltic intrusions, such as the Nipissing diabase of the Sudbury area, have added to the thickness of continental crust. Satellite magnetic surveys suggest that there are more such basaltic intrusions than previously realized; examples include the Bangui anomaly of central Africa and the Kentucky anomaly. Basaltic overplating from mafic dike swarms has repeatedly flooded continents; had it not been for erosion, they would be covered with basalt as Venus is today. The tectonic effects of basaltic volcanism on continents have only recently been realized. The World Stress Map project has discovered that continents are under horizontal compressive stress, caused by push from mid-ocean ridges, i.e., by basaltic volcanism. The stress fields are generally uniform over large intraplate areas, and could contribute to intraplate tectonism. Seafloor spreading has demonstrably been effective for at least 200 million years, and ridge push thus a contributor to tectonic activity for that long. Collectively, the petrologic and tectonic evolution of the Earth has been dominated for about 4 billion years by the 'second differentiation,' i.e., by basaltic magmatism.

Lowman, Paul D., Jr.

Modes of emplacement of basalt terrains and an analysis of mare volcanism in the Orientale Basin

Three distinctive types of basalt terrains can be recognized on earth on the basis of surface morphology: flood basalts, shield basalts, and plains basalts, each of which reflects unique styles of eruption and modes of emplacement. Two of these, flood basalts and plains basalts, appear to be important in the emplacement of mare basalts on the moon. Using surface features as identifying criteria, mare units in the Orientale Basin were examined and the following emplacement sequence was derived: (1) initial emplacement of impact melt in the basin center, (2) eruption of flood-type basalts in the basin center and approximately concurrent emplacement of plains type basalts in Lacus Veris, and (3) emplacement of plains type basalts in Lacus Autumni

Greeley, R.

Apollo 17 KREEPy basalts - Evidence for nonuniformity of KREEP

Breccia 72275 contains pristine KREEPy basalt clasts that are not found among other samples collected at Apollo 17. These basalts occur as discrete clasts and as clasts enclosed within basaltic microbreccias. Mineral and whole-rock chemical analyses reveal that the microbreccias are compositionally indistinguishable from the basalt clasts. Samples of the 72275 matrix also have the same compositions as the basalts and the basaltic microbreccias. 72275 was assembled in situ from a single flow or series of closely related flows of Apollo 17 KREEPy basalt before it was transported to the Apollo 17 site. As a rock type, Apollo 17 KREEPy basalts are distinct from Apollo 15 KREEP basalts. The Apollo 17 samples have lower REE concentrations, steeper negative slopes of the HREE, and are less magnesian than the Apollo 15 samples. The two basalt types cannot be related by fractional crystallization, partial melting, or assimilation. This is evidence for the compositional nonuniformity of KREEP as a function of geography.

Salpas, Peter A.

Flood basalt eruptions, comet showers, and mass extinction events

A chronology of initiation dates of the major continental flood basalt episodes has been established from compilation of published K-Ar and Ar-Ar ages of basaltic flows and related basic intrusions. The dating is therefore independent of the biostratigraphic and paleomagnetic time scales, and the estimated errors of the inititation dates are approximately + or - 4 pct. There are 11 distinct episodes of continental flood basalts known during the past 250 Myr. The data show that flood basalt episodes are generally relatively brief geologic events, with intermittent eruptions during peak output periods lasting ony 2 to 3 Myr or less. Statistical analyses suggest that these episodes may have occurred quasi-periodically with a mean cycle time of 32 + or - 1 Myr. The initiation dates of the flood basalts are close to the estimated dates of marine mass extinctions and impact-crater clusters. Although a purely internal forcing might be argued for the flood basalt volcanism, quasi-periodic comet impacts may be the trigger for both the flood basalts and the extinctions. Impact cratering models suggest that large-body impactors lead to deep initial cratering, and therefore may cause mantle disturbances and initiate mantle plume activity. The flood basalt episodes commonly mark the initiation or jump of a mantle hotspot, and are often followed by continental rifting and separation. Evidence from dynamical studies of impacts, occurrences of craters and hotspots, and the geochemistry of boundary layers is synthesized to provide a possible model of impact-generated volcanism. Flood basalt eruptions may themselves have severe effects on climate, and possibly on life. Impacts might, as a result, have led to mass extinctions through direct atmospheric disturbances, and/or indirectly through prolonged flood basalt volcanism.

Rampino, Michael R.

Some volcanologic aspects of Columbia River basalt volcanism relevant to the extinction controversy

The Columbia River Basalt Group is the youngest and most thoroughly studied flood-basalt province known; information about it should be relevant to questions about the possible relation of flood-basalt volcanism to mass extinctions. The group has a total volume of about 174,000 cu km and covers an area of about 164,000 sq km. It was erupted between 17.5 and 6 Ma, as measured by K-Ar and Ar-40/Ar-39 dates. Early eruptions formed the Imnaha Basalt. More than 85 percent of the group was produced during a 1.5 my period between 17 and 15.5 Ma, forming the Grande Ronde and greatly subordinate Picture Gorge Basalts. Later flows formed the Wanapum Basalt, which includes the well-known Roza Member, and the Saddle Mountains Basalt. Linear vent systems for many of the flows are known and are located only in the eastern third of the Columbia Plateau. No systematic migration of vents occurred throughout the 11.5 my period of activity; this and other considerations make it unlikely that the province is related to a hot spot. Model calculations based on observations that little cooling occurred during flow of hundreds of kilometers suggest eruption and emplacement durations of a few days. Some voluminous flows occur in all formations, but most such flows apparently were erupted during Grande Ronde time. The eruption and emplacement of more than 1,000 cu km of 1100 C basaltic lava on the surface within several days doubtless had at least local meteorologic effects. Whether the effects were broader can at present only be hypothesized. Grande Ronde Basalt and Picture Gorge Basalts contain moderately common but thin sedimentary interbeds between flows, whereas earlier and later formations contain numerous, locally thick sediment accumulations. Volcaniclastic debris derived from extra-plateau sources commonly occurs in the testbeds.

Swanson, Donald A.

The Mantle and Basalt-Crust Interaction Below the Mount Taylor Volcanic Field, New Mexico

The Mount Taylor Volcanic Field (MTVF) lies on the Jemez Lineament on the southeastern margin of the Colorado Plateau. The field is centered on the Mt. Taylor composite volcano and includes Mesa Chivato to the NE and Grants Ridge to the WSW. MTVF magmatism spans approximately 3.8-1.5 Ma (K-Ar). Magmas are dominantly alkaline with mafic compositions ranging from basanite to hy-basalt and felsic compositions ranging from ne-trachyte to rhyolite. We are investigating the state of the mantle and the spatial and temporal variation in basalt-crustal interaction below the MTVF by examining mantle xenoliths and basalts in the context of new mapping and future Ar-Ar dating. The earliest dated magmatism in the field is a basanite flow south of Mt. Taylor. Mantle xenolith-bearing alkali basalts and basanites occur on Mesa Chivato and in the region of Mt. Taylor, though most basalts are peripheral to the main cone. Xenolith-bearing magmatism persists at least into the early stages of conebuilding. Preliminary examination of the mantle xenolith suite suggests it is dominantly lherzolitic but contains likely examples of both melt-depleted (harzburgitic) and melt-enriched (clinopyroxenitic) mantle. There are aphyric and crystal-poor hawaiites, some of which are hy-normative, on and near Mt. Taylor, but many of the more evolved MTVF basalts show evidence of complex histories. Mt. Taylor basalts higher in the cone-building sequence contain >40% zoned plagioclase pheno- and megacrysts. Other basalts peripheral to Mt. Taylor and at Grants Ridge contain clinopyroxene and plagioclase megacrysts and cumulate-textured xenoliths, suggesting they interacted with lower crustal cumulates. Among the questions we are addressing: What was the chemical and thermal state of the mantle recorded by the basaltic suites and xenoliths and how did it change with time? Are multiple parental basalts (Si-saturated vs. undersaturated) represented and, if so, what changes in the mantle or in the tectonic regime allowed their coexistence or caused the transition?

Schrader, Christian M.

Valence State Partitioning of Cr and V Between Olivine-Melt and Pyroxene-Melt in Experimental Basalts of a Eucritic Composition

The partitioning of multivalent elements in basaltic systems can elucidate the oxygen fugacity (fO2) conditions under which basalts formed on planetary bodies (Earth, Moon, Mars, asteroids). Chromium and V are minor and trace elements in basaltic melts, partition into several minerals that crystallize from basaltic melts, exist in multiple valence states at differing fO2 conditions, and can therefore be used as oxybarometers for basaltic melts. Chromium is mostly 3+ in terrestrial basaltic melts at relatively high fO2 values (≥ IW+3.5), and mostly 2+ in melts at low fO2 values (≤ IW-1), such as those on the Moon and some asteroids. At intermediate fO2s, (i.e., IW-1 to IW+3.5), basaltic melts contain both Cr3+ and Cr2+. Vanadium in basaltic melts is mostly 4+ at high fO2, mostly 3+ at low fO2, and a mix of V3+ and V4+ at intermediate fO2 con-ditions. Understanding the partitioning of Cr and V into silicate phases with changing fO2 is therefore critical to the employment of Cr and V oxybarometers. In this abstract we examine the equilibrium partitioning of Cr and V between olivine/melt and pyroxene/melt in experimental charges of a eucritic composition produced at differing fO2 conditions. This study will add to the experimental data on DCr and DV (i.e., olivine/melt, pyroxene/melt) at differing fO2, and in turn these D values will be used to assess the fO2 of eucrite basalts and perhaps other compositionally similar planetary basalts.

Karner, J. M.

Chemistry of Venus’ Recent Basalts as Clues to its Ancient Past

Perhaps the most important question about Venus is whether it ever had a hydrosphere: liquid water, oceans, and thus an environment suitable for life as we know it. The D/H of Venus’ atmosphere suggests extensive water loss, and climate models may be consistent with global oceans. Rocks dating from that epoch may be preserved in Venus’ tesserae (and especially Ishtar Terra) – inferred to of felsic or silicic rock, which would suggest abundant water. However, the exact elemental compositions of tesserae (silicic or not) will be difficult to retrieve and most of Venus’ surface is basalt flows and volcanic constructs, inferred to be much younger than the oceanic epoch. Remotely sensed data are (and will be) ambiguous about the specific rock types that make up tesserae, and lander spacecraft are almost certain (in the near term) to avoid the rough and precipitous topography of the tesserae and touch down instead on flat, safe basaltic plains or volcanic rises. ‘Recent’ basalts at Venus’ surface could preserve chemical tracers of an ancient aqueous past, if their source regions (material that was re-melted) had been affected by water. This scenario occurs on Earth in Island Arc Basalts (IAB), where their compositions are thought to reflect aqueous alteration of parental midocean ridge basalts (MORB) and incorporation of oceanic sediments. Ancient Venus might have supported plate tectonic and thus have had IAB equivalents; absent plate tectonics, basalt affected by aqueous alteration could have been cycled into its mantle by burial under thick sections of later basalt. Our purpose is to suggest specific chemical clues in current basalts that would permit recognition of those with a history of aqueous interactions from those that did not. We compare Earth’s Ocean Island Basalts (OIB) that involved little water with IAB that show chemical effects ascribable to water. It is not clear that Venus’ basalts can be mapped into terrestrial tectonic settings; however, it seems reasonable that aqueous geochemical processes could have (had) similar effects on both planets.

A H Treiman

Gigaton commercial-scale carbon storage and mineralization potential in stacked Columbia River basalt reservoirs

This work presents a detailed supercritical CO 2 storage resource estimation for the stacked basalt reservoirs in the Grande Ronde Basalt of the Columbia River Basalt Group in eastern Washington and Oregon. The assessment aims to derisk the commercialization potential of geologic carbon storage in basalt by leveraging both structural and mineralization trapping of CO 2 in basalt. The structural closures formed by anticlinal ridges and synclinal valleys in Yakima Fold Belt are excellent physical traps to accommodate injected supercritical CO 2 . Rigorous hydraulic testing, well logs and simulation results from the Wallula Basalt Pilot #1 well showed the occurrence of 17 suitable permeable injection zones (up to 2,496 mD) intercalated with dense seals (~2.6E-10 mD) in the Grand Ronde Basalt. In addition, geochemical studies showed fast reactions between supercritical CO 2 and dissolved basalt minerals to form stable carbonates. In conclusion, our calculation indicates up to 40 gigatons (P90) of mineralization storage resources exist in the Grande Ronde Basalt reservoirs.

58 GEOSCIENCES

Sulfur in the Apollo 17 basalts and their source regions

Thirty-two Apollo 17 mare basalts have been analyzed for their total sulfur and metallic iron abundances. Sulfur abundances range from 1580 to 2770 microgram S/g with a median value of 1860 microgram S/g. Metallic iron abundances ranged from 0.033 to 0.21 wt.% Fe, with a mean value of 0.13 wt% Fe. The coarse-grained basalts contain more metallic iron than the fine-grained basalts. The metallic iron and sulfur abundances are not apparently related to the cooling rates of the basalts. A slight negative correlation exists between the concentrations of metallic iron and total sulfur for the Apollo 17 basalts. Sulfur content of the mare basalts increases with increasing degrees of fractionation whereas the metallic iron content decreases. Metallic iron in mare basalts may be ascribed to a variety of processes; at present the dominant process is unknown. The source regions for the Apollo 17 and 11 basalts were saturated with sulfur as compared to the Apollo 12 and 15 low titanium basalts which were not saturated.

Gibson, E. K., Jr.

Rb-Sr and Sm-Nd chronology and genealogy of mare basalts from the Sea of Tranquility

Rb-Sr and Sm-Nd ages of two Apollo 11 mare basalts, high-K basalt 10072 and low-K basalt 10062, are reported. Rb-Sr, Sm-Nd, and Ar-40-Ar-39 ages are in good agreement and indicate an extensive time interval for filling of the Sea of Tranquility, presumably by thin lava flows, in agreement with similar observations for the Ocean of Storms. Initial Sr and Nd isotopic compositions on Apollo 11 basalts reveal at least two parent sources producing basalts. The Sm-Nd isotopic data demonstrate that low-K and high-Ti basalts from Apollo 11 and 17 derived from distinct reservoirs, while low-Ti Apollo 15 mare basalt sources have Sm/Nd similar to the sources of Apollo 11 basalts. Groupings of mare basalt based on Ti content and on isotopic data do not coincide.

Papanastassiou, D. A.

Basalt generation at the Apollo 12 site. Part 2: Source heterogeneity, multiple melts, and crustal contamination

The petrogenesis of Apollo 12 mare basalts has been examined with emphasis on trace-element ratios and abundances. Vitrophyric basalts were used as parental compositions for the modeling, and proportions of fractionating phases were determined using the MAGFOX prograqm of Longhi (1991). Crystal fractionation processes within crustal and sub-crustal magma chambers are evaluated as a function of pressure. Knowledge of the fractionating phases allows trace-element variations to be considered as either source related or as a product of post-magma-generation processes. For the ilmenite and olivine basalts, trace-element variations are inherited from the source, but the pigeonite basalt data have been interpreted with open-system evolution processes through crustal assimilation. Three groups of basalts have been examined: (1) Pigeonite basalts-produced by the assimilation of lunar crustal material by a parental melt (up to 3% assimilation and 10% crystal fractionation, with an 'r' value of 0.3). (2) Ilmenite basalts-produced by variable degrees of partial melting (4-8%) of a source of olivine, pigeonite, augite, and plagioclase, brought together by overturn of the Lunar Magma Ocean (LMO) cumulate pile. After generation, which did not exhaust any of the minerals in the source, these melts experienced closed-system crystal fractionation/accumulation. (3) Olivine basalts-produced by variable degrees of partial melting (5-10%) of a source of olivine, pigeonite, and augite. After generation, again without exhausting any of the minerals in the source, these melts evolved through crystal accumulation. The evolved liquid counterparts of these cumulates have not been sampled. The source compositions for the ilmenite and olivine basalts were calculated by assuming that the vitrophyric compositions were primary and the magmas were produced by non-modal batch melting. Although the magnitude is unclear, evaluation of these source regions indicates that both be composed of early- and late-stage Lunar Magma Ocean (LMO) cumulates, requiring an overturn of the cumulate pile.

Neal, Clive R.

Sm-Nd and Rb-Sr Isotopic Studies of Meteorite Kalahari 009: An Old VLT Mare Basalt

Lunar meteorite Kalahari 009 is a fragmental basaltic breccia contain ing various very-low-Ti (VLT) mare basalt clasts embedded in a fine-g rained matrix of similar composition. This meteorite and lunar meteorite Kalahari 008, an anorthositic breccia, were suggested to be paired mainly due to the presence of similar fayalitic olivines in fragment s found in both meteorites. Thus, Kalahari 009 probably represents a VLT basalt that came from a locality near a mare-highland boundary r egion of the Moon, as compared to the typical VLT mare basalt samples collected at Mare Crisium during the Luna-24 mission. The concordant Sm-Nd and Ar-Ar ages of such a VLT basalt (24170) suggest that the extrusion of VLT basalts at Mare Crisium occurred 3.30 +/- 0.05 Ga ag o. Previous age results for Kalahari 009 range from approximately 4.2 Ga by its Lu-Hf isochron age to 1.70?0.04 Ga of its Ar-Ar plateau ag e. However, recent in-situ U-Pb dating of phosphates in Kalahari 009 defined an old crystallization age of 4.35+/- 0.15 Ga. The authors su ggested that Kalahari 009 represents a cryptomaria basalt. In this r eport, we present Sm-Nd and Rb-Sr isotopic results for Kalahari 009, discuss the relationship of its age and isotopic characteristics to t hose of other L-24 VLT mare basalts and other probable cryptomaria ba salts represented by Apollo 14 aluminous mare basalts, and discuss it s petrogenesis.

Shih, C.-Y.

Laboratory Simulated Acid-Sulfate Weathering of Basaltic Materials: Implications for Formation of Sulfates at Meridiani Planum and Gusev Crater, Mars

Acid-sulfate weathering of basaltic materials is a candidate formation process for the sulfate-rich outcrops and rocks at the MER rover Opportunity and Spirit landing sites. To determine the style of acid-sulfate weathering on Mars, we weathered basaltic materials (olivine-rich glassy basaltic sand and plagioclase feldspar-rich basaltic tephra) in the laboratory under different oxidative, acid-sulfate conditions and characterized the alteration products. We investigated alteration by (1) sulfuric-acid vapor (acid fog), (2) three-step hydrothermal leaching treatment approximating an open system and (3) single-step hydrothermal batch treatment approximating a "closed system." In acid fog experiments, Al, Fe, and Ca sulfates and amorphous silica formed from plagioclase-rich tephra, and Mg and Ca sulfates and amorphous silica formed from the olivine-rich sands. In three-step leaching experiments, only amorphous Si formed from the plagioclase-rich basaltic tephra, and jarosite, Mg and Ca sulfates and amorphous silica formed from olivine-rich basaltic sand. Amorphous silica formed under single-step experiments for both starting materials. Based upon our experiments, jarosite formation in Meridiani outcrop is potential evidence for an open system acid-sulfate weathering regime. Waters rich in sulfuric acid percolated through basaltic sediment, dissolving basaltic phases (e.g., olivine) and forming jarosite, other sulfates, and iron oxides. Aqueous alteration of outcrops and rocks on the West Spur of the Columbia Hills may have occurred when vapors rich in SO2 from volcanic sources reacted with basaltic materials. Soluble ions from the host rock (e.g., olivine) reacted with S to form Ca-, Mg-, and other sulfates along with iron oxides and oxyhydroxides.

Golden, D. C.

Derivation of Apollo 14 High-Al Basalts at Discrete Times: Rb-Sr Isotopic Constraints

Pristine Apollo 14 (A-14) high-Al basalts represent the oldest volcanic deposits returned from the Moon [1,2] and are relatively enriched in Al2O3 (>11 wt%) compared to other mare basalts (7-11 wt%). Literature Rb-Sr isotopic data suggest there are at least three different eruption episodes for the A-14 high-Al basalts spanning the age range approx.4.3 Ga to approx.3.95 Ga [1,3]. Therefore, the high-Al basalts may record lunar mantle evolution between the formation of lunar crust (approx.4.4 Ga) and the main basin-filling mare volcanism (<3.85 Ga) [4]. The high-Al basalts were originally classified into five compositional groups [5,6], and then regrouped into three with a possible fourth comprising 14072 based on the whole-rock incompatible trace element (ITE) ratios and Rb-Sr radiometric ages [7]. However, Rb-Sr ages of these basalts from different laboratories may not be consistent with each other because of the use of different 87Rb decay constants [8] and different isochron derivation methods over the last four decades. This study involved a literature search for Rb-Sr isotopic data previously reported for the high-Al basalts. With the re-calculated Rb-Sr radiometric ages, eruption episodes of A-14 high-Al basalts were determined, and their petrogenesis was investigated in light of the "new" Rb-Sr isotopic data and published trace element abundances of these basalts.

Hui. Hejiu

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.

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.

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.