18O/16O ratios in lunar fines and rocks

¹⁸O/¹⁶O ratios have been measured for Luna 20 and Apollo 15 fines and Apollo 15 rocks.Isotopic composition and fractionation between minerals are compared with previous results.Partial fluorination experiments on Luna 20 soil and Apollo 15021 extreme fines show large¹⁸O enrichments in grain surfaces. These results are discussed.     

Chemical features of the Luna 16 regolith sample

The Luna 16 regolith sample differs from Apollo 11, 12 and 14 regolith and basalt samples by having smaller negative Eu and Sr anomalies and nearly chondritic Eu/Sm and Eu/Sr ratios although the overall REE, Ba, Sr and U concentrations are 25 to 45 times chondrites. Major element data, in particular FeO vs. Al₂O₃, show that the Luna 16 regolith sample is composed of materials that follow a quantitatively different Fe/Al variation than do Apollo 11, 12, 14 and 15 samples. The small Eu and Sr anomalies and the displaced Fe/Al variation are two chemical features unique to the Luna 16 regolith sample. The Luna 16 regolith sample can contain little if any of the rock types abundant at Apollo sites, thus indicating that the unique chemical features are typical of local or nearby materials and indicate a separate petrogenetic province for major component rock types of the Luna 16 regolith.     

Lithic fragments,glasses and chondrules from Luna 16 fines

Bulk compositions of igneous and microbreccia lithic fragments, glasses, and chondrules from Luna 16 fines as well as compositions of minerals in basaltic lithic fragments were determined with the electron microprobe. Igneous lithic fragments and glasses are divided into two groups, the anorthositic-noritic-troctolitic (hereafter referred to as ANT) and basaltic groups. Chondrules are always of ANT composition and microbreccia lithic fragments are divided into groups 1 and 2. The conclusions reached may be summarized as follows: (1) Luna 16 fines are more similar in composition to Apollo 11 than to Apollo 12 and 14 materials (e.g. Apollo 11 igneous lithic fragments and glasses fall into similar ANT and basaltic groups; abundant norites in Luna 16 and Apollo 11 are not KREEP as in Apollo 12 and 14; Luna 16 basaltic lithic fragments may represent high-K and low-K suites as is the case for Apollo 11; rare colorless to greenish, FeO-rich and TiO₂-poor glasses were found in both Apollo 11 and Luna 16; Luna 16 spinels are similar to Apollo 11 spinels but unlike those from Apollo 12). (2) No difference was noted in the composition of lithic fragments, glasses and chondrules from Luna 16 core tube layers A and D. (3) Microbreccia lithic fragments of group 1 originated locally by mixing of high proportions of basaltic with small proportions of ANT materials. (4) Glasses are the compositional analogs to the lithic fragments and not to the microbreccias; most glasses were produced directly from igneous rocks. (5) Glasses show partial loss of Na and K due to vaporization in the vitrification process. (6) Luna 16 chondrules have ANT but not basaltic composition. It is suggested that either liquid droplets of ANT composition are more apt to nucleate from the supercooled state; or basaltic droplets have largely been formed in small and ANT droplets in large impact events (in the latter case, probability for homogeneous and inhomogeneous nucleation is larger. (7) No evidence for ferric iron and water-bearing minerals was found. (8) Occurrence of a great variety of igneous rocks in Luna 16 samples (anorthosite, noritic anorthosite, anorthositic norite, olivine norite, troctolite, and basalt) confirm our earlier conclusion that large-scale melting or partial melting to considerable depth and extensive igneous differentiation must have occurred on the moon.     

Mineralogy,petrology, and chemistry of a Luna 16 basaltic fragment,sample B-1

Luna 16 sample B-1 was the largest fragment (62 mg) obtained in the sample exchange with the USSR. Petrologic, mineralogic, and chemical investigations have been made on this fragment in conjunction with Rb-Sr and⁴⁰Ar/³⁹Ar investigations by our colleagues. Sample B-1 is a fine-grained ophitic basalt but is distinguished from the Apollo samples by containing a single pyroxene, predominantly pigeonitic, an ilmenite content (7%) intermediate to that of the Apollo 11 and 12 samples, and subequal amounts of pyroxene (50%) and plagioclase (40%). Chemically it is distinguished by a high Sr content (437 ppm) and a high K/U value (4700). The K-content (1396 ppm) is higher than that of Luna 16 soil sample A-2.     

Meteoritic and non-meteoritic trace elements in Luna 16 samples

Two Luna 16 soils have been analyzed for Ag, Au, Bi, Br, Cd, Co, Cs, Cu, Ga, Ge, In, Ur, Ni, Rb, Re, Sb, Se, Te, Tl, and Zn. A meteoritic component similar to that in Apollo 11 and 12 soils seems to be present, corresponding to ∼1.5 to 2% Cl chondrites or equivalent. It probably consists largely of micrometeorites. Three elements show strong enrichments compared to Apollo 11 and 12 soils: Cd (5× to 200×), Ag (5× to 10×), and Bi (3×). Presumably these elements were brought in by Cd-Ag-Bi rich material, similar to that in Unit VI of Apollo core 12028.     

Rare earth and other trace elements in historic azorean lavas

Rare earth element (REE) and other trace element compositions of 16 lavas from all historic and 2 prehistoric eruptions on 5 islands of the Azores Archipelago show notable intra-and inter-island differences. Fe enrichment and “compatible” element depletion due to fractional crystallization have been superimposed on variations established in the source area. Fractionation of La/Sm, U/Th, K/Na and “large ion lithophile” (LIL) element abundances are probably related to variable fusion of a source peridotite whose LIL element distribution cannot be exactly specified in view of its possible heterogeneity. Relative light-REE enrichment in basalt appears greatest on the “potassic” island São Miguel, the more sodic island Fayal and one lava from Pico, and least in basalts from the “sodic” islands Terceira, São Jorge and Pico. This variation is matched by most other LIL elements, although P shows unexpected enrichment in Terceira lavas, otherwise the least LIL element-enriched and most heavy-REE-enriched. Upper mantle phase chemistry is probably critical in establishing the patterns. In particular, P—REE covariance may reflect phase stabilities of apatite and (P-bearing) garnet in the upper mantle. Distribution patterns of REE in the historic lavas are similar to those of basalts from the Atlantic median rift at the crest of the Azores “platform”. Transition to light-REE-depleted rift-erupted basalts to the southwest is believed to be step-wise with increasing water depth, possibly indicating retention of a light-REE-rich phase in the residue from partial fusion as intersection of geotherm and peridotite solidus occur at lower pressures. The source mantle for the Azores basalts is probably light-REE- and LIL element-enriched but we find no evidence so far to suggest its emplacement by thermal “plume” activity.     

Major,minor and trace element abundances in samples from the Apollo 17 station 7 boulder: Implications for the origin of early lunar crustal rocks

Apollo 17 station 7 boulder consortia samples were analyzed for major and minor elements by a combined semimicro atomic absorption spectrophotometric and colorimetric procedure. Lithophile trace element abundances were determined by stable isotope dilution mass spectrometry. Three matrix types samples (77135, 77115, and 77075) were found to be KREEP-rich fragment-laden melts with analogues throughout the Apollo 17 landing site. Of the five clasts analyzed, at least one (77115,19, troctolite) is thought to be a cumulate; 77135, 77115, and 77075 are thought to have originated by impact fusion of material with similar composition. This original material may represent a partial melt of a parent material of the composition of an included, shocked norite breccia (77215).     

Isotopic and REE studies of lunar basalt 12038: implications for petrogenesis of aluminous mare basalts

We report Sr, Nd, and Sm isotopic studies of lunar basalt 12038, one of the so-called aluminous mare basalts. A precise internal Rb-Sr isochron yields a crystallization age of 3.35±0.09 AE and initial⁸⁷Sr/⁸⁶Sr=0.69922?2 (2σ error limits, 1AE=10⁹ years, λ(⁸⁷Rb)=0.0139AE^?1). An internal Sm-Nd isochron yields an age of 3.28±0.23AE and initial¹⁴³Nd/¹⁴⁴Nd=0.50764?28. Present-day¹⁴³Nd/¹⁴⁴Nd is less than the “chondritic” value, i.e. ?(Nd, 0)=?2.3±0.4 where ?(Nd) is the deviation of¹⁴³Nd/¹⁴⁴Nd from chondritic evolution, expressed as parts in 10⁴. At the time of crystallization ?(Nd, 3.2AE)=1.5±0.6.We have successfully modeled the evolution of the Sr and Nd isotopic compositions and the REE abundances within the framework of our earlier model for Apollo 12 olivine-pigeonite and ilmenite basalts. The isotopic and trace element features of 12038 can be modeled as produced by partial melting of a cumulate mantle source which crystallized from a lunar magma ocean with a chondrite-normalized REE pattern of constant negative slope. Chondrite-normalized La/Yb=2.2 for this hypothetical magma ocean pattern. A plot of I(Sr) versus ?(Nd) for the Apollo 12 basalts clearly shows the influence of varying proportions of olivine, clinopyroxene, orthopyroxene, and plagioclase in the basalt source regions. A small percentage of plagioclase (～5%) in the 12038 source apparently is responsible for low I(Sr) and ?(Nd) in this basalt. Aluminous mare basalts from Mare Crisium (Luna 24) and by inference Mare Fecunditatis (Luna 16) occupy locations on the I(Sr)-?(Nd) plot similar to that of 12038, implying that some basalts from three widely separated lunar regions came from plagioclase-bearing source regions. A summary of model calculations for mare basalts shows a record of lunar mantle solidification during the period when REE abundances in the lunar magma ocean increased from ～20× chondritic to >100× chondritic. Although there is a general trend from olivine to clinopyroxene-dominated source regions with progressive magma ocean evolution, significant mineralogical heterogeneities in mantle composition apparently formed at any given stage of evolution, as evidenced in particular by the three Apollo 12 magma types.     

Mariana Trough basalts (MTB): trace element and SrNd isotopic evidence for mixing between MORB-like and Arc-like melts

Mariana Trough basalt (MTB) glasses from zones of of active seafloor volcanism have incompatible trace element compositions which are intermediate between normal MORB and basaltic rocks from the active northern Mariana Island Arc (MIAB). The chemical variation is observed in trace elemental abundances and ratios such as LIL/LIL and LIL/HFS. MTB glasses with high LIL/HFS and Ba/Sm ratios, and low K/Rb, K/Ba, and Sm/Nd ratios have more enriched Sr and Nd isotopic compositions.Comparison of the SrNd isotopic compositions of MTB and MIAB suggests that the source region within the mantle wedge is heterogeneous. The diverse trace element and isotopic compositions of MTB glasses both within and between dredge sites near 18°N imply small-scale source heterogeneity. Correlation between Sm/Nd and¹⁴³Nd/¹⁴⁴Nd of the MTB glasses is interpreted as due to recent binary mixing, rather than closed system evolution of a common homogeneous source. Mixing of melts at or near the source region between a mantle component with long-term LREE and LIL element depletion (MORB-like) and a relatively enriched component with lower integrated¹⁴³Nd/¹⁴⁴Nd (Arc-like) is suggested by trends of the MTB data on ratio-ratio, ratio-element and element-element plots.     

Neutron capture on Gd and Sm in the Luna 16, G-2 soil

The Gd and Sm isotopic compositions have been measured in the Luna 16, G-2 soil. This sample has the largest low energy neutron fluence ψ = 5.9 × 10¹⁶n/cm² (E < 0.18eV) yet observed in a lunar sample. The ratio of the number of neutrons captured per atom by¹⁴⁹Sm to¹⁵⁷Gd is 0.76 which is distinct from the value of 0.86 observed at the Apollo 11, 12 and 14 sites. This indicates a softer neutron energy spectrum at the Sea of Plenty.     

Petrogenesis of Cenezoic volcanic rocks from the Aegean island arc

The Aegean volcanic arc formed in response to northeasterly subduction of the Mediterranean sea floor beneath the Aegean Sea. The active arc lies over 250 km from the Hellenic Trench in a region which has suffered considerable extension and subsidence since the mid-Tertiary. Suites of samples from the different volcanic centres making up the arc have been studied geochemically in order to assess lateral variations and to constrain the contribution of crustal contamination and sediment subduction in their petrogenesis.Lavas from all the major volcanic centres exhibit typical calc-alkaline major-element characteristics, and show enrichment in light REE and LIL elements but low contents of HFS elements. The enrichment in light REE is greater in the eastern (Nisyros, Kos) and western (Milos, Poros, Methana, Aegina) sectors of the arc (Ce_n/Yb_n=4) than in the central Santorini sector (Ce_n/Yb_n=2). All lavas have significant negative Eu anomalies and many have slight negative Ce anomalies. Less coherence is observed in the abundances and ratios of the other LIL elements, compared with the REE, along the island chain.Whereas the effects of crystal fractionation are evident in the trace-element patterns of lavas from individual islands, and are particularly well marked for Santorini, it is clear that there are consistent differences in trace-element abundances and ratios in the lavas of the various islands which reflect compositional differences in the mantle source and/or in melting conditions. Lavas from the eastern and western sectors have much higher levels of Ba and Sr but relatively lower Th, K and Rb than those from Santorini. Although some geochemical features could be explained through involvement of a component of subducted sediment in the source regions of the volcanoes, other element abundances and ratios indicate that this component must be very small. Detailed consideration of the inter-island geochemical variations suggests a complex make-up of the underlying lithosphere, resulting from a long history of subduction. In the region of Santorini, where crustal stretching is greatest, the underlying asthenosphere may be involved in magma production.     

A komatiite component in Apollo 16 highland breccias: implications for the nickel-cobalt systematics and bulk composition of the moon

The lunar crust at the Apollo 16 landing site contains substantial amounts of a “primitive component” in which the ferromagnesian group of elements is concentrated. The composition of this component can be retrieved via an analysis of mixing relationships displayed by lunar breccias. It is found to be a komatiite which is compositionally similar to terrestrial komatiites both in major and minor elements. The komatiite component of the lunar crust is believed to have formed by extensive degrees of melting of the lunar interior at depths greater than were involved in the formation of the lunar magma ocean which was parental to the crust. After formation of the anorthositic crust, it was invaded by extensive flows and intrusions of komatiite magma from these deeper source regions. The komatiites became intimately mixed with the anorthosite by intensive meteoroid impacts about 4.5 b.y. ago, thereby accounting for the observed mixing relationships displayed by the crust. The compositional similarity between lunar and terrestrial komatiites strongly implies a corresponding similarity between the compositions of their source regions in the lunar interior and the Earth's upper mantle. The composition of the lunar interior can be modelled more specifically by combining the komatiite composition with its liquidus olivine composition (as determined experimentally) in proportions chosen so as to produce a cosmochemically acceptable range of Mg/Si ratios for the bulk Moon. Except for higher FeO and lower Na₂O, the range of compositions thereby obtained for the bulk moon is very similar to the composition of the Earth's upper mantle.The effects of meteoritic contamination on the abundances of cobalt and nickel in lunar highland breccias were subtracted on the assumption that the contaminating projectiles were chondritic. The cobalt and nickel residuals thereby obtained were found to correlate strongly with the (Mg + Fe) content of the breccias, demonstrating that the Co and Ni are associated with the ferromagnesian component of the breccias and are genuinely indigenous to the Moon. The lunar highland Co and Ni residuals also display striking Ni/Co versus Ni correlations which follow a similar trend to those displayed by terrestrial basalts, picrites and komatiites. The lunar trends provide further decisive evidence of the indigenous nature of the Co and Ni residuals and suggest the operation of extensive fractionation controlled by olivine-liquid equilibria in producing the primitive component of the lunar breccias. Indigenous nickel abundances at the Apollo 14, 15 and 17 sites are much lower than at the Apollo 16 site, although rocks from all sites follow the same Ni/Co versus Ni trends. It is suggested that the primitive component at the Apollo 14, 15 and 17 sites was generally of basaltic composition, in contrast to the komatiitic nature of the Apollo 16 primitive component.     

Diffusion of rare gases of solar wind origin from lunar fines as bubbles

A diffusion mechanism is proposed which takes into account phenomena observed in ion-implanted solids, in particular the precipitation of rare gas in the form of bubbles and their migration. The composition of rare gases in the bubbles is inferred from the calculated distribution of solar wind rare gas ions as a function of depth in the grains. These calculations are made for the location and average composition of Apollo 11 samples. It is shown by analogy with experimental observations in ion-implanted solids that the bubbles would migrate towards the surface and that the diffusion constant for this migration would be strongly depth dependent. Relative abundances of rare gas nuclides remaining behind due to the resultant degassing are estimated for one Apollo 11 soil sample and are compared with observed relative abundances for this sample. A qualitative explanation of some of the experimental observations of Ducati et al. on individual lunar grains is also offered.     

In quest of lunar regolith breccias of exotic provenance: a uniquely anorthositic sample from the Fra Mauro (Apollo 14) highlands

Polymict samples can be used to establish mass-balance constraints regarding the bulk composition of the lunar crust, and to gauge the degree of regional heterogeneity in the composition of the lunar crust. The most ideally polymict type of sample is finely-mixed regolith (lunar soil), or its lithified equivalent, regolith breccia. Fortunately, lunar regolith breccias can occasionally be found at great distances from their points of origin — most of the known lunar meteorites are regolith breccias. We are searching for examples of exotic regolith samples among the Apollo regolith breccia collection. Most of the 21 Apollo regolith breccias analyzed for this study strongly resemble the local soils over which they were collected. Nine regolith breccias from Apollo 16 are surprisingly mature compared to previously-analyzed Apollo 16 regolith breccias, and six of the seven from Apollo 16 Station 5 have lower, more local-soil-like,mg ratios than previously analyzed regolith breccias from this station. Several of the Apollo 14 regolith breccias investigated show significantly highermg, and lower Al, than the local soils.The most interesting sample we have investigated is 14076,1, from a lithology that constitutes roughly half of a 2.0-g pebble. The presence of spherules indicates a regolith derivation for 14076,1, yet its highly aluminous (30 wt.% Al₂O₃) composition is clearly exotic to the 1.6-km traverse surface over which the Apollo 14 samples were collected. This sample resembles soils from the Descartes (Apollo 16) highlands far more than it does any other polymict sample from the Fra Mauro (Apollo 14) region. The I/_sFeO maturity index is extremely low, but this may be a result of thermal annealing. A variety of siderophile elements occur in 14076,1 at typical regolith concentrations. The chemistry of the second most aluminous regolith sample from Apollo 14, 14315, can only be roughly approximated as a mixture of local regolith and 14076,1-like material. However, the low a priori statistical probability for long-distance horizontal transport by impact cratering, along with the relatively high contents of incompatible elements in 14076,1 (despite its high Al content), suggest that this regolith breccia probably originated within a few hundred kilometers of the Appollo 14 site. If so, its compositional resemblance to ferroan anorthosite tends to suggest that the regional crust is, or originally was, far richer in ferroan anorthosite than implied by the meager statistics for pristine rocks from this site. Thus, 14076,1 tends to strengthen the hypothesis that ferroan anorthosite originated as the flotation crust of a global magmasphere.     

Lunar red spots: Possible pre-mare materials

Some anomalous red features observed on the moon by Whitaker are examined in detail. Crater counts and regional stratigraphy suggest that ages for these features are comparable to that of lunar highland material. Initial gamma-ray spectrometry indicates higher than average native radioactivity is associated with certain red areas. A possible explanation for these observations is that the red objects are the surface manifestation of highly radioactive pre-mare basalts (Apollo 14/KREEP/norite material). Conclusive proof of the nature of these objects will depend on the study of returned samples, making them ideal candidates for future space missions, especially for unmanned vehicles such as the Soviet Union's Luna 20.     

South Aegean volcanic arc: Geochemical variations and geotectonic implications

The Aegean volcanic arc is one of the most important geological structure of the Mediterranean area. It is a belt of volcanic centers consisting of products ranging from basaltic, andesitic, dacitic to rhyolitic in composition, all of them displaying a typical calc-alkaline chemical character. The most abundant rock types are represented by andesites and dacites. Minor amounts of basalts and rhyolites occur mainly in the central-eastern sector of the arc. The REE, Rb, Sr, Ba, Th, Ta, Hf, Zr, Ni, Co, V and Cr abundances determined in 27 representative samples from different centers suggest that: 1) the intermediate and acidic terms are products of crystal/liquid fractionation processes starting from basic parent magmas: 2) large variations in incompatible elements occur in the most basic samples that are interpreted as evidence for heterogeneously LIL element-enriched mantle source; 3) plagioclase played a role in the evolution of the volcanic centers of the eastern and central arc different from that played in the volcanoes of the western sector. Along the arc, the differences in the distribution of lithological types, in the volumes of erupted material, in the volcanological characteristics of the different centers as well as in the patterns of trace element distribution in the volcanites are considered to be connected with the prevailing tectonic regime affecting the various sectors of the arc.     

Petrogenesis of the Tanzawa plutonic complex, central Japan: Exposed felsic middle crust of the Izu–Bonin – Mariana arc

The Miocene Tanzawa plutonic complex, consisting mainly of tonalite intrusions, is exposed at the northern end of the Izu–Bonin – Mariana (IBM) arc system as a consequence of collision with the Honshu Arc. The Tanzawa plutonic rocks belong to the calc-alkaline series and exhibit a wide range of chemical variation, from 43 to 75 wt% SiO₂. They are characterized by relatively high Ba/Rb and Ce/Nb ratios, and low abundances of K₂O, LIL elements, and rare earth elements (REE). Their petrographic and geochemical features indicate derivation from an intermediate parental magma through crystal fractionation and accumulation processes, involving hornblende, plagioclase, and magnetite. The Tanzawa plutonic complex is interpreted to be the exposed middle crust of the IBM arc, which was uplifted during the collision. The mass balance calculations, combining data from melting experiments of hydrous basaltic compositions at lower-to-middle crustal levels, suggest that parental magma and ultramafic restite were generated by dehydration partial melting (∼ 45% melting) of amphibolite chemically similar to low-K tholeiitic basalt. Partial melting of hydrated mafic lower crust might play an important role in felsic middle-crust formation in the IBM arc.     

Targeting the impactors: siderophile element signatures of lunar impact melts from Serenitatis

Highly siderophile element compositions of lunar impact melt breccias provide a unique record of the asteroid population responsible for large cratering events in the inner Solar System. Melt breccias associated with the 3.89 Ga Serenitatis impact basin resolve at least two separate impact events. KREEP-rich melt breccias representing the Apollo 17 poikilitic suite are enriched in highly siderophile elements (3.6-15.8 ppb Ir) with CI-normalized patterns that are elevated in Re, Ru and Pd relative to Ir and Pt. The restricted range of lithophile element compositions combined with the coherent siderophile element signatures indicate formation of these breccias in a single impact event involving an EH chondrite asteroid, probably as melt sheet deposits from the Serenitatis Basin. One exceptional sample, a split from melt breccia 77035, has a distinctive lithophile element composition and a siderophile element signature more like that of ordinary chondrites, indicating a discrete impact event. The recognition of multiple impact events, and the clear signatures of specific types of meteoritic impactors in the Apollo 17 melt breccias, shows that the lunar crust was not comprehensively reworked by prior impacts from 3.9 to 4.5 Ga, an observation more consistent with a late cataclysm than a smoothly declining accretionary flux. Late accretion of enstatite chondrites during a 3.8-4.0 Ga cataclysm may have contributed to siderophile element heterogeneity on the Earth, but would not have made a significant contribution to the volatile budget of the Earth or oxidation of the terrestrial mantle. Siderophile element patterns of Apollo 17 poikilitic breccias become more fractionated with decreasing concentrations, trending away from known meteorite compositions to higher Re/Ir and Pd/Pt ratios. The compositions of these breccias may be explained by a two-stage impact melting process involving: (1) deep penetration of the Serenitatis impactor into meteorite-free lower crust, followed by (2) incorporation of upper crustal lithologies moderately contaminated by prior meteoritic infall into the melt sheet. Trends to higher Re/Ir with decreasing siderophile element concentrations may indicate an endogenous lunar crustal component, or a non-chondritic late accretionary veneer in the pre-Serenitatis upper crust.     

Transverse geochemical variations across the Antarctic Peninsula: Implications for the genesis of calc-alkaline magmas

Magnetic activity throughout the Antarctic Peninsula and the South Shetland Islands has been dominantly of a calc-alkaline nature for the last 200 Ma. Chemically, the plutonic and volcanic products are typical of a continental margin magmatic arc, similar to those from western South America. Within any one area, volcanic and plutonic rocks are compositionally indistinguishable, and all magmatic products show increasing SiO₂, and increasing K/Si, Rb/Si, Th/Si and to a lesser extent Ce/Si and La/Si ratios away from the proposed trench axis. The calc-alkaline basaltic compositions also have high large ion lithophile (LIL; e.g. K, Rb, Th)/high field strength (HFS; e.g. Zr, Nb, Ti) ratios relative to non-orogenic counterparts, and increasing LIL/HFS element ratios with increasing fractionation. It is proposed that the high LIL/HFS element ratios in basaltic and andesitic melts are primary features due to dehydration processes with the subducted slab and to fractionation of minor mineral phases from the melt. The increasing LIL/HFS element ratios in more acid rocks are probably due to removal of minor mineral phases from the melt. Although zone refining may contribute to the spatial variations across the peninsula, we have proposed that an enriched subcontinental mantle provides a viable alternative source for the observed K-h variations and for the increased LIL-element contents found in continental margin calc-alkaline magmas.     

Genesis of the Angra dos Reis and other achondritic meteorites

Major, minor and trace element abundances were determined in seven Angra dos Reis samples including whole rocks, fassaite (clinopyroxene), olivine and whitlockite separates via sequential instrumental neutron activation analysis. The chondritic normalized rare earth element (REE) abundance pattern for the Angra dos Reis clinopyroxene separates shows a concave downward shape with a small negative Eu anomaly. The strong fractionation between the light and the heavy REE in olivine separates could be attributed to the presence of islands of kirschsteinite in the olivines. The large-ion lithophile trace elements were highly enriched in the whitlockite separate as expected (e.g. La ≈ 370 ppm). The lower Hf and Sc abundances in whitlockite compared to that in the equilibrium “magma” could be the result of favorable partitioning of Hf and Sc in baddeleyite, which may have crystallized prior to or with whitlockite in the interstitial liquid. Comparison of whole rock with mineral separate data shows the presence of ～3% olivine, ～2.6% spinel and small amounts of metallic Ni-Fe and troilite in the whole rock.The trace element abundances in the derivative magma from which the Angra dos Reis clinopyroxene crystallized were estimated from the clinopyroxene data and the clinopyroxene mineral-liquid partition coefficients. From the derivative magma, the trace element abundances in the possible parent magmas were calculated by assuming that these parent magmas have undergone different degrees of clinopyroxene fractional crystallization to yield the Angra dos Reis derivative magma. Using the trace element abundances in these possible parent magmas, a two-stage crystal-liquid fractionation model with source material containing olivine, orthopyroxene and clinopyroxene is presented for the genesis of Angra dos Reis. Possible combinations of the degree of equilibrium non-modal partial melting, the source mineral composition and the initial element abundances required to generate possible Angra dos Reis parent magmas are calculated by the multilinear regression analysis method. Favorable solutions for this two-stage crystal-liquid fractionation model could be that Angra dos Reis crystallized at ～70% fractional crystallization of clinopyroxene from magmas generated by reasonable degrees of equilibrium partial melting (～7–10%) of deep-seated primitive source materials (olivine ～54–30%, orthopyroxene ～33–53%, and clinopyroxene ～13–17%) with trace element (Ba, Sr, REE and Sc) abundances ～3.5–4.7 × chondrites. These calculated REE abundances in the Angra dos Reis parent body are very similar to those suggested for the primordial moon (～3–5 × chondrites).Possible genetic relationships between Angra dos Reis and other achondrites, especially cumulate eucrites and nakhlites, are studied. Apparently, the unique Angra dos Reis could not be related to those achondrites by crystal-liquid fractionation of the same parent body.