A “chondritic” eucrite parent body: inference from trace elements

A total of 33 elements (Ag, Al, Au, Bi, Br, Cd, Ce, Co, Cr, Cs. Eu, Fe, Ge, Hf, Ir, Lu, Na, Ni, Os, Pd, Rb, Re, Sb, Se, Se, Si, Sm, Tb, Te, Tl, U, Yb and Zn) were analyzed by radiochemical and instrumental neutron activation in four eucrites: Juvinas (brecciated), Ibitira (vesicular, unbrecciated) and Moore County and Serra de Magé (cumulate, un brecciated).When arranged in order of volatility. Cl—normalized abundance patterns allow nebular and planetary effects to be distinguished. The stepped lithophile pattern reveals the dominance of nebular processes; in Ibitira, refractory elements (Hf, Lu, Tb, Ce, Sm, Yb, U, Eu) are (13.1 ± 0.7) × Cl chondrites; volatile elements (Rb. Cs, Br, Bi) are (6.0 + 1.5) × 10^?2 Cl. The depletion of Tl seems inherent to the eucrite parent body and is mirrored in the chalcophile elements by the marked deficit of Te relative to Se; apparently volatiles were accreted as a fractionated C3-like component. Consistent but subtle Cl-normalized abundance differences between eucrites (Serra de Magé < Moore County < Juvinas < Ibitira) result from crystal/liquid differentiation; Ibitira approximates the composition of an undifferentiated eucrite magma. The siderophile pattern retains little sign of nebular processes, but reflects planetary metal-silicate partition.The bulk composition of the eucrite parent body closely resembles that of H-chondrites, except for two features: moderately volatile elements (e.g. Na, K. Rb) are very much lower, apparently due to the accretion of more chondrule-like material; the metallic Fe-Ni content is only ~13%, even though total iron is very similar.     

Trace elements in ocean ridge basalt glasses: implications for fractionations during mantle evolution and petrogenesis

Seven well-documented and fresh glassy selvages from ocean floor basalt pillows were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Os, Pd, Rb, Re, Sb, Se, Te, Tl, U and Zn. The samples came from active spreading centers in the Indian and Atlantic Ocean. Glasses from DSDP Leg 24, site 238 (Indian Ocean) have a somewhat peculiar trace element pattern, but this is thought to reflect secondary processes operating at shallow depth, not an anomalous source region in the mantle. Our data rather indicate that heterogeneities in the mantle are confined to the highly incompatible lithophile elements.Chemical fractionations during petrogenesis of tholeiitic basalts are discussed in the light of literature data for primitive peridotitic upper mantle nodules. (Ir, Os), Au, Pd, Ni and Re are strongly fractionated from each other in igneous processes; the unfractionated chondritic mantle pattern thus imposes firm constraints on mantle evolution models. The potentially chalcophile elements Ag, Cd, In and Zn do not behave differently from lithophile elements of the same valency and comparable ionic radius. Residual sulfides are not abundant enough to efficiently control the partitioning of these elements during basalt petrogenesis. However, the poor coherence of Tl to Rb and U in ocean floor basalts could point to retention of Tl by residual sulfides during depletion of the MORB source regions. Sb is strongly depleted in the source regions of ocean ridge basalts; most likely, it was present as a highly incompatible Sb⁵⁺ cation. The limited Rb/Cs fractionation in oceanic tholeiites, as opposed to continental tholeiites and acidic rocks, appears to reflect the low abundance of volatile constituents and hydrous silicates in normal ocean ridge basalts.     

Petrochemistry and mineralogy of early Precambrian anorthositic rocks of the Limpopo belt, southern Africa

Two sections of the anorthosite ‘complex’ were examined at Messina, South Africa and at Pikwe, Botswana. Thirty XRF whole-rock analyses of samples in stratigraphic order show that alkalies at Messina increase upwards from leuco-gabbros to anorthosites, but no such correlation was found at Pikwe. Electron probe analyses of plagioclases in 33 samples indicate extensive normal zoning and variation (An₃₁-An₈₀) especially at Pikwe. The highest An-contents tend to vary monotonically with stratigraphic position, whereas the lowest values are erratic. Twenty-two amphibole analyses indicate that SiO₂, TiO₂ and MgO/FeO increase, decrease and increase, respectively, with height at Messina, but 22 analyses from Pikwe show no such trends. Their compositions are similar to those from the Fiskenaesset complex. Aluminous chromites are Fe-rich, also like the Fiskenaesset ones.

The Limpopo anorthositic rocks belong to a layered igneous body that was recrystallized by regional metamorphism and subjected to erratic metasomatism. The original Limpopo and Fiskenaesset bodies strongly resemble gabbroic and peridotitic relics in the Peninsular Ranges Batholith in S. California.     

R-mode factor analysis on enstatite chondrite analyses

R-mode factor analysis on 11 specimens of 9 enstatite chondrites, analysed for Ga, Se, Te, Zn, Cd, Bi, Tl, In, Sb, As, Co, showed three factors (rotated) to account for 92 per cent of the elemental variations (variance).Factor 1 dominates the first 8 elements listed, all volatile and mostly chalcophile: factors 2 and 3 express Sb and As variations, respectively, probably dependent on siderophile and less volatile behaviour; factors 1 and 2 contribute to Co.Factor-scores for individual meteorites indicate compositional differences (for these elements) between the E4 as against E5 and E6 stones (which are indistinguishable).Factor analysis of a second suite of 10 specimens analysed for Zn, Cd, Bi, Tl, In, Ag, Rb, Cs showed one factor to account for 93 per cent of the elemental variance. This expresses the association of Ag, Rb, Cs with the volatile-chalcophile factor.     

Volatile elements in chondrites: metamorphism or nebular fractionation?

Three of the most highly metamorphosed meteorites of their respective classes, Shaw (LL7), Karoonda (C5), and Coolidge (C4), were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Os, Pd, Rb, Re, Sb, Se, Te, Tl, U, and Zn. Comparison with data by Lipschutz and coworkers on artificially heated primitive meteorites shows that the natural metamorphism of meteorites cannot have taken place in a system open to volatiles. Shaw, metamorphosed at 1300°C for >10⁶ yr, is less depleted in In, Bi, Ag, Te, Zn, and Tl than Krymka heated at 1000°C for 1 week. Karoonda, metamorphosed at 600°C for many millennia, is less depleted in Bi and Tl than Allende heated at 600°C for 1 week.Data on primordial noble gases also show that the volatile-element patterns of ordinary and carbonaceous chondrites were established by nebular condensation, and changed little if at all during metamorphism. For enstatite chondrites, the evidence is still incomplete, but seems to favor a nebular origin of the volatile pattern.The general constancy of Tl/Rb, Tl/Cs and Tl/U ratios in terrestrial and lunar rocks suggests that loss of volatile metals such as Tl is rare during normal magmatism or metamorphism. Only impact melts show such loss with any frequency.     

Anorthosite formation by plagioclase flotation in ferrobasalt and implications for the lunar crust

The Sept Iles layered intrusion (Quebec, Canada) is dominated by a basal Layered Series made up of troctolites and gabbros, and by anorthosites occurring (1) at the roof of the magma chamber (100-500 m-thick) and (2) as cm- to m-size blocks in gabbros of the Layered Series. Anorthosite rocks are made up of plagioclase, with minor clinopyroxene, olivine and Fe-Ti oxide minerals. Plagioclase displays a very restricted range of compositions for major elements (An₆₈-An₆₀), trace elements (Sr: 1023-1071 ppm; Ba: 132-172 ppm) and Sr isotopic ratios (⁸⁷Sr/⁸⁶Sr_i: 0.70356-0.70379). This compositional range is identical to that observed in troctolites, the most primitive cumulates of the Layered Series, whereas plagioclase in layered gabbros is more evolved (An₆₀-An₃₈). The origin of Sept Iles anorthosites has been investigated by calculating the density of plagioclase and that of the evolving melts. The density of the FeO-rich tholeiitic basalt parent magma first increased from 2.70 to 2.75 g/cm³ during early fractionation of troctolites and then decreased continuously to 2.16 g/cm³ with fractionation of Fe-Ti oxide-bearing gabbros. Plagioclase (An₆₉-An₆₀) was initially positively buoyant and partly accumulated at the top of the magma chamber to form the roof anorthosite. With further differentiation, plagioclase (<An₆₀) became negatively buoyant and anorthosite stopped forming. Blocks of anorthosite (autoliths) even fell downward to the basal cumulate pile. The presence of positively buoyant plagioclase in basal troctolites is explained by the low efficiency of plagioclase flotation due to crystallization at the floor and/or minor plagioclase nucleation within the main magma body. Dense mafic minerals of the roof anorthosite are shown to have crystallized from the interstitial liquid.The processes related to floating and sinking of plagioclase in a large and shallow layered intrusion serve as a proxy to refine the crystallization model of the lunar magma ocean and explain the vertically stratified structure of the lunar crust, with (gabbro-)noritic rocks at the base and anorthositic rocks at the top. We propose that the lunar crust mainly crystallized bottom-up. This basal crystallization formed a mafic lower crust that might have a geochemical signature similar to the magnesian-suite without KREEP contamination, while flotation of some plagioclase grains produced ferroan anorthosites in the upper crust.     

Origin of Archean anorthosites: Evidence from the Bad Vermilion Lake anorthosite complex,Ontario

The Bad Vermilion Lake anorthosite complex (2,700 m.y.) is exposed over an area of about 100 km² near Rainy Lake, Ontario. As is typical of other Archean anorthosites, it is composed of coarse (1–30 cm across), equidimensional, euhedral to subhedral, calcic (An₈₀) plagioclase, in a finer grained mafic matrix. The amount of mafic matrix in individual samples ranges from none to about 70% by volume. The complex has been variably metamorphosed to greenschist facies. Zoisite, chlorite, and hornblende are abundant, but primary plagioclase is preserved in many places. The anorthosite complex is associated with gabbro and with mafic to felsic metavolcanic rocks, and is cut by tonalite plutons and by mafic dikes. Some gabbros contain local concentrations of Fe-Ti oxides and/or apatite, but no chromite. The mafic groundmass of the anorthositic rocks is similar in major and trace element chemistry, including rare earth elements, to the associated basaltic metavolcanics, suggesting that the anorthositic complex may have accumulated from a subvolcanic magma chamber which fed mafic lavas to the surface during its crystallization. Mafic flows and dikes chemically similar to the mafic metavolcanics contain plagioclase megacrysts akin to those of the anorthositic rocks, and thus may represent a link between the anorthosite complex and associated mafic lavas. Elongate pretectonic tonalite intrusions were comagmatic with the felsic metavolcanics, but not with the anorthosites or metabasalts. These silicic rocks may represent low-pressure partial melts of the mafic rocks. There is no direct or indirect evidence for significant volumes of ultramafic material at the present exposure level of the complex. An estimate of the bulk composition of all rocks presumed to be comagmatic with the anorthosites, including gabbros and mafic metavolcanics, is an aluminous basalt with about 20 wt.% Al₂O₃. This composition has REE abundances unlike those of typical Archean high-Al basalts and probably does not represent that of a primary or evolved melt. The possibility must be considered, therefore, that a substantial fraction of material comagmatic with the anorthosites has been separated from the complex, either by magmatic or tectonic processes.     

Moon and Earth : compositional differences inferred from siderophiles,volatiles, and alkalis in basalts

We have compared RNAA analyses of 18 trace elements in 25 low-Ti lunar and 10 terrestrial oceanic basalts. According to Ringwood and Kesson, the abundance ratio in basalts for most of these elements approximates the ratio in the two planets.Volatiles (Ag, Bi, Br, Cd, In, Sb, Sn, Tl, Zn) are depleted in lunar basalts by a nearly constant factor of 0.026 ± 0.013, relative to terrestrial basalts. Given the differences in volatility among these elements, this constancy is not consistent with models that derive the Moon's volatiles from partial recondensation of the Earth's mantle or from partial degassing of a captured body. It is consistent with models that derive planetary volatiles from a thin veneer (or a residuum) of C-chondrite material; apparently the Moon received only 2.6% of the Earth's endowment of such material per unit mass.Chalcogens (Se and Te) have virtually constant and identical abundances in lunar and terrestrial basalts, probably reflecting saturation with Fe(S, Se, Te) in the source regions.Siderophiles show diverse trends. Ni is relatively abundant in lunar basalts (4 × 10^?3 × Cl-chondrites), whereas Ir, Re, Ge, Au are depleted to 10^?4?10^?5× Cl. Except for Ir, these elements are consistently enriched in terrestrial basalts: Ni 3 × , Re 370 ×, Ge 330 × , Au 9 × . This difference apparently reflects the presence of nickel-iron phase in the lunar mantle, which sequesters these metals. On Earth, where such metal is absent, these elements partition into the crust to a greater degree. Though no lunar mantle rock is known, an analogue is provided by the siderophile-rich dunite 72417 (~0.1% metal) and the complementary, siderophile-poor troctolite 76535. The implied metal-siderophile distribution coefficients range from 10⁴ to 10⁶, and are consistent with available laboratory data.The evidence does not support the alternative explanation advanced by Ringwood—that Re was volatilized during the Moon's formation, and is an incompatible element (like La or W⁴⁺) in igneous processes. Re is much more depleted than elements of far greater volatility: (Re/U)_Cl～- 4 × 10^?6 vs (T1/U)_Cl = 1.3 × 10^?4, and Re does not correlate with La or other incompatibles.Heavy alkalis (K, Rb, Cs) show increasing depletion with atomic number. Cs/Rb ratios in lunar basalts, eucrites, and shergottites are 0.44, 0.36, and 0.65 × Cl, whereas the value for the bulk Earth is 0.15–0.26. These ratios fall within the range observed in LL and E6 chondrites. supporting the suggestion that the alkali depletion in planets, as in chondrites, was caused by localized remelting of nebular dust (= chondrule formation). Indeed, the small fractionation of K, Rb and Cs, despite their great differences in volatility, suggests that the planets, like the chondrites, formed from a mixture of depleted and undepleted material, not from a single, partially devolatilized material.     

Aubrites and diogenites: Trace element clues to their origin

We have analyzed by RNAA 25 aubrite and 9 diogenite samples for 13 to 29 siderophile, volatile, and lithophile trace elements. Both meteorite classes show a typically igneous siderophile element pattern, with Ir, Os, Re, Ge more depleted than Au, Ni, Pd, Sb. But aubrites tend to have about 10 × higher abundances (10^?3 ? 10 ^{? 4} × Cl for the first 4 and 10^?2?10^?3 × Cl for the last 4 siderophiles), apparently reflecting smaller metal/silicate distribution coefficients at lowerf(O₂), or less complete segregation of metal. Se is surprisingly abundant in aubrites (up to 0.4 × Cl), but Te is less so ($\text{Se}\text{Te}\text{? 5 × Cl}$), apparently due to its stronger siderophile character. Other volatiles (Ag, Zn, In, Cd, Bi, T1) show depletions intermediate between lunar dunite and the Earth's mantle.Of 7 aubrites analyzed for REE (Ce, Nd, Eu, Tb, Yb, Lu), 6 are depleted in REE (0.08?0.5 × Cl) and 5 show negative Eu anomalies (the exceptions are Bishopville and Mt. Egerton silicate). This supports an igneous origin, as already noted by Boynton and Schmitt (1972). No samples of the complementary, basaltic and feldspathic rocks have been found thus far, but one of our samples of Khor Temiki dark is a candidate for the basalt. It is 5?7 × enriched in REE and only slightly less so in Rb, Cs, and U. Though shocked and enriched in siderophiles to ~0.05 × Cl, it apparently represents a new meteorite class.Three diogenites analyzed for REE show very diverse patterns, from strongly depleted in light REE for Tatahouine (Ce = 0.01 × Cl) to flat for Garland (~2.5 × Cl). The data confirm the trends found by Fukuokaet al. (1977) as well as their interpretations.Factor analysis shows several parallel groupings for aubrites and diogenites: siderophiles (Re, Ir, Os, Pd, Ge), chalcophiles (Se, Te), volatiles (Ag, In, Tl) and incompatibles (U, REE, and Cs or Rb). But there are some differences for elements such as Ni, Sb, Cd, Bi, Au, and Zn, most of which behave more sensibly in aubrites than in diogenites.Several element pairs that differ greatly in volatility (Cs-U, Ge-Ir) correlate closely in aubrites, in approximately Cl-chondrite proportions. These correlations, and other lines of evidence, suggest strongly that aubrites originated by igneous processes in their parent body, not by direct nebular condensation. The source material may have resembled EL chondrites in oxidation state and depletion of refractories, metal, and volatiles.     

Ureilites: Trace element clues to their origin

Carbonaceous vein separates from Kenna and Haverö, as well as bulk Kenna, were analyzed by RNAA for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Pd, Os, Rb, Re, Sb, Se, Te, Tl. U, and Zn. The data are reviewed together with four earlier Chicago analyses of bulk ureilites. Linear regressions confirm the presence of two metal components, with the following Cl-normalized ratios: Ir/Ni = 14.6, ≤ 1; Ge/Ni = 5.4, 2.4; Au/Ni = 2.3, 0.9. The high-Ir component is enriched in vein separates and hence belongs to veins; the lowIr component belongs to the ultramafic rock. Vein material is enriched in all elements analyzed by us except Zn, and accounts for most of the C, noble gases, and presumably siderophiles in the meteorite. Most of the properties of ureilites apparently can be explained by the cumulate model of Berkley et al. (1980), with certain modifications. Comparison of ureilites with three other ultramafic rocks from different planets (Earth's mantle, lunar dunite, and Chassigny) suggests that the ureilite parent body had a primitive chondritic composition, similar to C3V chondrites but richer in metal and carbon. It melted, causing depletion of incompatibles to a mean abundance of ~0.02 × Cl and incomplete segregation of metal, FeS, and C. Fractional crystallization or melting of metal in the presence of S and C apparently can explain the fractionations of Ir, Re, Ni, Au, and perhaps Ge, obviating the need for extraneous sources of vein metal or unusual parent-body compositions. Noble gases from the parent material may have been retrapped in carbon during magmatism, provided the system was closed.     

H-chondrites: Trace element clues to their origin

We have analyzed 10 H-chondrites for 20 trace elements, using RNAA. The meteorites included 4 of petrologic type 4 and 2 each of types 3, 5 and 6.The data show that H-chondrites are not isochemical. H3's are depleted by some 10% not only in Fe (Dodd, 1976), but also in the siderophiles Os, Re, Ir, Ni, Pd, Au, and Ge. Moreover, the abundance pattern of siderophiles varies systematically with petrologic type. As similar fractionations of REE have been observed by Nakamura (1974), it appears that both the proportions and compositions of the main nebular condensates varied slightly during accretion of the H-chondrites. Thus the higher petrologic types are independent nebular products, not metamorphosed descendants of lower petrologic types.Abundances of highly volatile elements (Cs, Br, Bi, Tl, In, Cd, Ar³⁶) correlate with petrologic type, declining by ≤ 10^?3 from Type 3 to Type 6. The trends differ from those for artificially heated Type 3's (Ikramuddinet al., 1977b; Herzoget al., 1979), but agree passably with theoretical curves for nebular condensation. Apparently the low volatile contents of higher petrologic types are a primary feature, not the result of metamorphic loss.The mineralogy of chondrites suggests that they accreted between 405 K (absence of Fe₃O₄) and 560 K (presence of FeS), and the abundances of Tl, Bi, and In further restrict this interval to 420–500 K. Accretion at 1070 ± 100 K, as proposed by Hutchisonet al. (1979, 1980), leads to some extraordinary problems. Volatiles must be injected into the parent body after cooling, which requires permeation of the body by 10¹¹ times its volume of nebular gas. This process must also achieve a uniform distribution of the less volatile elements (Rb, Cu, Ag, Zn, Ga, Ge, Sn, Sb, Se, F), without freezeout in the colder outer layers.Factor analysis of our data shows 3 groupings: siderophiles (Os, Re, Ir, Ni, Pd, Au, and Ge), volatiles (Ag, Br, In, Cd, Bi, and Tl) and alkalis (Rb and Cs). The remaining 5 elements (U, Zn, Te, Se, and Sb) remain unassociated.     

Are C1 chondrites chemically fractionated? a trace element study

Six C1 chondrite samples and a C2 xenolith from the Plainview H5 chondrite were analyzed by radiochemical neutron activation for the elements Ag, Au, Bi, Br, Cd, Ce, Cs, Eu, Ge, In, Ir, Lu, Nd, Ni, Os, Pd, Pt, Rb, Re, Sb, Se, Sn, Tb, Te, Tl, Yb, and Zn. The data were combined with 9 earlier analyses from this laboratory and examined for evidence of chemical fractionation in C1 chondrites.A number of elements (Br, Rb, Cs, Au, Re, Os, Ni, Pd, Sb, Bi, In, Te) show small but correlated variations. Those of the first 8 probably reflect hydrothermal alteration in the meteorite parent body, whereas those of Sb, Bi, In, and Te may at least in part involve nebular processes. Br and Au show systematic abundance differences from meteorite to meteorite, which suggests hydrothermal transport on a kilometer scale. The remaining elements vary from sample to sample, suggesting transport on a centimeter scale.There is no conclusive evidence for nebular fractionation affecting C1 's. Though C1 chondrites have lower $\text{Zr}\text{Hf}$ and $\text{Ir}\text{Re}$ ratios than do other chondrite classes, these ratios vary in other classes, suggesting that those classes rather than C1's are fractionated. Three fractionation-prone REE—Ce, Eu, and Yb have essentially the same relative abundances in C1's and all other chondrite classes, and hence apparently are not fractionated in C1's. We did not confirm the large Tb and Yb variations in C1's reported by other workers.We present revised mean C1 abundances for 35 elements, based on the new data and a critical selection of literature data. Changes are generally less than 10%, except for Br, Rb, Ag, Sb, Te, Au, and the REE.The Plainview C2 xenolith has normal trace element abundances, except for 3 elements falling appreciably above the C2 range: Rb, Cs, and Bi. Hydrothermal alteration may be the reason for all 3, though nebular fractionation remains a possibility for Bi.     

Chemical fractionations in meteorites—X. Ureilites

Four ureilites (Dyalpur, Goalpara, Haverö, and Novo Urei) were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Rb, Re, Sb, Se, Te, Tl, and U. An attempt has been made to resolve the data into contributions from the parent ultramafic rock and the injected, carbon- and gas-rich vein material. Interelement correlations, supported by analyses of separated vein material (WANKE et al, 1972), suggest that the vein material is enriched about 10-fold in refractory Ir and Re over moderately volatile Ni and Au, and is low in volatiles except Ge, C, and noble gases. It appears to be a refractory-rich nebular condensate that precipitated carbon by surface catalytic reactions at ˜500K and trapped noble gases but few other volatiles. The closest known analogue is a Cr- and C-rich fraction from the Allende meteorite, highly enriched in heavy noble gases and noble metals. By analogy with Allende, the gas-bearing phase in ureilites may have been an Fe, Cr-sulfide.

The ultramafic rock contains siderophiles and chalcophiles (Ni, Au, Ge, S, Se) at ˜0.05 of Cl chondrite level, and highly volatile elements (Rb, Cs, Bi, Tl, Br, Te, In, Cd) at ˜0.01 Cl level. It probably represents the residue from partial melting of a C3V-like chondrite body, under conditions where phase separation was incomplete so that some liquid was retained. The vein material was injected into this rock at some later time.     

Terrestrial geochemistry of Cd,Bi, Tl,Pb, Zn and Rb

About 2000 common magmatic, metamorphic and sedimentary rocks and rockforming minerals contained in 465 individual samples have been analyzed for 6 trace metals and potassium with high precision, mainly by combined distillation and AAS methods. Estimates of average abundances in the continental crust are: 98 ppb Cd. 82 ppb Bi. 490 ppb Tl, 14.8 ppm Pb, 77 ppm Zn and 98 ppm Rb (K/Rb: 223). These averages are close to the mean concentrations of the 6 elements in sedimentary and in low to medium grade metamorphic rocks. In relation to the upper mantle the earth's crust has very effectively accumulated Rb, Pb, Tl (and Bi). Cd and Zn are equally distributed between the upper and lower crust. Bi, Tl, Rb, Pb and K are accumulated in the upper relative to the lower continental crust by factors between 3.5 and 1.4. This is mainly due to higher concentrations in granites and lower abundances in granulites relative to gneisses and schists. The five metals form large ions with bulk coefficients less than one for the partition between metamorphic rocks and anatectic granitic melts. The major hosts of Rb, Tl, Pb and Bi in rocks are minerals with 8- to 12-coordinated sites such as mica, K-feldspar, plagioclase etc. (except for some preference of Bi for sphene and apatite). As examples of significant correlations those of Pb with Tl, K, Bi and Rb in mafic rocks and of Bi with K, Rb, Tl and Pb in sedimentary rocks can be reported. In granites and gneisses hydroxyl containing Fe²⁺-Mg-silicates are major host minerals for Zn and Cd. Except in some carbonate rocks Cd has no preference for Ca minerals.     

“Mysterite” : a late condensate from the solar nebula

We have attempted to clarify the nature of “mysterite”, a material that had been postulated to explain the overabundance of Tl, Bi and Ag in certain chondrites. Four dark clasts and a vein sample from the H6 chondrite Supuhee were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Os, Rb, Re, Sb, Se, Te, Tl and Zn. One of the clasts is enriched in all volatile elements, while the other 4 samples are enriched only in the siderophile volatiles Ag, Bi and Tl. The enrichments range up to 100 times typical H6 chondrite abundances. The proportions of Ag, Bi, Tl suggest the presence of at least two, Tl-rich and Tl-poor, varieties of mysterite ($\text{Tl}\text{Bi}\text{= 7.2}$ and <0.1). The former seems to dominate in Supuhee and Krymka, and the latter in Mezö-Madaras. Apparently mysterite is a late condensate from the solar nebula that collected volatiles left behind by earlier generations of chondrites. It was incorporated in Supuhee and perhaps in other chondrites (mainly of low petrologic types) during brecciation events.     

Plagioclase twin laws and fabrics in three specimens of anorthosite

Twinning patterns and petrofabrics of plagioclases are examined in three specimens of anorthosite from the Bushveld Complex, the Quebec Massif, and the Fiskenaesset Complex. Their plagioclases have petrographical characteristics exhibiting their different petrogeneses.In an anorthosite from the Bushveld Complex, plagioclase grains are twinned after the albite-Carlsbad, pericline, albite and Carlsbad laws. Frequency percentage of the albite-Carlsbad and Carlsbad laws reaches 43% Plagioclase grains in the adcumulate layers are developed with their composition plane (010) subparallel to the cumulate plane, whereas those in the heteradcumulate layers are developed with their composition plane (010) subperpendicular to the cumulate plane.In an equigranular anorthosite from the Quebec Massif, plagioclase grains are polysynthetically twinned after the albite and pericline laws with rare examples of the albite-Carlsbad and Carlsbad laws. Frequency percentage of the latter two laws is only 1% together. Some regularities are recognized in the petrofabrics of c-axis and (010) plane.In a calcic anorthosite from the Fiskenaesset Complex, plagioclase grains are polysynthetically twinned, exclusively according to the pericline law or a combination of pericline and albite laws. The pericline law is predominant and reaches 64% and this twinning pattern cleaarly differs from that of the former two anorthosites.     

Luna 20 soil: abundance of 17 trace elements

Luna 20 soil is remarkably similar to Apollo 16 soil, in its content of 17 mainly volatile or siderophile elements: Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Rb, Re, Sb, Se, Te, Tl, U, and Zn. Like other highland soils, it seems to contain an ancient meteoritic component of fractionated, volatile-poor composition. The bulk soil has a high $\text{Tl}\text{Cs}$ ratio (9.4 × 10^?2), similar to that in Apollo 16 soils (5.4 × 10^?2), but higher than that in samples from other sites (1.1 × 10^?2). It is severely contaminated with Ag, Cd, Re, and Sb, judging from a comparison with a 1.7 mg soil breccia sample from the coarse fraction of the soil.     

Meteoritic trace elements in lunar rock 14321, 184

The 16 trace elements (Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Rb, Re, Sb, Se, Te, Tl and Zn) were measured by radiochemical neutron activation analysis in six samples of 14321, 184: microbreccia-2 (15), microbreccia-3 (14A, 16A and 19A), basaltic clast (1A), and light matrix material (9A). The 14321 microbreccias typically contain a siderophile-rich ancient meteoritic component, poor in volatiles, which is characterized by low $\text{Ir}\text{Au}$ and $\text{Re}\text{Au}$ ratios (0.25-0.38 and 0.34-0.50, respectively, normalized to Cl). This component also occurs in Apollo 12 KREEP glasses, norite fractions of Apollo 14 1–2 mm soils, Apennine Front breccias, and Cayley Formation material, and may represent ejecta from the Imbrian basin.The basaltic clast 14321, 184-1A closely resembles 14053 in trace element content, and both are 5–10 times higher than mare basalts in volatile trace elements (Br, Cd, Tl). The light matrix material contains 9.2 ± 0.5 per cent of microbreccias, judging from its siderophile content.     

Feldspathic lunar meteorites and their implications for compositional remote sensing of the lunar surface and the composition of the lunar crust

We present new compositional data for six feldspathic lunar meteorites, two from cold deserts (Yamato 791197 and 82192) and four from hot deserts (Dhofar 025, Northwest Africa 482, and Dar al Gani 262 and 400). The concentrations of FeO (or Al₂O₃) and Th (or any other incompatible element) together provide first-order compositional information about lunar polymict samples (breccias and regoliths) and regions of the lunar surface observed from orbit. Concentrations of both elements on the lunar surface have been determined from data acquired by orbiting spacecraft, although the derived concentrations have large uncertainties and some systematic errors compared to sample data. Within the uncertainties and errors in the concentrations derived from orbital data, the distribution of FeO and Th concentrations among lunar meteorites, which represent ∼18 source regions on the lunar surface, is consistent with that of 18 random samples from the surface. Approximately 11 of the lunar meteorites are low-FeO and low-Th breccias, consistent with large regions of the lunar surface, particularly the northern farside highlands. Almost all regoliths from Apollo sites, on the other hand, have larger concentrations of both elements because they contain Fe-rich volcanic lithologies from the nearside maria and Th-rich lithologies from the high-Th anomaly in the northwestern nearside. The feldspathic lunar meteorites thus offer our best estimate of the composition of the surface of the feldspathic highlands, and we provide such an estimate based on the eight most well-characterized feldspathic lunar meteorites. The variable but high (on average) Mg/Fe ratio of the feldspathic lunar meteorites compared to ferroan anorthosites confirms a hypothesis that much of the plagioclase at the surface of the feldspathic highlands is associated with high-Mg/Fe feldspathic rocks such as magnesian granulitic breccia, not ferroan anorthosite. Geochemically, the high-Mg/Fe breccias appear to be unrelated to the mafic magnesian-suite rocks of the Apollo collection. Models for the formation of the upper lunar crust as a simple flotation cumulate composed mainly of ferroan anorthosite do not account for the complexity of the crust as inferred from the feldspathic lunar meteorites.     

Sr isotopes and trace element geochemistry of the impact melt and target rocks at the Mistastin Lake crater,Labrador

The Mistastin Lake meteorite crater lies completely within a batholith composed of mangerite and adamellite with lenses of anorthosite and is located in central Labrador. The multivariate statistical technique of correspondence analysis was used to summarize the relationships between the different rock units for the trace elements Nb, Zr, Y, Sr, Rb, Th, Pb, Zn, Cu, Ni. The samples of impact melt form a linear array of points on a factor plot joining the anorthosite samples to the mangerite and adamellite samples. This indicates that the various melt samples can be formed as a result of the complete fusion of different proportions of anorthosite and granitic rocks. A least-squares mixing model utilizing the average trace element composition of the four rock types indicates that an average melt rock can be formed by mixing 60% anorthosite, 38% mangerite and 2% adamellite. An isochron obtained on the combined mangerite and adamellite units of the batholith gives an age of 1347 ±15 m.y. (1σ) with an initial ratio of 0.7082 ± 0.0003. The anorthosite samples plot below the isochron and the melt rocks fall along a mixing line joining the locus of anorthosite points to an average granite sample on the isochron. This is a further indication that the melt was formed by melting of anorthosite and granitic rocks that form the local geological environment.