Sm-Nd isotopic evolution of chondrites and achondrites,II

The¹⁴⁷Sm¹⁴³Nd and¹⁴⁶Sm¹⁴²Nd isotope systematics have been investigated in five chondrites and the achondrites Moama and Angra dos Reis (ADOR). The new chondrite data and those we have reported before are all consistent with our previously reported reference values for CHUR (“chondritic uniform reservoir”) of (¹⁴³Nd/¹⁴⁴Nd)_CHUR⁰ = 0.511847 and (¹⁴⁷Sm/¹⁴⁴Nd)_CHUR⁰ = 0.1967. Most of the bulk chondrites analyzed have ¹⁴³Nd/¹⁴⁴Nd and ¹⁴⁷Sm/¹⁴⁴Nd within 0.5 ε-units and 0.15% of the CHUR values, respectively. This strongly suggests that the CHUR evolution is now known to within these error limits throughout the history of the solar system. The St. Severin chondrite yields an SmNd internal isochron age of T = 4.55 ± 0.33AE and an initial ε_Nd = 0.11 ? 0.26. Much larger variations in Sm/Nd ratios were measured in mineral separates of the Moama and ADOR achondrites. Thus, very precise ages of 4.46 ± 0.03AE and4.564 ± 0.037AE were obtained for these meteorites, respectively. The initial ε_Nd values obtained for Moama and ADOR are 0.03 ? 0.25and0.14 ? 0.20, respectively. The values obtained on these meteorites are fully consistent with the CHUR evolution curve. Initial ε_Nd data on terrestrial igneous and meta-igneous rocks demonstrates that positive initial ε_Nd values occur throughout the past 4 AE. This confirms our earlier report that a light rare earth element-depleted layer has existed throughout most of the Earth history and is the source of present-day mid-ocean ridge basalts. The inferred shape of the ε_Nd vs. age curve for the depleted mantle suggests profound changes in tectonic regimes with time; in particular, it suggests a much higher rate of recycling of continental materials into the mantle during the Archean as compared to later time periods.¹⁴⁶Sm¹⁴²Nd systematics of ADOR and Moama are supportive of the hypothesis that¹⁴⁶Sm was present in the early solar system and suggests a ¹⁴⁶Sm/¹⁴⁴Sm ratio of about 0.01 for the solar system ～ 4.56 AE ago. This inferred high¹⁴⁶Sm abundance cannot be explained as a late injection from a supernova and must be due to galactic nucleo-synthesis.     

SmNd isotopic systematics of Enderby Land granulites and evidence for the redistribution of Sm and Nd during metamorphism

Measurements of¹⁴³Nd/¹⁴⁴Nd and¹⁴⁷Sm/¹⁴⁴Nd are reported for whole rocks and mineral separates from granulites of the Napier Complex at Fyfe Hills. Charnockites, leuconorites and gabbros yield a whole rock SmNd isochron age of3060 ± 160m.y. and an initial¹⁴³Nd/¹⁴⁴Nd ratio of0.50776 ± 10 (?_Nd(3060m.y.) = ?2.0 ± 1.8). The negative ?_Nd value and the presence of geologically induced dispersion in the data suggest that the isochron age does not represent the time of primary crystallization of the complex but instead indicates a time of later redistribution of Sm and Nd and partial re-equilibration of¹⁴³Nd/¹⁴⁴Nd ratios. This probably occurred during the upper granulite facies metamorphism which has also been dated at～ 3100m.y. by RbSr and UPb zircon studies [1]. Coexisting clinopyroxene, apatite and total rock fractions in two adjacent samples define an approximately linear array corresponding to an age of 2300 ± 300 m.y. This array indicates that redistribution of Sm and Nd and re-equilibration of¹⁴³Nd/¹⁴⁴Nd ratios occurred on an intermineral scale during the upper amphibolite to lower granulite facies metamorphism at～ 2450m.y.Due to the resetting of the SmNd system on both whole rock and mineral scales, the primary crystallization age of the igneous protolith is not well constrained by the present data, although it is clearly3100m.y. If it is assumed that the complex was derived initially from a depleted mantle reservoir(?_Nd(T) ? 2), evolution of the negative ?_Nd value of ?2.0 with the observed Sm/Nd ratios requires a prehistory of～ 380m.y. This implies a primary age of～ 3480m.y. However, substantially older primary ages can be inferred if the source reservoirs had?_Nd(T) > 2 and/or substantial reductions in the Sm/Nd ratio occurred in whole rocks during the granulite facies metamorphism at 3100 m.y. Such an inferred reduction in the Sm/Nd ratio may have been the result of preferential loss of Sm relative to Nd, or introduction of a low Sm/Nd fluid with?_Nd ≥ 0 during granulite facies metamorphism.     

Isotope geochemistry of xenoliths from East Africa: Implications for development of mantle reservoirs and their interaction

Pb, Nd and Sr isotope analyses together with U, Pb, Sm, Nd, Rb and Sr concentrations have been obtained for separated phases of lherzolite and bulk rock mafic granulite xenoliths in Recent volcanics from Tanzania. A garnet lherzolite from the Lashaine vent has yielded the least radiogenicPb(²⁰⁶Pb/²⁰⁴Pb= 15.55) and Nd(¹⁴³Nd/¹⁴⁴Nd= 0.51127; ?_Nd⁰ = ?26.7) isotope compositions recorded so far for an ultramafic xenolith, and ⁸⁷Sr/⁸⁶Sr= 0.83604. The Pb isotope compositions of the mafic granulites are variable 15.77<²⁰⁶Pb/²⁰⁴Pb<17.50 and some show evidence for depletion of U relative to Pb up to 2.0 Ga ago. Overall the isotope results suggest that the mantle part of the continental lithosphere beneath Tanzania has components that have undergone a complex history that includes major chemical fractionations ca. 2.0 Ga ago. A phlogopite-amphibole vein from the Pello Hill sample has Sr, Nd and Pb isotope compositions similar to those of mid-ocean ridge basalts, indicating both a young emplacement age for the vein material and a source which had an isotopic signature characteristic of depleted mantle.The Sr, Nd and Pb isotope systematics of ultramafic xenoliths do not conform with those of MORB, particularly in terms of their PbSr, and NdPb relationships. In this regard they are similar to some ocean islands and could be a viable source material for some ocean island basalts at least. The mantle part of the continental lithosphere is as likely to contain recycled components derived from the continental crust as are other regions of mantle. If the mantle part of continental lithosphere is invoked as a source for ocean islands, it does not negate the possibility that substantial recycled components are involved.     

Nd isotopic systematics and chemistry of Central Australian sapphirine granulites: an example of rare earth element mobility

Lower Proterozoic sapphirine-bearing and associated granulites from Central Australia exhibit the greatest range of present-day¹⁴³Nd/¹⁴⁴Nd ratios (∈_Nd(O)= ?26.5 to +112.3) yet reported for rocks believed to be cogenetic. The Nd isotopic data and REE abundances of these rocks demonstrate extreme fractionation of the rare earths during the formation of stratiform CuPbZn sulfide deposits with which they are closely associated. Field relationships, petrography and chemistry of the sapphirine granulites suggest that their protoliths comprised chlorite-rich rocks which were generated by hydrothermal alteration of a range of rock types prior to metamorphism; calculations employing REE abundances of the sapphirine granulites and associated rocks, combined with bulk solid-fluid distribution coefficient data yield high fluid/rock ratios, consistent with a pre-metamorphic hydrothermal origin for the unusual REE patterns. The SmNd data for these rocks define an age of 1760±75Ma, which is significantly younger than the crust formation age of the terrain ( 2070±125Ma) but indistinguishable from the RbSr whole rock age for granulite facies metamorphism (1790±35Ma). These data are interpreted in terms of major hydrothermal fractionation of the rare earths shortly (perhaps tens of millions of years) before granulite facies metamorphism, followed by redistribution of Nd isotopes or small fractionations of the Sm/Nd ratio during the granulite facies event, and possibly also during intense retrogression which reset RbSr whole rock and UPb zircon and monazite systematics at about 1700 Ma.     

The provenance and crustal residence ages of British sediments in relation to palaeogeographic reconstructions

24 SmNd isotope analyses of fine-grained Phanerozoic and modern clastic sediments from Britain and Quebec are presented. In combination with published data, they have been used to calculate “crustal residence ages” (t_CR) and to assess the provenance of the British sedimentary mass. Sediments now preserved on either side of the suture formed by the closure of the Iapetus Ocean ca. 400 Ma ago were derived from isotopically distinct source regions. Sediments north of the suture are characterised by1.7 < t_CR < 2.8 Ga, whereas those to the south exhibit a smaller range and an average value of 1.6 Ga. The northern and southern source regions were most probably Laurentia and Gondwana respectively. It seems likely that a third source, perhaps Baltica, provided the lower Palaeozoic Southern Uplands succession. Sediments deposited in southern Britain after the closure of Iapetus were derived mainly from the recycling of older sediments. The tectonic rearrangements which occurred during the Phanerozoic are not reflected in the SmNd isotopic structure of the southern British sedimentary mass, suggesting that the Caledonian and Hercynian orogenies, and even the Grenville orogeny, involved minimal accretion of new mantle-derived material into the British and adjacent continental crust. SmNd analyses of fine-grained clastic sediments provide a powerful sedimentological tool for elucidating palaeogeography, clastic source areas, sediment recycling and maturity, and some aspects of sediment transport.     

Hydrothermal Mn-deposits of the Franciscan Assemblage,II. Isotope and trace element geochemistry,and implications for hydrothermal convection at spreading centers

Major element, trace element and Sr, Nd, Pb and O isotopic data for a Franciscan Mn-deposit suggest an origin by seafloor hydrothermal circulation. Based onQ-mode factor analysis the cherts and Mn-lenses of the Blue Jay mine formed from a combination of 4 components representing 1 biogenic, 1 hydrothermal, and 2 detrital sources. RbSr, UThPb and O isotopic systematics in the Mn-lenses were affected by input from the hydrothermal circulation of material leached from the underlying basalts. Nd isotopic compositions in both cherts and Mn-lenses are identical and within the range measured for Pacific Ocean water suggesting the REE were not mobilized by hydrothermal activity. Correlation of δ¹⁸O with SiO₂ and MnO₂ in the Mn-lenses implies the lenses formed by simple mixing of hydrothermally derived Mn-oxides with seawater and biogenic silica. δ¹⁸O of the cherts is both uniform and depleted relative to DSDP Jurassic cherts but similar to microquartz-bearing cherts of the Monterey Formation: this suggests that diagenetic activity exerted more control on oxygen isotope compositions then hydrothermal alteration or metamorphism. Finally, a well defined RbSr isochron of158 ± 5Myr was obtained for these cherts and opens the possibility of determining absolute radiometric ages for similar cherts throughout the geologic record.     

SmNd study of Archean alkalic rocks from the Superior Province of the Canadian Shield

The Abitibi Volcanic Belt in eastern Superior Province of the Canadian Shield is the largest continuous greenstone belt in the world and is a key example of late Archean crust. This belt has, in general, suffered a low intensity of metamorphism and deformation, and, as a result, the stratigraphy and geology are well established. Tholeiitic and calc-alkaline series of igneous rocks are present in this belt in about equal proportions. However, the undersaturated potassic and leucitic volcanics of the Timiskaming Group are a unique feature of this belt.SmNd systematics were determined for twelve Timiskaming volcanic rocks. These rocks show nepheline, diopside and/or olivine plus leucite in the norm and a highly fractionated REE pattern. Sm and Nd concentrations range from 25 to 160 and 45 to 300 times the chondritic abundance, respectively. The Sm and Nd isotopic data yield an isochron age of 2702±105Ma for these volcanic rocks with an initial ε_Nd of +1.9±1.6. This age establishes the Timiskaming alkalic rock to be one of the oldest of their kind. From stratigraphic relations, 2705 Ma is an upper limit for the age and the ε_Nd values of +1.8 to +2.2 at this age for the twelve rocks are also upper limits. Further, this small but positive ε_Nd value for the isochron, when compared to other mantle-derived Archean rocks in the Superior Province, indicates that the Archean mantle was heterogeneous beneath the Canadian Shield and that the Timiskaming alkalic lavas were derived from a depleted mantle.     

Morphology versus UPb systematics in zircon: a high-resolution isotopic study of a zircon population from a Variscan dike in the Central Alps

UPb isotopic measurements on individual zircon crystals combined with morphological analyses permit the identification of three distinct components within the zircon population of the Saedelhorn diorite, a Variscan dike from the western Gotthard (Central Alps, Switzerland): (i) 94% of the grains in the zircon population are elongate crystals with pronounced skeletal morphology indicative of rapid growth from a supercooled melt. (ii) 5% of the population consist of turbid, mostly subhedral zircons frequently showing D-type morphology (classification according to Pupin and Turco [1]) and elevated uranium contents compared to the skeletal variety. Single-crystal and multi-grain UPb isotopic data of group (i) and (ii) zircons define an intrusion age of 293 +5/−4 m.y. for the dike. (iii) Rare, transparent zircon crystals (<1% of the zircon population) yield apparent UPb ages in the range of 370–490 m.y. and display morphological and isotopic characteristics closely resembling those of a Caledonian orthogneiss intruded by the dike. This implies presence of assimilated wall-rock components in the macroscopically homogeneous dike sample.A comparison of the data obtained by conventional analysis of multi-grain zircon fractions and those obtained by grain-by-grain analysis demonstrates that age resolution is considerably improved by single-crystal UPb dating. Furthermore, quantitative identification of zircon components assimilated by the ascending magma along its path to the present level of exposure is feasible by the latter technique. Since it is likely that such zircon grains are common to a broad variety of magma types, valuable information on age and composition of crustal layers not accessible to direct observation may readily become available by application of precise micro-analytical techniques.Low initial¹⁴³Nd/¹⁴⁴Nd(ε_Nd = −2.7) at the time of intrusion of the Saedelhorn dike requires the magma to be derived partially or totally from a crustal source. For this crustal precursor, a model age of 1050 m.y. (T_DM) is obtained, indicating that Proterozoic crust was involved in the petrogenesis of the Variscan intrusives of the Gotthard area.     

Correlated Nd,Sr and Pb isotope variation in Walvis Ridge basalts and implications for the evolution of their mantle source

Basement intersected in DSDP holes 525A, 528 and 527 on the Walvis Ridge consists of submarine basalt flows and pillows with minor intercalated sediments. These holes are situated on the crest and mid and lower northwest flank of a NNW-SSE-trending ridge block which would have closely paralleled the paleo mid-ocean ridge [13, 14]. The basalts were erupted approximately 70 m.y. ago, an age equivalent to that of immediately adjacent oceanic crust in the Angola Basin and consistent with formation at the paleo mid-ocean ridge [14]. The basalt types vary from aphyric quartz tholeiites on the ridge crest to highly plagioclase phyric olivine tholeiites on the ridge flank. These show systematic differences in incompatible trace element and isotopic composition. Many element and isotope ratio pairs form systematic trends with the ridge crest basalts at one end and the highly phyric ridge flank basalts at the other.The low ¹⁴³Nd/¹⁴⁴Nd (0.51238), ²⁰⁶Pb/²⁰⁴Pb (17.54), ²⁰⁸Pb/²⁰⁴Pb (15.47), ²⁰⁸Pb/²⁰⁴Pb (38.14) and high⁸⁷Sr/⁸⁶Sr (0.70512) ratios of the ridge crest basalts suggest derivation from an old Nd/Sm-, Rb/Sr- and Pb/U-enriched mantle source. This isotopic signature is similar to that of alkaline basalts on Tristan de Cunha but offset to significantly lower Nd and Pb isotopic ratios. The isotopic ratio trends may be extrapolated beyond the ridge flank basalts with higher¹⁴³Nd/¹⁴⁴Nd (0.51270), ²⁰⁶Pb/²⁰⁴Pb (18.32), ²⁰⁷Pb/²⁰⁴Pb (15.52), ²⁰⁸Pb/²⁰⁴Pb (38.77) and lower ⁸⁷Sr/⁸⁶Sr (0.70417) ratios in the direction of increasingly Nd/Sm-, Rb/Sr- and Pb/U-depleted source compositions. These isotopic correlations are equally consistent with mixing od depleted and enriched end member melts or partial melting of an inhomogenous, variably enriched mantle source. However, observe ZrBaNbY interelement relationships are inconsistent with any simple two-component model of magma mixing, as might result from the rise of a lower mantle plume through the upper mantle. Incompatible element and Pb isotopic systematics also preclude extensive involvement of depleted (N-type) MORB material or its mantle sources. In our preferred petrogenetic model the Walvis Ridge basalts were derived by partial melting of mantle similar to an enriched (E-type) MORB source which had become heterogeneous on a small scale due to the introduction of small-volume melts and metasomatic fluids.     

Rare earth element geochemistry of garnet lherzolite and megacrystalline nodules from minette of the Colorado plateau province

Mineral and whole-rock REE abundances in garnet lherzolite and megacrystalline nodules from The Thumb display broad correlations with major element compositions. Lherzolites with > 12 modal % clinopyroxene plus garnet (“high-CaAl lherzolites”) have relatively flat chondrite-normalized whole-rock REE patterns. Lherzolites poor in clinopyroxene and garnet (“low-CaAl lherzolites”) have lower HREE in clinopyroxenes and garnets and higher whole-rock LREE/HREE. It is concluded that the low-CaAl lherzolites may have undergone LREE metasomatism after depletion of the major element compositions by partial melting and that much of the garnet now present was originally dissolved in aluminous orthopyroxene. The high-CaAl lherzolites may be interpreted either as primordial mantle samples or as products of equilibration with very LREE-enriched liquids. The “megacrystalline” nodules are medium- to ultracoarse-grained intergrowths and megacrysts with mineral compositions similar to discrete nodule suites in kimberlites. The REE abundances of the megacrystalline minerals are consistent with an origin as cumulates from magma with extremely fractionated REE, similar to minette or kimberlite.The patterns of correlation of REE and major elements in this inclusion suite are similar to the patterns observed in the garnet lherzolite and discrete nodule suites of southern African kimberlites. Both of the subcontinental mantle provinces represented by these suites contain three distinct petrogenetic components: refractory garnet lherzolite enriched in LREE and depleted in HREE, fertile garnet lherzolite with generally chondritic REE abundances, and a suite of ultracoarse minerals precipitated from magma with extremely fractionated REE generally similar to the host magmas.     

Mineral age patterns in ca. 3700 my old rocks from West Greenland

KAr,⁴⁰Ar³⁹Ar and RbSr dates are reported for minerals from the ca. 3700 my-old Amîtsoq and Isua gneisses of the Godthaabsfjord area of West Greenland. KAr dates on biotites and hornblendes range from about 1900 to 3500 my, with hornblendes having a much narrower range (ca. 2250–2750 my) than biotites. One biotite from Isua gives an impossibly high KAr date of 4940 my.⁴⁰Ar³⁹Ar mineral dates are in close agreement with conventional KAr dates over the entire range of apparent age values. The presence of minor amounts of excess argon is observed in the hornblendes, but radiogenic and excess argon in the biotites are completely homogenised and cannot be differentiated.Rb-Sr measurements on biotites are closely concordant and show that all biotites were completely open to diffusion of radiogenic⁸⁷Sr at about 1600–1700 my. This is the first proof of a regional thermal event at this time in the Archaean of West Greenland, although similar dates are well known from the Proterozoic belts to the north and south.The evidence suggests that those KAr biotite dates greater than about 2700–2800 my result from excess radiogenic argon incorporated during a thermal event of about this age or, more probably, during the 1600–1700 my Sr isotope homogenisation event. Scatter of mineral dates below about 2700 my could also be due, at least in part, to overprinting by the 1600–1700 my event.KAr mineral dates and an Rb-Sr mineral isochron from a pegmatite associated with the last major rock-forming event in the Godthaabsfjord area, namely the Qo?rqut granite, indicate an age of emplacement of 2580 ± 30 my.     

Composition of the core,II. Effect of high pressure on solubility of FeO in molten iron

An experimental and theoretical investigation of the effect of pressure on the solubility of FeO in molten iron has been carried out. Analyses of shock-wave compression data on iron oxides combined with measurements of the FeO bond length in “metallic” oxides suggest that the partial molar volume of FeO(V^*) dissolved in molten iron is substantially smaller than that of molten wüstite. Hence the effect of high pressure should be to increase the solubility of FeO in molten iron at a given temperature. This inference is confirmed by an experimental investigation of the effect of pressure on the position of the FeFeO eutectic. Thermodynamic calculations based on these experiments yield an estimate forV^* which is in reasonable agreement with the theoretical estimates. The experimental value ofV^* is used to calculate the effect of high pressure upon the FeFeO phase diagram. Solubility of FeO in molten iron increases sharply with pressure, the liquid immiscibility region contracts and disappears around 20 GPa and it is predicted that the FeFeO phase diagram should resemble a simple eutectic system above about 20 GPa. Analogous calculations predict that the solubility of FeO in molten iron in equilibrium with magnesiowüstite (Mg_0.8Fe_0.2)O at 2500°C increase from 14 mol.%(P = 0) to above 25 mol.% at 20 GPa. If the core formed by segregation of metallic iron originally dispersed throughout the earth, it seems inevitable that it would dissolved large amounts of FeO, thereby accounting for the observation that the density of the outer core is substantially smaller than that of pure iron under correspondingP, T conditions.     

Hafnium/rare earth element fractionation in the sedimentary system and crustal recycling into the Earth's mantle

Among long-lived radioactive parent-daughter element pairs, the ratio Lu/Hf is strongly fractionated relative to constant Sm/Nd in the Earth's sedimentary system. This is caused by high resistance to chemical weathering of the mineral zircon (Zr,Hf)SiO₄. Zircon-bearing sandy sediments on and near continents have very low Lu/Hf, while deep-sea clays have up to three times the chondritic Lu/Hf ratio. Turbidity currents mechanically carry the low-Lu/Hf sandy material onto the ocean floor. The results are important for the crust-to-mantle recycling discussion, where most recycled materials would be subducted oceanic sediments. Such sediment should be capable of explaining the HfNd mantle isotopic variation by mixing with peridotite, but in fact any average pelagic sediment has Nd/Hf and Lu/Hf too high to allow mixing curves to pass through the Hf/Nd isotopic array. The array could only be reproduced by subduction of turbidite sandstone with pelagic sediment in the approximate ratio 1.2 to 1, and by maintaining a good mixture between the two components. At least today, turbidites are available for subduction only at locations quite different and distant from those where pelagic sediments may be recycled; furthermore, mantle isotopic variation shows that the mantle often cannot mix itself well enough to homogenize these widely-separated sedimentary components to the degree required. The Lu/Hf fractionations place a severe restriction on the ability of recycled sediments to explain mantle isotopic patterns.     

The effect of initial230Th disequilibrium on young UPb ages: the Makalu case,Himalaya

Comparative UPb dating of zircon, xenotime and monazite from two different samples of the Himalayan “Makalu” granite shows the two U decay series to be in disequilibrium, particularly in monazite. This disequilibrium is due to excess or deficit amounts of radiogenic²⁰⁶Pb which originate from an excess or deficit of²³⁰Th, respectively, occurring initially in the mineral. Such an initial disequilibrium is caused by UTh fractionation between the crystallising mineral and the magma. Therefore, the UPb ages of Th-rich minerals such as monazite (and allanite) have to be corrected for excess²⁰⁶Pb due to excess²³⁰Th, whereas Th-poor minerals such as zircon and xenotime require a correction for a deficit of²⁰⁶Pb due to deficiency of²³⁰Th. The extent of this correction depends on the degree of ThU fractionation and on the age of the rock. For the two monazite populations analysed here, these excess amounts of²⁰⁶Pb were, with reference to the amount of radiogenic²⁰⁶Pb, 8–10% and 15–20% respectively, and less than 1% for zircon and xenotime. The varying degrees of Th enrichment relative to U in monazite show that the ThU partition coefficients for this mineral are not constant within a single granite. Furthermore, for monazite there is evidence for excess amounts of radiogenic²⁰⁷Pb originating from the decay of initial excess²³¹Pa, also enriched during crystal growth.The very low Th/U ratios of 0.196 and 0.167, determined for thetwo whole rocks from which the minerals have been extracted, substantiate the view that granite formation is a fundamental mechanism for ThU fractionation in continental crust.The different ages of 21.9 ± 0.2m.y. and24.0 ± 0.4m.y., obtained by averaging the corrected²³⁸U²⁰⁶Pb ages of the monazites, suggest that the apparently homogeneous Makalu granite was generated over a period of at least 2 m.y.     

Interpretation of Nd,Sr and Pb isotope data from Archean migmatites in Lofoten-Vesterålen,Norway

Sm-Nd data for the Archean granulite and amphibolite facies migmatites of Langøy and Hinnøy in Vesterålen are presented which indicate that their protoliths formed ～2.6 AE ago. Rubidium and U loss during a granulite facies metamorphism at ～1.8 AE caused serious disturbance of total-rock U-Pb and Rb-Sr systems. Therefore these systems do not provide any precise age information for the granulite facies migmatites. For the amphibolite facies migmatites of Vesterålen both SmNd, RbSr and PbPb total-rock systems give model ages of ～2.6 AE. The results on both granulite and amphibolite facies rocks are thus in agreement. Previous interpretations based on PbPb data, which indicated an age of 3.41 AE for the Archean terrane of Vesterålen, are not valid.One SmNd model age from the granulite facies migmatites at Moskenesøy in Lofoten indicates that the protoliths of these migmatites formed ～2.0 AE ago and are thus not related to the Vesterålen migmatites.     

Major-element vapor fractionation on the lunar surface: An unusual lithic fragment from the Luna 20 fines

A 250-μm fragment in the Luna 20 fines has a very fine-grained “igneous” texture and has the composition (wt.%): SiO₂, 41.1; TiO₂, 0.35; Al₂O₃, 27.2; Cr₂O₃, 0.14; FeO, 4.2; MnO, 0.06; MgO, 8.5; CaO, 17.8; Na₂O, 0.05; and K₂O < 0.02. It contains ～ 65% plagioclase An_99–100, ～ 15% olivine Fo₉₀, ～ 2% Mg-Al spinel and the remainder an unusual interstitial phase with composition SiO₂, 34.8; TiO₂, 1.78; Al₂O₃, 18.3; Cr₂O₃, 0.04; FeO, 14.1; MnO, 0.22; MgO, 5.0; CaO, 24.1; Na₂O, 0.34; K₂O < 0.02. This fragment probably represents a portion of a normal highland rock (anorthositic norite) which was heated to a very high temperature by impact, lost volatiles including SiO₂, and then partially crystallized. The observed phases and their inferred crystallization sequence are consistent with experimental results in the system CaOMgOAl₂O₃SiO₂ (Schairer and Yoder, 1969), assuming the unusual phase to be a residual glass. This type of internal fractionation, leading to silica depletion in the residuum, is different from that normally observed in lunar rocks and is attributed to slightly lower bulk SiO₂ resulting from vapor fractionation due to impact (which also results in lower Na₂O and other volatiles). Because differentiation of the type shown by this fragment is rare in lunar materials, we infer that such major-element vapor fractionation is uncommon on the surface of the moon. The experimental CaOMgOAl₂O₃SiO₂ phase relations also have a bearing on the lunar model proposed by D.L. Anderson in 1973: his “refractory” original lunar composition would differentiate to produce silica deficient liquids, like the unusual phase in our fragment, rather than the normal lunar crustal rocks.     

The chronology of the Nakhla achondritic meteorite

A well-defined internal RbSr isochron has been determined for the unbrecciated Nakhla achondrite, defining an age T = (1.24 ± 0.01) AE and an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70254 ± 0.00003. The excellence of fit to the isochron shows that a very thorough Sr isotopic equilibration took place at this time between all phases of the meteorite. Recent petrological observations indicate that the age most probably represents the time of an igneous crystallization event on the parent body of Nakhla. The age shows that we may no longer assume that major chemical and physical differentiation processes took place only in early solar system history. The RbSr systematics are shown not to require late formation of the Nakhla parent body. Geochemical similarities between Nakhla and the earth are discussed.     

Inherited isotope systems and the source region pre-history of early Caledonian granites in the Dalradian Series of Scotland

RbSr and UPb isotope analyses are reported for two pre-metamorphic Caledonian granites which intrude Dalradian rocks in the Central Highlands of Scotland. These data indicate that the origin of the granitic magmas involved partial fusion of old crustal material.UPb systems of zircon size and magnetic fractions from the Ben Vuirich granite are strongly discordant. However, U/Pb isotopic ratios precisely define a chord which intersects concordia at 514_?7⁺⁶ m.y. and 1316_?25⁺²⁶ m.y. Geological constraints suggest that the lower intersection records the post-F₂, pre-M₃ emplacement age of the granite. The upper intersection reflects the presence of old zircon xenocrysts incorporated into the granite magma without complete isotopic resetting. The ultimate source of these xenocrysts is probably a metamorphic basement complex which formed about 1320 m.y. ago, but the immediate source region of the granites could have been Dalradian sediments derived therefrom.RbSr whole-rock systems of the Ben Vuirich granite are also strongly discordant, although 8 out of 13 data points scatter about an “errorchron” of 564 ± 24 m.y. with an initial⁸⁷Sr/⁸⁶Sr ratio of about 0.716. This is interpreted as a spurious result due to incomplete homogenization of Sr isotopes in the source region during partial fusion. Initial⁸⁷Sr/⁸⁶Sr ratios at the time of emplacement indicated by the zircon data ranged from 0.7173 to 0.7191. Whole-rock samples from the Dunfallandy Hill granite have Rb/Sr ratios 2–3 times higher than those from Ben Vuirich and define a reasonably good isochron age of 491 ± 15 m.y. with an initial⁸⁷Sr/⁸⁶Sr of 0.7185 ± 0.0008. This may date granite emplacement or subsequent resetting of the high Rb/Sr rocks during Caledonian metamorphism. RbSr systematics indicate that the crustal source regions of these and other Caledonian granites separated from the upper mantle at least ca. 800 m.y. ago and probably ca. 1300 m.y. ago, thus confirming the interpretation of the upper intersection age of the zircon UPb data.     

RbSr dating of the Yatsushiro granite and gneiss,Kyushu, Japan

RbSr measurements on the Yatsushiro granite and gneiss, which had been considered stratigraphically to be of possible Precambrian age, are reported. The whole rock isochron for the granite gives an age of 352 ± 8 my with a low initial⁸⁷Sr/⁸⁶Sr ratio of 0.7037 ± 0.0006. Data for constituent minerals of the granites are dispersed irregularly around the whole rock isochron (possibly by later tectonic events). For the gneiss, a metamorphic event around 410 my is indicated by the muscovite RbSr ages. The present results do not support the possibility that the Yatsushiro granite and gneiss are Precambrian in age.     

U–Th–Pb and Rb–Sr systematics of Apollo 17 boulder 7 from the North Massif of the Taurus-Littrow Valley

Portions of highland breccia boulder 7 collected during the Apollo 17 mission were studied using UThPb and RbSr systematics. A RbSr internal isochron age of3.89 ± 0.08b.y. with an initial⁸⁷Sr/⁸⁶Sr of0.69926 ± 0.00008 was obtained for clast 1 (77135,57) (a troctolitic microbreccia). A troctolitic portion of microbreccia clast 77215,37 yielded a UPb internal isochron of3.8 ± 0.2b.y. and an initial²⁰⁶Pb/²⁰⁷Pb of 0.69. These internal isochron age are interpreted as reflecting metamorphic events, probably related to impacts, which reset RbSr and UPb mineral systems of older rocks.Six portions of boulder 7 were analyzed for U, Th, and Pb as whole rocks. Two chemical groups appear to be defined by the U, Th, and Pb concentration data. Chemical group A is characterized by U, Th, and Pb concentrations and²³⁸U/²⁰⁴Pb values which are higher than those of group B. Group A rocks have typical²³²Th/²³⁸U ratios of ～ 3.85, whereas-group B rocks have unusually high Th/U values of ～ 4.1.Whole-rock UPb and PbPb ages are nearly concordant. Two events appear to be reflected in these data — one at ～ 4.4 b.y. and one at ～ 4.5 b.y. The chemical groupings show no correlation with documented ages. The old ages of ～ 4.4 b.y. and ～ 4.5 b.y. may, like the younger ～ 4.0 b.y. ages, be related to basin excavation events.