The oxygen isotope composition, petrology and geochemistry of mare basalts: Evidence for large-scale compositional variation in the lunar mantle

To investigate the formation and early evolution of the lunar mantle and crust we have analysed the oxygen isotopic composition, titanium content and modal mineralogy of a suite of lunar basalts. Our sample set included eight low-Ti basalts from the Apollo 12 and 15 collections, and 12 high-Ti basalts from Apollo 11 and 17 collections. In addition, we have determined the oxygen isotopic composition of an Apollo 15 KREEP (K - potassium, REE - Rare Earth Element, and P - phosphorus) basalt (sample 15386) and an Apollo 14 feldspathic mare basalt (sample 14053). Our data display a continuum in bulk-rock δ¹⁸O values, from relatively low values in the most Ti-rich samples to higher values in the Ti-poor samples, with the Apollo 11 sample suite partially bridging the gap. Calculation of bulk-rock δ¹⁸O values, using a combination of previously published oxygen isotope data on mineral separates from lunar basalts, and modal mineralogy (determined in this study), match with the measured bulk-rock δ¹⁸O values. This demonstrates that differences in mineral modal assemblage produce differences in mare basalt δ¹⁸O bulk-rock values. Differences between the low- and high-Ti mare basalts appear to be largely a reflection of mantle-source heterogeneities, and in particular, the highly variable distribution of ilmenite within the lunar mantle. Bulk δ¹⁸O variation in mare basalts is also controlled by fractional crystallisation of a few key mineral phases. Thus, ilmenite fractionation is important in the case of high-Ti Apollo 17 samples, whereas olivine plays a more dominant role for the low-Ti Apollo 12 samples.Consistent with the results of previous studies, our data reveal no detectable difference between the Δ¹⁷O of the Earth and Moon. The fact that oxygen three-isotope studies have been unable to detect a measurable difference at such high precisions reinforces doubts about the giant impact hypothesis as presently formulated.     

The case against early melting of the bulk of the Moon

Recent data suggest that the source region of mare basalts became compositionally closed at 4.42 Gy. presumably some 170 My. after the Moon accreted. Thermal-history models indicate that the outer part of the Moon could not have cooled to temperatures low enough to cause closure unless only the outer few hundred kilometers were initially molten. A total early lunar differentiation is therefore prohibited. The bulk of the Moon was therefore pristine and undifferentiated at the time of mare basalt formation. bl     

Trace element partitioning between ilmenite, armalcolite and anhydrous silicate melt: Implications for the formation of lunar high-Ti mare basalts

We performed a series of experiments at high pressures and temperatures to determine the partitioning of a wide range of trace elements between ilmenite (Ilm), armalcolite (Arm) and anhydrous lunar silicate melt, to constrain geochemical models of the formation of titanium-rich melts in the Moon. Experiments were performed in graphite-lined platinum capsules at pressures and temperatures ranging from 1.1 to 2.3 GPa and 1300-1400 °C using a synthetic Ti-enriched Apollo ‘black glass’ composition in the CaO-FeO-MgO-Al₂O₃-TiO₂-SiO₂ system. Ilmenite-melt and armalcolite-melt partition coefficients (D) show highly incompatible values for the rare earth elements (REE) with the light REE more incompatible compared to the heavy REE ( 0.0020 ± 0.0010 to 0.069 ± 0.010 for ilmenite; 0.0048 ± 0.0023 to 0.041 ± 0.008 for armalcolite). D values for the high field strength elements vary from highly incompatible for Th, U and to a lesser extent W (for ilmenite: 0.0013 ± 0.0008, 0.0035 ± 0.0015 and 0.039 ± 0.005, and for armalcolite 0.008 ± 0.003, 0.0048 ± 0.0022 and 0.062 ± 0.03), to mildly incompatible for Nb, Ta, Zr, and Hf (e.g. 0.28 ± 0.05 and : 0.76 ± 0.07). Both minerals fractionate the high field strength elements with D_Ta/D_Nb and D_Hf/D_Zr between 1.3 and 1.6 for ilmenite and 1.3 and 1.4 for armalcolite. Armalcolite is slightly more efficient at fractionating Hf from W during lunar magma ocean crystallisation, with D_Hf/D_W = 12-13 compared to 6.7-7.5 for ilmenite. The transition metals vary from mildly incompatible to compatible, with the highest compatibilities for Cr in ilmenite (D ∼ 7.5) and V in armalcolite (D ∼ 8.1). D values show no clear variation with pressure in the small range covered.Crystal lattice strain modelling of D values for di-, tri- and tetravalent trace elements shows that in ilmenite, divalent elements prefer to substitute for Fe while armalcolite data suggest REE replacing Mg. Tetravalent cations appear to preferentially substitute for Ti in both minerals, with the exception of Th and U that likely substitute for the larger Fe or Mg cations. Crystal lattice strain modelling is also used to identify and correct for very small (∼0.3 wt.%) melt contamination of trace element concentration determinations in crystals.Our results are used to model the Lu-Hf-Ti concentrations of lunar high-Ti mare basalts. The combination of their subchondritic Lu/Hf ratios and high TiO₂ contents requires preferential dissolution of ilmenite or armalcolite from late-stage, lunar magma ocean cumulates into low-Ti partial melts of deeper pyroxene-rich cumulates.     

Non-chondritic Sm/Nd ratio in the terrestrial planets: Consequences for the geochemical evolution of the mantle-crust system

Super-chondritic ¹⁴²Nd signatures are ubiquitous in terrestrial, Martian and lunar samples, and indicate that the terrestrial planets may have accreted from material with Sm/Nd ratio higher than chondritic. This contradicts the long-held view that chondrites represent a reference composition for the ¹⁴⁷Sm-¹⁴³Nd system. Using coupled ¹⁴⁶Sm-¹⁴²Nd and ¹⁴⁷Sm-¹⁴³Nd systematics in planetary samples, we have proposed a new set of values for the ¹⁴⁷Sm/¹⁴⁴Nd and ¹⁴³Nd/¹⁴⁴Nd ratios of the bulk silicate Earth (Caro et al., 2008). Here, we revise the Bulk Silicate Earth estimates for the ⁸⁷Rb-⁸⁷Sr and ¹⁷⁶Lu-¹⁷⁶Hf systems using coupled Sr-Nd-Hf systematics in terrestrial rocks. These estimates are consistent with Hf-Nd systematics in lunar samples. The implications of a slightly non-chondritic silicate Earth with respect to the geochemical evolution of the mantle-crust system are then examined. We show that the Archean mantle has evolved with a composition indistinguishable from that of the primitive mantle until about 2 Gyr. Positive ε¹⁴³Nd and ε¹⁷⁶Hf values ubiquitous in the Archean mantle are thus accounted for by the non-chondritic Sm/Nd and Lu/Hf composition of the primitive mantle rather than by massive early crustal formation, which solves the paradox that early Archean domains only have a limited extension in the present-day continents. The Sm-Nd and Lu-Hf evolution of the depleted mantle for the past 3.5 Gyr can be entirely explained by continuous extraction of the continents from a well-mixed mantle. Thus, in contrast to the chondritic Earth model, Sm-Nd mass balance relationships can be satisfied without the need to call upon hidden reservoirs or layered mantle convection. This new Sm-Nd mass balance yields a scenario of mantle evolution consistent with trace element and noble gas systematics. The high ³He/⁴He mantle component is associated with ¹⁴³Nd/¹⁴⁴Nd compositions indistinguishable from the bulk silicate Earth, suggesting that the less degassed mantle sources did not experience significant fractionation for moderately incompatible elements.     

Nd/Nd and Sm/Nd stratigraphy of Upper Ordovician epeiric sea carbonates

Stratigraphic changes in the ε_Nd of epeiric sea carbonates from central North America track the submergence history of the interior craton during the Late Ordovician. Fluctuations in sea level changed the Nd isotope balance of the epeiric sea by modifying the flux of Nd weathered from the highlands of the Taconic Orogen (ε_Nd = −6 to −9) and from the low relief Precambrian basement (ε_Nd = −22 to −15) of the Transcontinental Arch and Canadian Shield. Transgressions over the Arch and Shield, which diminished the weathering flux of Nd from the Precambrian basement, are recorded as positive shifts in the ε_Nd profiles of carbonates. Negative ε_Nd shifts reflect regression and reexposure of the Precambrian basement to erosion. Correlation of Upper Ordovician carbonates by use of the ε_Nd profiles demonstrates the potential for Nd isotope stratigraphy. Comparison of stratigraphic variations in carbonate Sm/Nd ratios with sea level curves, conodont paleoecology, and the ε_Nd profiles suggest that our observed variations in Sm/Nd ratios are related to changes in depth. Increasing Sm/Nd ratios correlate with increasing depth, whereas decreasing Sm/Nd ratios correlate with decreasing depth. This relationship between Sm/Nd ratios and depth suggests Sm/Nd profiles have potentially wide applications in understanding the paleoceanography of ancient epeiric seas.     

Petrogenesis of picritic mare magmas: Constraints on the extent of early lunar differentiation

Calculations of isobaric batch, polybaric batch, and polybaric fractional melting have been carried out on a variety of proposed lunar and terrestrial source region compositions. Results show that magmas with a generally tholeiitic character—plagioclase and high-Ca pyroxene crystallize before low-Ca pyroxene reflecting relatively high Al₂O₃ concentrations (>12 wt%)—are the inevitable consequence of anhydrous partial melting of source regions composed primarily of olivine and two pyroxenes with an aluminous phase on the solidus. Low-Al₂O₃ magmas (<10 wt%), as typified by the green picritic glasses in the lunar maria require deep (700–1000 km), low-Al₂O₃ source regions without an aluminous phase. The difference between primitive and depleted mantle beneath mid-ocean ridges amounts to less than 0.1 wt% Al₂O₃, whereas formation of the green glass source region requires a net loss of between 1.5 and 2.5 wt% Al₂O₃. Basalt extraction cannot account for fractionations of this magnitude. Accumulation of olivine and pyroxene at the base of a crystallizing magma ocean is, however, an effective method for producing the necessary Al₂O₃ depletions. Both olivine-rich and pyroxene-rich source regions can produce the picritic magmas, but mixing calculations show that both types of source region are likely to be hybrids consisting of an early- to intermediate-stage cumulate (olivine plus enstatite) and a later stage cumulate assemblage. Mass balance calculations show that refractory element-enriched bulk Moon compositions contain too much Al₂O₃ to allow for the deep low-Al₂O₃ source regions even after extraction of an Al₂O₃-rich (26–30 wt%) crust between 50 and 70 km thick.     

Activated release of alkalis during the vesiculation of molten basalts under high vacuum: implications for lunar volcanism

Knudsen cell-quadrupole mass spectrometry was used to study the high-temperature vaporization of Hawaiian basalts, plagioclase, tektites, and samples from the Allende meteorite. Procedures are described by which mass loss rates and vapor pressures of Na and K were measured quantitatively.Gas-rich glassy basalts were observed to vesiculate under vacuum over the 900–1000°C region and simultaneously evaporate alkalis in nonequilibrium fashion at rates (units of μg/g/hr) of approximately 200–300 Na and 75–250 K. Degassed residues of the same basalts demonstrated equilibrium evaporation rates (over the same temperature range) of 60–120 Na and 30–60 K. The gas-deficient plagioclase and tektite sample showed only equilibrium vaporization with rates of 60 Na, 10 K (plagioclase) and 10 Na, 5K (tektites) at 900–1000°C. The Allende meteorite vaporized at rates of 2400 Na and 200 K at 900–1000°C, possibly by the reaction of Na₂O and K₂O with C or S₂, or by the thermal decomposition of nepheline or sodalite.The nonequilibrium vaporization of alkalis from the gas-rich basalts is attributed to vigorous agitation of the melt during its vesiculation by a gas phase composed principally of SO₂, CO₂, H₂O, CO, and H₂S. The major gases released from the Allende meteorite at 900–1000°C are, in order of decreasing abundance, CO, S₂, CO₂, H₂O, SO₂, and H₂S.It is proposed that nonequilibrium vaporization of alkalis during the vesiculation of lunar lavas was responsible for the production of alkali-rich vapors which subsequently deposited plagioclase crystals in the vugs of lunar rocks. The vesiculative, nonequilibrium vaporization of Na and K during a lunar volcanic eruption should be expected to occur at a high rate upon initial extrusion of the lava into vacuum but then decrease by a factor of approximately three when degassing is nearing completion. Vaporization losses remain inadequate to explain the uniformly low alkali concentrations in lunar basalts.     

海洋Nd同位素演化及古洋流循环示踪研究

海洋Nd同位素演化已经成为示踪陆源风化输入和洋流循环改变的最重要的手段之一,得到了越来越多的应用,并取得了许多重要的成果。海水的Nd同位素组成主要受陆源输入物质控制,热液输入几乎可以忽略。由于Nd在海洋中的停留时间(约500～1000a)略小于海水的平均混合时间(约1500a),且各洋盆有不同的Nd同位素风化输入,因此现代各大洋海水具有不同的Nd同位素组成。在陆源输入稳定的情况下,可以利用海水的Nd同位素组成和演化来示踪水体的混合或洋流循环的改变。目前主要依靠对海洋中水成铁锰结壳、海洋钙质有孔虫壳体、磷酸质鱼骨头或鱼牙齿化石以及沉积物中铁锰氧化物组分等的研究来恢复和反演古海水的Nd同位素组成和演化。4种分析材料各有其优缺点。其中,通过对水成铁锰结壳的Nd同位素分析,基本建立了各大洋新生代以来的主要洋流的Nd同位素组成的长尺度演化。通过有孔虫壳体、鱼化石碎片和沉积物中Fe-Mn氧化物组分可以进行高时间分辨率的古海水Nd同位素演化示踪。利用海水Nd同位素演化可以示踪古洋流通道的开启或闭合,以及获得水体交换的直接信息,为研究构造运动与气候变化之间的关系提供指示。同时,将海水Nd同位素演化与气候变化的指标结合起来,可以用于示踪各种气候条件下洋流循环的改变,将洋流循环的改变与气候变化联系起来,研究两者之间的成因关系。对表层水体的Nd同位素组成的研究则可以示踪不同气候条件下大陆陆源风化输入的改变。     

Ordovician igneous and metamorphic units in southeastern Puna: New U–Pb and Sm–Nd data and implications for the evolution of northwestern Argentina

New field, petrological, geochemical, and geochronological data (U–Pb and Sm–Nd) for Ordovician rock units in the southeastern Puna, NW Argentina, indicate two lithostratigraphic units at the eastern–northeastern border of salar Centenario: (1) a bimodal volcanosedimentary sequence affected by low- to medium-grade metamorphism, comprising metasediments associated with basic and felsic metavolcanic rocks, dated 485 ± 5 Ma, and (2) a plutonic unit composed of syenogranites to quartz-rich leucogranites with U–Pb zircon ages between 462 ± 7 and 475 ± 5 Ma. Felsic metavolcanic and plutonic rocks are peraluminous and show similar geochemical differentiation trends. They also have similar Sm–Nd isotopic compositions (T_DM model ages of 1.54–1.78 Ga; ε_Nd(T) values ranging from −3.2 to −7.5) that suggest a common origin and derivation of the original magmas from older (Meso-Paleoproterozoic?) continental crust. Mafic rocks show ε_Nd(T) ranging from +2.3 to +2.5, indicating a depleted mantle source. The data presented here, combined with those in the literature, suggest Ordovician magmatism mainly recycles preexisting crust with minor additions of juvenile mantle-derived material.     

Capture of interplanetary bodies in geocentric orbits and early lunar evolution

During the accretion of planets such as Earth, which are formed by collisional accretion of plan-etesimals, the probability of capture of interplanetary bodies in planetocentric orbits is calculated following the approach of Hills (1973) and the n-body simulation, using simplectic integration method. The simulation, taking an input mass equal to about 50% of the present mass of the inner planets, distributed over a large number of planetoids, starting at 4 M y after the formation of solar system, yielded four inner planets within a period of 30 M y. None of these seed bodies, out of which the planets formed, remained at this time and almost 40% mass was transferred beyond 100 AU. Based on these calculations, we conclude that ∼ 1.4 times the mass of the present inner planets was needed to accumulate them. The probability of capture of planetoids in geocentric orbits is found to be negligible. The result emphasizes the computational difficulty in ’probability of capture’ of planetesimals around the Earth before the giant impact. This conclusion, however, is in contradiction to the recent observations of asteroids being frequently captured in transient orbits around the Earth, even when the current population of such interplanetary bodies is smaller by several orders of magnitude compared to the planetary accumulation era.     

Sm／Nd Evolution of Upper Mantle and Continental Crust：Constraints on Gowth Rates of the Continental Crust

A new approach to the investigation of the Sm/Nd evolution of the upper mantle directly from the data on lherzolite xenoliths is described in this paper.It is demonstrated that the model age TCHUR of an unmetasomatic iherzolite zenolith ca represent the mean depletion age of its mantle source, thus presenting a correlation trend between f^Sm/Nd and the mean depletion age of the upper mantle from the data on xenoliths.This correlation trend can also be derived from the data on river suspended loads as well as from granitoids.Based on the correlation trend mentioned above and mean depletion ages of the upper mantle at various geological times, an evolution curve for the mean f^Sm/Nd value of the upper mantle through geological time has been established.It is suggested that the upwilling of lower mantle material into the upper mantle and the recycling of continental crust material during the Archean were more active ,thus maintaining fairly constantf^Sm/Nd and εNd values during this time period. Similarly ,an evolution curve for the mean f^Sm/Nd value of the continental crust through geological time has also been established from the data of continental crust material.In the light of both evolution curves for the upper mantle and continental crust ,a growth curve for the continental crust has been worked out ,suggesting that :(1)about 30%(in volume )of the present crust was present as the continental crust at 3.8 Ga ago ;(2)the growth rate was much lower during the Archean ;and (3)the Proterozoic is another major period of time during which the continental crust wsa built up .     

Isotopic and geochemical systematics in Tertiary-Recent basalts from southeastern Australia and implications for the evolution of the sub-continental lithosphere

Tertiary-Recent Tasmanian and Newer (Victoria/South Australia) basalts range from quartz tholeiite to olivine melilitite and show systematic increases in their incompatible element abundances with increasing degree of silica undersaturation. These two basalt provinces show similar relative abundances of rare earth elements (REE), differences in the relative concentrations of Rb, Ba, Th, K and Nb, and distinct, restricted isotopic compositions. The Tasmanian basalts have ${}^{87}\text{Sr}{}^{86}\text{Sr}$ from 0.7026 to 0.7034, and ?_Nd from + 7.5 to + 5.8; the Newer basalts have higher ${}^{87}\text{Sr}{}^{86}\text{Sr}$ from 0.7038 to 0.7045, and lower ?_Nd from +4.2 to + 1.7. The range in Sr and Nd isotope compositions can be denned by primary magma compositions for both provinces, using Mg-values, Ni content and the presence of spinel lherzolite nodules. Major and trace element and Sr, Nd and Pb isotope compositions are uniform on a scale of up to 50 km for four separate Newer basanite centers. The chemical and isotopic data are consistent with a model whereby tholeiitic basalts are derived by large degrees of partial melting from a chemically uniform but isotopically variable source, and generation of undersaturated, alkaline basalts by smaller degrees of partial melting of the same source. No isotopic or geochemical evidence was found which would suggest that the more evolved basalts have been contaminated by continental crust.In contrast to tholeiitic and alkalic basalts from Hawaii, there is a continuous spectrum of isotope compositions for the Newer tholeiitic to alkalic basalts. A model is proposed for the generation of these basalts involving mixtures of hotspot mantle plume-derived melt and lithospheric mantle-derived melt, where observed differences between ocean island and continental alkaline basalts are attributed to differences between the sub-oceanic and sub-continental lithospheric mantles. Isotopic differences between tholeiitic and alkalic basalts are interpreted to be due to varying degrees of exchange and mixing between the hotspot plume and lithospheric mantle melt components. The model is consistent with the generation of these basalts from a source which has been recently enriched in the LREE.     

Komatiites of the Onverwacht Group,S. Africa: REE geochemistry,Sm/Nd age and mantle evolution

Komatiites of the Tjakastad Subgroup of the Onverwacht Group (S. Africa) were dated by the Sm/Nd method. A whole-rock isochron yields an age of 3.56±0.24 (2) AE, with initial ¹⁴³Nd/¹⁴⁴Nd ratio of 0.50818±23 (2), corresponding to _Nd(T)= + 1.9±4.5. This age is interpreted as the time of initial Onverwacht volcanism. This result agrees with earlier Sm/Nd data of Hamilton et al. (1979) and is consistent with the Rb-Sr result of Jahn and Shih (1974).Komatiites may be divided into 3 groups based on the typology of heavy REE distributions (Jahn and Gruau 1981). According to this scheme, the Onverwacht komatiites of the present study belong to two groups: the predominant Group II rocks showing (Gd/Yb)_N1.4, CaO/Al₂O₃ = 1.33, Al₂O₃/TiO₂10.6; and the subordinate Group III rocks with (Gd/Yb)_N<1.0; CaO/Al₂O₃0.6 and A1₂O₃/ TiO₂40. This contrasting feature is best explained by garnet fractionation within the mantle sources.Younger komatiites (2.7 AE) from Finland, Canada, Rhodesia, and Australia have (Gd/Yb)_N1.0, CaO/ Al₂O₃<1.1 and Al₂O₃/TiO₂21 based on 58 analyses. These ratios are nearly chondritic or of the bulk earth value (Anders 1977). It appears that some late Archean komatiites are different in chemistry from many early Archean komatiites. This may imply that the upper mantle chemistry has evolved through Archean times. However, the age connotation of the chemical parameters, such as CaO/Al₂O₃, (Gd/Yb)_N or Al₂O₃/TiO₂ ratio has not been firmly established. The characteristic high CaO/Al₂O₃ or (Gd/Yb)_N ratios in many Onverwacht Group rocks can also be explained as a result of local short-term mantle heterogeneity.     

月海盆地线性构造展布及其成因分析

综合多源遥感数据识别提取月球正面南北纬50°之间的线性构造,重点分析月岭和月溪的影像特征、分布规律和时空关系,结合月海沉降模型分析两者的成因机制,结合地形和重力场数据预测影响月岭类型的因素。研究表明,在质量瘤盆地,月岭和月溪存在明显的时空关系和构造成因联系,两者主要由月海沉降产生的局部应力引起,前月海时期盆地的均衡状态和月海充填的几何形状可能影响了月岭的分布类型。     

High-precision Measurements of the 143Nd/144Nd Isotope Ratio in Certified Reference Materials without Nd and Sm Separation by MC-ICP-MS

A precise and accurate method for the determination of 143 Nd/144 Nd isotope ratio without Nd and Sm separation by multiple collector inductively coupled plasma mass spectrometry is demonstrated in this paper.     

月海盆地线性构造展布及其成因分析

综合多源遥感数据识别提取月球正面南北纬50°之间的线性构造,重点分析月岭和月溪的影像特征、分布规律和时空关系,结合月海沉降模型分析两者的成因机制,结合地形和重力场数据预测影响月岭类型的因素。研究表明,在质量瘤盆地,月岭和月溪存在明显的时空关系和构造成因联系,两者主要由月海沉降产生的局部应力引起,前月海时期盆地的均衡状态和月海充填的几何形状可能影响了月岭的分布类型。     

Geochemistry, petrology and ages of the lunar meteorites Kalahari 008 and 009: New constraints on early lunar evolution

Kalahari 008 and 009 are two lunar meteorites that were found close to each other in Botswana. Kalahari 008 is a typical lunar anorthositic breccia; Kalahari 009 a monomict breccia with basaltic composition and mineralogy. Based on minor and trace elements Kalahari 009 is classified as VLT (very-low-Ti) mare basalt with extremely low contents of incompatible elements, including the REE. The Lu-Hf data define an age of 4286 ± 95 Ma indicating that Kalahari 009 is one of the oldest known basalt samples from the Moon. It provides evidence for lunar basalt volcanism prior to 4.1 Ga (pre-Nectarian) and may represent the first sample from a cryptomare. The very radiogenic initial ¹⁷⁶Hf/¹⁷⁷Hf (εHf = +12.9 ± 4.6), the low REE, Th and Ti concentrations indicate that Kalahari 009 formed from re-melting of mantle material that had undergone strong incompatible trace element depletion early in lunar history. This unusually depleted composition points toward a hitherto unsampled basalt source region for the lunar interior that may represent a new depleted endmember source for low-Ti mare basalt volcanism. Apparently, the Moon became chemically very heterogeneous at an early stage in its history and different cumulate sources are responsible for the diverse mare basalt types.Evidence that Kalahari 008 and 009 may be paired includes the similar fayalite content of their olivine, the identical initial Hf isotope composition, the exceptionally low exposure ages of both rocks and the fact that they were found close to each other. Since cryptomaria are covered by highland ejecta, it is possible that these rocks are from the boundary area, where basalt deposits are covered by highland ejecta. The concentrations of cosmogenic radionuclides and trapped noble gases are unusually low in both rocks, although Kalahari 008 contains slightly higher concentrations. A likely reason for this difference is that Kalahari 008 is a polymict breccia containing a briefly exposed regolith, while Kalahari 009 is a monomict brecciated rock that may never have been at the surface of the Moon.Altogether, the compositions of Kalahari 008 and 009 permit new insight into early lunar evolution, as both meteorites sample lunar reservoirs hitherto unsampled by spacecraft missions. The very low Th and REE content of Kalahari 009 as well as the depletion in Sm and the lack of a KREEP-like signature in Kalahari 008 point to a possible source far from the influence of the Procellarum-KREEP Terrane, possibly the lunar farside.     

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.     

Nature of magnetic grains in basalts and implications for palaeomagnetism

Journal of Earth System Science - Investigations involving temperature dependence of low-field susceptibility and of low- and high-field hysteresis have been carried out on more than one thousand...