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1.
Oxygen and iron isotope analyses of low-Ti and high-Ti mare basalts are presented to constrain their petrogenesis and to assess stable isotope variations within lunar mantle sources. An internally-consistent dataset of oxygen isotope compositions of mare basalts encompasses five types of low-Ti basalts from the Apollo 12 and 15 missions and eight types of high-Ti basalts from the Apollo 11 and 17 missions. High-precision whole-rock δ18O values (referenced to VSMOW) of low-Ti and high-Ti basalts correlate with major-element compositions (Mg#, TiO2, Al2O3). The observed oxygen isotope variations within low-Ti and high-Ti basalts are consistent with crystal fractionation and match the results of mass-balance models assuming equilibrium crystallization. Whole-rock δ56Fe values (referenced to IRMM-014) of high-Ti and low-Ti basalts range from 0.134‰ to 0.217‰ and 0.038‰ to 0.104‰, respectively. Iron isotope compositions of both low-Ti and high-Ti basalts do not correlate with indices of crystal fractionation, possibly owing to small mineral-melt iron fractionation factors anticipated under lunar reducing conditions.The δ18O and δ56Fe values of low-Ti and the least differentiated high-Ti mare basalts are negatively correlated, which reflects their different mantle source characteristics (e.g., the presence or absence of ilmenite). The average δ56Fe values of low-Ti basalts (0.073 ± 0.018‰, n = 8) and high-Ti basalts (0.191 ± 0.020‰, n = 7) may directly record that of their parent mantle sources. Oxygen isotope compositions of mantle sources of low-Ti and high-Ti basalts are calculated using existing models of lunar magma ocean crystallization and mixing, the estimated equilibrium mantle olivine δ18O value, and equilibrium oxygen-fractionation between olivine and other mineral phases. The differences between the calculated whole-rock δ18O values for source regions, 5.57‰ for low-Ti and 5.30‰ for high-Ti mare basalt mantle source regions, are solely a function of the assumed source mineralogy. The oxygen and iron isotope compositions of lunar upper mantle can be approximated using these mantle source values. The δ18O and δ56Fe values of the lunar upper mantle are estimated to be 5.5 ± 0.2‰ (2σ) and 0.085 ± 0.040‰ (2σ), respectively. The oxygen isotope composition of lunar upper mantle is identical to the current estimate of Earth’s upper mantle (5.5 ± 0.2‰), and the iron isotope composition of the lunar upper mantle overlaps within uncertainty of estimates for the terrestrial upper mantle (0.044 ± 0.030‰).  相似文献   

2.
Ilmenite has played an important role in the petrogenesis of lunar high-Ti picritic magmas, and armalcolite is another high-Ti oxide that was first discovered on the moon. In this study, we examined the thermodynamic stability of ilmenite and armalcolite in the context of lunar cumulate mantle overturn. Two starting compositions were explored, an ilmenite-bearing dunite (olivine + ilmenite) and an ilmenite-bearing harzburgite (olivine + orthopyroxene + ilmenite). Experiments were conducted using a 19.05 mm piston-cylinder apparatus at temperatures of 1235-1475 °C and pressures of 1-2 GPa. In runs with the ilmenite-bearing dunite mixture, ilmenite is stable in the subsolidus assemblage at least up to 1450 °C and 2 GPa. In runs with the ilmenite-bearing harzburgite starting mixture, ilmenite is stable at pressures greater than 1.4 GPa, and armalcolite is stable at lower pressures. Solidi for both starting compositions were determined, and the phase boundary between ilmenite- and armalcolite-bearing harzburgite was shown to have little dependence on temperature. During lunar cumulate overturn, sinking ilmenite formed near the end of lunar magma ocean solidification transforms into armalcolite when in contact with harzburgite cumulates at depths of less than 280 km in the lunar mantle. Inefficient overturn could leave isolated, inhomogeneously distributed pockets of armalcolite-bearing harzburgite in the upper lunar mantle, underlain by an ilmenite-bearing lower lunar mantle. These high-Ti oxide-bearing harzburgitic pockets can serve as potential sources for the generation of high-Ti magmas through partial melting or through assimilation of high-Ti minerals during transport of low-Ti picritic magmas in the lunar mantle.FeO-MgO exchange between olivine and either ilmenite or armalcolite was also examined in this study. We found the FeO-MgO distribution coefficient to be effectively independent of temperature for the pressures, temperatures, and compositions explored, with an average value of 0.179 ± 0.008 for olivine/ilmenite and 0.319 ± 0.021 for olivine/armalcolite. Given the bulk composition of an overturned lunar cumulate mantle, our measured FeO-MgO distribution coefficients can be used to estimate the Mg# of coexisting minerals in armalcolite- or ilmenite-bearing harzburgite and dunite in the overturned lunar mantle. Finally, the transformation from ilmenite-bearing harzburgite to armalcolite-bearing harzburgite results in a density increase of up to 2%. Large armalcolite-bearing cumulate bodies in the upper lunar mantle may be detectable in future lunar geophysical experiments.  相似文献   

3.
The nature of the source of continental flood basalts (CFB) is a highly debated topic. Proposed mantle sources for CFBs, including both high- and low-Ti basalts, include subcontinental lithospheric mantle (SCLM), asthenospheric mantle, and deep, plume-related mantle. Re-Os isotope systematics can offer important constraints on the sources of both ocean island basalts (OIB) and CFB, and may be applied to distinguish different possible melt sources. This paper reports the first Re-Os isotope data for the Late Permian Emeishan large igneous province (LIP) in Southwest China. Twenty one CFB samples including both low- and high-Ti basalts from five representative sites within the Emeishan LIP have been analyzed for Os, Nd, and Pb isotopic compositions. The obtained Os data demonstrate that crustal assimilation affected Os isotopic compositions of some Emeishan basalt samples with low Os concentrations but not all of the samples, and the Emeishan basalts with high Os contents likely experienced the least crustal contamination. The low and high-Ti basalts yield distinct Os signatures in terms of 187Os/188Os and Os content. The low-Ti basalt with the highest Os concentration (400 ppt) has a radiogenic Os isotopic composition (γOs(t), +6.5), similar to that of plume-derived OIB. Because the Os isotopic composition of basalts with relatively high Os concentrations (typically >50 ppt) likely represents that of their mantle source, this result implies a plume-derived origin for the low-Ti basalts. On the other hand, the high-Ti basalts with high Os concentration (over 50 ppt) have unradiogenic Os isotopic signatures (γOs(t) values range from −0.8 to −1.4), suggesting that a subcontinental lithosphere mantle (SCLM) component most likely contributed to the generation of these magmas. Combining Pb and Nd isotopic tracers with the Os data, we demonstrate that the low-Ti basaltic magmas in the Emeishan CFB were mainly sourced from a mantle plume reservoir, whereas the high-Ti basaltic magmas were most likely derived from a SCLM reservoir or were contaminated by a significant amount of lithospheric mantle material during plume-related magma ascent through the SCLM.  相似文献   

4.
It is widely accepted that basaltic magmas are products of partial fusion of periodotite within planetary mantles. As such, they provide valuable insights into the composition, structure, and processes of planetary interiors. Those compositions which approach primary melt compositions provide the most direct information about planetary interiors and serve as a starting point to understand basaltic evolution. Within the collection of lunar samples returned by the Apollo and Luna missions are homogeneous, picritic glass beads of volcanic origin. These picritic glasses are our closest approximations to primary magmas. As such, these glass beads provide a unique perspective concerning the origin of mare basalts, the characteristics of the lunar interior, and processes in the early differentiation of the Moon. We have obtained trace element data for these picritic glasses using SIMS techniques. These data and literature isotopic and experimental data on the picritic glasses are placed within the framework of mare basaltic magmatism.The volcanic glasses are very diverse in their trace element characteristics, for example, they have a wide range of REE pattern shapes and concentrations. Like the crystalline mare basalts, all picritic glasses have a negative Eu anomaly. Unlike the crystalline mare basalts, there is little correlation between the size of the Eu anomaly and overall REE concentrations. Trace element differences among the various glasses suggests that a KREEP component was incorporated into their mantle source. This implies large scale mixing of the “Lunar Magma Ocean”-derived cumulate pile. Subtle differences among glasses suggest that local mixing of sources may also have been an important process. Preservation of subtle chemical differences in the picritic glasses and crystalline basalts may be interpreted as indicating that they were produced by small to moderate degrees of partial melting and that the lunar mantle did not experience extensive melting during episodes of mare volcanism.Several lines of evidence are consistent with the view that the picritic glasses were derived from mantle sources that were compositionally distinct from the sources for crystalline mare basalts. These are parallel, but no common, liquid lines of descent; chemical differences between picritic glasses and the more primitive crystalline mare basalts; experimental studies indicating that the picritic glasses are multiply saturated at depths greater than that of the mare basalts; differences in lead isotopic data; and the mode of eruption (i.e., fire fountaining for glass beads). These data also provide circumstantial evidence that suggests that the picritic glasses were derived from a source somewhat more volatile-rich than that of the mare basalts.Several petrogenetic models are suggested by the trace element characteristics of the picritic glasses:
  • 1.(1) Partial melting of heterogeneous lunar mantle at depths greater than 300 km to produce the parental magmas (picritic) for both the mare basalts and picritic glasses. Picritic magmas represented by glass beads were erupted to the surface with small degrees of fractional crystallization while mare basalts were produced by larger degrees of fractional crystallization (15–30%) of similar (but not identical) picritic magmas.
  • 2.(2) Picritic magmas represented by the glass beads were generated at depths greater than 400 km in a volatile-enriched (relative to the mare basalt source) heterogeneous mantle while mare basalts are fractional crystallization products of picritic magmas generated at depths of less than 400 km.
  • 3.(3) The picritic magmas represented by the glass beads represent polybaric melting that initiated at depths of at least 1000 km. A primitive mantle component or less processed cumulate mantle components may have been involved in the generation of the picritic glasses in any of these models.
  相似文献   

5.
Northern Brazil contains remnants of Mesozoic flood basalts and hypabyssal rocks that were apparently emplaced during tectonism related to opening of the Atlantic Ocean. Analyses and new K-Ar ages reveal that this 700x250 km Maranhão province (5°–8°S) has low-Ti basalts (1.1 wt% TiO2) in the western part that range about 160 to 190 Ma, and high-Ti basalts (3.4–4.4 wt% TiO2) in the eastern part about 115–122 Ma. Low-Ti basalt compositions are less evolved and have a smaller range, Mg# 62-56, than the high-Ti basalts, Mg# 44–33. General characteristics of the least evolved members of low- and high-Ti groups include, respectively, Zr 100 and 250 ppm, Sr 225 and 475 ppm, Ba 200 and 500 ppm, Nb 10 and 26 ppm, Y 29 and 36 ppm, La/Yb(n) 4.2 and 8.8, where La(n) is 30 and 90. Overall compositions resemble the low- and high-Ti basaltic rocks of the Mesozoic Serra Geral (Paraná) province in southern Brazil. The Maranhão low-Ti basalts have more radiogenic Sr and Pb and higher 18O than the high-Ti basalts. Respectively, low- vs high-Ti: Sr26–54 vs 15–18; 206Pb/204Pb=18.25–.78 vs 18.22–.24; and 18O 8.9–12.6 vs 6.5–8.6. Nd isotopes overlap: Nd–1.6 to –3.8 vs –2.1 to –3. Ages, compositions, and isotopes indicate that the low- and high-Ti groups had independent parentages from enriched subcontinental mantle. However, both groups can be modeled from one source composition if low-Ti basalt isotopes reflect crustal contamination, and if the parentages for each group were picritic liquids that represent either higher (for low-Ti) or lower (for high-Ti) percentages of melting of that single source. When comparing Pb isotopes of Maranhão and Serra Geral high-Ti basalts (uncontaminated) to evaluate the DUPAL anomaly, Maranhão has Pb 7/4=4.6–11, and Pb 8/4=72–87; Serra Geral has Pb 7/4=10–13, and Pb 8/4=95–125. The small difference is not enough to conform to DUPAL contours, and is inconsistent with large-scale isotopic heterogeneity of mantle beneath Brazil prior to rifting of South America from Africa. Maranhão low-Ti magmas probably relate to the opening of central North Atlantic, and high-Ti magmas to the opening of equatorial Atlantic. The proposed greater percentage of source melting for low-Ti basalts may reflect a Triassic-Jurassic hotspot, while lesser melting for high-Ti magmas may relate to Cretaceous decompressional (rifting) melting.  相似文献   

6.
New data is presented for five evolved, low-Ti lunar mare basalt meteorites from the LaPaz Icefield, Antarctica, LAP 02205, LAP 02224, LAP 02226, LAP 02436, and LAP 03632. These basalts have nearly identical mineralogies, textures, and geochemical compositions, and are therefore considered to be paired. The LaPaz basalts contain olivine (Fo64-2) and pyroxene (Fs32Wo8En60 to Fs84-86Wo15En2-0) crystals that record extreme chemical fractionation to Fe-enrichment at the rims, and evidence for silicate liquid immiscibility and incompatible element enrichment in the mesostasis. The basalts also contain FeNi metals with unusually high Co and Ni contents, similar to some Apollo 12 basalts, and a single-phase network of melt veins and fusion crusts. The fusion crust has similar chemical characteristics to the whole rock for the LaPaz basalts, whereas the melt veins represent localized melting of the basalt and have an endogenous origin. The crystallization conditions and evolved nature of the LaPaz basalts are consistent with fractionation of olivine and chromite from a parental liquid similar in composition to some olivine-phyric Apollo 12 and Apollo 15 basalts or lunar low-Ti pyroclastic glasses. However, the young reported ages for the LaPaz mare basalts (∼2.9 Ga) and their relative incompatible element enrichment compared to Apollo mare basalts and pyroclastic glasses indicate they cannot be directly related. Instead, the LaPaz mare basalts may represent fractionated melts from a magmatic system fed by similar degrees of partial melting of a mantle source similar to that of the low-Ti Apollo mare basalts or pyroclastic glasses, but which possessed greater incompatible element enrichment. Despite textural differences, the LaPaz basalts and mare basalt meteorite NWA 032 have similar ages and compositions and may originate from the same magmatic system on the Moon.  相似文献   

7.
An Apollo 17 picritic orange glass composition has been used to experimentally investigate the conditions at which graphite would oxidize to form a CO-rich gas, and ultimately produce lunar fire-fountain eruptions. Isothermal decompression experiments run above the A17 orange glass liquidus temperature (>1350 °C) suggest that the initial CO-rich gas phase produced by graphite oxidation would be generated during magma ascent at a pressure of 40 MPa, 8.5 km beneath the lunar surface. Additional experiments with 2000 ppm S and 1000 ppm Cl showed that the presence of these dissolved gas species would not affect the depth of graphite oxidation, verifying that the first volcanic gas phase would be generated by the oxidation of graphite.A simple ideal chemical mixing model for calculating melt FeO activity in a Fe-metal/silicate melt system was tested with a series of 0.1 MPa controlled oxygen fugacity experiments. Agreement between the model and experiments allows the model to be used to calculate oxygen fugacity in picritic lunar glass compositions such as the A17 orange glass. Using this model in a reanalysis of chemical equilibria between the natural A17 orange glass melt and the metal spherules (Fe85Ni14Co1) trapped within the glass beads indicates a log oxygen fugacity of −11.2, 0.7 log units, more oxidized than previous estimates. At the A17 orange glass liquidus temperature (1350 ± 5 °C), this fO2 corresponds to a minimum pressure of 41 MPa on the graphite–C–O surface. The fact that the same critical graphite oxidation pressure was determined in decompression experiments and from the Fe–FeO activity model for the natural A17 orange glass–metal assemblage strongly supports this pressure (8.5 km depth) for volcanic gas formation in lunar basalts. Generation of a gas by oxidation of C in ascending magma is likely to have been important in getting dense lunar magmas to the surface as well as in generating fire-fountain eruptions. The vesicles common in many lunar basalts and the ubiquitous Fe-metal in these rocks are also likely generated by the oxidation of carbon. The presence of carbon in the lunar basalts and the recent discovery of ppm levels of water in lunar basalts indicate that at least parts of the lunar interior still contained volatiles at 3.9 bybp.  相似文献   

8.
We report results of experiments constraining oxygen isotope fractionations between CO2 vapor and Na-rich melilitic melt at 1 bar and 1250 and 1400°C. The fractionation factor constrained by bracketed experiments, 1000.lnαCO2-Na melilitic melt, is 2.65±0.25 ‰ (±2σ; n=92) at 1250°C and 2.16±0.16 ‰ (2σ; n=16) at 1400°C. These values are independent of Na content over the range investigated (7.5 to 13.0 wt. % Na2O). We combine these data with the known reduced partition function ratio of CO2 to obtain an equation describing the reduced partition function ratio of Na-rich melilite melt as a function of temperature. We also fit previously measured CO2-melt or -glass fractionations to obtain temperature-dependent reduced partition function ratios for all experimentally studied melts and glasses (including silica, rhyolite, albite, anorthite, Na-rich melilite, and basalt). The systematics of these data suggest that reduced partition function ratios of silicate melts can be approximated either by using the Garlick index (a measure of the polymerization of the melt) or by describing melts as mixtures of normative minerals or equivalent melt compositions. These systematics suggest oxygen isotope fractionation between basalt and olivine at 1300°C of approximately 0.4 to 0.5‰, consistent with most (but not all) basalt glass-olivine fractionations measured in terrestrial and lunar basalts.  相似文献   

9.
Northeast Africa 003 (NEA 003) is a lunar meteorite found as a two paired stones (6 and 118 g) in Libya, 2000 and 2001. The main portion (∼75 vol%) of the 118 g meteorite, used for this study, (NEA 003-A) consists of mare-basalt and a smaller adjacent portion (∼25 vol%) is a basaltic breccia (NEA 003-B). NEA 003-A has a coarse-grained magmatic texture consisting mainly of olivine, pyroxene and plagioclase. The late-stage mineral association is composed mainly of elongated plagioclase, ilmenite, troilite, fayalite, Si-K-rich glass, apatite, and a rare SiO2 phase. Other accessory minerals include ulvöspinel, chromite, and trace Fe-Ni metal. Olivine and pyroxene contain shock-induced fractures, and plagioclase is completely converted into maskelynite.The Fe/Mn values of the whole rock, olivines and pyroxenes, and the bulk-rock oxygen isotopic composition provide evidence for the lunar origin of NEA 003-A meteorite. This is further supported by the presence of Fe-Ni metal and the anhydrous mineral association.NEA 003-A is geochemically and petrographically distinct from previously described mare-basalt meteorites and is not paired with any of them. The petrography and major element composition of NEA 003-A is similar to the composition of low-Ti olivine mare basalts from Apollo 12 and olivine-normative basalts from Apollo 15. The NEA 003-A meteorite shows obvious geochemical similarities in trace elements contents with Apollo 15 olivine-normative basalts and could represent a yet unknown geochemically primitive member of the olivine-normative basalt series. The meteorite is depleted in rare earth elements (REE) and incompatible trace elements indicating a primitive character of the parental magma. The bulk-rock chemical composition demonstrates that the parent melt of NEA 003-A was not contaminated with KREEP components as a result of magma mixing or assimilation processes. Results of crystallization modelling and low minimum cooling rate estimates (∼0.07 °C/h) suggest that the parent melt of NEA 003-A crystallized in the lower part of a lava flow containing cumulate olivine (∼10%) and was probably derived from more primitive picritic magma by fractional crystallization processes.Sm-Nd dating yields an age of 3.09 ± 0.06 Ga which corresponds to the period of lower Eratosthenian lunar volcanic activity, and the near-chondritic εNd value of −0.4 ± 0.3 indicates that the meteorite could be derived from a slightly enriched mantle source similar to the Apollo 15 green glasses. Ar-Ar step release results are inconsistent with Sm-Nd ages suggesting that NEA 003-A was exposed to one or more impact events. The most extensive event took place at 1.8 Ga and the shock intensity was likely between 28 and 45 GPa. The absence of solar Ar suggests that NEA 003-A has not been directly exposed at the lunar surface but the cosmic ray exposure age of 209 ± 6 Ma suggests that NEA 003-A resided in the upper regolith for part of its history.  相似文献   

10.
The sulfur concentration at pyrrhotite- and anhydrite-saturation in primitive hydrous basaltic melt of the 2001-2002 eruption of Mt. Etna was determined at 200 MPa, T = 1050-1250 °C and at log fO2 from FMQ to FMQ+2.2 (FMQ is Fayalite-Magnetite-Quartz oxygen buffer). At 1050 °C Au sample containers were used. A double-capsule technique, using a single crystal olivine sample container closed with an olivine piston, embedded in a sealed Au80Pd20 capsule, was developed to perform experiments in S-bearing hydrous basaltic systems at T > 1050 °C. Pyrrhotite is found to be a stable phase coexisting with melt at FMQ-FMQ+0.3, whereas anhydrite is stable at FMQ+1.4-FMQ+2.2. The S concentration in the melt increases almost linearly from 0.12 ± 0.01 to 0.39 ± 0.02 wt.% S at FeS-saturation and from 0.74 ± 0.01 to 1.08 ± 0.04 wt.% S at anhydrite-saturation with T ranging from 1050-1250 °C. The relationships between S concentration at pyrrhotite and/or anhydrite saturation, MgO content of the olivine-saturated melt, T, and log fO2 observed in this study and from previous data are used to develop an empirical model for estimating the magmatic T and fO2 from the S and MgO concentrations of H2O-bearing olivine-saturated basaltic melts. The model can also be used to determine maximum S concentrations, if fO2 and MgO content of the melt are known. The application of the model to compositions of melt inclusions in olivines from Mt. Etna indicates that the most primitive magmas trapped in inclusions might have been stored at log fO2 slightly higher than FMQ+1 and at T = 1100-1150 °C, whereas more evolved melts could have been trapped at T ? 1100 °C. These values are in a good agreement with the estimates obtained by other independent methods reported in the literature.  相似文献   

11.
The paper reports data on the geology and tectono-magmatic reactivation of the Norilsk area and on the stratigraphy and geochemistry of its volcanic sequence, with the discussion of the sources and genesis of the ore magmas and the scale of the ore-forming process. According to the geochemistry of the lavas and intrusive rocks (Ti concentration and the La/Sm and Gd/Yb ratios), two types of the parental magmas are recognized: high-Ti magmas of the OIB type (from bottom to top, suites iv, sv, and gd of phase 1) and low-Ti magmas (suites hk, tk, and nd of phase 2 and suites mr-mk of phase 3), which were derived from the lithospheric mantle. The magmatic differentiation of the parental low-Ti magma of the tk type into a magma of the nd type was associated with the derivation of an evolved magma of the nd type, which was depleted in ore elements, and an ore magma, which was a mixture of silicate and sulfide melts, protocrysts of silicate minerals, and chromite. Judging from their geochemical parameters, the intrusions of the lower Norilsk type were comagmatic with the lavas of the upper part of the nd suite, and the ore-bearing intrusions of the upper Norilsk type were comagmatic with the lavas of the mr-mk suites. When the ore-bearing intrusions were emplaced, their magmas entrained droplets of sulfide melt and protocrysts of olivine and chromite and brought them to the modern magmatic chamber. These protocrysts are xenogenic with respect to the magma that formed the intrusions. In certain instances (Talnakh and Kharaelakh intrusions), the moving magma entrained single portions of sulfide magma, which were emplaced as individual subphases. The experimental study of the peridotite-basalt-fluid system shows that mantle reservoirs with protoliths of subducted oceanic crustal material could serve as sources of relatively low-temperature (1250–1350°C) high-Ti magnesian magmas of the rifting stage from an olivine-free source.  相似文献   

12.
The lunar meteorite Northwest Africa (NWA) 032 is a low-Ti basalt that has incompatible-element abundances and Th/Sm ratios characteristic of the involvement of late stage magma ocean crystallization products (urKREEP) in its petrogenesis. This sample is very fine-grained and contains terrestrial weather products. A progressive leaching procedure was therefore developed and applied to magnetic separates and whole rock fractions to obtain Rb-Sr and Sm-Nd ages. Although many of the leachates, as well as the unleached mineral and whole rock fractions contain terrestrial alteration products, selected residue fractions yield concordant Rb-Sr and Sm-Nd ages. Rubidium-Sr isotopic analyses yield an age of 2947 ± 16 Ma with an initial 87Sr/86Sr of 0.700057 ± 17. These characteristics indicate NWA 032 is derived from a source region with an 87Rb/86Sr ratio of 0.044 ± 0.001. This value is higher than all but those determined for KREEP basalts, and suggests that NWA 032 is derived from a source region that has higher incompatible-element abundances than other low-Ti basalts. Samarium-neodymium isotopic analysis yield a concordant age of 2931 ± 92 Ma and an initial εNd of +9.71 ± 0.74 corresponding to a source region with 147Sm/144Nd ratio of 0.246 ± 0.004. The initial Nd isotopic composition stands in contrast to the initial Sr isotopic composition by requiring NWA 032 to be derived from a source with lower incompatible-element abundances than most low-Ti basalts. The source of NWA 032 is therefore unlike those of other lunar basalts.Modeling of magma ocean cumulate formation demonstrates that unlike other low-Ti basalt source regions the NWA 032 source is a mixture of olivine, pigeonite, and clinopyroxene bearing cumulates and only a small amount of urKREEP. Furthermore, unlike other mare basalt sources, the NWA 032 source does not contain appreciable quantities of plagioclase. Partial melting models demonstrate that the incompatible-element characteristics of the NWA 032 result from formation by smaller degrees of partial melting than other mare basalts. Thus, the incompatible-element geochemical signature that is observed in NWA 032 appears to reflect the combined effects of generation from an unusual plagioclase-free incompatible-element-depleted source region by very small degrees of partial melting. This study demonstrates that both the presence of urKREEP in the source region and small degrees of partial melting generate magmas with similar, but not identical, incompatible-element characteristics. In addition, it underscores the fact that there is significantly more geochemical diversity on the Moon than is represented by samples collected by the American and Soviet lunar missions.  相似文献   

13.
Lunar rocks are inferred to tap the different fossil cumulate layers formed during crystallisation of a lunar magma ocean (LMO). A coherent dataset, including Zr isotope data and high precision HFSE (W, Nb, Ta, Zr, Hf) and REE (Nd, Sm, Lu) data, all obtained by isotope dilution, can now provide new insights into the processes active during LMO crystallisation and during the petrogenesis of lunar magmas. Measured 92Zr and 91Zr abundances agree with the terrestrial value within 0.2 ε-units. Incompatible-trace-element enriched rocks from the Procellarum KREEP Terrane (PKT) display Nb/Ta and Zr/Hf above the bulk lunar value (ca. 17), and mare basalts display lower ratios, generally confirming the presence of complementary enriched and depleted mantle reservoirs on the Moon. The full compositional spectrum of lunar basalts, however, also requires interaction with ilmenite-rich layers in the lunar mantle. Notably, the high-Ti mare basalts analysed display the lowest Nb/Ta and Zr/Hf of all lunar rocks, and also higher Sm/Nd at similar Lu/Hf than low-Ti basalts. The high-Ti basalts also exhibit higher and strongly correlated Ta/W (up to 25) and Hf/W (up to 140), at similar W contents, which is difficult to reconcile with ortho- and clinopyroxene-controlled melting. Altogether, these patterns can be explained via assimilation of up to ca. 20% of ilmenite- and clinopyroxene-rich LMO cumulates by more depleted melts from the lower lunar mantle. Direct melting of ilmenite-rich cumulates or the possible presence of residual metals in the lunar mantle both cannot easily account for the observed Ta/W and Hf/W patterns. Cumulate assimilation is also a viable mechanism that can partially buffer the Lu/Hf of mare basalts at relatively low values while generating variable Sm/Nd. Thus, the dichotomy between low Lu/Hf of lunar basalts and high time integrated source Lu/Hf as inferred from Hf isotope compositions can potentially be explained. The proposed assimilation model also has important implications for the short-lived nuclide chronology of the Earth-Moon system. The new Hf/W and Ta/W data, together with a compilation of existing W-Th-U data for lunar rocks, indicate that the terrestrial and lunar mantles are indistinguishable in their Hf/W. Virtually identical εW and Hf/W in the terrestrial and lunar mantle suggest a strong link between final core-mantle equilibration on Earth and the Moon forming giant impact. Previously, linear arrays of lunar samples in 182W vs. Hf/W and 142Nd vs. Sm/Nd spaces have been interpreted as isochrons, arguing for LMO crystallisation as late as 250 Myrs after solar system formation. Based on the proposed assimilation model, the 182W and 142Nd in many lunar magmas can be shown to be decoupled from their ambient Hf/W and Sm/Nd source compositions. As a consequence, the 182W vs. Hf/W and 142Nd vs. Sm/Nd arrays would constitute mixing lines rather than isochrons. Hence, the lunar 182Hf-182W and 146Sm-142Nd data would be fully consistent with an “early” crystallisation age of the LMO, even as early as 50 Myrs after solar system formation when the Moon was probably formed.  相似文献   

14.
Apatite has been analyzed from mare basalts, the magnesian-suite, the alkali-suite, and KREEP-rich impact-melt rocks using an electron probe microanalysis routine developed specifically for apatite. We determined that all the lunar apatite grains analyzed are predominantly fluorine rich; however, they also contain varying concentrations of chlorine and a missing structural component that, after ruling out other possibilities, we attribute to OH. Apatite grains from mare basalts are compositionally distinct from the apatite grains in the magnesian-suite, the alkali-suite, and KREEP-rich impact-melt rocks, which all had similar apatite compositions. Apatite grains in mare basalts are depleted in chlorine, and many of the analyzed grains have stoichiometry that suggests a significant OH component (i.e., >0.08 structural formula units), whereas apatite grains in the magnesian suite, alkali suite, and KREEP-rich impact melts are enriched in chlorine and do not typically have a missing structural component that could be attributed to OH− (within the detection limit of 0.08 sfu). From these data, we infer that residual liquids in the mare basalts were enriched in H2O and fluorine relative to chlorine at the time of apatite crystallization, whereas residual liquids in magnesian-suite, alkali-suite, and KREEP-rich impact melts were enriched in chlorine relative to H2O and fluorine at the time of apatite crystallization. The relative volatile abundance that we determined for the mare basalts is identical to the previously determined relative volatile abundance for the lunar picritic glasses. This result indicates that the observed relative volatile abundance signature of the picritic glass source is the same as that in the mare basalt source regions. The magnesian-suite, alkali-suite, and KREEP-rich impact-melt rocks likely reflect a volatile source with different volatile abundances than the sources of mare volcanics. Moreover, the magnesian-suite, alkali-suite, and KREEP-rich impact-melt rocks may reveal the relative volatile abundance of urKREEP, the residual melt of the magma ocean. This difference in relative magmatic volatile abundance among the lithologic groups investigated cannot be explained by degassing of a single source composition (relative to magmatic volatiles). The most reasonable explanation for the compositional disparity is a difference in the relative volatile abundances in the magmatic source regions of the Moon. Therefore, we conclude that the Moon has a heterogeneous distribution of magmatic volatiles within its interior, with a chemical divide (with respect to magmatic volatiles) existing between magmas that arise by partial melting of the lunar mantle and magmas that have seen significant contamination by a KREEP component.  相似文献   

15.
The Paran continental flood basalt province is a voluminousbimodal volcanic sequence, with <5% silicic rocks (‘rhyolites’)lying on top of the basalts, concentrated towards the SouthAtlantic margin. Petrographically, the rhyolites have an anhydrousmineralogy (plagioclase, pyroxene, Fe–Ti oxides), and.two distinct groups are defined on the basis of phenocryst abundance.The Palmas group rhyolites are almost aphyric (<5% phenocrysts),in contrast to the plagioclase-rith Chapec group rhyolites(<25% phenocrysts). The plagioclase and clinopyroxene phenocrystsin the Palmas group rhyolites are rounded and poorly preserved,and are compositionally less evolved than those in the Chapecgroup. Calculated eruption temperatures are unusually high forsilicic magmas (950–1100C), and lie within the rangeof temperatures for the associated flood basalts. Chemically,the Palmas and Chapec group rhyolites are clearly distinguishable,with the most striking feature being the higher high field strengthelements, notably Ti, in the Chapec group. This mirrors thewell-documented low- and high-Ti division of the Paran basalts,and in addition there is a geographic correlation between thelow- and high- Ti basalt and rhyolite provinces, with high-Tivolcanics predominating in the north of the Paran Basin, andlow-Ti in the south. The Chapec group have Sr and Nd isotoperatios which overlap with those of the high-Ti basalts (87Sr/86Sr1300•705–0•708), whereas the Palmas group exhibita range towards high Sr isotope ratios (87Sr/86Sr130 0•714–0•727),continuing the trend of the low-Ti basalts to more radiogenicvalues. This suggests that assimilation of radiogenic materialhas occurred. Both rhyolite groups plot away from the isotopicfields for crustal basement types beneath the Paran, thus anorigin by simple crustal melting is discounted. Based on petrographic,chemical and isotopic data, petrogenetic models for the tworhyolite groups are developed, focusing on the clear geneticlink between the Palmas rhyolites and the low-Ti basalts, andthe Chapec rhyolites and the high-Ti basalts. The Chapec rhyolitesare modelled as partial melts ( 30%) of underplated high-Tibasalts, rather than fractionates, primarily because of thetime gap between eruption of the high-Ti basalts and Chapecrhyolites. However, the Palmas rhyolites are almost coeval withthe low-Ti basalts, and are modelled as the products of open-systemfractional crystallization from these low-Ti basaltic magmas.In addition, this low-Ti suite shows a continuous trend frombasalt to rhyolite in highly incompatible elements such as Zrand Hf consistent with a liquid line of descent, whereas thehigh-Ti magmas have a substantial gap in the concentration ofthese elements between the basalts and rhyolites. Experimentaldata support the derivation of both Paran rhyolite groups frombasaltic parents with moderately low water contents. Pressurecalculations suggest shallower ponding for the Palmas magmasthan for the Chapec magma (<5 kbar vs 5–15 kbar),and the style of eruption inferred for the two groups is explosive(rheoignimbritic) for the Palmas group, and effusive (lava flows)for the Chapec group. KEY WORDS: Paran; Brazil; rhyolits; petrogenesis; geochemistry *Corresponding author  相似文献   

16.
Near liquidus experiments on peridotite and other olivine normative compositions from 1.7 to 6 GPa confirm the applicability of exchange-based empirical models of Ni and Co partitioning between olivine and silicate liquids with compositions close to the liquidus of peridotite. Given that most estimates of lunar bulk composition are peridotitic, the partitioning models thus lend themselves to calculation of olivine compositions produced during the early stages of magma ocean crystallization. Calculation of olivine compositions produced by fractional crystallization of a model lunar magma ocean, initially 700 km deep, reveals a prominent maximum in Ni concentration versus fraction crystallized or Mg’ (molar MgO/(MgO + FeO)), but a pattern of monotonically increasing Co concentration. These patterns qualitatively match the puzzling patterns of Ni and Co concentrations observed in lunar rocks in which forsteritic olivines in magnesian suite cumulates have lower Ni and Co abundances than do less magnesian olivines from low-Ti mare basalts, and olivines from the ferroan anorthosite suite (FAS) have lower Ni, but similar Co to mare basalt olivines.The Ni and Co abundances in olivines from the magnesian suite cumulates can be reconciled in terms of fractional crystallization of a deep magma ocean which initially produces a basal dunite comprised of the hottest and most magnesian olivine overlain by an olivine-orthopyroxene (harzburgite) layer that is in turn overlain by an upper zone of plagioclase-bearing cumulates. The ultramafic portion of the cumulate pile overturns sending the denser harzburgite layer, which later becomes a portion of the green glass source region, to the bottom of the cumulate pile with Ni- and Co-rich olivine. Meanwhile, the less dense, but hottest, most magnesian olivines with much lower Ni and Co abundances are transported upward to the base of the plagioclase-bearing cumulates where subsequent heat transfer leads to melting of mixtures of primary dunite, norite, and gabbronorite with KREEP (a K-REE-P enriched component widely believed to be derived from the very latest stage magma ocean liquid). These hybrid melts have Al2O3, Ni, and Co abundances and Mg’ appropriate for parent magmas of the magnesian suite. Ni and Co abundances in the FAS are consistent with either direct crystallization from the magma ocean or crystallization of melts of primary dunite-norite mixtures without KREEP.  相似文献   

17.
Miller Range (MIL) 05035 is a lunar gabbroic meteorite. The mineralogy, Fe/Mn ratios in olivine and pyroxene, bulk-rock chemical composition and the bulk oxygen isotope values (δ17O = 2.86-2.97‰ and δ18O = 5.47-5.71‰) are similar to those of other mare basalts, and are taken as supporting evidence for a lunar origin for this meteorite. The sample is dominated by pyroxene grains (54-61% by area mode of thin section) along with large plagioclase feldspar (25-36% by mode) and accessory quartz, ilmenite, spinel, apatite and troilite. The bulk-rock major element composition of MIL 05035 indicates that the sample has a very low-Ti (VLT) to low-Ti lunar heritage (we measure bulk TiO2 to be 0.9 Wt.%) and has low bulk incompatible trace element (ITE) concentrations, akin to samples from the VLT mare basalt suite. To account for these geochemical characteristics we hypothesize that MIL 05035’s parental melt was derived from a mantle region dominated by early cumulates of the magma ocean (comprised principally of olivine and orthopyroxene). MIL 05035 is likely launch paired with the Asuka-881757 and Yamato-793169 basaltic lunar meteorites and the basaltic regolith breccia MET 01210. This group of meteorites (Y/A/M/M) therefore may be a part of a stratigraphic column consisting of an upper regolith environment underlain by a coarsening downwards basalt lava flow.  相似文献   

18.
Leone Melluso  John J. Mahoney  Luigi Dallai   《Lithos》2006,89(3-4):259-274
Near-primitive picritic basalts in the northwestern Deccan Traps have MgO > 10 wt.% and consist of two groups (low-Ti and high-Ti) with markedly different incompatible element and Nd–Sr–Pb isotope characteristics. Many elemental characteristics of the low-Ti picritic basalts are similar to those of transitional or normal ocean ridge basalts. However, values of ratios like Ba/Nb (13–30) and Ce/Pb (4–11), and isotopic ratios (e.g., εNd(t) + 0.3 to − 6.3, (207Pb/204Pb)t 15.63–15.75 at (206Pb/204Pb)t 18.19–18.84, δ18Oolivine as high as + 6.2‰) are far-removed from ocean-ridge-type values, indicating a significant contribution from continental crust. The crustal signature could represent crustal contamination of ascending magmas; alternatively, it could represent a minor component within the Indian lithospheric mantle of anciently subducted sedimentary material or fluids derived from subducted material. In contrast, the high-Ti picritic basalts are chemically and isotopically rather similar to recent shield lavas of the Réunion hotspot (e.g., εNd(t) + 2 to + 4) and to volcanic rocks along the postulated pre-Deccan track of this hotspot in Pakistan. Neither type of picritic basalt is parental to the voluminous flows comprising the bulk of the Deccan Traps. However, many of the Deccan primary magmas could have been derived from mixtures of a high-Ti-type, Réunion-like source component and a component more similar to, or even more incompatible-element-depleted than, average ocean-ridge mantle.  相似文献   

19.
Delineation of low pressure phase equilibria in the composition space relevant to titaniferous lunar basalts demonstrates a significant degree of control by those equilibria on the compositions of the basalts. The existence of two distinct chemical groups of basalts (high and low-K) which cannot be related one to the other by fractional crystallization at any pressure, suggests that melting is responsible for the two groups. Consideration of the pressure shift required to produce the differences between groups constrains magma segregation to have occurred in the outer 150 km of the Moon. It is difficult to relate low-Ti and high-Ti basalts to the same source region. The preferred source region of high-Ti basalts, based on phase equilibrium considerations, is a late ilmenite-rich cumulate produced from the residual liquid of the primordial differentiation of the outer portions of the Moon. This ilmenite-rich layer is sandwiched between the lunar feldspathic crust and a complementary mafic cumulate.  相似文献   

20.
The Maymecha-Kotuy area, comprising ～70,000 km2 of the northern part of the Siberian flood-basalt province, is of unusual interest because it appears to be the only such province in the world where high-Ti, alkaline-ultramafic rocks with associated carbonatites predominate over basaltic extrusive and intrusive rocks. New field and geochemical studies of the igneous rocks of this area were initiated with the goals of (1) correlating them with the magmatic formations of the well-studied Noril'sk area and (2) reconstructing the entire magmatic evolution of Siberian flood-basalt volcanism.

This report presents the first complete stratigraphic section for the volcanic sequence of the Maymecha River Basin (the most extensive in the Maymecha-Kotuy area), based on flow-by-flow mapping and sample collection. The geochemical and lithologic characteristics of the volcanic and intrusive rocks are thoroughly documented and show an unusually broad range in composition–e.g., SiO2 and MgO contents range from 40 to 70 and from <1 to 38 wt%, respectively. New geochemical data, considered together with earlier paleomagnetic data, indicate that as much as 3000 m of the Maymecha-Kotuy sequence consists of lavas younger than those preserved near Noril'sk. Thus, the combined thickness of the lavas and tuffs that constitute the Siberian flood-basalt province is estimated as ～6500 m. As at Noril'sk, the volcanic sequence lies with unconformity on sedimentary rocks of the Tungusskaya Series. At Maymecha, the sequence begins with a major, basaltic-tuff unit and an overlying suite of low-Ti, tholeiitic basalts, but the magmatism then became more diverse, with several alternations of low-Ti and high-Ti lavas, and evolved to eruption of high-Ti trachybasalts, melanephelinites, trachyandesites, trachytes, trachydacites, and trachyrhyodacites. The uppermost ～1400 m of the sequence consists of high-Ti, limburgitic and picritic lavas, as well as Mg-rich (23 to 38 wt%), high-Ti, meymechitic lavas, apparently unique in the world. Graphic evidence of the volcanic nature of the meymechites is presented here for the first time.

The numerous dikes and several sills of the Maymecha River Basin are subdivided into seven types, which can be geochemically related to the volcanic sequence and in some cases can be reliably correlated with magmatic rocks of the Noril'sk area. Preliminary indications are that the complex body commonly referred to as the Guli intrusion is, in fact, an intrusive-volcanic complex occupying ～2000 km2, in which a large, laccolithic intrusive mass of dunitic to peridotitic rocks was breached by a central volcanic edifice from which flowed ankaratrite and picritic ankaratrite lavas. Cutting the ankaratrites and picritic ankaratrites of the complex, but intimately related to it, is a variety of intrusive, alkaline rock types and two carbonatite bodies that may be related to a central feeder zone.

We recognize four magma types as products of Siberian flood-basalt volcanism and refer to them herein as low-Ti-I, low-Ti-2, moderate-Ti, and high-Ti. In contrast to the Noril'sk area, where high-Ti magmas constitute <1 vol% of the igneous rocks, their proportion is ～50 vol% in the Maymecha River Basin. These high-Ti rocks can be subdivided into trachybasaltic, melanephelinitic, and meymechitic rock series; clearly related to these series, judging from trace-element characteristics, are associated trachyandesitic, trachytic, and felsic lavas. In general, the trachyandesitic, trachytic, and felsic lavas appear to be related to the trachybasaltic series through fractionation, but some of the felsic tuffs display characteristics that suggest their relation to the melanephelinitie series. Previous investigators have concluded that meymechitic magma formed by low degrees of mantle-peridotite melting (<7%) at pressures corresponding to depths of 250 to 300 km. The distinctions between the trachybasaltic, melanephelinitic, and meymechitic rock series must relate to different sources and conditions of melting. It is remarkable that no geochemical signature of crustal contamination can be recognized for any of the high-Ti rocks, including the felsic lavas and tuffs. We conclude that the alternation of low-Ti and high-Ti magma types observed in the lower half of the volcanic sequence in the Maymecha River Basin resulted from repetitive expulsion from discrete mantle sources through independent plumbing systems.  相似文献   

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