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1.
An accurate assessment of the bulk chemical composition of Mars is fundamental to understanding planetary accretion, differentiation, mantle evolution, the nature of the igneous parent rocks that were altered to produce sediments on Mars, and the initial concentrations of volatiles such as H, Cl and S, important constituents of the Martian surface. This paper reviews the three main approaches that have been used to estimate the bulk chemical composition of Mars: geochemical/cosmochemical, isotopic, and geophysical. The standard model is one developed by Wänke and Dreibus in a series of papers, which is based on compositions of Martian meteorites. Since their groundbreaking work, substantial amounts of data have become available to allow a reassessment of the composition of Mars from elemental data, including tests of the basic assumptions in the geochemical models. The results adjust some of the concentrations in the Wänke–Dreibus model, but in general confirm its accuracy. Bulk silicate Mars has roughly uniform depletion of moderately volatile elements such as K (0.6 × CI), and strong depletion of highly volatile elements (e.g., Tl). The highly volatile elements are within uncertainties uniformly depleted at about 0.06 CI abundances. The highly volatile chalcophile elements are likewise roughly uniformly depleted, but with more scatter, with normalized abundances of 0.03 CI. Bulk planetary H2O is much higher than estimated previously: it appears to be slightly less than in Earth, but D/H is similar in Earth and Mars, indicating a common source of water-bearing material in the inner solar system. K/Th ranges from ∼3000 to ∼5000 among the terrestrial planets, a small range compared to CI chondrites (19,000). FeO varies throughout the inner solar system: ∼3 wt% in Mercury, 8 wt% in Earth and Venus, and 18 wt% in Mars. These differences can be produced by varying oxidation conditions, hence do not suggest the terrestrial planets were formed from fundamentally different materials. The broad chemical similarities among the terrestrial planets indicate substantial mixing throughout the inner solar system during planet formation, as suggested by dynamical models.  相似文献   

2.
The 182Hf-182W systematics of meteoritic and planetary samples provide firm constraints on the chronology of the accretion and earliest evolution of asteroids and terrestrial planets and lead to the following succession and duration of events in the earliest solar system. Formation of Ca,Al-rich inclusions (CAIs) at 4568.3 ± 0.7 Ma was followed by the accretion and differentiation of the parent bodies of some magmatic iron meteorites within less than ∼1 Myr. Chondrules from H chondrites formed 1.7 ± 0.7 Myr after CAIs, about contemporaneously with chondrules from L and LL chondrites as shown by their 26Al-26Mg ages. Some magmatism on the parent bodies of angrites, eucrites, and mesosiderites started as soon as ∼3 Myr after CAI formation and may have continued until ∼10 Myr. A similar timescale is obtained for the high-temperature metamorphic evolution of the H chondrite parent body. Thermal modeling combined with these age constraints reveals that the different thermal histories of meteorite parent bodies primarily reflect their initial abundance of 26Al, which is determined by their accretion age. Impact-related processes were important in the subsequent evolution of asteroids but do not appear to have induced large-scale melting. For instance, Hf-W ages for eucrite metals postdate CAI formation by ∼20 Myr and may reflect impact-triggered thermal metamorphism in the crust of the eucrite parent body. Likewise, the Hf-W systematics of some non-magmatic iron meteorites were modified by impact-related processes but the timing of this event(s) remains poorly constrained.The strong fractionation of lithophile Hf from siderophile W during core formation makes the Hf-W system an ideal chronometer for this major differentiation event. However, for larger planets such as the terrestrial planets the calculated Hf-W ages are particularly sensitive to the occurrence of large impacts, the degree to which impactor cores re-equilibrated with the target mantle during large collisions, and changes in the metal-silicate partition coefficients of W due to changing fO2 in differentiating planetary bodies. Calculated core formation ages for Mars range from 0 to 20 Myr after CAI formation and currently cannot distinguish between scenarios where Mars formed by runaway growth and where its formation was more protracted. Tungsten model ages for core formation in Earth range from ∼30 Myr to >100 Myr after CAIs and hence do not provide a unique age for the formation of Earth. However, the identical 182W/184W ratios of the lunar and terrestrial mantles provide powerful evidence that the Moon-forming giant impact and the final stage of Earth’s core formation occurred after extinction of 182Hf (i.e., more than ∼50 Myr after CAIs), unless the Hf/W ratios of the bulk silicate Moon and Earth are identical to within less than ∼10%. Furthermore, the identical 182W/184W of the lunar and terrestrial mantles is difficult to explain unless either the Moon consists predominantly of terrestrial material or the W in the proto-lunar magma disk isotopically equilibrated with the Earth’s mantle.Hafnium-tungsten chronometry also provides constraints on the duration of magma ocean solidification in terrestrial planets. Variations in the 182W/184W ratios of martian meteorites reflect an early differentiation of the martian mantle during the effective lifetime of 182Hf. In contrast, no 182W variations exist in the lunar mantle, demonstrating magma ocean solidification later than ∼60 Myr, in agreement with 147Sm-143Nd ages for ferroan anorthosites. The Moon-forming giant impact most likely erased any evidence of a prior differentiation of Earth’s mantle, consistent with a 146Sm-142Nd age of 50-200 Myr for the earliest differentiation of Earth’s mantle. However, the Hf-W chronology of the formation of Earth’s core and the Moon-forming impact is difficult to reconcile with the preservation of 146Sm-142Nd evidence for an early (<30 Myr after CAIs) differentiation of a chondritic Earth’s mantle. Instead, the combined 182W-142Nd evidence suggests that bulk Earth may have superchondritic Sm/Nd and Hf/W ratios, in which case formation of its core must have terminated more than ∼42 Myr after formation of CAIs, consistent with the Hf-W age for the formation of the Moon.  相似文献   

3.
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   

4.
Samples returned from the surface of planetary bodies are both complementary to orbital and in situ observations and provide a unique perspective for understanding the nature and evolution of that body. This unique perspective is based on the scale the sample is viewed (mm-Å), the ability to manipulate the sample, the capability to analyze the sample at high precision and accuracy, and the ability to significantly modify experiments as logic and technology dictates over an extended period of time (decades). Unlike the Apollo missions, robotic sample return missions in the next decade will result in the return of relatively small sample mass. Such robotically returned samples are scientifically more valuable if they can be placed within a planetary context through orbital observations and if information concerning planetary-scale processes and conditions can be extracted from them. Conversely, samples give remotely sensed data ground truth. That is, they act as a “calibration standard” for these data allowing a much enhanced global view to be constructed.The Moon is an example that illustrates how information can be extracted from small samples and then extended to planetary and solar system scales. Three examples from the Moon illustrate this point. First, multi-analytical and experimental studies of minute (10-500 μm) glass beads representing near-primary magmas provide constraints on the composition and condition of the lunar mantle, the style of early planetary differentiation, the history and character of early mantle dynamics and melting, and the isolation of the lunar mantle from late-stages of lunar accretion. Second, trace element analysis of individual mineral grains via ion microprobe and isotopic analysis of small rock fragments representing some of the oldest and youngest periods of lunar magmatism illustrate their usefulness for both fingerprinting distinct episodes of lunar magmatism and reconstructing the evolution of lunar magmatism. Third, mechanisms for primitive planetary mantles degassing and volatile transport on airless bodies can be understood by the analysis of volatile coatings on glass and mineral fragments in the lunar regolith.As many of our insights about the Moon are based on samples that primarily were collected within a limited lunar terrain, our understanding of the Moon is somewhat biased. Future scientifically strategic sampling targets are young mare basalts (Roris basalt in Oceanus Procellarum), far-side mare basalts (Mare Moscoviense), large pyroclastic deposits and potential mantle xenoliths (Aristarchus plateau, Rima Bode) major unsampled crustal lithologies outside the Procellarum KREEP terrane (central peak in Tsiolkovsky crater, South-pole Aitken basin), basin and crater melt sheets (South-pole Aitken basin, Giordano Bruno) and H deposits in permanently shaded areas (South-pole Aitken basin). Sampling these locations would further our understanding of processes at work during the early evolution of the terrestrial planets, provide a comprehensive history of endogenous (e.g., primary volcanic degassing) and exogenous (e.g., solar wind, galactic cosmic rays, volatiles from comets) volatile reservoirs and volatile transport and would provide unique historical information about events and processes that affected the entire inner solar system, a record obscured on the Earth and Mars.  相似文献   

5.
We have used a recently developed quantitative pyrolysis-Fourier transform infrared spectroscopy method to measure the production of water and carbon dioxide during 250 °C desorption and 1000 °C gasification steps for a range of carbonaceous chondrites. Greater yields of water and carbon dioxide during gasification are associated with meteorites believed to have experienced more aqueous alteration on their asteroid parent body (i.e. gas yields for petrographic type 1 > type 2 > type 3). Volatile yields most likely reflect quantities of hydrated mineral phases and partially oxidised organic matter. Methane was not detected in the gasification products of the meteorites, allowing an upper limit on its production of around 100 ppm to be calculated based on the sensitivity of the pyrolysis-Fourier transform infrared spectroscopy technique employed. When considered alongside rates of infall of cosmic dust throughout Earth history, the data can be used to evaluate the production of volatiles during the thermal ablation of dust upon atmospheric entry, and to estimate their contribution to a terrestrial planet’s atmosphere and hydrosphere. Over the long term, it appears that contributions of this nature to the Earth’s volatile inventory are small, although production rates are calculated to have been substantially higher before and during the Late Heavy Bombardment of 3.8-4.0 Ga. Moreover, ablation of carbonaceous chondritic material does not appear to be a plausible source of the atmospheric methane budget of Mars.  相似文献   

6.
Multiple lines of evidence show that the Rb-Sr, Sm-Nd, and Ar-Ar isotopic systems individually give robust crystallization ages for basaltic (or diabasic) shergottite Northwest Africa (NWA) 1460. In contrast to other shergottites, NWA 1460 exhibits minimal evidence of excess 40Ar, thus allowing an unambiguous determination of its Ar-Ar age. The concordant Rb-Sr, Sm-Nd, and Ar-Ar results for NWA 1460 define its crystallization age to be 346 ± 17 Ma (2σ). In combination with petrographic and trace element data for this specimen and paired meteorite NWA 480, these results strongly refute the suggestion by others that the shergottites are ∼4.1 Ga old. Current crystallization and cosmic-ray exposure (CRE) age data permit identification of a maximum of nine ejection events for Martian meteorites (numbering more than 50 unpaired specimens as of 2008) and plausibly as few as five such events. Although recent high resolution imaging of the Martian surface has identified limited areas of sparsely cratered terrains, the meteorite data suggest that either these areas are representative of larger areas from which the meteorites might come, or that the cratering chronology needs recalibration. Time-averaged 87Rb/86Sr = 0.16 for the mantle source of the parent magma of NWA 1460/480 over the ∼4.56 Ga age of the planet is consistent with previously estimated values for bulk silicate Mars in the range 0.13-0.16, and similar to values of ∼0.18 for the “lherzolitic” shergottites. Initial εNd for NWA 1460/480 at 350 ± 16 Ma ago was +10.6 ± 0.5, which implies a time-averaged 147Sm/144Nd of 0.217 in the Martian mantle prior to mafic melt extraction, similar to values of 0.211-0.216 for the “lherzolitic” shergottites. These time-averaged values do not imply a simple two-stage mantle/melt evolution, but must result from multiple episodes of melt extractions from the source regions. Much higher “late-stage” εNd values for the depleted shergottites imply similar processes carried to a greater degree. Thus, NWA 1460/480, the “lherzolitic” shergottites and perhaps EET 79001 give the best (albeit imperfect) estimate of the Sr- and Nd-isotopic characteristics of bulk silicate Mars.  相似文献   

7.
The discrepancy between the impact records on the Earth and Moon in the time period, 4.0-3.5 Ga calls for a re-evaluation of the cause and localization of the late lunar bombardment. As one possible explanation, we propose that the time coverage in the ancient rock record is sufficiently fragmentary, so that the effects of giant, sterilizing impacts throughout the inner solar system, caused by marauding asteroids, could have escaped detection in terrestrial and Martian records. Alternatively, the lunar impact record may reflect collisions of the receding Moon with a series of small, original satellites of the Earth and their debris in the time period about 4.0-3.5 Ga. The effects on Earth of such encounters could have been comparatively small. The location of these tellurian moonlets has been estimated to have been in the region around 40 Earth radii. Calculations presented here, indicate that this is the region that the Moon would traverse at 4.0-3.5 Ga, when the heavy and declining lunar bombardment took place. The ultimate time limit for the emergence of life on Earth is determined by the effects of planetary accretion--existing models offer a variety of scenarios, ranging from low average surface temperature at slow accretion of the mantle, to complete melting of the planet followed by protracted cooling. The choice of accretion model affects the habitability of the planet by dictating the early evolution of the atmosphere and hydrosphere. Further exploration of the sedimentary record on Earth and Mars, and of the chemical composition of impact-generated ejecta on the Moon, may determine the choice between the different interpretations of the late lunar bombardment and cast additional light on the time and conditions for the emergence of life.  相似文献   

8.
Volcanic suites from Wawa greenstone belts in the southern Superior Province comprise an association of typical late Archean arc volcanic rocks including adakites, magnesian andesites (MA), niobium-enriched basalts (NEB), and ‘normal’ tholeiitic to calc-alkaline basalts to rhyolites. The adakites represent melts from subducted oceanic crust and all other suites were derived from the mantle wedge above the subducting oceanic lithosphere. The magnesian andesites are interpreted to be the product of hybridization of adakite melts with arc mantle wedge peridotite. The initial ?Hf values of the ∼2.7 Ga Wawa adakites (+3.5 to +5.2), magnesian andesites (+2.6 to +5.1), niobium-enriched basalts (+4.4 to +6.6), and ‘normal’ tholeiitic to calc-alkaline arc basalts (+5.3 to +6.4) are consistent with long-term depleted mantle sources. The niobium-enriched basalts and ‘normal’ arc basalts have more depleted ?Hf values than the adakites and magnesian andesites. The initial ?Nd values in the magnesian andesites (+0.4 to +2.0), niobium-enriched basalts (+1.4 to +2.4), and ‘normal’ arc tholeiitic to calc-alkaline basalts (+1.6 to +2.9) overlap with, but extend to lower values than, the slab-derived adakites (+2.3 to +2.8). The lower initial ?Nd values in the mantle-wedge-derived suites, particularly in the magnesian andesites, are attributed to recycling of an Nd-enriched component with lower ?Nd to the mantle wedge. As a group, the slab-derived adakites plot closest to the 2.7 Ga depleted mantle value in ?Nd versus ?Hf space, additionally suggesting that the Nd-enriched component in the mantle wedge did not originate from the 2.7 Ga slab-derived melts. Accordingly, we suggest that the enriched component had been added to the mantle wedge at variable proportions by recycling of older continental material. This recycling process may have occurred as early as 50-70 Ma before the initiation of the 2.7 Ga subduction zone. The selective enrichment of Nd in the sources of the Superior Province magmas can be explained by experimental studies and geochemical observations in modern subduction systems, indicating that light rare earth elements (e.g., La, Ce, Sm, Nd) are more soluble than high field strength elements (e.g., Zr, Hf, Nb, Ta) in aqueous fluids that are derived from subducted slabs. As a corollary, we suggest that the recycled Nd-enriched component was added to the mantle source of the Wawa arc magmas by dehydration of subducted sediments.  相似文献   

9.
The timescale of accretion and differentiation of asteroids and the terrestrial planets can be constrained using the extinct 182Hf-182W isotope system. We present new Hf-W data for seven carbonaceous chondrites, five eucrites, and three shergottites. The W isotope data for the carbonaceous chondrites agree with the previously revised 182W/184W of chondrites, and the combined chondrite data yield an improved ?W value for chondrites of −1.9 ± 0.1 relative to the terrestrial standard. New Hf-W data for the eucrites, in combination with published results, indicate that mantle differentiation in the eucrite parent body (Vesta) occurred at 4563.2 ± 1.4 Ma and suggest that core formation took place 0.9 ± 0.3 Myr before mantle differentiation. Core formation in asteroids within the first ∼5 Myr of the solar system is consistent with the timescales deduced from W isotope data of iron meteorites. New W isotope data for the three basaltic shergottites EETA 79001, DaG 476, and SAU 051, in combination with published 182W and 142Nd data for Martian meteorites reveal the preservation of three early formed mantle reservoirs in Mars. One reservoir (Shergottite group), represented by Zagami, ALH77005, Shergotty, EETA 79001, and possibly SAU 051, is characterized by chondritic 142Nd abundances and elevated ?W values of ∼0.4. The 182W excess of this mantle reservoir results from core formation. Another mantle reservoir (NC group) is sampled by Nakhla, Lafayette, and Chassigny and shows coupled 142Nd-182W excesses of 0.5-1 and 2-3 ? units, respectively. Formation of this mantle reservoir occurred 10-20 Myr after CAI condensation. Since the end of core formation is constrained to 7-15 Myr, a time difference between early silicate mantle differentiation and core formation is not resolvable for Mars. A third early formed mantle reservoir (DaG group) is represented by DaG 476 (and possibly SAU 051) and shows elevated 142Nd/144Nd ratios of 0.5-0.7 ? units and ?W values that are indistinguishable from the Shergottite group. The time of separation of this third reservoir can be constrained to 50-150 Myr after the start of the solar system. Preservation of these early formed mantle reservoirs indicates limited convective mixing in the Martian mantle as early as ∼15 Myr after CAI condensation and suggests that since this time no giant impact occurred on Mars that could have led to mantle homogenization. Given that core formation in planetesimals was completed within the first ∼5 Myr of the solar system, it is most likely that Mars and Earth accreted from pre-differentiated planetesimals. The metal cores of Mars and Earth, however, cannot have formed by simply combining cores from these pre-differentiated planetesimals. The 182W/184W ratios of the Martian and terrestrial mantles require late effective removal of radiogenic 182W, strongly suggesting the existence of magma oceans on both planets. Large impacts were probably the main heat source that generated magma oceans and led to the formation metallic cores in the terrestrial planets. In contrast, decay of short-lived 26Al and 60Fe were important heat sources for melting and core formation in asteroids.  相似文献   

10.
We report Si isotopic data on a suite of terrestrial mantle-derived samples, meteorites and a lunar sample. Our data on co-existing mantle minerals, peridotites and basalts demonstrate lack of any resolvable high temperature fractionation during igneous processes. We show that the δ30Si of the bulk silicate Earth (BSE) is identical, within analytical uncertainties, to carbonaceous and ordinary chondrites (CHUR). Based on our data the difference between δ30SiBSE and δ30SiCHUR is 0.035 ± 0.035. Whole-rock differentiated meteorites from different parent bodies (Mars, Vesta) and a lunar breccia sample also show similar δ30Si suggesting broad-scale Si isotope homogeneity in the inner Solar System with an average δ29Si = −0.20 ± 0.01 and δ30Si = −0.39 ± 0.02 relative to the NBS28 Si isotope standard.A difference between δ30SiBSE and δ30SiCHUR of 0.035, as observed in our study, translates to less than 1.67 wt.% Si in the core considering a continuous accretion model whereas estimates using a batch model are even lower. Within uncertainties (±0.035‰) in the δ30Si difference between the BSE and CHUR, a maximum of 3.84 wt.% Si could be present in the Earth’s core whereas at δ30SiBSE-δ30SiCHUR = 0, there is no requirement of Si in the Earth’s core. Such low Si in the core necessitates the presence of other light elements in the core to explain its density deficit. Our data also places constraints on the oxidation state of the Earth’s mantle during core segregation. The uncertainties in estimating the concentration of oxidized Fe in the mantle during the first 90% of accretion arise from uncertainties in the estimates of the equilibrium partition coefficient of silicon between metal and silicate at conditions relevant to core formation. For δ30SiBSE-δ30SiCHUR = 0.035 ± 0.035, the concentration of oxidized Fe in the mantle during the first 90% of accretion could be as low as ∼1%. However, at δ30SiBSE-δ30SiCHUR = 0, the Si isotope data do not require any change in the mantle concentration of oxidized Fe during accretion from the present day value of 6.26%.  相似文献   

11.
Excesses of 182W have previously been measured in samples from the Moon and Mars, and can be derived from high Hf/W regions in their interiors during their early histories. Although planetary mantles will have superchondritic Hf/W after core formation, the extent to which high Hf/W regions could be generated by magmatic fractionation has not been evaluated. In order to address the latter possibility, we have carried out experiments from 100 MPa to 10.0 GPa, 1150 to 1850°C, at oxygen fugacities near the IW (iron-wüstite) buffer, and measured partition coefficients for W and Hf for plagioclase-liquid, olivine-liquid, orthopyroxene-liquid, clinopyroxene-liquid, garnet-liquid, and metal-liquid pairs. Clinopyroxene and garnet are both capable of fractionating Hf from W during magmatic crystallization or mantle melting, and minor variations in the measured D’s can be attributed to crystal chemical effects. Excesses of 182W and 142Nd in lunar samples can be explained by fractionation of Hf from W, and Sm from Nd (by ilmenite and clinopyroxene) during crystallization of the latest stages of a lunar magma ocean. Correlations of εW with εNd in martian samples could be a result of early silicate fractionation in the martian mantle (clinopyroxene and/or garnet).  相似文献   

12.
Aqueous extraction contributes to the formation and weathering of planetary materials and renders electrolytes such as phosphate available for biology. In this context, the solubility of phosphate is measured in planetary materials, represented by the Mars meteorites Nakhla, Dar al Gani 476 (DaG 476), Elephant Morraine 79001 (EETA 79001), and terrestrial analogs, and in the Murchison CM2 and Allende CV3 carbonaceous chondrites. The Mars meteorites contain high levels of phosphate that is readily extracted by water, up to 15 mg kg−1 in Nakhla and DaG 476 and 38 mg kg−1 in EETA 79001, while the terrestrial analogs and the carbonaceous chondrites contain 0.5 to 6 mg kg−1. Correspondingly, high phosphate concentrations of 4 to >28 mg L−1 are obtained in extracts of the Mars meteorites at high solid/solution ratios, exceeding the concentrations of 0.4 to 2.0 mg L−1 in the extracts of the terrestrial analogs. A wide range of planetary conditions, including N2 and CO2 atmospheres, solid/solution ratios of 0.01 to 1.0 kg L−1, extraction times of 1 to 21 d, and temperatures of 20 to 121°C affect the amounts of extractable phosphate by factors of only 2 to 5 in most materials. Phosphate-fixing capacity and exchangeable phosphate are assessed by the isotopic exchange kinetics (IEK) method, which quantifies the amount of P isotopically exchangeable within 1 min (E1min) and between 1 min and 3 months (E1min-3m) and the amount of P that cannot be exchanged within 3 months (E>3m). The IEK results show that the DaG 476 Mars meteorite and terrestrial analogs have low P-fixing capacities, while the carbonaceous chondrites have high P-fixing capacities. Aqueous processing under early planetary CO2 atmospheres has large effects on the available phosphate. For example, the fraction of total P that is exchangeable in 3 months increases from 1.6 to 11%, 13 to 51.6%, and 43.9 to 90.4% in the DaG 476 Mars meteorite, Allende, and Murchison, respectively. The results show that solutions with high phosphate concentrations can form in the pores of planetary lava ash and basalts and in carbonaceous asteroids and meteorites. These solutions can help prebiotic synthesis and early microbial nutrition. The Martian and carbonaceous chondrite materials contain sufficient phosphate for space-based agriculture.  相似文献   

13.
Uranium-lead ratios (commonly represented as 238U/204Pb = μ) calculated for the sources of martian basalts preserve a record of petrogenetic processes that were active during early planetary differentiation and formation of martian geochemical reservoirs. To better define the range of μ values represented by the source regions of martian basalts, we completed U-Pb elemental and isotopic analyses on whole rock, mineral and leachate fractions from the martian meteorite Queen Alexandra Range 94201 (QUE 94201). The whole rock and silicate mineral fractions have unradiogenic Pb isotopic compositions that define a narrow range (206Pb/204Pb = 11.16-11.61). In contrast, the Pb isotopic compositions of weak HCl leachates are more variable and radiogenic. The intersection of the QUE 94201 data array with terrestrial Pb in 206Pb/204Pb-207Pb/204Pb-208Pb/204Pb compositional space is consistent with varying amounts of terrestrial contamination in these fractions. We calculate that only 1-7% contamination is present in the purified silicate mineral and whole rock fractions, whereas the HCl leachates contain up to 86% terrestrial Pb. This terrestrial Pb contamination generated a 206Pb-207Pb array in the QUE fractions that appears to represent an ancient age, which contrasts with a much younger crystallization age of 327 ± 10 Ma derived from Rb-Sr and Sm-Nd isochrons (Borg L. E., Nyquist L. E., Taylor L. A., Wiesmann H. and Shih C. -Y. (1997) Constraints on Martian differentiation processes from Rb-Sr and Sm-Nd isotopic analyses of the basaltic shergottite QUE 94201. Geochim. Cosmochim. Acta61, 4915-4931). Despite the contamination, and accepting 327 ± 10 Ma as the crystallization age, we use the U-Pb data to determine the initial 206Pb/204Pb of QUE 94201 to be 11.086 ± 0.008 and to calculate the μ value of its mantle source to be 1.82 ± 0.01. The μ value calculated for the QUE 94201 source is the lowest determined for any martian basalt source, and, when compared to the highest values determined for martian basalt sources, indicates that μ values in martian source reservoirs vary by at least a factor of two. Additionally, the range of source μ values indicates that the μ value of bulk silicate Mars is approximately three. The amount of variation in the μ values of the mantle sources (μ ∼ 2-4) is greater than can be explained by igneous processes involving silicate phases alone. We suggest the possibility that a small amount of sulfide crystallization may generate greater extents of U-Pb fractionation during formation of the mantle sources of martian basalts.  相似文献   

14.
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   

15.
The suggestion that radon could be used as a radioactive tracer of regolith-atmosphere exchanges and as a proxy for subsurface water on Mars, as well as its indirect detection in the Martian atmosphere by the rover Opportunity, have raised the need for a better characterization of its production process and transport efficiency in the Martian soil. More specifically, a proper estimation of radon exhalation rate on Mars requires its emanation factor and diffusion length to be determined. The dependence of the emanation factor as a function of pore water content (at 267 and 293 K) and the dependence of the adsorption coefficient on temperature, specific surface area and nature of the carrier gas (He, He + CO2) have been measured on a Martian soil analogue (Hawaiian palagonitized volcanic ash, JSC Mars-1), whose radiometric analysis has been performed. An estimation of radon diffusion lengths on Mars is provided and is used to derive a global average emanation factor (2-6.5%) that accounts for the exhalation rate inferred from the 210Po surface concentration detected on Martian dust and from the 214Bi signal measured by the Mars Odyssey Gamma Ray Spectrometer. It is found to be much larger than emanation factors characterizing lunar samples, but lower than the emanation factor of the palagonite samples obtained under dry conditions. This result probably reflects different degrees of aqueous alteration and could indicate that the emanation factor is also affected by the current presence of pore water in the Martian soil. The rationale of the “radon method” as a technique to probe subsurface water on Mars, and its sensitivity to soil parameters are discussed. These experimental data are useful to perform more detailed studies of radon transport in the Martian atmosphere using Global Climate Models and to interpret neutron and gamma data from Mars Odyssey Gamma Ray Spectrometer.  相似文献   

16.
The seven nakhlite meteorites are augite-rich igneous rocks that formed in flows or shallow intrusions of basaltic magma on Mars. They consist of euhedral to subhedral crystals of augite and olivine (to 1 cm long) in fine-grained mesostases. The augite crystals have homogeneous cores of Mg′=63% and rims that are normally zoned to iron enrichment. The core-rim zoning is cut by iron-enriched zones along fractures and is replaced locally by ferroan low-Ca pyroxene. The core compositions of the olivines vary inversely with the steepness of their rim zoning - sharp rim zoning goes with the most magnesian cores (Mg′=42%), homogeneous olivines are the most ferroan. The olivine and augite crystals contain multiphase inclusions representing trapped magma. Among the olivine and augite crystals is mesostasis, composed principally of plagioclase and/or glass, with euhedra of titanomagnetite and many minor minerals. Olivine and mesostasis glass are partially replaced by veinlets and patches of iddingsite, a mixture of smectite clays, iron oxy-hydroxides and carbonate minerals. In the mesostasis are rare patches of a salt alteration assemblage: halite, siderite, and anhydrite/gypsum. The nakhlites are little shocked, but have been affected chemically and biologically by their residence on Earth.Differences among the chemical compositions of the nakhlites can be ascribed mostly to different proportions of augite, olivine, and mesostasis. Compared to common basalts, they are rich in Ca, strongly depleted in Al, and enriched in magmaphile (incompatible) elements, including the LREE. Nakhlites contain little pre-terrestrial organic matter. Oxygen isotope ratios are not terrestrial, and are different in anhydrous silicates and in iddingsite. The alteration assemblages all have heavy oxygen and heavy carbon, while D/H values are extreme and scattered. Igneous sulfur had a solar-system isotopic ratio, but in most minerals was altered to higher and lower values. High precision analyses show mass-independent fractionations of S isotopes. Nitrogen and noble gases are complex and represent three components: two mantle sources (Chas-E and Chas-S), and fractionated Martian atmosphere.The nakhlites are igneous cumulate rocks, formed from basaltic magma at ∼1.3 Ga, containing excess crystals over what would form from pure magma. After accumulation of their augite and olivine crystals, they were affected (to various degrees) by crystallization of the magma, element diffusion among minerals and magma, chemical reactions among minerals and magma, magma movement among the crystals, and post-igneous chemical equilibration. The extent of these modifications varies, from least to greatest, in the order: MIL03346, NWA817, Y000593, Nakhla=Governador Valadares, Lafayette, and NWA998.Chemical, isotopic, and chronologic data confirm that the nakhlites formed on Mars, most likely in thick lava flows or shallow intrusions. Their crystallization ages, referenced to crater count chronologies for Mars, suggest that the nakhlites formed on the large volcanic constructs of Tharsis, Elysium, or Syrtis Major. The nakhlites were suffused with liquid water, probably at ∼620 ma. This water dissolved olivine and mesostasis glass, and deposited iddingsite and salt minerals in their places. The nakhlites were ejected from Mars at ∼10.75 Ma by an asteroid impact and fell to Earth within the last 10,000 years.Although the nakhlites are enriched in incompatible elements, their source mantle was strongly depleted. This depletion event was ancient, as the nakhlites’ source mantle was fractionated while short-lived radionuclides (e.g., ) were still active. This differentiation event may have been core formation coupled with a magma ocean, as is inferred for the moon.  相似文献   

17.
Impact cratering was an important — even dominant — process affecting the crustal evolution of the small terrestrial planets. The fundamental highlands/maria dichotomy of the Moon's surface can be traced to a late heavy bombardment by basin-forming, asteroid-sized bodies which produced not only a topographic division in the lunar crust but also localized the later eruptions of mare basalts. Major impact basins with diameters in excess of 200 km are recognized throughout the inner solar system from Mars to Mercury. Similar craters must have formed on the Earth prior to 4 Ga ago, and the minimum number of such basin-forming impacts can be calculated by scaling from the observed (minimum) number preserved on the Moon. When allowance is made for differences in impact velocity, gravitational cross-section and the effects of gravity on crater diameter, it is found that at least 50% of a presumed global sialic crust would have been converted into impact basins by 4 Ga ago. Among the effects resulting from the impact of an asteroidal object on the early crust were: (a) establishment of a topographic dichotmy of 3–4 km (after isostatic adjustment), (b) pressure-release partial melting of the upper mantle and rapid flooding of the basin floor by basalt, and (c) enhancement of thermal gradients in the sub-basin lithosphere and upper asthenosphere. Comparative planetary data such as impact scaling can be used as important constraints on models of the early terrestrial crust. For example, the topography resulting from impact bombardment produced discrete oceans and dry land by 4 Ga ago, making unreasonable models of a globe-encircling ocean on the Earth after that time.  相似文献   

18.
Liquid Fe metal-liquid silicate partition coefficients for the lithophile and weakly-siderophile elements Ta, Nb, V, Cr, Si, Mn, Ga, In and Zn have been measured in multianvil experiments performed from 2 to 24 GPa, 2023-2873 K and at oxygen fugacities of −1.3 to −4.2 log units relative to the iron-wüstite buffer. Compositional effects of light elements dissolved in the metal liquid (S, C) have been examined and experiments were performed in both graphite and MgO capsules, specifically to address the effect of C solubility in Fe-metal on siderophile element partitioning. The results were used to examine whether there is categorical evidence that a significant portion of metal-silicate equilibration occurred under very high pressures during core-mantle fractionation on Earth. Although the depletion of V from the mantle due to core formation is significantly greater than that of Nb, our results indicate that both elements have similar siderophile tendencies under reducing conditions at low pressures. With increasing pressure, however, Nb becomes less siderophile than V, implying that average metal-silicate equilibration pressures of at least 10-40 GPa are required to explain the Nb/V ratio of the mantle. Similarly the moderately-siderophile, volatile element ratios Ga/Mn and In/Zn are chondritic in the mantle but both volatility and core-mantle equilibration at low pressure would render these ratios strongly sub-chondritic. Our results indicate that pressures of metal-silicate partitioning exceeding 30-60 GPa would be required to render these element ratios chondritic in the mantle. These observations strongly indicate that metal-silicate equilibration must have occurred at high pressures, and therefore support core-formation models that involve deep magma oceans. Moreover, our results allow us to exclude models that envisage primarily low-pressure (<1 GPa) equilibration in relatively small planetary bodies. We also argue that the core cannot contain significant U as this would require metal-silicate equilibration at oxygen fugacities low enough for significant amounts of Ta to have also been extracted from the mantle. Likewise, as In is more siderophile than Pb but similarly volatile and also quite chalcophile it would have been difficult for Pb to enter the core without reversing the relative depletions of these elements in the mantle unless metal-silicate equilibration occurred at high pressures >20 GPa.  相似文献   

19.
The Antarctic lunar meteorite Meteorite Hills (MET) 01210 is a polymict regolith breccia, dominantly composed of mare basalt components. One relatively large (2.7 × 4.7 mm) basalt clast in MET 01210 (MET basalt) shows remarkable mineralogical similarities to the lunar-meteorite crystalline mare basalts Yamato (Y)-793169, Asuka (A)-881757, and Miller Range (MIL) 05035. All four basalts have similar rock texture, mineral assemblage, mineral composition, pyroxene crystallization trend, and pyroxene exsolution lamellae. The estimated TiO2 contents (∼2.0 wt%) of the MET basalt and MIL 05035 are close to the bulk-rock TiO2 contents of Y-793169 and A-881757. These similarities suggest that Y-793169, A-881757, MIL 05035, and the MET basalt came from the same basalt flow, which we designate the YAMM basalt. The source-basalt pairing of the YAMM is also supported by their similar REE abundances, crystallization ages (approx. 3.8-3.9 Ga), and isotopic compositions (low U/Pb, low Rb/Sr, and high Sm/Nd). The pyroxene exsolution lamellae, which are unusually coarse (up to a few microns) by mare standards, imply a relatively slow cooling in an unusually thick lava and/or subsequent annealing within a cryptomare. Reported noble gas and CRE data with close launch ages (∼1 Ma) and ejection depths (deeper than several meters) among the four meteorites further indicate their simultaneous ejection from the moon. Despite the marginally close terrestrial ages, pairing in the conventional Earth-entry sense seems unlikely because of the remote recovery sites among the YAMM meteorites.The high abundance (68%) of mare components in MET 01210 estimated from a two-component mixing model calculation could have resulted from either lateral mixing at a mare-highland boundary or vertical mixing in a cryptomare. The proportion of mare materials in MET 01210 is greater than in Apollo core samples at the mare-highland boundary. The burial depth (>several meters deep) inferred from the lack of surface irradiation of MET 01210 exceeds the typical mare regolith thickness (a few meters). Thus, the source of the YAMM meteorites is likely a terrain of locally high mare-highland mixing within a cryptomare. We searched for a possible source crater of the YAMM meteorites within the well-defined cryptomare, based on the multiple constraints obtained from this study and published data. An unnamed 1.4 km-diameter crater (53°W, 44.5°S) on the floor of the Schickard crater is the most suitable source for the YAMM meteorites.The 238U/204Pb (μ) value of the YAMM basalts is extremely low, relative to those of the Apollo mare basalts, but comparable to those of the Luna 24 very low-Ti basalts. The low-μ source indicates a derivation from a less differentiated mantle with a lack of KREEP components. Although the chemical sources of materials and heat source of melting might be independent, the heat source that generated the source magma of the YAMM and Luna 24 basalts may not be related to KREEP, unlike the case of the Apollo basalts. The distinct chemical and isotopic compositions of mantle sources between the Apollo basalts and the YAMM/Lunar 24 basalts imply differences in mantle composition and thermal evolution between the Procellarum KREEP Terrane (PKT) and non-PKT regions of the nearside.  相似文献   

20.
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   

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