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1.
Highly siderophile elements (HSEs) can be used to understand accretion and core formation in differentiated bodies, due to their strong affinity for FeNi metal and sulfides. Coupling experimental studies of metal–silicate partitioning with analyses of HSE contents of Martian meteorites can thus offer important constraints on the early history of Mars. Here, we report new metal–silicate partitioning data for the PGEs and Au and Re across a wide range of pressure and temperature space, with three series designed to complement existing experimental data sets for HSE. The first series examines temperature effects for D(HSE) in two metallic liquid compositions—C‐bearing and C‐free. The second series examines temperature effects for D(Re) in FeO‐bearing silicate melts and FeNi‐rich alloys. The third series presents the first systematic study of high pressure and temperature effects for D(Au). We then combine our data with previously published partitioning data to derive predictive expressions for metal–silicate partitioning of the HSE, which are subsequently used to calculate HSE concentrations of the Martian mantle during continuous accretion of Mars. Our results show that at midmantle depths in an early magma ocean (equivalent to approximately 14 GPa, 2100 °C), the HSE contents of the silicate fraction are similar to those observed in the Martian meteorite suite. This is in concert with previous studies on moderately siderophile elements. We then consider model calculations that examine the role of melting, fractional crystallization, and sulfide saturation/undersaturation in establishing the range of HSE contents in Martian meteorites derived from melting of the postcore formation mantle. The core formation modeling indicates that the HSE contents can be established by metal–silicate equilibrium early in the history of Mars, thus obviating the need for a late veneer for HSE, and by extension volatile siderophile elements, or volatiles in general.  相似文献   

2.
Volatile element concentrations in planets are controlled by many factors such as precursor material composition, core formation, differentiation, magma ocean and magmatic degassing, and late accretionary processes. To better constrain the role of core formation, we report new experiments defining the effect of temperature, and metallic S and C content on the metal-silicate partition coefficient (or D(i) metal/silicate) of the volatile siderophile elements (VSE) Bi, Cd, In, and Sn. Additionally, the effect of pressure on metal-silicate partitioning between 1 and 3 GPa, and olivine-melt partitioning at 1 GPa have been studied for Bi, Cd, In, Sn, As, Sb, and Ge. Temperature clearly causes a decrease in D(i) metal/silicate for all elements. Sulfur and C have a large influence on activity coefficients in metallic Fe liquids, with C causing a decrease in D(i) metal/silicate, and S causing an increase. Pressure has only a small effect on D(Cd), D(In), and D(Ge) metal/silicate. Depletions of Bi, Cd, In, and Sn in the terrestrial and Martian mantles are consistent with high PT core formation and metal-silicate equilibrium at the high temperatures indicated by previous studies. A late Hadean matte would influence Bi the most, due to its high D(sulfide/silicate) ~2000, but segregation of a matte would only reduce the mantle Bi content by 50%; all other less chalcophile elements (e.g., Sn, In, and Cd) would be minimally affected. The lunar depletions of highly VSE require a combination of core formation and an additional depletion mechanism—most likely the Moon-forming giant impact, or lunar magma ocean degassing.  相似文献   

3.
Elemental abundances for volatile siderophile and chalcophile elements for Mars inform us about processes of accretion and core formation. Such data are few for Martian meteorites, and are often lacking in the growing number of desert finds. In this study, we employed laser ablation inductively coupled plasma–mass spectrometry (LA‐ICP‐MS) to analyze polished slabs of 15 Martian meteorites for the abundances of about 70 elements. This technique has high sensitivity, excellent precision, and is generally accurate as determined by comparisons of elements for which literature abundances are known. However, in some meteorites, the analyzed surface is not representative of the bulk composition due to the over‐ or underrepresentation of a key host mineral, e.g., phosphate for rare earth elements (REE). For other meteorites, the range of variation in bulk rastered analyses of REE is within the range of variation reported among bulk REE analyses in the literature. An unexpected benefit has been the determination of the abundances of Ir and Os with a precision and accuracy comparable to the isotope dilution technique. Overall, the speed and small sample consumption afforded by this technique makes it an important tool widely applicable to small or rare meteorites for which a polished sample was prepared. The new volatile siderophile and chalcophile element abundances have been employed to determine Ge and Sb abundances, and revise Zn, As, and Bi abundances for the Martian mantle. The new estimates of Martian mantle composition support core formation at intermediate pressures (14 ± 3 GPa) in a magma ocean on Mars.  相似文献   

4.
Kevin Righter 《Icarus》2002,158(1):1-13
The issue of whether the Moon has a small metallic core is reexamined in light of new information: improved dynamical modeling, new constraints on core size, and high temperature and pressure metal-silicate partition coefficients. Addressed specifically is the question of whether the Moon's siderophile element budget can be explained by derivation of the Moon from a differentiated impactor or proto-Earth (stage 1), followed by formation of a small metallic core within the Moon (stage 2). If the Moon is made of mantle material from either a “hot” impactor or a “warm” impactor or proto-Earth, a small metallic core (0.7 to 2 mass%) is predicted. If the Moon is made from mantle material from a “hot” proto-Earth, the lunar mantle would be more depleted in W or Re than is observed. Scenarios in which the Moon is made from impactor or proto-Earth mantle material that has equilibrated with metal at low pressures and temperatures (“cold” scenarios) would yield a much larger metallic core than observed. Finally, the greater depletions of Ni, Mo, and Re in the Moon (relative to the Earth) can be explained by low PT and reduced metal-silicate equilibrium in an impactor without later core formation in the Moon (i.e., no stage 2), but depletions of Co, Ga, and W cannot. Altogether, geochemically unlikely or geophysically inadequate non-metallic core alternatives, substantial geophysical evidence for a metallic core, and the successful models presented here for siderophile element depletions all favor the presence of a small lunar metallic core. Previous geochemical objections to an impactor origin of the Moon are eliminated because siderophile element concentrations in the lunar mantle are consistent with separation of a small core from a bulk Moon derived from impactor mantle material.  相似文献   

5.
The depletion of volatile siderophile elements (VSE) Sn, Ag, Bi, Cd, and P in mantles of differentiated planetary bodies can be attributed to volatile‐depleted precursor materials (building blocks), fractionation during core formation, fractionation into and retention in sulfide minerals, and/or volatile loss associated with magmatism. Quantitative models to constrain the fractionation due to core formation have not been possible due to the lack of activity and partitioning data. Interaction parameters in Fe‐Si liquids have been measured at 1 GPa, 1600 °C and increase in the order Cd (~6), Ag (~10), Sn (~28), Bi (~46), and P (~58). These large and positive values contrast with smaller and negative values in Fe‐S liquids indicating that any chalcophile behavior exhibited by these elements will be erased by dissolution of a small amount of Si in the metallic liquid. A newly updated activity model is applied to Earth, Mars, and Vesta. Five elements (P, Zn, Sn, Cd, and In) in Earth's primitive upper mantle can largely be explained by metal‐silicate equilibrium at high PT conditions where the core‐forming metal is a Fe‐Ni‐S‐Si‐C metallic liquid, but two other—Ag and Bi—become overabundant during core formation and require a removal mechanism such as late sulfide segregation. All of the VSE in the mantle of Mars are consistent with core formation in a volatile element depleted body, and do not require any additional processes. Only P and Ag in Vesta's mantle are consistent with combined core formation and volatile‐depleted precursors, whereas the rest require accretion of chondritic or volatile‐bearing material after core formation. The concentrations of Zn, Ag, and Cd modeled for Vesta's core are similar to the concentration range measured in magmatic iron meteorites indicating that these volatile elements were already depleted in Vesta's precursor materials.  相似文献   

6.
Abstract— This study explores the controls of oxygen fugacity and temperature on the solubilities of Fe, Ni, Co, Mo, and W in natural eucritic liquids to better constrain the formation of eucritic melts. The solubilities of all five elements in molten silicate in equilibrium with FeNiCo‐, FeMo‐, and FeW‐ alloys increase with increasingly oxidizing conditions and decrease with decreasing temperatures. In applying these data to formation scenarios of the eucrite parent body, we find that the siderophile element abundances in eucrites (meteoritic basalts) cannot be explained by a single‐step partialmelting process from a chondritic, metal‐containing source. The Ni content of the partial melt is too high, and the W and Mo contents are too low compared to the abundances in eucritic meteorites. But Fe, Ni, and Co concentrations in eucrites can be modeled by metal‐silicate equilibrium during more or less complete melting of the eucrite parent body with subsequent fractional crystallization of olivine and orthopyroxene. However, the computed values of Mo are still too low and those of W too high when compared with Mo and W abundances in eucritic meteorites. One possibility is that the Mo and W partition coefficients strongly depend on pressure, although the howardite‐eucrite‐diogenite (HED) parent body only had a minimal pressure gradient (maximum interior pressure = 0.1 GPa). Alternatively, sulfides may have played some role in establishing Mo abundances.  相似文献   

7.
Abstract– Pd and Ag partitioning between liquid Fe metallic sulfide and liquid silicate under plausible magma ocean conditions constrains potential core 107Ag content and the origin of observed Pd and Ag mantle abundances. DPdmetallic sulfide/silicate (element concentration in metallic liquid/concentration in silicate liquid) in our experiments is insensitive to S content and temperature, but increases with total Pd content. DPdmetallic sulfide/silicate at low Pd concentration ranges from approximately 150–650. Metallic sulfide Pd content and silicate Pd content anticorrelate in our study. A curved silicate saturation surface in the Fe sulfide–silicate Pd ternary can explain both the metallic sulfide–silicate Pd anticorrelation and interstudy differences in DPdmetallic sulfide/silicate behavior. The size and shape of the curved silicate phase volume may respond to physical and chemical conditions, reducing the general applicability of D calculations. Ag becomes decreasingly siderophile as S increases: DAgmetallic sulfide/silicate decreases from 144 at 0 wt% S to 2.5 at 28 wt% S added to the starting metal sulfide liquid. Model calculations indicate that 1% core material incorporated into the Hawai’ian plume would yield a 107Ag signature on the surface smaller than detectable by current analytical techniques. Observed Pd and Ag mantle depletions relative to bulk Earth are consistent with depletions calculated with the data from this study for a magma ocean scenario without additional accretionary input after core formation.  相似文献   

8.
Abstract— Pyroxene structural data, along with analyses of titanomagnetite, fayalite and mesostasis of the new nakhlite Miller Range (MIL) 03346, define equilibration near 1 bar, 1100 °C, and oxygen fugacity near the FMQ buffer. There is a clear progression of oxygen fugacity (fO2) in Martian meteorites from reduced Allan Hills (ALH) 84001 to intermediate shergottites to oxidized nakhlites. This trend can be explained by polybaric graphite‐CO‐CO2 equilibria in the Martian mantle. Shergottites would have formed at pressures between 1.2 and 3.0 GPa, and nakhlite parent liquids formed at pressures >3.0 GPa, consistent with geochemical and petrologic data for the shergottites and nahklites. Carbon buffering in the Martian mantle could be responsible for variation in fO2 in Martian meteorites (rather than assimilation or crustal interaction), as well as C‐H‐O fluids that could be the source of ˜30 ppb CH4 detected by recent spacecraft missions. The conundrum of an oxidized current mantle and basalts, but reduced early mantle during core‐mantle equilibrium exists for both the Earth and Mars. A polybaric buffering role for graphite can explain this discrepancy for Mars, and thus it may not be necessary to have an oxidation mechanism like the dissociation of MgFe‐perovskite to account for the oxidized terrestrial mantle.  相似文献   

9.
Knowledge of Martian igneous basaltic compositions is crucial for constraining mantle evolution, including early differentiation and mantle convection. Primitive magmas provide direct information about their mantle source regions, but most Martian meteorites either contain cumulate olivine or crystallized from fractionated melts. The recently discovered Martian meteorite Northwest Africa (NWA) 5789 is an olivine‐phyric shergottite. NWA 5789 has special significance among the Martian meteorites because it appears to represent one of the most magnesian Martian magmas known, other than Yamato (Y) 980459. Its most magnesian olivine cores (Fo85) are in Mg‐Fe equilibrium with a magma of the bulk rock composition, suggesting that the bulk represents a magma composition. Based on the Al/Ti ratio of its pyroxenes, we infer that the rock began to crystallize at a high pressure consistent with conditions in Mars’ lower crust/upper mantle. It continued and completed its crystallization closer to the surface, where cooling was rapid and produced a mesostasis of radiating sprays of plagioclase and pyroxene. The mineralogy, petrology, mineral chemistry, and bulk rock composition of NWA 5789 are very similar to those of Y‐980459. The similarities between the two meteorites suggest that NWA 5789 (like Y‐980459) represents a primitive, mantle‐derived magma composition. They also suggest the possibility that NWA 5789 and Y‐980459 formed in the same lava flow. However, based on the mineralogy and texture of its mesostasis, NWA 5789 must have cooled more slowly than Y‐980459. NWA 5789 will help elucidate the igneous geology and geochemistry of Mars.  相似文献   

10.
We conducted a petrologic study of apatite within 12 Martian meteorites, including 11 shergottites and one basaltic regolith breccia. These data were combined with previously published data to gain a better understanding of the abundance and distribution of volatiles in the Martian interior. Apatites in individual Martian meteorites span a wide range of compositions, indicating they did not form by equilibrium crystallization. In fact, the intrasample variation in apatite is best described by either fractional crystallization or crustal contamination with a Cl‐rich crustal component. We determined that most Martian meteorites investigated here have been affected by crustal contamination and hence cannot be used to estimate volatile abundances of the Martian mantle. Using the subset of samples that did not exhibit crustal contamination, we determined that the enriched shergottite source has 36–73 ppm H2O and the depleted source has 14–23 ppm H2O. This result is consistent with other observed geochemical differences between enriched and depleted shergottites and supports the idea that there are at least two geochemically distinct reservoirs in the Martian mantle. We also estimated the H2O, Cl, and F content of the Martian crust using known crust‐mantle distributions for incompatible lithophile elements. We determined that the bulk Martian crust has ~1410 ppm H2O, 450 ppm Cl, and 106 ppm F, and Cl and H2O are preferentially distributed toward the Martian surface. The estimate of crustal H2O results in a global equivalent surface layer (GEL) of ~229 m, which can account for at least some of the surface features on Mars attributed to flowing water and may be sufficient to support the past presence of a shallow sea on Mars' surface.  相似文献   

11.
Abstract— Phase equilibrium experiments have been performed on a synthetic analog of the Gusev plains basalt composition from the Spirit landing site on Mars. Near‐liquidus phase relations were determined over the pressure range of 0.1 to 1.5 GPa and at temperatures from 1125 to 1390 °C in a piston cylinder apparatus and 1 atm gas mixing furnace. The composition is multiply saturated with olivine, orthopyroxene, and spinel near its liquidus at 1320 °C and 1.0 GPa, or 85 km depth on Mars, placing an upper limit constraint on the thickness of the Martian lithosphere at the time of eruption. Our experimental work suggests that the Gusev basalts are anhydrous batch melts of a primitive Martian mantle similar to the composition estimated by Dreibus and Wänke (1984). The temperature of multiple saturation indicates the persistence of high mantle potential temperatures on Mars, similar to those on the modern Earth, until at least the very latest Noachian (3.7 Ga). These high mantle temperatures would be responsible for persistent basaltic volcanism throughout the southern highlands during the first billion years of Mars's history. The source for Gusev basalts differs strongly from the source for shergottite meteorites, reinforcing the idea of the absence of global mantle convection and mixing on Mars. The existence of a relatively primitive mantle reservoir requires that at least part of the mantle underwent little modification during early planetary differentiation.  相似文献   

12.
Abstract— If Vesta is the parent body of the howardite, eucrite, and diogenite (HED) meteorites, then geo-chemical and petrologic constraints for the meteorites may be used in conjunction with astronomical constraints for the size and mass of Vesta to (1) determine the size of a possible metal core in Vesta and (2) model the igneous differentiation and internal structure of Vesta. The density of Vesta and petrologic models for HED meteorites together suggest that the amount of metal in the parent body is <25 mass%, with a best estimate of ～5%, assuming no porosity. For a porosity of up to 5% in the silicate fraction of the asteroid, the permissible metal content is <30%. These results suggest that any metal core in the HED parent body and Vesta is not unusually large. A variety of geochemical and other data for HED meteorites are consistent with the idea that they originated in a magma ocean. It appears that diogenites formed by crystal accumulation in a magma ocean cumulate pile and that most noncumulate eucrites (excepting such eucrites as Bouvante and Statinem) formed by subsequent crystallization of the residual melts. Modelling results suggest that the HED parent body is enriched in rare earth elements by a factor of ～2.5–3.5 relative to CI-chondrites and that it has approximately chondritic Mg/Si and Al/Sc ratios. Stokes settling calculations for a Vesta-wide, nonturbulent magma ocean suggest that early-crystallizing magnesian olivine, orthopyroxene, and pigeonite would have settled relatively quickly, permitting fractional crystallization to occur, but that later-crystallizing phases would have settled (or floated) an order of magnitude more slowly, allowing, instead, a closer approach to equilibrium crystallization for the more evolved (eucritic) melts. This would have inhibited the formation of a plagioclase-flotation crust on Vesta. Plausible models for the interior of Vesta, which are consistent with the data for HED meteorites and Vesta, include a metal core (<130 km radius), an olivine-rich mantle (～65–220 km thick), a lower crustal unit (～12–43 km thick) composed of pyroxenite, from which diogenites were derived, and an upper crustal unit (～23–42 km thick), from which eucrites originated. The present shape of Vesta (with ～60 km difference in the maximum and minimum radius) suggests that all of the crustal materials, and possibly some of the underlying olivine from the mantle, could have been locally excavated or exposed by impact cratering.  相似文献   

13.
Abstract— Isotopic and trace element compositions of Martian meteorites show that early differentiation of Mars produced complementary crustal and mantle reservoirs that were sampled by later magmatic events. This paper describes a mass balance model that estimates the rare earth element (REE) content and thickness of the crust of Mars from the compositions of shergottites. The diverse REE and Nd isotopic compositions of shergottites are most easily explained by variable addition of light rare earth element (LREE)–enriched crust to basaltic magmas derived from LREE-depleted mantle source regions. Antarctic shergottites EET 79001, ALH 77005, LEW 88516, and QUE 94201 all have strongly LREE-depleted patterns and positive initial 143Nd isotopic compositions, which is consistent with the generation of these magmas from depleted mantle sources and little or no interaction with enriched crust. In contrast, Shergotty and Zagami have negative initial 143Nd isotopic compositions and less pronounced depletions of the LREE, which have been explained by incorporation of enriched crustal components into mantle-derived magmas (Jones, 1989; Longhi, 1991; Borg et al., 1997). The mass balance model presented here derives the REE composition of the crustal component in Shergotty by assuming it represents a mixture between a mantle-derived magma similar in composition to EET 79001A and a LREE-enriched crustal component. The amount of crust in Shergotty is constrained by mixing relations based on Nd-isotopic compositions, which allows the REE pattern of the crustal component to be calculated by mass balance. The effectiveness of this model is demonstrated by the successful recovery of important characteristics of the Earth's continental crust from terrestrial Columbia River basalts. Self-consistent results for Nd-isotopic compositions and REE abundances are obtained if Shergotty contains ～10–30% of LREE-enriched crust with >10 ppm Nd. This crustal component would have moderately enriched LREE (Sm/Nd = 0.25–0.27; 147Sm/144Nd = 0.15–0.17; La/Yb = 2.7–3.8), relatively unfractionated heavy rare earth elements (HREE), and no Eu anomaly. Crust with these characteristics can be produced from a primitive lherzolitic Martian mantle by modest amounts (2–8%) of partial melting, and it would have a globally averaged thickness of <45 km, which is consistent with geophysical estimates. Mars may serve as a laboratory to investigate planetary differentiation by extraction of a primary basaltic crust.  相似文献   

14.
Abstract— We investigated the transfer of meteorites from Mars to Earth with a combined mineralogical and numerical approach. We used quantitative shock pressure barometry and thermodynamic calculations of post‐shock temperatures to constrain the pressure/temperature conditions for the ejection of Martian meteorites. The results show that shock pressures allowing the ejection of Martian meteorites range from 5 to 55 GPa, with corresponding post‐shock temperature elevations of 10 to about 1000 °C. With respect to shock pressures and post‐shock temperatures, an ejection of potentially viable organisms in Martian surface rocks seems possible. A calculation of the cooling time in space for the most highly shocked Martian meteorite Allan Hills (ALH) 77005 was performed and yielded a best‐fit for a post‐shock temperature of 1000 °C and a meteoroid size of 0.4 to 0.6 m. The final burial depths of the sub‐volcanic to volcanic Martian rocks as indicated by textures and mineral compositions of meteorites are in good agreement with the postulated size of the potential source region for Martian meteorites during the impact of a small projectile (200 m), as defined by numerical modeling (Artemieva and Ivanov 2004). A comparison of shock pressures and ejection and terrestrial ages indicates that, on average, highly shocked fragments reach Earth‐crossing orbits faster than weakly shocked fragments. If climatic changes on Mars have a significant influence on the atmospheric pressure, they could account for the increase of recorded ejection events of Martian meteorites in the last 5 Ma.  相似文献   

15.
Abstract— Thirteen phosphate minerals are found in IIIAB iron meteorites. Four of these (sarcopside, graftonite, johnsomervilleite, and galileiite) constitute the majority of occurrences. The IIIB iron meteorites are confined to occurrences of only these four phosphates. The IIIA iron meteorites may contain one or more of these four phases; they may also contain other rarer phosphates, and silica (in two instances) and a silicate rock (in one instance). Thus, the IIIA lithophile chemistry is more varied than that of the IIIB meteorites. Based on petrographic relations, sarcopside appears to be the first phosphate to form. Graftonite is probably formed by recrystallization of sarcopside. Johnsomervilleite and galileiite exsolved as enclaves in sarcopside or graftonite at lower temperatures, although some of these also nucleated as separate crystals. The IIIAB phosphates are carriers of a group of incompatible lithophile elements: Fe, Mn, Na, Ca, and K, and, rarely, Mg as well as Pb. These elements (and O) were concentrated in a residual, S-rich liquid during igneous fractional crystallization of the IIIAB core mass. The phosphates formed by oxidation of P as the core solidified and excluded O, which increased its partial pressure in the residual liquid. The trace siderophile trends in bulk IIIAB metal are paralleled by a mineralogical trend of the phosphate minerals that formed. For IIIAB meteorites with low-Ir contents in the metal, the phosphates are mainly Fe-Mn phases; at intermediate Ir values, more Na-bearing phosphates appear; at the highest Ir values, the rarer Na-, K-, Mg-, Cr-, and Pb-bearing phosphates appear. The absence of significant amounts of Mg, Si, Al, and Ti suggest depletion of these elements in the core by the overlying mantle.  相似文献   

16.
Abstract— The Martian meteorite Yamato (Y‐) 980459 is an olivine‐phyric shergottite. It has a very primitive character and may be a primary melt of the Martian mantle. We have conducted crystallization experiments on a synthetic Y‐980459 composition at Martian upper mantle conditions in order to test the primary mantle melt hypothesis. Results of these experiments indicate that the cores of the olivine megacrysts in Y‐980459 are in equilibrium with a melt of bulk rock composition, suggesting that these megacrysts are in fact phenocrysts that grew from a magma of the bulk rock composition. Multiple saturation of the melt with olivine and a low‐calcium pyroxene occurs at approximately 12 ± 0.5 kbar and 1540 ± 10°C, suggesting that the meteorite represents a primary melt that separated from its mantle source at a depth of ?100 km. Several lines of evidence suggest that the Y‐980459 source underwent extensive melting prior to and/or during the magmatic event that produced the Y‐980459 parent magma. When factored into convective models of the Martian interior, the high temperature indicated for the upper Martian mantle and possibly high melt fraction for the Y‐980459 magmatic event suggests a significantly higher temperature at the core‐mantle boundary than previously estimated.  相似文献   

17.
Abstract— The age, structure, composition, and petrogenesis of the martian lithosphere have been constrained by spacecraft imagery and remote sensing. How well do martian meteorites conform to expectations derived from this geologic context? Both data sets indicate a thick, extensive igneous crust formed very early in the planet's history. The composition of the ancient crust is predominantly basaltic, possibly andesitic in part, with sediments derived from volcanic rocks. Later plume eruptions produced igneous centers like Tharsis, the composition of which cannot be determined because of spectral obscuration by dust. Martian meteorites (except Allan Hills 84001) are inferred to have come from volcanic flows in Tharsis or Elysium, and thus are not petrologically representative of most of the martian surface. Remote‐sensing measurements cannot verify the fractional crystallization and assimilation that have been documented in meteorites, but subsurface magmatic processes are consistent with orbital imagery indicating thick crust and large, complex magma chambers beneath Tharsis volcanoes. Meteorite ejection ages are difficult to reconcile with plausible impact histories for Mars, and oversampling of young terrains suggests either that only coherent igneous rocks can survive the ejection process or that older surfaces cannot transmit the required shock waves. The mean density and moment of inertia calculated from spacecraft data are roughly consistent with the proportions and compositions of mantle and core estimated from martian meteorites. Thermal models predicting the absence of crustal recycling, and the chronology of the planetary magnetic field agree with conclusions from radiogenic isotopes and paleomagnetism in martian meteorites. However, lack of vigorous mantle convection, as inferred from meteorite geochemistry, seems inconsistent with their derivation from the Tharsis or Elysium plumes. Geological and meteoritic data provide conflicting information on the planet's volatile inventory and degassing history, but are apparently being reconciled in favor of a periodically wet Mars. Spacecraft measurements suggesting that rocks have been chemically weathered and have interacted with recycled saline groundwater are confirmed by weathering products and stable isotope fractionations in martian meteorites.  相似文献   

18.
We performed shock recovery experiments on an olivine‐phyric basalt at shock pressures of 22.2–48.5 GPa to compare with shock features in Martian meteorites (RBT 04261 and NWA 1950). Highly shocked olivine in the recovered basalt at 39.5 and 48.5 GPa shows shock‐induced planar deformation features (PDFs) composed of abundant streaks of defects. Similar PDFs were observed in olivine in RBT 04261 and NWA 1950 while those in NWA 1950 were composed of amorphous lamellae. Based on the present results and previous studies, the width and the abundance of lamellar fine‐structures increased with raising shock pressure. Therefore, these features could be used as shock pressure indicators while the estimated pressures may be lower limits due to no information of temperature dependence. For Martian meteorites that experienced heavy shocks, the minimum peak shock pressures of RBT 04261 and NWA 1950 are estimated to be 39.5–48.5 GPa and 48.5–56 GPa, respectively, which are found consistent with those estimated by postshock temperatures expected by the presence of brown olivine. We also investigated shock‐recovered basalts preheated at 750 and 800 °C in order to check the temperature effects on shock features. The results indicate a reduction in vitrifying pressure of plagioclase and a pressure increase for PDFs formation in olivine. Further temperature‐controlled shock recovery experiments will provide us better constraints to understand and to characterize various features found in natural shock events.  相似文献   

19.
Abstract— Noble gas data from Martian meteorites have provided key constraints about their origin and evolution, and their parent body. These meteorites have witnessed varying shock metamorphic overprinting (at least 5 to 14 GPa for the nakhlites and up to 45–55 GPa (e.g., the lherzolitic shergottite Allan Hills [ALH] A77005), solar heating, cosmic‐ray exposure, and weathering both on Mars and Earth. Influences on the helium budgets of Martian meteorites were evaluated by using a new data set and literature data. Concentrations of 3He, 4He, U, and Th are measured and shock pressures for same sample aliquots of 13 Martian meteorites were determined to asses a possible relationship between shock pressure and helium concentration. Partitioning of 4He into cosmogenic and radiogenic components was performed using the lowest 4He/3He ratio we measured on mineral separates (4He/3He = 4.1, pyroxene of ALHA77005). Our study revealed significant losses of radiogenic 4He. Systematics of cosmogenic 3He and neon led to the conclusion that solar radiation heating during transfer from Mars to Earth and terrestrial weathering can be ruled out as major causes of the observed losses of radiogenic helium in bulk meteorites. For bulk rock we observed a correlation of shock pressure and radiogenic 4He loss, ranging between ?20% for Chassigny and other moderately shocked Martian meteorites up to total loss for meteorites shocked above 40 GPa. A steep increase of loss occurs around 30 GPa, the pressure at which plagioclase transforms to maskelynite. This correlation suggests significant 4He loss induced by shock metamorphism. Noble gas loss in rocks is seen as diffusion due to (1) the temperature increase during shock loading (shock temperature) and (2) the remaining waste heat after adiabatic unloading (post shock temperature). Modeling of 4He diffusion in the main U, Th carrier phase apatite showed that post‐shock temperatures of ?300 °C are necessary to explain observed losses. This temperature corresponds to the post‐shock temperature calculated for bulk rocks shocked at about 40 GPa. From our investigation, data survey, and modeling, we conclude that the shock event during launch of the meteorites is the principal cause for 4He loss.  相似文献   

20.
Abstract— The relative abundances of the highly siderophile elements (HSE) Os, Ir, Ru, Pt, Rh, and Pd in relatively pristine lherzolites differ from solar abundance ratios and are several orders of magnitude higher than predicted for equilibrium distribution between metal/silicate (core‐mantle). The samples are characterized by a mean Ca/Al ratio of 1.18 ± 0.09 σM and a mean Ca/Si ratio of 0.10 ± 0.01 σM, overlapping with a mean Ca/Al of 1.069 ± 0.044 σM and a mean Ca/Si of 0.081 ± 0.023 σM found in chondrites (Wasson and Kallemeyn 1988). Interestingly, the CI‐normalized abundance pattern shows decreasing solar system normalized abundances with increasing condensation temperatures. The abundance of the moderately volatile element Pd is about 2x higher than those in the most refractory siderophiles Ir and Os. Thus, the HSE systematics of upper mantle samples suggest that the late bombardment, which added these elements to the accreting Earth, more closely resembles materials of highly reduced EH or EL chondrites than carbonaceous chondrites. In fact, the HSE in the Earth mantle are even more fractionated than the enstatite chondrites—an indication that some inner solar system materials were more highly fractionated than the latter.  相似文献   

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