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1.
The Antarctic shergottite EETA79001 is believed to be an impact-ejected fragment of the planet Mars. Samples of the carbonate (white druse) and the basaltic (lithology A) components from this meteorite have been found to contain amino acids at a level of approximately 1 ppm and 0.4 ppm, respectively. The detected amino acids consist almost exclusively of the L-enantiomers of the amino acids commonly found in proteins, and are thus terrestrial contaminants. There is no indication of the presence of alpha-aminoisobutyric acid, one of the most abundant amino acids in several carbonaceous chondrites. The relative abundances of amino acids in the druse material resemble those in Antarctic ice, suggesting that the source of the amino acids may be ice meltwater. The level of amino acids in EETA79001 druse is not by itself sufficient to account for the 600-700 ppm of volatile C reported in druse samples and suggested to be from endogenous martian organic material. However, estimates of total terrestrial organic C present in the druse material based on our amino acid analyses and the organic C content of polar ice can account for most of the reported putative organic C in EETA79001 druse.  相似文献   

2.
火星生命研究的进展与前景   总被引：3，自引：0，他引：3  
关于火星是否存在或曾经存在生命的争论由来已久。有人以ALH84001火星陨石新鲜破裂面上的大量碳酸盐小球体和多环芳香烃（PAHs）为主要依据，推论火星至少在13～36亿 aBP前很可能有生命形态存在。然而，很多人认为ALH84001陨石的各种特性可以是非生物成因的。由于地球上的生物在超过115℃的温度下很难存活（火星可与之类比），争论的焦点逐渐集中在碳酸盐球体的形成温度上。也有研究者关注该陨石上有机物质的来源问题。对ALH84001陨石的综合学科研究提出了互相矛盾的证据。综述了自1996年以来在国外各种主要期刊上发表的关于 ALH84001陨石与火星生命的研究成果（也包括了一些对其他火星陨石的研究），认为目前尚不能断言火星生命存在与否。对火星继续深入探索以获取进一步的证据是十分必要的。以美国国家航空和宇航局（NASA）Odys sey宇宙飞船起始的火星探测计划将引发新一轮火星生命研究的热潮。  相似文献   

3.
H isotope measurements of carbonate, phosphate, feldspathic and mafic glasses, and post-stishovite silica phase in the shergottites Zagami, Shergotty, SaU 005, DaG 476, ALHA 77005 and EETA 79001, as well as in Chassigny and ALH 84001, show that all these phases contain deuterium-enriched water of extraterrestrial origin. The minerals and glasses analyzed may contain an initial primary hydrogen component, but their isotopic composition was modified to varying degrees by three different processes: interaction with a fractionated exchangeable water reservoir on Mars, hydrogen devolatilization by impact melting, and terrestrial contamination. Positive correlations between δD and water abundance in feldspathic glass and post-stishovite silica in Zagami, Shergotty, and SaU 005 is indicative of mixing of a high δD component (3000-4000‰) and a less abundant, low δD component (∼0‰). The high δD component is primarily derived from the Martian exchangable reservoir, but may also have been influenced by isotopic fractionation associated with shock-induced hydrogen loss. The low δD component is either a terrestrial contaminant or a primary “magmatic” component. The negative correlation between δD and water abundances in mafic and feldspathic glasses in ALH 84001, ALHA 77005, and EETA 79001 is consistent with the addition of a low δD terrestrial contaminant to a less abundant high-deuterium Martian component. The low δD of magmatic glass in melt inclusions suggests that the δD of Martian parent magma was low and that the initial H isotope signature of Mars may be similar to that of Earth.  相似文献   

4.
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   

5.
The magnetites and sulfides located in the rims of carbonate globules in the Martian meteorite ALH84001 have been claimed as evidence of past life on Mars. Here, we consider the possibility that the rims were formed by dissolution and reprecipitation of the primary carbonate by the action of water. To estimate the rate of these solution-precipitation reactions, a kinetic model of magnesite-siderite carbonate dissolution was applied and used to examine the physicochemical conditions under which these rims might have formed. The results indicate that the formation of the rims could have taken place in < 50 yr of exposure to small amounts of aqueous fluids at ambient temperatures. Plausible conditions pertaining to reactions under a hypothetical ancient Martian atmosphere (1 bar CO2), the modern Martian atmosphere (8 mbar CO2), and the present terrestrial atmosphere (0.35 mbar CO2) were explored to constrain the site of the process. The results indicated that such reactions likely occurred under the latter two conditions. The possibility of Antarctic weathering must be entertained, which, if correct, would imply that the plausibly biogenic minerals (single-domain magnetite of characteristic morphology and sulfide) reported from the rims may be the products of terrestrial microbial activity. This model is discussed in terms of the available isotope data and found to be compatible with the formation of ALH84001 rims. Particularly, anticorrelated variations of radiocarbon with δ13C indicate that carbonate in ALH84001 was affected by solution-precipitation reactions immediately after its initial fall (∼13,000 yr ago) and then again during its recent exposure prior to collection.  相似文献   

6.
Using transmission electron microscopy (TEM), we have analyzed magnetite (Fe3O4) crystals acid-extracted from carbonate globules in Martian meteorite ALH84001. We studied 594 magnetites from ALH84001 and grouped them into three populations on the basis of morphology: 389 were irregularly shaped, 164 were elongated prisms, and 41 were whisker-like. As a possible terrestrial analog for the ALH84001 elongated prisms, we compared these magnetites with those produced by the terrestrial magnetotactic bacteria strain MV-1. By TEM again, we examined 206 magnetites recovered from strain MV-1 cells. Natural (Darwinian) selection in terrestrial magnetotactic bacteria appears to have resulted in the formation of intracellular magnetite crystals having the physical and chemical properties that optimize their magnetic moment. In this study, we describe six properties of magnetite produced by biologically controlled mechanisms (e.g., magnetotactic bacteria), properties that, collectively, are not observed in any known population of inorganic magnetites. These criteria can be used to distinguish one of the modes of origin for magnetites from samples with complex or unknown histories. Of the ALH84001 magnetites that we have examined, the elongated prismatic magnetite particles (similar to 27% of the total) are indistinguishable from the MV-1 magnetites in five of these six characteristics observed for biogenically controlled mineralization of magnetite crystals.  相似文献   

7.
New petrologic and bulk geochemical data for the SNC-related (Martian) meteorite ALH84001 suggest a relatively simple igneous history overprinted by complex shock and hydrothermal processes. ALH84001 is an igneous orthopyroxene cumulate containing penetrative shock deformation textures and a few percent secondary extraterrestrial carbonates. Rare earth element (REE) patterns for several splits of the meteorite reveal substantial heterogeneity in REE abundances and significant fractionation of the REEs between crushed and uncrushed domains within the meteorite. Complex zoning in carbonates indicates nonequilibrium processes were involved in their formation, suggesting that CO2-rich fluids of variable composition infiltrated the rock while on Mars. We interpret petrographic textures to be consistent with an inorganic origin for the carbonate involving dissolution-replacement reactions between CO2-charged fluids and feldspathic glass in the meteorite. Carbonate formation clearly postdated processes that last redistributed the REE in the meteorite.  相似文献   

8.
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   

9.
Shock veins and melt pockets in Lithology A of Martian meteorite Elephant Moraine (EETA) 79001 have been investigated using electron microprobe (EM) analysis, petrography and X-ray Absorption Near Edge Structure (XANES) spectroscopy to determine elemental abundances and sulfur speciation (S2− versus S6+). The results constrain the materials that melted to form the shock glasses and identify the source of their high sulfur abundances. The XANES spectra for EETA79001 glasses show a sharp peak at 2.471 keV characteristic of crystalline sulfides and a broad peak centered at 2.477 keV similar to that obtained for sulfide-saturated glass standards analyzed in this study. Sulfate peaks at 2.482 keV were not observed. Bulk compositions of EETA79001 shock melts were estimated by averaging defocused EM analyses. Vein and melt pocket glasses are enriched in Al, Ca, Na and S, and depleted in Fe, Mg and Cr compared to the whole rock. Petrographic observations show preferential melting and mobilization of plagioclase and pyrrhotite associated with melt pocket and vein margins, contributing to the enrichments. Estimates of shock melt bulk compositions obtained from glass analyses are biased towards Fe- and Mg- depletions because, in general, basaltic melts produced from groundmass minerals (plagioclase and clinopyroxene) will quench to a glass, whereas ultramafic melts produced from olivine and low-Ca pyroxene megacrysts crystallize during the quench. We also note that the bulk composition of the shock melt pocket cannot be determined from the average composition of the glass but must also include the crystals that grew from the melt - pyroxene (En72-75Fs20-21Wo5-7) and olivine (Fo75-80). Reconstruction of glass + crystal analyses gives a bulk composition for the melt pocket that approaches that of lithology A of the meteorite, reflecting bulk melting of everything except xenolith chromite.Our results show that EETA79001 shock veins and melt pockets represent local mineral melts formed by shock impedance contrasts, which can account for the observed compositional anomalies compared to the whole rock sample. The observation that melts produced during shock commonly deviate from the bulk composition of the host rock has been well documented from chondrites, rocks from terrestrial impact structures and other Martian meteorites. The bulk composition of shock melts reflects the proportions of minerals melted; large melt pockets encompass more minerals and approach the whole rock whereas small melt pockets and thin veins reflect local mineralogy. In the latter, the modal abundance of sulfide globules may reach up to 15 vol%. We conclude the shock melt pockets in EETA79001 lithology A contain no significant proportion of Martian regolith.  相似文献   

10.
A simple synthesis of various forms of calcium carbonate with spherical and 'floral' morphologies is reported. Vaterite formation occurs at approximately 25 degrees C, aragonite at approximately 70 degrees C and calcite at about approximately 80 degrees C. These are produced when CO2 is reacted with an aqueous solution of calcium chloride in the presence of ammonia. These conditions may have existed at the surface of Mars in the past, leading us to conclude that such mineral formations may be common there. Although the initial phases are modified over time with changing temperature and pressure conditions, they still influence the final morphology of the carbonates observed. A comparison of these structures with those found in the Martian meteorite ALH84001 suggests, but does not confirm, a non-biogenic origin for the ALH84001 carbonates.  相似文献   

11.
The carbonates in martian meteorite ALH84001 preserve a record of aqueous processes on Mars at 3.9 Ga, and have been suggested to contain signatures of ancient martian life. The conditions of the carbonate formation environment are critical for understanding possible evidence for life on Mars, the history of water on Mars, and the evolution of the martian atmosphere. Despite numerous studies of petrographic relationships, microscale oxygen isotope compositions, microscale chemical compositions, and other minerals associated with the carbonates, formation models remain relatively unconstrained. Microscale carbon isotope analyses of ALH84001 carbonates reveal variable δ13C values ranging from +27 to +64‰. The isotopic compositions are correlated with chemical composition and extent of crystallization such that the Mg-poor, early-formed carbonates are relatively 13C depleted and the Mg-rich, later forming carbonates, are 13C enriched. These data are inconsistent with many of the previously proposed environments for carbonate formation, and a new set of hypotheses are proposed. Specifically, two new models that account for the data involve low temperature (<100°C) aqueous processes: (1) the carbonates formed during mixing of two fluids derived from separate chemical and isotopic reservoirs; or (2) the carbonates formed from high pH fluids that are exposed to a CO2-rich atmosphere and precipitate carbonate, similar to high pH springs on Earth.  相似文献   

12.
Oxygen isotope ratios of merrillite and chlorapatite in the Martian meteorites ALH84001 and Los Angeles have been measured by ion microprobe in multicollector mode. δ18O values of phosphate minerals measured in situ range from ∼3 to 6‰, and are similar to Martian meteorite whole-rock values, as well as the δ18O of igneous phosphate on Earth. These results suggest that the primary, abiotic, igneous phosphate reservoir on Mars is similar in oxygen isotopic composition to the basaltic phosphate reservoir on Earth. This is an important first step in the characterization of Martian phosphate reservoirs for the use of δ18O of phosphate minerals as a biomarker for life on Mars. Cumulative textural, major-element, and isotopic evidence presented here suggest a primary, igneous origin for the phosphates in Los Angeles and ALH84001; textural and chemical evidence suggests that phosphates in ALH84001 were subsequently shock-melted in a later event.  相似文献   

13.
Small, discoid globules and networks of magnesium-iron-calcium carbonates occur within impact-produced fracture zones in the ALH84001 Martian meteorite. Because these carbonates contain or are associated with the hydrocarbons, single-domain magnetite and iron-sulfide grains, and purported microfossils that collectively have been cited as evidence for ancient Martian life, it is critically important to understand their formation. Previous hypotheses for the origin of the carbonates involve either alteration of the rock by hydrothermal fluids at relatively low temperatures, or formation from a CO2-rich vapor at high temperatures. This paper explores an alternative mechanism–direct precipitation from a ponded evaporating brine infiltrating into fractures in the floor of an impact crater. Such a model can be reconciled with the observed carbonate compositional zoning and extreme stable-isotopic fractionations. If the carbonates formed in this manner, this removes a possible obstacle to the proposed existence of microbial remains in ALH84001; however, the cited evidence for life can be better explained by inorganic processes expected from brines in an evaporating alkaline lake, with an overprint of shock metamorphism and subsequent contamination by organic matter after falling to Earth.  相似文献   

14.
The oxygen (δ18O, δ17O) and carbon (δ13C, FMOD14C-the fraction of modern 14C) isotopic compositions of carbonate were measured for a set of paired Antarctic CM chondrites (EET 96006, EET 96016, EET 96017, and EET 96019). While the oxygen isotopic compositions do not plot on the terrestrial fractionation line and indicate that a component of the carbonate minerals has an extraterrestrial origin, they also do not fall on the array defined for carbonates by CM falls and are thus consistent with the presence of a terrestrial carbonate component. The δ13C and FMOD14C measurements of carbonate suggest the presence of at least two carbon sources: carbonate derived from atmospheric CO2 that is inferred to have been produced as a result of silicate weathering reactions and carbonate derived from another carbon source that is either old or non-atmospheric. The relationships between oxygen and carbon isotope data provide additional constraints on the weathering process, and allow the possibility that rock-dominated weathering of the meteorite caused the oxygen isotopic composition of Antarctic water added to the meteorite to evolve away from the terrestrial mass-fractionation array, leading to formation of low temperature terrestrial alteration products that do not lie on the terrestrial fractionation line.  相似文献   

15.
ALH84001, a cataclastic cumulate orthopyroxenite meteorite from Mars, has been dated by Ar-Ar stepped heating and laser probe methods. Both methods give ages close to 3,900 Ma. The age calculated is dependent on assumptions made about 39Ar recoil effects and on whether significant quantities of 40Ar from the Martian atmosphere are trapped in the meteorite. If, as suggested by xenon and nitrogen isotope studies, Martian atmospheric argon is present, then it must reside predominantly in the K-rich phase maskelynite. Independently determined 129Xe abundances in the maskelynite can be used to place limits on the concentration of the atmospheric 40Ar. These indicate a reduction of around 80 Ma to ages calculated on the assumption that no Martian atmosphere is present. After this correction, the nominal ages obtained are: 3940 +/- 50, 3870 +/- 80, and 3970 +/- 100 Ma. by stepped heating, and 3900 +/- 90 Ma by laser probe (1 sigma statistical errors), giving a weighted mean value of 3,920 Ma. Ambiguities in the interpretation of 39Ar recoil effects and in the contribution of Martian atmospheric 40Ar lead to uncertainties in the Ar-Ar age which are difficult to quantify, but we suggest that the true value lies somewhere between 4,050 and 3,800 Ma. This age probably dates a period of annealing of the meteorite subsequent to the shock event which gave it its cataclastic texture. The experiments provide the first evidence of an event occurring on Mars coincident with the time of the late heavy bombardment of the Moon and may reflect a similar period of bombardment in the Southern Highlands of Mars. Whether the age determined bears any relationship to the time of carbonate deposition in ALH84001 is not known. Such a link depends on whether the temperature associated with the metasomatic activity was sufficient to cause argon loss from the maskelynite and/or whether the metasomatism and metamorphism were linked in time through a common heat source.  相似文献   

16.
我国南极陨石研究与展望   总被引：2，自引：0，他引：2  
继1998～2000年我国第15、16次南极科考队在南极格罗夫山发现32块陨石之后，2002～2003年第19次科考队成立了以回收陨石为中心任务的格罗夫山综合考察分队，在同一地区成功回收4448块陨石。我国的南极陨石回收工作不但实现了零的突破，而且成为继日本和美国之后拥有南极陨石数量最多的国家之一。通过对第15、16次队回收的32块陨石以及第19次队4448块陨石中的38块代表性样品的化学一岩石类型划分工作,除平衡型普通球粒陨石外，发现了2块火星陨石、2块橄辉无球粒陨石、6块非平衡L3型陨石、4块碳质球粒陨石和1块非平衡型顽辉石球粒陨石等特殊类型陨石。本文主要介绍了南极陨石的回收和研究进展，以及我国在南极格罗夫山回收陨石的情况和已取得的初步研究成果。同时对我国今后的陨石回收与研究工作提出初步设想。  相似文献   

17.
南极陨石的研究发现，有几个碳质球粒陨石富含与ＣＩ陨石类似的含水层状硅酸盐集合体及其角砾，其氧同位素比值也与ＣＩ接近，因而称之为类Ｃ１陨石。类Ｃ１陨石与Ｃ１陨石的区别是：类Ｃ１陨石中的含水层状硅酸盐既以基质的形式产出，也出现在球粒中；类Ｃ１陨石中含有球粒及有关组分，如球粒碎块、矿物集合体等。每个陨石中所含这些组分的数量不同，其矿物的成分也差别很大，从而说明它们形成的星云环境不同。因此笔者认为类Ｃ１陨  相似文献   

18.
南极陨石的研究发现，有几个碳质球粒陨石富含与Ｃ１陨石类似的含水层状硅酸盐集合体及其角砾．其氧同位素比值也与Ｃ１接近，因而称之为类Ｃ１陨石。类Ｃ１陨石与Ｃ１陨石的区别是：类Ｃ１陨石中的含水层状硅酸盐既以基质的形式产出，也出现在球粒中；类Ｃ１陨石中含有球粒及有关组分，如球粒碎块、矿物集合体等。每个陨石中所含这些组分的数量不同，其矿物的成分也差别很大，从而说明它们形成的星云环境不同。因此笔者认为类Ｃ１陨石可能是小行星区星云盘外层的星云凝聚物受到不同程度水化作用后吸积形成的陨石。  相似文献   

19.
Martian meteorite Allan Hills (ALH) 84001 contains sub-micron magnetite grains, suggested to be of biogenic origin, in its globules of Fe-Mg carbonate mineral. There is disagreement on whether the low Mg content of the magnetite could only arise from biological metabolism ( [Treiman, 2003] and [Thomas-Keprta et al., 2009]). However, constraints on the magnetite’s biogenicity are far less certain than had been inferred. The thermochemical bases for the equilibrium calculations are reviewed in detail; there are inconsistencies and gaps in fundamental data for siderite, macromolecular carbons, and magnesioferrite. The calculations of Treiman (2003), assuming formation of magnetite via “siderite = magnetite + CO2 + CO”, are incorrect because of a flaw in the computer code used. The corrected location of this equilibrium (Thomas-Keprta et al., 2009) is no longer crucial, because of recent finds that the magnetite grains are associated with macromolecular carbon; this implies that the dominant magnetite-forming reaction was “siderite = magnetite + CO2 + C”. From the location of this equilibrium, using the corrected computer code and best available thermochemical data, the Mg-poor magnetite grains (and macromolecular carbon) in carbonates in ALH 84001 could have formed by decomposition of the carbonates at geologically reasonable pressures and temperatures. The low-Mg compositions of the magnetite grains remain consistent with an abiotic origin within the known geological history of ALH 84001.  相似文献   

20.
Thermal decomposition of siderite has been proposed as a source of magnetite in martian meteorites. Laboratory experiments were conducted to evaluate the possibility that this process might also result in abiotic synthesis of organic compounds. Siderite decomposition in the presence of water vapor at 300°C generated a variety of organic products dominated by alkylated and hydroxylated aromatic compounds. The results suggest that formation of magnetite by thermal decomposition of siderite on the precursor rock of the martian meteorite ALH84001 would have been accompanied by formation of organic compounds and may represent a source of extraterrestrial organic matter in the meteorite and on Mars. The results also suggest that thermal decomposition of siderite during metamorphism could account for some of the reduced carbon observed in metasedimentary rocks from the early Earth.  相似文献   

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