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1.
Abstract— In a study of the isotopic signatures of trapped Xe in shock-produced glass of shergottites and in ALH 84001, we observe three components: (1) modern Martian atmospheric Xe that is isotopically mass fractionated relative to solar Xe, favoring the heavy isotopes, (2) solar-like Xe, as previously observed in Chassigny, and (3) an isotopically fractionated (possibly ancient) component with little or no radiogenic 129Xerad. In situ-produced fission and spallation components are observed predominantly in the high-temperature steps. Heavy N signatures in ALH 84001, EET 79001 and Zagami reveal Martian atmospheric components. The low-temperature release of ALH 84001 shows evidence for the presence of a light N component (δ15N ≤ -21%), which is consistent with the component observed in the other Shergotty, Nakhla and Chassigny (SNC) group meteorites. The highest observed 129Xe/130Xe ratio of 15.60 in Zagami and EET 79001 is used here to represent the present Martian atmospheric component, and the isotopic composition of this component is compared with other solar system Xe signatures. The 129Xe/130Xe ratios in ALH 84001 are lower but appear to reflect varying mixing ratios with other components. The consistently high 129Xe/130Xe ratios in rocks of different radiometric ages suggest that Martian atmospheric Xe evolved early on. As already concluded in earlier work, only a small fission component is observed in the Martian atmospheric component. Assuming that a chondritic 244Pu/129I initial ratio applies to Mars, this implies that either Pu-derived fission Xe is retained in the solid planet (in fact, in situ-produced fission Xe is observed in ALH 84001) or may reflect a very particular degassing history of the planet.  相似文献   

2.
Heterogeneities in terrestrial samples for 182W/183W and 142Nd/144Nd are only preserved in Hadean and Archean rocks while heterogeneities in 129Xe/130Xe and 136Xe/130Xe persist to very young mantle‐derived rocks. In contrast, meteorites from Mars show that the Martian mantle preserves heterogeneities in 182W/183W and 142Nd/144Nd up to the present. As a consequence of the probable “deep magma ocean” core formation process, we assume that the Earth and Mars both had a very early two‐mantle‐reservoir structure with different initial extinct nuclide isotopic compositions (different 182W/183W, 142Nd/144Nd, 129Xe/130Xe, 136Xe/130Xe ratios). Based on this assumption, we developed a simple stochastic model to trace the evolution of a mantle with two initially distinct layers for the extinct isotopes and its development into a heterogeneous mantle by convective mixing and stretching of these two layers. Using the extinct isotope system 182Hf‐182W, we find that the mantles of Earth and Mars exhibit substantially different mixing or stirring rates. This is consistent with Mars having cooled faster than the Earth due to its smaller size, resulting in less efficient mantle mixing for Mars. Moreover, the mantle stirring rate obtained for Earth using 182Hf‐182W is consistent with the mantle stirring rate of ~500 Myr constrained by the long‐lived isotope system, 87Rb‐87Sr and 147Sm‐143Nd. The apparent absence of 182W/183W isotopic heterogeneity in modern terrestrial rocks is attributed to very active mantle stirring which reduced the 182W/183W isotopic heterogeneity to a relatively small scale (~83 m for a mantle stirring rate of 500 Myr) compared to the common sampling scale of terrestrial basalts (~30 or 100 km). Our results also support the “deep magma ocean” core formation model as being applicable to both Mars and Earth.  相似文献   

3.
We report new data from Pesyanoe‐90,1 (dark lithology) on the isotopic signature of solar wind (SW) Xe as recorded in this enstatite achondrite which represents a soil‐breccia of an asteroidal regolith. The low temperature (≤800°C) steps define the Pesyanoe‐S xenon component, which is isotopically consistent with SW Xe reported for the lunar regolith. This implies that the SW Xe isotopic signature was the same at two distinct solar system locations and, importantly, also at different times of solar irradiation. Further, we compare the calculated average solar wind “SW‐Xe” signature to Chass‐S Xe, the indigenous Xe observed in SNC (Mars) meteorites. Again, a close agreement between these compositions is observed, which implies that a mass‐dependent differential fractionation of Xe between SW‐Xe and Chass‐S Xe is >1.5%o per amu. We also observe fractionated (Pesyanoe‐F) Xe and Ar components in higher temperature steps and we document a fission component due to extinct 244Pu. Interestingly, the Pesyanoe‐F Xe component is revealed only at the highest temperatures (>1200°C). The Pesyanoe‐F gas reveals Xe isotopic signatures that are consistent with lunar solar energetic particles (SEP) data and may indicate a distinct solar energetic particle radiation as was inferred for the moon. However, we cannot rule out fractionation processes due to parent body processes. We note that ratios 36Ar/38Ar≤5 are also consistent with SEP data. Calculated abundances of the fission component correlate well with radiogenic 40Ar concentrations, revealing rather constant 244Pu/K ratios in Pesyanoe, and separates thereof, and indicate that both components were retained. We identify a nitrogen component (δ15N = 44%o) of non‐solar origin with an isotopic signature distinct from indigenous N (δ15N = ?33%o). While large excesses at 128Xe and 129Xe are observed in the lunar regolith samples, these excesses in Pesyanoe are small. On the other hand, significant 126Xe isotopic excesses, comparable to relative excesses observed in lunar soils and breccias, are prominent in the intermediate temperature steps of Pesyanoe‐90,1.  相似文献   

4.
Noble gases in the five angrites Northwest Africa (NWA) 1296, 2999, 4590, 4801, and 4931 were analyzed with total melting and stepwise heating methods. The noble gases consist of in situ components: spallogenic, radiogenic, nucleogenic, and fission. Cosmic-ray exposure ages of the angrites (including literature data) spread uniformly from <0.2 to 56 Ma, and coarse-grained angrites have longer exposure ages than fine-grained angrites. It is implied that the parent bodies from which the two subgroups of angrites were ejected are different and have distinct orbital elements. The 244Pu-136Xe relative ages of the angrites obtained by using 244Pu/150Nd ratios are as old as that of Angra dos Reis, reflecting their early formation. On the other hand, another method to obtain 244Pu-136Xe relative ages, using fission 136Xe, spallogenic 126Xe, and Ba/REE ratios, yields systematically older 244Pu-136Xe ages than those obtained by using 244Pu/150Nd ratios, which is explained by apparently high Ba/REE ratios caused by Ba contamination during terrestrial weathering. The 244Pu/238U ratio at 4.56 Ga of angrites is estimated as 0.0061 ± 0.0028, which is consistent with those for chondrules, chondrites, achondrites, and a terrestrial zircon. It is suggested that initial 244Pu/238U ratio has been spatially homogeneous at least in the inner part of the early solar system.  相似文献   

5.
《Icarus》1987,71(2):225-240
Based on our new and previous determinations of halogens in SNC meteorites, the bulk concentrations of halogens in the SPB, which is thought to be Mars, are estimated. The two-component model for the formation of terrestrial planets as proposed byA. E. Ringwood (Geochem. J. 11, 111–135 (1977) andOn the Origin of the Earth and Moon, Springer-Verlag, New York, 1979) andH. Wa¨nke (Philos. Trans. Roy. Soc. London, Ser. A 303, 287–302 (1981) is further substantiated. It is argued that almost all of the H2O added to Mars during its homogeneous accretion was converted on reaction with metallic Fe to H2, which escaped. By comparing the solubilities of H2O and HCl in molten silicates, the amount of H2O left in the mantle of Mars at the end of accretion can be related to the abundance of Cl. In this way an H2O content in the Martian mantle of 36 ppm is obtained, corresponding to an ocean covering the whole planet to a depth of about 130 m.The huge quantities of H2 produced by the reaction of H2O with metallic iron should also have removed other volatile species by hydrodynamic escape. Thus it is postulated that the present atmospheres of Venus, Earth, and Mars were formed by degassing the interiors of the planets, after the production of H2 had ceased, i.e., after metallic iron was no longer available. It is also postulated that the large differences in the amounts of primordial rare gases in the atmospheres of Venus, Earth, and Mars are due mainly to different loss factors.Except for gaseous species, Mars is found to be richer in volatile (halogens) and moderately volatile elements than the Earth. The resulting low release factor of40Ar for Mars is attributed to a low degree of fractionation, leading to a relatively small crustal enrichment of even the most incompatible elements like K.  相似文献   

6.
We analyzed noble gases in nine individual chondrules, an assemblage of small chondrules, and four whole‐rock samples of the Allende CV3 chondrite. Major elements were also determined for five chondrules. The cosmic ray exposure ages are calculated from cosmogenic 3He to be 5.17 ± 0.38 and 5.15 ± 0.25 Myr for the averages of the chondrules and whole rocks, respectively, showing no significant pre‐exposure evidence for the studied chondrules. Large amounts of 36Ar, 80,82Kr, and 128Xe produced by neutron capture are observed in most samples; the abundances of these nuclides are correlated among the samples. The epithermal neutron flux and neutron slowing down density are calculated based on [80Kr]n, from which a sample depth of about 30 cm can be calculated. The measured chondrules contain variable amounts of radiogenic 129Xe. The abundance ratios of radiogenic 129Xe to neutron capture–produced 128Xe are rather constant among the studied chondrules; four chondrules give more precise ratios at the high‐temperature fractions, ranging from 1920 ± 80 to 2280 ± 140, which corresponds to a time difference of 3.9 ± 2.4 Myr. It is noticeable that most chondrules also contain 244Pu‐derived fission Xe. The average 244Pu/238U ratio for nine chondrules is 0.0069 ± 0.0018, which agrees well with the preferred ratio reported for chondrites.  相似文献   

7.
A new composition of primordial terrestrial xenon is derived, on the assumption that it lies on an extension of the mixing line between solar Xe and anomalous (CCF) Xe in carbonaceous chondrites. With this composition, the apparent fission components in atmospheric and well gas Xe become larger, and resemble 244Pu fission xenon.  相似文献   

8.
Abstract— Considerable evidence points to a martian origin of the SNC meteorites. Noble gas isotopic compositions have been measured in most SNC meteorites. The 129Xe/132Xe vs. 84Kr/132Xe ratios in Chassigny, most shergottites, and lithology C of EETA 79001 define a linear array. This array is thought to be a mixing line between martian mantle and martian atmosphere. One of the SNC meteorites, Nakhla, contains a leachable component that has an elevated 129Xe/132Xe ratio relative to its 84Kr/132Xe ratio when compared to this approximately linear array. The leachable component probably consists in part of iddingsite, an alteration product produced by interaction of olivine with aqueous fluid at temperatures lower than 150 °C. The elevated Xe isotopic ratio may represent a distinct reservoir in the martian crust or mantle. More plausibly, it is elementally fractionated martian atmosphere. Formation of sediments fractionates the noble gases in the correct direction. The range of sediment/atmosphere fractionation factors is consistent with the elevated 129Xe/132Xe component in Nakhla being contained in iddingsite, a low temperature weathering product. The crystallization age of Nakhla is 1.3 Ga. Its low-shock state suggests that it was ejected from near the surface of Mars. As liquid water is required for the formation of iddingsite, these observations provide further evidence for the near surface existence of aqueous fluids on Mars more recently than 1.3 Ga.  相似文献   

9.
M. Ozima  Y.N. Miura 《Icarus》2004,170(1):17-23
Surface-correlated noble gases in lunar soils are primarily implanted SW (solar wind) noble gases. However, they also include apparently orphan radiogenic 40Ar, 129Xe, and 244Pu-derived fission Xe in excess of plausible primordial solar origin. These orphan radiogenic components are usually assigned a lunar origin, in a scenario in which radiogenic noble gases produced in the lunar interior were degassed into the transient atmosphere and then re-implanted to the lunar surface together with SW. There are some quantitative difficulties with this scenario, however, and it requires special constraints on the degassing history of the Moon that have not emerged from more general thermal history models. We therefore urge consideration of alternative hypotheses. As a possible source for the orphan radiogenic noble gases, we have examined planetary pollution of the Sun, as suggested by studies of extrasolar planetary systems (e.g., Murray et al., 2001, Astrophys. J. 555, 801-815; Israelian et al., 2001, Nature 411, 163-166). Pollution of the Sun by 2M⊕ (two Earth mass) planetary materials (Murray et al., 2001, Astrophys. J. 555, 801-815) is likely not significant for Ar but could be important to account for orphan Xe in the Moon.  相似文献   

10.
Abstract— Possible evidence for the presence of 248Cm in the early Solar System was reported from fission gas studies (Rao and Gopalan, 1973) and recently from studies of very high nuclear track densities (≥ 5 × 10g cm?2) in the merrillite of the H4 chondrite Forest Vale (F. V.) (Pellas et al., 1987). We report here an analysis of the isotopic abundances of xenon in F. V. phosphates and results of track studies in phosphate/pyroxene contacts. The fission xenon isotopic signature clearly identifies 244Pu as the extinct progenitor. We calculate an upper limit 248Cm/244Pu < 1.5 × 10?3 at the beginning of Xe retention in F. V. phosphates. This corresponds to an upper limit of the ratio 248Cm/235U ≤ 5 × 10?5, further constraining the evidence for any late addition of freshly synthesized actinide elements just prior to Solar System formation. The fission track density observed after annealing the phosphates at 290 °C (1 hr, which essentially erases spallation recoil tracks) is also in agreement with the 244Pu abundance inferred from fission Xe. The spallation recoil tracks produced during the 76 Ma cosmic-ray exposure account for the very high track density in merrillites.  相似文献   

11.
Analysis of abundance patterns of rare gases Ne22, Ar36, Kr84 and Xe130 on Earth and in ordinary and carbonaceous chondrites is presented. A mechanism of chemical adsorption of rare gases at the planetesimal stage during their accretion is proposed to generate the abundance pattern of the heavy rare gases on the Earth. The calculated values for Xe and Kr agree well with the observed values whereas for Ar, the agreement is poor.  相似文献   

12.
Abstract The 244Pu-fission-136Xe retention ages of howardites, eucrites, and diogenites (HEDs) show that these meteorites have retained Xe since they were formed about 4500 Ma ago. For the Garland diogenite and the Millbillillie eucrite, we obtain fission Xe ages of 4525 ± 40 Ma and 4486 ± 40 Ma, respectively. If Xe isotope data reported by other workers are also considered, we conclude that the monomict equilibrated eucrites Camel Donga, Juvinas, and Millbillillie formed about 40 Ma later than Pasamonte, a polymict unequilibrated eucrite. Stannern, a monomict equilibrated brecciated eucrite, yields a 244Pu-136Xe age of 4442 Ma. The 40K-40Ar retention ages fall, for most HEDs, into the 1000–4000 Ma age range, indicating that 40Ar is generally not well retained. The good retentivity for Xe of HEDs allows us to study primordial trapped Xe in these meteorites. Except for Shalka, in which other authors found Kr and Xe from terrestrial atmospheric contamination only, we present for the first time Kr and Xe isotopic data for diogenites. We studied Ellemeet, Garland, Ibbenbühren, Shalka, and Tatahouine. We show that Tatahouine contains two types of trapped Xe: a terrestrial contamination acquired by an irreversible adsorption process and released at pyrolysis temperatures up to 800 °C, and indigenous primordial Xe released primarily between 800 °C and 1200 °C. The isotopic composition of this primordial Xe is identical to that proposed earlier to be present in primitive achondrites and termed U-Xe or “primitive” Xe, but it has not been directly observed in achondrites until now. This type of primitive Xe is important for understanding the evolution of other Xe reservoirs in the Solar System. Terrestrial atmospheric Xe (corrected for fission Xe and radiogenic Xe from outgassing of the Earth) is related to it by a mass dependent fractionation favoring the heavier Xe isotopes. This primitive Xe is isotopically very similar to solar Xe except for 134Xe and 136Xe. Solar Xe appears to contain an enrichment of unknown origin for these isotopes relative to the primitive Xe.  相似文献   

13.
The radiogenic and primordial noble gas content of the atmospheres of Venus, Earth, and Mars are compared with one another and with the noble gas content of other extraterrestial samples, especially meteorites. The fourfold depletion of 40Ar for Venus relative to the Earth is attributed to the outgassing rates and associated tectonics and volcanic styles for the two planets diverging significantly within the first billion or so years of their history, with the outgassing rate for Venus becoming much less than that for the Earth at subsequent times. This early divergence in the tectonic style of the two planets may be due to a corresponding early onset of the runaway greenhouse on Venus. The 16-fold depletion of 40Ar for Mars relative to the Earth may be due to a combination of a mild K depletion for Mars, a smaller fraction of its interior being outgassed, and to an early reduction in its outgassing rate. Venus has lost virtually all of its primordial He and some of its radiogenic He. The escape flux of He may have been quite substantial in Venus' early history, but much diminished at later times, with this time variation being perhaps strongly influenced by massive losses of H2 resulting from efficient H2O loss processes.Key trends in the primordial noble gas content of terrestial planetary atmospheres include (1) a several orders of magnitude decrease in 20Ne and 36Ar from Venus to Earth to Mars; (2) a nearly constant 20Ne/36Ar ratio which is comparable to that found in the more primitive carbonaceous chondrites and which is two orders of magnitude smaller than the solar ratio; (3) a sizable fractionation of Ar, Kr, and Xe from their solar ratios, although the degree of fractionation, especially for 36Ar/132Xe, seems to decrease systematically from carbonaceous chondrites to Mars to Earth to Venus; and (4) large differences in Ne and Xe isotopic ratios among Earth, meteorites, and the Sun. Explaining trends (2), (2) and (4), and (1) pose the biggest problems for the solar-wind implantation, primitive atmosphere, and late veneer hypotheses, respectively. It is suggested that the grain-accretion hypothesis can explain all four trends, although the assumptions needed to achieve this agreement are far from proven. In particular, trends (1), (2), (3), and (4) are attributed to large pressure but small temperature differences in various regions of the inner solar system at the times of noble gas incorporation by host phases; similar proportions of the host phases that incorporated most of the He and Ne on the one hand (X) and Ar, Kr, and Xe on the other hand (Q); a decrease in the degree of fractionation with increasing noble-gas partial pressure; and the presence of interstellar carriers containing isotopically anomalous noble gases.Our analysis also suggests that primordial noble gases were incorporated throughout the interior of the outer terrestial planets, i.e., homogeneous accretion is favored over inhomogeneous accretion. In accord with meteorite data, we propose that carbonaceous materials were key hosts for the primordial noble gases incorporated into planets and that they provided a major source of the planets' CO2 and N2.  相似文献   

14.
Abstract— The flux of galactic cosmic rays (GCR) in the solar system appears to change with time. Based on the abundances in iron meteorites of cosmogenic nuclides of different half lives, Lavielle et al. (1999) found that the GCR flux increased in recent times (<100 Ma) by about 38% compared to average flux in the past 150 Ma to 700 Ma ago. A promising technique for calibrating the GCR flux during the past ?50 Ma, based on the 129I and 129Xe pair of nuclides, was discussed earlier (Marti 1986; Murty and Marti 1987). The 129I‐129Xen chronometer provides a shielding‐independent system as long as the exposure geometry remained fixed. It is especially suitable for large iron meteorites (Te‐rich troilite) because of the effects by the GCR secondary neutron component. Although GCR‐produced Xe components were identified in troilites, several issues require clarifications and improvements; some are reported here. We developed a procedure for achieving small Xe extraction blanks which are required to measure indigenous Xe in troilites. The 129Xe and 131Xe excesses (129Xen, 131Xen) due to neutron reactions in Te are correlated in a stepwise release run during the troilite decomposition. Our data show that indigenous Xe in troilite of Cape York has isotopic abundances consistent with ordinary chondritic Xe (OC‐Xe), in contrast to a terrestrial signature which was reported earlier. Two methods are discussed which assess and correct for an interfering radiogenic 129Xer component from extinct 129I. The corrected 129Xen concentration in troilite D4 of Cape York yields a cosmic ray exposure (CRE) age of 82 ± 7 Ma consistent, within uncertainties, with reported data (Murty and Marti 1987; Marti et al. 2004).  相似文献   

15.
The presence of methane on Mars is of great interest, since one possibility for its origin is that it derives from living microbes. However, CH4 in the martian atmosphere also could be attributable to geologic emissions released through pathways similar to those occurring on Earth. Using recent data on methane degassing of the Earth, we have estimated the relative terrestrial contributions of fossil geologic methane vs. modern methane from living methanogens, and have examined the significance that various geologic sources might have for Mars.Geologic degassing includes microbial methane (produced by ancient methanogens), thermogenic methane (from maturation of sedimentary organic matter), and subordinately geothermal and volcanic methane (mainly produced abiogenically). Our analysis suggests that ～80% of the “natural” emission to the terrestrial atmosphere originates from modern microbial activity and ～20% originates from geologic degassing, for a total CH4 emission of ～28.0×107 tonnes year?1.Estimates of methane emission on Mars range from 12.6×101 to 57.0×104 tonnes year?1 and are 3–6 orders of magnitude lower than that estimated for Earth. Nevertheless, the recently detected martian, Northern-Summer-2003 CH4 plume could be compared with methane expulsion from large mud volcanoes or from the integrated emission of a few hundred gas seeps, such as many of those located in Europe, USA, Mid-East or Asia. Methane could also be released by diffuse microseepage from martian soil, even if macro-seeps or mud volcanoes were lacking or inactive. We calculated that a weak microseepage spread over a few tens of km2, as frequently occurs on Earth, may be sufficient to generate the lower estimate of methane emission in the martian atmosphere.At least 65% of Earth’s degassing is provided by kerogen thermogenesis. A similar process may exist on Mars, where kerogen might include abiogenic organics (delivered by meteorites and comets) and remnants of possible, past martian life. The remainder of terrestrial degassed methane is attributed to fossil microbial gas (～25%) and geothermal-volcanic emissions (～10%). Global abiogenic emissions from serpentinization are negligible on Earth, but, on Mars, individual seeps from serpentinization could be significant. Gas discharge from clathrate-permafrost destabilization should also be considered.Finally, we have shown examples of potential degassing pathways on Mars, including mud volcano-like structures, fault and fracture systems, and major volcanic edifices. All these types of structures could provide avenues for extensive gas expulsion, as on Earth. Future investigations of martian methane should be focused on such potential pathways.  相似文献   

16.
We show that the surface of a planet growing by planetesimal impact is heated over the melting temperature of the surface materials due to the blanketing effect of an impact induced H2O atmosphere with the present H2O abundance of the Earth even when the accretion time is as long as 108 years. Hence, a magma ocean covering the entire surface was formed on the Earth and Moon and other terrestrial planets during their formations.  相似文献   

17.
The evidence forin situ produced fission xenon from244Pu in rock 14321 is presented. The inferred abundance ratio244Pu/238U is found to be consistent with values observed in a meteorite. Data from a stepwise release of the xenon permits a characterization of the trapped component, which can be shown to be distinct from solar xenon. We discuss the evidence for the presence of fission gases and of uncorrelated radiogenic argon in this and in other Apollo 14 rocks and some implications regarding their origin.Paper dedicated to Prof. Harold C. Urey on the occasion of his 80th birthday on 29 April 1973.  相似文献   

18.
Carbon and oxygen isotopes show no large anomalies on Venus (10–15%) or Mars (<5%); the high value of15N/14N found on Mars is explained by non-thermal escape of nitrogen. The isotopes of non-radiogenic noble gases in the atmosphere of Mars exhibit abundance patterns similar to those in the primordial component of meteoritic gases and in the Earth's atmosphere. This implies that gas fractionation took place in the inner solar nebula prior to planet formation. The relatively high value of129Xe on Mars emphasizes its deficiency on Earth, implying a difference in accretion histories of volatiles for the two planets. In the outer solar system, we find normal isotope ratios for nitrogen and carbon on Jupiter, and for carbon on Saturn, but precision is low (±15% at best). Controversy exists about the correct value of D/H, with current estimates ranging from 2.3±1.1 to 5.1±0.7×10–5. Planetary missions planned for the next few years should add considerably to the quantity and quality of these data.Paper presented at the Conference on Protostars and Planets, held at the Planetary Science Institute, University of Arizona, Tucson, Arizona, between January 3 and 7, 1978.  相似文献   

19.
A hypothesis is considered in which the 36Ar found on Venus is of solar origin. This possibility is quantitatively discussed within the framework of present theories of planetary accumulation by sweep up of planetesimals under gas-free conditions. Solar wind implantation of 36Ar would take place by irradiation of accumulating material during the first ≈105 years of planetary growth, provided that the flux of solar wind was enhanced by a factor of ≈100 at that time. Enrichment of Venus in implanted gas would be a consequence of the irradiated material being initially confined to the innermost edge of the radially opaque circusolar planetesimal disk predicted by these theories. The observed atmospheric data require a Ne/Ar fractionation by a factor of ≈100 during the planetesimal stage. It is also necessary that there be very little mixing of irradiated planetesimals from the inner edge of disk to the distance (≈1 AU) at which the Earth formed. The hypothesis can be tested by measurement of the abundance of Kr and Xe in the Venus atmosphere. Venera data indicate a terrestrial 36Ar/Kr ratio, in disagreement with the solar wind hypothesis. In contrast, the Pioneer experiments find a lower limit to this ratio, well above the terrestrial value, that is compatible with the hypothesis. These experiments also show that Venus' 36Ar/Xe ratio does not correspond to the so-called “planetary” trapped inert gas composition. The inert of Venus could be related to result of admixture of gas with solar composition. The inert gas on Venus could be related to that found in enstatite chondrites.  相似文献   

20.
Abstract— The C contents and isotopic compositions of four eucrites, four diogenites and two howardites have been determined. Stepped heating in an O atmosphere was employed to convert selectively different carbonaceous materials to CO2 gas at various temperatures. This technique successfully distinguishes between terrestrial contaminants and indigenous C. With the exception of the Kapoeta howardite, the howardite, eucrite, and diogenite (HED) meteorites contain ～10–30 ppm indigenous C with δ13C between ?29% and ?19%. Kapoeta (a regolith breccia) has an elevated C content and δ13C, due to the presence of 13C-enriched carbonate minerals (δ13C ～ +20%) in CM2- or CR2-like clasts. The range in δ13C displayed by HED samples is similar to that of other solar system basalts, such as lunar rocks and Martian meteorites but distinctly different from that of the terrestrial mantle. The diogenites have a slightly lower total C yield and higher δ13C than the eucrites, which is a result of degassing of trapped CO/CC2/CO2–3 from the silicate lattice during metamorphism or annealing. However, three out of the four diogenites studied appear to contain a discrete component, possibly of graphitic C coating silicate grains, that is seemingly unaffected by the extended annealing period experienced by the diogenites. It is possible that this component might host the indigenous primitive Xe recently identified in diogenites.  相似文献   

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