Polycyclic aromatic hydrocarbons (PAHs) in Antarctic Martian meteorites, carbonaceous chondrites, and polar ice

Recent analyses of the carbonate globules present in the Martian meteorite ALH84001 have detected polycyclic aromatic hydrocarbons (PAHs) at the ppm level (McKay et al., 1996). The distribution of PAHs observed in ALH84001 was interpreted as being inconsistent with a terrestrial origin and were claimed to be indigenous to the meteorite, perhaps derived from an ancient martian biota. We have examined PAHs in the Antarctic shergottite EETA79001, which is also considered to be from Mars, as well as several Antarctic carbonaceous chondrites. We have found that many of the same PAHs detected in the ALH84001 carbonate globules are present in Antarctic carbonaceous chondrites and in both the matrix and carbonate (druse) component of EETA79001. We also investigated PAHs in polar ice and found that carbonate is an effective scavenger of PAHs in ice meltwater. Moreover, the distribution of PAHs in the carbonate extract of Antarctic Allan Hills ice is remarkably similar to that found in both EETA79001 and ALH84001. The reported presence of L-amino acids of apparent terrestrial origin in the EETA79001 druse material (McDonald and Bada, 1995) suggests that this meteorite is contaminated with terrestrial organics probably derived from Antarctic ice meltwater that had percolated through the meteorite. Our data suggests that the PAHs observed in both ALH84001 and EETA79001 are derived from either the exogenous delivery of organics to Mars or extraterrestrial and terrestrial PAHs present in the ice meltwater or, more likely, from a mixture of these sources. It would appear that PAHs are not useful biomarkers in the search for extinct or extant life on Mars.     

Xenon and other noble gases in shergottites

We have determined the isotopic composition of the xenon component trapped in EETA 79001 lithologies B and C, which we refer to as SPB-xenon. SPB-xenon is isotopically distinct from known xenon reservoirs, but differs in regular fashion. Normalized to ¹³²Xe, the light isotope ratios are indistinguishable from air, the ¹²⁹Xe/¹³²Xe ratio is about 2.4, and ¹³⁴Xe and ¹³⁶Xe are enhanced relative to the terrestrial atmosphere or AVCC. The apparent heavy-isotope enrichments are not generated by in situ fission and there is no spectral evidence for the presence of ²⁴⁴Pu fission xenon. However, the xenon composition does match that of fractionated AVCC except at ¹²⁹Xe, and consequently may be derived from or related to that component. ALHA 77005, Shergotty and EETA 79001 lithology A also have enhanced ¹²⁹Xe/¹³²Xe ratios in most temperature steps, and are seemingly consistent with varying mixtures of SPB-xenon and terrestrial xenon.Our results for neon and argon in EETA 79001 confirm earlier results on the exposure ages. We have also verified that the trapped ³⁸Ar/³⁶Ar ratio in lithology C is apparently substantially different from the terrestrial or meteoritic value. Krypton in EETA 79001,C is more fractionated with respect to AVCC than is terrestrial krypton and in the opposite direction as xenon. EETA 79001,C contains excess ⁸⁰Kr (and perhaps ⁸²Kr and ¹²⁸Xe), presumably from neutron capture on bromine and iodine, but these neutron captures do not appear to have occurred by in situ processes.     

Beryllium-10 contents of shergottites,nakhlites, and Chassigny

Accelerator mass spectrometry gives the following ¹⁰Be contents (dpm/kg) for the SNC meteorites: Shergotty, 13.0 ± 1.5 and 17.3 ± 2.7; Zagami, 18.6 ± 2.5 and 20.0 ± 3.2; ALHA 77005, 15 ± 3; EETA 79001A, 7.8 ± 1.1 and 6.3 ± 0.5; EETA 79001B, 8.5 ± 1.1; Nakhla, 19.7 ± 3.3; Lafayette, 18.1 ± 2.5; Governador Valadares, 25.6 ± 3.6; Chassigny, 20.5 ± 3.1. The ¹⁰Be contents of the NC meteorites indicate that significant accumulation of cosmogenic nuclides occurred in decimeter rather than planetary-size bodies. The agreement of the ³He, ²¹Ne, and ¹⁰Be exposure ages of the shergottites also supports small-body irradiation. A long terrestrial age for EETA 79001 appears unlikely.     

Martian regolith in Elephant Moraine 79001 shock melts? Evidence from major element composition and sulfur speciation

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 (En_72-75Fs_20-21Wo_5-7) and olivine (Fo_75-80). 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.     

Exposure history of shergottites

The cosmogenic nuclides ³⁶Cl (t_1/2 = 3.0 × 10⁵ years). ²⁶Al (7.05 × 10⁵ years). ¹⁰Be (1.6 × 10⁶ years) and ⁵³Mn (3.7 × 10⁶ years) were measured in three shergottites, ALHA 77005, EETA 79001, and Shergotty by accelerator mass spectrometry and neutron activation. The cosmogenic nuclide data constrain the history and origin of shergottites. ALHA 77005 was ejected from its parent body about 2.7 My ago and was exposed to cosmic rays as a body of 5–6 cm radius. Solar cosmic ray produced ²⁶A1 and ⁵³Mn were first clearly observed in this meteorite. The exposure age of EETA 79001 was 0.6 My and the preatmospheric radius was about 15 cm. The exposure age of Shergotty was calculated to be 2.2 My and the preatmospheric size was about 10–15 cm in radius. The terrestrial age of ALHA 77005 was 0.2 My and that of EETA 79001 was less than 0.06 My. All cosmogenic nuclide data indicate that the three shergottites were never exposed to cosmic rays in their parent bodies, whether that parent body was Mars or an asteroid. All shergottites were ejected from greater than a 3 m depth in their parent bodies. The ejection of EETA 79001 was a different event from that of the other shergottites.     

Magnetic studies on Shergotty and other SNC meteorites

Hysteresis measurements on three shergottite and two nakhlite meteorites indicate single domain grain size behavior for the highly shocked Shergotty, Zagami, and EETA 79001 meteorites, with more multidomain-like behavior for the unshocked Nakhla and Governador Valadares meteorites. High viscosity and initial susceptibility for Antarctic shergottite ALHA 77005 indicate the presence of superparamagnetic grains in this specimen. Thermomagnetic curves likewise reveal a range of oxidation states for the high ulvospinel titanomagnetite grains which dominate the magnetic properties of these first five meteorites. Thermomagnetic analysis indicate Shergotty and Zagami as the least initially oxidized, while EETA 79001 appears to be the most oxidized. Cooling of the meteorite samples from high temperature in air results in a substantial increase in magnetization due to the production of magnetite through oxidation exsolution of titanomagnetite. However, vacuum heating substantially suppresses this process, and in the case of EETA 79001 and Nakhla, results in a rehomogenization of the titanomagnetite grains.Remanence measurements on several subsamples of Shergotty and Zagami meteorites reveal a large variation in intensity that does not seem related to the abundance of remanence carriers. The other meteorites carry only weak remanence, suggesting weak magnetizing fields as the source of their magnetic signal. A paleointensity experiment on a weakly magnetized subsample of Shergotty reveals a low temperature component of magnetization acquired in a field of 2,000 gammas. Also present was a high temperature component reflecting a paleo-field strength of between 250 and 1,000 gammas, depending on the nature and degree of alteration that the sample may have undergone with heating. This is consistent with an earlier paleointensity estimate of 1,000 gammas for ALHA 77005. The weak field environment that these meteorites seem to reflect is consistent with either a Martian or asteroidal body origin, but inconsistent with a terrestrial origin.     

Nuclear tracks,Sm isotopes and neutron capture effects in the Elephant Morraine shergottite

Nuclear track studies, uranium concentration measurements and Sm-isotope studies have been performed on both lithologies A and B of the Elephant Morraine shergottite, BETA 79001. Track studies show that EETA 79001 was a rather small object in space with a preatmospheric radius of 12 ± 2 cm, corresponding to a preatmospheric mass of 28 ± 13 kg. Phosphates have U-concentrations ranging from 0.3 to 1.3 ppm. There are occasional phosphates with excess fission tracks, possibly produced from neutron induced fission of U and Th, during the regolith exposure in the shergottite parent body (SPB). Sm-isotope studies, while not showing any clear cut excess in ¹⁵⁰Sm, enable us to derive meaningful upper limits to thermal neutron fluences of 2 to 3 × 10¹⁵ n/cm², during a possible regolith irradiation. These limits are consistent with the track data and also enable us to derive an upper limit to the neutron exposure age of EETA 79001 of 55 Myr in the SPB regolith.     

The sources of water in Martian meteorites: clues from hydrogen isotopes

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.     

Terrestrial Kr-Kr ages of Antarctic meteorites

The production rate of ³⁸Ar in meteorites—P(38)—has been determined, as a function of the sample's chemical composition, from ⁸¹Kr-Kr exposure ages of four eucrite falls. The cosmogenic ⁷⁸Kr/⁸³Kr ratio is used to estimate the shielding dependence of P(38).

From the “true” ³⁸Ar exposure ages and the apparent ⁸¹Kr-Kr exposure ages of nine Antarctic eucrite finds, terrestrial ages are calculated. They range from about 3 × 10⁵ a (Pecora Escarpment 82502) to very recent falls (Thiel Mountains 82502). Polymict eucrites from the Allan Hills (A78132, A79017 and A81009) have within the limits of error the same exposure age (15.2 × 10⁶ a) and the same terrestrial age (1.1 × 10⁵ a). This is taken as strong evidence that these meteorites are fragments of the same fall. A similar case are the Elephant Moraine polymict eucrites A79005, A79006 and 82600 with an exposure age of 26 × 10⁶ a and a terrestrial age of 1.8 × 10⁵ a. EETA79004 may be different from this group because its exposure age and terrestrial age are 21 × 10⁶ a and 2.5 × 10⁵ a, respectively.

The distribution of terrestrial ages of Allan Hills meteorites is discussed. Meteorites from this blue ice field have two sources: Directly deposited falls and meteorites transported to the Allan Hills inside the moving Antarctic ice sheet. During the surface residence time meteorites decompose due to weathering processes. The weathering “half-life” is about 1.6 × 10⁵ a. From the different age distributions of Allan Hills and Yamato meteorites, it is concluded that meteorite concentrations of different Antarctic ice fields need different explanations.     

A reexamination of amino acids in lunar soils: implications for the survival of exogenous organic material during impact delivery

Using a sensitive high performance liquid chromatography technique, we have analyzed both the hot water extract and the acid hydrolyzed hot water extract of lunar soil collected during the Apollo 17 mission. Both free amino acids and those derived from acid labile precursors are present at a level of roughly 15 ppb. Based on the D/L amino acid ratios, the free alanine and aspartic acid observed in the hot water extract can be entirely attributed to terrestrial biogenic contamination. However, in the acid labile fraction, precursors which yield amino acids are apparently present in the lunar soil. The amino acid distribution suggests that the precursor is probably solar wind implanted HCN. We have evaluated our results with regard to the meteoritic input of intact organic compounds to the moon based on an upper limit of < or = 0.3 ppb for alpha-aminoisobutyric acid, a non-protein amino acid which does not generally occur in terrestrial organisms and which is not a major amino acid produced from HCN, but which is a predominant amino acid in many carbonaceous chondrites. We find that the survival of exogenous organic compounds during lunar impact is < or = 0.8%. This result represents an example of minimum organic impact survivability. This is an important first step toward a better understanding of similar processes on Earth and on Mars, and their possible contribution to the budget of prebiotic organic compounds on the primitive Earth.     

Water-extractable and exchangeable phosphate in Martian and carbonaceous chondrite meteorites and in planetary soil analogs

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 (E_1min) and between 1 min and 3 months (E_1min-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.     

Noble gases and nitrogen in Martian meteorites Dar al Gani 476, Sayh al Uhaymir 005 and Lewis Cliff 88516: EFA and extra neon

Meteorite “finds” from the terrestrial hot deserts have become a major contributor to the inventory of Martian meteorites. In order to understand their nitrogen and noble gas components, we have carried out stepped heating experiments on samples from two Martian meteorites collected from hot deserts. We measured interior and surface bulk samples, glassy and non-glassy portions of Dar al Gani 476 and Sayh al Uhaymir 005. We have also analyzed noble gases released from the Antarctic shergottite Lewis Cliff 88516 by crushing and stepped heating. For the hot desert meteorites significant terrestrial Ar, Kr, Xe contamination is observed, with an elementally fractionated air (EFA) component dominating the low temperature releases. The extremely low Ar/Kr/Xe ratios of EFA may be the result of multiple episodes of trapping/loss during terrestrial alteration involving aqueous fluids. We suggest fractionation processes similar to those in hot deserts to have acted on Mars, with acidic weathering on the latter possibly even more effective in producing elementally fractionated components. Addition from fission xenon is apparent in DaG 476 and SaU 005. The Ar-Kr-Xe patterns for LEW 88516 show trends as typically observed in shergottites - including evidence for a crush-released component similar to that observed in EETA 79001. A trapped Ne component most prominent in the surface sample of DaG 476 may represent air contamination. It is accompanied by little trapped Ar (²⁰Ne/³⁶Ar > 50) and literature data suggest its presence also in some Antarctic finds. Data for LEW 88516 and literature data, on the other hand, suggest the presence of two trapped Ne components of Martian origin characterized by different ²⁰Ne/²²Ne, possibly related to the atmosphere and the interior. Caution is recommended in interpreting nitrogen and noble gas isotopic signatures of Martian meteorites from hot deserts in terms of extraterrestrial sources and processes. Nevertheless our results provide hope that vice-versa, via noble gases and nitrogen in meteorites and other relevant samples from terrestrial deserts, Martian secondary processes can be studied.     

Amino acid abundances and stereochemistry in hydrothermally altered sediments from the Juan de Fuca Ridge, northeastern Pacific Ocean.

The Juan de Fuca Ridge is a hydrothermally active, sediment covered, spreading ridge situated a few hundred kilometres off the west coast of North America in the northeastern Pacific Ocean. Sediments from seven sites drilled during the Ocean Drilling Program (ODP) Legs 139 and 168 were analyzed for total hydrolyzable amino acids (THAA), individual amino acid distributions, total organic C (TOC) and total N (TN) contents. The aim was to evaluate the effects of hydrothermal stress on the decomposition and transformation of sedimentary amino acids. Hydrolyzable amino acids account for up to 3.3% of the total organic C content and up to 12% of the total N content of the upper sediments. The total amounts of amino acids decrease significantly with depth in all drilled holes. This trend is particularly pronounced in holes with a thermal gradient of around 0.6 degrees C/m or higher. The most abundant amino acids in shallow sediments are glycine, alanine, lysine, glutamic acid, valine and histidine. The changes in amino acid distributions in low temperature holes are characterized by increased relative abundances of non-protein beta-alanine and gamma-aminobutyric acid. In high temperature holes the amino acid compositions are characterized by high abundances of glycine, alanine, serine, ornithine and histidine at depth. D/L ratios of samples with amino acid distributions similar to those found in acid hydrolysates of kerogen, indicate that racemization rates of amino acids bound by condensation reactions may be diminished.     

珠江中下游颗粒有机质的碳氮℃稳定同位素、氨基酸和木质素组成及其地球化学意义

从东江到珠江口采集了悬浮颗粒物,通过测定总有机质的元素（TOC、TN）、同位素（δ13C、δ15N）组成以及生物标志物（氨基酸、木质素）等地球化学性质,来揭示颗粒有机质的来源和组成。结果表明,浮游生物（13%-52%）和土壤（45%-77%）是珠江颗粒有机质的主要来源,植物（0%-11%）对颗粒物的贡献较小。颗粒有机质含有高比例的氨基酸碳（TAAC）,说明浮游生物对颗粒物的重要性。氨基酸的降解指数（DI）在-0.51到0.79之间,说明这些水生来源有机质的降解程度比较小。木质素的降解参数（Ad/Al、3,5-BD/V）较大,表明珠江颗粒有机碳的陆源来源主要是土壤。在颗粒物中检测到了少量的二氨基庚二酸（Dapa）,说明细菌对颗粒有机碳也有所贡献。不同环境中颗粒物的木质素组成主要与颗粒物丰度和粒径有关：（1）相对于河流,水库颗粒物中的木质素含量显著偏低,降解程度更高;（2）相对于中游,下游颗粒物丰度较高,木质素含量较高。     

The Shergotty Consortium and SNC meteorites: An overview

The Shergotty meteorite has a multi-phase (magmatic and shock) history. While the Shergotty picture is complex, consortium studies have advanced our knowledge and understanding of Shergotty and shergottites, nakhlites and Chassigny (SNC) meteorites. Martian origin for the SNC meteorites is strongly favored by several workers from the evidence of trapped noble gases and nitrogen compositions in glasses (lithology C) of the EETA 79001 meteorite, which compare well with the Martian atmosphere analysis made by the Viking Spacecraft. The parent body is about 2 to 4 times richer in volatiles (Cl, Br, Na, K, Rb, Zn, F, Pb, etc.) than the Earth. Consortium studies on Shergotty show very low thermoluminescence, no deformation of tracks, cosmic ray exposure age of about 2.5 million years (m.y.), a pre-atmospheric size of about 12 cm radius, and apparently one shock event at 30 GPa pressure that converted plagioclase to maskelynite. The crystallization age of Shergotty by the Sm-Nd method is 360 ± 16 m.y. The Rb-Sr age for Shergotty is reported as 166 m.y. and the Pb-U age as about 200 m.y. Interpretations of age-dating and exposure scenarios are controversial and may require further studies.At least two scenarios for the ejection of SNC meteorites are possible: 1) ejection as a large body (>6 m size) by a single impact on Mars and then multiple breakup in the asteroidal belt at about 11 m.y. for Chassigny and nakhlites, at 2.5 m.y. for Shergotty, Zagami and ALHA 77005, and at 0.6 m.y. for EETA 79001; and 2) ejection of small objects (<0.5 m size) by multiple impacts on the Martian terrain at 11, 2.5 and 0.6 m.y. with no breakup in space.     

Noble gas contents of shergottites and implications for the Martian origin of SNC meteorites

Isotopic concentrations of the noble gases have been measured in several different phases of Elephant Moraine A79001 and in whole rock samples of Zagami and Allan Hills A77005, three meteorites which belong to the rare group of SNC achondrites that may have originated from the planet Mars. Shocked phases of EETA79001 contain a trapped Ar, Kr, and Xe component characterized by ${}^{84}\text{Kr}{}^{132}\text{Xe}$ ～15, ${}^{40}\text{Ar}{}^{36}\text{Ar}\text{> 2000}$, ${}^{129}\text{Xe}{}^{132}\text{Xe ≥ 2}$, and ${}^4\text{He}{}^{40}\text{Ar}\text{≤ 0.1}$. These elemental and isotopic ratios are unlike those for any other noble gas component except analyses of the Martian atmosphere made by Viking spacecraft. The isotopic composition of the trapped Kr shows an approximate 1% per mass unit enrichment of lighter isotopes compared to terrestrial Kr, and the traped Xe may show either a fission component or a fractionated enrichment of heavier isotopes compared to terrestrial Xe. It is hypothesized that these gases represent a portion of the Martian atmosphere which was shock-implanted into EETA79001, and that they constitute direct evidence of a Martian origin for the shergottite meteorites. Cosmic ray-produced gases in the eight known SNC meteorites form three distinct groups with exposure ages of ～11 MY (Chassigny and the nakhlites), ～2.6 MY (Shergotty, Zagami, and ALHA77005), and ～0.5 MY (EETA79001). These ages suggest three distinct events and cannot have been produced by irradiation for a common time under greatly different shielding. Comparison of cosmogenic ${}^3\text{He}{}^{21}\text{Ne}$ measured in EETA79001 with two independent models for the production of this ratio as a function of shielding indicates that this meteorite was irradiated in space as a relatively small object. If the SNC meteorites were ejected from Mars ～ 180 My ago, the shock age of the shergottites, they must have been relatively large objects (>6 meters diameter) which experienced at least three space collisions to initiate cosmic ray exposure. Ejection from Mars by three events at the times of initiation of cosmic ray exposure would permit the ejected objects to have been much smaller (<1 meter diameter), but would require three such events on 1.3 Gy Martian terraine in the past ～10 MY and would not explain the common 180 MY shock age seen in all four shergottites.     

Non-racemic amino acids in the Murray and Murchison meteorites.

Small (1.0-9.2%) L-enantiomer excesses were found in six alpha-methyl-alpha-amino alkanoic acids from the Murchison (2.8-9.2%) and Murray (1.0-6.0%) carbonaceous chondrites by gas chromatography-mass spectroscopy of their N-trifluoroacetyl or N-pentafluoropropyl isopropyl esters. These amino acids [2-amino-2,3-dimethylpentanoic acid (both diastereomers), isovaline, alpha-methyl norvaline, alpha-methyl valine, and alpha-methyl norleucine] are either unknown or rare in the terrestrial biosphere. Enantiomeric excesses were either not observed in the four alpha-H-alpha-amino alkanoic acids analyzed (alpha-amino-n-butyric acid, norvaline, alanine, and valine) or were attributed to terrestrial contamination. The substantial excess of L-alanine reported by others was not found in the alanine in fractionated extracts of either meteorite. The enantiomeric excesses reported for the alpha-methyl amino acids may be the result of partial photoresolution of racemic mixtures caused by ultraviolet circularly polarized light in the presolar cloud. The alpha-methyl-alpha-amino alkanoic acids could have been significant in the origin of terrestrial homochirality given their resistance to racemization and the possibility for amplification of their enantiomeric excesses suggested by the strong tendency of their polymers to form chiral secondary structure.     

Volume of Antarctic Ice at the Last Glacial Maximum, and its impact on global sea level change

The volume of Antarctic ice at the Last Glacial Maximum is a key factor for calculating the past contribution of melting ice sheets to Late Pleistocene global sea level change. At present, there are large uncertainties in our knowledge of the extent and thickness of the formerly expanded Antarctic ice sheets, and in the timing of their release as meltwater into the world’s oceans. This paper reviews the four main approaches to determining former Antarctic ice volume, namely glacial geology, glacio-isostatic studies, glaciological modelling, and ice core analysis and attempts to reconcile these to give a ‘best estimate’ for ice volume. In the Ross Sea there was a major expansion of grounded ice at the Last Glacial Maximum, accounting for 2.3–3.2 m of global sea level. At some time in the Weddell Sea a large grounded ice sheet corresponding to c. 2.7 m of global sea level extended to the shelf break. However, this ice expansion has not yet been confidently dated and may not relate to the Last Glacial Maximum. Around East Antarctica there was thickening and advance offshore of ice in coastal regions. Ice core evidence suggests that the interior of East Antarctica was either close to its present elevation or thinner during the last glacial so the effect of East Antarctica on sea level depends on the net balance between marginal thickening and interior thinning. Suggested East Antarctic contributions vary from a 3–5.5 m lowering to a 0.64 m rise in global sea level. The Antarctic Peninsula ice sheet thickened and extended offshore at the Last Glacial Maximum, with a sea level equivalent contribution of c. 1.7 m. Thus, the Antarctic ice sheets accounted for between 6.1 and 13.1 m of global sea level fall at the Last Glacial Maximum. This is substantially less than has been suggested by most previous studies but the maximum figure matches well with one modelling estimate. The timing of Antarctic deglaciation is not well known. In the Ross Sea, terrestrial evidence suggests deglaciation may have begun at c. 13,000 yr BP¹ but that grounded ice persisted until c. 6,500 yr BP. Marine evidence suggests the western Ross Sea was deglaciated by c. 11,500 yr BP. Deglaciation of the Weddell Sea is poorly constrained. Grounded ice in the northern Antarctic Peninsula had retreated by c. 13,000 yr BP, and further south deglaciation occurred sometime prior to c. 6,000 yr BP. Many parts of coastal East Antarctica apparently escaped glaciation at the LGM, but in those areas that were ice-covered deglaciation was underway by 10,000 yr BP. With existing data, the timing of deglaciation shows no firm relation to northern hemisphere-driven sea level rise. This is probably due partly to lack of Antarctic dating evidence but also to the combined influence of several forcing mechanisms acting during deglaciation.     

Summary and implications of reported amino acid concentrations in the Murchison meteorite

A study of literature reports of the concentrations of amino acids in extracts from the Murchison meteorite shows that many of the concentration ratios are constant. There are two possible interpretations of these ratios. One is that they are controlled by the pathways through which the amino acids formed, from which it follows that the amino acids are distributed in the same proportions throughout the meteorite. The other interpretation is that the ratios result from the analytical procedures used to extract the amino acids from the meteorite. These methods rely heavily on high-temperature (100 degrees C) aqueous extraction and subsequent high-temperature acid hydrolysis. A correlation was observed in the present study between the relative concentrations of several amino acids in the meteorite extracts and their relative aqueous solubilities at 100 degrees C (alanine, valine, leucine, isoleucine, norleucine, aspartic acid, glutamic acid and glycine). The extract solutions are dilute, and far from the saturation limits, but these correlations suggest that the sampling procedure affects directly the reported concentrations for these amino acids. Ratios of the concentration of serine to those of glycine are also constant but cannot be accounted for solely by relative solubilities, and, as suggested elsewhere, serine as well as phenylalanine and methionine may be terrestrial contaminants. Data for beta-alanine, alpha-aminobutyric acid, proline, sarcosine, alloisoleucine, beta-aminoisobutyric acid, beta-aminobutyric acid, and threonine also show constant abundances relative to glycine, but lack of solubility data at extraction conditions prohibits evaluating the extent of possible sampling bias for these amino acids. If the extraction process does not bias the results, and all extractable amino acids are removed from meteorite samples, then the properties of amino acids which control both their solubilities and their concentrations in the meteorite need to be established. The possibility of sampling bias needs to be tested experimentally before concluding that extraction is complete, and that the constant relative abundances indicate that the relative concentrations of amino acids are homogeneous in the meteorite.