Thermal stability of water and hydroxyl on the surface of the Moon from temperature-programmed desorption measurements of lunar analog materials

The adsorption of molecular water onto lunar analog materials was investigated under ultra-high vacuum with the goal to better understand the thermal stability and evolution of water on the lunar surface. Temperature-programmed desorption (TPD) experiments show that lunar-analog basaltic-composition glass is hydrophobic, with water-water interactions dominating over surface chemisorption. This suggests that lunar agglutinates will tend not to adsorb water at temperatures above where water clusters and multilayer ice forms. The basalt JSC-1A lunar mare analog, which is a complex mixture of minerals and glass, adsorbs water above 180 K with an adsorption profile that extends to 400 K, showing evidence for a continuum of water adsorption sites. Bancroft albite adsorbs more water, more strongly, than JSC-1A, with a well-defined desorption peak near 225 K. This suggests that mineral surfaces will adsorb more water than mare or mature (glassy, agglutinate rich) surfaces and may explain the association of water with fresh feldspathic craters at high latitudes. The activation energies for the thermal desorption of water from these materials were determined, and along with values from the literature, used to model the grain-to-grain migration of water within the lunar regolith. These models suggest that a combination of recombinative desorption of hydroxyl along with molecular desorption of water and its subsequent migration within and out of the regolith may explain observed diurnal variations in the distribution of water and hydroxyl on the illuminated Moon.     

A propensity for n‐ω‐amino acids in thermally altered Antarctic meteorites

Abstract– Asteroids and their fragments have impacted the Earth for the last 4.5 Gyr. Carbonaceous meteorites are known to contain a wealth of indigenous organic molecules, including amino acids, which suggests that these meteorites could have been an important source of prebiotic organic material during the origins of life on Earth and possibly elsewhere. We report the detection of extraterrestrial amino acids in thermally altered type 3 CV and CO carbonaceous chondrites and ureilites recovered from Antarctica. The amino acid concentrations of the thirteen Antarctic meteorites ranged from 300 to 3200 parts‐per‐billion (ppb), generally much less abundant than in amino acid‐rich CI, CM, and CR carbonaceous chondrites that experienced much lower temperature aqueous alteration on their parent bodies. In contrast to low‐temperature aqueously altered meteorites that show complete structural diversity in amino acids formed predominantly by Strecker–cyanohydrin synthesis, the thermally altered meteorites studied here are dominated by small, straight‐chain, amine terminal (n‐ω‐amino) amino acids that are not consistent with Strecker formation. The carbon isotopic ratios of two extraterrestrial n‐ω‐amino acids measured in one of the CV chondrites (δ¹³C approximately ?25‰) are consistent with ¹³C‐depletions observed previously in hydrocarbons produced by Fischer‐Tropsch type reactions. The predominance of n‐ω‐amino acid isomers in thermally altered meteorites hints at cosmochemical mechanisms for the preferential formation and preservation of a small subset of the possible amino acids.     

Molecular distribution, 13C‐isotope,and enantiomeric compositions of carbonaceous chondrite monocarboxylic acids

The water‐soluble organic compounds in carbonaceous chondrite meteorites constitute a record of the synthetic reactions occurring at the birth of the solar system and those taking place during parent body alteration and may have been important for the later origins and development of life on Earth. In this present work, we have developed a novel methodology for the simultaneous analysis of the molecular distribution, compound‐specific δ¹³C, and enantiomeric compositions of aliphatic monocarboxylic acids (MCA) extracted from the hot‐water extracts of 16 carbonaceous chondrites from CM, CR, CO, CV, and CK groups. We observed high concentrations of meteoritic MCAs, with total carbon weight percentages which in some cases approached those of carbonates and insoluble organic matter. Moreover, we found that the concentration of MCAs in CR chondrites is higher than in the other meteorite groups, with acetic acid exhibiting the highest concentration in all samples. The abundance of MCAs decreased with increasing molecular weight and with increasing aqueous and/or thermal alteration experienced by the meteorite sample. The δ¹³C isotopic values of MCAs ranged from ?52 to +27‰, and aside from an inverse relationship between δ¹³C value and carbon straight‐chain length for C₃–C₆ MCAs in Murchison, the ¹³C‐isotopic values did not correlate with the number of carbon atoms per molecule. We also observed racemic compositions of 2‐methylbutanoic acid in CM and CR chondrites. We used this novel analytical protocol and collective data to shed new light on the prebiotic origins of chondritic MCAs.     

A chemical sequence of macromolecular organic matter in the CM chondrites

Abstract— A new organic parameter is proposed to show a chemical sequence of organic matter in carbonaceous chondrites, using carbon, hydrogen, and nitrogen concentrations of solvent‐insoluble and high‐molecular weight organic matter (macromolecules) and the molecular abundance of solvent‐extractable organic compounds. The H/C atomic ratio of the macromolecule purified from nine CM chondrites including the Murchison, Sayama, and seven Antarctic meteorites varies widely from 0.11 to 0.72. During the H/C change of ?0.7 to ?0.3, the N/C atomic ratio remains at ?0.04, followed by a sharp decline from ?0.040 to ?0.017 between H/C ratios from ?0.3 to ?0.1. The H/CN/C sequence shows different degrees of organic matter thermal alteration among these chondrites in which the smaller H/C‐N/C value implies higher alteration levels on the meteorite parent body. In addition, solvent‐extractable organic compounds such as amino acids, carboxylic acids, and polycyclic aromatic hydrocarbons are abundant only in chondrites with macromolecular H/C values >?0.5. These organic compounds were extremely depleted in the chondrites with a macromolecular H/C value of <?0.5. Possibly, most solvent‐extractable organic compounds could have been lost during the thermal alteration event that caused the H/C ratio of the macromolecule to fall below 0.4.     

Compound‐specific carbon,nitrogen, and hydrogen isotopic ratios for amino acids in CM and CR chondrites and their use in evaluating potential formation pathways

Abstract– Stable hydrogen, carbon, and nitrogen isotopic ratios (δD, δ¹³C, and δ¹⁵N) of organic compounds can reveal information about their origin and formation pathways. Several formation mechanisms and environments have been postulated for the amino acids detected in carbonaceous chondrites. As each proposed mechanism utilizes different precursor molecules, the isotopic signatures of the resulting amino acids may indicate the most likely of these pathways. We have applied gas chromatography with mass spectrometry and combustion isotope ratio mass spectrometry to measure the compound‐specific C, N, and H stable isotopic ratios of amino acids from seven CM and CR carbonaceous chondrites: CM1/2 Allan Hills (ALH) 83100, CM2 Murchison, CM2 Lewis Cliff (LEW) 90500, CM2 Lonewolf Nunataks (LON) 94101, CR2 Graves Nunataks (GRA) 95229, CR2 Elephant Moraine (EET) 92042, and CR3 Queen Alexandra Range (QUE) 99177. We compare the isotopic compositions of amino acids in these meteorites with predictions of expected isotopic enrichments from potential formation pathways. We observe trends of decreasing δ¹³C and increasing δD with increasing carbon number in the α‐H, α‐NH₂ amino acids that correspond to predictions made for formation via Strecker‐cyanohydrin synthesis. We also observe light δ¹³C signatures for β‐alanine, which may indicate either formation via Michael addition or via a pathway that forms primarily small, straight‐chain, amine‐terminal amino acids (n‐ω‐amino acids). Higher deuterium enrichments are observed in α‐methyl amino acids, indicating formation of these amino acids or their precursors in cold interstellar or nebular environments. Finally, individual amino acids are more enriched in deuterium in CR chondrites than in CM chondrites, reflecting different parent‐body chemistry.     

Extraterrestrial amino acids identified in metal‐rich CH and CB carbonaceous chondrites from Antarctica

Carbonaceous chondrites contain numerous indigenous organic compounds and could have been an important source of prebiotic compounds required for the origin of life on Earth or elsewhere. Extraterrestrial amino acids have been reported in five of the eight groups of carbonaceous chondrites and are most abundant in CI, CM, and CR chondrites but are also present in the more thermally altered CV and CO chondrites. We report the abundance, distribution, and enantiomeric and isotopic compositions of simple primary amino acids in six metal‐rich CH and CB carbonaceous chondrites that have not previously been investigated for amino acids: Allan Hills (ALH) 85085 (CH3), Pecora Escarpment (PCA) 91467 (CH3), Patuxent Range (PAT) 91546 (CH3), MacAlpine Hills (MAC) 02675 (CBb), Miller Range (MIL) 05082 (CB), and Miller Range (MIL) 07411 (CB). Amino acid abundances and carbon isotopic values were obtained by using both liquid chromatography time‐of‐flight mass spectrometry and fluorescence, and gas chromatography isotope ratio mass spectrometry. The δ¹³C/¹²C ratios of multiple amino acids fall outside of the terrestrial range and support their extraterrestrial origin. Extracts of CH chondrites were found to be particularly rich in amino acids (13–16 parts per million, ppm) while CB chondrite extracts had much lower abundances (0.2–2 ppm). The amino acid distributions of the CH and CB chondrites were distinct from the distributions observed in type 2 and 3 CM and CR chondrites and contained elevated levels of β‐, γ‐, and δ‐amino acids compared to the corresponding α‐amino acids, providing evidence that multiple amino acid formation mechanisms were important in CH and CB chondrites.     

An upper limit to the abundance of lightning-produced amino acids in the Jovian water clouds

The effect of excess hydrogen on the synthesis of amino acids, by high-temperature shock waves in a hydrogen/methane/ammonia/water vapor mixture, was studied experimentally. The energy efficiency results, together with the best estimate of the lightning energy dissipation rate on Jupiter, from the Voyager data, were used to calculate an upper limit to the rate of amino acid production by lightning in the Jovian water clouds. Using reasonable values for the eddy diffusion coefficients within and below the water clouds, the column abundance of lightning-produced amino acids in the clouds was estimated to be 6.2 × 10^?6 cm-am. Hence, concentration of amino acids in water droplets would be 8 × 10^?8 mole liter^?1.     

Observations of water vapor ions at the lunar surface

The Apollo 14 Suprathermal Ion Detector Experiment observed a series of bursts of 48.6 eV water vapor ions at the lunar surface during a 14-h period on March 7, 1971. The maximum flux observed was 10⁸ ions cm^–2 s^–1 sr^–1. These ions were also observed at Apollo 12, 183 km to the west. Evaluation of specific artificial sources including the Apollo missions and the Russian Lunokhod leads to the conclusion that the water vapor did not come from a man-made source. Natural sources exogenous to the Moon such as comets and the solar wind are also found to be inadequate to explain the observed fluxes. Consequently, these water vapor ions appear to be of lunar origin.Paper dedicated to Prof. Harold C. Urey on the occasion of his 80th birthday on 29 April 1973.     

On the survivability of an enantiomeric excess of amino acids in comet nuclei during the decay of26Al and other radionuclides

We present a computer model calculation for the racemization of a possible excess of amino acids in the icy fraction of comet nuclei bring about by ionizing radiation released during the decay of²⁶Al,⁴⁰K,²³⁵U,²³⁸U and²³²Th. The model takes into account a total of 110 chemical reactions, of which 91 are needed to explain the radiation chemical processing of the major constituents of comet nuclei (Navarro-Gonzálezet al., 1992) and 19 are necessary to simulate the radiolysis of glycine/alanine mixtures in aqueous solutions (Navarro-Gonzálezet al., 1994 and 1996). It is predicted that an enantiomeric excess of alanine would not be destroyed by radioracemization during the decay of embedded radionuclides. Nevertheless, this enantiomeric excess could be attenuated by the formation of racemic amino acids in the interior of comet nuclei as a result of the radiation-induced polymerization of HCN.     

Numerical calculations of the longevity of impact oases on Titan

A promising setting for the formation of interesting prebiotic molecules on Titan is the transient liquid water environment formed by a comet impact, as originally suggested by Thompson and Sagan (1992, in: Symposium on Titan, ESA SP, vol. 338, p. 167). The impact melt (water or a water-ammonia mixture) generated in such an event can react with the abundant photochemical hydrocarbons and nitriles deposited on the surface of Titan to form more complex molecules such as purines and amino acids. We use a finite-difference thermal conduction code to calculate how long it takes for realistic liquid deposits in crater floors to freeze in the Titan environment. Our results suggest that 15 km diameter craters can sustain liquid water or water-ammonia environments for ∼¹⁰²-10³ yr and 150 km craters can sustain them for ∼¹⁰³-10⁴ yr. We discuss the implications of these timescales for organic chemistry on Titan.     

Spectroscopic Observations of Comet C/1996 B2 (Hyakutake) with the Caltech Submillimeter Observatory

The apparition of Comet C/1996 B2 (Hyakutake) offered an unexpected and rare opportunity to probe the inner atmosphere of a comet with high spatial resolution and to investigate with unprecedented sensitivity its chemical composition. We present observations of over 30 submillimeter transitions of HCN, H¹³CN, HNC, HNCO, CO, CH₃OH, and H₂CO in Comet Hyakutake carried out between 1996 March 18 and April 9 at the Caltech Submillimeter Observatory. Detections of the H¹³CN (4–3) and HNCO (16_0,16–15_0,15) transitions represent the first observations of these species in a comet. In addition, several other transitions, including HCN (8–7), CO (4–3), and CO (6–5) are detected for the first time in a comet as is the hyperfine structure of the HCN (4–3) line. The observed intensities of the HCN (4–3) hyperfine components indicate a line center optical depth of 0.9 ± 0.2 on March 22.5 UT. The HCN/HNC abundance ratio in Comet Hyakutake at a heliocentric distance of 1 AU is similar to that measured in the Orion extended ridge— a warm, quiescent molecular cloud. The HCN/H¹³CN abundance ratio implied by our observations is 34 ± 12, similar to that measured in giant molecular clouds in the galactic disk but significantly lower than the Solar System¹²C/¹³C ratio. The low HCN/H¹³CN abundance ratio may be in part due to contamination by an SO₂line blended with the H¹³CN (4–3) line. In addition, chemical models suggest that the HCN/H¹³CN ratio can be affected by fractionation during the collapse phase of the protosolar nebula; hence a low HCN/H¹³CN ratio observed in a comet is not inconsistent with the solar system¹²C/¹³C isotopic ratio. The abundance of HNCO relative to water derived from our observations is (7 ± 3) × 10⁻⁴. The HCN/HNCO abundance ratio is similar to that measured in the core of Sagittarius B2 molecular cloud. Although a photo-dissociative channel of HNCO leads to CO, the CO produced by HNCO is a negligible component of cometary atmospheres. Production rates of HCN, CO, H₂CO, and CH₃OH are presented. Inferred molecular abundances relative to water are typical of those measured in comets at 1 AU from the Sun. The exception is CO, for which we derive a large relative abundance of 30%. The evolution of the HCN production rate between March 20 and March 30 suggests that the increased activity of the comet was the cause of the fragmentation of the nucleus. The time evolution of the H₂CO emission suggests production of this species from dust grains.     

Enumeration, isolation, and characterization of ultraviolet (UV-C) resistant bacteria from rock varnish in the Whipple Mountains, California

The in situ search for life on Mars requires an understanding of the possible habitats available and the types of microbes that inhabit such environments on Earth. Rock varnish is ubiquitous in terrestrial deserts and has been suggested to exist on Mars. Data reported here show that there are very high numbers of bacteria (¹⁰⁷-¹⁰⁸ g⁻¹ dry wt) associated with rock varnish collected in the hot desert of the Whipple Mountains, south of Death Valley, CA, USA. Some of the bacteria identified in the rock varnish from the Whipple Mountains are resistant to UV-C exposure. This suggests that habitats like rock varnish, if they occur in the martian polar regions where liquid water may be available, may provide niches for radiation-resistant life forms such as the bacteria observed in the Whipple Mountains varnish ecosystem. The UV-resistant microbes isolated represent a diverse group of genera, but all are from the order Actinomycetales (the genera Arthrobacter, Curtobacterium, Geodermatophilus, and Cellulomonas). They are metabolically versatile heterotrophs capable of growing on a variety of simple sugars, amino acids, organic acids and aromatic acids as sole carbon and energy sources.     

Cometary glycine detected in samples returned by Stardust

Abstract— Our previous analysis of cometary samples returned to Earth by NASA's Stardust spacecraft showed several amines and amino acids, but the origin of these compounds could not be firmly established. Here, we present the stable carbon isotopic ratios of glycine and ε‐amino‐n‐caproic acid (EACA), the two most abundant amino acids identified in Stardust‐returned foil samples measured by gas chromatography‐mass spectrometry coupled with isotope ratio mass spectrometry. The δ¹³C value for glycine of +29 ± 6‰ strongly suggests an extraterrestrial origin for glycine, while the δ¹³C value for EACA of ?25 ± 2‰ indicates terrestrial contamination by Nylon‐6 during curation. This represents the first detection of a cometary amino acid.     

Carbon isotopic composition of acetic acid generated by hydrous pyrolysis of macromolecular organic matter from the Murchison meteorite

Abstract— Low molecular weight monocarboxylic acids, including acetic acid, are some of the most abundant organic compounds in carbonaceous chondrites. So far, the ¹³C‐ and D‐enriched signature of water‐extractable carboxylic acids has implied an interstellar contribution to their origin. However, it also has been proposed that monocarboxylic acids could be formed by aqueous reaction on the meteorite parent body. In this study, we conducted hydrous pyrolysis of macromolecular organic matter purified from the Murchison meteorite (CM2) to examine the generation of monocarboxylic acids with their stable carbon isotope measurement. During hydrous pyrolysis of macromolecular organic matter at 270–330 °C, monocarboxylic acids with carbon numbers ranging from 2 (C₂) to 5 (C₅) were detected, acetic acid (CH₃COOH; C₂) being the most abundant. The concentration of the generated acetic acid increased with increasing reaction temperature; up to 0.48 mmol acetic acid/g macromolecular organic matter at 330 °C. This result indicates that the Murchison macromolecule has a potential to generate at least ?0.4 mg acetic acid/g meteorite, which is about four times higher than the amount of water‐extractable acetic acid reported from Murchison. The carbon isotopic composition of acetic acid generated by hydrous pyrolysis of macromolecular organic matter is ?‐27‰ (versus PDB), which is much more depleted in ¹³C than the water‐extractable acetic acid reported from Murchison. Intramolecular carbon isotope distribution shows that methyl (CH₃‐)‐C is more enriched in ¹³C relative to carboxyl (‐COOH)‐C, indicating a kinetic process for this formation. Although the experimental condition of this study (i.e., 270–330 °C for 72 h) may not simulate a reaction condition on parent bodies of carbonaceous chondrite, it may be possible to generate monocarboxylic acids at lower temperatures for a longer period of time.     

Enceladus: A hypothesis for bringing both heat and chemicals to the surface

The eruptive plumes and large heat flow (～15 GW) observed by Cassini in the South Polar Region of Enceladus may be expressions of hydrothermal activity inside Enceladus. We hypothesize that a subsurface ocean is the heat reservoir for thermal anomalies on the surface and the source of heat and chemicals necessary for the plumes. The ocean is believed to contain dissolved gases, mostly CO₂ and is found to be relatively warm (～0 °C). Regular tidal forces open cracks in the icy crust above the ocean. Ocean water fills these fissures. There, the conditions are met for the upward movement of water and the dissolved gases to exsolve and form bubbles, lowering the bulk density of the water column and making the pressure at its bottom less than that at the top of the ocean. This pressure difference drives ocean water into and up the conduits toward the surface. This transportation mechanism supports the thermal anomalies and delivers heat and chemicals to the chambers from which the plumes erupt. Water enters these chambers and there its bubbles pop and loft an aerosol mist into the ullage. The exiting plume gas entrains some of these small droplets. Thus, nonvolatile chemical species in ocean water can be present in the plume particles. A CO₂ equivalent-gas molar fraction of ～4 × 10^?4 for the ocean is sufficient to support the circulation. A source of heat is needed to keep the ocean warm at ～0 °C (about two degrees above its freezing point). The source of heat is unknown, but our hypothesis is not dependent on any particular mechanism for producing the heat.     

The heartbeat of the volcano: The discovery of episodic activity at Prometheus on Io

The temporal signature of thermal emission from a volcano is a valuable clue to the processes taking place both at and beneath the surface. The Galileo Near Infrared Mapping Spectrometer (NIMS) observed the volcano Prometheus, on the jovian moon Io, on multiple occasions between 1996 and 2002. The 5 micron (μm) brightness of this volcano shows considerable variation from orbit to orbit. Prometheus exhibits increases in thermal emission that indicate episodic (though non-periodic) effusive activity in a manner akin to the current Pu'u 'O'o-Kupaianaha (afterwards referred to as the Pu'u 'O'o) eruption of Kilauea, Hawai'i. The volume of material erupted during one Prometheus eruption episode (defined as the interval from minimum thermal emission to peak and back to minimum) from 6 November 1996 to 7 May 1997 is estimated to be ∼0.8 km³, with a peak instantaneous volumetric flux (effusion rate) of ∼140 m³ s⁻¹, and an averaged volumetric flux (eruption rate) of ∼49 m³ s⁻¹. These quantities are used to model subsurface structure, magma storage and magma supply mechanisms, and likely magma chamber depth. Prometheus appears to be supplied by magma from a relatively shallow magma chamber, with a roof at a minimum depth of ∼2-3 km and a maximum depth of ∼14 km. This is a much shallower depth range than sources of supply proposed for explosive, possibly ultramafic, eruptions at Pillan and Tvashtar. As Prometheus-type effusive activity is widespread on Io, shallow magma chambers containing magma of basaltic or near-basaltic composition and density may be common. This analysis strengthens the analogy between Prometheus and Pu'u 'O'o, at least in terms of eruption style. Even though the style of eruption appears to be similar (effusive emplacement of thin, insulated, compound pahoehoe flows) the scale of activity at Prometheus greatly exceeds current activity at Pu'u 'O'o in terms of volume erupted, area covered, and magma flux. Whereas the estimated magma chamber at Prometheus dwarfs the Pu'u 'O'o magma chamber, it fits within expectations if the Pu'u 'O'o chamber were scaled for the greater volumetric flux and lower gravity of Io. Recent volumetric eruption rates derived from Galileo data for Prometheus were considerably smaller than the rate that produced the extensive flows formed in the ∼17 years between the Voyager and Galileo missions. These smaller eruption rates, coupled with the fact that flows are not expanding laterally, may mean that the immediate heat source that generates the Prometheus plume is simultaneously running out of available volatiles and the thermal energy that drives mobilization of volatiles. This raises the question of whether the current Prometheus eruption is in its last throes.     

Molecular and isotopic analyses of Tagish Lake alkyl dicarboxylic acids

Abstract— The Tagish Lake meteorite soluble organic suite has a general composition that differs from those of both CI and CM chondrites. These differences suggest that distinct processes may have been involved in the formation of different groups of organics in meteorites. Tagish Lake alkyl dicarboxylic acids have a varied, abundant distribution and are, with carboxylated pyridines, the only compounds to have an occurrence comparable to that of the Murchison meteorite. This study has undertaken their molecular and isotopic characterization, with the aim to understand their origin and to gain insights into the evolutionary history of the meteorite parent body. Tagish Lake alkyl dicarboxylic acids are present as a homologous series of saturated and unsaturated species with three‐ through ten‐carbon atom chain length. Linear saturated acids are predominant and show decreasing amounts with increasing chain length. A total of 44 of these compounds were detected with the most abundant, succinic acid, present at ?40 nmol/g meteorite. Overall the molecular distribution of Tagish Lake dicarboxylic acids shows a remarkable compound‐to‐compound correspondence with those observed in the Murchison and Murray meteorites. In both Tagish Lake and Murchison, the imides of the more abundant dicarboxylic acids were also observed. The hydrogen and carbon isotopic compositions of individual Tagish Lake dicarboxylic acids were determined and compared to those of the corresponding acids in the Murchison meteorite. All δD and δ¹³C values for Tagish Lake acids are positive and show a substantial isotopic enrichment. δD values vary from, approximately, +1120%_o for succinic acid to +1530%_o for methyl glutaric acid. δ¹³C values ranged from +12.6%_o for methyl glutaric acid to +22.9%_o for glutaric acid, with adipic acid having a significantly lower value (+5.5%_o). Murchison dicarboxylic acid showed similar isotopic values: their δ5¹³C values were generally higher by an average 17% and δD values were lower for succinic and glutaric acids, possibly due to contamination. The molecular and isotopic data collected for these compounds restrict their possible origin to processes, either interstellar or of very cold nebular regions, that produced significant isotopic enrichments. Saturated or partially unsaturated nitriles and dinitriles appear to be good precursor candidates as their hydrolysis, upon water exposure, would produce dicarboxylic acids and other carboxylated species found in Tagish Lake. This evolutionary course could possibly include pre‐accretionary processes.     

Pyrolysis of simple amino acids and nucleobases: survivability limits and implications for extraterrestrial delivery

The idea of extraterrestrial delivery of organic matter to the early Earth is strongly supported by the detection of a large variety of organic compounds in the interstellar medium, comets, and carbonaceous chondrites. Whether organic compounds essential for the emergence and evolution of life, particularly amino acids and nucleic acid bases found in the meteorites, can be efficiently delivered by other space bodies is unclear and depends primarily on capability of the biomolecules to survive high temperatures during atmospheric deceleration and impacts to the terrestrial surface. In the present study we estimated survivability of simple amino acids (glycine, Lalanine, α-aminoisobutyric acid, L-valine and L-leucine), purines (adenine and guanine) and pyrimidines (uracil and cytosine) under rapid heating to temperatures of 400-1000°C under N₂ or CO² atmosphere. We have found that most of the compounds studied cannot survive the temperatures substantially higher than 700°C; however at 500600°C, the recovery can be at a percent level (or even 10%-level for adenine, uracil, alanine, and valine). The final fate of amino acids and nucleobases during the atmospheric deceleration and surface impacts is discussed depending on such factors as size of the space body, nature and altitude of the heating, chemical composition of the space body and of the atmosphere.     

Comet 9P/Tempel 1: Sublimation beneath the dust cover

In the current work we analyze properties of the dust mantle, its thickness and thermal conductivity, necessary to reproduce observed rate of water production of Comet 9P/Tempel 1. For this purpose we considered simplified shape of the comet nucleus approximated by the symmetric prolate ellipsoid with smooth surface. We have performed simulations, using models with dust mantle of the thickness either constant, but nonuniform (Model A), or evolving (Model B). The simulated profiles of water production versus time were compared with observations. In addition, we compared the calculated surface temperature with the real temperatures derived from IR observations (the Deep Impact mission). This new double-stage verification procedure, shows that our model A is a good representation for the nucleus of Comet Tempel 1. This indicates, that the dust mantle thickness should be nonuniform, but does not change significantly with time. We show, that reproducing observed high temperatures of the nucleus requires dust mantle, that is almost everywhere thick and has extremely low thermal inertia. The latter should be close to zero as already predicted by others. The agreement between the simulated and measured water production can be obtained when the dust is regionally thin and has the thermal inertia higher than average, according to our simulations about 100 W s^1/2 K⁻¹ m⁻². Such regions should be located in the south hemisphere of the nucleus.     

Extraterrestrial amino acids and L‐enantiomeric excesses in the CM2 carbonaceous chondrites Aguas Zarcas and Murchison

The abundances, distributions, enantiomeric ratios, and carbon isotopic compositions of amino acids in two fragments of the Aguas Zarcas CM2 type carbonaceous chondrite fall and a fragment of the CM2 Murchison meteorite were determined via liquid chromatography time‐of‐flight mass spectrometry and gas chromatography isotope ratio mass spectrometry. A suite of two‐ to six‐carbon aliphatic primary amino acids was identified in the Aguas Zarcas and Murchison meteorites with abundances ranging from ~0.1 to 158 nmol/g. The high relative abundances of α‐amino acids found in these meteorites are consistent with a Strecker‐cyanohydrin synthesis on these meteorite parent bodies. Amino acid enantiomeric and carbon isotopic measurements in both fragments of the Aguas Zarcas meteorites indicate that both samples experienced some terrestrial protein amino acid contamination after their fall to Earth. In contrast, similar measurements of alanine in Murchison revealed that this common protein amino acid was both racemic (D ≈ L) and heavily enriched in ¹³C, indicating no measurable terrestrial alanine contamination of this meteorite. Carbon isotope measurements of two rare non‐proteinogenic amino acids in the Aguas Zarcas and Murchison meteorites, α‐aminoisobutyric acid and D‐ and L‐isovaline, also fall well outside the typical terrestrial range, confirming they are extraterrestrial in origin. The detections of non‐terrestrial L‐isovaline excesses of ~10–15% in both the Aguas Zarcas and Murchison meteorites, and non‐terrestrial L‐glutamic acid excesses in Murchison of ~16–40% are consistent with preferential enrichment of circularly polarized light generated L‐amino acid excesses of conglomerate enantiopure crystals during parent body aqueous alteration and provide evidence of an early solar system formation bias toward L‐amino acids prior to the origin of life.