K2O‐rich trapped melt in olivine in the Nakhla meteorite: Implications for petrogenesis of nakhlites and evolution of the Martian mantle

We used new analytical and theoretical methods to determine the major and minor element compositions of the primary trapped liquid (PTLs) represented by melt inclusions in olivine and augite in the Martian clinopyroxenite, Nakhla, for comparison with previously proposed compositions for the Nakhla (or nakhlite) parent magma. We particularly focused on obtaining accurate K₂O contents, and on testing whether high K₂O contents and K₂O/Na₂O ratios obtained in previous studies of melt inclusions in olivine in Nakhla could have been due to unrepresentative sampling, systematic errors arising from electron microprobe techniques, late alteration of the inclusions, and/or boundary layer effects. Based on analyses of 35 melt inclusions in olivine cores, the PTL in olivine, PTL_oliv, contained (by wt) approximately 47% SiO₂, 6.3% Al₂O₃, 9.6% CaO, 1.8% K₂O, and 0.9% Na₂O, with K₂O/Na₂O = 2.0. We infer that the high K₂O content of PTL_oliv is not due to boundary layer effects and represents a real property of the melt from which the host olivine crystallized. This melt was cosaturated with olivine and augite. Its mg# is model‐dependent and is constrained only to be ≥19 (equilibrium Fo = 40). Based on analyses of 91 melt inclusions in augite cores, the PTL in augite, PTL_aug, contained (by wt) 53–54% SiO₂, 7–8% Al₂O₃, 0.8–1.1% K₂O, and 1.1–1.4% Na₂O, with K₂O/Na₂O = 0.7–0.8. This K₂O content and K₂O/Na₂O ratio are significantly higher than inferred in studies of melt inclusions in augite in Nakhla by experimental rehomogenization. PTL_aug was saturated only with augite, and in equilibrium with augite cores of mg# 62. PTL_aug represents the Nakhla parent magma, and does not evolve to PTL_oliv by fractional crystallization. We therefore conclude that olivine cores in Nakhla (and, by extension, other nakhlites) are xenocrystic. We propose that PTL_oliv and PTL_aug were generated from the same source region. PTL_oliv was generated first and emplaced to form olivine‐rich cumulate rocks. Shortly thereafter, PTL_aug was generated and ascended through these olivine‐rich cumulates, incorporating fragments of wallrock that became the xenocrystic olivine cores in Nakhla. The Nakhla (nakhlite) mantle source region was pyroxenitic with some olivine, and could have become enriched in K relative to Na via metasomatism. A high degree of melting of this source produced the silica‐poor, alkali‐rich magma PTL_oliv. Further ascension and decompression of the source led to generation of the silica‐rich, relatively alkali‐poor magma PTL_aug. Potassium‐rich magmas like those involved in the formation of the nakhlites represent an important part of the diversity of Martian igneous rocks.     

Experimental petrology of the basaltic shergottite Yamato‐980459: Implications for the thermal structure of the Martian mantle

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

A review of volatiles in the Martian interior

Multiple observations from missions to Mars have revealed compelling evidence for a volatile‐rich Martian crust. A leading theory contends that eruption of basaltic magmas was the ultimate mechanism of transfer of volatiles from the mantle toward the surface after an initial outgassing related to the crystallization of a magma ocean. However, the concentrations of volatile species in ascending magmas and in their mantle source regions are highly uncertain. This work and this special issue of Meteoritics & Planetary Science summarize the key findings of the workshop on Volatiles in the Martian Interior (Nov. 3–4, 2014), the primary open questions related to volatiles in Martian magmas and their source regions, and the suggestions of the community at the workshop to address these open questions.     

Ultraviolet irradiation of naphthalene in H2O ice: Implications for meteorites and biogenesis

Abstract— The polycyclic aromatic hydrocarbon (PAH) naphthalene was exposed to ultraviolet radiation in H₂O ice under astrophysical conditions, and the products were analyzed using infrared spectroscopy and high‐performance liquid chromatography. As we found in our earlier studies on the photoprocessing of coronene in H₂O ice, aromatic alcohols and ketones (quinones) were formed. The regiochemistry of the reactions is described and leads to specific predictions of the relative abundances of various oxidized naphthalenes that should exist in meteorites if interstellar ice photochemistry influenced their aromatic inventory. Since oxidized PAHs are present in carbon‐rich meteorites and interplanetary dust particles (IDPs), and ubiquitous in and fundamental to biochemistry, the delivery of such extraterrestrial molecules to the early Earth may have played a role in the origin and evolution of life.     

Neutron Capture Isotopes in the Martian Regolith and Implications for Martian Atmospheric Noble Gases

Impact-produced glasses in some martian meteorites have trapped significant amounts of the recent martian atmosphere. From literature data, we estimate that ∼9% of the trapped ⁸⁰Kr in these meteorites was produced from neutron capture on ⁷⁹Br. Estimates of neutron fluences made from ⁸⁰Kr and ¹⁴⁹Sm for bulk samples of meteorite EET79001 indicate that ⁸⁰Kr excesses in the impact glass were not produced in situ. Theoretical calculations independently predict production of a large neutron-capture component of ⁸⁰Kr and ³⁶Ar in the martian regolith, and part of this component presumably escaped into the martian atmosphere. These calculations were made by using the Los Alamos High-Energy Transport Code to calculate the fluxes of galactic cosmic ray (GCR)-produced thermal neutrons as a function of depth in the uppermost 500 g cm⁻² of the martian surface, and by adopting average Cl, Br, and I concentrations of the upper martian surface of ∼0.3%, ∼20 ppm, and ∼0.5 ppm, respectively. Combining these data with the appropriate neutron-capture cross sections, we calculate Mars global production rates of ⁸⁰Kr_n=2.4×10¹⁶atoms sec⁻¹, ³⁶Ar_n=5.5×10¹⁸ atoms sec⁻¹, and ¹²⁸Xe_n=3×10¹³ atoms sec⁻¹. Calculated global production rates of spallogenic ⁸⁰Kr_sp, and ³⁶Ar_sp, are smaller by factors of ∼770 and ∼29, respectively. It would require ∼330 Myr to produce an amount of ⁸⁰Kr_n equivalent to the amount inferred to be present today in the martian atmosphere (∼2.5×10³² atoms). Production of these neutron-capture components probably has occurred over the past ∼4 Gyr, as only an atmospheric pressure substantially higher than today's would appreciably decrease the neutron flux in the regolith. Thus, most of the neutron-capture noble gases produced over time probably remain in the martian regolith and would make sensitive indicators of the time period a sample has resided near the martian surface. Assuming mixing of the martian surface to an average depth of 100 m, the predicted average regolith concentrations of ⁸⁰Kr_n, ³⁶Ar_n, and ¹²⁸Xe_n are ∼4×10⁻⁹ cm⁻³ g⁻¹, ∼1×10⁻⁶ cm³ g⁻¹, and ∼5×10⁻¹² cm³ g⁻¹, respectively. If similar fractions of these neutron-capture isotopes have escaped into the atmosphere, they would comprise ∼3% and ∼0.2% of the present atmospheric inventories of ³⁶Ar and ¹²⁸Xe, respectively. The fractional excess of ⁸⁰Kr_n in ancient martian meteorite ALH84001 appears similar to that in shock-glass phases of young shergottite meteorites. If ALH84001 acquired its atmospheric gases ∼4 Gyr ago, this implies that, prior to that time, halogens were greatly concentrated at the martian surface by crustal formational and weathering processes, impacts efficiently degassed the regolith, and Mars did not have a significant atmosphere to shield the surface.     

Magnetic properties of Martian meteorites: Implications for an ancient Martian magnetic field

Abstract— The magnetic properties of samples of seven Martian meteorites (EET 79001, Zagami, Nakhla, Lafayette, Governador Valadares, Chassigny and ALH 84001) have been investigated. All possess a weak, very stable primary natural remanent magnetization (NRM), and some have less stable secondary components. In some cases, the latter are associated with magnetic contamination of the samples, imparted since their recovery, and with viscous magnetization, acquired during exposure of the meteorites to the geomagnetic field since they fell. The magnetic properties are carried by a small content (<1%) of titanomagnetite and, in ALH 84001, possibly by magnetite as well. The most likely source of the primary NRM is a thermoremanent magnetization acquired when the meteorite material last cooled from a high temperature in the presence of a magnetic field. Current evidence is that this was 1.3 Ga ago for the nakhlites and Chassigny and 180 Ma for shergottites: the time of the last relevant cooling of ALH 84001 is not presently known. Preliminary estimates of the strength of the magnetizing field are in the range 0.5–5 üT, which is at least an order of magnitude greater than the present field. It is tentatively concluded that the magnetic field was generated by a dynamo process in a Martian core with appropriate structure and properties.     

On the abundance of NO2 in the Martian atmosphere

Spectrophotometric scans of Mars and the Moon in the region 4000–5000 Å were obtained and ratioed. No evidence of any absorption greater than 3% is visible in the Martian spectrum. Using our own laboratory spectra of NO₂ as well as the published work of Hall and Blacet (1952) we confirm Marshall's (1964) upper limit of 8 μm atmospheres (0.0008 cm amagat) for the abundance of NO₂ in the atmosphere of Mars.     

History of Martian volatiles: Implications for organic synthesis

A theoretical reconstruction of the history of Martian volatiles indicates that Mars probably possessed a substantial reducing atmosphere at the outset of its history and that its present tenous and more oxidized atmosphere is the result of extensive chemical evolution. As a consequence, it is probable that Martian atmospheric chemical conditions, now hostile with respect to abiotic organic synthesis in the gas phase, were initially favorable. Evidence indicating the chronology and degradational history of Martian surface features, surface mineralogy, bulk volatile content, internal mass distribution, and thermal history suggests that Mars catastrophically developed a substantial reducing atmosphere as the result of rapid accretion. This atmosphere probably persisted—despite the direct and indirect effects of hydrogen escape—for a geologically short time interval during, and immediately following, Martian accretion. That was the only portion of Martian history when the atmospheric environment could have been chemically suited for organic synthesis in the gas phase. Subsequent gradual degrassing of the Martian interior throughout Martian history could not sustain a reducing atmosphere due to the low intensity of planet-wide orogenic activity and the short atmospheric mean residence time of hydrogen on Mars. During the post-accretion history of Mars, the combined effects of planetary hydrogen escape, solar-wind sweeping, and reincorporation of volatiles into the Martian surface produced and maintained the present atmosphere.     

Expanding the application of the Eu‐oxybarometer to the lherzolitic shergottites and nakhlites: Implications for the oxidation state heterogeneity of the Martian interior

Abstract— Experimentally rehomogenized melt inclusions from the nakhlite Miller Range 03346 (MIL 03346) and the lherzolitic shergottite Allan Hills 77005 (ALH 77005) have been analyzed for their rare earth element (REE) concentrations in order to characterize the early melt compositions of these Martian meteorites and to calculate the oxygen fugacity conditions they crystallized under. D(Eu/Sm)_{pyroxene/melt} values were measured at 0.77 and 1.05 for ALH 77005 and MIL 03346, respectively. These melts and their associated whole rock compositions have similar REE patterns, suggesting that whole rock REE values are representative of those of the early melts and can be used as input into the pyroxene Eu‐oxybarometer for the nakhlites and lherzolitic shergottites. Crystallization fO₂ values of IW + 1.1 (ALH 77005) and IW + 3.2 (MIL 03346) were calculated. Whole rock data from other nakhlites and lherzolitic shergottites was input into the Eu‐oxybarometer to determine their crystallization fO₂ values. The lherzolitic shergottites and nakhlites have fO₂ values that range from IW + 0.4 to 1.6 and from IW + 1.1 to 3.2, respectively. These values are consistent with some previously determined fO₂ estimates and expand the known range of fO₂ values of the Martian interior to four orders of magnitude. The origins of this range are not well constrained. Possible mechanisms for producing this spread in fO₂ values include mineral/melt fractionation, assimilation, shock effects, and magma ocean crystallization processes. Mineral/melt partitioning can result in changes in fO₂ from the start to the finish of crystallization of 2 orders of magnitude. In addition, crystallization of a Martian magma ocean with reasonable initial water content results in oxidized, water‐rich, late‐stage cumulates. Sampling of these oxidized cumulates or interactions between reduced melts and the oxidized material can potentially account for the range of fO₂ values observed in the Martian meteorites.     

Flares of H2O maser radio line in the sources GDD 25 and Sgr B2

Special Astrophysical Observatory, USSR Academy of Sciences; Byurakan Astrophysical Observatory. Translated from Astrofizika, Vol. 30, No. 1, pp. 121–127, January–February, 1989.     

New estimates for Io eruption temperatures: Implications for the interior

The initial interpretation of Galileo data from Jupiter's moon, Io, suggested eruption temperatures . Tidal heating models have difficulties explaining Io's prodigious heat flow if the mantle is , although we suggest that temperatures up to may be possible. In general, Io eruption temperatures have been overestimated because the incorrect thermal model has been applied. Much of the thermal emission from high-temperature hot spots comes from lava fountains but lava flow models were utilized. We apply a new lava fountain model to the highest reported eruption temperature, the SSI observation of the 1997 eruption at Pillan. This resets the lower temperature limit for the eruption from 1600 to . Additionally, viscous heating of the magma may have increased eruption temperature by as a result of the strong compressive stresses in the ionian lithosphere. While further work is needed, it appears that the discrepancy between observations and interior models is largely resolved.     

Nature of the Martian uplands: Effect on Martian meteorite age distribution and secondary cratering

Abstract— Martian meteorites (MMs) have been launched from an estimated 5–9 sites on Mars within the last 20 Myr. Some 80–89% of these launch sites sampled igneous rock formations from only the last 29% of Martian time. We hypothesize that this imbalance arises not merely from poor statistics, but because the launch processes are dominated by two main phenomena: first, much of the older Martian surface is inefficient in launching rocks during impacts, and second, the volumetrically enormous reservoir of original cumulate crust enhances launch probability for 4.5 Gyr old rocks. There are four lines of evidence for the first point, not all of equal strength. First, impact theory implies that MM launch is favored by surface exposures of near‐surface coherent rock (≤10² m deep), whereas Noachian surfaces generally should have ≥10² m of loose or weakly cemented regolith with high ice content, reducing efficiency of rock launch. Second, similarly, both Mars Exploration Rovers found sedimentary strata, 1–2 orders of magnitude weaker than Martian igneous rocks, favoring low launch efficiency among some fluvial‐derived Hesperian and Noachian rocks. Even if launched, such rocks may be unrecognized as meteorites on Earth. Third, statistics of MM formation age versus cosmic‐ray exposure (CRE) age weakly suggest that older surfaces may need larger, deeper craters to launch rocks. Fourth, in direct confirmation, one of us (N. G. B.) has found that older surfaces need larger craters to produce secondary impact crater fields (cf. Barlow and Block 2004). In a survey of 200 craters, the smallest Noachian, Hesperian, and Amazonian craters with prominent fields of secondaries have diameters of ?45 km, ?19 km, and ?10 km, respectively. Because 40% of Mars is Noachian, and 74% is either Noachian or Hesperian, the subsurface geologic characteristics of the older areas probably affect statistics of recognized MMs and production rates of secondary crater populations, and the MM and secondary crater statistics may give us clues to those properties.     

Siderophile and chalcophile element abundances in shergottites: Implications for Martian core formation

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

Martian planetwide crater distributions: Implications for geologic history and surface processes

Population-density maps of craters in three size ranges (0.6 to 1.2 km, 4 to 10 km, and >20 km in diameter) were compiled for most of Mars from Mariner 9 imagery. These data provide: historical records of the eolian processes (0.6 to 1.2 km craters); stratigraphic, relative, and absolute timescales (4 to 10 km craters); and a history of the early postaccretional evolution of the uplands (> 20 km craters).Based on the distribution of large craters (>20 km diameters), Mars is divisible into two general classes of terrain, densely cratered and very lightly cratered—a division remarkably like the uplands-maria dichotomy of the moon. It is probable that this bimodal character in the density distribution of large craters arose from an abrupt transition in the impact flux rate from an early intense period associated with the tailing off of accretion to an extended quiescent epoch, not from a void in geological activity during much of Mars' history. Radio-isotope studies of Apollo lunar samples show that this transition occurred on the moon in a short time.The intermediate-sized craters (4 to 10 km diameter) and the small-sized craters (0.6 to 1.2 km diameter) appear to be genetically related. The smaller ones are apparently secondary impact craters generated by the former. Most of the craters in the larger of these two size classes appear fresh and uneroded, although many are partly buried by dust mantles. Poleward of the 40° parallels the small fresh craters are notably absent owing to these mantles. The density of small craters is highest in an irregular band centered at 20°S. This band coincides closely with (1) the zone of permanent low-albedo markings; (2) the “wind equator” (the latitude of zero net north or south transport at the surface); and (3) a band that includes a majority of the small dendritic channels. Situated in the southermost part of the equatorial unmantled terrain which extends from about 40°N to 40°S, this band is apparently devoid of even a thin mantle. Because this belt is also coincident with the latitutde of maximum solar insolation (periapsis occurs near summer solstice), we suggest that this band arises from the asymmetrical global wind patterns at the surface and that the band probably follows the latitude of maximum heating which migrates north and south from 25°N to 25°S within the unmantled terrain on a 50,000 year timescale.The population of intermediate-sized craters (4–10 km diameter) appears unaffected by the eolian mantles, at least within the ±45° latitudes. Hence the local density of these craters is probably a valid indicator of the relative age of surfaces generated during the period since the uplands were intensely bombarded and eroded. It now appears that the impact fluxes at Mars and the moon have been roughly the same over the last 4 b.y. because the oldest postaccretional, mare-like surfaces on Mars and the moon display about the same crater density. If so, the nearness of Mars to the asteroid belt has not generated a flux 10 to 25 times greater than the lunar flux. Whereas the lunar maria show a variation of about a factor of three in crater density from the oldest to the youngest major units, analogous surfaces on Mars show a variation between 30 and 50. This implies that periods of active eolian erosion, tectonic evolution, volcanic eruption, and possibly fluvial modification have been scattered throughout Martian history since the formation and degradation of the martian uplands and not confined to small, ancient or recent, epochs. These processes are surely active on the planet today.     

Insights into the Martian mantle: The age and isotopics of the meteorite fall Tissint

The recent witnessed fall of the meteorite Tissint represents the delivery of a pristine new sample from the surface of Mars. This meteorite provides an unprecedented opportunity to study a variety of aspects about the planet's evolution. Using the Rb–Sr and Sm–Nd isotopic systems, we determined that Tissint, a depleted shergottite, has a crystallization age of 574 ± 20 Ma, an initial ε¹⁴³Nd = +42.2 ± 0.5, and an initial ⁸⁷Sr/⁸⁶Sr = 0.700760 ± 11. These initial Nd and Sr isotopic compositions suggest that Tissint originated from a mantle source on Mars that is distinct from the source reservoirs of the other Martian meteorites. The known crystallization ages, geochemical characteristics, ejection ages, and ejection dynamics of Tissint and other similarly grouped Martian meteorites suggest that they are likely derived from a source crater up to approximately 90 km in diameter with an age of approximately 1 Ma that is located on terrain that is approximately 600 million years old.     

Implications of abundant hygroscopic minerals in the Martian regolith

Converging lines of evidence suggest that a significant portion of the Martian surface fines may consist of salts and smectite clays. Salts can form stoichiometric hydrates as well as eutectic solutions with depressed freezing points; clays contain bound water of constitution and adsorb significant quantities of water from the vapor phase. The formation of ice may be suppressed by these minerals in some regions on Mars, and their presence in abundance would imply important consequences for atmospheric and geologic processes and the prospects for exobiology.     

The chlorine isotopic composition of Martian meteorites 1: Chlorine isotope composition of Martian mantle and crustal reservoirs and their interactions

The Martian meteorites record a wide diversity of environments, processes, and ages. Much work has been done to decipher potential mantle sources for Martian magmas and their interactions with crustal and surface environments. Chlorine isotopes provide a unique opportunity to assess interactions between Martian mantle‐derived magmas and the crust. We have measured the Cl‐isotopic composition of 17 samples that span the range of known ages, Martian environments, and mantle reservoirs. The ³⁷Cl of the Martian mantle, as represented by the olivine‐phyric shergottites, NWA 2737 (chassignite), and Shergotty (basaltic shergottite), has a low value of approximately ?3.8‰. This value is lower than that of all other planetary bodies measured thus far. The Martian crust, as represented by regolith breccia NWA 7034, is variably enriched in the heavy isotope of Cl. This enrichment is reflective of preferential loss of ³⁵Cl to space. Most basaltic shergottites (less Shergotty), nakhlites, Chassigny, and Allan Hills 84001 lie on a continuum between the Martian mantle and crust. This intermediate range is explained by mechanical mixing through impact, fluid interaction, and assimilation‐fractional crystallization.     

Coupling the atmosphere with interior dynamics: Implications for the resurfacing of Venus

We calculated 2D and 3D mantle convection models for Venus using digitized atmosphere temperatures from the model of Bullock and Grinspoon (Bullock, M.A., Grinspoon, D.H. [2001]. Icarus 150, 19–37) to study the interaction between interior dynamics and atmosphere thermal evolution. The coupling between atmosphere and interior occurs through mantle degassing and the effect of varying concentrations of the greenhouse gas H₂O on the surface temperature. Exospheric loss of hydrogen to space is accounted for as a H₂O sink. The surface temperature enters the mantle convection model as a boundary condition.Our results suggest a self-consistent feedback mechanism between the interior and the atmosphere resulting in spatial–temporal surface renewal. Greenhouse warming of the atmosphere results in an increase in the surface temperature. Whenever the surface temperature reaches a critical value, the viscosity difference across the lithosphere becomes smaller than about 10⁵ and the surface becomes locally mobile. The critical surface temperature depends on the activation energy for mantle creep, the stress exponent in the non-Newtonian mantle rheology law, and the mantle temperature. Surface renewal together with surface lava flow may explain why the surface of Venus is young on average, i.e. not older than a few hundred million years.The mobilization of the near-surface lithosphere increases the rate of heat removal from the mantle and thereby the interior cooling rate. The enhanced cooling results in a reduction of the water outgassing rates. As a consequence of decreasing water concentrations in the atmosphere, the surface temperature decreases. Our model calculations suggest that Venus should have been geologically active until recently. This is in agreement with several lines of observational evidence from thermal emissivity measurements and crater distribution analyses.     

H2O maser pumping: The effect of quasi-resonance energy transfer in collisions between H2 and H2O molecules

The effect of quasi-resonance energy transfer in collisions between H₂ and H₂O molecules in H₂O maser sources is investigated. New data on the state-to-state rate coefficients for collisional transitions for H₂O and H₂ molecules are used in the calculations. The results of ortho-H₂O level population inversion calculations for the 22.2-, 380-, 439-, and 621-GHz transitions are presented. The ortho-H₂O level population inversion is shown to depend significantly on the population distribution of the para-H₂ J = 0 and 2 rotational levels. The possibility of quasi-resonance energy transfer in collisions between H₂ molecules at highly excited rotational-vibrational levels and H₂O molecules is considered. The quasi-resonance energy transfer effect can play a significant role in pumping H₂O masers in the central regions of active galactic nuclei and in star-forming regions.     

Constraints on the water,chlorine, and fluorine content of the Martian mantle

Previous estimates of the volatile contents of Martian basalts, and hence their source regions, ranged from nearly volatile‐free through estimates similar to those found in terrestrial subduction zones. Here, we use the bulk chemistry of Martian meteorites, along with Martian apatite and amphibole chemistry, to constrain the volatile contents of the Martian interior. Our estimates show that the volatile content of the source region for the Martian meteorites is similar to the terrestrial Mid‐Ocean‐Ridge Mantle source. Chlorine is enriched compared with the depleted terrestrial mantle but is similar to the terrestrial enriched source region; fluorine is similar to the terrestrial primitive mantle; and water is consistent with the terrestrial mantle. Our results show that Martian magmas were not volatile saturated; had water/chlorine and water/fluorine ratios ~0.4–18; and are most similar, in terms of volatiles, to terrestrial MORBs. Presumably, there are variations in volatile content in the Martian interior as suggested by apatite compositions, but more bulk chemical data, especially for fluorine and water, are required to investigate these variations. Finally, the Noachian Martian interior, as exemplified by surface basalts and NWA 7034, may have had higher volatile contents.