Infrared imaging spectroscopy of Mars: H2O mapping and determination of CO2 isotopic ratios

High-resolution infrared imaging spectroscopy of Mars has been achieved at the NASA Infrared Telescope Facility (IRTF) on June 19-21, 2003, using the Texas Echelon Cross Echelle Spectrograph (TEXES). The areocentric longitude was 206°. Following the detection and mapping of hydrogen peroxide H₂O₂ [Encrenaz et al., 2004. Icarus 170, 424-429], we have derived, using the same data set, a map of the water vapor abundance. The results appear in good overall agreement with the TES results and with the predictions of the Global Circulation Model (GCM) developed at the Laboratory of Dynamical Meteorology (LMD), with a maximum abundance of water vapor of 3±1.5×¹⁰⁻⁴(17±9 pr-μm). We have searched for CH₄ over the martian disk, but were unable to detect it. Our upper limits are consistent with earlier reports on the methane abundance on Mars. Finally, we have obtained new measurements of CO₂ isotopic ratios in Mars. As compared to the terrestrial values, these values are: (¹⁸O/¹⁷O)[M/E] = 1.03 ± 0.09; (¹³C/¹²C)[M/E] = 1.00 ± 0.11. In conclusion, in contrast with the analysis of Krasnopolsky et al. [1996. Icarus 124, 553-568], we conclude that the derived martian isotopic ratios do not show evidence for a departure from their terrestrial values.     

Simultaneous mapping of H2O and H2O2 on Mars from infrared high-resolution imaging spectroscopy

New maps of martian water vapor and hydrogen peroxide have been obtained in November-December 2005, using the Texas Echelon Cross Echelle Spectrograph (TEXES) at the NASA Infra Red Telescope facility (IRTF) at Mauna Kea Observatory. The solar longitude Ls was 332° (end of southern summer). Data have been obtained at 1235-1243 cm⁻¹, with a spectral resolution of 0.016 cm⁻¹ (R=8×¹⁰⁴). The mean water vapor mixing ratio in the region [0°-55° S; 345°-45° W], at the evening limb, is 150±50 ppm (corresponding to a column density of 8.3±2.8 pr-μm). The mean water vapor abundance derived from our measurements is in global overall agreement with the TES and Mars Express results, as well as the GCM models, however its spatial distribution looks different from the GCM predictions, with evidence for an enhancement at low latitudes toward the evening side. The inferred mean H₂O₂ abundance is 15±10 ppb, which is significantly lower than the June 2003 result [Encrenaz, T., Bézard, B., Greathouse, T.K., Richter, M.J., Lacy, J.H., Atreya, S.K., Wong, A.S., Lebonnois, S., Lefèvre, F., Forget, F., 2004. Icarus 170, 424-429] and lower than expected from the photochemical models, taking in account the change in season. Its spatial distribution shows some similarities with the map predicted by the GCM but the discrepancy in the H₂O₂ abundance remains to be understood and modeled.     

CO2 Snow on Mars and Early Earth: Experimental Constraints

Greenhouse warming due to carbon dioxide atmospheres may be responsible for maintaining the early Earth's surface temperature above freezing and may even have allowed for liquid water on early Mars. However, the high levels of CO₂ required for such warming should have also resulted in the formation of CO₂ clouds. These clouds, depending on their particle size, could lead to either warming or cooling. The particle size in turn is determined by the nucleation and growth conditions. Here we present laboratory studies of the nucleation and growth of carbon dioxide on water ice under martian atmospheric conditions. We find that a critical saturation, S=1.34, is required for nucleation, corresponding to a contact parameter between solid water and solid carbon dioxide of m=0.95. We also find that after nucleation occurs, growth of CO₂ is very rapid, and we report the growth rates at a number of supersaturations. Because growth would be expected to continue until the CO₂ pressure is lowered to its vapor pressure, we expect particles larger than those being currently suggested for the present and past martian atmospheres. Using this information in a microphysical model described in a companion paper, we find that CO₂ clouds are best described as “snow,” having a relatively small number of large particles.     

Mars CO2 cycle: Effects of airborne dust and polar cap ice emissivity

Mars General Circulation Model (GCM) simulations are presented to illustrate the importance of the ice emissivity of the seasonal CO₂ polar caps in regulating the effects of airborne dust on the martian CO₂ cycle. Simulated results show that atmospheric dust suppresses CO₂ condensation when the CO₂ ice emissivity is high but enhances it when the CO₂ ice emissivity is low. This raises the possibility that the reason for the repeatable nature of the CO₂ cycle in the presence of a highly variable dust cycle is that the CO₂ ice emissivity is “neutral” - the value that leads to no change in CO₂ condensation with changing atmospheric dust. For this GCM, the “neutral” emissivity is approximately 0.55, which is low compared to observed cap emissivities. This inconsistency poses a problem for this hypothesis. However, it is clear that the CO₂ ice emissivity is a critical physical parameter in determining how atmospheric dust affects the CO₂ cycle on Mars.     

Long-term spectroscopic observations of Mars using IRTF/CSHELL: Mapping of O2 dayglow, CO, and search for CH4

Long-term spectroscopic observations of the O₂ dayglow at 1.27 μm result in a map of the latitudinal and seasonal behavior of the dayglow intensity for the full martian year. The O₂ dayglow is a sensitive tracer of Mars' photochemistry, and this map reflects variations of Mars' photochemistry at low and middle latitudes. It may be used to test photochemical models. Long-term observations of the CO mixing ratio have been also combined into the seasonal-latitudinal map. Seasonal and latitudinal variations of the mixing ratios of CO and the other incondensable gases (N₂, Ar, O₂, and H₂) discovered in our previous work are caused by condensation and sublimation of CO₂ to and from the polar regions. They reflect dynamics of the atmosphere and polar processes. The observed map may be used to test global circulation models of the martian atmosphere. The observed global abundances of CO are in reasonable agreement with the predicted variations with the 11-year solar cycle. Despite the perfect observing conditions, methane has not been detected using the IRTF/CSHELL with a 3σ upper limit of 14 ppb. This upper limit does not rule out the value of 10 ppb observed using the Canada-France-Hawaii Telescope and the Mars Express Planetary Fourier Spectrometer.     

Subvisible CO2 ice clouds detected in the mesosphere of Mars

The formation of CO₂ ice clouds in the upper atmosphere of Mars has been suggested in the past on the basis of a few temperature profiles exhibiting portions colder than CO₂ frost point. However, the corresponding clouds were never observed. In this paper, we discuss the detection of the highest clouds ever observed on Mars by the SPICAM ultraviolet spectrometer on board Mars Express spacecraft. Analyzing stellar occultations, we detected several mesospheric detached layers at about 100 km in the southern winter subtropical latitudes, and found that clouds formed where simultaneous temperature measurements indicated that CO₂ was highly supersaturated and probably condensing. Further analysis of the spectra reveals a cloud opacity in the subvisible range and ice crystals smaller than 100 nm in radius. These layers are therefore similar in nature as the noctilucent clouds which appear on Earth in the polar mesosphere. We interpret these phenomena as CO₂ ice clouds forming inside supersaturated pockets of air created by upward propagating thermal waves. This detection of clouds in such an ultrararefied and supercold atmosphere raises important questions about the martian middle-atmosphere dynamics and microphysics. In particular, the presence of condensates at such high altitudes begs the question of the origin of the condensation nuclei.     

Near-infrared spectra of laboratory H2O-CH4 ice mixtures

We present 1.25-19 μm infrared spectra of pure solid CH₄ and H₂O/CH₄=87, 20, and 3 solid mixtures at temperatures from 15 to 150 K. We compare and contrast the absorptions of CH₄ in solid H₂O with those of pure CH₄. Changes in selected peak positions, profiles, and relative strength with temperature are presented, and absolute strengths for absorptions of CH₄ in solid H₂O are estimated. Using the two largest (ν₃+ν₄) and (ν₁+ν₄) near-IR absorptions of CH₄ at 2.324 and 2.377 μm (4303 and 4207 cm⁻¹), respectively, as examples, we show that peaks of CH₄ in solid H₂O are at slightly shorter wavelength (higher frequency) and broader than those of pure solid CH₄. With increasing temperature, these peaks shift to higher frequency and become increasingly broad, but this trend is reversible on re-cooling, even though the phase transitions of H₂O are irreversible. It is to be hoped that these observations of changes in the positions, profiles, and relative intensities of CH₄ absorptions with concentration and temperature will be of use in understanding spectra of icy outer Solar System bodies.     

A sensitive search for SO2 in the martian atmosphere: Implications for seepage and origin of methane

Mars was observed near the peak of the strongest SO₂ band at 1364-1373 cm⁻¹ with resolving power of 77,000 using the Texas Echelon Cross Echelle Spectrograph on the NASA Infrared Telescope Facility. The observation covered the Tharsis volcano region which may be preferable to search for SO₂. The spectrum shows absorption lines of three CO₂ isotopomers and three H₂O isotopomers. The water vapor abundance derived from the HDO lines assuming D/H = 5.5 times the terrestrial value is 12±1.0 pr. μm, in agreement with the simultaneous MGS/TES observations of 14 pr. μm at the latitudes (50° S to 10° N) of our observation. Summing of spectral intervals at the expected positions of sixteen SO₂ lines puts a 2σ upper limit on SO₂ of 1 ppb. SO₂ may be emitted into the martian atmosphere by seepage and is removed by three-body reactions with OH and O. The SO₂ lifetime, 2 years, is longer than the global mixing time 0.5 year, so SO₂ should be rather uniformly distributed across Mars. Seepage of SO₂ is less than 15,000 tons per year on Mars which is smaller than the volcanic production of SO₂ on the Earth by a factor of 700. Because CH₄/SO₂ is typically 10⁻⁴-10⁻³ in volcanic gases on the Earth, our results show seepage is unlikely to be the source of the recently discovered methane on Mars and therefore strengthen its biogenic origin.     

Yearly and seasonal variations of low albedo surfaces on Mars in the OMEGA/MEx dataset: Constraints on aerosols properties and dust deposits

The time variations of spectral properties of dark martian surface features are investigated using the OMEGA near-IR dataset. The analyzed period covers two Mars years, spanning from early 2004 to early 2008 (includes the 2007 global dust event). Radiative transfer modeling indicates that the apparent albedo variations of low to mid-latitude dark regions are consistent with those produced by the varying optical depth of atmospheric dust as measured simultaneously from the ground by the Mars Exploration Rovers. We observe only a few significant albedo changes that can be attributed to surface phenomena. They are small-scaled and located at the boundaries between bright and dark regions. We then investigate the variations of the mean particle size of aerosols using the evolution of the observed dark region spectra between 1 and 2.5 μm. Overall, we find that the observed changes in the spectral slope are consistent with a mean particle size of aerosols varying with time between 1 and 2 μm. Observations with different solar zenith angles make it possible to characterize the aerosol layer at different altitudes, revealing a decrease of the particle size of aerosols as altitude increases.     

CO2 clouds, CAPE and convection on Mars: Observations and general circulation modeling

The thermal emission spectrometer (TES) and the radio science (RS) experiment flying on board the Mars Global Surveyor (MGS) spacecraft have made observations of atmospheric temperatures below the saturation temperature of carbon dioxide (CO₂). This supersaturated air provides a source of convective available potential energy (CAPE), which, when realized may result in vigorous convective mixing. To this point, most Mars atmospheric models have assumed vertical mixing only when the dry adiabatic lapse rate is exceeded. Mixing associated with the formation of CO₂ clouds could have a profound effect on the vertical structure of the polar night, altering the distribution of temperature, aerosols, and gasses.Presented in this work are estimates of the total planetary inventory of CAPE and the potential convective energy flux (PCEF) derived from RS and TES temperature profiles. A new Mars Global Circulation Model (MGCM) CO₂ cloud model is developed to better understand the distribution of observed CAPE and its potential effect on Martian polar dynamics and heat exchange, as well as effects on the climate as a whole. The new CO₂ cloud model takes into account the necessary cloud microphysics that allow for supersaturation to occur and includes a parameterization for CO₂ cloud convection. It is found that when CO₂ cloud convective mixing is included, model results are in much better agreement with the observations of the total integrated CAPE as well as total column non-condensable gas concentrations presented by Sprague et al. [2005a, GRS measurements of Ar in Mars’ atmosphere, American Astronomical Society, DPS meeting #37, #24.08, and 2005b, Distribution and Abundance of Mars’ Atmospheric Argon, 36th Annual Lunar and Planetary Science Conference, #2085] When the radiative effects of water ice clouds are included the agreement is further improved.     

Mapping the mesospheric CO2 clouds on Mars: MEx/OMEGA and MEx/HRSC observations and challenges for atmospheric models

This study presents the latest results on the mesospheric CO₂ clouds in the martian atmosphere based on observations by OMEGA and HRSC onboard Mars Express. We have mapped the mesospheric CO₂ clouds during nearly three martian years of OMEGA data yielding a cloud dataset of ∼60 occurrences. The global mapping shows that the equatorial clouds are mainly observed in a distinct longitudinal corridor, at seasons L_s = 0-60° and again at and after L_s = 90°. A recent observation shows that the equatorial CO₂ cloud season may start as early as at L_s = 330°. Three cases of mesospheric midlatitude autumn clouds have been observed. Two cloud shadow observations enabled the mapping of the cloud optical depth (τ = 0.01-0.6 with median values of 0.13-0.2 at λ = 1 μm) and the effective radii (mainly 1-3 μm with median values of 2.0-2.3 μm) of the cloud crystals. The HRSC dataset of 28 high-altitude cloud observations shows that the observed clouds reside mainly in the altitude range ∼60-85 km and their east-west speeds range from 15 to 107 m/s. Two clouds at southern midlatitudes were observed at an altitude range of 53-62 km. The speed of one of these southern midlatitude clouds was measured, and it exhibited west-east oriented speeds between 5 and 42 m/s. The seasonal and geographical distribution as well as the observed altitudes are mostly in line with previous work. The LMD Mars Global Climate Model shows that at the cloud altitude range (65-85 km) the temperatures exhibit significant daily variability (caused by the thermal tides) with the coldest temperatures towards the end of the afternoon. The GCM predicts the coldest temperatures of this altitude range and the season L_s = 0-30° in the longitudinal corridor where most of the cloud observations have been made. However, the model does not predict supersaturation, but the GCM-predicted winds are in fair agreement with the HRSC-measured cloud speeds. The clouds exhibit variable morphologies, but mainly cirrus-type, filamented clouds are observed (nearly all HRSC observations and most of OMEGA observations). In ∼15% of OMEGA observations, clumpy, round cloud structures are observed, but very few clouds in the HRSC dataset show similar morphology. These observations of clumpy, cumuliform-type clouds raise questions on the possibility of mesospheric convection on Mars, and we discuss this hypothesis based on Convective Available Potential Energy calculations.     

The rotational temperature and column density of H3 in Uranus

H₃⁺ emission from Uranus has been observed repeatedly for over a decade. However, the details of the emission mechanisms are still poorly understood. In this paper, we discuss our findings from the observations we made in September 2000 and September 2001. The spectrum of Uranus was recorded at the NASA Infrared Telescope Facility using the SpeX instrument between 3 and 5 μm, with a resolving power of 1000. The 3.4–4.1 μm range permits a determination of both the H₃⁺ column density and its rotational temperature. The H₃⁺ emission, measured at 3.986 μm in the 0.8×3.7 arcsec aperture, was 0.031 Jy in September 2000 and 0.053 Jy in September 2001. The rotational temperature was found to be 560±40 K and 640±40 K in 2000 and 2001 respectively, with corresponding column densities of 5.1 (+3.2,−1.4) 10¹¹ and 4.0 (+1.8,−1.0) 10¹¹ cm⁻². These results extend the baseline for the variability study of the H₃⁺ emission (Astrophys. J. 524 (1999) 1059). Previous observations between 1992 and 1998 seemed to indicate a correlation between the H₃⁺ intensity and the solar cycle. The current data for 2000 and 2001 appear to be consistent with this general tendency.     

Airglow on Mars: Some model expectations for the OH Meinel bands and the O2 IR atmospheric band

This work presents model calculations of the diurnal airglow emissions from the OH Meinel bands and the O₂ IR atmospheric band in the neutral atmosphere of Mars. A time-dependent photochemical model of the lower atmosphere below 80 km has been developed for this purpose. Special emphasis is placed on the nightglow emissions because of their potential to characterize the atomic oxygen profile in the 50-80 km region. Unlike on Earth, the OH Meinel emission rates are very sensitive to the details of the vibrational relaxation pathway. In the sudden death and collisional cascade limits, the maximum OH Meinel column intensities for emissions originating from a fixed upper vibrational level are calculated to be about 300 R, for transitions v^′=9→v^′?8, and 15,000 R, for transitions v^′=1→v^′=0, respectively. During the daytime the 1.27 μm emission from O₂(), primarily formed from ozone photodissociation, is of the order of MegaRayleighs (MR). Due to the long radiative lifetime of O₂(), a luminescent remnant of the dayglow extends to the dark side for about two hours. At night, excited molecular oxygen is expected to be produced through the three body reaction O + O + CO₂. The column emission of this nighttime component of the airglow is estimated to amount to 25 kR. Both nightglow emissions, from the OH Meinel bands and the O₂ IR atmospheric band, overlap in the 50-80 km region. Photodissociation of CO₂ in the upper atmosphere and the subsequent transport of the atomic oxygen produced to the emitting layer are revealed as key factors in the nightglow emissions from these systems. The Mars 5 upper constraint for the product [H][O₃] is revised on the basis of more recent values for the emission probabilities and collisional deactivation coefficients.     

High-resolution spectroscopy of Saturn at 3 microns: CH4, CH3D, C2H2, C2H6, PH3, clouds, and haze

We report observation and analysis of a high-resolution 2.87-3.54 μm spectrum of the southern temperate region of Saturn obtained with NIRSPEC at Keck II. The spectrum reveals absorption and emission lines of five molecular species as well as spectral features of haze particles. The ν₂+ν₃ band of CH₃D is detected in absorption between 2.87 and 2.92 μm; and we derived from it a mixing ratio approximately consistent with the Infrared Space Observatory result. The ν₃ band of C₂H₂ also is detected in absorption between 2.95 and 3.05 μm; analysis indicates a sudden drop in the C₂H₂ mixing ratio at 15 mbar (130 km above the 1 bar level), probably due to condensation in the low stratosphere. The presence of the ν₃+ν₉+ν₁₁ band of C₂H₆ near 3.07 μm, first reported by Bjoraker et al. [Bjoraker, G.L., Larson, H.P., Fink, U., 1981. Astrophys. J. 248, 856-862], is confirmed, and a C₂H₆ condensation altitude of 10 mbar (140 km) in the low stratosphere is determined. We assign weak emission lines within the 3.3 μm band of CH₄ to the ν₇ band of C₂H₆, and derive a mixing ratio of 9±4×¹⁰⁻⁶ for this species. Most of the C₂H₆ 3.3 μm line emission arises in the altitude range 460-620 km (at ∼μbar pressure levels), much higher than the 160-370 km range where the 12 μm thermal molecular line emission of this species arises. At 2.87-2.90 μm the major absorber is tropospheric PH₃. The cloud level determined here and at 3.22-3.54 is 390-460 mbar (∼30 km), somewhat higher than found by Kim and Geballe [Kim, S.J., Geballe, T.R., 2005. Icarus 179, 449-458] from analysis of a low resolution spectrum. A broad absorption feature at 2.96 μm, which might be due to NH₃ ice particles in saturnian clouds, is also present. The effect of a haze layer at about 125 km (∼12 mbar level) on the 3.20-3.54 μm spectrum, which was not apparent in the low resolution spectrum, is clearly evident in the high resolution data, and the spectral properties of the haze particles suggest that they are composed of hydrocarbons.     

A sensitive search for nitric oxide in the lower atmospheres of Venus and Mars: Detection on Venus and upper limit for Mars

High-resolution spectra of Venus and Mars at the NO fundamental band at 5.3 μm with resolving power ν/δν=76,000 were acquired using the TEXES spectrograph at NASA IRTF on Mauna Kea, Hawaii. The observed spectrum of Venus covered three NO lines of the P-branch. One of the lines is strongly contaminated, and the other two lines reveal NO in the lower atmosphere at a detection level of 9 sigma. A simple photochemical model for NO and N at 50-112 km was coupled with a radiative transfer code to simulate the observed equivalent widths of the NO and some CO₂ lines. The derived NO mixing ratio is 5.5±1.5 ppb below 60 km and its flux is . Predissociation of NO at the (0-0) 191 nm and (1-0) 183 nm bands of the δ-system and the reaction with N are the only important loss processes for NO in the lower atmosphere of Venus. The photochemical impact of the measured NO abundance is significant and should be taken into account in photochemical modeling of the Venus atmosphere. Lightning is the only known source of NO in the lower atmosphere of Venus, and the detection of NO is a convincing and independent proof of lightning on Venus. The required flux of NO is corrected for the production of NO and N by the cosmic ray ionization and corresponds to the lightning energy deposition of . For a flash energy on Venus similar to that on the Earth (∼¹⁰⁹ J), the global flashing rate is ∼90 s⁻¹ and ∼6 km⁻² y⁻¹ which is in reasonable agreement with the existing optical observations. The observed spectrum of Mars covered three NO lines of the R-branch. Two of these lines are contaminated by CO₂ lines, and the line at 1900.076 cm⁻¹ is clean and shows some excess over the continuum. Some photochemical reactions may result in a significant excitation of NO (v=1) in the lowest 20 km on Mars. However, quenching of NO (v=1) by CO₂ is very effective below 40 km. Excitation of NO (v=1) in the collisions with atomic oxygen is weak because of the low temperature in the martian atmosphere, and we do not see any explanation of a possible emission of NO at 5.3 μm. Therefore the data are treated as the lack of absorption with a 2 sigma upper limit of 1.7 ppb to the NO abundance in the lower atmosphere of Mars. This limit is above the predictions of photochemical models by a factor of 3.     

The 2.9-4.2 micron spectrum of Saturn: Clouds and CH4, PH3, and NH3

We have used synthetic spectra to analyze a medium resolution 2.9-4.2 μm spectrum of Saturn's temperate region observed at UKIRT using CGS4. The synthetic spectra include CH₄, PH₃, and NH₃ lines, for which mixing ratios were adopted from recent Cassini results. The observed absorption features in the spectrum are well accounted for by lines of these molecular species formed 22 +/− 8 km above the 1 bar pressure level at ∼610 mbar. The influence of optically thin haze particles at higher altitudes on the spectrum is not pronounced, with higher spectral resolution probably required to constrain the effects of haze in this wavelength region. Fluorescent line emission by CH₄ in its ν₃ and ν₃+ν₄−ν₄ bands, detected in the 3.2-3.5 μm region, originates between 400 km (∼0.06 mbar) and 800 km (∼0.01 μbar) above the 1 bar level, with peak contributions from the two major contributing bands at 550 km (∼3 μbar) and 700 km (∼0.1 μbar), respectively.     

Geologic context of in situ rocky exposures in Mare Serpentis, Mars: Implications for crust and regolith evolution in the cratered highlands

Global acquisition of infrared spectra and high-resolution visible and infrared imagery has enabled the placement of compositional information within stratigraphic and geologic context. Mare Serpentis, a low albedo region located northwest of Hellas Basin, is rich in spectral and thermophysical diversity and host to numerous isolated exposures of in situ rocky material. Most martian surfaces are dominated by fine-grained particulate materials that bear an uncertain compositional and spatial relationship to their source. Thus location and characterization of in situ rock exposures is important for understanding the origin of highland materials and the processes which have modified those materials. Using spectral, thermophysical and morphologic information, we assess the local and regional stratigraphy of the Mare Serpentis surface in an effort to reconstruct the geologic history of the region. The martian highlands in Mare Serpentis are dominated by two interspersed surface units, which have distinct compositional and thermophysical properties: (1) rock-dominated surfaces relatively enriched in olivine and pyroxene, and depleted in high-silica phases, and (2) sediment or indurated material depleted in olivine and pyroxene, with relatively higher abundance of high-silica phases. This is a major, previously unrecognized trend which appears to be pervasive in the Mare Serpentis region and possibly in other highland areas. The detailed observations have led us to form two hypotheses for the relationship between these two units: either (1) they are related through a widespread mechanical and/or chemical alteration process, where less-mafic plains materials are derived from the mafic bedrock, but have been compositionally altered in the process of regolith formation, or (2) they are stratigraphically distinct units representing separate episodes of upper crust formation. Existing observations suggest that the second scenario is more likely. In this scenario, plains materials represent older, degraded, and possibly altered, “basement” rock, whereas the rocky exposures represent later additions to the crust and are probably volcanic in origin. These hypotheses should be further testable with decimeter-resolution imagery and meter-resolution short wavelength infrared spectra.     

Methane on Mars: A product of H2O photolysis in the presence of CO

We suggest that the methane observed on Mars can be formed by photolysis of water vapor in the presence of CO, in addition to possible geological sources, rather than biologically.     

Limits on the trapping of atmospheric CH4 in martian polar ice analogs

Recent detection of methane (CH₄) on Mars has generated interest in possible biological or geological sources, but the factors responsible for the reported variability are not understood. Here we explore one potential sink that might affect the seasonal cycling of CH₄ on Mars - trapping in ices deposited on the surface. Our apparatus consisted of a high-vacuum chamber in which three different Mars ice analogs (water, carbon dioxide, and carbon dioxide clathrate hydrates) were deposited in the presence of CH₄ gas. The ices were monitored for spectroscopic evidence of CH₄ trapping using transmission Fourier-Transform Infrared (FT-IR) spectroscopy, and during subsequent sublimation of the ice films the vapor composition was measured using mass spectrometry (MS). Trapping of CH₄ in water ice was confirmed at deposition temperatures <100 K which is consistent with previous work, thus validating the experimental methods. However, no trapping of CH₄ was observed in the ice analogs studied at warmer temperatures (140 K for H₂O and CO₂ clathrate, 90 K for CO₂ snow) with approximately 10 mTorr CH₄ in the chamber. From experimental detection limits these results provide an upper limit of 0.02 for the atmosphere/ice trapping ratio of CH₄. If it is assumed that the trapping mechanism is linear with CH₄ partial pressure and can be extrapolated to Mars, this upper limit would indicate that less than 1% is expected to be trapped from the largest reported CH₄ plume, and therefore does not represent a significant sink for CH₄.     

Jupiter's hydrocarbon polar brightening: Discovery of 3-micron line emission from south polar CH4, C2H2, and C2H6

Jupiter exhibits bright H⁺₃ auroral arcs at 3-4 microns that cool the hot (>1000 K) ionosphere above the ∼¹⁰−7 bar level through the infrared bands of this trace constituent. Below the ¹⁰−7 bar level significant cooling proceeds through infrared active bands of CH₄, C₂H₂, and C₂H₆. We report the discovery of 3-micron line emission from these hydrocarbon species in spectra of the jovian south polar region obtained on April 18 and 20, 2006 (UT) with CGS4 on the United Kingdom Infrared Telescope. Estimated cooling rates through these molecules are 7.5×¹⁰−3, 1.4×¹⁰−3, and , respectively, for a total nearly half that of H⁺₃. We derive a temperature of 450 ± 50 K in the ¹⁰−7-¹⁰−5 bar region from the C₂H₂ lines.