ALH84001, a cumulate orthopyroxenite member of the martian meteorite clan

Abstract— ALH84001, originally classified as a diogenite, is a coarse-grained, cataclastic, orthopyroxenite meteorite related to the martian (SNC) meteorites. The orthopyroxene is relatively uniform in composition, with a mean composition of Wo_3.3En_69.4Fs_27.3. Minor phases are euhedral to subhedral chromite and interstitial maskelynite, An_31.1Ab_63.2Or_5.7, with accessory augite, Wo_42.2En_45.1Fs_12.7, apatite, pyrite and carbonates, Cc_11.5Mg_58.0Sd_29.4Rd_1.1. The pyroxenes and chromites in ALH84001 are similar in composition to these phases in EETA79001 lithology A megacrysts but are more homogeneous. Maskelynite is similar in composition to feldspars in the nakhlites and Chassigny. Two generations of carbonates are present, early (pre-shock) strongly zoned carbonates and late (post-shock) carbonates. The high Ca content of both types of carbonates indicates that they were formed at moderately high temperature, possibly ～700 °C. ALH84001 has a slightly LREE-depleted pattern with La 0.67x and Lu 1.85x CI abundances and with a negative Eu anomaly (Eu/Sm 0.56x CI). The uniform pyroxene composition is unusual for martian meteorites, and suggests that ALH84001 cooled more slowly than did the shergottites, nakhlites or Chassigny. The nearly monomineralic composition, coarse-grain size, homogenous orthopyroxene and chromite compositions, the interstitial maskelynite and apatite, and the REE pattern suggest that ALH84001 is a cumulate orthopyroxenite containing minor trapped, intercumulus material.     

Fabrication and response of high concentration SIMPLE superheated droplet detectors with different liquids

The combined measurement of dark matter interactions with different superheated liquids has recently been suggested as a cross-correlation technique in identifying WIMP candidates. We describe the fabrication of high concentration superheated droplet detectors based on the light nuclei liquids C₃F₈, C₄F₈, C₄F₁₀ and CCl₂F₂, and investigation of their irradiation response with respect to C₂ClF₅. The results are discussed in terms of the basic physics of superheated liquid response to particle interactions, as well as the necessary detector qualifications for application in dark matter search investigations. The possibility of heavier nuclei SDDs is explored using the light nuclei results as a basis, with CF₃I provided as an example.     

Petrology,geochemistry, and cosmic‐ray exposure age of Iherzolitic shergottite Northwest Africa 1950

Northwest Africa (NWA) 1950 is a new member of the lherzolitic shergottite clan of the Martian meteorites recently found in the Atlas Mountains. The petrological, mineralogical, and geochemical data are very close to those of the other known lherzolitic shergottites. The meteorite has a cumulate gabbroic texture and its mineralogy consists of olivine (Fo₆₆ to Fo₇₅), low and high‐Ca pyroxenes (En₇₈Fs₁₉Wo₂‐En₆₀Fs₂₆W₁₄; En₅₃Fs₁₆Wo₃₁‐En₄₅Fs₁₄Wo₄₁), and plagioclase (An₅₇Ab₄₁Or₁ to An₄₀Ab₅₇Or₃; entirely converted into maskelynite during intense shock metamorphism). Accessory minerals include phosphates (merrillite), chromite and spinels, sulfides, and a glass rich in potassium. The oxygen isotopic values lie on the fractional line defined by the other SNC meteorites (Δ¹⁷O = 0.312 %o). The composition of NWA 1950 is very similar to the other lherzolitic shergottites and suggests an origin from the same magmatic system, or at least crystallization from a close parental melt. Cosmogenic ages indicate an ejection age similar to those of the other lherzolitic shergottites. The intensity of the shock is similar to that observed in other shergottites, as shown by the occurrence of small melt pockets containing glass interwoven with stishovite.     

Experimental impact shock chemistry on planetary icy satellites

We present new experimental results on impact shock chemistry into icy satellites of the outer planets. Icy mixtures of pure water ice with CO₂, Na₂CO₃, CH₃OH, and CH₃OH/(NH₄)₂SO₄ at 77 K were ablated with a powerful pulsed laser—a new technique used to simulate shock processes which can occur during impacts. New products were identified by GC-MS and FTIR analyses after laser ablation. Our results show that hydrogen peroxide is formed in irradiated H₂O/CO₂ ices with a final concentration of 0.23%. CO and CH₃OH were also detected as main products. The laser ablation of frozen H₂O/Na₂CO₃ generates only CO and CO₂ as destruction products from the salt. Pulsed irradiation of water ice containing methanol leads also to the formation of CO and CO₂, generates methane and more complex molecules containing carbonyl groups like acetaldehyde, acetone, methyl formate, and a diether, dimethyl formal. The last three compounds are also produced when adding ammonium sulfate to H₂O/CH₃OH ice, but acetone is more abundant. The formation of two hydrocarbons, CH₄ and C₂H₆ is observed as well as the production of three nitrogen compounds, nitrous oxide, hydrogen cyanide, and acetonitrile.     

Stratospheric observations of NO3 and its experimental and theoretical distribution between 20 and 40 km

A simultaneous night-time observation of NO₃ and 0₃ has been made by means of a balloon-borne spectrophotometer pointing at the rising planet Venus. The spectrum recorded between 642 and 672 nm makes it possible to determine the NO₃ and O₃ absorptions in the 662 nm band and the Chappuis bands, respectively. The NO₃ vertical distribution is deduced, and is found to reach a peak of (3.4 ± 0.4) 10⁷ molecules cm^?3at 35 km. Such an observational result can be interpreted in terms of a theoretical profile deduced from a one-dimension time-dependant photochemical model which takes account of the night-time stratospheric NO₂, NO₃ and N₂O₅ constituents and the latest kinetic and photochemical data for the rate constants.     

Crystal chemistry of merrillite from Martian meteorites: Mineralogical recorders of magmatic processes and planetary differentiation

Merrillite is a ubiquitous accessory phase in a variety of Martian meteorite lithologies. The Martian merrillites exhibit a positive correlation between Mg# and Na and a negative correlation between Mg# and both Mn and vacancies in the octahedral Na‐site. Their REE patterns are varied and range from LREE‐depleted to LREE‐enriched. The dominant cation substitutions in the Martian merrillites are Fe²⁺_{VI Mg‐site}?Mg²⁺_{VI Mg‐site} and Ca²⁺_{VI Na‐site} +  □_{VI Na‐site}?2Na⁺_{VI Na‐site}. The REE substitution into the 8‐fold coordinated Ca‐site is accommodated by the coupled substitution Ca_{VIII Ca‐site} + (Na)_{VI Na‐site} ?(Y³⁺ + REE³⁺)_{VIII Ca‐site} + □_{VI Na‐site}. The REE substitution is significantly more prevalent in lunar merrillite and can be used as a “fingerprint” to distinguish lunar from Martian meteorites. The substitution of OH^? (whitlockite) and/or F^? (bobdownsite) for O^2? on one of the phosphate tetrahedrons appears to be rather insignificant. The correlations among Na, Mg#, Mn, and Na‐site vacancies are linked to the premerrillite crystallization history of the melt and the crystal chemical behavior of the Mg‐ and Na‐sites. The former reflects the sequence and extent of plagioclase and pyroxene crystallization. The differences in REE pattern shapes among the merrillites reflect source regions for the Martian basalts and the shapes are not greatly perturbed by the crystallization history. The occurrence of merrillite does not imply low‐volatile component in the Martian magmas. However, the low whitlockite and bobdownsite contents suggest that these samples were not altered by hydrothermal fluids and therefore not reset owing to aqueous fluid interactions. Consequently, the young ages of the shergottites are probably true igneous crystallization ages.     

Anion chemistry on Titan: A possible route to large N-bearing hydrocarbons

The reaction of CN^? with cyanoacetylene (HC₃N), has been studied as a function of the HC₃N pressure in a quadrupole tandem mass spectrometer. The mass spectra revealed the fast depletion of the CN^? parent ion and formation of larger anions of rapidly growing size. Most of the ions observed were found to belong to two series of products: (HC₃N)_x·C_2p+1N^? and (HC₃N)_x·C_2pN^? resulting from the sequential additions of HC₃N molecules and loss of HCN or HCCN molecules. The mechanism and energetics of the first two reaction steps are briefly discussed. The laboratory data are compared with those from the Cassini CAPS-ELS spectrometer. It is believed that the reactions observed could account for the growth of anions in Titan’s ionosphere.     

Laboratory studies on the reactions between Chlorine,Sulfur Dioxide,and Oxygen: Implications for the Venus Stratosphere

The title reaction was studied by photolyzing mixtures of Cl₂ and SO₂ with and without O₂ present in an atmosphere of N₂, using Fourier transform infrared spectrophotometry to monitor reactants and products. In the absence of oxygen, sulfur dioxide is quantitatively converted to sulfuryl chloride. With 10 to 150 Torr O₂ present H₂SO₄ is produced as well as SO₂Cl₂. When a number of speculative reactions inferred from these experiments are added to a published model for Venus stratospheric chemistry, it emerges that SO₂Cl₂ is a key reservoir species for chlorine and that the reaction between Cl and So₂ provides an important cycle for destroying O₂ and converting SO₂ to H₂So₄. The modified model could provide a possible solution to the photochemistry of the Venus stratosphere if the mixing ratio of chlorine on Venus were as high as 8 ppm.     

Carbon dioxide segregation in 1:4 and 1:9 CO2:H2O ices

The mid-infrared spectra of mixed vapor deposited ices of CO₂ and H₂O were studied as a function of both deposition temperature and warming from 15 to 100 K. The spectra of ices deposited at 15 K show marked changes on warming beginning at 60 K. These changes are consistent with CO₂ segregating within the ice matrix into pure CO₂ domains. Ices deposited at 60 and 70 K show a greater degree of segregation, as high as 90% for 1:4 CO₂:H₂O ice mixtures deposited at 70 K. As the ice is warmed above 80 K, preferential sublimation of the segregated CO₂ is observed. The kinetics of the segregation process is also examined. The segregation of the CO₂ as the ice is warmed corresponds to temperatures at which the structure of the water ice matrix changes from the high density amorphous phase to the low density amorphous phase. We show how these microstructural changes in the ice have a profound effect on the photochemistry induced by ultraviolet irradiation. These experimental results provide a framework in which observations of CO₂ on the icy bodies of the outer Solar System can be considered.     

Computing molecular complexes in earth's and other atmospheres

There has been a considerable research interest in molecular aggregates, complexes or clusters, relevant to Earth's and other planetary atmospheres. Consequently, a considerable amount of data has been obtained in laboratory observations and also in computations. This report surveys our recent and ongoing computations of several such systems of atmospheric significancy, both systems with relatively weak and relatively strong bonding interactions. Among them, several types of homo- and hetero-dimers with importance to Earth's atmosphere: (H₂O)₂, (N₂)₂, N₂O₂, , (O₂)₂, or (O₃)₂. Dimer of carbon dioxide (CO₂)₂ is computed owing to its supposed significancy in the atmosphere of Venus. Systems with stronger bonding are represented by ClONO₂H⁺ and 2,3,7,8-tetrachlorodibenzo-p-dioxin. The report also discusses computational tools, combining advanced quantum-chemical methods with statistical-mechanical treatments. The structure, energetics, and vibrations of the complexes are evaluated at correlated ab initio levels. The computations typically show several minimum-energy structures and their relative populations are sensitive to temperature. The computed dimerization equilibrium constants are of a special interest as a critical stability measure and an input information for evaluations of the altitude population profiles in the atmosphere. A special attention is paid to the temperature enhancement of clustering degree in saturated vapors. This interesting paradox represents a product of atmospheric studies though it is actually a phenomenon of a more general physico-chemical validity.     

Photochemistry of minor constituents in the troposphere

Altitude profiles for the number densities of NO, NO₂, NO₃, N₂O₅, HNO₂, CH₃O, CH₃O₂, H₂CO, OH, and HO₂ are calculated as a function of time of day with a steady-state photochemical model in which the altitude profiles for the number densities of H₂O, CH₄, H₂, CO, O₃, and the sum of NO and NO₂ are fixed at values appropriate to a summer latitude of 34°. Average daily profiles are calculated for the long-lived species, HNO₃, H₂O₂, and CH₃O₂H.The major nitrogen compound HNO₃ may have a number density approaching 5 × 10¹¹ molecules cm^?3 at the surface, although an effective loss path due to collisions with particulates could greatly reduce this value.The number density of OH remains relatively unchanged in the first 6 km and reaches 1 × 10⁷ molecules cm^?3 at noon, while the number density of HO₂ decreases throughout the lower troposphere from its noontime value of 8 × 10⁸ molecules cm^?3 at the surface.H₂O₂ and H₂CO both have number densities in the ppb range in the lower troposphere.Owing to decreasing temperature and water concentration, the production of radicals and their steady-state number densities decrease with altitude, reaching a noontime minimum of 1 × 10⁸ molecules cm^?3 for OH and 3 × 10⁷ molecules cm^?3 for HO₂ at the tropopause. The related minor species show even sharper decreases with increasing altitude.The primary path for interconverting OH and HO₂ serves as the major sink for CO and leads to a tropospheric lifetime for CO of ~0.1 yr.Another reaction cycle, the oxidation of CH₄, is quite important in the lower troposphere and leads to the production of H₂CO along with the destruction of CH₄ for which a tropospheric lifetime of ~2 yr is estimated.The destruction of H₂CO that was produced in the CH₄ oxidation cycle provides the major source of CO and H₂ in the atmosphere.     

Studies of proton-irradiated SO2 at low temperatures: Implications for lo

The infrared absorption spectrum from 3.3 to 27 μm (3030-370 cm^?) of SO₂ ice films has been measured at 20 and 88°K before and after 1-MeV proton irradiation. The radiation flux was chosen to simulate the estimated flux of Jovian magnetospheric 1-MeV protons incident on Io. After irradiation, SO₃ is identified as the dominant molecule synthesized in the SO₂ ice. This is also the case after irradiation of composite samples of SO₂ with sulfur, or disulfites. Darkening was observed in irradiated SO₂ ice and in irradiated S₈ pellets. Photometric and spectral measurements of the thermoluminescence of irradiated SO₂ have been made during warming. The spectrum appears as a broad band with a maximum at 4450 Å. Analysis of the luminescence data suggests that, at Ionian temperatures, irradiated SO₂ ice would not be a dominant contributor to posteclipse brightening phenomena. After warming to room temperature, a form of SO₃ remains along with a sulfate and S₈. Based on these experiments, it is reasonable to propose that small amounts of SO₃ may exist on the surface of Io as a result of irradiation synthesis in SO₂ frosts.     

Microwave Remote Sensing of the Temperature and Distribution of Sulfur Compounds in the Lower Atmosphere of Venus

A multi-wavelength radio frequency observation of Venus was performed on April 5, 1996, with the Very Large Array to investigate potential variations in the vertical and horizontal distribution of temperature and the sulfur compounds sulfur dioxide (SO₂) and sulfuric acid vapor (H₂SO₄(g)) in the atmosphere of the planet. Brightness temperature maps were produced which feature significantly darkened polar regions compared to the brighter low-latitude regions at both observed frequencies. This is the first time such polar features have been seen unambiguously in radio wavelength observations of Venus. The limb-darkening displayed in the maps helps to constrain the vertical profile of H₂SO₄(g), temperature, and to some degree SO₂. The maps were interpreted by applying a retrieval algorithm to produce vertical profiles of temperature and abundance of H₂SO₄(g) given an assumed sub-cloud abundance of SO₂. The results indicate a substantially higher abundance of H₂SO₄(g) at high latitudes (above 45°) than in the low-latitude regions. The retrieved temperature profiles are up to 25 K warmer than the profile obtained by the Pioneer Venus sounder probe at altitudes below 40 km (depending on location and assumed SO₂ abundance). For 150 ppm of SO₂, it is more consistent with the temperature profile obtained by Mariner 5, extrapolated to the surface via a dry adiabat. The profiles obtained for H₂SO₄(g) at high latitudes are consistent with those derived from the Magellan radio occultation experiments, peaking at around 8 ppm at an altitude of 46 km and decaying rapidly away from that altitude. At low latitudes, no significant H₂SO₄(g) is observed, regardless of the assumed SO₂ content. This is well below that measured by Mariner 10 (Lipa and Tyler 1979, Icarus39, 192-208), which peaked at ∼14 ppm near 47 km. Our results favor ≤100 ppm of SO₂ at low latitudes and ≤50 ppm in polar regions. The low-latitude value is statistically consistent with the results of Bézard et al. (1983, Geophs. Res. Lett.20, 1587-1590), who found that a sub-cloud SO₂ abundance of 130±40 ppm best matched their observations in the near-IR. The retrieved temperature profile and higher abundance of H₂SO₄(g) in polar regions are consistent with a strong equatorial-to-polar, cloud-level flow due to a Hadley cell in the atmosphere of Venus.     

Silicon negative ion chemistry in the atmosphere-in situ and laboratory measurements

The results of a rocket-borne mass spectrometer measurement indicate that large concentrations of negative ions exist above the bottom of the atmospheric atomic oxygen layer. A large majority of these ions have a mass greater than 100 amu. In addition, an ion at mass 76 was observed with concentrations too large to be CO₄^?. In order to explain these features, a number of reactions involving silicon oxide negative ions have been measured in a flowing afterglow system. The ion SiO₃^? is produced by reaction of O₃^?, and CO₃^?, with SiO. The SiO₃^? ion is extremely stable and does not react measurably with NO, NO₂, CO, CO₂, O₃ or O. Since meteoroid ablation produces a large silicon input into the atmosphere, it appears possible that the ions observed at mass 76 may be SiO₃^?. Possible production mechanisms for this ion as well as the heavy ions are discussed.     

Monte Carlo modeling of neutral gas and dust in the coma of Comet 1P/Halley

The neutral gas environment of a comet is largely influenced by dissociation of parent molecules created at the surface of the comet and collisions of all the involved species. We compare the results from a kinetic model of the neutral cometary environment with measurements from the Neutral Mass Spectrometer and the Dust Impact Detection System onboard the Giotto spacecraft taken during the fly-by at Comet 1P/Halley in 1986. We also show that our model is in good agreement with contemporaneous measurements obtained by the International Ultraviolet Explorer, sounding rocket experiments, and various ground based observations.The model solves the Boltzmann equation with a Direct Simulation Monte Carlo technique (Tenishev, V., Combi, M., Davidsson, B. [2008]. Astrophys. J. 685, 659-677) by tracking trajectories of gas molecules and dust grains under the influence of the comet’s weak gravity field with momentum exchange among particles modeled in a probabilistic manner. The cometary nucleus is considered to be the source of dust and the parent species (in our model: H₂O, CO, H₂CO, CO₂, CH₃OH, C₂H₆, C₂H₄, C₂H₂, HCN, NH₃, and CH₄) in the coma. Subsequently our model also tracks the corresponding dissociation products (H, H₂, O, OH, C, CH, CH₂, CH₃, N, NH, NH₂, C₂, C₂H, C₂H₅, CN, and HCO) from the comet’s surface all the way out to 10⁶ km.As a result we are able to further constrain cometary the gas production rates of CO (13%), CO₂ (2.5%), and H₂CO (1.5%) relative to water without invoking unknown extended sources.     

ROEDDERITE IN THE QINGZHEN (EH3) CHONDRITE

The rare mineral roedderite, (Na_1.09 K_0.89 Ca_0.02)_2.00 (Mg_4.71 Fe_0.27)_4.98 (Si_11.80 Al_0.09)_11.89 O₃₀ has been found in accessory amounts in the highly unequilibrated enstatite chondrite, Qingzhen. It occurs in association with minor amounts of albite and SiO₂ as inclusions within the metal or sulfide phases of metal-sulfide assemblages. The roedderite crystals are connected through oxide and silicate veins to the surrounding matrix. The presence of glass coated vesicles on the surface of the assemblages strongly suggests that roedderite originated in the presence of a fluid phase, presumably during post-accretional planetary processes.     

Possibilities for the detection of hydrogen peroxide-water-based life on Mars by the Phoenix Lander

The Phoenix Lander landed on Mars on 25 May 2008. It has instruments on board to explore the geology and climate of subpolar Mars and to explore if life ever arose on Mars. Although the Phoenix mission is not a life detection mission per se, it will look for the presence of organic compounds and other evidence to support or discredit the notion of past or present life.The possibility of extant life on Mars has been raised by a reinterpretation of the Viking biology experiments [Houtkooper, J. M., Schulze-Makuch, D., 2007. A possible biogenic origin for hydrogen peroxide on Mars: the Viking results reinterpreted. International Journal of Astrobiology 6, 147-152]. The results of these experiments are in accordance with life based on a mixture of water and hydrogen peroxide instead of water. The near-surface conditions on Mars would give an evolutionary advantage to organisms employing a mixture of H₂O₂ and H₂O in their intracellular fluid: the mixture has a low freezing point, is hygroscopic and provides a source of oxygen. The H₂O₂-H₂O hypothesis also explains the Viking results in a logically consistent way. With regard to its compatibility with cellular contents, H₂O₂ is used for a variety of purposes in terran biochemistry. The ability of the anticipated organisms to withstand low temperatures and the relatively high water vapor content of the atmosphere in the Martian arctic, means that Phoenix will land in an area not inimical to H₂O₂-H₂O-based life. Phoenix has a suite of instruments which may be able to detect the signatures of such putative organisms.     

Formation of a mass distribution of objects. ii. mergings in a two-component set of particles

The random quantity ξ, the number of pairwise mergings for a two-component sample N = N₁ + N₂, N₂≤ N₁, is found under the assumption that mergings only between particles of different types are possible. Let T₀,T₁,T₂,..., T_m, ... be a sequence of times. We then have a discrete approximation of the process of mergings by a uniform Markov chain. Translated from Astrofizika, Vol. 43, No. 1, pp. 137-142, January–March, 2000.     

Spectro-imaging observations of Jupiter's 2-μm auroral emission. I. H3 distribution and temperature

We report on spectro-imaging infrared observations of Jupiter's auroral zones, acquired in October 1999 and October 2000 with the FTS/BEAR instrument at the Canada-France-Hawaii Telescope. The use of narrow-band filters at 2.09 and 2.12 μm, combined with high spectral resolution (0.2 cm⁻¹), allowed us to map emission from the H₂S₁(1) quadrupole line and from several H₃⁺ lines. The H₂ and H₃⁺ emission appears to be morphologically different, especially in the north, where the latter notably exhibits a “hot spot” near 150°-170° System III longitude. This hot spot coincides in position with the region of increased and variable hydrocarbon, FUV and X-ray emission, but is not seen in the more uniform H₂S₁(1) emission. We also present the first images of the H₂ emission in the southern polar region. The spectra include a total of 14 H₃⁺ lines, including two hot lines from the 3ν₂-ν₂ band, detected on Jupiter for the first time. They can be used to determine H₃⁺ column densities, rotational (T_rot) and vibrational (T_vib) temperatures. We find the mean T_vib of the v₂=3 state to be lower (960±50 K) than the mean T_rot in v₂=2 (1170±75 K), indicating an underpopulation of the v₂=3 level with respect to local thermodynamical equilibrium. Rotational temperatures and associated column densities are generally higher and lower, respectively, than inferred previously from ν₂ observations. This is a likely consequence of a large positive temperature gradient in the sub-microbar auroral atmosphere. While the signal-to-noise is not sufficient to take full advantage of the 2-D capabilities of the observations, the search for correlations between line intensities, T_vib and column densities, indicates that variations in line intensities are mostly due to correlated variations in the H₃⁺ column densities. The thermostatic role played by H₃⁺ at ionospheric levels may provide an explanation. The exception is the northern “hot spot,” which exhibits a T_vib about 250 K higher than other regions. A partial explanation might invoke a homopause elevation in this region, but a fully consistent scenario is not yet available. The different distributions of the H₂ and H₃⁺ emission are equally difficult to explain.     

An estimate of the temperature and abundance of CH4 and other molecules in the atmosphere of Uranus

We present a preliminary analysis of CH₄ absorptions near 6800 Å in new high resolution spectra of Uranus. A curve of growth analysis of the data yields a rotational temperature near 100 K and a CH₄/H₂ ratio that is 1 to 3 times that expected for a solar type composition. The long pathlengths of CH₄, apparently demanded by absorptions near 4700 Å, are qualitatively shown to be the result of line formation in a deep, predominantly Rayleigh scattering atmosphere in which continuum absorption is a strong function of wavelength. The analysis of the CH₄ also yields a minimum value for the effective pressure of line formation (～ 2 atm). This value is shown to be twice that expected on Uranus if the atmosphere were predominantly H₂. It is speculated that large amounts of some otherwise optically inert gas is present in the Uranus atmosphere. N₂ is suggested as a possible candidate since there are cosmogonic reasons why Uranus should contain large amounts of N relative to C, He, and H, and also because the pressure-induced pure rotation spectrum of N₂ could possibly account for the low brightness temperatures that have recently been observed at 33 and 350 μm. If N₂ is present the planet probably possesses a surface at the 10–100 atmosphere level.