Oxygen and carbon isotope ratios in the martian atmosphere

Oxygen and carbon isotope ratios in the martian CO₂ are key values to study evolution of volatiles on Mars. The major problems in spectroscopic determinations of these ratios on Mars are uncertainties associated with: (1) equivalent widths of the observed absorption lines, (2) line strengths in spectroscopic databases, and (3) thermal structure of the martian atmosphere during the observation. We have made special efforts to reduce all these uncertainties. We observed Mars using the Fourier Transform Spectrometer at the Canada–France–Hawaii Telescope. While the oxygen and carbon isotope ratios on Mars were byproducts in the previous observations, our observation was specifically aimed at these isotope ratios. We covered a range of 6022 to 6308 cm⁻¹ with the highest resolving power of ν/δν=3.5×10⁵ and a signal-to-noise ratio of 180 in the middle of the spectrum. The chosen spectral range involves 475 lines of the main isotope, 184 lines of ¹³CO₂, 181 lines of CO¹⁸O, and 119 lines of CO¹⁷O. (Lines with strengths exceeding 10⁻²⁷ cm at 218 K are considered here.) Due to the high spectral resolution, most of the lines are not blended. Uncertainties of retrieved isotope abundances are in inverse proportion to resolving power, signal-to-noise ratio, and square root of the number of lines. Laboratory studies of the CO₂ isotope spectra in the range of our observation achieved an accuracy of 1% in the line strengths. Detailed observations of temperature profiles using MGS/TES and data on temperature variations with local time from two GCMs are used to simulate each absorption line at various heights in each part of the instrument field of view and then sum up the results. Thermal radiation of Mars' surface and atmosphere is negligible in the chosen spectral range, and this reduces errors associated with uncertainties in the thermal structure on Mars. Using a combination of all these factors, the highest accuracy has been achieved in measuring the CO₂ isotope ratios: ¹³C/¹²C = 0.978 ± 0.020 and ¹⁸O/¹⁶O = 1.018 ± 0.018 times the terrestrial standards. Heavy isotopes in the atmosphere are enriched by nonthermal escape and sputtering, and depleted by fractionation with solid-phase reservoirs. The retrieved ratios show that isotope fractionation between CO₂ and oxygen and carbon reservoirs in the solid phase is almost balanced by nonthermal escape and sputtering of O and C from Mars.     

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.     

Atmospheric Corrections Using MODTRAN for TOA and Surface BRDF Characteristics from High Resolution Spectroradiometric/ Angular Measurements from a Helicopter Platform

l. IntroductionThe cIassicaI definition of bi--directional reflectance--distribution function (BRDF) is aderivative, distribution function, relatlng the irradiance incident from one given direction tolts contribution to the radiance renected in another direct1on (N1codemus et al., l977).f r (0,, rp,; 0,, rp, )= dL, (0,, P,; 0,, 9,; E, )/ dE, (0,, 9,) [sr-- 1 ], (l)where 0 (zenith angle) and 9 (azimuth angle) together indicate a direction, the subscr1pt i indi-cates quantities associated wi…     

Venera 9, 10: Is there a dust ring around Venus?

Four surveys in which the geometrical parameters were suitable for observations on weak scattering objects were carried out by the Venera 9, 10 orbiters using 3000–8000 Å spectrometers. The results of one survey can be explained by a dust layer at the height of sighting h = 100–700 km. Its absence in other sessions suggests a ring structure. The spectrum of dust scattering is a power function of the wavelength with the index varying from ?2.1 at 100km to ?1.3 at 500km. A method is proposed for obtaining the optical thickness, density and size distribution of dust particles from the scattering spectra. For m > 10^?14 g the number of dust particles with a mass higher than m is proportional to m^?1.3. The radial optical thickness τ is 0.7 × 10^?5 at 5000 Å assuming the geometric thickness δ to be 100 km. The maximum optical thickness along the normal to the plane of the ring is τ_n = 4 × 10^?6. The mass of the ring is 20 tons or 5 × 10^?3 g cm^?1 per unit circumference length; the maximum mass in a column normal to the ring plane is 10^?10g cm^?2; the maximum density (for δ = 100 km) is 10^?17 g cm^?3. A satellite of Venus gradually destroyed by temperature effects and by meteorite streams and plasma fluxes is suggested as the source of dust in the ring. One of 1 km radius could sustain such a ring for a billion years. The zodiacal light intensity near Venus is estimated.     

热液金刚石压腔在地质流体研究中的应用

热液金刚石压腔(HDAC)是专为模拟地壳温压条件下的地质作用而设计的，它尤其适用于观测水或其它流体与地质物质之间的相互作用。HDAC可时-190～1200℃，0～10GPa的热液体系进行实验，并可在实验的温压条件下．用各种先进的光学方法分析样品，更可以把实验的全程录像存档。充满流体的HDAC本身就可当做是一个人工合成的流体包裹体。因此它可以用来研究流体的状态方程和相关系。它又可时其它流体包裹体样品施加外压力，因此在热分析的过程中可免除包裹体的膨胀或爆破的困境。HDAC可应用到颇为宽广的温压范围，它已被广泛地用来观测各种化学体系的临界现象，包括在地质方面特别有用的含水硅酸盐体系。HDAC也可与同步辐射X光源相结合，而取得各种金属或稀土元素水溶液的x射线吸收精细结构(X-ray absorption fine structure；XAFS)光谱，因而时在热液里的金属或稀土元素络合物的组分和结构提供了最基本的资料。然而，X光的强度在透过金刚石时，因绕射和吸收而大大地减弱，因此应用一般的HDAC来获取那些吸收边在10keV以下的元素的XAFS光谱颇为困难。目前已有两种改良式的HDAC解除了这方面的困难，而时在元素周期表上的第一排过渡性金属元素和稀土元素的水溶液，提供清晰的XAFS光谱。这些资料可用来研究金属或稀土元素络合物在地质热液里的特性，及其在元素迁移和成矿作用方面的效应。而这些元素在地质应用方面特别重要。     

Comment on “Methane on Mars: A product of H2O photolysis in the presence of CO” by A. Bar-Nun and V. Dimitrov

Bar-Nun and Dimitrov [Bar-Nun, A., Dimitrov, V., 2006. Icarus 181, 320-322] suggested a sequence of reactions to form methane on Mars. These reactions are based on the study of products in the N₂-CO-H₂O mixture irradiated at 185 nm. The suggested scheme was not quantitatively justified by chemical kinetics. One of the key reactions is effectively blocked by O₂ in the martian atmosphere, and another key reaction does not exist. There are no pathways for effective formation of methane in the martian atmosphere.     

Nightside ionosphere of Venus

Venera 9, 10 measurements of the nightside ionospheric profile and the night airglow were used for investigating ionosphere formation processes. The upper ionospheric layer may be formed by HeI 584 Å radiation; the lower layer by meteorite ionization. Upper limits on the electron energy flux, <4 × 10⁸eV cm⁻² s⁻¹, the helium ion flux <10⁷ cm⁻² s⁻¹, the nitric oxide mixing ratio, <1.5 × 10⁻⁴ and the atomic sulphur mixing ratio, <10⁻⁶, are deduced for ionospheric altitudes.     

Excitation of the oxygen nightglow on the terrestrial planets

A scheme of excitation, quenching, and energy transfer processes in the oxygen nightglow on the Earth, Venus, and Mars has been developed based on the observed nightglow intensities and vertical profiles, measured reaction rate coefficients, and photochemical models of the nighttime atmospheres of the Venus and Mars. The scheme involves improved radiative lifetimes of some band systems, calculated yields of the seven electronic states of O₂ in termolecular association, and rate coefficients of seven processes of electronic quenching of the Herzberg states of O₂, which are evaluated by fitting to the nightglow observations. Electronic quenching of the vibrationally excited Herzberg states by O₂ and N₂ in the Earth's nightglow is a quarter of total collisional removal of the O₂(A, A′) states and a dominant branch for the O₂(c) state. The scheme supports the conclusion by Steadman and Thrush (1994) that the green line is excited by energy transfer from the O₂(A³Σ_u⁺, v≥6) molecules, and the inferred rate coefficient of this transfer is 1.5×10⁻¹¹ cm³ s⁻¹. The O₂ bands at 762 nm and 1.27 μm are excited directly, by quenching of the Herzberg states, and by energy transfer from the O₂(⁵Π_g) state. Quenching of the O₂ band at 762 nm excites the band at 1.27 μm as well. Effective yield of the O₂(a¹Δ_g) state in termolecular association on Venus and Mars is ∼0.7. Quantitative assessments of all these processes have been made. A possible reaction of O₂(c¹Σ_u⁻)+CO is a very minor branch of recombination of CO₂ on Venus and Mars. Night airglow on Mars is calculated for typical conditions of the nighttime atmosphere. The calculated vertical intensity of the O₂ band at 1.27 μm is 13 kR, far below the recently reported detections.     

On the structure of Mars' atmosphere at 120–220 km

Altitude dependences of [CO₂] and [CO₂⁺] are deduced from Mariner 6 and 7 CO₂⁺ airglow measurements. CO₂ densities are also obtained from n_e radio occultation measurements. Both [CO₂] profiles are similar and correspond to the model atmosphere of Barth et al. (1972) at 120 km, but at higher altitudes they diverge and at 200–220 km the obtained [CO₂] values are three times less the model. Both the airglow and radio occultation observations show that a correction factor of 2.5 should be included into the values for solar ionization flux given by Hinteregger (1970). The ratio of [CO₂⁺]/n_e is 0.15–0.2 and, hence, [O]/[CO₂] is ～3% at 135 km. An atmospheric and ionospheric model is developed for 120–220 km. The calculated temperature profile is characterized by a value of T ≈ 370°K at h ? 220 km, a steep gradient (～2°/km) at 200-160 km, a bend in the profile at 160 km, a small gradient (～0.7°/km) below and a value of T ≈ 250°K at 120 km. The upper point agrees well with the results of the Lyman-α measurements; the steep gradient may be explained by molecular viscosity dissipation of gravity and acoustical waves (the corresponding energy flux is 4 × 10^?2 erg cm^?2sec^?1 at 180 km). The bend at 160 km may be caused by a sharp decrease of the eddy diffusion coefficient and defines K ≈ 2 × 10⁸cm²sec^?1; and the low gradient gives an estimate of the efficiency of the atmosphere heating by the solar radiation as ? ≈ 0.1.