Helium on Mars and Venus: EUVE observations and modeling

Long-exposure spectroscopy of Mars and Venus with the Extreme Ultraviolet Explorer (EUVE) has revealed emissions of He 584 Å on both planets and He 537 Å/O⁺ 539 Å and He⁺ 304 Å on Venus. Our knowledge of the solar emission at 584 Å, eddy diffusion in Mars' upper atmosphere, electron energy distributions above Mars' ionopause, and hot oxygen densities in Mars' exosphere has been significantly improved since our analysis of the first EUVE observation of Mars [Krasnopolsky, Gladstone, 1996, Helium on Mars: EUVE and Phobos data and implications for Mars' evolution, J. Geophys. Res. 101, 15,765-15,772]. These new results and a more recent EUVE observation of Mars are the motivation for us to revisit the problem in this paper. We find that the abundance of helium in the upper atmosphere, where the main loss processes occur, is similar to that in the previous paper, though the mixing ratio in the lower and middle atmosphere is now better estimated at 10±6 ppm. Our estimate of the total loss of helium is almost unchanged at 8×¹⁰²³ s⁻¹, because a significant decrease in the loss by electron impact ionization above the ionopause is compensated by a higher loss in collisions with hot oxygen. We neglect the outgassing of helium produced by radioactive decay of U and Th because of the absence of current volcanism and a very low upper limit to the seepage of volcanic gases. The capture of solar wind α-particles is currently the only substantial source of helium on Mars, and its efficiency remains at 0.3. A similar analysis of EUV emissions from Venus results in a helium abundance in the upper atmosphere which is equal to the mean of the abundances measured previously with two optical and two mass spectrometers, and a derived helium mixing ratio in the middle and lower atmosphere of 9±6 ppm. Helium escape by ionization and sweeping out of helium ions by the solar wind above the ionopause is smaller than that calculated by Prather and McElroy [1983, Helium on Venus: implications for uranium and thorium, Science 220, 410-411] by a factor of 3. However, charge exchange of He⁺ ions with CO₂ and N₂ between the exobase and ionopause and collisions with hot oxygen ignored previously add to the total loss which appears to be at the level of 10⁶ cm⁻² s⁻¹ predicted by Prather and McElroy [1983, Science 220, 410-411]. The loss of helium is compensated by outgassing of helium produced by radioactive decay of U and Th and by the capture of the solar wind α-particles with an efficiency of 0.1. We also compare our derived α-particle capture efficiencies for Mars and Venus with observed X-ray emissions resulting from the charge exchange of solar wind heavy ions with the extended atmospheres on both planets [Dennerl et al., 2002, Discovery of X-rays from Venus with Chandra, Astron. Astrophys. 386, 319-330; Dennerl, 2002, Discovery of X-rays from Mars with Chandra, Astron. Astrophys. 394, 1119-1128]. The emissions from both disk and halo on Mars agree with our calculated values; however, we do not see a reasonable explanation for the X-ray halo emission on Venus. The ratio of the charge exchange efficiencies derived from the disk X-ray emissions of Mars and Venus is similar to the ratio of the capture efficiencies for these planets. The surprisingly bright emission of He⁺ at 304 Å observed by EUVE and Venera 11 and 12 suggests that charge exchange in the flow of the solar wind α-particles around the ionopause is much stronger than in the flow of α-particles into the ionosphere.     

The UV spectrum of the binary system TY Pyx

A detailed list and analysis of line identifications of five UV spectra of the RS CVn-type binary system TY Pyxidis are presented. These spectra are recorded at different phases with the International Ultraviolet Explorer (IUE). Two of them are in the wavelength range1235–1950 Å while the other three in the range2700–3110 Å.The far-UV spectrum of TY Pyx is mainly an emission spectrum dominated by the emission lines of the ions:Ci, Oi, Cii, Siii, Heii, Alii, and Feiii. We also pointed out the existence of a Feiii [34] line in absorption.The UV spectrum between 2700–3110 Å is dominated by weak absorption lines. Two satellite components are indicated for many lines, which correspond to the two stars of the system, in the two out of the three spectra (LWP 13386 and LWP 13347).Violet emission wings are observed for Fei [1], Tii [1],Oiv [1], and Siiii [1]. The UV spectrum of TY Pyx is also characterized by the multi-structure of Mgii [1] resonance lines.Based on data from the International Ultraviolet Explorer, de-archived from the Villafranca Data Archive of the European Space Agency.     

Noble gases in planetary atmospheres: Implications for the origin and evolution of atmospheres

The radiogenic and primordial noble gas content of the atmospheres of Venus, Earth, and Mars are compared with one another and with the noble gas content of other extraterrestial samples, especially meteorites. The fourfold depletion of ⁴⁰Ar for Venus relative to the Earth is attributed to the outgassing rates and associated tectonics and volcanic styles for the two planets diverging significantly within the first billion or so years of their history, with the outgassing rate for Venus becoming much less than that for the Earth at subsequent times. This early divergence in the tectonic style of the two planets may be due to a corresponding early onset of the runaway greenhouse on Venus. The 16-fold depletion of ⁴⁰Ar for Mars relative to the Earth may be due to a combination of a mild K depletion for Mars, a smaller fraction of its interior being outgassed, and to an early reduction in its outgassing rate. Venus has lost virtually all of its primordial He and some of its radiogenic He. The escape flux of He may have been quite substantial in Venus' early history, but much diminished at later times, with this time variation being perhaps strongly influenced by massive losses of H₂ resulting from efficient H₂O loss processes.Key trends in the primordial noble gas content of terrestial planetary atmospheres include (1) a several orders of magnitude decrease in ²⁰Ne and ³⁶Ar from Venus to Earth to Mars; (2) a nearly constant ²⁰Ne/³⁶Ar ratio which is comparable to that found in the more primitive carbonaceous chondrites and which is two orders of magnitude smaller than the solar ratio; (3) a sizable fractionation of Ar, Kr, and Xe from their solar ratios, although the degree of fractionation, especially for ³⁶Ar/¹³²Xe, seems to decrease systematically from carbonaceous chondrites to Mars to Earth to Venus; and (4) large differences in Ne and Xe isotopic ratios among Earth, meteorites, and the Sun. Explaining trends (2), (2) and (4), and (1) pose the biggest problems for the solar-wind implantation, primitive atmosphere, and late veneer hypotheses, respectively. It is suggested that the grain-accretion hypothesis can explain all four trends, although the assumptions needed to achieve this agreement are far from proven. In particular, trends (1), (2), (3), and (4) are attributed to large pressure but small temperature differences in various regions of the inner solar system at the times of noble gas incorporation by host phases; similar proportions of the host phases that incorporated most of the He and Ne on the one hand (X) and Ar, Kr, and Xe on the other hand (Q); a decrease in the degree of fractionation with increasing noble-gas partial pressure; and the presence of interstellar carriers containing isotopically anomalous noble gases.Our analysis also suggests that primordial noble gases were incorporated throughout the interior of the outer terrestial planets, i.e., homogeneous accretion is favored over inhomogeneous accretion. In accord with meteorite data, we propose that carbonaceous materials were key hosts for the primordial noble gases incorporated into planets and that they provided a major source of the planets' CO₂ and N₂.     

First measurement of helium on Mars: implications for the problem of radiogenic gases on the terrestrial planets

108 +/- 11 photons of the martian He 584-angstroms airglow detected by the Extreme Ultraviolet Explorer satellite during a 2-day exposure (January 22-23, 1993) correspond to the effective disk average intensity of 43 +/- 10 Rayleigh. Radiative transfer calculations, using a model atmosphere appropriate to the conditions of the observation and having an exospheric temperature of 210 +/- 20 K, result in a He mixing ratio of 1.1 +/- 0.4 ppm in the lower atmosphere. Nonthermal escape of helium is due to electron impact ionization and pickup of He+ by the solar wind, to collisions with hot oxygen atoms, and to charge exchange with molecular species with corresponding column loss rates of 1.4 x 10(5), 3 x 10(4), and 7 x 10(3) cm-2 sec-1, respectively. The lifetime of helium on Mars is 5 x 10(4) years. The He outgassing rate, coupled with the 40Ar atmospheric abundance and with the K:U:Th ratio measured in the surface rocks, is used as input to a single two-reservoir degassing model which is applied to Mars and then to Venus. A similar model with known abundances of K, U, and Th is applied to Earth. The models for Earth and Mars presume loss of all argon accumulated in the atmospheres during the first billion years by large-scale meteorite and planetesimal impacts. The models show that the degassing coefficients for all three planets may be approximated by function delta = delta (0)(t(0)/t)1/2 with delta (0) = 0/1, 0.04, and 0.0125 Byr-1 for Earth, Venus, and Mars, respectively. After a R2 correction this means that outgassing processes on Venus and Mars are weaker than on Earth by factors of 3 and 30, respectively. Mass ratios of U and Th are almost the same for all three planets, while potassium is depleted by a factor of 2 in Venus and Mars. Mass ratios of helium and argon are close to 5 x 10(-9) and 2 x 10(-8) g/g in the interiors of all three planets. The implications of these results are discussed.     

The ultraviolet spectrum of the binary system KS Persei (HD 30353)

Nine high- and low-resolution IEU spectra at different orbital phases during different cycles, of the hydrogen-poor single-lined spectroscopic binary KS per (HD 30353) have been studied. The near-UV spectrum is characterized by the presence of several lines of once ionized metals which show the same orbital RV shifts observed in the visual range. The MgII resonance lines present a sharp interstellar + circumstellar core and an emission peak at about 83 and 92 km s^–1. The far UV spectrum is characterized by the presence of strong absorptions of the resonance lines ofNV,CIV, SiIV, SiIII.Direct determination of the IS extinction from the 2200 Å feature givesE(B-V)=0.33. A comparison of corrected logarithmic continuous energy distribution with the theoretical models by Kurucz, indicates that the companion is a hot star,T _e=15000 K; logg=4. A comparison with the recent UV work ofv Sgr, shows that, KS Per is very similar tov Sgr.Based on observations by the International Ultraviolet Explorer (IUE) collected at the Villafrance Satellite Tracking Station and obtained from the IUE data bank.     

Martian volatiles: Their degassing history and geochemical fate

Observations of Mars and cosmochemical considerations imply that the total inventory of degassed volatiles on Mars is 10² to 10³ times that present in Mars' atmosphere and polar caps. The degassed volatiles have been physically and chemically incorporated into a layer of unconsolidated surface rubble (a “megaregolith”) up to 2km thick. Tentative lines of evidence suggest a high concentration (～5g/cm²) of ⁴⁰ Ar in the atmosphere of Mars. If correct, this would be consistent with a degassing model for Mars in which the Martian “surface” volatile inventory is presumed identical to that of Earth but scaled to Mars' smaller mass and surface area. The implied inventory would be: (⁴⁰Ar) = 4g/cm², (H₂O) = 1 × 10⁵g/cm², (CO₂) = 7 × 10³g/cm², (N₂) = 3 × 10²g/cm², (Cl) = 2 × 10³g/cm², and (S) = 2 × 10²g/cm². Such a model is useful for testing, but differences in composition and planetary energy history may be anticipated between Mars and Earth on theoretical grounds. Also, the model demands huge regolith sinks for the volatiles listed.If the regolith were in physical equilibrium with the atmosphere, as much as 2 × 10⁴g/cm² of H₂O could be stored in it as hard-frozen permafrost, or 5 × 10⁴g/cm² if equilibrium with the atmosphere were inhibited. Spectral measurements of Martian regolith material and laboratory measurement of weathering kinetics on simulated regolith material suggest large amounts of hydrated iron oxides and clay minerals exist in the regolith; the amount of chemically bound H₂O could be from 1 × 10⁴ to 4 × 10⁴g/cm². In an Earth-analogous model, a 2 km mixed regolith must contain the following concentrations of other volatile-containing compounds by weight: carbonates = 1.5%, nitrates = 0·3%, chlorides = 0.6%, and sulfates = 0.1%. Such concentrations would be undetectable by current Earth-based spectral reflectance measurements, and (except the nitrates) formation of the “required” amounts of these compounds could result from interaction of adsorbed H₂O and ice with primary silicates expected on Mars. Most of the CO₂ could be physically adsorbed on the regolith.Thus, maximum amounts of H₂O and other volatiles which could be stored in the Mars regolith are marginally compatible with those required by an Earth-analogous model, although a lower atmospheric ⁴⁰Ar concentration and regolith volatile inventory would be easier to reconcile with observational constraints. Differences in the ratios of H₂O and other volatiles to ⁴⁰Ar between surface volatiles on the real Mars and on an Earth-analogous Mars could result from and reflect differences in bulk composition and time history of degassing between Mars and Earth. Models relating Viking-observable parameters, e.g., (⁴⁰Ar) and (³⁶Ar), to the time history and overall intensity of Mars degassing are given.     

The UV spectrum of the binary system SZ Psc

In this paper we study the far-UV as well as the UV spectrum of the spectroscopic binary system SZ Psc in the wavelength ranges 1235–1950 Å and 2710–3090 Å, respectively, from spectra obtained with the International Ultraviolet Explorer (IUE). The UV spectrum of SZ Psc is mainly an emission spectrum. The short wavelength region includes emission lines formed from the low chromosphere to the transition region (e.g., Siiv,Civ, andNv) and also a deep and broad absorption line of Feii.The Mgii[1] resonance doublet at about 2800 Å presents a P Cygni profile and a multiple structure with two emission and two absorption satellite components. We also present the emission measure diagram in the temperature region 4.4T _e <53.     

Mars’ atmospheric 40Ar: A tracer for past crustal erosion

Noble gas ⁴⁰Ar may be used as a tracer of the past evolution of volatiles in Mars’ crust, mantle and atmosphere. ⁴⁰Ar is formed by the radioactive decay of ⁴⁰K in the mantle and in the crust and is released from the mantle to the atmosphere due to volcanism and from the crust by erosion such as eolian and hydrothermal erosion. Furthermore, ⁴⁰Ar can escape from the atmosphere into space via atmospheric escape mechanisms. The evolution of the atmospheric abundance of ⁴⁰Ar thus depends on these three processes whose efficiencies vary with time.In the present study we reconsider atmospheric escape mechanism efficiencies and describe various possible scenarios of the evolution of ⁴⁰Ar with a model describing the three main reservoirs of ⁴⁰Ar, the mantle, crust and atmosphere. First, we show that atmospheric escape, which is stronger in the early evolution, does not significantly influence the present abundance of the atmospheric ⁴⁰Ar. In the early evolution the atmospheric concentration of ⁴⁰Ar is very low as the outgassing of ⁴⁰Ar from the mantle occurs relatively late in the martian evolution. Thus, the atmospheric ⁴⁰Ar concentration is essentially a tracer of Mars’ outgassing history and not of the escape processes. Second, using the results of the most recent published crustal formation models, the calculated present ⁴⁰Ar atmospheric abundance is smaller than its observed value. This discrepancy may be explained by a significant ⁴⁰Ar supply from the crust by erosion (16–30% of the ⁴⁰Ar content of the upper first 10 km of crust). The knowledge of the fraction of crustal ⁴⁰Ar outgassed to the atmosphere is an important constraint for any future global modelling of past Mars’ hydrothermal activity aiming at better characterizing the role of subsurface aqueous alteration processes in Mars climate evolution. One of the main sources of the uncertainty of these results is the present uncertainty in the measured atmospheric ⁴⁰Ar value (±20%). More precise measurements of ⁴⁰Ar and ³⁶Ar in the martian atmosphere are therefore required to better constrain the model.     

The UV spectrum of the Be star 88 Herculis

In this paper, we give a detailed list and analysis of line identifications of the UV spectrum of the Be star 88 Her in the wavelength range 1958–3002 Å recorded in 1984, 23 May with the International Ultraviolet Explorer (IUE). The spectrum is crowded by shell absorptions lines, mostly those of singly ionized iron peak elements.The detailed analysis of the radial velocities measured in the whole spectral range 1100–3002 Å is also given.     

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 Martian PFS average spectrum: Comparison with ISO SWS

The evaluation of the planetary Fourier spectrometer performance at Mars is presented by comparing an average spectrum with the ISO spectrum published by Lellouch et al. [2000. Planet. Space Sci. 48, 1393.]. First, the average conditions of Mars atmosphere are compared, then the mixing ratios of the major gases are evaluated. Major and minor bands of CO₂ are compared, from the point of view of features characteristics and bands depth. The spectral resolution is also compared using several solar lines. The result indicates that PFS radiance is valid to better than 1% in the wavenumber range 1800-4200 cm⁻¹ for the average spectrum considered (1680 measurements). The PFS monochromatic transfer function generates an overshooting on the left-hand side of strong narrow lines (solar or atmospheric). The spectral resolution of PFS is of the order of 1.3 cm⁻¹ or better. A large number of narrow features to be identified are discovered.     

Jovian auroral spectroscopy with FUSE: analysis of self-absorption and implications for electron precipitation

High-resolution (∼0.22 Å) spectra of the north jovian aurora were obtained in the 905-1180 Å window with the Far Ultraviolet Spectroscopic Explorer (FUSE) on October 28, 2000. The FUSE instrument resolves the rotational structure of the H₂ spectra and the spectral range allows the study of self-absorption. Below 1100 Å, transitions connecting to the v^″?2 levels of the H₂ ground state are partially or totally absorbed by the overlying H₂ molecules. The FUSE spectra provide information on the overlying H₂ column and on the vibrational distribution of H₂. Transitions from high-energy H₂ Rydberg states and treatment of self-absorption are considered in our synthetic spectral generator. We show comparisons between synthetic and observed spectra in the 920-970, 1030-1080, and 1090-1180 Å spectral windows. In a first approach (single-layer model ), the synthetic spectra are generated in a thin emitting layer and the emerging photons are absorbed by a layer located above the source. It is found that the parameters of the single-layer model best fitting the three spectral windows are 850, 800, and 800 K respectively for the H₂ gas temperature and 1.3×¹⁰¹⁸, 1.5×¹⁰²⁰, and 1.3×¹⁰²⁰ cm−2 for the H₂ self-absorbing vertical column respectively. Comparison between the H₂ column and a 1-D atmospheric model indicates that the short-wavelength FUV auroral emission originates from just above the homopause. This is confirmed by the high H₂ rovibrational temperatures, close to those deduced from spectral analyses of H⁺₃ auroral emission. In a second approach, the synthetic spectral generator is coupled with a vertically distributed energy degradation model, where the only input is the energy distribution of incoming electrons (multi-layer model ). The model that best fits globally the three FUSE spectra is a sum of Maxwellian functions, with characteristic energies ranging from 1 to 100 keV, giving rise to an emission peak located at 5 μbar, that is ∼100 km below the methane homopause. This multi-layer model is also applied to a re-analysis of the Hopkins Ultraviolet Telescope (HUT) auroral spectrum and accounts for the H₂ self-absorption as well as the methane absorption. It is found that no additional discrete soft electron precipitation is necessary to fit either the FUSE or the HUT observations.     

The Unusual Absorption Line Spectrum of Quasar SDSS J2220+0109

We report the Balmer broad absorption lines (BALs) in the quasar SDSS J2220 + 0109 discovered from the SDSS data, and present a detailed analysis of the peculiar absorption line spectrum, including the He I* multiplet at λλ3189, 3889 arising from the metastable 2³s-state helium and the Balmer Hα and Hβ lines from the excited hydrogen H I of n = 2 level, which are rarely seen in quasar spectra, as well as many absorption lines arising from the excited Fe II* of the levels 7 955 cm⁻¹, 13 474 cm⁻¹ and 13 673 cm⁻¹ in the wavelength range 3100∼3300 Å. Ca II H, K absorption line doublets also clearly appear in the SDSS spectrum. All absorption lines show a similar blueshifted velocity structure of Δv ≈ − 1500 ∼ 0 km·s⁻¹ relative to the quasar's systematic redshift determined from the emission lines. Detailed analysis suggests that the Balmer absorption lines should arise from the partially ionized region with a column density of N_HI ≈ 10²¹ cm⁻² for an electron density of ne ∼ 10⁶ cm⁻³; and that the hydrogen n = 2 level may be populated via collisional excitation with Lyα pumping.     

The far UV spectrum of the O4V ((f)) star 9 Sagittarii

A detailed list of line identifications of the far UV spectrum of the O4V((f)) star 9 Sagittarii (HD 164794) in the wavelength range 1174-2000 Å is presented. The identification is based on two spectra recorded in 1981 (on 16 April—SWP 13729 and on 24 August—SWP 14805) by the International Ultraviolet Explorer (IUE). In the list many unclassified lines are included. The radial velocities of all lines, classified and unclassified, are measured for both spectra and the mean velocities for different ions are discussed.     

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.     

FIRST RESULTS OF THE SUMER TELESCOPE AND SPECTROMETER ON SOHO – I. Spectra and Spectroradiometry

SUMER – the Solar Ultraviolet Measurements of the Emitted Radiation instrument on the Solar and Heliospheric Observatory (SOHO) – observed its first light on January 24, 1996, and subsequently obtained a detailed spectrum with detector B in the wavelength range from 660 to 1490 Å (in first order) inside and above the limb in the north polar coronal hole. Using detector A of the instrument, this range was later extended to 1610 Å. The second-order spectra of detectors A and B cover 330 to 805 Å and are superimposed on the first-order spectra. Many more features and areas of the Sun and their spectra have been observed since, including coronal holes, polar plumes and active regions. The atoms and ions emitting this radiation exist at temperatures below 2 × 10⁶ K and are thus ideally suited to investigate the solar transition region where the temperature increases from chromospheric to coronal values. SUMER can also be operated in a manner such that it makes images or spectroheliograms of different sizes in selected spectral lines. A detailed line profile with spectral resolution elements between 22 and 45 mÅ is produced for each line at each spatial location along the slit. From the line width, intensity and wavelength position we are able to deduce temperature, density, and velocity of the emitting atoms and ions for each emission line and spatial element in the spectroheliogram. Because of the high spectral resolution and low noise of SUMER, we have been able to detect faint lines not previously observed and, in addition, to determine their spectral profiles. SUMER has already recorded over 2000 extreme ultraviolet emission lines and many identifications have been made on the disk and in the corona.     

Effects of ion excitation on charge transfer reactions of the Mars, Venus, and Earth ionospheres

The absolute reaction cross sections and reaction rate coefficients as a function of photoionisation energy for 25 ion-molecule reactions (charge transfer reactions except for one) have been measured between the most abundant species present as ions or neutral in the Mars, Venus and Earth ionospheres: O₂, N₂, NO, CO, Ar and CO₂.This study shows the strong influence of electronic as well as vibrational internal energy on most ion-molecule reactions. In particular endothermic charge transfer reactions are driven by electronic excitation of O₂⁺ and NO⁺ ions in their a⁴Π_u and a³Σ⁺ metastable states, respectively. Moreover, it is shown that lifetimes of these metastable states are sufficient to survive the mean free path in the lowest part of ionospheres and therefore express their enhanced reactivity. The reactions of O₂⁺ with NO as well as the reactions of CO₂⁺ with NO, O₂, CO and to a less extent N₂ are driven by vibrational excitation. N₂⁺ and CO⁺ reactions vary much less with photon energy than the other ones, except for the case of reactions with Ar. The effects of the molecular ion internal energy content on their reactivity must be included in the ionospheric models for most of the reactions investigated in the present work. It is also the case for the effect of collision energy on the CO⁺+M reactions as we expect that a significant proportion of these CO⁺ could be produced with translational energy by dissociation of doubly charged CO₂²⁺, in particular in the Mars ionosphere. Recommended effective rate constant values are given as a function of VUV photon energy.     

The antiquity indicator argon‐40/argon‐36 for lunar surface samples calibrated by uranium‐235‐xenon‐136 dating

Abstract— Several solar gas rich lunar soils and breccias have trapped ⁴⁰Ar/³⁶Ar ratios >10, although solar Ar is expected to yield a ratio of <0.01. Radiogenic ⁴⁰Ar produced in the lunar crust from ⁴⁰K decay was outgassed into the lunar atmosphere, ionized, accelerated in the electromagnetic field of the solar wind, and reimplanted into lunar surface material. The ⁴⁰Ar loss rate depends on the decreasing abundance of ⁴⁰K. In order to calibrate the time dependence of the ⁴⁰Ar/³⁶Ar ratio in lunar surface material, the period of reimplantation of lunar atmospheric ions and of solar wind Ar was determined using the ²³⁵U‐¹³⁶Xe dating method that relies on secondary cosmic‐ray neutron‐induced fission of ²³⁵U. We identified the trapped, fissiogenic, and cosmogenic noble gases in lunar breccia 14307 and lunar soils 70001‐8, 70181, 74261, and 75081. Uranium and Th concentrations were determined in the 74261 soil for which we obtain the ²³⁵U‐¹³⁶Xe time of implantation of 3.25^+0.38_‐0.60 Ga ago. On the basis of several cosmogenic noble gas signatures we calculate the duration of this near surface exposure of 393 ± 45 Ma and an average shielding depth below the lunar surface of 73 ± 7 g/cm². A second, recent exposure to solar and cosmic‐ray particles occurred after this soil was excavated from Shorty crater 17.2 ± 1.4 Ma ago. Using a compilation of all lunar data with reliable trapped Ar isotopic ratios and pre‐exposure times we infer a calibration curve of implantation times, based on the trapped⁴⁰ Ar/³⁶Ar ratio. A possible trend for the increase with time of the solar ³He/⁴He and ²⁰Ne/²²Ne ratios of about 12%/Ga and about 2%/Ga, respectively, is also discussed.     

S xi Emission Lines in Active Region Spectra Obtained with the Solar euv Rocket Telescope and Spectrograph (Serts)

Theoretical electron density sensitive emission line ratios involving a total of eleven 2s ²2p ²–2s2p ³ transitions in Sxi between 187 and 292 Å are presented. A comparison of these with solar active region observations obtained during rocket flights by the Solar EUV Rocket Telescope and Spectrograph (SERTS) reveals generally good agreement between theory and experiment. However, the 186.87 Å line is masked by fairly strong Fexii emission at the same wavelength, while 239.83 Å is blended with an unknown feature, and 285.58 Å is blended with possibly Niv 285.56 Å. In addition, the 191.23 Å line appears to be more seriously blended with an Fexiii feature than previously believed. The presence of several new Sxi lines is confirmed in the SERTS spectra, at wavelengths of 188.66, 247.14 and 291.59 Å, in excellent agreement with laboratory measurements. In particular, the detection of the 2s ²2p ^{2 3} P ₁ –2s2p ^{3 3} P _0,1 transitions at 242.91 Å is the first time (to our knowledge) that this feature has been identified in the solar spectrum. The potential usefulness of the Sxi line ratios as electron density diagnostics for the solar transition region and corona is briefly discussed.     

Detection Of Soft X-Ray Emission From Comet C/1995 O1 (Hale–Bopp)

We report the detection of soft X-rays from comet C/1995 O1 (Hale-Bopp) by the Low Energy Concentrator Spectrometer (LECS) on-board the X-ray satellite, BeppoSAX. The observations took place on 1996 September 10–11 approximately 1 day after a large dust outburst (Schulz et al., 1997–1999). After correcting for the comets motion, a 7σ enhancement was found centered (2.1 ± 1.3) x 10⁵ km from the position of the nucleus, in the general solar direction. The total X-ray luminosity in the 0.1–2.0 keV energy band is 5 x 10¹⁶ erg s⁻¹ which is at least a factor of ∼ 3 greater than measured by the Extreme Ultraviolet Explorer (EUVE)4 days later and suggests that the bulk of the emission measured by the LECS is related to the dust outburst. The extracted LECS spectrum is well fit by a thermal bremsstrahlung-like distribution of temperature of 0.29 ± 0.06 keV - consistent with that observed in other comets. We find no evidence for fluorescent carbon or oxygen emission and place 95% confidence limits of 1.0 x 10¹⁵ and 7.8 x 10¹⁵ erg s⁻¹ to narrow line emission at 0.28 and 0.53 keV, respectively. We calculate that if such lines are present, they constitute at most 18% of the 0.1–2.0 keV continuum luminosity. This revised version was published online in July 2006 with corrections to the Cover Date.