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1.
Hydroxyl nightglow is intensively studied in the Earth atmosphere, due to its coupling to the ozone cycle. Recently, it was detected for the first time also in the Venus atmosphere, thanks to the VIRTIS-Venus Express observations. The main Δν=1, 2 emissions in the infrared spectral range, centred, respectively, at 2.81 and 1.46 μm (which correspond to the (1-0) and (2-0) transitions, respectively), were observed in limb geometry (Piccioni et al., 2008) with a mean emission rate of 880±90 and 100±40 kR (1R=106 photon cm−2 s−1 (4πster)−1), respectively, integrated along the line of sight. In this investigation, the Bates-Nicolet chemical reaction is reported to be the most probable mechanism for OH production on Venus, as in the case of Earth, but HO2 and O may still be not negligible as mechanism of production for OH, differently than Earth. The nightglow emission from OH provides a method to quantify O3, HO2, H and O, and to infer the mechanism of transport of the key species involved in the production. Very recently, an ozone layer was detected in the upper atmosphere of Venus by the SPICAV (Spectroscopy for Investigation of Characteristics of the Atmosphere of Venus) instrument onboard Venus Express (Montmessin et al., 2009); this discovery enhances the importance of ozone to the OH production in the upper atmosphere of Venus through the Bates-Nicolet mechanism. On Venus, OH airglow is observed only in the night side and no evidence has been found whether a similar emission exists also in the day side. On Mars it is expected to exist both on the day and night sides of the planet, because of the presence of ozone, though OH airglow has not yet been detected.In this paper, we review and compare the OH nightglow on Venus and Earth. The case of Mars is also briefly discussed for the sake of completeness. Similarities from a chemical and a dynamical point of view are listed, though visible OH emissions on Earth and IR OH emissions on Venus are compared.  相似文献   

2.
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(A3Σu+, 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(5Πg) state. Quenching of the O2 band at 762 nm excites the band at 1.27 μm as well. Effective yield of the O2(a1Δg) 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(c1Σu−)+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.  相似文献   

3.
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.  相似文献   

4.
While CO, HCl, and HF, that were considered in the first part of this work, have distinct absorption lines in high-resolution spectra and were detected four decades ago, the lines of HDO, OCS, and SO2 are either very weak or blended by the telluric lines and have not been observed previously by ground-based infrared spectroscopy at the Venus cloud tops. The H2O abundance above the Venus clouds is typically below the detection limit of ground-based IR spectroscopy. However, the large D/H ratio on Venus facilitates observations of HDO. Converted to H2O with D/H ≈ 200, our observations at 2722 cm−1 in the Venus afternoon show a H2O mixing ratio of ∼1.2 ppm at latitudes between ±40° increasing to ±60° by a factor of 2. The observations in the early morning reveal the H2O mixing ratio that is almost constant at 2.9 ppm within latitudes of ±75°. The measured H2O mixing ratios refer to 74 km. The observed increase in H2O is explained by the lack of photochemical production of sulfuric acid in the night time. The recent observations at the P-branch of OCS at 4094 cm−1 confirm our detection of OCS. Four distributions of OCS along the disk of Venus at various latitudes and local times have been retrieved. Both regular and irregular components are present in the variations of OCS. The observed OCS mixing ratio at 65 km varies from ∼0.3 to 9 ppb with the mean value of ∼3 ppb. The OCS scale height is retrieved from the observed limb darkening and varies from 1 to 4 km with a mean value of half the atmospheric scale height. SO2 at the cloud tops has been detected for the first time by means of ground-based infrared spectroscopy. The SO2 lines look irregular in the observed spectra at 2476 cm−1. The SO2 abundances are retrieved by fitting by synthetic spectra, and two methods have been applied to determine uncertainties and detection limits in this fitting. The retrieved mean SO2 mixing ratio of 350 ± 50 ppb at 72 km favors a significant increase in SO2 above the clouds since the period of 1980-1995 that was observed by the SOIR occultations at Venus Express. Scale heights of OCS and SO2 may be similar, and the SO2/OCS ratio is ∼500 and may be rather stable at 65-70 km under varying conditions on Venus.  相似文献   

5.
In 1999, observations of the Venus nightglow with the Keck I telescope showed that the 5577 Å oxygen green line was a significant feature, comparable in intensity to the terrestrial green line. Subsequent measurements have been carried out at the Apache Point Observatory (APO) and again at Keck I, confirming the presence of the line with substantially varying intensity. The Herzberg II emission intensity, from the O2(c-X) transition, was found to have an intensity near 3 kR in one APO run, comparable to the value found on all previous measurements. Thus, of the three oxygen features seen at Venus—the green line, the Herzberg II emission system, and the 1.27-μ 0-0 band of the IR atmospheric system—the first is quite variable, the second is relatively constant, while the third also shows large variations. The reaction between O2(, v=0) and CO is considered as a possible mechanism to explain green line production and its variability, as well as the variability of the 1.27-μ emission and the stability of the CO2 atmosphere. This reaction may catalyze CO2 recombination some five orders of magnitude faster than the slow three-body O + CO reaction.  相似文献   

6.
Ultraviolet (UV) nightglow data from the SPICAV instrument (SPectroscopy for the Investigation of the Characteristics of the Atmosphere of Venus) onboard the Venus Express spacecraft, currently in orbit around Venus, are presented. In its extended source mode, SPICAV has shown that the Venus nightglow in the UV contains essentially Lyman-α and Nitric Oxide (NO) emissions. In the stellar mode, when the slit of the spectrometer is removed, an emission is also observed at the limb in addition to the stellar spectrum. A forward model allows us to identify this feature as being an NO emission. Due to radiative recombination of N and O atoms produced on the dayside of Venus, and transported to the nightside, NO nightglow provides important constraints to the Solar-to-Anti Solar thermospheric circulation prevailing above 90 km. The forward model presented here allows us to derive the altitude of the peak of emission of the NO layer, found at 113.5±6 km, as well as its scale height, of 3.4±1 km and its brightness. The latter is found to be very variable with emissions between 19 Kilo-Rayleigh (kR) and 540 kR. In addition, the NO nightglow is sometimes very patchy, as we are able to observe two distinct emission zones in the field of view. Finally, systematic extraction of this emission from stellar occultations extends the database of the NO emission already reported elsewhere using limb observations.  相似文献   

7.
Variations of the upper cloud boundary and the CO, HF, and HCl mixing ratios were observed using the CSHELL spectrograph at NASA IRTF. The observations were made in three sessions (October 2007, January 2009, and June 2009) at early morning and late afternoon on Venus in the latitude range of ±60°. CO2 lines at 2.25 μm reveal variations of the cloud aerosol density (∼25%) and scale height near 65 km. The measured reflectivity of Venus at low latitudes is 0.7 at 2.25 μm and 0.028 at 3.66 μm, and the effective CO2 column density is smaller at 3.66 μm than those at 2.25 μm by a factor of 4. This agrees with the almost conservative multiple scattering at 2.25 μm and single scattering in the almost black aerosol at 3.66 μm. The expected difference is just a factor of (1 − g)−1 = 4, where g = 0.75 is the scattering asymmetry factor for Venus’ clouds. The observed CO mixing ratio is 52 ± 4 ppm near 08:00 and 40 ± 4 ppm near 16:30 at 68 km, and the higher ratio in the morning may be caused by extension of the CO morningside bulge to the cloud tops. The observed weak limb brightening in CO indicates an increase of the CO mixing ratio with altitude. HF is constant at 3.5 ± 0.2 ppb at 68 km in both morningside and afternoon observations and in the latitude range ±60°. Therefore the observations do not favor a bulge of HF, though HF is lighter than CO. Probably a source in the upper atmosphere facilitates the bulge formation. The recent measurements of HCl near 70 km are controversial (0.1 and 0.74 ppm) and require either a strong sink or a strong source of HCl in the clouds. The HCl lines of the (2-0) band are blended by the solar and telluric lines. Therefore we observed the P8 lines of the (1-0) band at 3.44 μm. These lines are spectrally clean and result in the HCl mixing ratio of 0.40 ± 0.03 ppm at 74 km. HCl does not vary with latitude within ±60°. Our observations support a uniformly mixed HCl throughout the Venus atmosphere.  相似文献   

8.
Venus was observed at 2.4 and 3.7 μm with a resolving power of 4×104 using the long-slit high-resolution spectrograph CSHELL at NASA IRTF. The observations were made along a chord that covered a latitude range of ± 60° at a local time near 8:00. The continuous reflectivity and limb brightening at 2.4 μm are fitted by the clouds with a single scattering albedo 1−a=0.01 and a pure absorbing layer with τ=0.09 above the clouds. The value of 1−a agrees with the refractive index of H2SO4 (85%) and the particle radius of 1 μm. The absorbing layer is similar to that observed by the UV spectrometer at the Pioneer Venus orbiter. However, its nature is puzzling. CO2 was measured using its R32 and R34 lines. The retrieved product of the CO2 abundance and airmass is constant at 1.9 km-atm along the instrument slit in the latitude range of ± 60°. The CO mixing ratio (measured using the P21 line) is rather constant at 70 ppm, and its variations of ∼10% may be caused by atmospheric dynamics. The observed value is higher than the 50 ppm retrieved previously from a spectrum of the full disk, possibly, because of some downward extension of the mesospheric morningside bulge of CO. The observations of the HF R3 line reveal a constant HF mixing ratio of 3.5±0.5 ppb within ± 60° of latitude, which is within the scatter in the previous measurements of HF. OCS has been detected for the first time at the cloud tops by summing 17 lines of the P-branch. The previous detections of OCS refer to the lower atmosphere at 30-35 km. The retrieved OCS mixing ratio varies with a scale height of 1 to 3 km. The mean OCS mixing ratio is ∼2 ppb at 70 km and ∼14 ppb at 64 km. Vertical motions in the atmosphere may change the OCS abundance. The detected OCS should significantly affect Venus' photochemistry. A sensitive search for H2S using its line at 2688.93 cm−1 results in a 3 sigma upper limit of 23 ppb, which is more restrictive than the previous limit of 100 ppb.  相似文献   

9.
The vertical profile of H2SO4 vapor is calculated using current atmospheric and thermodynamic data. The atmospheric data include the H2O profiles observed at 70-112 km by the SOIR solar occultations, the SPICAV-UV profiles of the haze extinction at 220 nm, the VeRa temperature profiles, and a typical profile of eddy diffusion. The thermodynamic data are the saturated vapor pressures of H2O and H2SO4 and chemical potentials of these species in sulfuric acid solutions. The calculated concentration of sulfuric acid in the cloud droplets varies from 85% at 70 km to a minimum of 70% at 90 km and then gradually increasing to 90-100% at 110 km. The H2SO4 vapor mixing ratio is ∼10−12 at 70 and 110 km with a deep minimum of 3 × 10−18 at 88 km. The H2O-H2SO4 system matches the local thermodynamic equilibrium conditions up to 87 km. The column photolysis rate of H2SO4 is 1.6 × 105 cm−2 s−1 at 70 km and 23 cm−2 s−1 at 90 km. The calculated abundance of H2SO4 vapor at 90-110 km and its photolysis rate are smaller than those presented in the recent model by Zhang et al. (Zhang, X., Liang, M.C., Montmessin, F., Bertaux, J.L., Parkinson, C., Yung, Y.L. [2010]. Nat. Geosci. 3, 834-837) by factors of 106 and 109, respectively. Assumptions of 100% sulfuric acid, local thermodynamic equilibrium, too warm atmosphere, supersaturation of H2SO4 (impossible for a source of SOX), and cross sections for H2SO4·H2O (impossible above the pure H2SO4) are the main reasons of this huge difference. Significant differences and contradictions between the SPICAV-UV, SOIR, and ground-based submillimeter observations of SOX at 70-110 km are briefly discussed and some weaknesses are outlined. The possible source of high altitude SOX on Venus remains unclear and probably does not exist.  相似文献   

10.
We present revised tremolite powder thermal decomposition kinetics using previous and newly acquired data from longer time (years instead of months) and lower temperature experiments (<1073 K). We also present kinetic results for decomposition of millimeter- to centimeter-sized tremolite grains. Natural tremolite samples were heated at ambient pressure in flowing CO2 or N2 gas from 1023-1238 K. The tremolite decomposition products are a physical mixture of two pyroxene solid solutions (with the bulk composition Dp59En41), a silica polymorph, and water vapor. Decomposition rates were calculated by using the mass loss of the heated samples. Tremolite crystals and crystalline powder decompositions follow different but related Avrami-Erofe'ev (nucleation and growth) kinetic models. The rate equations for thermal decomposition of tremolite crystalline powder and the larger crystal grains are log10kpowder (h−1)=18.69(±0.19)−23,845(±833)/T and log10kcrystal (h−1)=19.82(±0.07)−25,670(±916)/T. The associated apparent activation energies are 456(±16) kJ mol−1 and 491(±18) kJ mol−1, respectively. We propose a decomposition mechanism and suggest that decomposition and dehydroxylation occur simultaneously. The rate-limiting step is proposed to be structural rearrangement of the amphibole structure to the two pyroxenes and silica. This step and the overall decomposition rate are predicted to be independent of pressure from 1 to 100 bars. These kinetic analyses strengthen our previous conclusion (Johnson and Fegley, 2000, Icarus 146, 301-306) that if hydrous minerals, such as tremolite, formed on Venus during a wetter past, then these minerals could still exist at current conditions on Venus' surface today.  相似文献   

11.
An analysis of ion data from 390 Venus Express, VEX, orbits demonstrates that the flow of solar wind- and ionospheric ions near Venus is characterized by a marked asymmetry. The flow asymmetry of solar wind H+ and ionospheric O+ points steadily in the opposite direction to the planet’s orbital motion, and is most pronounced near the Pole and in the tail/nightside region. The flow asymmetry is consistent with aberration forcing, here defined as lateral forcing induced by the planet’s orbital motion. In addition to solar wind forcing by the radial solar wind expansion, Venus is also subject a lateral/aberration forcing induced by the planet’s orbital motion transverse to the solar wind flow.The ionospheric response to lateral solar wind forcing is analyzed from altitude profiles of the ion density, ion velocity and ion mass-flux. The close connection between decreasing solar wind H+ mass-flux and increasing ionospheric O+ mass-flux, is suggestive of a direct/local solar wind energy and momentum transfer to ionospheric plasma. The bulk O+ ion flow is accelerated to velocities less than 10 km/s inside the dayside/flank Ionopause, and up to 6000 km in the tail. Consequently, the bulk O+ outflow does not escape, but remains near Venus as a fast (km/s) O+ zonal wind in the Venus polar and nightside upper ionosphere. Furthermore, the total O+ mass-flux in the Venus induced magnetosphere, increases steadily downward to a maximum of 2 × 10−14 kg/(m2 s) at ≈400 km altitude, suggesting a downward transport of energy and momentum. The O+, and total mass-flux, decay rapidly below 400 km. With no other plasma mass-flux as replacement, we argue that the reduction of ion mass-flux is caused by ion-neutral drag, a transfer of ion energy and momentum to neutrals, implying that the O+ plasma wind is converted to a neutral (thermosphere) wind at Venus. Incidentally, such a neutral wind would go in the same direction as the Venus atmosphere superrotation.  相似文献   

12.
We analyze EUV spatially-resolved dayglow spectra obtained at 0.37 nm resolution by the UVIS instrument during the Cassini flyby of Venus on 24 June 1999, a period of high solar activity level. Emissions from OI, OII, NI, CI and CII and CO have been identified and their disc average intensity has been determined. They are generally somewhat brighter than those determined from the observations made with the HUT spectrograph at a lower activity level, We present the brightness distribution along the foot track of the UVIS slit of the OII 83.4 nm, OI 98.9 nm, Lyman-ß + OI 102.5 nm and NI 120.0 nm multiplets, and the CO C-X and B-X Hopfield-Birge bands. We make a detailed comparison of the intensities of the 834 nm, 989 nm, 120.0 nm multiplets and CO B-X band measured along the slit foot track on the disc with those predicted by an airglow model previously used to analyze Venus and Mars ultraviolet spectra. This model includes the treatment of multiple scattering for the optically thick OI, OII and NI multiplets. It is found that the observed intensity of the OII emission at 83.4 nm is higher than predicted by the model. An increase of the O+ ion density relative to the densities usually measured by Pioneer Venus brings the observations and the modeled values into better agreement. The calculated intensity variation of the CO B-X emission along the track of the UVIS slit is in fair agreement with the observations. The intensity of the OI 98.9 nm emission is well predicted by the model if resonance scattering of solar radiation by O atoms is included as a source. The calculated brightness of the NI 120 nm multiplet is larger than observed by a factor of ∼2-3 if photons from all sources encounter multiple scattering. The discrepancy reduces to 30-80% if the photon electron impact and photodissociation of N2 sources of N(4S) atoms are considered as optically thin. Overall, we find that the O, N2 and CO densities from the empirical VTS3 model provide satisfactory agreement between the calculated and the observed EUV airglow emissions.  相似文献   

13.
John E. Moores  Peter H. Smith 《Icarus》2011,211(2):1129-1149
A chamber was constructed to simulate the boundary between the ice table, regolith and atmosphere of Mars and to examine fractionation between H2O and HDO during sublimation under realistic martian conditions of temperature and pressure. Thirteen experimental runs were conducted with regolith overlying the ice. The thickness and characteristic grain size of the regolith layer as well as the temperature of the underlying ice was varied. From these runs, values for the effective diffusivity, taking into account the effects of adsorption, of the regolith were derived. These effective diffusivities ranged from 1.8 × 10−4 m2 s−1 to 2.2 × 10−3 m2 s−1 for bare ice and from 2.4 × 10−11 m2 s−1 to 2.0 × 10−9 m2 s−1 with an adsorptive layer present. From these, latent heats of adsorption of 8.6 ± 2.6 kJ mol−1 and 9.3 ± 2.8 kJ mol−1 were derived at ice-surface temperatures above 223 ± 8 K and 96 ± 28 kJ mol−1 and 104 ± 31 kJ mol−1 respectively for H2O and HDO were derived at colder temperatures. For temperatures below 223 K, the effective diffusivity of HDO was found to be lower than the diffusivity of H2O by 40% on average, suggesting that the regolith was adsorptively fractionating the sublimating gas with a fractionation factor of 1.96 ± 0.74. Applying these values to Mars predicts that adsorbed water on the regolith is enriched in HDO compared to the atmosphere, particularly where the regolith is colder. Based on current observations, the D/H ratio of the regolith may be as high as 21 ± 8 times VSMOW at 12°S and LS = 357° if the regolith is hydrated primarily by the atmosphere, neglecting any hydration from subsurface ice.  相似文献   

14.
F. Altieri  L. Zasova  G. Bellucci  B. Gondet 《Icarus》2009,204(2):499-511
We present a method to derive the 2D maps of the O2 (a1Δg) airglow emission at 1.27 μm from the OMEGA/MEx nadir observations. The OMEGA imaging capabilities allow monitoring the 2D distribution, daily and seasonal variation of the O2 emission intensities with a detection limit of 4 MR. The highest values, of the order of ∼31 MR, are found on the south pole for 11 h < LT < 13 h, during the early spring (186° < Ls < 192°) of martian year (MY) 27, according to the Mars Year numbering scheme of Clancy et al. [Clancy, R.T., Wolff, M.J., Christensen, P.R., 2003. Mars aerosol studies with the MGS TES emission phase function observations: Optical depths, particle sizes, and ice cloud types versus latitude and solar longitude. J. Geophys. Res. 108. doi: 10.1029/2003JE002058]. In the polar regions the day-by-day variability, associated with polar vortex turbulences, is obtained of the order of 30-50% as predicted by the model [Lefévre, F., Lebonnois, S., Montmessin, F., Forget, F., 2004. Three-dimensional modeling of ozone on Mars. J. Geophys. Res. 109, E07004. doi: 10.1029/2004JE002268] and found by SPICAM [Perrier, S., Bertaux, J.-L., Lebonnois, S., Korablev, O., Fedorova, A., 2006. Global distribution of total ozone on Mars from SPICAM/MEX UV measurements. J. Geophys. Res. 111, E09S06. doi: 10.1029/2006JE002681]. In the considered set of data a maximum of the O2 emission is observed between 11 h and 15 h LT in the latitude range 70-85° during early spring on both hemispheres, while for the southern autumn-winter season a maximum is found between 50° and 60° in the southern hemisphere for MY28. Increase of intensity of the O2 emission observed from Ls 130° to 160° at southern high latitudes may be explained by increase of solar illumination conditions in the maps acquired during the considered period.Atmospheric waves crossing the terminator on the southern polar regions are observed for the first time during the MY28 early spring. The spatial scale of the waves ranges from 100 to 130 km, and the intensity fluctuations are of the order of 4MR.This study confirms the high potentiality of O2 (a1Δg) day glow as a passive tracer of the martian atmosphere dynamics at high latitudes.  相似文献   

15.
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16.
B. Gundlach  S. Kilias  E. Beitz  J. Blum 《Icarus》2011,214(2):717-723
Coagulation models assume a higher sticking threshold for micrometer-sized ice particles than for micrometer-sized silicate particles. However, in contrast to silicates, laboratory investigations of the collision properties of micrometer-sized ice particles (in particular, of the most abundant H2O-ice) have not been conducted yet. Thus, we used two different experimental methods to produce micrometer-sized H2O-ice particles, i.e. by spraying H2O droplets into liquid nitrogen and by spraying H2O droplets into a cold nitrogen atmosphere. The mean particle radii of the ice particles produced with these experimental methods are (1.49 ± 0.79) μm and (1.45 ± 0.65) μm. Ice aggregates composed of the micrometer-sized ice particles are highly porous (volume filling factor: ? = 0.11 ± 0.01) or rather compact (volume filling factor: ? = 0.72 ± 0.04), depending on the method of production. Furthermore, the critical rolling friction force of FRoll,ice = (114.8 ± 23.8) × 10−10 N was measured for micrometer-sized ice particles, which exceeds the critical rolling friction force of micrometer-sized SiO2 particles . This result implies that the adhesive bonding between micrometer-sized ice particles is stronger than the bonding strength between SiO2 particles. An estimation of the specific surface energy of micrometer-sized ice particles, derived from the measured critical rolling friction forces and the surface energy of micrometer-sized SiO2 particles, results in γice = 0.190 J m−2.  相似文献   

17.
K. Jockers  S. Szutowicz  T. Bonev 《Icarus》2011,215(1):153-185
Axisymmetric models of the outgassing of a cometary nucleus have been constructed. Such models can be used to describe a nucleus with a single active region. The models may include a solar zenith angle dependence of the outgassing. They retrieve the outgassing flux at distances from the nucleus where collisions between molecules are unimportant, as function of the angle with respect to the outgassing axis. The observed emissions must be optically thin. Furthermore the models assume that the outflow speed at large distance from the nucleus does not depend on direction. The value of the outflow speed is retrieved. The models are applied to CN images and HCN spectra of Comet 2P/Encke, obtained nearly simultaneously in November 2003 with the 2 m optical telescope on Mount Rozhen, Bulgaria, and with the 10 m Heinrich Hertz Submillimeter Telescope on Mount Graham, Arizona, USA. According to Sekanina (1988), Astron. J. 95, 911-924, at that time a single outgassing source was active. Input parameters to the models like the rotation period of the nucleus and a small correction to Sekanina’s rotation axis are determined from a simpler jet position angle model. The rotation is prograde with a sideric period of 11.056 ± 0.024 h, in agreement with literature values. The best fit model has an outflow speed of 0.95 ± 0.04 km s−1. The same value has been derived from the corkscrew appearing in the CN images. The location of the outgassing axis is at colatitude δa = 7.4° ± 2.9° and longitude λa = 235° ± 17° (a definition of zero longitude is provided). Comet Encke’s outgassing corresponds approximately to the longitudinally averaged solar input on a spherical nucleus (i.e. very likely comes from deeper layers) but with some deficiency of outgassing at mid-latitudes and non-zero outgassing from the dark polar cap. The presence of gas flow from the dark polar cap is explained as evidence of gas flow across the terminator. The models rely mostly on the CN images. The HCN spectra are more noisy. They provide information how to determine the best fit outflow velocity and the sense of rotation. The model HCN spectra are distinctly non-Gaussian. Within error limits they are consistent with the observations. Models based solely on the HCN spectra are also presented but, because of the lower quality of the data and the unfavorable observing geometry, yield inferior results. As a by-product we determine the CN parent life time from our CN observations. The solar EUV and Lyα radiation field at the time of our observations is taken into account.  相似文献   

18.
Radio spectroscopic observations of Comet 19P/Borrelly were performed during the 1994 apparition and at, and near, the time of the Deep Space 1 flyby in 2001. HCN, CS, CH3OH, and H2CO were detected using the 30-m telescope of the Institut de Radioastronomie Millimétrique and the James Clerk Maxwell Telescope, and their production rates relative to water are estimated to be 0.06-0.11, 0.07, 1.7, and 0.4%, respectively. Only upper limits are derived for H2S and CO. The upper limit for CO/H2O (<15%) is not very constraining, while the upper limit for the H2S/H2O ratio of 0.45% is near the bottom of the range of values measured for other comets. Observations of the OH radical at the Nançay radio telescope provide water production rates a few weeks before the 1994 and 2001 perihelia. Observations of the 110-101 water line at 557 GHz with the Odin satellite yield a water production rate of (2.5±0.5)×1028 s−1 on September 22, 2001, at the time of the Deep Space 1 encounter, and (3.3±0.6)×1028 s−1 averaged over the September 22-24, 2001 period. The line shapes are asymmetric and blueshifted by V0∼−0.18 km s−1 for the best observed HCN lines recorded one week after perihelion. The HCN line shapes, and the similar OH and HCN velocity shifts over the September-November 1994 and August-September 2001 periods, favor anisotropic outgassing towards the Sun. Strong outgassing directed along the primary dust jet seen on visible images is not excluded by the HCN line shapes, but unrealistically high gas expansion velocities are required to explain the line shapes in that case.  相似文献   

19.
We analyze FUV spatially-resolved dayglow spectra obtained at 0.37 nm resolution by the UVIS instrument during the Cassini flyby of Venus. We use a least-squares fit method to determine the brightness of the OI emissions at 130.4 and OI 135.6 nm, and of the bands of the CO fourth positive system which are dominated by fluorescence scattering. We compare the brightness observed along the UVIS foot track of the two OI multiplets with that deduced from a model of the excitation of these emissions by photoelectron impact on O atoms and resonance scattering of the solar 130.4 nm emission. The large optical thickness 130.4 nm emission is accounted for using a radiative transfer model. The airglow intensities are calculated along the foot track and found to agree with the observed 130.4 nm brightness within ∼10%. The modeled OI 135.6 nm brightness is also well reproduced by the model. The oxygen density profile of the VTS3 model is found to be consistent with the observations. We find that self-absorption of the (0, v″) bands of the fourth positive emission of CO is important and we derive a CO vertical column of about 6.4 × 1015 cm−2 in close agreement with the value provided by the VTS3 empirical atmospheric model.  相似文献   

20.
Jacques Gustin  Ian Stewart 《Icarus》2010,210(1):270-283
This study reports the analysis of far ultraviolet (FUV) limb spectra of the airglow of Saturn in the 1150-1850 Å spectral window, obtained with the Ultraviolet Imaging Spectrograph (UVIS) onboard Cassini, spanning altitudes from −1200 to 4000 km. The FUV limb emission consists of three main contributions: (1) H Ly-α peaking at 1100 km with a brightness of 0.8 kilo-Rayleighs (kR), (2) reflected sunlight longward of 1550 Å which maximizes at −950 km with 16.5 kR and (3) H2 bands in the 1150-1650 Å bandwidth, peaking at 1050 km reaching a maximum of 3.9 kR.A vertical profile of the local H2 volume emission rate has been derived using the hydrocarbon density profiles from a model of the Saturn equatorial atmosphere. It is well matched by a Chapman function, characterized by a maximum value of 3.5 photons cm−3 s−1 in the 800-1650 Å UV bandwidth, peaking at 1020 km.Comparisons between the observed spectra and a first-order synthetic airglow H2 model in the 1150-1650 Å bandwidth show that the spectral shape of the H2 bands is accounted for by solar fluorescence and photoelectron excitation. The best fits are obtained with a combination of H2 fluorescence lines and 20 eV electron impact spectra, the latter contributing ∼68% of the total H2 airglow emission.  相似文献   

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