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1.
The quenching rate kN2 of O(1D) by N2 and the specific recombination rate α1D of O2+ leading to O(1D) are re-examined in light of available laboratory and satellite data. Use of recent experimental values for the O(1D) transition probabilities in a re-analysis of AE-C satellite 6300 Å airglow data results in a value for kN2 of 2.3 × 10?11 cm3s?1 at thermospheric temperatures, in excellent agreement with the laboratory measurements. This implies a value of JO2 = 1.5 × 10?6s?1 for the O2 photodissociation rate in the Schumann-Runge continuum. The specific recombination coefficient α1D = 2.1 × 10?7cm3s?1 is also in agreement with the laboratory value. Implications for the suggested N(2D) + O2 → O(1D) + NO reaction are discussed.  相似文献   

2.
In an updating of energy characteristics of lightnings on Venus obtained from Venera-9 and -10 optical observations, the flash energy is given as 8 × 108 J and the mean energy release of lightnings is 1 erg cm?2 s which is 25 times as high as that on the Earth. Lightnings were observed in the cloud layer. The stroke rate in the near-surface atmosphere is less than 5 s?1 over the entire planet if the light energy of the stroke exceeds 4 × 105 J and less than 15 s?1 for (1–4) × 105 J.The average NO production due to lightnings equals 5 × 108 cm?2 s?1, the atomic nitrogen production is equal to 7 × 109 cm?2s?1,the N flux toward the nightside is 3.2 × 109 cm?2s?1, the number densities [N] = 3 × 107cm?3 and [NO] = 1.8 × 106cm?3 at 135 km. Almost all NO molecules in the upper atmosphere vanish interacting with N and the resulting NO flux at 90-80 km equals 5 × 105cm?2s?1, which is negligibly small as compared with lightning production. If the predissociation at 80–90 km is regarded as the single sink of NO, its mixing ratio, fNO, is 4 × 10?8, for the case of a surface sink fNO = 0.8 × 10?9 at 50 km. Excess amounts, fNO ? 4 × 10?8, may exist in the thunderstorm region.  相似文献   

3.
Incoherent scatter observations of the ionospheric F1 layer above Saint-Santin (44.6°N) are analyzed after correction of a systematic error at 165 and 180 km altitude. The daytime valley observed around 200 km during summer for low solar activity conditions is explained in terms of a downward ionization drift which reaches ?30 m s?1 around 180 km. Experimental determinations of the ion drift confirm the theoretical characteristics required for the summer daytime valley as well as for the winter behaviour without a valley. The computations require an effective dissociative recombination rate of 2.3 × 10?7 (300/Te)0.7 (cm3s?1) and ionizing fluxes compatible with solar activity conditions at the time when the valley is observed.  相似文献   

4.
In this paper we confirm an earlier finding that the reaction
constitutes a major source of OI 6300 Å dayglow. The rate coefficient for this reaction is found to be consistent with an auroral result, namely k1 ≈ 6 × 10?12cm3s?1. We correct an error in an earlier publication and demonstrate that reaction (1) is consistent with the laboratory determined quenching rate for the reaction
where k2 = 2.3 × 10?11cm3s?1. Dissociative recombination of O+2 with electrons is found to be a major daytime source in summer above ~220 km.  相似文献   

5.
Previous studies based on radio scintillation measurements of the atmosphere of Venus have identified two regions of small-scale temperature fluctuations located in the vicinity of 45 and 60 km. A global study of the fluctuations near 60 km, which are consistent with wind-shear-generated turbulence, was conducted using the Pioneer Venus measurements. The structure constants of refractive index fluctuations cn2 and temperature fluctuations cT2 increase poleward, peak near 70° latitude, and decrease over the pole; cn2 varies from 2 × 10?15 to 1.5 × 10?14m23 and cT2 from 4 × 10?3 to 7 × 10?2°K2m?23. These results indicate greater turbulent activity at the higher latitudes. In the region near 45 km the refractive index fluctuations and the corresponding temperature fluctuations are substantially lower. Based on the analysis of one representative occultation measurement, cn2 = 2 × 10?16m?23and cT2 = 7.3 × 10?4°K2m?23 in the 45-km region. The fluctuations in this region also appear to be consistent with wind-shear-generated turbulence. The turbulence level is considerably weaker than that at 60 km; the energy dissipation rate ε is 4.9 × 10?5m2sec?3 and the small-scale eddy diffusion coefficient K is 2 × 103 cm2 sec?1.  相似文献   

6.
Radiative recombination of N and O provides a significant source for auroral emission in the γ and δ bands of NO with selective population of vibrational levels in the A2Σ+ and C2Π states. This mechanism may account for emissions detected near 2150 Å. Models are derived for the auroral ionosphere and include estimates for the concentrations of N and NO. The concentration of NO is estimated to have a value of about 108 cm?1 near 140 km in an IBC III aurora. The corresponding density for N is about 5 × 107cm?3 and the concentration ratio NO+O2+ has a value of about 5.5.  相似文献   

7.
It is shown that Titan's surface and plausible atmospheric thermal opacity sources—gaseous N2, CH4, and H2, CH4 cloud, and organic haze—are sufficient to match available Earth-based and Voyager observations of Titan's thermal emission spectrum. Dominant sources of thermal emission are the surface for wavelenghts λ ? 1 cm, atmospheric N2 for 1 cm ? λ ? 200 μm,, condensed and gaseous CH4 for 200 μm ? λ ? 20 μm, and molecular bands and organic haze for λ ? 20 μm. Matching computed spectra to the observed Voyager IRIS spectra at 7.3 and 52.7° emission angles yields the following abundances and locations of opacity sources: CH4 clouds: 0.1 g cm? at a planetocentric radius of 2610–2625 km, 0.3 g cm?2 at 2590–2610 km, total 0.4 ± 0.1 g cm–2 above 2590 km; organic haze: 4 ± 2 × 10?6, g cm, ?2 above 2750 km; tropospheric H2: 0.3 ± 0.1 mol%. This is the first quantitative estimate of the column density of condensed methane (or CH4/C2H6) on Titan. Maximum transparency in the middle to far IR occurs at 19 μm where the atmospheric vertical absorption optical depth is ?0.6 A particle radius r ? 2 μm in the upper portion of the CH4 cloud is indicated by the apparent absence of scattering effects.  相似文献   

8.
The photodissociation of water vapour in the mesosphere depends on the absorption of solar radiation in the region (175–200 nm) of the O2 Schumann-Runge band system and also at H-Lyman alpha. The photodissociation products are OH + H, OH + H, O + 2H and H2 + O at Lyman alpha; the percentages for these four channels are 70, 8, 12 and 10%, respectively, but OH + H is the only channel between 175 and 200 nm. Such proportions lead to a production of H atoms corresponding to practically the total photodissociation of H2O, while the production of H2 molecules is only 10% of the H2O photodissociation by Lyman alpha.The photodissociation frequency (s?1) at Lyman alpha can be expressed by a simple formula
JLyαH2O=4.5 ×10?61+0.2F10.7?65100exp[?4.4 ×10?19 N0.917]
where F10.7 cm is the solar radioflux at 10.7 cm and N the total number of O2 molecules (cm?2), and when the following conventional value is accepted for the Lyman alpha solar irradiance at the top of the Earth's atmosphere (Δλ = 3.5 A?) qLyα,∞ = 3 × 1011 photons cm?2 s1?.The photodissociation frequency for the Schumann-Runge band region is also given for mesospheric conditions by a simple formula
JSRB(H2O) = JSRB,∞(H2O) exp [?10?7N0.35]
where JSRB,∞(H2O) = 1.2 × 10?6 and 1.4 × 10?6 s?1 for quiet and active sun conditions, respectively.The precision of both formulae is good, with an uncertainty less than 10%, but their accuracy depends on the accuracy of observational and experimental parameters such as the absolute solar irradiances, the variable transmittance of O2 and the H2O effective absorption cross sections. The various uncertainties are discussed. As an example, the absolute values deduced from the above formulae could be decreased by about 25-20% if the possible minimum values of the solar irradiances were used.  相似文献   

9.
The paper gives the results of detailed studies of the frequency spectra Ss(?) of the chain of the wave packets Fs(t) of geomagnetic pulsations PC-1 recorded at the Novolazarevskaya station. The bulk of the energy of Fs(t) is concentrated in the vicinity of the central frequencies ?s0 of spectra—the carrier frequencies of the signals. The velocity V0 ≌ 6.103km s?1 of the flux of protons generating these signals correspond to them. The spectra of the signals have oscillations—“satellites” irregularly distributed in frequency. These satellites, as the authors believe, testify to the presence of the individual groups of protons of low concentration whose velocities vary within 103–104 km s?1.Their energy is only of the order of 10?2–10?3 of the energy of the main proton flux. Clearly pronounced maxima on double and triple frequencies ? = 2?s0and 3?s0 are detected. They show that the generation of pulsations PC-1 is accompanied by the generation on the overtones of wave packets called in this paper “two-fold” and “three-fold” pulsations PC-1. Intensive symmetrical satellites of a modulation character have been discovered on frequencies ?±sK. Frequency differences Δ?sK± = ¦?s0 ? ?sK±¦ = (0.011,0.022 and 0.035) Hz correspond to them. The authors believe that the values of Δ?±sK are resonance frequencies of the magnetospheric cavity in which geomagnetic pulsations PC-1 are generated. It is established that the values of Δ?±sK coincide closely with the carrier frequencies of geomagnetic pulsations PC-3 and PC-4 generated in the magnetosphere. This leads to the conclusion that the resonance oscillations of the magnetospheric cavity are their source. Thus, the generation of geomagnetic pulsations of different types and resonance oscillations in the magnetosphere are integrated into a unified process. The importance of the results obtained and the necessity to check further their trustworthiness and universality, using experimental data gathered in different conditions, is stressed.  相似文献   

10.
Measurements of N2+ and supporting data made on the Atmosphere Explorer-C satellite in the ionosphere are used to study the charge exchange process
O+(2D)+N2kN+2+O
The equality k = (5 ± 1.7) × 10?10cm3s?1. This value lies close to the lower limit of experimental uncertainty of the rate coefficient determined in the laboratory. We have also investigated atomic oxygen quenching of O+(2D) and find that the rate coefficient is 2 × 10?11 cm3s?1 to within approximately a factor of two.  相似文献   

11.
In March 1979, the spectrum of Venus was recorded in the far infrared from the G.P. Kuiper Airborne Observatory when the planet subtended a phase angle of 62°. The brightness temperature was observed to be 275°K near 110 cm?1, dropping to 230°K near 270 cm?1. Radiance calculations, using temperature and cloud structure formation from the Pioneer Venus mission and including gaseous absorption by the collision-induced dipole of CO2, yield results consistently brighter than the observations. Supplementing the spectral data, Pioneer Venus OIR data at similar phase angles provide the constraint that any additional infrared opacity must be contained in the upper cloud, H2SO4 to the Pioneer-measured upper cloud structure serves to reconcile the model spectrum and the observations, but cloud microphysics strongly indicates that such a high particle density haze (N ? 1.6 × 107cm?3) is implausible. The atmospheric environment is reviewed with regard to the far infrared opacity and possible particle distribution modifications are discussed. We conclude that the most likely possibility for supplementing the far-infrared opacity is a population of large particles (r ? 1 μm) in the upper cloud with number densities less than 1 particle cm?3 which has remained undetected by in situ measurements.  相似文献   

12.
A sounding rocket was flown during the predawn on 17 January, 1976 from Uchinoura, Japan, to measure directly the behaviour of the conjugate photoelectrons at magnetically low latitudes. On board the rocket were an electron energy analyzer, 630 nm airglow photometer, and plasma probes to measure electron density and temperature. The incoming flux of the photoelectrons was measured in the altitude range between 210 and 340 km. The differential flux at the top of the atmosphere was determined to be F = (1.3 ± 0.4) × 1011exp[?E(eV)12] electron · m?2 · sr?1 · s?1 in the energy range 10 ? E ? 50 eV. The emission rate of the 630 nm airglow was observed in the altitude range between 90 and 360 km. The apparent emission rate observed at 80 km was 32 ± 5 R. From a theoretical calculation of the optical excitation rate using the observed electron flux data along with a model distribution of atomic oxygen, it was estimated that more than 65% of the emission could be produced by direct impact of the photoelectrons with atomic oxygen in the thermosphere between 200 and 360 km. Using the observed electron density and the model distribution of oxygen molecules the residual of the emission was ascribed to the excitation of O(1D) through dissociative recombination, O2++eO1 + O7. The direct collisional excitation by ambient electrons is estimated to be negligibly small at the level of observed electron temperature.  相似文献   

13.
A recent determination by D. R. Bates of the Rayleigh scattering cross section (σRS) for air from 0.2 to 1 μm leads to a simple empirical formula (λ in μm) σRS = 4.02 × 10?28λ4+xcm2 where x = 0.389λ + 0.09426λ ? 0.3228 for the spectral region 0.2 μm < λ < 0.55 μm ; the accuracy is within ±0.5%. From the visible at 0.55 μm to the infrared (i.r.) at 1 μm, the same accuracy can be obtained using a constant value, x = 0.04. The formula accounts for the degree of depolarization which varies with the wavelength according to the latest determination by Bates.  相似文献   

14.
Branching ratios σ(O03PO+2D0)σ(O03PO+4S0) and σ(O03PO+2P0)σ (O03P4S0) are calculated at 584 Å and 304 A employing the close-coupling approximation to compute the photoionization cross section values. The coupled channels include the states dominated by the ground configuration 1s22s2p3 of O+and the next excited configuration ls22s2p4. It is found that the partial c section σ(2D0) decreases more rapidly than σ(2P0), and at the lower wavelength 304 Å, the ratio σ(2D0)σ(4S0) < σ(2P0)σ(4S0). Present results at 304 Å differ considerably from previous work.  相似文献   

15.
A mechanism has been proposed for uv-accelerated desorption from Fe2+ sites on mineral surfaces that satisfies kinetic constraints determined in the laboratory by Huguenin. The process is an integral step of the photochemical weathering mechanism for producing dust on Mars, and it now appears that it may play primary roles in stabilizing CO2 against dissociation by sunlight and in controlling the oxidation state of the atmosphere. We propose that adsorption occurs at octahedrally coordinated Fe2+ surface sites to form seven-coordinate transition-state complexes. These complexes acquire 16–18 kcal mole?1 of ligand field stabilization energy. During illumination (λ ≤ 0.35 μm), electrons are photoemitted from the surfaced Fe2+, temporarily oxidizing them to Fe3+. Fe3+ has no ligand field stabilization energy, and the complexes lose 16–18 kcal mole?1 of stabilization energy. This is a large fraction of the 19- to 28-kcal mole?1 activation energy for dissociating the complexes, and desorption should proceed spontaneously. The gases that were observed to undergo adsorption-photodesorption include O2, CO2, CO, H2O, N2, and Ar. Photodesorption can drive several catalytic reactions, one of which is the oxidation of CO to CO2. The rate of this reaction should be limited by the supply of CO and O2 to the surface to ~2 × 1012 cm?2 sec?1 (column photodissociation rate of CO2). By including this surface reaction in models of Martian atmospheric CO2 chemistry, CO2 can be stabilized against photodissociation with eddy diffusion coefficients of only 3 × 105?1 × 107 cm2 sec?1 below 40 km, raising to ~ 109 cm2 sec?1 at 140 km. Odd hydrogen is not needed to catalyze the oxidation of CO below 40 km, and odd hydrogen mixing ratios need only to be fH ? 10?10 to depress ozone concentrations below the observed upper limit in equatorial regions. Another catalytic reaction that should be driven by photodesorption on Mars is 20H?(ads)H2O + 12O2(g) + 2e?crystal. This is an important source of atmospheric O2, amounting to 7 × 1013?2 × 1017 O2 molecules cm?2 yr?1, and it could have a significant effect on atmospheric oxidation state.  相似文献   

16.
The calculated radiative lifetime of the metastable ion is 6.4 × 10?3s. Used in conjunction with the results of measurements by Erdman, Espy and Zipf this sets 1.3 × 10?18 cm2 as the upper limit to the cross section for the formation of N+(5S) in e - N2 collisions at 100eV which leaves the possibility that the process is responsible for the λ2145A? feature in auroras only just open. The cross section for the formation of N+(5S) in e — N collisions is large. However for this process to lead to the observed intensity of λ2145A? relative to λ3914A? the N:N2 abundance ratio would have to be as high as 1.6 × 10?2.  相似文献   

17.
Simultaneous measurements of the 6300 Å airglow intensity, the electron density profile, and F-region ion temperatures and vertical ion velocities taken at the Arecibo Observatory in March 1971 are utilized in the height integrated continuity equation to extract the number of photons'of 6300 Å emitted per recombination. After accounting for quenching of O(1D) and the electrons lost via NO+ recombination, the efficiency of O(1D) production by the dissociative recombination of O2+ is determined to be 0.6 ± 0.2 including cascading from the O(1S) state. The uncertainty includes both random measurement errors and estimates of possible systematic errors.  相似文献   

18.
A major loss process for the metastable species, O+(2D), in the thermosphere is quenching by electrons
O+(2D) + e → O+(4S) + e
.To date no laboratory measurement exists for the rate coefficient of this reaction. Thermospheric models involving this process have thus depended on a theoretically calculated value for the rate coefficient and its variation with electron temperature. Earlier studies of the O+(2D) ion based on the Atmosphere Explorer data gathered near solar minimum, could not quantify this process. However, Atmosphere Explorer measurements made during 1978 exhibit electron densities that are significantly enhanced over those occurring in 1974, due to the large increases that have occurred in the solar extreme ultraviolet flux. Under such conditions, for altitudes ? 280 km, the electron quenching process becomes the major loss mechanism for O+(2D), and the chemistry of the N+2 ion, from which the O+(2D) density is deduced, simplifies to well determined processes. We are thus able to use the in situ satellite measurements made during 1978 to derive the electron quenching rate coefficient. The results confirm the absolute magnitude of the theoretical calculation of the rate coefficient, given by the analytical expression k(Te) = 7.8 × 10?8 (Te/300)?0.5cm3s?1. There is an indication of a stronger temperature dependence, but the agreement is within the error of measurement.  相似文献   

19.
Laboratory cross-section data on the excitation of the OII(2s 2p44P → 2s2 2p34S; λ834 Å) resonance transition and on the production of O+ and O2+ ions by electron impact on atomic oxygen are used to show that the ratio σ(λ834 A?)σ(O+ + O2+) is nearly constant for incident electron energies > 50 eV. Under auroral conditions, the total electron-ion pair production rate from electron impact on O can be inferred from λ834 Å volume emission rate measurements using the result that η(O+ + O2+)$?8.4η(λ834 A?). These findings, along with earlier work on the simultaneous ionization-excitation of the 1 Neg (0,0) band of N2+ and the 1 Neg (1, 0) band of O+2, allow the specific ionization rates for the principal atmospheric constituents (O+, O+2, N+2), for the multiply-ionized species (O2+, O2+2, N2+2), and for the dissociatively produced atomic ions to be inferred in aurora from remote satellite observations.  相似文献   

20.
A magnetic type mass spectrometer has been flown on two ESRO sounding rockets from ESRANGE (Kiruna 68°N) on February 25 and 26, 1970. The first launch was at sunset (16:33 UT) and the second the next morning, during sunrise (04:47 UT). For both flights the solar zenith angle was approximately 98°. The instrument was measuring simultaneously the neutral gas and positive ion composition and the total ion density. In this paper the results of the ion composition measurements are presented. For both flights the main ion constituents measured between approximately 110–220 km were O+, NO+ and O2+. Only at sunset were N+ and N2+ detected above 200 km. In spite of the identical solar UV-radiation, pronounced sunset/sunrise variations in the positive ion composition were found. The total ion densities at sunrise were between 5×103 and 5 × 104 ions cm?3 and therefore too high to be explained without a night-time ionization by precipitated particles. At sunrise the NO+ and O2+ profiles show a correlated wavelike structure with three pronounced almost equally spaced layers in the E-region. Only the highest layer is present in the O+ profile. Locally enhanced field aligned ionization originated by particle precipitation and an E × B instability are the most likely source for this structure. In the E- and lower F-regions the NO+O2+ ration increased overnight from values around 7 at sunset to 15 at sunrise, correlated with an increase of the local magnetic activity index K from 0+ to 2°. This could be explained if the NO density and magnetic activity are correlated.  相似文献   

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