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  • 1
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    Requirements for the early atmosphere of Mars from nitrogen isotope ratios (1993)
    In:  CASI
    Details
    Publication Date: 2013-08-31
    Description: The N escape models of Fox and Dalgarno and Fox required the presence of a dense, early CO2 atmosphere to inhibit fractionation of the N isotopes N-15 and N-14. The computed photochemical escape fluxes are so large at the present that the isotope ratio measured by Viking (about 1.62x terrestrial) can be produced in about 1.5 b.y. This model was refined in several ways. It was updated to incorporate the variation of the escape fluxes with increases in the solar fluxes at earlier times according to the model of Zahnle and Walker. As expected, this exacerbates the problem with overfractionation, but not greatly. Most of the escape and fractionation of the N occurs in the last 1.5 b.y., when the solar flux was only slightly different from the present. The dense early atmosphere must persist only a bit longer in order to reproduce the measured isotope ratio. The model was also modified to take into account changes in the O mixing ratio with time in the past, assuming that the O abundance is proportional to the square root of the solar flux. Although the production rate of O from photodissociation of CO2 scales as the solar flux, the strength of the winds and other mixing processes also increases with the solar flux, resulting in possibly more effective transport of O to the lower atmosphere where it is destroyed by catalytic and three-body recombination mechanisms.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Workshop on Early Mars: How Warm and How Wet?, Part 1; p 11-12
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  • 2
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    Nitrogen escape from Mars (1992)
    In:  CASI
    Details
    Publication Date: 2013-08-29
    Description: The mass spectrometer on the Viking spacecraft measured anomalous N-15:N-14 ratio of about 1.62 times the terrestrial value. This enhancement presumably results from differential escape of N-15. The escape of N is non-thermal and potential escape mechanisms include photodissociation, photoionization, and electron impact dissociative ionization of N2, and ion-molecule reactions and dissociative recombination of N2(+). The authors propose some calculations to explain the N ratio, but even with all escape mechanisms considered, the ratios don't balance. This leads to the assumption that some other escape mechanisms must exist that are unexplained.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Workshop on the Martian Surface and Atmosphere Through Time; p 53-54
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  • 3
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    Mars atmospheric loss and isotopic fractionation by solar-wind-induced sputtering and photochemical escape (1993)
    In:  CASI
    Details
    Publication Date: 2013-08-31
    Description: We examine the effects of loss of Mars atmospheric constituents by solar-wind-induced sputtering and by photochemical escape during the last 3.8 b.y. Sputtering is capable of efficiently removing all species from the upper atmosphere including the light noble gases; N is removed by photochemical processes as well. Due to diffusive separation (by mass) above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species with the lighter mass being preferentially lost. For C and O, this allows us to determine the size of nonatmospheric reservoirs that mix with the atmosphere; these reservoirs can be CO2 adsorbed in the regolith or H2O in the polar ice caps. We have constructed both simple analytical models and time-dependent models of the loss from and supply of volatiles to the Martian atmosphere.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Mars: Past, Present, and Future. Results from the MSATT Program, Part 1; p 21
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  • 4
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    Mars atmosphere loss and isotopic fractionation by solar-wind-induced sputtering and photochemical escape (1993)
    In:  CASI
    Details
    Publication Date: 2013-08-31
    Description: The effects of loss of Mars atmospheric constituents by solar-wind-induced sputtering and by photochemical escape during the last 3.8 b.y. were examined. Sputtering is capable of efficiently removing all species from the upper atmosphere, including the light noble gases; N also is removed by photochemical processes. Due to the diffusive separation by mass above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species, with the lighter mass being preferentially lost. For C and O, this allows us to determine the size of nonatmospheric reservoirs that mix with the atmosphere; these reserviors can be accounted for by exchange with CO2 adsorbed in the regolith and with H2O in the polar ice deposits. Both simple analytical models and time-dependent models of the loss of volatiles from and supply to the Martian atmosphere were constructed. Both Ar and Ne require continued replenishment from outgassing over geologic time.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Workshop on Early Mars: How Warm and How Wet?, Part 1; p 14-15
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  • 5
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    The production and escape of nitrogen atoms on Mars (1992)
    In:  CASI
    Details
    Publication Date: 2013-08-29
    Description: The lack of agreement between our previously computed values and those measured by Viking of the N-15:N-14 isotope enhancement ratio has led us to reevaluate our model of the Martian ionosphere. In previous models, we were unable to reproduce the ion profiles measured by the RPA on Viking using electron temperatures that were higher that the ion temperatures. When we increased the electron temperatures to 2500-3000 K and with a zero flux upper boundary condition, the ion densities at high altitudes exceeded the measured values by a large factor. We found that we can better fit the observed profiles if we impose a loss process at the upper boundary of our model. If the horizontal fluxes of ions do not constitute a net loss of ions, then the escape of N due to dissociative recombination is also inhibited and better agreement with the measured isotope ratio is found. The production of escaping nitrogen atoms is closely related to the production of thermospheric odd nitrogen; therefore, the densities of NO measured by Viking provide a convenient check on our nitrogen escape model. Our standard model NO densities are less that the measured values by a factor of 2-3, as are those of previous models. We find that reasonable agreement can be obtained by assuming that the rate coefficient for loss of odd nitrogen in the reaction of N with NO is smaller at temperatures that prevail in the lower Martian thermosphere than the standard value, which applies to temperatures of 200-400 K. Other aspects of this investigation are presented.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Papers Presented to the Workshop on the Evolution of the Martian Atmosphere; p 13-14
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  • 6
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    Mars atmospheric loss and isotopic fractionation by pick-up-ion sputtering and photochemical escape (1994)
    In:  Other Sources
    Details
    Publication Date: 2019-01-25
    Description: We examine the effects of loss of constituents of the Martian atmosphere due to sputtering by solar-wind pick-up ions and photochemical escape during the last 3.8 billion years. Sputtering is capable of efficiently removing species from the upper atmosphere to space, including the light noble gases; nitrogen and oxygen are removed by both sputtering ad photochemical processes. Due to diffusive separation (by mass) above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species, with the lighter isotope being preferentially lost. This allows current measurements of the isotopic ratios to be used as a measure of the atmospheric evolution as integrated over geologic time. For carbon and oxygen, isotopic fractionation is buffered by exchange of atmospheric species with non-atmospheric reservoirs of CO2 and H2O. This allows us to determine the size of the non-atmospheric reservoirs which are capable of mixing with the atmosphere; these reservoirs can be CO2 absorbed in the regolith and/or H2O in the polar ice caps. Such an exchangeable reservoir is required in order to keep the fractionation of the atmospheric gases as low as is observed.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Inst., Conference on Deep Earth and Planetary Volatiles; p 19
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  • 7
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    The vibrational distribution of N2(+) in the terrestrial ionosphere (1985)
    In:  Other Sources
    Details
    Publication Date: 2019-06-28
    Description: The densities and vibrational distributions of N2(+) in the X2sigma g +, A2Pi u and B2sigma u + states in the daytime terrestrial ionosphere are computed for both low and high solar activity. Altitude profiles of the relative populations of the vibrational levels of N2(+) X2sigma g + are presented. The fraction of vibrationally excited N2(+) varies from 5 percent at 100 km to 50 percent at 450 km. Several models are examined in which loss of N2(+)(v) is enhanced for v greater than 0 and in which various assumptions are made about the vibrational distributions produced in charge transfer reactions. The N2(+) densities are significantly reduced if N2(+)(v) reacts with O at rates which are near gas-kinetic. Vibrational distributions of the A2pi u and B2sigma u + states are also presented, as well as volume emission rates and integrated overhead intensities of the major bands of the Meinel and first negative systems.
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research (ISSN 0148-0227); 90; 7557-756
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  • 8
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    Studies of the role of metastables and doubly ionized species in the chemical and thermal structure of the Venusian and Martian ionospheres (1981)
    In:  CASI
    Details
    Publication Date: 2019-06-28
    Description: Models of the upper atmospheres of Mars and Venus were constructed using Viking and Pioneer Venus data. The neutral densities, with the exception of NO, N(4S), N(2D) and N(2P) were taken from the measured values, along with the neutral, ion, and electron temperatures. Using solar fluxes and relevant cross sections, the production rates of ions and neutral fragments by photo and electron impact processes were computed. These production rates were combined with chemical production rates and loss along with one dimensional transport eddy diffusion, molecular and ambi polar diffusion, and thermal diffusion, to determine the densities of ions and odd nitrogen species. Preliminary calculations show that the chemistry of metastables and doubly ionized species is important in the ionospheres of Mars and Venus. Production of N(+) in metastable reactions is particularly important, and it explains the discrepancy between the measurements of earlier models. Production of CO(+) is also affected. Reactions of O(++) and O(+)(2D) with N2 have important consequences for the escape rate of atomic nitrogen from the Martian atmosphere.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: NASA-CR-164329
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  • 9
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    A stratospheric chemical instability (1982)
    In:  Other Sources
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    Publication Date: 2019-06-28
    Description: The equations which determine partitioning of Cl(x) in steady state have multiple (three) solutions under conditions which might arise in the high-latitude winter stratosphere. Two of these solutions are stable, one is unstable, to infinitesimal perturbations. The relative stability of solutions is examined by subjecting the system to finite perturbations. The more stable solution is found to eliminate the less stable when semi-infinite volumes of the two solutions are placed in contact. The high-ClO, low NO2 solution is more stable under most conditions. Transitions from less to more stable states are slow in winter but may occur more rapidly when the seasonal variation of insolation is taken into account.
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research; 87; Dec. 20
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  • 10
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    The chemistry of metastable species in the Venusian ionosphere (1982)
    In:  Other Sources
    Details
    Publication Date: 2019-06-28
    Description: Reactions of metastable species are important in determining the densities of minor ions in the Venusian ionosphere. Calculations are carried out in which the coupled continuity and momentum equations are solved for twelve ions and four neutral species in the dayside ionosphere, including O(+)(2D), O(2P), N(2D), and N(2P). Altitude profiles of these metastable species are presented. Their reactions are shown to be a significant source of several minor ions, especially N2(+), CO(+), and N(+). The discrepancies which existed between model and measured densities of these ions are resolved.
    Keywords: LUNAR AND PLANETARY EXPLORATION
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