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Shimazaki, T.

Publications and source records attributed to Shimazaki, T..

At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1985

Radiative relaxation of molecular vibration of the nitric oxide molecule as a possible source of the infrared Shuttle glow

A model calculation to predict infrared Shuttle flow due to the radiative relaxation of vibration of the NO molecule is presented. Space Shuttles hit atmospheric NO molecules at a very high speed and excite vibrational and rotational motions up to the temperature of 54,000 K. With the electric dipole radiation of delta v = 1, 2, 3, and particularly 4 (v is the vibrational quantum number), the excited NO molecules emit infrared radiation before they collide with other molecules. The total radiation power is estimated to be 170 A micro-W, where A is the cross-section area of the Shuttle in sq m if no adsorption of the NO molecule takes place on the Shuttle surface. The intensity of each infrared line is calculated as a function of time, including all vibrational states up to v = 35.

Mizushima, M.↗
NASA NTRS1985

Shuttle glow emissions due to radiative relaxation of highly vibrationally excited NO molecules produced by surface reflection

A new mechanism is proposed for the Space Shuttle glow, which is due to the radiative relaxation of ambient nitric-oxide molecules that are excited to very high vibrational levels by collisions with the Shuttle surface. Many of the particles colliding with the Shuttle surface at a very high speed (about 8 km/sec) would bounce off, exciting vibrational and rotational motions of molecules up to the level of vibrational quantum number v not greater than 35. Radiative transfer from these high levels should cause emissions in the spectrum range from infrared (IR) to visible red depending upon the transition paths. A perturbation method is used to calculate the transition probability and the emission intensity for the transitions of Delta-v not greater than 4. The result indicates that the Delta-v not greater than 4 transitions from high vibrational levels dominates the other transitions; the Delta-v = 4 transitions generally occur at the IR range.

Shimazaki, T.↗
NASA NTRS1984

The dayside Venus ionosphere. II - Combined numerical model of ion and neutral composition above 120 km

The median vertical profile of ion densities for the dayside Venusian ionosphere obtained by the orbiter retarding potential analyzer (ORPA) is simulated by one-dimensional model calculations. The model includes both neutral and ionic chemistry, eddy and molecular diffusion for neutral constituents, and ion-plasma diffusion for ionic constituents. The electron and ion temperatures measured by the ORPA are used to calculate the plasma diffusion coefficients and scale heights for ions. The predicted O2(+) densities below about 200 km agree particularly well with observations by the ORPA, but the model values are significantly less than those measured by the orbiter ion mass spectrometer. The observed ion composition is interpreted in terms of densities of the neutral atmosphere and its composition.

Shimazaki, T.↗
NASA NTRS1984

The photochemical time constants of minor constituents and their families in the middle atmosphere

A comprehensive formula is worked out for the photochemical time constant of minor constituents in the middle atmosphere. The formula is particularly useful for evaluating the time constants for families of some chemical species that are strongly coupled by rapid exchange reactions. Height profiles of photochemical time constants are calculated for individual species and their families based on the chemical reaction rate constants recommended in the recent WMO and JPL reports. Potential exchange reactions among various family members are discussed, and the effects of the choice of family membership on the time constant are evaluated.

Shimazaki, T.↗
NASA NTRS1981

A model of temporal variations in ozone density in the Martian atmosphere

Temporal variations of the ozone density profile in the Martian atmosphere at high latitudes are calculated for the course of a Martian year, taking into account seasonal and diurnal variations in temperature, water vapor and solar radiation. Calculations are based on a model including 35 neutral photochemical reactions, and vertical eddy diffusion using a time step of 12 min for the region from the surface to 240 km altitude. Results are found to be in better agreement with Mariner 9 observations of the time and magnitude of the seasonal maximum than previous model calculations. The diurnal variation is predicted to be small near the solstices, with the nighttime ozone density greater than the daytime and the magnitude of the difference dependent on season. Opposite temporal variations are predicted for ozone densities above and below about 25 km, and an ozone density maximum at 35-40 km is obtained. It is suggested that the effects of an aerosol layer may not be important in enhancing predicted ozone concentration, and may even decrease it.

Shimazaki, T.↗
NASA NTRS1979

The seasonal variation of ozone density in the Martian atmosphere

A one-dimensional, time-dependent model has been developed to investigate seasonal variations in ozone density in the Martian atmosphere. The model utilizes data for atmospheric temperature, pressure, and water vapor abundance observed by Viking. The results indicate that a high ozone density is not produced near the winter solstice but is in rather late winter, when the amount of water vapor is still small and the solar radiation can penetrate more deeply. A similar condition met in early winter does not necessarily produce a high ozone density because of the predicted higher HO2 density. Seasonal variations in ozone abundance are discussed in terms of the abundances of H2O and H2 and the seasonal variations in their reaction products H2O2 and HOx. The roles of transport, the effects of ozone loss to the surface, and the differences between northern and southern hemisphere ozone distributions are also discussed.

Shimazaki, T.↗
NASA NTRS1979

A simplified method for calculating the atmospheric heating rate by absorption of solar radiation in the stratosphere and mesosphere

Calculations of the atmospheric heating rate by absorption of solar radiation by O3, H2O, and CO2 are reported. The method needs only seven parameters for each molecule and is particularly useful for heating calculations in three-dimensional global circulation models below 80 km. Applying the formula to the observed distributions of O3, H2O, and CO2 produces reasonable latitudinal and seasonal variations in the heating rate. The calculated heating rate, however, is sensitive to the global distributions of the absorbing gases, and uncertainties in the O3 distribution above approximately 50 km and the H2O distribution below approximately 20 km may seriously affect the global distributions of the heating rate in these regions.

Shimazaki, T.↗
NASA NTRS1978

Thermal structure of the primitive ionosphere

Exospheric neutral and electron temperatures have been estimated for the primitive upper atmosphere and ionosphere with various oxygen content in the scheme of our previous model (Shimizu and Shimazaki, 1976). The exospheric neutral temperature has been shown to be rather insensitive to the change of oxygen content, justifying our previous assumption for the temperature variation, while the exospheric electron temperature has been found to be quite sensitive to the compositional change, mainly owing to the strong dependence of electron density on the oxygen concentration.

Ashihara, O.↗
NASA NTRS1977

The NASA Ames Research Center one- and two-dimensional stratospheric models. Part 2: The two-dimensional model

The two-dimensional model of stratospheric constituents is presented in detail. The derivation of pertinent transport parameters and the numerical solution of the species continuity equations, including a technique for treating the stiff differential equations that represent the chemical kinetic terms, and appropriate methods for simulating the diurnal variations of the solar zenith angle and species concentrations are discussed. Predicted distributions of tracer constituents (ozone, carbon 14, nitric acid) are compared with observed distributions.

Whitten, R. C.↗
NASA NTRS1977

Simplified methods for calculating photodissociation rates

Simplified methods for calculating the transmission of solar UV radiation and the dissociation coefficients of various molecules are compared. A significant difference sometimes appears in calculations of the individual band, but the total transmission and the total dissociation coefficients integrated over the entire SR (solar radiation) band region agree well between the methods. The ambiguities in the solar flux data affect the calculated dissociation coefficients more strongly than does the method. A simpler method is developed for the purpose of reducing the computation time and computer memory size necessary for storing coefficients of the equations. The new method can reduce the computation time by a factor of more than 3 and the memory size by a factor of more than 50 compared with the Hudson-Mahle method, and yet the result agrees within 10 percent (in most cases much less) with the original Hudson-Mahle results, except for H2O and CO2. A revised method is necessary for these two molecules, whose absorption cross sections change very rapidly over the SR band spectral range.

Shimazaki, T.↗
NASA NTRS1976

Evolution of the ionosphere

Studies were made of the electron density profiles at various stages of atmospheric evolution, with the assumption that the atmospheric composition has changed due to the gradual increase of oxygen while the nitrogen level has remained constant. The result of model calculations indicates that when the oxygen content is less than about 1% of the present earth's atmosphere level, the major ions in the F2 region will change from O(+) to N(+). The maximum number density of N(+) ions reaches approximately 10 million per cu cm because of the absence of a rapid loss mechanism for N(+). The height of the N(+) ion density peak is much lower than the height of the F2 layer peak of the current ionosphere.

Shimizu, M.↗
NASA NTRS1976

A comparison of one-dimensional theoretical models of stratospheric minor constituents

The density profiles of stratospheric minor constituents are compiled from several one-dimensional theoretical models that have appeared in the literature. The models are compared with each other and also with observations if data are available. The similarity and disparity of the models are clarified and discussed. If a large difference exists among the models, attempts are made to interpret it as much as possible in terms of the physical and chemical data employed in each model. The inadequacy of one-dimensional models in calculating the realistic ozone density distributions and the problems related to it are briefly discussed.

Shimazaki, T.↗
NASA NTRS1973

Theoretical model of vertical distributions of CO and CH4 in the mesosphere and upper stratosphere.

Carbon compounds (CO and CO2) and methane are added to an existing computer program (Shimazaki and Laird, 1970, 1972), which calculates diurnal variations in density distributions of pure oxygen compounds, hydrogen compounds, and nitrogen compounds. For the present model calculations, the original program was modified to calculate the steady-state profiles for all constituents, and then these solutions were used as the initial condition for solving the time-dependent equations. The effects of chemical reactions and vertical eddy diffusion transport on the CH4 and CO concentrations above 40 km, where one-dimensional treatment may not be too inappropriate, are discussed. Some of the 15 constituents included in the computer program interact with CO and CH4 chemically, and CH4 is more sensitive to the eddy diffusion coefficient than any other constituent. Therefore it is easier to determine the most appropriate profile of the eddy diffusion coefficient by comparing the model profile with the observations for CH4.

Shimazaki, T.↗
NASA NTRS1973

On the theoretical model for vertical ozone density distributions in the mesosphere and upper stratosphere.

Calculations based on an improved, time-dependent theoretical model for the vertical ozone density distribution in the upper atmosphere are shown to clarify the cause and determine the appearance precondition for the depression at the 70-85 km altitude region in the ozone density distribution suggested by several theoretical models and only sometimes experimentally observed. It is concluded that the depression develops at night through the effects of hydrogen-oxygen and nitrogen-oxygen reactions, as well as those of eddy diffusion transports.

Shimazaki, T.↗
NASA NTRS1972

Seasonal effects on distributions of minor neutral constituents in the mesosphere and lower thermosphere.

Calculations have been made of the diurnal variations in minor neutral constituents in the mesosphere and lower thermosphere for the condition of 60 deg latitude, summer and winter. Excited molecular oxygen has been added, and the effects of absorption of Schumann-Runge bands have been taken into account. The results show significant seasonal differences, which may be interpreted mainly in terms of the difference of penetration of solar radiation and the duration of sunlit hours. However, the comparison of the observed seasonal and diurnal variations in the airglow emissions from hydroxyl, atomic oxygen (5577 A), and excited molecular oxygen with those calculated from models suggests that effects of large-scale meridional circulation (horizontal and vertical transports) may be important in explaining these observations. It is shown that the concentration of the constituents whose main loss mechanism is recombination with atomic oxygen decreases sharply above 80 km.

Shimazaki, T.↗