Engineering topics

Minschwaner, K.

Publications and source records attributed to Minschwaner, K..

10 records

NASA NTRS2003

SPARC-IGAC Symposium on Climate-Chemistry Interactions. Climate Feedback by Water Vapor in the Tropical Upper Troposphere

The strong greenhouse forcing by atmospheric water vapor is expected to play an important role in shaping the direction of any future changes in climate. We present calculations that provide a new perspective on the sensitivity of upper tropospheric water vapor to changes in surface temperature. Equilibrium states of our atmospheric model show unambiguously that as the surface warms, changes in the vertical distribution and temperature of detraining air parcels from tropical convection lead to higher water vapor mixing ratios in the upper troposphere. However, the increase in mixing ratio is not as large as the increase in saturation mixing ratio due to warmer environmental temperatures, so that the relative humidity decreases. Our analysis suggests that models that maintain a fixed relative humidity are likely overestimating the magnitude of the water vapor feedback.

Dessler, A. E.↗

NASA NTRS1997

Infrared Radiative Forcing and Atmospheric Lifetimes of Trace Species Based on Observations from UARS

Observations from instruments on the Upper Atmosphere Research Satellite (UARS) have been used to constrain calculations of infrared radiative forcing by CH4, CCl2F2 and N2O, and to determine lifetimes Of CCl2F2 and N2O- Radiative forcing is calculated as a change in net infrared flux at the tropopause that results from an increase in trace gas amount from pre-industrial (1750) to contemporary (1992) times. Latitudinal and seasonal variations are considered explicitly, using distributions of trace gases and temperature in the stratosphere from UARS measurements and seasonally averaged cloud statistics from the International Satellite Cloud Climatology Project. Top-of-atmosphere fluxes calculated for the contemporary period are in good agreement with satellite measurements from the Earth Radiation Budget Experiment. Globally averaged values of the radiative forcing are 0.536, 0.125, and 0.108 W m-2 for CH4, CCl2F2, and N2O, respectively. The largest forcing occurs near subtropical latitudes during summer, predominantly as a result of the combination of cloud-free skies and a high, cold tropopause. Clouds are found to play a significant role in regulating infrared forcing, reducing the magnitude of the forcing by 30-40% compared to the case of clear skies. The vertical profile of CCl2F2 is important in determining its radiative forcing; use of a height-independent mixing ratio in the stratosphere leads to an over prediction of the forcing by 10%. The impact of stratospheric profiles on radiative forcing by CH4 and N2O is less than 2%. UARS-based distributions of CCl2F2 and N2O are used also to determine global destruction rates and instantaneous lifetimes of these gases. Rates of photolytic destruction in the stratosphere are calculated using solar ultraviolet irradiances measured on UARS and a line-by-line model of absorption in the oxygen Schumann-Runge bands. Lifetimes are 114 +/- 22 and 118 +/- 25 years for CCl2F2 and N2O, respectively.

Minschwaner, K.↗

NASA NTRS1996

Bulk Properties of Isentropic Mixing into the Tropics in the Lower Stratosphere

Timescales for mixing of midlatitude air into the tropical lower stratosphere are deduced from observations of long-lived tracers N2O and CCl3F. Bulk mixing between tropical and midlatitude regions is assumed to be isentropic and relatively slow compared with local mixing within each region. The mean value of the mixing timescale ranges from 12 to 18 months near 20 km. There is a tendency for shorter mixing times at higher and lower altitudes, although vertical profiles of mixing cannot be definitively established by the data. A more robust quantity is given by the fraction of midlatitude air entrained into the tropical upwelling region. Implied mixing fractions exceed 50% above 22 km.

Minschwaner, K.↗

NASA NTRS1996

The Effects of Tropical Cirrus Clouds on the Abundance of Lower Stratospheric Ozone

The distribution of many chemical constituents of the atmosphere (e.g., ozone) is at least partially determined by the. distribution of net radiative heating in the atmosphere. In this paper, we demonstrate the significant effect of high cirrus clouds on the net radiative heating of the tropical lower stratosphere. A model of tropical lower stratospheric ozone is then used to demonstrate the sensitivity of calculated ozone to the varying cloud cover used in the model. We conclude that calculated ozone is sensitive to the inclusion of clouds In models and that models of the atmosphere should include a realistic description of tropical cirrus clouds in order to accurately simulate the chemical composition of the atmosphere.

Dessler, A. E.↗

NASA NTRS1996

The Effects of Tropical Cirrus Clouds on the Abundance of Lower Stratospheric Ozone

The distribution of many chemical constituents of the atmosphere (e.g., ozone) is at least partially determined by the, distribution of net radiative heating in the atmosphere. In this paper, we demonstrate the significant effect of high cirrus clouds on the net radiative heating of the tropical lower stratosphere. A model of tropical lower stratospheric ozone is then used to demonstrate the sensitivity of calculated ozone to the varying cloud cover used in the model. We conclude that calculated ozone is sensitive to the inclusion of clouds in models and that models of the atmosphere should include a realistic description of tropical cirrus clouds in order to accurately simulate the chemical composition of the atmosphere.

Dessler, A. E.↗

NASA NTRS1996

The Effects of Tropical Cirrus Clouds on the Abundance of Lower Stratospheric Ozone

The distribution of many chemical constituents of the atmosphere (e.g., ozone) is at least partially determined by the distribution of net radiative heating in the atmosphere. In this paper, we demonstrate the significant effect of high cirrus clouds on the net radiative heating of the tropical lower stratosphere. A model of tropical lower stratospheric ozone is then used to demonstrate the sensitivity of calculated ozone to the varying cloud cover used in the model. We conclude that calculated ozone is sensitive to the inclusion of clouds in models and that models of the atmosphere should include a realistic description of tropical cirrus clouds in order to accurately simulate the chemical composition of the atmosphere.

Dessler, A. E.↗

NASA NTRS1996

Quantifying Transport Between the Tropical and Mid-Latitude Lower Stratosphere

Because exchange with the tropics is slower than multi-dimensional models generally assume, ozone at mid-latitudes apears to be more sensitive to elevated levels of industrial chlorine than currently predicted. Nevertheless, approximately 45% of air in the tropical ascent region at 21 km has been entrained from mid-latitudes, implying that emissions from supersonic aircraft could deplete ozone in the middle stratosphere.

stratosphere↗

NASA NTRS1993

Absorption of solar radiation by O2 - Implications for O3 and lifetimes of N2O, CFCl3, and CF2Cl2

An accurate line-by-line model is used to evaluate effects of absorption in the Schumann-Runge bands of O2 on transmission of UV radiation. The model is used to evaluate rates of photolysis for N2O, CFCl3, and CF2Cl2, and to infer global loss rates and instantaneous lifetimes appropriate for 1980. A parameterized version of the line-by-line model enabling rapid evaluation of transmission in the Schumann-Runge region is described. Photochemical calculations employing the parameterization and constrained by data from the Atmospheric Trace Molecule Spectroscopy experiment are used to examine the budget of odd oxygen. Consistent with previous studies, it is shown that photochemical loss of odd oxygen exceeds production by photolysis of O2 for altitudes above 40 km. The imbalance between production and loss is shown to be consistent with a source of odd oxygen proportional to the product of the mixing ratio and photolysis rate of ozone, which suggests that processes involving vibrationally excited O2 may play an important role in production of odd oxygen.

Minschwaner, K.↗

NASA NTRS1993

Ultraviolet O2 transmittance - AURIC implementation

A new spectrally precise approach to Schumann-Runge synthesis has been devised, employing nine (9) different spectral arrays containing polynomial coefficients. The coefficients were fit to calculated cross sections obtained from a detailed Schumann-Runge model that incorporates the most recent high resolution spectroscopic data for a temperature range between 130 and 500K. This large data base is being used to reexamine the existing parameterizations of UV transmission and photolysis. In addition, it is now possible to extend atmospheric radiance codes further into the ultraviolet. Initial implementation has been accomplished for the MODTRAN code as part of the eventual development of AURIC, the Atmospheric Ultraviolet Radiance Integrated Code.

Anderson, G. P.↗

NASA NTRS1992

Polynomial coefficients for calculating O2 Schumann-Runge cross sections at 0.5/cm resolution

O2 cross sections from 49,000 to 57,000/cm have been fitted with temperature dependent polynomial expressions, providing an accurate and efficient means of determining Schumann-Runge band cross sections for temperatures between 130 and 500 K. The least squares fits were carried out on a 0.5/cm spectral grid, using cross sections obtained from a Schumann-Runge line-by-line model that incorporates the most recent spectroscopic data. The O2 cross sections do not include the underlying Herzberg continuum, but they do contain contributions from the temperature dependent Schumann-Runge continuum. The cross sections are suitable for use in UV transmission calculations at high spectral resolution. They should also prove useful for updating existing parameterizations of ultraviolet transmission and O2 photolysis.

Minschwaner, K.↗