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At least 37 records · Page 2

Evidence from the limb infrared monitor of the stratosphere for nonlocal thermodynamic equilibrium in the nu2 mode of mesospheric water vapour and the nu3 mode of stratospheric nitrogen dioxide

Data from the 6.9-micron H2O channel and the 6.2-micron NO2 channel of the Nimbus 7 Limb Infrared Monitor of the Stratosphere (LIMS) have been used to investigate the daytime enhancement to H2O; the high concentration of H2O sometimes observed in the polar night mesosphere; and the high ratio of daytime to nighttime NO2 in the upper stratosphere. These three phenomena deviate noticeably from the predictions of photochemical theory. The 20 to 30 percent diurnal variation in stratospheric H2O apparent in LIMS data cannot be reconciled with a photochemical lifetime in excess of four months. This is attributed to departure from local thermodynamic equilibrium of daytime emission which had not been accounted for in retrievals. Speculative possibilities of NLTE emission from the H2O nu2 and NO2 nu3 hot bands are discussed. It is found that the nonthermal emission from NO2 significantly affects retrieval of H2O in the polar nighttime and NO2 in the daytime stratosphere at low latitudes.

Kerridge, Brian J.

Effects on stratospheric ozone from high-speed civil transport: Sensitivity to stratospheric aerosol loading

The potential impact of high-speed civil transport (HSCT) aircraft emissions on stratospheric ozone and the sensitivity of these results to changes in aerosol loading are examined with a two-dimensional model. With aerosols fixed at background levels, calculated ozone changes due to HSCT aircraft emissions range from negligible up to 4-6% depletions in column zone at northern high latitudes. The magnitude of the ozone change depends mainly on the NO(x) increase due to aircraft emissions, which depends on fleet size, cruise altitude, and engine design. The partitioning of the odd nitrogen species in the lower stratosphere among NO, NO2, N2O5, is strongly dependent on the concentration of sulfuric acid aerosol particles, and thus the sensitivity of O3 to NO(x) emissions changes when the stratospheric aerosol loading changes. Aerosol concentrations 4 times greater than background levels have not been unusual in the last 2 decades. Our model results show that a factor of 4 increase in aerosol loading would significantly reduce the calculated ozone depletion due to HSCT emissions. Because of the neutral variabiltiy of stratospheric aerosols, the possible impact of HSCT emissions on ozone must be viewed as a range of possible results.

Weisenstein, Debra K.

Airborne Brightness Temperature Measurements of the Polar Winter Troposphere as Part of the Airborne Arctic Stratosphere Experiment 2 and the Effect of Brightness Temperature Variations on the Diabatic Heating in the Lower Stratosphere

In this paper we report radiometric measurements of tropospheric brightness temperatures obtained during the AASE 2 experiment. These measurements represent the first attempt to characterize effective radiative temperatures as seen from above the troposphere during the Arctic winter. The reported measurements include brightness temperatures at 6.7 and 10.5 micrometers as seen from the NASA DC-8 aircraft flying at about 11 km altitude. We also present radiative transfer calculations to estimate the effect of tropospheric brightness temperature on the lower stratospheric heating rates. Because of the recent massive eruption of the Pinatubo volcano, we also discuss the effects of a volcanic aerosol layer. It is concluded that small particles like the volcanic aerosol or PSCs type 1 do not affect stratospheric heating rates by much; on the other hand, larger particles, PSCs types 2 and 3, may have significant effects on heating rates and consequently on dynamics of the lower stratosphere. The dynamical effects of local stratospheric temperature variations are briefly discussed.

Valero, Francisoco P. J.

Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O and O3

The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta about 330-380 K near 40N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta =352-364 K. Temperatures on the 355 K surface at 20-40 N were low enough to dehydrate air to these values. while most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta <362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

Hintsa, E. J.

Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O and O3

The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta-330-380 K near 40 N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta=352-364 K. Temperatures on the 355 K surface at 20-40 N were low enough to dehydrate air to these values. While most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta<362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

Hintsa, E. J.

Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O, and O3

The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta approximately 330-380 K near 40 N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta = 352-364 K. Temperatures on the 355 K surface 20-40 N were low enough to dehydrate air to these values. While most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta < 362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

Hintsa, E. J.

Troposphere-to-Stratosphere Transport in the Lowermost Stratosphere from Measurements of H2O, CO2, N2O and O3

The origin of air in the lowermost stratosphere is investigated with measurements from the NASA ER-2 aircraft. Air with high water vapor mixing ratios was observed in the stratosphere at theta = 330-380 K near 40 N in May 1995, indicating the influence of intrusions of tropospheric air. Assuming that observed tracer-tracer relationships reflect mixing lines between tropospheric and stratospheric air masses, we calculate mixing ratios of H2O (12-24 ppmv) and CO2 for the admixed tropospheric air at theta = 352-364 K. Temperatures on the 355 K surface at 20-40 N were low enough to dehydrate air to these values. While most ER-2 CO2 data in both hemispheres are consistent with tropical or subtropical air entering the lowermost stratosphere, measurements from May 1995 for theta < 362 K suggest that entry of air from the midlatitude upper troposphere can occur in conjunction with mixing processes near the tropopause.

Hintsa, E. J.

Composite Materials With Uncured Epoxy Matrix Exposed in Stratosphere During NASA Stratospheric Balloon Flight

A cassette of uncured composite materials with epoxy resin matrixes was exposed in the stratosphere (40 km altitude) over three days. Temperature variations of -76 to 32.5C and pressure up to 2.1 torr were recorded during flight. An analysis of the chemical structure of the composites showed, that the polymer matrix exposed in the stratosphere becomes crosslinked, while the ground control materials react by way of polymerization reaction of epoxy groups. The space irradiations are considered to be responsible for crosslinking of the uncured polymers exposed in the stratosphere. The composites were cured on Earth after landing. Analysis of the cured composites showed that the polymer matrix remains active under stratospheric conditions. The results can be used for predicting curing processes of polymer composites in a free space environment during an orbital space flight.

Kondyurin, Alexey

Sub-Seasonal Forecasting of the Stratospheric Wave Events, Sudden Stratospheric Warmings, and Their Influence on the Troposphere

Stratospheric wave events and major sudden stratospheric warming (SSW) events are well captured in high-resolution global forecasts out to 10 days. Tropospheric influences of SSW include statistically significant shifts in the storm tracks and associated surface temperature and precipitation pattern changes. Since these events can in turn influence the troposphere on time scales of 30-60 days the ability to predict these events and the subsequent long-term response on time scales beyond 10 days is of interest. Here we examine the prediction of stratospheric wave events and their evolution using the NASA GMAO (Global Modeling and Assimilation Office) Sub-Seasonal to Seasonal (S2S) system. This is a recently released subseasonal to seasonal forecast system, GEOS-S2S version 2.1. Compared to GMAO's previous system, the new version runs at higher atmospheric resolution (approximately 1/2 degree globally), contains a substantially improved model of the cryosphere, includes additional interactive aerosol model components, and the ocean data assimilation system has been replaced with a Local Ensemble Transform Kalman Filter. Results are based on a comprehensive series of hindcasts starting from the year 2000. They show that while the S2S system is not as accurate at 10 days in forecasting major SSW events as the NASA GMAO Forward Processing system, it can usefully predict stratospheric anomalies out to 20 days and the subsequent stratospheric/tropospheric evolution beyond 30 days.

Coy, L.

Connections Between the Stratosphere and Surface Weather Associated with the Stratospheric Sudden Warming in Early 2018

A major Stratospheric Sudden Warming (SSW) occurred on 11 February 2018. This was the first major SSW since January 2013 and the first split-vortex SSW since January 2009. We examine the SSW and the tropospheric connections using the NASA MERRA-2 reanalysis (1980-2018) and the NASA GEOS Forward Processing (FP) system. A strong tropospheric wave forcing event in January 2018 displaced the stratospheric vortex off the pole. This displaced vortex persisted until the major SSW vortex split in February. At the time of the major SSW split vortex event the MERRA-2 100 hPa meridional heat flux, a measure of the tropospheric forcing on the stratosphere, attained record high values, associated with a strong tropospheric ridge over the US west coast and wave disturbances over the North Atlantic and Asia. The near-real-time GEOS-FP system forecasted the major SSW event with high skill out to 10 days. The analyses also show that after, the SSW, a steady circulation anomaly persisted over the European sector and the transient weather systems were concentrated over the North American continent, under the stronger of the two split vortices. The propagation of these synoptic-scale vortices around the deep, quasi-stationary vortex that extended from the surface into the stratosphere, is well illustrated in animations of extreme temperature changes near the surface over North America. A quantitative analysis of these synoptic waves and their propagation will examine their signatures in potential vorticity and other fields.

Pawson, S.

Stratospheric Water Vapor Observations From the International Space Station By the Stratospheric Aerosol and Gas Experiment III (Sage III/ISS)

The Stratospheric Aerosol and Gas Experiment III has routinely observed the upper atmosphere from the International Space Station (SAGE III/ISS) since June 2017. An important greenhouse gas and molecule affecting chemistry cycles, water vapor is among the vertical profiles of trace gases measured by SAGE III/ISS. This makes SAGE III/ISS the youngest of the current fleet of space-based instruments capable of measuring the vertical distribution of stratospheric water vapor (SWV). The SWV record is mature, a candidate for multi-instrument datasets, e.g. Stratospheric Water and Ozone Satellite Homogenized (SWOOSH) dataset, and shows promise within the GEOS Constituent Data Assimilation System. This presentation reviews the variations in SWV observed by SAGE III/ISS over the past half-decade. Variations highlighted include phase changes of the Quasi-biennial Oscillation (QBO), seasonal and monsoonal moisture patterns, and terrestrial events such as the recent January 2022 Hunga Tonga eruption that perturbed the SWV in spectacular fashion.

stratospheric water vapor

The distribution of odd nitrogen in the lower stratosphere and possible perturbations caused by stratospheric air transport

In the lower stratosphere a significant production of odd nitrogen results from the reaction N2O + O(D-1) yields 2NO. Since the transport is relatively slow, odd nitrogen builds up with a maximum mixing ratio of 2 x 10 to the minus 8th power at 30 Km. Profiles of odd nitrogen, for different latitudes, winter and summer, are computed from one-dimensional transport models. Variations with latitude are small. Horizontal transport is therefore not believed to alter our results significantly. In order to evaluate the effect of odd nitrogen upon the ozone layer, NO(x) profiles are calculated. OH is here a key component, since it converts NO2 to HNO3. In the region where ozone is determined by chemistry rather than by transport (above 25 km), NO2 is found to be relatively abundant. The effect of stratospheric transport on the NO(x) distribution is shown to depend critically upon the height of emission. The effect increases by a factor of 5 or more for a change of flight level from 18 km to 23 km. This strong dependence should be duely considered when future stratospheric transport is discussed.

Isaksen, I. S. A.

Two-dimensional monthly average ozone balance from limb infrared monitor of the stratosphere and stratospheric and mesospheric sounder data

For many years, atmospheric scientists have been concerned with the balance of ozone production and loss terms in the upper stratosphere. Crutzen and Schmailzl (1983) found that the ozone loss was higher than the ozone production in the upper stratosphere. In the present investigation, previous studies are used as a basis in the conduction of a two-dimensional calculation of the production and loss of ozone. The monthly and zonally averaged loss and production rates for ozone are computed using recent Nimbus 7 satellite measurements of stratospheric constituents and accepted reaction and photodissociation rates. It is found that ozone has a loss rate which is about 40-60 percent higher than the production in the photochemical region.

Jackman, C. H.

Concentrations and uncertainties of stratospheric trace species inferred from limb infrared monitor of the stratosphere data. I - Methodology and application to OH and HO2. II - Monthly averaged OH, HO2, H2O2, and HO2NO2

Difficulties arise in connection with the verification of multidimensional chemical models of the stratosphere. The present study shows that LIMS data, together with a photochemical equilibrium model, may be used to infer concentrations of a variety of zonally averaged trace Ox, OHx, and NOx species over much of the stratosphere. In the lower stratosphere, where the photochemical equilibrium assumption for HOx species breaks down, inferred concentrations should still be accurate to about a factor of 2 for OH and 2.5 for HO2. The algebraic nature of the considered model makes it possible to see easily to the first order the effect of variation of any model input parameter or its uncertainty on the inferred concontration of the HOx species and their uncertainties.

Kaye, J. A.

Chemistry and transport in a three-dimensional stratospheric model - Chlorine species during a simulated stratospheric warming

The distributions in the stratosphere of a variety of chemical species were calculated for a 6-day period during the February 1979 stratospheric major warming, using winds derived from a spectral forecast model which included O(x), NO(x), HO(x), and ClO(x) chemistries as well as longitudinally varying reaction rate coefficients and photolysis rates for these molecules. The results obtained indicate a particular importance of chemistry and transport for the Cl-containing species ClO, ClONO2, HCl, and HOCl. Dynamical effects dominate the variability of HCl, while diurnal effects dominate that of ClONO2 and ClO. The effects of strong planetary wave activity may be seen in terms of large longitudinal variability of the total HCl and ClONO columns in the stratosphere; in the middle and high northern latitudes, it is sufficiently large to exceed the diurnal variability of the column.

Kaye, Jack A.

Airborne lidar observations in the wintertime Arctic stratosphere - Polar stratospheric clouds

Polar stratospheric cloud (PSC) distributions in the wintertime Arctic stratosphere and their optical characteristics were measured with a multiwavelength airborne lidar system as part of the 1989 Airborne Arctic Stratospheric Expedition. PSCs were observed on 10 flights between January 6 and February 2, 1989, into the polar vortex. The PSCs were found in the 14-27 km altitude range in regions where the temperatures were less than 195 K. Two types of aerosols with different optical characteristics (Types 1a and 1b) were observed in PSCs thought to be composed of nitric acid trihydrate. Water ice PSCs (Type 2) were observed to have high scattering ratios (greater than 10) and high aerosol depolarizations (greater than 10 percent) at temperatures less than 190 K.

Browell, E. V.

Stratospheric aerosol optical depth observed by the Stratospheric Aerosol and Gas Experiment. II - Decay of the El Chichon and Ruiz volcanic perturbations

The decay of the El Chichon perturbation to the optical depth of stratospheric aerosols at 1.02 micron, 0.525 micron, and 0.453 micron is calculated from the Stratospheric Aerosol and Gas Experiment II (SAGE II) data set for the period December 1984 to December 1988. It is found that the perturbed optical depths at middle and higher latitudes of both hemispheres exhibited an exponential decay superimposed by a seasonal oscillation with a maximum and a minimum occurring in local winter and local summer, respectively. Microphysical processes and variation of the tropopause height alone cannot explain this seasonal change of optical depth. The magnitudes of the exponential component at higher latitudes were, in general, larger than those at lower latitudes. For optical depths in tropical regions, the seasonal oscillations were small and were disturbed by the eruption of Nevado del Ruiz on November 13, 1985. The increase in the ratio of optical depth at 0.525 micron to that at 1.02 micron from about 2.0 at the beginning of 1985 to about 3.5 at the end of 1988 indicates the average size of aerosol particles in the stratosphere is diminishing since the eruption of El Chichon. The 1/e folding time for El Chichon decay derived from the SAGE II data set is in reasonably good agreement with those derived by other methods.

Yue, G. K.

The minor stratospheric warming of January 1989 - Results from STRATAN, a stratospheric-tropospheric data assimilation system

Using a stratospheric-tropospheric data assimilation system, referred to as STRATAN, a minor sudden stratospheric warming that occurred in January 1989 is investigated. The event had a maximum influence on the stratospheric circulation near 2 hPa. The zonal mean circulation reversed briefly in the polar region as the temperature increased 34 K in 3 days. The cause of the warming is shown to be the rapid development and subsequent movement of a warm anomaly, which initially developed in the midlatitudes. The development of the warm anomaly is caused by adiabatic descent, and the dissipation by radiative cooling. A brief comparison with the NMC analysis and temperature sounding data is also presented.

Steenrod, Stephen D.