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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 91 records · Page 5
All sourcesNASA NTRSDOE OSTI
NASA NTRS1983

Vertical distribution of scattering hazes in Titan's upper atmosphere

Radial intensity scans of a Voyager 2 high phase angle image of Titan have been inverted to yield vertical extinction profiles at 1 deg intervals around the limb. A detached haze layer with peak particle number densities of about 0.2 cu/cm exists at all latitudes south of about 45 N, and at an altitude of 300-350 km. The optical depth 0.01 level lies at a radius of 2932 + or - 5 km at the equator and at a radius of 2915 + or - 10 km over the poles (altitudes of 357 + or - 5 and 340 + or - 10 km, respectively). In addition to the haze layer at 300-350 km, there is a small enhancement in the extinction at about 450 km which exists at all latitudes between 75 deg S and about 60 deg N.

Rages, K.↗
NASA NTRS2018

A Singular Value Decomposition Framework for Retrievals with Vertical Distribution Information from Greenhouse Gas Column Absorption Spectroscopy Measurements

We describe a variation of the Optimal Estimation (OE) method for greenhouse gas remote sensing retrievals using a singular value decomposition (SVD) and an uninformative prior. The SVD method is capable of discerning vertical information in column integrated absorption measurements. While traditional Bayesian optimal estimation (OE) assumes a prior distribution in order to regularize the inversion problem, the SVD approach identifies principal components that can be retrieved from the measurement without explicitly specifying a prior mean and prior covariance matrix. We discuss the method, illustrate its use on an integrated path differential absorption CO2 lidar measurement model, and compare it to traditional optimal estimation using numerical simulations. In the absence of forward model error, the mathematics behind the SVD method guarantee it to be bias-free, which is confirmed by the numerical simulations. In contrast, traditional OE retrievals exhibit bias when the prior mean used in the retrieval differs from the true mean. While the SVD approach can be used for most trace gas retrievals, it is particularly useful for situations where prior knowledge of the trace gas profile is poor. The SVD analysis is also useful in illustrating how vertical information is treated by the traditional OE approach.

Ramanathan, Anand K.↗
NASA NTRS1975

The vertical distribution of soluble gases in the troposphere

The thermodynamic properties of several water-soluble gases are reviewed to determine the likely effect of the atmospheric water cycle on their vertical profiles. It is found that gaseous HCl, HNO3, and HBr are sufficiently soluble in water to suggest that their vertical profiles in the troposphere have a similar shape to that of water vapor. It is predicted that HCl, HNO3, and HBr exhibit a steep negative gradient with altitude roughly equal to the altitude gradient of water vapor. Therefore, ground-based sources of inorganic chlorine, odd nitrogen, and inorganic bromine compounds are not likely to affect the stratosphere directly in the mean. Calculations also show that while SO2 and NH3 are significantly affected by the atmospheric water cycle, their abundances may not decrease with altitude as rapidly as does that of water vapor.

Stedman, D. H.↗
NASA NTRS1980

The vertical distribution of tropospheric ammonia

A one-dimensional tropospheric photochemical model is used to simulate measured profiles of NH3 obtained with the Infrared Heterodyne Radiometer. The relative roles of homogeneous loss, heterogeneous loss, and vertical eddy transport are discussed in terms of selecting parameters which best fit the measurements. The best fit was obtained for a vertical eddy diffusion coefficient of 200,000/sq cm per sec or greater (corresponding to a characteristic vertical transport time in excess of about 35 days), and a characteristic heterogeneous loss time in excess of 10 days. The characteristic homogeneous chemical loss time was found to be about 40 days at the surface and decreased to about 180 days at 10 km, and not very sensitive to model chemical perturbations. Increased ground-level concentrations of NH3 to about 10 ppb, compared to background surface concentrations of about 1 ppb, were measured several weeks after application of ammonium nitrate fertilizer. This suggests that the volatilization of ammonium nitrate fertilizer is rapid, and an important source of NH3. Because of the characteristic times for the loss mechanisms, synoptic time-scale phenomena may play an important role in determining the tropospheric distribution of NH3 concentrations.

Levine, J. S.↗
NASA NTRS2006

What does Reflection from Cloud Sides tell us about Vertical Distribution of Cloud Droplet Sizes?

Cloud development, the onset of precipitation and the effect of aerosol on clouds depend on the structure of the cloud profiles of droplet size and phase. Aircraft measurements of cloud profiles are limited in their temporal and spatial extent. Satellites were used to observe cloud tops not cloud profiles with vertical profiles of precipitation-sized droplets anticipated from CloudSat. The recently proposed CLAIM-3D satellite mission (cloud aerosol interaction mission in 3-D) suggests to measure profiles of cloud microphysical properties by retrieving them from the solar and infrared radiation reflected or emitted from cloud sides. Inversion of measurements from the cloud sides requires rigorous understanding of the 3-dimentional(3-D) properties of clouds. Here we discuss the reflected sunlight from the cloud sides and top at two wavelengths: one nonabsorbing to solar radiation (0.67 microns) and one with liquid water efficient absorption of solar radiation (2.1 microns). In contrast to the plane-parallel approximation, a conventional approach to all current operational retrievals, 3-D radiative transfer is used for interpreting the observed reflectances. General properties of the radiation reflected from the sides of an isolated cloud are discussed. As a proof of concept, the paper shows a few examples of radiation reflected from cloud fields generated by a simple stochastic cloud model with the prescribed vertically resolved microphysics. To retrieve the information about droplet sizes, we propose to use the probability density function of the droplet size distribution and its first two moments instead of the assumption about fixed values of the droplet effective radius. The retrieval algorithm is based on the Bayesian theorem that combines prior information about cloud structure and microphysics with radiative transfer calculations.

Marshak, A.↗
NASA NTRS2005

What Does Reflection from Cloud Sides Tell Us About Vertical Distribution of Cloud Droplet Sizes?

Cloud development, the onset of precipitation and the effect of aerosol on clouds depend on the structure of the cloud profiles of droplet size and phase. Aircraft measurements of cloud profiles are limited in their temporal and spatial extent. Satellites were used to observe cloud tops not cloud profiles with vertical profiles of precipitation-sized droplets anticipated from Cloudsat. The recently proposed CLAIM-3D satellite mission (cloud aerosol interaction mission in 3D) suggests to measure profiles of cloud microphysical properties by retrieving them from the solar and infrared radiation reflected or emitted from cloud sides. Inversion of measurements from the cloud sides requires rigorous understanding of the 3-dimensional (3D) properties of clouds. Here we discuss the reflected sunlight from the cloud sides and top at two wavelengths: one nonabsorbing to solar radiation (0.67 micrometers) and one with liquid water efficient absorption of solar radiation (2.1 micrometers). In contrast to the plane-parallel approximation, a conventional approach to all current operational retrievals, 3D radiative transfer is used for interpreting the observed reflectances. General properties of the radiation reflected from the sides of an isolated cloud are discussed. As a proof of concept, the paper shows a few examples of radiation reflected from cloud fields generated by a simple stochastic cloud model with the prescribed vertically resolved microphysics. To retrieve the information about droplet sizes, we propose to use the probability density function of the droplet size distribution and its first two moments instead of the assumption about fixed values of the droplet effective radius. The retrieval algorithm is based on the Bayesian theorem that combines prior information about cloud structure and microphysics with radiative transfer calculations.

Marshak, Alexander↗
NASA NTRS1982

Determination of the horizontal and vertical distribution of clouds from infrared satellite sounding data

A numerical algorithm, based on a physical inversion of the radiative transfer equation, is developed to retrieve the global distribution of the horizontal cloud cover, the cloud-top pressure levels and their temperature. The algorithm makes use of infrared and microwave temperature sounding data to derive the clear-column vertical temperature profiles and then uses the same infrared sounding data to obtain the corresponding cloud parameters. Experimental verification of this method is carried out using data from the High resolution Infrared Sounder (HIRS) and the Microwave Sounding Unit (MSU) operating on the NOAA weather satellite system.

Chahine, M. T.↗
NASA NTRS2000

Vertical Distributions of PH3 in Saturn from Observations of Its 1-0 and 3-2 Rotational Lines

Far-infrared Fourier-transform spectrometer measurements of the 1-0 and 3-2 PH3 transitions in Saturn's disk near 267 and 800 GHz (8.9 and 26.7/cm), respectively, were analyzed simultaneously to derive a global mean profile for the PH3 vertical mixing ratio between 100 and 600 mbar total pressure. The far-infrared spectrum is relatively free from spectral interlopers, suffers minimal absorption or scattering by atmospheric particulates, and contains intrinsically weak PH3 lines that are sensitive to a range of atmospheric depths. The combined spectra are inconsistent with a uniform tropospheric mixing ratio, even with a stratospheric cut-off. They are consistent with a volume mixing ratio of PH3 that drops from 1.2 x 10(exp -5) at 645 mbar pressure to a value of 4.1 x 10(exp -7) at 150 mbar pressure, a decrease that is linear is log abundance vs log pressure. The mixing ratio could drop even more quickly at atmospheric pressures below 150 mbar and still be consistent with the data. The mixing ratio may well remain constant with depth for pressures above 630 mbar. The maximum PH3 mixing ratio in this model is consistent with a [P]/[H] ratio in the deep atmosphere that is about a factor of 10 higher than solar composition. Such a model is consistent with rapid mixing up to the radiative-convective boundary and transport by, for example, vertical waves just above this boundary. In the best fitting model, the eddy diffusion coefficient is approximately 10(exp 4) sq cm near 630 mbar, and it must increase with altitude. The predominant PH3 loss mechanisms are direct photolysis by UV radiation and scavenging by H atoms produced by the photolysis.

Orton, G. S.↗
NASA NTRS2014

Past Changes in the Vertical Distribution of Ozone Part 1: Measurement Techniques, Uncertainties and Availability

Peak stratospheric chlorofluorocarbon (CFC) and other ozone depleting substance (ODS) concentrations were reached in the mid- to late 1990s. Detection and attribution of the expected recovery of the stratospheric ozone layer in an atmosphere with reduced ODSs as well as efforts to understand the evolution of stratospheric ozone in the presence of increasing greenhouse gases are key current research topics. These require a critical examination of the ozone changes with an accurate knowledge of the spatial (geographical and vertical) and temporal ozone response. For such an examination, it is vital that the quality of the measurements used be as high as possible and measurement uncertainties well quantified. In preparation for the 2014 United Nations Environment Programme (UNEP)/World Meteorological Organization (WMO) Scientific Assessment of Ozone Depletion, the SPARC/IO3C/IGACO-O3/NDACC (SI2N) Initiative was designed to study and document changes in the global ozone profile distribution. This requires assessing long-term ozone profile data sets in regards to measurement stability and uncertainty characteristics. The ultimate goal is to establish suitability for estimating long-term ozone trends to contribute to ozone recovery studies. Some of the data sets have been improved as part of this initiative with updated versions now available. This summary presents an overview of stratospheric ozone profile measurement data sets (ground and satellite based) available for ozone recovery studies. Here we document measurement techniques, spatial and temporal coverage, vertical resolution, native units and measurement uncertainties. In addition, the latest data versions are briefly described (including data version updates as well as detailing multiple retrievals when available for a given satellite instrument). Archive location information for each data set is also given.

stratospheric ozone layer measurement↗
NASA NTRS2005

Short-term, seasonal and interannual variability of the vertical distribution of water vapor observed by AIRS

The Atmospheric Infrared Sounder (AIRS) consists of a suite of instruments on board the Aqua spacecraft which retrieve atmospheric parameters over the globe at radiosonde quality on a daily basis in non-precipitating fields of view with less than 80% cloud cover. Although quantitative global measurements of water vapor have been available since the 1980's, the vertical resolution of these measurements was very coarse. AIRS provides global coverage amounting to 324,000 precipitable water vapor profiles with spatial resolution at nadir of 45 km and a vertical resolution in the troposphere of 2 km.

remote sounding↗
NASA NTRS1988

The origin and vertical distribution of carbon monoxide in Jupiter

Six clearly-resolved lines of the CO 1-0 vibration-rotation band near 4.7 microns have been observed in Jupiter at a resolution of 0.07/cm. CO is not found to be concentrated in the stratosphere, but is shown to be present in the troposphere at a mole fraction of 1.6 + or - 0.3 x 10 to the -9th, suggesting that rapid vertical mixing is the source of CO. Results indicate that the global oxygen abundance in Jupiter's gaseous envelope below the cloud-forming regions must be near the solar value, and that intervening clouds with an optical depth of 0.5-4 are present above the line-forming region.

Noll, Keith S.↗
NASA NTRS1990

Temporal and vertical distribution of acidity and ionic composition in clouds - Comparison between modeling results and observations

Cyclic temporal variations of pH and ionic concentration in sampled clouds which traversed the Mt. Mitchell State Park (North Carolina) site during the summers of 1986, 1987, and 1988 are reported. These clouds typically had a measured pH minimum during their initial and final stages. The cause of this basic cylic pattern is attributed to sampling at different vertical levels of the cloud. This is substantiated by visual observations made while sampling. The results also suggest that the measured pH patterns do not always exhibit minima during the formative and dissipative stages of the cloud, apparently in response to the underlying dynamical processes. The relationship between temporal pH measurements made at a stationary site to vertical cloud levels provides insights into the physical processes (e.g., nucleation scavenging near cloud base, dry air entrainment near cloud top) influencing the observed cloud-water chemistry on a real-time basis and would improve cloud chemistry models.

Defelice, T. P.↗
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 NTRS2022

Updated Trends of the Stratospheric Ozone Vertical Distribution in the 60°S-60°N Latitude Range Based on the LOTUS Regression Model

This study presents an updated evaluation of stratospheric ozone profile trends in the 60°S - 60°N latitude range over the 2000 - 2020 period using an updated version of the Long-term Ozone Trends and Uncertainties in the Stratosphere (LOTUS) regression model that was used to evaluate such trends up to 2016 for the last WMO Ozone Assessment (2018). In addition to the derivation of detailed trends as a function of latitude and vertical coordinates, the regressions are performed with the data sets averaged over broad latitude bands, i.e., 60°S–35°S, 20°S–20°N and 35°N–60°N. The same methodology as in the last Assessment is applied to combine trends in these broad latitude bands in order to compare the results with the previous studies. Longitudinally resolved merged satellite records are also considered in order to provide a better comparison with trends retrieved from ground-based records, e.g., lidar, ozone sondes, Umkehr, microwave and Fourier Transform Infrared (FTIR) spectrometers at selected stations where long-term time series are available. The study includes a comparison with trends derived from the REF-C2 simulations of the Chemistry Climate Model Initiative (CCMI-1). This work confirms past results showing an ozone increase in the upper stratosphere, which is now significant in the three broad latitude bands. The increase is largest in the northern and southern hemisphere midlatitudes, with ~2.2%/decade at ~2.1 hPa, and ~2.1%/decade at ~3.2 hPa respectively, compared to ~1.6%/decade at ~2.6 hPa in the tropics. New trend signals have emerged from the records, such as a significant decrease of ozone in the tropics around 35 hPa and a non-significant increase of ozone in the southern midlatitudes at about 20 hPa. Non-significant negative ozone trends are derived in the lowermost stratosphere, with the most pronounced trends in the tropics. While a very good agreement is obtained between trends from merged satellite records and the CCMI-1 REF-C2 simulation in the upper stratosphere, observed negative trends in the lower stratosphere are not reproduced by models at southern and, in particular, at northern midlatitudes, where models report an ozone increase. However, the lower stratospheric trend uncertainties are quite large, for both measured and modelled trends. Finally, 2000-2020 stratospheric ozone trends derived from the ground-based and longitudinally resolved satellite records are in reasonable agreement over the European Alpine and tropical regions, while at the Lauder station in the southern hemisphere mid-latitudes they show some differences.

Stratospheric ozone trends↗
NASA NTRS2017

Ground-Based High Spectral Resolution Lidar Observation of Aerosol Vertical Distribution in the Summertime Southeast United States

As part of the Southeast United States-based Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys (SEAC4RS), and collinear with part of the Southeast Atmosphere Study, the University of Wisconsin High Spectral Resolution Lidar system was deployed to the University of Alabama from 19 June to 4 November 2013. With a collocated Aerosol Robotic Network (AERONET) sun photometer, a nearby Chemical Speciation Network (PM2.5) measurement station, and near daily ozonesonde releases for the August-September SEAC4RS campaign, the site allowed the regions first comprehensive diurnal monitoring of aerosol particle vertical structure. A 532nm lidar ratio of 55 sr provided good closure between aerosol backscatter and AERONET (aerosol optical thickness, AOT). A principle component analysis was performed to identify key modes of variability in aerosol backscatter. ''Fair weather'' days exhibited classic planetary boundary layer structure of a mixed layer accounting for approx. 50% of AOT and an entrainment zone providing another 25%. An additional 5-15% of variance is gained from the lower free troposphere from either convective detrainment or frequent intrusions of western United States biomass burning smoke. Generally, aerosol particles were contained below the 0 C level, a common level of stability in convective regimes. However, occasional strong injections of smoke to the upper troposphere were also observed, accounting for the remaining 10-15% variability in AOT. Examples of these common modes of variability in frontal and convective regimes are presented, demonstrating why AOT often has only a weak relationship to surface PM2.5 concentration.

HSRL↗
NASA NTRS2011

Vertical Distribution of Water at Phoenix

Phoenix results, combined with coordinated observations from the Mars Reconnaissance Orbiter of the Phoenix lander site, indicate that the water vapor is nonuniform (i.e., not well mixed) up to a calculated cloud condensation level. It is important to understand the mixing profile of water vapor because (a) the assumption of a well-mixed atmosphere up to a cloud condensation level is common in retrievals of column water abundances which are in turn used to understand the seasonal and interannual behavior of water, (b) there is a long history of observations and modeling that conclude both that water vapor is and is not well-mixed, and some studies indicate that the water vapor vertical mixing profile may, in fact, change with season and location, (c) the water vapor in the lowest part of the atmosphere is the reservoir that can exchange with the regolith and higher amounts may have an impact on the surface chemistry, and (d) greater water vapor abundances close to the surface may enhance surface exchange thereby reducing regional transport, which in turn has implications to the net transport of water vapor over seasonal and annual timescales.

Phoenix↗
NASA NTRS2002

Precipitation Recycling and the Vertical Distribution of Local and Remote Sources of Water for Precipitation

Precipitation recycling is defined as the amount of water that evaporates from a region that precipitates within the same region. This is also interpreted as the local source of water for precipitation. In this study, the local and remote sources of water for precipitation have been diagnosed through the use of passive constituent tracers that represent regional evaporative sources along with their transport and precipitation. We will discuss the differences between this method and the simpler bulk diagnostic approach to precipitation recycling. A summer seasonal simulation has been analyzed for the regional sources of the United States Great Plains precipitation. While the tropical Atlantic Ocean (including the Gulf of Mexico) and the local continental sources of precipitation are most dominant, the vertically integrated column of water contains substantial water content originating from the Northern Pacific Ocean, which is not precipitated. The vertical profiles of regional water sources indicate that local Great Plains source of water dominates the lower troposphere, predominantly in the PBL. However, the Pacific Ocean source is dominant over a large portion of the middle to upper troposphere. The influence of the tropical Atlantic Ocean is reasonably uniform throughout the column. While the results are not unexpected given the formulation of the model's convective parameterization, the analysis provides a quantitative assessment of the impact of local evaporation on the occurrence of convective precipitation in the GCM. Further, these results suggest that local source of water is not well mixed throughout the vertical column.

Bosilovich, Michael G.↗