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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 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1992

Large-scale variability of ozone and aerosols in the summertime Arctic and sub-Arctic troposphere

The results of mesoscale and large-scale studies of the distribution of aerosols and O3 using primarily an airborne DIAL system are reported. The tropospheric composition at high latitudes is found to be strongly influenced by stratospheric intrusions. Regions of low-aerosol scattering and enhanced O3 mixing ratios are correlated with descending air from the lower stratosphere. Over 37 percent of the troposphere along the flight track at latitudes higher than 57 deg N had significantly enhanced O3 levels due to stratospheric intrusions, and in the 4-6 km latitude range the tropospheric extent of the enhanced O3 exceeded 56 percent. Ozone mixing ratios of 80 ppbv at 6 km are common, with vertical O3 gradients of over 11 ppbv/km observed across the base of strong intrusions. In the mixed layer over the tundra, O3 was in the 25-35 ppbv range with a gradient of 5.5 ppbv/km, while in the continental polar air masses, the average gradient in the lower troposphere is 7.4 ppbv/km, indicating more downward transport of O3 at higher latitudes.

Browell, E. V.↗
NASA NTRS1994

Annual variability of ozone along alpine hillsides

Over a period of more than two years (March 1989 till June 1991) ozone and nitrogen dioxide have been monitored along twelve alpine hillsides in the Austrian alps. The profiles had a height-resolution of 100 m and cover a range between 400 m and 1800 m asl, that is 100 m to 1100 m above the bottom of the valleys. They were situated in remote rural areas as well as in the vicinity of polluted urban and industrial areas. Both trace gases were monitored by means of integral chemical (SAM-surface active monitor) methods with a measuring cycle of two weeks. The concentration of ozone exhibits a substantial annual variation over the entire height range. In summer, highest ozone levels are observed near the ground and at the top of the mountains, whereas in winter the maxima are found mainly in the crest regions. The overall ozone burden shows a relative maximum near the temperature inversion layer in the valleys and an absolute maximum at the crest.

Putz, Erich↗
NASA NTRS2001

Vertical Distribution and Variability of Ozone During July 1999 Over Andenes, Norway

Ozonesonde measurements of the polar atmosphere obtained at Andenes, Norway during July 1999 showed unusual characteristics when compared with mid- or low-latitude ozone profiles. A minimum of two ozonesondes each day were released, one in late afternoon and one in early evening. A very well-defined ledge in the ozone profile corresponding to the tropopause appears to form as a result of transport. The ozone amount increases four to five times, from about 30 nb at the tropopause to 120 nb at a pressure about 10-20 hPa lower. The typical peak ozone value, although at a higher altitude than the ledge, appears at a much lower pressure (approx. 140 hPa) than found in midor low-latitudes (approx. 18-25 hPa), Total column ozone amounts are consistently higher than 300 DU. Analysis of the variation with regard to wind conditions will be discussed.

Schmidlin, F. J.↗
NASA NTRS2010

Interannual Variability of Ozone in the Winter Lower Stratosphere and the Relationship to Lamina and Irreversible Transport

We use the high-resolution dynamic limb sounder (HIRDLS) high-vertical resolution ozone profiles in the northern hemisphere lower stratosphere to examine the meridional transport out of the tropics. We focus on February 2005.2007 when there are differences in the dynamical background in the lower stratosphere due to the states of the quasibiennial oscillation and polar vortex. HIRDLS data reveal a large number of low ozone laminae that have the characteristics of tropical air at midlatitudes. More laminae are observed in February in 2006 than in 2005 or 2007. Because laminae can form, move out of the tropics, and return to the tropics without mixing into the midlatitude ozone field, the number of laminae is not directly related to the net transport. We use equivalent latitude coordinates to discriminate between reversible and irreversible laminar transport. The equivalent latitude analysis shows greater irreversible transport between the tropics and lower midlatitudes in both 2005 and 2007 compared to 2006 despite the higher number of laminae observed in 2006. Our conclusion that there was more irreversible transport of tropical air into the lower midlatitudes in 2005 and 2007 is supported by equivalent length analysis of mixing using microwave limb sounder N2O measurements. This study shows that reversibility must be considered in order to infer the importance of lamination to net transport.

Olsen, Mark A.↗
NASA NTRS1989

The vertical ozone distribution during maximum and minimum solar activity

To study the latitude variation of ozone vertical distribution the complex experiment was carried out in February to July 1985 between 40 deg N to 70 deg S at the Pacific and the Indian Oceans. The great bulk of their data network were taken by the optical rocket ozonometers at the Southern Hemisphere. The results were compared with reference models containing the most extensive set of ozone observations from VS satellites between 1978 and 1982. To analyze latitude-season ozone variability at fixed altitude levels the experimental ozone concentration data were confirmed with model equatorial data. To compare the experimental data with reference model data, analogous model values were calculated. The results of calculation indicated a good agreement between experimental and reference model data of relative latitude-season variations of ozone concentration. Maximum variability is observed at 50 km in the equator and not exceeded 15 percent in the other regions at all altitude levels.

Kokin, G. A.↗
NASA NTRS2015

The Global Structure of UTLS Ozone in GEOS-5: A Multi-Year Assimilation of EOS Aura Data

Eight years of ozone measurements retrieved from the Ozone Monitoring Instrument (OMI) and the Microwave Limb Sounder, both on the EOS Aura satellite, have been assimilated into the Goddard Earth Observing System version 5 (GEOS-5) data assimilation system. This study thoroughly evaluates this assimilated product, highlighting its potential for science. The impact of observations on the GEOS-5 system is explored by examining the spatial distribution of the observation-minus-forecast statistics. Independent data are used for product validation. The correlation coefficient of the lower-stratospheric ozone column with ozonesondes is 0.99 and the bias is 0.5%, indicating the success of the assimilation in reproducing the ozone variability in that layer. The upper-tropospheric assimilated ozone column is about 10% lower than the ozonesonde column but the correlation is still high (0.87). The assimilation is shown to realistically capture the sharp cross-tropopause gradient in ozone mixing ratio. Occurrence of transport-driven low ozone laminae in the assimilation system is similar to that obtained from the High Resolution Dynamics Limb Sounder (HIRDLS) above the 400 K potential temperature surface but the assimilation produces fewer laminae than seen by HIRDLS below that surface. Although the assimilation produces 5 - 8 fewer occurrences per day (up to approximately 20%) during the three years of HIRDLS data, the interannual variability is captured correctly. This data-driven assimilated product is complementary to ozone fields generated from chemistry and transport models. Applications include study of the radiative forcing by ozone and tracer transport near the tropopause.

GEOS-5↗
NASA NTRS2020

Global-scale distribution of ozone in the remote troposphere from ATom and HIPPO airborne field missions

Ozone is a key constituent of the troposphere, where it drives photochemical processes, impacts air quality, and acts as a climate forcer. Large-scale in situ observations of ozone commensurate with the grid resolution of current Earth system models are necessary to validate model outputs and satellite retrievals. In this paper, we examine measurements from the Atmospheric Tomography (ATom; four deployments in 2016–2018) and the HIAPER Pole-to-Pole Observations (HIPPO; five deployments in 2009–2011) experiments, two global-scale airborne campaigns covering the Pacific and Atlantic basins. ATom and HIPPO represent the first global-scale, vertically resolved measurements of O3 distributions throughout the troposphere, with HIPPO sampling the atmosphere over the Pacific and ATom sampling both the Pacific and Atlantic. Given the relatively limited temporal resolution of these two campaigns, we first compare ATom and HIPPO ozone data to longer-term observational records to establish the representativeness of our dataset. We show that these two airborne campaigns captured on average 53 %, 54 %, and 38 % of the ozone variability in the marine boundary layer, free troposphere, and upper troposphere–lower stratosphere (UTLS), respectively, at nine well-established ozonesonde sites. Additionally, ATom captured the most frequent ozone concentrations measured by regular commercial aircraft flights in the northern Atlantic UTLS. We then use the repeated vertical profiles from these two campaigns to confirm and extend the existing knowledge of tropospheric ozone spatial and vertical distributions throughout the remote troposphere. We highlight a clear hemispheric gradient, with greater ozone in the Northern Hemisphere, consistent with greater precursor emissions and consistent with previous modeling and satellite studies. We also show that the ozone distribution below 8 km was similar in the extra-tropics of the Atlantic and Pacific basins, likely due to zonal circulation patterns. However, twice as much ozone was found in the tropical Atlantic as in the tropical Pacific, due to well-documented dynamical patterns transporting continental air masses over the Atlantic. Finally, we show that the seasonal variability of tropospheric ozone over the Pacific and the Atlantic basins is driven year-round by transported continental plumes and photochemistry, and the vertical distribution is driven by photochemistry and mixing with stratospheric air. This new dataset provides additional constraints for global climate and chemistry models to improve our understanding of both ozone production and loss processes in remote regions, as well as the influence of anthropogenic emissions on baseline ozone.

ATom, aircraft profiles, Atlantic pollution, ozone↗
NASA NTRS2000

Recent Changes in Tropospheric Ozone in the Tropics

This paper presents a detailed characterization of tropical tropospheric column ozone variability on time scales varying from a few days to a solar cycle. The study is based on more than 20 years (1979 to the present) of tropospheric column ozone time series derived from the convective cloud differential (CCD) method using total ozone mapping spectrometer (TOMS) data. Results indicate three distinct regions in the tropics with distinctly three different zonal characteristics related to seasonal, interannual and solar variabilities. These three regions are the eastern Pacific, Atlantic, and western Pacific. Tropospheric column ozone in the Atlantic region peaks at about the same time (September-October) from 20 N to 20 S. The amplitude of the annual cycle, however, varies from about 3 to 6 Dobson unit (DU) from north to south of the equator. In comparison, the annual cycle in both the eastern and western Pacific is generally week and the phase varies from peak values in March and April in the northern hemisphere to September and October in the southern hemisphere. The interannual pattern in the three regions are also very different. The Atlantic region indicates a quasi biennial oscillation in the tropospheric column ozone which is out of phase with the stratospheric ozone. This is consistent with the photochemical control of this region caused by high pollution and high concentration of ozone producing precursors. The observed pattern, however, does not seem to be related to the interannual variability in ozone precursors related to biomass burning. Instead, it appears to be a manifestation of the UV modulation of upper tropospheric chemistry on a QBO time scale caused by stratospheric ozone. During El Nino events, there is anomalously low ozone in the eastern Pacific and high values in the western Pacific indicating the effects of convectively driven transport. The observed increase of 10-20 DU in tropospheric column ozone in the Indonesian region in the western Pacific during the recent 1997-1998 El Nino was associated with large-scale forest fires which may have contributed 5-10 DU of the total increase.

Chandra, S.↗
NASA NTRSDate not supplied

Regional and Seasonal Trends in Tropical Ozone from SHADOZ Profiles: Reference for Models and Satellite Products

Understanding lowermost stratosphere (LMS) ozone variability is an important topic in the trends and climate assessment communities because of feedbacks among changing temperature, dynamics, water vapor and ozone. LMS evaluations are usually based on satellite observations. Free tropospheric (FT) ozone assessments typically rely on profiles from commercial aircraft. Ozonesonde measurements constitute an independent dataset encompassing both LMS and FT. We used Southern Hemisphere Additional Ozonesondes (SHADOZ) data from 1998-2019 in the GSFC Multiple Linear Regression (MLR) model to analyze monthly mean FT and LMS ozone across five well-distributed tropical sites, three based on combination of nearby individual stations (Figure 1). Our findings: (1) both FT (defined as 5-15 km) and LMS (15-20 km) ozone trends exhibit marked regional and seasonal variability. (2) Stations with the largest FT ozone increases, in the equatorial Americas and western Pacific/east Indian Ocean, show these trends most strongly in February-May when there is convectively-driven wave activity. (3) LMS ozone losses are greatest in the 2nd half of the year (solid lines in Figure 2) when the losses are correlated with an increase in tropopause height (TH) as derived from SHADOZ radiosonde data. ( 4) When the upper FT and LMS are defined by tropopause-relative coordinates, the LMS ozone trend calculated by MLR becomes insignificant, as shown in the dashed lines in Figure 2. Thus, the 20-year decline in tropical LMS ozone reported in recent satellite- and model-based studies does not point to a chemical loss but is rather a signature of a tropopause that has been perturbed by a changing climate. Output based on our regional and monthly averaged FT and LMS ozone trends will be available as a reference for satellite- and model-based analyses.

Free Tropospheric (FT) ozone assessments↗
NASA NTRS2005

Separating the Chemical and Dynamical Contributions to the Ozone Change

Statistical analysis is used to extract the sensitivity of ozone to changes in stratospheric chlorine due to emissions of chlorofluorcarbons from the observed ozone record. The statistical analysis relies on a model that accounts for natural variations in ozone including the seasonal cycle, the solar cycle, variations in aerosols due to volcanic eruption, and the quasi- biennial oscillation, A noise term includes contributions to ozone variability due to inter-annual variability in the stratospheric circulation not due to the quasi-biennial oscillation, The residual circulation varies due to variability in planetary wave forcing, and studies using meteorological analyses show that the build-up of ozone over the winter is correlated with the planetary wave Eliassen-Palm flux. This variability in the residual circulation is not included in the statistical model, and contributes to the apparent ozone sensitivity to chlorine derived from observations for 1979 - 2000. We have investigated these relationships using multi-decadal simulations of our off-line chemistry and transport model (CTM). Our simulations use meteorological fields output from a 50 year simulation of a general circulation model (GCM). A 50 climatology specifies the sea surface temperatures to produce the GCM simulation. The CTM was used with these winds to produce two simulations, one in which the boundary conditions for chlorofluorcarbons and other source gases vary as specified for 1973-2022 by the Scenario A2 of the World Meteorological Organization ozone assessment, and the second with source gases fixed to their 1979 values. The same statistical analysis used to derive trends from observations is applied to the CTM output. When applied to the difference between the two simulations the statistical analysis provides a more precise measure of the ozone sensitivity to chlorine change. We are testing ways of including the interannual variability in the residual circulation in the statistical model so that we can derive the same result from the Scenario A2 simulation as is obtained when the statistical analysis is applied to the difference between the two simulations. This should provide direction as to how to account for the changes in ozone due to interannual variability in the residual circulation in the statistical model that is applied to the observed data record.

Douglass, Anne R.↗
NASA NTRS1994

Global QBO in circulation and ozone. Part 1: Reexamination of observational evidence

Observational evidence for a global quasi-biennial oscillation (QBO) pattern is reviewed. In particular, the presence of an extratropical, as well as an equatorial, component of the QBO signal in column ozone is established. It is found that the ozone interannual variability is such that as one moves away from the Tropics, the frequency spectrum of the anomaly changes from one that is dominated by the equatorial QBO frequency of 1/30 mo to a two-peak spectrum around the two frequencies: 1/30 mo and 1/20 mo. Instead of treating the 1/20 mo frequency as a separate phenomenon to be filtered away in extracting the QBO in the extratropics, as was previously done, the authors argue that both peaks are integral parts of the extratropical QBO phenomenon. The 1/20 mo frequency happens to be the difference combination of the QBO frequency 1/30 mo and the annual frequency 1/12 mo. Therefore, it can represent the result of the QBO modulating an annual cycle. The authors suggest that previous methods of extracting the extratropical QBO signal severely underestimated the contribution of the QBO to the interannual variability of ozone when data are filtered to pass only the component with the period of equatorial QBO. Further, it is argued that the transport of equatorial QBO ozone anomaly by a non-QBO circulation can at most account for 6-8 Dobson units (DU) of the observed interannual variability of column ozone in the extratropics. The remaining variability (up to 20 DU) probably cannot be produced without an anomaly in the transporting circulation in the extratropics.

Tung, K. K.↗
NASA NTRS2000

Reducing The Station-to Station Variability of Umkehr Ozone Trends Using SAGE Measurements

This proposed research sought to use SAGE I and II ozone and aerosol measurements to reduce the variability in ozone trends, principally, but not exclusively, in layer 8 (40 km) derived from multiple Umkehr stations. Building on our experience with both SAGE and Umkehr data, we proposed to commence at the very beginning of the Umkehr process (measured radiance ratios) and proceed through the fitting and inversion processes in conjunction with radiative transfer calculations to establish a consistent, reliable time series of Umkehr ozone profiles at a number of stations. We expected to be able to reconcile the present discrepancies between SAGE and Umkehr trends in the upper stratosphere and, in particular, to reduce the variability in trend estimates among mid-latitude Umkehr stations.

Newchurch, Mike↗
NASA NTRS1984

Spatial variability of total ozone at high latitudes in winter

The spatial variability of total ozone at high latitudes in winter is explained by the vertical structure of planetary-scale waves. The location of the maximum in total ozone is governed by the phase shift with height of the waves, while the amplitude of the maximum depends on the phase and also on the vertical and horizontal mean-zonal ozone gradients.

Kurzeja, R. J.↗
NASA NTRS2003

Tropospheric Ozone Over a Tropical Atlantic Station in the Northern Hemisphere: Paramaribo, Surinam (6 deg N, 55 deg W)

We present an analysis of 2.5 years of weekly ozone soundings conducted at a new monitoring station in Paramaribo, Surinam (6 deg N,55 deg W). This is currently one of only three ozone sounding stations in the northern hemisphere (NH) tropics, and the only one in the equatorial Atlantic region. Paramaribo is part of the Southern Hemisphere ADditional Ozone Sounding program (SHADOZ). Due to its position close to the equator, the Inter Tropical Convergence Zone (ITCZ) passes over Paramaribo twice per year, which results in a semi-annual seasonality of many parameters including relative humidity and ozone. The dataset from Paramaribo is used to: (1) evaluate ozone variability relative to precipitation, atmospheric circulation patterns and biomass burning; (2) contrast ozone at the NH equatorial Atlantic with that at nearby southern hemisphere (SH) stations Natal (6 deg S,35 deg W) and Ascension (8 deg S,14 deg W); (3) compare the seasonality of tropospheric ozone with a satellite-derived ozone product: Tropical Tropospheric Ozone Columns from the Modified Residual method (MR-TTOC). We find that Paramaribo is a distinctly Atlantic station. Despite its position north of the equator, it resembles nearby SH stations during most of the year. Transport patterns in the lower and middle troposphere during February and March differ from SH stations, which leads to a seasonality of ozone with two maxima. MR-TTOC over Paramaribo does not match the observed seasonality of ozone due to the use of a SH ozone sonde climatology in the MR method. The Paramaribo ozone record is used to suggest an improvement for northern hemisphere MR-TTOC retrievals. We conclude that station Paramaribo shows unique features in the region, and clearly adds new information to the existing SHADOZ record.

Peters, W.↗
NASA NTRSDate not supplied

Atmospheric Formaldehyde Trend and Its Source Attributions in the Recent Decades

Formaldehyde (CH 2 O) is one of the most important reactive trace gases in the atmosphere with an important role in tropospheric chemistry and in the control of surface air quality. Sources of CH 2 O includes direct emissions and in situ production from the oxidation of volatile organic compounds (VOCs). In this study, we investigate spatial-temporal variations in atmospheric CH 2 O and how changes in CH 2 O couple with tropospheric ozone variability during the past two decades using recently available retrievals from the Ozone Monitoring Instrument (OMI) aboard NASA’s Aura satellite and the RefD1 simulation from the NASA Goddard Earth Observing System Chemistry Climate Model (GEOSCCM). Our initial analysis provides evidence of significant increases in atmospheric CH 2 O concentrations over several of the world’s major anthropogenic regions, including China, India, and the Middle East, and several biomass burning regions, including South America, southern Africa, boreal regions and Indonesia. We furthermore will identify regional source contributions to CH 2 O trends, including anthropogenic VOCs emissions, biogenic isoprene emissions and open fires. In particular, we will focus on anthropogenic emission regions to examine the role of changing anthropogenic VOC emissions on CH 2 O abundance.

Atmospheric Formaldehyde↗