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At least 451 records · Page 25

Results from NASA's Near Real Time Ozone Data Assimilation Systems

Organizations in Europe, Australia, and the United States have recently broadened constituent assimilation activities beyond water vapor, which has been assimilated for years in the numerical weather prediction applications. Many of these activities have focused on ozone, with some efforts focused on the entire suite of reactive constituents that control the ozone distribution. This talk will draw from results from the near real-time ozone data assimilation system being run by NASA's Data Assimilation Office. This system utilizes ozone observations from both the TOMS and the SBUV instrument to generate global synoptic maps of ozone. The initial application of this product is to provide ozone fields to assist in the atmospheric corrections' that are necessary for the retrieval of information from other NASA instruments. The validation of the ozone assimilation system shows that the assimilated product agrees well with independent HALOE and ozonesonde observations. Aside from providing a global synoptic map, there is verifiable geophysical information at higher vertical resolution than either of the date types input into the system. This talk will establish the validation results and enumerate applications of the ozone data assimilation system. Results from exploratory research will be presented. The applications being considered include estimates of tropospheric ozone, provision of ozone fields for interactive retrievals, use of analysis increments from the assimilation to evaluate model performance, and development of long-term consistent three-dimensional global ozone fields. The results from the exploratory studies are promising, and help demonstrate how assumptions made in the development of the ozone assimilation impact the other applications. For instance, RMS errors in the current product are large near the tropopause, which is sensitive to the specification of vertical correlation functions, which in turns impacts the amount of ozone analyzed to be in the troposphere. How these sensitivities impact the different applications will also be discussed.

Rood, Richard B.↗

Optical effects of polar stratospheric clouds on the retrieval of TOMS total ozone

Small areas of sharply reduced ozone density appear frequently in the maps produced from polar region total ozone mapping spectrometer (TOMS) data. These mini-holes are of the order of 1000 km in extent with a lifetime of a few days. On the basis of measurements from ground-based instruments, balloon-borne ozonesondes, and simultaneous measurements of aerosol and ozone concentrations during aircraft flights in the Arctic and Antarctic regions, the appearance of polar stratospheric clouds (PSCs) are frequently associated with false reductions in ozone derived from the TOMS albedo data. By combining radiative transfer calculations with the observed PSC and ozone data, it is shown that PSCs located near or above the ozone density maximum (with optical thickness greater than 0.1) can explain most of the differences between TOMS ozone data and ground or in situ ozone measurements. Several examples of real and false TOMS mini-hole phenomenon are investigated using data from the 1989 Airborne Arctic Stratospheric Expedition (AASE) and from balloon flights over Norway and Sweden.

Torres, O.↗

Variability of ozone near the tropopause from GASP data

The first 22 months of ozone data from the Global Atmospheric Sampling Program are summarized. Variations in space and time were examined at nearly all scales permitted by the data. Case studies in the tropics suggest that local ozone maxima may be found in or near clouds. Preliminary seasonal mean maps of ozone during spring are presented for the Northern Hemisphere. In the troposphere over the United States during summer there is a distinct midcontinental ozone maximum. There is a diurnal variation in ozone in the upper troposphere and the daily range is about 5 ppbv. Correlations between ozone and other variables are given for the synoptic-scale and on a hemispheric scale. The possible bearing of these results on ozone transport computations is discussed.

Nastrom, G. D.↗

Ozone Climatology

The primary role of models in the assessment process is to predict changes to ozone. It is crucial therefore that the ability of the models to reproduce the actual distribution of ozone be tested. Historically, maps of the ozone column (latitude by month) have been used for this purpose. In MM I a climatology was developed for the vertical distribution of ozone for 15-60 km, based on SBUV data for 1979-80. SBUV profiles are reported with vertical resolution of approx. 5 km, but the true resolution is lower, approx. 8 km above the ozone maximum and approx. 15 km for 10-25 km. The climatology was considered valid to about 20-30% at 20 km and to 50% at 15 km. Comparisons were made with models in mixing ratio (ppm), which emphasizes the middle and upper stratosphere. A new ozone climatology was developed for the vertical distribution of ozone for MM II. Our goal was to develop a product that could be used to evaluate models in the lower stratosphere, the region where most of the ozone column resides and where most of the ozone loss is occurring, as well as the middle and upper stratosphere.

Logan, Jennifer A.↗

Contribution of TOMS to Earth Science- An Overview

The TOMS instrument was launched on the Nimbus-7 satellite in Oct 1978 with the goal of understanding the meteorological influences on the ozone column. The nominal lifetime of the instrument was 1 year. However, in response to the concern over possible man-made influences on the ozone layer NASA continued to nurse the instrument for 13.5 years and launched a major program to produce accurate trend quality dataset of ozone. Despite severe optical degradation and other significant anomalies that developed in the instrument over its lifetime, the effort turned out to be a tremendous success. In 1984, TOMS took center stage as the primary provider of Antarctic ozone hole maps to the world community; it continues to play that role until today. An unexpected benefit of the close attention paid to improving the TOMS data quality was that several atmospheric constituents that interfere with ozone measurement were also identified and meticulously converted into long-term datasets of their own. These constituents include clouds, volcanic S02, aerosols, and ocean phytoplankton. In addition, the high quality of the basic datasets made it possible to produce global maps of surface UV and tropospheric ozone. In most cases there are no other sources of these data sets. Advanced UV instruments currently under development in the US and Europe will continue to exploit the TOMS-developed techniques for several decades.

Bhartia, P. K.↗

Applications of Constituent Data Assimilation Systems

Organizations in Europe, Australia, and the United States have recently broadened constituent assimilation activities beyond that water vapor, which has been assimilated for years in the numerical weather prediction community. Many of these activities have focused on ozone, with some efforts focused on the entire suite of reactive constituents that control the ozone distribution. This talk will draw from results from the near real-time ozone data assimilation system being run by NASA's Data Assimilation Office. This system utilizes ozone observations from both the TOMS and the SBUV instrument to generate global synoptic maps of ozone. The initial application of this product is to provide ozone fields to assist in the atmospheric corrections' that are necessary for the retrieval of information from other NASA instruments. The validation of the ozone assimilation system shows that the assimilated product agrees well with independent HALOE and ozonesonde observations. This suggests that the product is of sufficient quality to be extended to other applications. This talk will enumerate these other applications and present initial results from exploratory research. The applications being considered include estimates of tropospheric ozone, provision of ozone fields for interactive retrievals, use of analysis increments from the assimilation to evaluate model performance, and development of long-term consistent three-dimensional global ozone fields. The results from the exploratory studies are promising, and help demonstrate how assumptions made in the p development of the ozone assimilation impact the other applications. For instance, RMS errors in the current product are large near the tropopause, which is sensitive to the specification of vertical correlation functions, which in turns impacts the amount of ozone analyzed to be in the troposphere. How these sensitivities impact the different applications will also be discussed.

Rood, Richard B.↗

Remote Sensing of Tropospheric Ozone and Its Precursors

Global and regional mapping of tropospheric ozone and its precursors using the Tropospheric Emission Spectrometer and its forerunner - the Airborne Emission Spectrometer - will be discussed.

ozone troposphere spectrometry Tropospheric Emissi↗

The significance of biomass burning as a source of carbon monoxide and ozone in the Southern Hemisphere tropics - A satellite analysis

Carbon monoxide mixing ratios obtained by the October 1984 Measurement of Air Pollution from Satellites (MAPS) experiment are compared with the distribution of October 1984 Total Ozone Mapping Spectrometer (TOMS) ozone concentrations. The TOMS and MAPS data show coincident high values of ozone and carbon monoxide over central South America and southeastern Africa. The 1984 MAPS data are also compared with tropospheric ozone concentrations derived from 6 years of TOMS and Stratospheric Aerosol and Gas Experiment (SAGE) I and II measurements. Examination of the October climatological distribution of tropospheric ozone also reveals high concentrations over central South America and southeastern Africa. These coincident high values of CO and ozone in the rural southern tropics are most likely due to biomass burning and the subsequent transport of CO and ozone by large-scale weather patterns. It appears that both CO and ozone are being transported thousands of kilometers from their source regions by the prevailing winds.

Watson, Catherine E.↗

A TOMS-Based View of Tropical Tropospheric Ozone (OTTO) From Large Fires Associated with the 1997-1998 El Nino

Since the launch of Earth-Probe TOMS in July 1 996, we have been producing tropical tropospheric ozone (TTO) maps (10S - 10N), in gridded format, l x 2 degrees, in near-real time. These images, along with images from the full ADEOS-TOMS record of TTO (Sept. 1996 - May 1997) can be viewed on a homepage: http://metosrv2.umd,edu/-tropo). The TTO maps, based on the modified-residual method of Hudson and Thompson [1998], have been validated using ozonesondes from Ascension (8S, 15W), Nairobi (2S, 36E) and American Samoa (14S, 171W). The fires associated with El Nino-induced dryness are exhibited regionally as high tropospheric ozone column (> 60 Dobson Units) with high absorbing aerosol (smoke) signal in TOMS [J. R. Herman, personal communication, 1998]. Episodes of high TTO in 1997-98 will be shown. Regional TTO over Indonesia during the 1997-98 period will be highlighted and comparisons will be made with TTO in that region taken from the 1979-92 Nimbus/TOMS TTO record.

Thompson, Anne M.↗

Atmospheric Physics

The possibility of extending the atmospheric observation from space is discussed. Observations of the earth's limb from GEO at microwave frequencies, global mapping of ozone, charged particle precipitation, photochemical reactions, spectral emissions from the atmosphere, microwave measurements, and radio probing of the atmosphere and ionosphere, which were not feasible prior to the availability of the shuttle because of the antenna limitations, may be readily carried out from the space stations.

Source record↗

Synoptic and chemical evolution of the Antarctic vortex in winter and spring, 1987

The dynamical evolution of the vortex at least up to 50 mb is dominated by synoptic scales in the troposphere. In particular, there is a clear response when poleward extension of tropospheric anticyclones from latitudes of 40 and 50 S to 70 and 80 S occurs. This response is evident in isentropic potential vorticity maps, TOMS ozone fields and SAM II polar stratospheric clouds. An important feature of the high latitude Southern Hemisphere lower stratosphere is a transition at potential temperatures in the 390 to 400 K range. This transition, the vortopause, is clearly marked in aircraft profiles of O3, H2O, N2O and ClO at latitudes 68 to 72 S near the Antarctic peninsula, and also cross-sections of potential vorticity and potential temperature; above it, the isopleths are more closely spaced than below it. The aircraft measurements of H2O, O3, NO sub y, N2O, ClO, and whole air data are examined in material coordinates, theta and P sub theta, backed up by trajectory analysis. The evolution of the chemical mixing ratios is examined in these coordinates as a function of time from mid-August to late September. Conclusions are drawn about the rates of change and their causes. The meteorological and aircraft data are examined for evidence of the following kinds of motion with respect to the vortex: ingress of air aloft, subsidence, peeling off of air to lower latitudes, and folding of the vortopause. Conclusions are presented regarding the evidence for a chemical sink of ozone above and below theta = 400 K, and whether the vortex has a mass flow through it, or if the chemical sink operates on a fixed mass of air. Implications for mid-latitudes are briefly considered in the light of the conclusions.

Tuck, A. F.↗

Convective lofting links Indian Ocean air pollution to paradoxical South Atlantic ozone maxima

We describe a broad resolution of the Atlantic Parado concerning the seasonal and geographic distribution, of tropical tropospheric ozone. We highlight periods of significant maximum tropospheric O3 for Jan.- April, 1999, exploiting satellite estimates and SHADOZ (Southern Hemisphere Additional Ozonesondes). Trajectory analyses connecting sondes and Total Tropospheric Ozone (TTO) maps suggest a complex influence from the Indian Ocean: beginning with mixed combustion sources, then low level transport, cumulonimbus venting, possible stratospheric input, and finally high-level transport to the west, with possible mixing over Africa. For the Jan.-March highest column-O3 periods in the Atlantic, distinct sounding peaks trace to specific NO sources, especially lightning, while in the same episodes, recurring every 20-50 days, more diffuse buildups of Indian-to-Atlantic pollution make important contributions.

Chatfield, R. B.↗

Investigations of Stratosphere-Troposphere Exchange of Ozone Derived From MLS Observations

Daily high-resolution maps of stratospheric ozone have been constructed using observations by MLS combined with trajectory information. These fields are used to determine the extratropical stratosphere-troposphere exchange (STE) of ozone for the year 2005 using two diagnostic methods. The resulting two annual estimates compare well with past model- and observational-based estimates. Initial analyses of the seasonal characteristics indicate that significant STE of ozone in the polar regions occurs only during spring and early summer. We also examine evidence that the Antarctic ozone hole is responsible for a rapid decrease in the rate of ozone STE during the SH spring. Subtracting the high-resolution stratospheric ozone fiom OMI total column measurements creates a high-resolution tropospheric ozone residual (HTOR) product. The HTOR fields are compared to the spatial distribution of the ozone STE. We show that the mean tropospheric ozone maxima tend to occur near locations of significant ozone STE. This suggests that STE may be responsible for a significant fraction of many mean tropospheric ozone anomalies.

Olsen, Mark A.↗

Global distribution of total ozone derived from Nimbus 3 satellite during April July, 1969 and its implication to upper tropospheric circulation

Utilizing a stepwise multiple regression scheme, monthly mean global maps of total ozone are produced from the spectral intensity measurements made by the infrared interferometer spectrometer (IRIS) onboard the Nimbus 3 satellite for the period April 18 to July 22, 1969. These maps show that over the equatorial regions total ozone increases steadily from April to July. Further, latitudinal variation of total ozone derived from these maps shows that the ozone increases at all latitudes over the Southern Hemisphere uniformly from April to July while over the Northern Hemisphere the monthly decrease at all latitudes is nonuniform. In general, these maps bear a close resemblance to the upper tropospheric circulation. It is observed that the total ozone is best correlated with the 200 mb geopotential heights. This relationship enables the utilization of total ozone as a quasi-stream function to determine geostrophic winds at 200 mb level. Further, even at low latitudes where the total ozone does not bear simple relationship to the geopotential heights the course of the easterly jet stream with the help of the ozone measurements can be identified.

Prabhakara, C.↗

Ozone Loss From Quasi-Conservative Coordinate Mapping During the 1999-2000 SOLVE Campaign

During the winter of 1999-2000, the Sage III Ozone Loss and Validation Experiment (SOLVE) field experiment took place in Kiruna, Sweden. The purpose of SOLVE was to examine ozone depletion mechanisms in the Arctic stratosphere (from about 10 to 50 km altitude) during the winter and early spring, when a band of strong winds (the 'polar vortex') circle the pole. Measurements of stratospheric ozone were made by several different kinds of instruments in different meteorological situations. We analyzed these data using the 'quasi-conservative coordinate mapping' technique, in which the measurements are analyzed in terms of meteorological properties ('potential temperature' and 'potential vorticity') which tend not to change very much over a few days. This technique reduces or removes the changes that are associated with the polar vortex moving around. Over longer time periods, potential temperature and potential vorticity change as air cools and descends within the polar vortex. We account for these changes by calculating the trajectories of air parcels, and this enables us to extend the analysis over a ten-week period from January 10 to March 17, 2000. Using data from the NASA ER-2 aircraft, from the DIAL and AROTEL laser sounders on the NASA DC-8 aircraft, and balloon-borne ozonesondes, our analysis reveals changes in ozone which, because we have removed the effects of polar vortex motion and the descending air, indicate chemical destruction of ozone in early 2000. We find a peak decline rate of approximately 0.03 ppmv/day near 470 K of potential temperature (near 20 km) in mid-January which sinks in altitude to around 440 K (near 18 km) in mid-March.

Lait, L. R.↗

Probing planetary pollution from space

The data sets obtained from instruments that have measured carbon monoxide and tropospheric ozone from space are reviewed. These instruments include a gas cell correlation radiometer named MAPS (Measurement of Air Pollution from Satellites), the Total Ozone Mapping Spectrometer, and the Stratospheric Aerosol and Gas Experiment. Particular attention is given to differential absorption lidar technology which can determine the vertical distribution of aerosols and selected trace gases with considerably more resolution than passive remote sensing techniques. The current plans for monitoring pollution from spaceborne platforms are also discussed.

Fishman, Jack↗

Mapping Yearly Fine Resolution Global Surface Ozone through the Bayesian Maximum Entropy Data Fusion of Observations and Model Output for 1990–2017

Estimates of ground-level ozone concentrations are necessary to determine the human health burden of ozone. To support the Global Burden of Disease Study, we produce yearly fine resolution global surface ozone estimates from 1990 to 2017 through a data fusion of observations and models. As ozone observations are sparse in many populated regions, we use a novel combination of the M3Fusion and Bayesian Maximum Entropy (BME) methods. With M3Fusion, we create a multi-model composite by bias-correcting and weighting nine global atmospheric chemistry models based on their ability to predict observations (8,834 sites globally)in each region and year. BME is then used to integrate observations, such that estimates match observations at each monitoring site with the observational influence decreasing smoothly across space and time until the output matches the multi-model composite. After estimating at 0.5° resolution using BME, we add fine spatial detail from an additional model, yielding estimates at 0.1° resolution. Observed ozone is predicted more accurately (R2=0.81 at test point, 0.63 at 0.1°,0.62 at 0.5°) than the multi-model mean (R2=0.28 at 0.5°). Global ozone exposure is estimated to be increasing, driven by highly populated regions of Asia and Africa, despite decreases in the United States and Russia.

environmental modeling↗