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At least 541 records · Page 30
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NASA NTRS1978

The effect of increased carbon dioxide concentrations on stratospheric ozone

Consideration is given to the influence on ozone of an increased carbon dioxide concentration, for which a measurable growth has been observed in the recent past. Increased carbon dioxide can indirectly affect ozone by perturbing atmospheric temperatures, which will alter ozone production, whose rate displays a fairly strong temperature dependence. This paper presents one-dimensional model results for the steady state ozone behavior when the CO2 concentration is twice its ambient level; the results account for coupling between chemistry and temperature. When the CO2 level doubled, the total ozone burden increased in relation to the ambient burden by 1.2-2.5%, depending on the vertical diffusion coefficient used. Above 30 km, ozone concentrations were larger than the ambient values, a maximum increase of 16% being reached at 43 km. In this region the relative variations were insensitive to the choice of diffusion coefficient. Below 30 km, ozone concentrations were smaller than the unperturbed values and were sensitive to the vertical diffusion profile in this region (10-30 km).

Boughner, R. E.↗
NASA NTRS1978

Long period time variations of ozone in the lower stratosphere

Observations of total ozone at a number of stations in the Northern Hemisphere show an increase during the period 1961-1970 followed by a decrease of ozone during the 1970's, at least at many stations in Central Europe. It is well known that total ozone is highly correlated with ozone in the lower stratosphere. Analysis of the trends of ozone based on data derived from balloon-borne ozonesondes during the period 1967-75 at four stations in Central Europe shows that most of the ozone variations occurred in the lower stratosphere with relatively little contribution from tropospheric changes or those above the ozone peak. Possible meteorological origins of these decade type variations will be discussed.

London, J.↗
NASA NTRS1978

Distribution of atmospheric ozone and how it is measured

The total amount of ozone in a vertical column has been measured spectroscopically at near ultraviolet and visible wavelengths, using ground- and satellite-based instruments. The vertical distribution of ozone from the surface up to approximately 100 km has been measured by a variety of techniques - chemical and optical - and from a number of observing platforms, including balloon, rocket, and satellite platforms. The various methods presently used for determining the atmospheric ozone distribution are reviewed, along with a discussion of their advantages and disadvantages. The observed average distribution of total ozone for the period 1958-1975 shows the expected geographic and seasonal variations. The variations of total ozone, including hemispheric differences, are clearly associated with large-scale circulation processes in the lower stratosphere. Approximately ten years of observations of the vertical ozone distribution, up through the ozone maximum, also show geographic and seasonal variations strongly related to the lower stratosphere circulation. The distribution above the maximum, however, results from the interaction of photochemistry and stratospheric motions.

London, J.↗
NASA NTRS1979

Utilization of 100 mb midlatitude height fields as an indicator of sampling effects on total ozone variations

Midlatitude 100-mb height fields are employed to determine the effects of ground based sampling locations on measurements of variations in the total ozone content of the atmosphere. The precision of the zonal average heights computed by the technique of Angell and Korshover (1978) from data over ozone sampling areas at 50 deg N is compared to the zonal average computed from the entire data set. Linear regressions of ozone contents determined by an analysis of backscatter UV satellite data with respect to 100 mb heights are utilized to transform zonal differences in height to ozone levels. The zonal average total ozone sampling error is found to be on the order of 2% for midlatitudes of the Northern hemisphere, indicating that the general shape of ozone trends determined by ground-based observations appears to be real and the increase of ozone from the mid-1960's to the early 1970's may be greater than previously suggested.

Miller, A. J.↗
NASA NTRS1979

Numerical simulation of ozone production, transport and distribution with a global atmospheric general circulation model

The production, transport, and distribution of ozone are simulated for a January with a global atmospheric general circulation model. In this model, the ozone influences the radiational heating and the photochemical ozone production and destruction, the radiational heating influences the atmospheric circulation, and the circulation redistributes the ozone. The model has simulated the synoptic and time-averaged observed large-scale fields of temperature, mass, and velocity in the troposphere and stratosphere, although with deficiencies which are seen in the time-averaged O3 distribution. Transport of ozone in the summer and winter hemispheres, in different seasons, and in various latitudes is discussed, and it is concluded that the divergence of the ozone transport maintains it below its photochemical equilibrium concentration in the tropics and subtropics, and the convergence of the ozone transport maintains it above its photochemical equilibrium concentration in the middle and high latitudes of both hemispheres. Thus, both the atmospheric motions and the O3 photochemistry determine the O3 sources and sinks.

Schlesinger, M. E.↗
NASA NTRS1981

Two-dimensional model studies of the effect of supersonic aircraft operations on the stratospheric ozone content

For a fleet of 250 aircraft, the change in the ozone column is predicted to be very close to zero; in fact, the ozone overburden may actually increase as a result of show that above 25 to 30 km the ozone abundance decreases via catalytic destruction, but at lower heights it increases, mainly as a result of coupling with odd hydrogen species. Water vapor released in the engine exhaust is predicted to cause ozone decreases; for the hypothetical engines used in the study, the total column ozone changes due to water vapor emission largely offset the predicted ozone increases due to NOx emission. The actual effect of water vapor may be less than calculated because present models do not include thermal feedback. Feedback refers to the cooling effect of additional water vapor that would tend to slow the NOx reactions which destroy ozone.

Whitten, R. C.↗
NASA NTRS1981

Global ozone long-term trends from satellite measurements and the response to solar activity variations

Analysis of global ozone variations for the period April 1970 to December 1975 was performed by using the reprocessed Nimbus 4 backscattered ultraviolet (BUV) measurements of total ozone. A correlation coefficient of 0.97 is found between the 6-month running mean of global mean total ozone (filtered for mean semiannual, annual, and quasibiennial variations) and the 10.7-cm solar activity index. Correcting ozone for a time-dependent latitudinal bias relative to Dobson ozone measurements reduces to 2-3% the global mean ozone variation over the solar cycle. The solar ultraviolet variability required in a one-dimensional time-dependent radiative photochemical model to account for the observed ozone variation appears to be consistent with recent solar UV observations.

Keating, G. M.↗
NASA NTRS1981

Characteristics of space and ground based total ozone observing systems investigated by intercomparison of Nimbus 4 Backscattered Ultraviolet /BUV/ data with Dobson and M-83 results

The Nimbus 4 Backscattered Ultraviolet (BUV) experiment data has been reprocessed to provide a near global data set covering the seven years from 1970 to 1977. The data set is the result of a three year effort by the Ozone Processing Team which included review and correction of the spacecraft ephemeris, instrument calibration, and processing algorithms. The accuracy of the resulting total ozone determinations compares well with that of ground based data. An important application of the global BUV data set is to use it in determining long term trends in global total ozone. However, in order to identify long term trends in ozone, it is necessary to eliminate first long-term drift in the instrument calibration. A follow on experiment, the Solar Backscattered Ultraviolet/Total Ozone Mapping Spectrometer, (SBUV/TOMS), was flown on Nimbus 7 launched in October 1978. The SBUV provides information about both total ozone and vertical ozone profiles for a 200 km square field of view.

Fleig, A. J.↗
NASA NTRS1981

The validation of LIMS ozone profiles using correlative rocket, ECC, and Dobson data sets

The Limb Infrared Monitor of the Stratosphere (LIMS) experiment is a limb scanning infrared sounder designed to measure vertical temperature profiles and the concentrations of key chemical compounds which are important in the stratospheric ozone-nitrogen photochemistry. Preliminary ozone profiles are being intercompared with correlative rocket and balloonsonde ozone data sets as part of the Nimbus 7 LIMS data validation activity. The LIMS ozone retrievals extend from the lower mesosphere to the tropopause (or cloud-top altitudes). In this paper, preliminary statistics of comparisons of ECC (electrochemical concentration cell) ozonesonde and rocket ozone profiles with LIMS ozone profiles are presented. ECC ozonesonde data taken at times of LIMS overpasses are also used to extend the LIMS retrieval down to ground level. Each combined profile is then integrated to obtain total column ozone. These integrated results are compared to Dobson data obtained at approximately the same time and location.

Remsberg, E. E.↗
NASA NTRS1983

A two-dimensional photochemical model of the atmosphere. I Chlorocarbon emissions and their effect on stratospheric ozone

A two-dimensional photochemical model is used to examine changes to the ozone layer caused by emissions of CFCl3, CF2Cl2, CH3CCl3 and CCl4. The influence of a possible secular increase in tropospheric methane up to 2 percent per year was found to be small, although it acts to mask decreases in total ozone caused by the chlorocarbons. Increasing NO(x) emissions caused by industralization also tend to mask decreases in total ozone and may have caused total ozone to increase by about 1 percent. The model-calculated ozone decreases are estimated to be about 3 percent by 1980. This estimate is higher than estimates by similar models, although it is noted that CCl4 and CH3CCl3 emissions are included in the model in addition to CFCl3 and CF2Cl2. This is significant because the model indicates that CCl4 has dominated the ozone depletions so far, and knowledge of the historical emission rate of CCl4 to the atmosphere is incomplete. There remain sufficient significant disagreements between theoretical and observed concentrations and variabilities, particularly for odd nitrogen and ClO, to caution against assigning too much confidence in the calculated ozone depletion.

Gidel, L. T.↗
NASA NTRS1983

Baseline ozone results from 1923 to 1955

Baseline total atmospheric ozone values from the year 1923 to 1955 are reported which have been derived from observations of the solar constant made by Smithsonian Institution sites in both the Northern and Southern Hemispheres. Ozone was determined from absorption by the broad, weak Chappuis band near 0.6 microns as measured on 1194 days at Mt. Montezuma, Chile and 970 days at Table Mountain, California. Results show systematic changes on the order of 25 percent in the ozone level at Montezuma with a time scale of 10-20 years, although the previously reported 30 percent decrease between 1920-1930 and 1940-1950 is found to have been erroneous. Comparisons of ozone data with geomagnetic indices and sunspot number show a suggestive correlation of ozone with sunspot number, although the relation is not borne out by comparison of ozone and sunspot cycles, or by Fourier analysis. Comparison of ozone data in the Chappuis band obtained by a modern filter-wheel radiometer with that obtained from a Dobson spectrometer at Mauna Loa Observatory shows Chappuis band measurements to be 14 percent lower.

Angione, R. J.↗
NASA NTRS1984

The vertical distribution of ozone in the mesosphere and lower thermosphere

An assessment is made of the ability of current theory to explain the phenomenology of upper atmospheric ozone as revealed by the sizeable body of measurements presently available. The chemical processes affecting the vertical distribution of ozone are reviewed, and simple analytical expressions for the ozone concentrations at different altitudes are derived which approximate the key elements of the ozone chemistry. These equations provide simple explanations of the sensitivity of model computations to the choice of rate constants and climatological patterns. Model calculations are compared with a detailed measurement of an ozone profile, and the model is modified to assess the variation in ozone expected to result from perturbations in key climatological processes. These predictions are then compared with the variability observed in midlatitude measurements in order to verify the model description of ozone processes in the upper atmosphere.

Allen, M.↗
NASA NTRS1984

Intercomparison of the Nimbus 7 SBUV/TOMS total ozone data sets with Dobson and M83 results

Two years of SBUV/TOMS (Solar Backscattered Ultraviolet/Total Ozone Mapping Spectrometer) data spanning the period November 1978 to October 1980 have been processed and compared with ground-based ozone measurements made at 62 Dobson spectrophotometer and 18 M83 filter photometer ozone stations. Results show that the satellite ozone values are consistently smaller than those measured by the stations; most of this difference is probably due to an error in the currently accepted ozone absorption cross sections at ultraviolet wavelengths. Dobson-derived ozone amounts agree extremely well with those derived from each of the satellite instruments. Long-term stability of the ozone derived by the two instruments is expected to be better than 0.5 percent per year.

Bhartia, P. K.↗
NASA NTRS1984

An analysis of the annual cycle in upper stratospheric ozone

The mid-latitude upper stratospheric ozone profiles obtained by the solar backscatter ultraviolet instrument on the Nimbus 7 satellite show a clear annual cycle both in the absolute ozone amounts between 0.98 and 15.6 mbar and in the magnitude of disturbances that reveal themselves as longitudinal structure. At the lowest pressure analyzed a winter maximum in ozone exists, but as one progresses downward in altitude a shift in the temporal phase of the annual cycle occurs in the vicinity of 3 to 4 mbar. Comparison of the observed behavior with the predictions of a one-dimensional photochemical model shows a systematic tendency for calculated ozone amount to be 20-27 percent below the data for pressures less than 7.8 mbar. The chemical model successfully predicts the change in phase of the annual cycle, although at a pressure greater than observed. Diagnosis of model results shows the observed shift to be closely coupled to the magnitude of the ozone column density near 3-4 mbar. The wavelength-dependent attenuation of the solar radiation field by ozone alters the relative magnitude of the molecular oxygen and ozone dissociation rates, leading to a change in the temporal phase of the annual cycle.

Frederick, J. E.↗
NASA NTRS1986

In situ stratospheric ozone measurements by long path UV absorption - Developments and interpretation

A high-sensitivity, in situ UV absorption ozone sensor has been developed for use in the stratosphere. The instrument couples 254-nm radiation from a low-pressure mercury discharge lamp into a 40-pass White cell to attain a high-sensitivity ozone absorption measurement. Preflight/postflight laboratory tests utilizing an ozone source coupled to a laboratory UV ozone photometer in a fast-flow system as well as in-flight diagnostics verify the successful operation of the instrument. Evidence is presented to verify that in situ UV absorption ozone photometers can measure stratospheric ozone with better than 3 percent precision and 5 percent accuracy, provided proper attention is given to both the thermal field surrounding the gondola and the ambient pressure measurements. Ozone data are compared with modeled profiles in the 28- to 40-km region. An assessment of the disagreement between observations and modeled profiles is given along with suggestions for future experiments designed to constrain photochemical models.

Weinstock, E. M.↗
NASA NTRS1986

Atlas of TOMS ozone data collected during the Genesis of Atlantic Lows Experiment (GALE), 1986

Data from the TOMS (Total Ozone Mapping Spectrometer) instrument aboard the Nimbus-7 satellite were collected daily in real time during the GALE (Genesis of Atlantic Lows Experiment) from January 15 through March 15, l986. The TOMS ozone data values were processed into GEMPAK format and transferred from the Goddard Space Flight Center to GALE operations in Raleigh-Durham, NC, in as little as three hours for use, in part, to direct aircraft research flights recording in situ measurements of ozone and water vapor in areas of interest. Once in GEMPAK format, the ozone values were processed into gridded form using the Barnes objective analysis scheme and contour plots of the ozone created. This atlas provides objectively analyzed contour plots of the ozone for each of the sixty days of GALE as well as four-panel presentations of the ozone analysis combined on the basis of GALE Intensive Observing Periods (IOP's).

Larko, David E.↗
NASA NTRS1986

Derivation of photochemical information near 1 mbar from ozone and temperature data

An analysis procedure has been developed for derivation of information about the photochemical behavior of ozone near 1 mbar by explicitly accounting for the dynamical transport terms in the continuity equation for perturbations from the zonal mean. The procedure is shown to be valid using data from a numerical transport model and is then applied to LIMS ozone and temperature data, using geostrophic winds to estimate the transport terms. The data study is restricted to March at 2, 1, and 0.7 mbar. Because the temperature deviations are dynamically produced, large temperature deviations are associated with significant ozone transport terms. The anticorrelation between the deviations of ozone and temperature disappears when the transport terms are small. The derived photochemical information is compared to photochemical theory. Although there is overall agreement in the magnitude as well as the latitude, altitude, and time dependencies, discrepancies are suggested which may be related to the long-standing failure of photochemical models to calculate ozone accurately near 1 mbar. The theory suggests that the addition of Cl(x) to the stratosphere will affect the relationship of ozone and temperature at 2 and 1 mbar. Comparison of the photochemical information derived from future ozone and temperature measurements with the results of the present analysis should provide a critical test of the photochemical scheme thought to describe the behavior of odd chlorine in the stratosphere.

Douglass, Anne R.↗
NASA NTRS1987

Net ozone photochemical production over the eastern and central North Pacific as inferred from GTE/CITE 1 observations during fall 1983

The role of photochemistry in the budget of tropospheric ozone is studied. Measurements of O3, NO, CO, H2O vapor, and temperature obtained during the fall of 1983 during the GTE/CITE project over the eastern and central North Pacific Ocean are analyzed. The effect of altitude on the measurements is discussed. The analysis reveals a correlation between ozone and NO levels; both increase in concentration and variability with altitude. It is observed that an additional source of secondary importance associated wih CO-rich air parcels exists. A photochemical model is utilized to calculate the net rate of ozone production by photochemical reactions. A net photochemical source of ozone in the free troposphere and a net sink in the boundary layer are detected. The relation between the ozone source in the free troposphere and NO is examined. It is estimated that photochemistry provides a net ozone source to the free troposphere overlying the eastern and central North Pacific Ocean of about 5 x 10 to the 10th molecules/sq cm sec and a net sink of ozone to the boundary layer overlying this region of about 3 x 10 to the 10th molecules/sq cm sec.

Chameides, W. L.↗