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Browell, E. V.

Publications and source records attributed to Browell, E. V..

At least 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1992

Summertime photochemistry of the troposphere at high northern latitudes

Budgets of O3, NO(x), and NO(y), and acetic acid in the Arctic Boundary Layer Expedition (ABLE 3A) flight region are constructed using photochemical model statistics based on aircraft observations. A Lagrangian model is used to reconstruct the photochemical history of two aged biomass fire plumes sampled by the ABLE 3A aircraft. It is shown that anthropogenic influence on O3 levels in the Arctic may manifest itself not by long-range transport of pollution-derived O3, but rather by a decrease of the regional photochemical sink due to the presence of small amounts of NO(x). The low concentrations of NO(x) measured in ABLE 3A were sufficient to reduce the rate of photochemical loss appreciably relative to a NO(x)-free atmosphere, thus increasing the O3 lifetime. It is shown that decomposition of PAN can account for most of the NO(x) measured below 4-km altitude, but for only 20 percent at 6-km altitude. A lifetime of 29 days is estimated for NO(y) in the ABLE 23A flight region.

Jacob, D. J.↗
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 NTRS1992

Deposition of ozone to tundra

Eddy correlation measurements of O3 deposition fluxes to tundra during the Arctic Boundary Layer Expedition (ABLE 3A) are reported. The mean O3 deposition velocity was 0.24 cm/s in the daytime and 0.12 cm/s at night. The day-to-day difference in deposition velocity was driven by both atmospheric stability and surface reactivity. The mean surface resistance to O3 deposition was 2.6 s/cm in the daytime and 3.4 s/cm at night. The relatively low surface resistance at night is attributed to light-insensitive uptake of O3 at dry upland tundra surfaces. The small day-tonight difference in surface resistance is attributed to additional stomatal uptake by wet meadow tundra plants in the daytime. The mean O3 deposition flux to the world north of 60 deg N in July-August is estimated at 8.2 x 10 exp 10 molecules/sq cm/s. Suppression of photochemical loss by small anthropogenic inputs of nitrogen oxides could have a major effect on O3 concentrations in the summertime Arctic troposphere.

Jacob, D. J.↗
NASA NTRS1992

Summertime tropospheric observations related to N(x)O(y) distributions and partitioning over Alaska - Arctic Boundary Layer Expedition 3A

Measurements of NO, NO2, PAN and NO(y) are presented for the summertime middle/lower troposphere over northern high latitudes. Chemical signatures from concurrent measurements of O3, CO, C2H2, C2H6, C3H8, C2Cl4, and H2O are used to characterize factors affecting the budget and distribution of N(x)O(y) in the Arctic and Sub-Arctic tropospheric air masses sampled over Alaska during the NASA Arctic Boundary Layer Expedition (ABLE 3A). The results implicate biomass burning in Siberia as the probable source of about one-third of the NO(y) abundance within the middle lower troposphere over Alaska and the downward transport of air from altitude in the vicinity of the tropopause as a major contributor to the abundance of NO(y) within the lower 6 km column over Alaska.

Sandholm, S. T.↗
NASA NTRS1992

Lidar Measurements of Aerosol and Ozone Distributions During the 1992 Airborne Arctic Stratospheric Expedition

The LaRC airborne lidar system was operated from the ARC DC-8 aircraft during the 1992 Airborne Arctic Stratospheric Expedition (ASEE-2) to investigate the distribution of stratospheric aerosols and O3 across the Arctic vortex from Jan. to Mar. 1992. Monthly flights were made across the Arctic vortex from Anchorage, Alaska, to Stavanger, Norway, and then back to Bangor, Maine, and additional round-trip flights north into the vortex were made each month from either Stavanger or Bangor depending on the location of the vortex that month. The airborne lidar system uses the differential absorption lidar (DIAL) technique at laser wavelengths of 301.5 and 310.8 nm to measure O3 profiles above the DC-8 over the 12-25 km altitude range. Lidar measurements of aerosol backscatter and depolarization profiles over the 12-30 km altitude range are made simultaneously with the O3 measurements using infrared (IR) and visible (VIS) laser wavelengths of 603 and 1064 nm, respectively. The measurements of Pinatubo aerosols, polar stratospheric clouds, and O3 made with the airborne DIAL system during the AASE-2 expedition and to chemical and dynamical process that contribute to O3 depletion in the wintertime Arctic stratosphere.

Browell, E. V.↗
NASA NTRS1992

Observations of reduced ozone concentrations in the tropical stratosphere after the eruption of Mt. Pinatubo

Two independent sets of data, one of aerosols from an airborne lidar system, and one of ozone from ozonesonde measurements indicate that significant ozone decreases may have happened as a result of the injection of debris by the Mt. Pinatubo volcano in June 1991. The amount of this reduction maximizes at 24-25 km, near the peak of the aerosol distribution, though a deficit is seen throughout the lower stratosphere between 19 and 28 km. The greatest differences observed prior and subsequent to the eruptions at these altitudes is 18-20 percent.

Grant, W. B.↗
NASA NTRS1991

Tropospheric water vapor measurements with an airborne lidar system

A differential absorption lidar system has been developed for the remote measurement of atmospheric water vapor and aerosol distributions from an aircraft. The first extensive observations of H2O and aerosols in the lower troposphere made with this system are briefly discussed.

Browell, E. V.↗
NASA NTRS1990

Airborne lidar observations in the wintertime Arctic stratosphere - Ozone

Large-scale distributions of ozone (O3) were measured with an airborne lidar system as part of the 1989 Airborne Arctic Stratospheric Expedition. Measurements of O3 distributions were obtained between January 6 and February 15, 1989, on 15 long-range flights into the polar vortex from the Solar Air Station, Norway. The observed O3 distribution was found to clearly indicate the edge of the polar vortex and to be an effective tracer of dynamical processes in the lower stratosphere. On the last two flights of the expedition, large regions with reduced O3 levels were observed by the lidar inside the polar vortex. Ozone had decreased by as much as 17 percent in the center of these areas, and using the in situ measurements made on the ER-2 aircraft, it was concluded that this decline was due to chemical O3 destruction.

Browell, E. V.↗
NASA NTRS1990

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.↗
NASA NTRS1990

An analysis of lidar observations of polar stratospheric clouds

Lidar observations by Browell et al. (1990) are interpreted using single scattering calculations for nonspherical particles and aerosol microphysical calculations. Many of the lidar observations are consistent with particles containing 10 ppbv of condensed nitric acid vapor and an equivalent mass of water. The lidar observations of these Type 1 clouds identify two subtypes, whose properties are deduced. Type 1b particles are spherical, or nearly spherical, and typically have radii near 0.5 micron; Type 1a particles are not spherical, and have a spherical volume equivalent radius exceeding 1.0 micron. Several factors may cause variations in the size of the particles. The most significant factors are the cooling rate and the degree to which the air parcels cool below the condensation point. Specific examples in which cooling rate and cooling point may have led to variations in particle size are found in the Browell et al. (1990) data set. Condensation of 1 ppmm of water or less is quantitatively sufficient to account for the magnitude of the lidar backscatter observed from water ice clouds. The ice particles are not spherical in shape. The sizes of particles in water ice clouds cannot be determined because they are much larger than the wavelength of the lidar.

Toon, Owen B.↗
NASA NTRS1990

A study of the H2O absorption line shifts in the visible spectrum region due to air pressure

Results of measured and calculated shift coefficients are presented for 170 absorption lines of H2O in five vibrational-rotational bands. The measurements have been carried out using highly sensitive laser spectrometers with a resolution of at least 0.01/cm; the calculations are based on the Anderson-Tsao-Curnutte-Frost method. Good agreement is obtained between the theoretical and experimental values of the shift coefficients of H2O lines due to N2, O2, and air pressure.

Grossmann, B. E.↗
NASA NTRS1990

Differential absorption lidar detection of ozone in the troposphere and lower stratosphere

The DIAL technique for deriving O3 profiles from lidar measurements is discussed. Examples of a variety of O3 and aerosol measurements are presented from studies of (1) photochemically produced O3 in the summertime over the eastern United States and in biomass burning plumes during the dry season over the Amazon Basin of Brazil; (2) vertical O3 transport from the mixed layer into the free troposphere via cloud dynamics and from the stratosphere into the troposphere via tropopause fold events; and (3) O3 depletion in the O3 hole over Antarctica. The NASA airborne DIAL system is considered to be an advanced field system.

Browell, E. V.↗
NASA NTRS1989

Measurements of size and composition of particles in polar stratospheric clouds from infrared solar absorption spectra

Results are presented on polar stratospheric cloud (PSC) observations, based on IR measurements of solar extinction, made by the airborne JPL Mark IV interferometer during the Airborne Antarctic Ozone Expedition in 1987, together with the instrumentation and the theoretical aspects of data analysis. Thirty-three PSC cases were analyzed and categorized into two types, I and II, which were found to occur at different altitudes during September. Type I clouds, seen at altitudes above 15 km, contained particles with radii of about 0.5 micarons and nitric acid concentrations greater than 40 percent, while type II clouds, found usually below 15 km, contained particles with radii of 6 microns and larger, composed of water ice. In addition, particles of larger than the 15-micron-size detection limit were encounterd.

Kinne, S.↗
NASA NTRS1989

Intercomparison of ozone measurements over Antarctica

Measurements of the abundances of ozone over Antarctica in August and September 1987 obtained during the Airborne Antarctic Ozone Experiment are intercompared. These measurements of ozone concentrations and total column abundance were obtained by three satellite instruments, two IR and one UV column-measuring instruments aboard the DC-8, one in situ DC-8, and two in situ ER-2 instruments, an upward looking lidar aboard the DC-8, and ozone sondes from four sites in Antarctica. This paper presents a summary of the ozone data, using the data and accuracies given by the individual investigators in the individual papers in this issue, without any attempt to critically review or evaluate the data. In general, very good agreement (within about 10-20 percent, limited by natural variability) among the various techniques was found, with no systematic biases detected. These observations confirm the low ozone amounts reported in the Antarctic stratosphere.

Margitan, J. J.↗
NASA NTRS1989

Implications of AAOE observations for proposed chemical explanations of the seasonal and interannual behavior of Antarctic ozone

Model simulations were used to investigate the seasonal and interannual behavior of ozone for different choices of initial odd nitrogen concentration in July and different assumptions on the heterogeneous reactions, with particular consideration given to the possible contribution of chlorine chemistry to the ozone hole phenomenon. The numerical experiments were selected based on the simulations of the observed trace gas concentrations during the Airborne Antarctic Ozone Experiment in 1987. In all cases considered, the catalytic cycle associated with the formation and photolysis of Cl2O2 could account for more than half of the photochemical removal of O3 within the Antarctic vortex through mid-September. The reaction of BrO with ClO, which accounts for 15-20 percent of O3 removal in the same period, tends to play a more important role toward the end of September, when the concentration of ClO is expected to decrease. No simple relationship was found between the increase in chlorine lavel and the interannual decrease in Antarctic O3.

Ko, M. K. W.↗
NASA NTRS1989

Diagnostic studies of the Antarctic vortex during the 1987 Airborne Antarctic Ozone Experiment - Ozone miniholes

Localized rapid reductions in total ozone (miniholes), which were observed during the Airborne Antarctic Ozone Experiment, are studied with particular attention given to meteorological aspects. It is suggested that miniholes are forced by tropospheric weather features and that they are largely reversible distortions to the airflow around the vortex. The relationship between the miniholes and upper tropospheric and lower stratospheric synoptic-scale disturbances is studied. Trajectory calculations are presented which demonstrate the exchange of air from low latitudes with air from within the vortex, with the vortex air subsequently moving to lower latitudes.

Mckenna, D. S.↗
NASA NTRS1988

Ozone measurements in the troposphere of an Amazonian rain forest environment

Ozone concentration profiles from the ground to above the stratospheric peak were obtained in an equatorial rain forest environment near Manaus in the Amazon Basin between July and August of 1985. The peak ozone concentration (4.4 x 10 to the 22 molecules/cu cm) was found at 20 mbar (26.6 km). A major pollution (biomass-burning) event which occurred near the end of the experiment was responsible for large changes in ozone concentration.

Kirchhoff, V. W. J. H.↗