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.

Airborne lidar observations in the wintertime Arctic stratosphere: Polar stratospheric clouds

Wavelet analysis is applied to airborne infrared lidar data to obtain an objective determination of boundaries in aerosol backscatter that are associated with boundary layer structure. This technique allows high-resolution spatial variability of planetary boundary layer height and other structures to be derived in complex, multilayered atmospheres. The technique is illustrated using data from four different lidar systems deployed on four different field campaigns. One case illustrates high-frequency retrieval of the top of a strongly convective boundary layer. A second case illustrates the retrieval of multiple layers in a complex, stably stratified region of the lower troposphere. The method is easily modified to allow for varying aerosol distributions and data quality. Two more difficult cases, data that contain a great deal of instrumental noise and a cloud-topped convective layer, are described briefly. The method is also adaptable to model analysis, as is shown via application to large eddy ...

An Objective Method for Deriving Atmospheric Structure from Airborne Lidar Observations

An overview of the Transport and Atmospheric Chemistry near the Equator-Atlantic (TRACE A) field mission is presented. TRACE A was conducted to provide a comprehensive investigation of the chemical composition, transport, and chemistry of the atmosphere over the tropical South Atlantic Ocean and the adjacent South American and African continents. Measurements for TRACE A consisted of a remote sensing component to derive tropospheric ozone and biomass burning patterns, an airborne atmospheric chemistry component to determine the composition of the air in the most pristine areas of our research domain as well as to characterize the photochemistry and transport of trace gas emissions from both fire and biogenic sources, a series of ozonesonde observations, and an enhanced radiosonde network and airborne meteorological measurements that provided information about the transport of trace gases and the physical processes that were responsible for their observed distributions. The data were interpreted through the use of both photochemical and meteorological numerical models. The picture that emerges from TRACE A is that widespread biomass burning in both South America and southern Africa is the dominant source of the precursor gases necessary for the formation of the huge amounts of ozone over the South Atlantic Ocean. In addition, however, the meteorology in this region of the world is favorable for the accumulation of these pollutants over the tropical Atlantic basin so that photochemical processes produce large quantities of ozone in situ. The generation of ozone occurs over scales of thousands of kilometers and is unusually enhanced in the upper troposphere where relatively high concentrations of nitrogen oxides (NOx) prevail. This latter finding suggests that convective processes (or other lifting mechanisms) may play an important role in the generation of tropospheric ozone or that there may be an additional significant upper tropospheric source of NOx, such as from lightning.

NASA GTE TRACE A experiment (September–October 1992): Overview

The NASA Global Tropospheric Experiment (GTE) Transport and Atmospheric Chemistry Near the Equator-Atlantic (TRACE A) expedition was conducted September 21 through October 26, 1992, to investigate factors responsible for creating the seasonal South Atlantic tropospheric ozone maximum. During these flights, fine aerosol (0.1–3.0 μm) number densities were observed to be enhanced roughly tenfold over remote regions of the tropical South Atlantic and greater over adjacent continental areas, relative to northern hemisphere observations and to measurements recorded in the same area during the wet season. Chemical and meteorological analyses as well as visual observations indicate that the primary source of these enhancements was biomass burning occurring within grassland regions of north central Brazil and southeastern Africa. These fires exhibited fine aerosol (N) emission ratios relative to CO (dN/dCO) of 22.5 ± 9.7 and 23.6 ± 15.1 cm−3 parts per billion by volume (ppbv)−1 over Brazil and Africa, respectively. Convection coupled with counterclockwise flow around the South Atlantic subtropical anticyclone subsequently distributed these aerosols throughout the remote South Atlantic troposphere. We calculate that dilute smoke from biomass burning produced an average tenfold enhancement in optical depth over the continental regions as well as a 50% increase in this parameter over the middle South Atlantic Ocean; these changes correspond to an estimated net cooling of up to 25 W m−2 and 2.4 W m−2 during clear-sky conditions over savannas and ocean respectively. Over the ocean our analyses suggest that modification of CCN concentrations within the persistent eastern Atlantic marine stratocumulus clouds by entrainment of subsiding haze layers could significantly increase cloud albedo resulting in an additional surface radiative cooling potentially greater in magnitude than that caused by direct extinction of solar radiation by the aerosol particles themselves.

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Aerosols from biomass burning over the tropical South Atlantic region: Distributions and impacts

Investigations of the kinematics of the lower stratospheric Arctic vortex during the winter of 1991-1992 using the contour advection with surgery technique reveal three distinct events in which there was substantial intrusion of midlatitude air into the vortex, in apparent contradiction of the view that the polar vortex constitutes an isolated air mass. Two of these events, in late January and mid-February, were well documented. They were predicted in high-resolution forecasts by the European Centre for Medium-Range Weather Forecasts, most clearly in experimental forecasts with reduced diffusion. Direct confirmation of the presence of the intrusions and of their calculated locations was provided by aerosol observations from the airborne differential absorption laser lidar aboard the NASA DC-8, taken as part of the second Airborne Arctic Stratospheric Expedition campaign; aerosol-rich air of midlatitude origin was seen in the expected position of the intrusions. The reality of the February event was also confirmed by in situ measurements from the NASA ER-2. Such events may be significant for the chemical processes taking place within the winter vortex. The intrusions were evidently related to the meteorology of the northern stratosphere during this winter and in particular to persistent tropospheric blocking over the northeastern Atlantic Ocean and western Europe and concomitant ridging into the lower stratospheric vortex in this region. Nevertheless, preliminary investigations have indicated that such events are not uncommon in other northern hemisphere winters, although no such events were found in the southern hemisphere during the Antarctic winter of 1987.

Intrusions into the lower stratospheric Arctic vortex during the winter of 1991–1992

The differential absorption lidar (DIAL) technique for deriving O/sub 3/ profiles from lidar measurements is discussed. The US National Aeronautics and Space Administration's airborne DIAL system is described, and examples of a broad range of O/sub 3/ and aerosol measurements are presented from a number of field experiments. The airborne and ground-based DIAL measurements discussed demonstrate the outstanding capability of lidar for conducting O/sub 3/ investigations throughout the troposphere and lower stratosphere under widely different atmospheric conditions. >

E.V. Browell

Papers

Differential absorption lidar sensing of ozone