Lamont R. Poole

The CALIPSO Mission: A Global 3D View of Aerosols and Clouds

Aerosols and clouds have important effects on Earths climate through their effects on the radiation budget and the cycling of water between the atmosphere and Earths surface. Limitations in our understanding of the global distribution and properties of aerosols and clouds are partly responsible for the current uncertainties in modeling the global climate system and predicting climate change. The CALIPSO satellite was developed as a joint project between NASA and the French space agency CNES to provide needed capabilities to observe aerosols and clouds from space. CALIPSO carries CALIOP, a two-wavelength, polarization-sensitive lidar, along with two passive sensors operating in the visible and thermal infrared spectral regions. CALIOP is the first lidar to provide long-term atmospheric measurements from Earths orbit. Its profiling and polarization capabilities offer unique measurement capabilities. Launched together with the CloudSat satellite in April 2006 and now flying in formation with the A-train satellite constellation, CALIPSO is now providing information on the distribution and properties of aerosols and clouds, which is fundamental to advancing our understanding and prediction of climate. This paper provides an overview of the CALIPSO mission and instruments, the data produced, and early results.

The role of aerosol variations in anthropogenic ozone depletion at northern midlatitudes

Aerosol surface area distributions inferred from satelliteborne 1-μm extinction measurements are used as input to a two-dimensional model to study the effects of heterogeneous chemistry upon anthropogenic ozone depletion at northern midlatitudes. It is shown that short-term (interannual) and longer-term (decadal) changes in aerosols very likely played a substantial role along with trends in anthropogenic chlorine and bromine in both triggering the ozone losses observed at northern midlatitudes in the early 1980s and increasing the averaged long-term ozone depletions of the past decade or so. The use of observed aerosol distributions enhances the calculated ozone depletion due to halogen chemistry below about 25 km over much of the past decade, including many periods not generally thought to be affected by volcanic activity. Direct observations (especially the relationships of NO X /NO Y and ClO/Cl y ratios to aerosol content) confirm the key aspects of the model chemistry that is responsible for this behavior and demonstrate that aerosol changes alone are not a mechanism for ozone losses in the absence of anthropogenic halogen inputs to the stratosphere. It is also suggested that aerosol-induced ozone changes could be confused with 11-year solar cycle effects in some statistical analyses, resulting in an overestimate of the trends ascribed to solar activity. While the timing of the observed ozone changes over about the past 15 years is in remarkable agreement with the model predictions that explicitly include observed aerosol changes, their magnitude is about 50% larger than calculated. Possible chemical and dynamical causes of this discrepancy are explored. On the basis of this work, it is shown that the timing and magnitude of future ozone losses at midlatitudes in the northern hemisphere are likely to be strongly dependent upon volcanic aerosol variations as well as on future chlorine and bromine loading.

A global climatology of stratospheric aerosol surface area density deduced from Stratospheric Aerosol and Gas Experiment II measurements: 1984–1994

A global climatology of stratospheric aerosol surface area density has been developed using the multiwavelength aerosol extinction measurements of the Stratospheric Aerosol and Gas Experiment (SAGE) II for 1984–1994. The spatial and temporal variability of aerosol surface area density at 15.5, 20.5, and 25.5 km are presented as well as cumulative statistical distributions as a function of altitude and latitude. During this period, which encompassed the injection and dissipation of the aerosol associated with the June 1991 Mount Pinatubo eruption as well as the low loading period of 1989–1991, aerosol surface area density varied by more than a factor 30 at some altitudes. Aerosol surface area density derived from SAGE II and from the University of Wyoming optical particle counters are compared for 1991–1994 and are shown to be in generally good agreement though some differences are noted. An extension of the climatology using single-wavelength measurements by the Stratospheric Aerosol Measurement II (1978–1994) and SAGE (1979–1981) instruments is also presented.

Heterogeneous chlorine chemistry in the tropopause region

Satellite observations of cloud optical depths and occurrence frequencies are used as input to a two-dimensional numerical model of the chemistry and dynamics of the atmosphere to study the effects of heterogeneous reactions on cloud surfaces upon chemical composition and ozone depletion in the tropopause region. Efficient reactions of ClONO2 with HCl and H2O, and of HOCl with HCl, are likely to take place on the surfaces of cirrus clouds [Borrmann et al., 1996] and perturb chlorine chemistry, much as they do on polar stratospheric clouds present at higher altitudes and colder temperatures. Because of the very low predicted background abundances of ClO near the tropopause, such reactions could enhance the local ClO mixing ratios by up to 30-fold at midlatitudes. Substantial perturbations are also predicted for related chemical species (e.g., HCl, HOCl, ClONO2, NO2, HO2) in the midlatitude and tropical tropopause regions due to these heterogeneous reactions. If cirrus clouds occur with sufficient frequency and spatial extent, they could influence not only the chemical composition but also the ozone depletion in the region near the tropopause. Because of variations in observed cloud occurrence frequency and in photochemical and dynamical timescales, the presence of cirrus clouds likely has its largest effect on ozone near the midlatitude tropopause of the northern hemisphere in summer.

Comparison of reflectance with backscatter and absorption parameters for turbid waters

The relation of reflectance to backscatter and absorption parameters is investigated for waters more turbid than those of previous investigations. Experimental data are examined for river waters in which beam attenuation values range from 8.9 to 18.9 m(_1) at 550 nm. Attenuation, absorption, backscatter, and irradiance reflectance spectral properties are presented for wavelengths between 450 and 800 nm. Comparisons of reflectance with backscatter to absorption ratio and backscatter with absorption plus backscatter ratio indicate that data for turbid waters do not fit linear or polynomial models which are presently available in the literature.

Role of aerosol variations in anthropogenic ozone depletion in the polar regions

A climatology of aerosol surface area inferred from satellite measurements is used as input in a two-dimensional model to study the long-term evolution of polar ozone depletion, especially the Antarctic ozone hole. It is found that volcanic aerosol inputs very likely modulate the severity of the ozone hole. In particular, the rapid deepening of the ozone hole in the early 1980s, as seen, for example, in the Halley Bay total ozone measurements, was probably caused by accelerated heterogeneous chemistry associated with an increase in aerosol surface area due to volcanic injection combined with the anthropogenic perturbation of stratospheric chlorine. This is further substantiated by the large Antarctic ozone decline observed and modeled after the eruption of Mount Pinatubo. A number of factors that influence the ozone hole are also investigated, including the effect of liquid versus frozen aerosol, the effects of denitrification and dehydration, the role of HO x in HCl and ClONO 2 recovery, and the effect of chlorine partitioning at the start of winter. Denitrification tends to slightly increase modeled ozone loss, primarily between about 17 and 25 km late in the season, while dehydration tends to decrease the amount of ozone depletion. However, temperature and aerosol amount have the strongest control on the model ozone loss for a given chlorine loading. These findings suggest that future Arctic ozone depletion could be severe in unusually cold winters or years with large volcanic aerosol surface area.

Ozone depletion at mid-latitudes: Coupling of volcanic aerosols and temperature variability to anthropogenic chlorine

Satellite observations of total ozone at 40–60°N are presented from a variety of instruments over the time period 1979–1997. These reveal record low values in 1992–3 (after Pinatubo) followed by partial but incomplete recovery. The largest post-Pinatubo reductions and longer-term trends occur in spring, providing a critical test for chemical theories of ozone depletion. The observations are shown to be consistent with current understanding of the chemistry of ozone depletion when changes in reactive chlorine and stratospheric aerosol abundances are considered along with estimates of wave-driven fluctuations in stratospheric temperatures derived from global temperature analyses. Temperature fluctuations are shown to make significant contributions to model calculated northern mid-latitude ozone depletion due to heterogeneous chlorine activation on liquid sulfate aerosols at temperatures near 200–210K (depending upon water vapor pressure), particularly after major volcanic eruptions. Future mid-latitude ozone recovery will hence depend not only on chlorine recovery but also on temperature trends and/or variability, volcanic activity, and any trends in stratospheric sulfate aerosol.

The potential for ozone depletion in the Arctic polar stratosphere

The nature of the Arctic polar stratosphere is observed to be similar in many respects to that of the Antarctic polar stratosphere, where an ozone hole has been identified. Most of the available chlorine (HCl and ClONO2) was converted by reactions on polar stratospheric clouds to reactive ClO and Cl2O2 throughout the Arctic polar vortex before midwinter. Reactive nitrogen was converted to HNO3, and some, with spatial inhomogeneity, fell out of the stratosphere. These chemical changes ensured characteristic ozone losses of 10 to 15% at altitudes inside the polar vortex where polar stratospheric clouds had occurred. These local losses can translate into 5 to 8% losses in the vertical column abundance of ozone. As the amount of stratospheric chlorine inevitably increases by 50% over the next two decades, ozone losses recognizable as an ozone hole may well appear.

Use of stratospheric aerosol properties as diagnostics of Antarctic vortex processes

Physical properties of the stratospheric aerosol population are inferred from cloud-free SAGE II multiwavelength extinction measurements in the Antarctic during late summer (February/March) and spring (September/October, November). Seasonal changes in these properties are used to infer physical processes occurring in the Antarctic stratosphere over the course of the winter. The analysis suggests that the apparent springtime cleansing of the Antarctic stratosphere is the result of aerosol redistribution through subsidence of the polar vortex air mass and sedimentation of large polar stratospheric cloud particles. The analysis also suggests that vortex processes are responsible for a significant downward transport of aerosol through the tropopause.

In Situ Observations of Aerosol and Chlorine Monoxide After the 1991 Eruption of Mount Pinatubo: Effect of Reactions on Sulfate Aerosol

Highly resolved aerosol size distributions measured from high-altitude aircraft can be used to describe the effect of the 1991 eruption of Mount Pinatubo on the stratospheric aerosol. In some air masses, aerosol mass mixing ratios increased by factors exceeding 100 and aerosol surface area concentrations increased by factors of 30 or more. Increases in aerosol surface area concentration were accompanied by increases in chlorine monoxide at mid-latitudes when confounding factors were controlled. This observation supports the assertion that reactions occurring on the aerosol can increase the fraction of stratospheric chlorine that occurs in ozone-destroying forms.