Abstract

Abstract. Processes occurring in the tropical upper troposphere (UT), the Tropical Transition Layer (TTL), and the lower stratosphere (LS) are of importance for the global climate, for stratospheric dynamics and air chemistry, and for their influence on the global distribution of water vapour, trace gases and aerosols. In this contribution we present aerosol and trace gas (in-situ) measurements from the tropical UT/LS over Southern Brazil, Northern Australia, and West Africa. The instruments were operated on board of the Russian high altitude research aircraft M-55 "Geophysica" and the DLR Falcon-20 during the campaigns TROCCINOX (Araçatuba, Brazil, February 2005), SCOUT-O3 (Darwin, Australia, December 2005), and SCOUT-AMMA (Ouagadougou, Burkina Faso, August 2006). The data cover submicron particle number densities and volatility from the COndensation PArticle counting System (COPAS), as well as relevant trace gases like N2O, ozone, and CO. We use these trace gas measurements to place the aerosol data into a broader atmospheric context. Also a juxtaposition of the submicron particle data with previous measurements over Costa Rica and other tropical locations between 1999 and 2007 (NASA DC-8 and NASA WB-57F) is provided. The submicron particle number densities, as a function of altitude, were found to be remarkably constant in the tropical UT/LS altitude band for the two decades after 1987. Thus, a parameterisation suitable for models can be extracted from these measurements. Compared to the average levels in the period between 1987 and 2007 a slight increase of particle abundances was found for 2005/2006 at altitudes with potential temperatures, Θ, above 430 K. The origins of this increase are unknown except for increases measured during SCOUT-AMMA. Here the eruption of the Soufrière Hills volcano in the Caribbean caused elevated particle mixing ratios. The vertical profiles from Northern hemispheric mid-latitudes between 1999 and 2006 also are compact enough to derive a parameterisation. The tropical profiles all show a broad maximum of particle mixing ratios (between Θ≈340 K and 390 K) which extends from below the TTL to above the thermal tropopause. Thus these particles are a "reservoir" for vertical transport into the stratosphere. The ratio of non-volatile particle number density to total particle number density was also measured by COPAS. The vertical profiles of this ratio have a maximum of 50% above 370 K over Australia and West Africa and a pronounced minimum directly below. Without detailed chemical composition measurements a reason for the increase of non-volatile particle fractions cannot yet be given. However, half of the particles from the tropical "reservoir" contain compounds other than sulphuric acid and water. Correlations of the measured aerosol mixing ratios with N2O and ozone exhibit compact relationships for the tropical data from SCOUT-AMMA, TROCCINOX, and SCOUT-O3. Correlations with CO are more scattered probably because of the connection to different pollution source regions. We provide additional data from the long distance transfer flights to the campaign sites in Brazil, Australia, and West-Africa. These were executed during a time window of 17 months within a period of relative volcanic quiescence. Thus the data represent a "snapshot picture" documenting the status of a significant part of the global UT/LS fine aerosol at low concentration levels 15 years after the last major (i.e., the 1991 Mount Pinatubo) eruption. The corresponding latitudinal distributions of the measured particle number densities are presented in this paper to provide data of the UT/LS background aerosol for modelling purposes.

Highlights

  • In the upper troposphere and lower stratosphere (UT/LS) aerosols influence the radiative budget and the actinic fluxes for photochemical reactions, serve as condensation nuclei for altocumulus and cirrus cloud formation (Kramer et al, 2009), and provide sites for heterogeneous chemical reactions (Borrmann et al, 1997).Of particular importance for many of the aerosol and cloud related processes in the tropics is the so-called Tropical Transition Layer (TTL) within the UT/LS

  • In this contribution we present aircraft-borne in-situ measurements of submicron particle abundance and volatility from the 9 to 12 km altitude range, the UT/LS, and the TTL over Southern Brazil (TROCCINOX campaign, 2005), West Africa (SCOUT-AMMA, including balloon-borne measurements from Niger, 2006), and Northern Australia (SCOUTO3, 2005)

  • The transfer flights from Europe to the tropical campaign locations showed that at potential temperature levels above 367 K the ambient particle number densities range from 20 cm−3 at higher latitudes to values around 100 cm−3 in the tropics and that the geographical distribution of the particle abundance was rather homogeneous along the different latitude bands

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Summary

Introduction

In the upper troposphere and lower stratosphere (UT/LS) aerosols influence the radiative budget and the actinic fluxes for photochemical reactions, serve as condensation nuclei for altocumulus and cirrus cloud formation (Kramer et al, 2009), and provide sites for heterogeneous chemical reactions (Borrmann et al, 1997). More recently Froyd et al (2010), presented air-borne mass spectrometric composition measurements of ice residues from tropical cirrus and subvisible cirrus clouds They concluded that most ice residuals consisted of internal mixtures of neutralised sulphate and some organics (similar to liquid sulphuric acid droplets) and that mineral dust or other heterogeneous nuclei do not play a role in cirrus formation. Based on recent laser ablation mass spectrometric in-situ measurements in the TTL over Costa Rica, Froyd et al (2009) showed that significant numbers of particles with sizes above 500 nm contain oxidised organic compounds They conclude that the chemical composition of these larger particles in the tropical TTL depends on tropical dynamics, regional sources (implying boundary layer processes as well) and the occurrence of overshooting cumulonimbus clouds. The measurements presented here originate from local flights of the M-55 “Geophysica” and the German DLR Falcon-20 research aircraft during the campaigns: TROCCINOX (from Aracatuba, Brazil; Schumann, 2005), SCOUT-O3 (based in Darwin, Australia; Vaughan et al, 2008; Brunner et al, 2009), and SCOUT-AMMA

Aug 2006 16 Aug 2006 flight period until
Atmospheric background in 2005 and 2006
Instrumentation for submicron particle and trace gas measurements
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Summary and conclusions
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