Abstract

Abstract. Aerosol variations and trends over different land and ocean regions from 1980 to 2009 are analyzed with the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model and observations from multiple satellite sensors and available ground-based networks. Excluding time periods with large volcanic influence, aerosol optical depth (AOD) and surface concentration over polluted land regions generally vary with anthropogenic emissions, but the magnitude of this association can be dampened by the presence of natural aerosols, especially dust. Over the 30-year period in this study, the largest reduction in aerosol levels occurs over Europe, where AOD has decreased by 40–60% on average and surface sulfate concentrations have declined by a factor of up to 3–4. In contrast, East Asia and South Asia show AOD increases, but the relatively high level of dust aerosols in Asia reduces the correlation between AOD and pollutant emission trends. Over major dust source regions, model analysis indicates that the change of dust emissions over the Sahara and Sahel has been predominantly driven by the change of near-surface wind speed, but over Central Asia it has been largely influenced by the change of the surface wetness. The decreasing dust trend in the North African dust outflow region of the tropical North Atlantic and the receptor sites of Barbados and Miami is closely associated with an increase of the sea surface temperature in the North Atlantic. This temperature increase may drive the decrease of the wind velocity over North Africa, which reduces the dust emission, and the increase of precipitation over the tropical North Atlantic, which enhances dust removal during transport. Despite significant trends over some major continental source regions, the model-calculated global annual average AOD shows little change over land and ocean in the past three decades, because opposite trends in different land regions cancel each other out in the global average, and changes over large open oceans are negligible. This highlights the necessity for regional-scale assessment of aerosols and their climate impacts, as global-scale average values can obscure important regional changes.

Highlights

  • Aerosols affect earth’s energy budget by scattering and absorbing solar and terrestrial radiation and by altering cloud properties and lifetimes

  • We show the spatial patterns of global aerosol spatial distributions from multiple satellite data sets and the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model (Sect. 4.1), multi-decadal variations of regional aerosol optical depth (AOD) and aerosol surface mass concentrations over land (Sect. 4.2) and ocean (Sect. 4.3), and spatial patterns of AOD change over two time segments during the past 30 years (Sect. 4.4)

  • Over land regions dominated by pollution aerosols, the 30-year AOD and surface concentration trends are generally consistent with the direction of the regional pollutant emission changes

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Summary

Introduction

Aerosols affect earth’s energy budget by scattering and absorbing solar and terrestrial radiation and by altering cloud properties and lifetimes. They influence weather, air quality, atmospheric chemistry, and biogeochemical cycles. Anthropogenic activities have caused considerable changes in aerosol composition and loading, and will continue to do so in the future (e.g., Leibensperger et al, 2012; Sillmann et al, 2013). Historical emission inventories have estimated that trends in anthropogenic emission are closely tied to economic growth, population density, and technological development, which may explain the regional aerosol variability shown in the long-term satellite data records. Understanding the cause of aerosol trends in terms of human activities or natural variability is key to projecting the earth system’s response to future changes

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