Abstract

The impact of aerosol spatio-temporal variability on the Arctic radiative budget is not fully constrained. This case study focuses on the intra-Arctic modification of long-range transported aerosol and its direct aerosol radiative effect (ARE). Different types of air-borne and ground-based remote sensing observations (from Lidar and sun-photometer) revealed a high tropospheric aerosol transport episode over two parts of the European Arctic in April 2018. By incorporating the derived aerosol optical and microphysical properties into a radiative transfer model, we assessed the ARE over the two locations. Our study displayed that even in neighboring Arctic upper tropospheric levels, aged aerosol was transformed due to the interplay of removal processes (nucleation scavenging and dry deposition) and alteration of the aerosol source regions (northeast Asia and north Europe). Along the intra-Arctic transport, the coarse aerosol mode was depleted and the visible wavelength Lidar ratio (LR) increased significantly (from 15 to 64–82 sr). However, the aerosol modifications were not reflected on the ARE. More specifically, the short-wave (SW) atmospheric column ARE amounted to +4.4 - +4.9 W m−2 over the ice-covered Fram Strait and +4.5 W m−2 over the snow-covered Ny-Ålesund. Over both locations, top-of-atmosphere (TOA) warming was accompanied by surface cooling. These similarities can be attributed to the predominant accumulation mode, which drives the SW radiative budget, as well as to the similar layer altitude, solar geometry, and surface albedo conditions over both locations. However, in the context of retreating sea ice, the ARE may change even along individual transport episodes due to the ice albedo feedback.

Highlights

  • As anthropogenic climate change drives major modifications in the Arctic environment, Arctic aerosol and its related feedback mechanisms are inextricably affected

  • Our study focused on a persistent aerosol transport episode, which was synergistically identified by remote sensing systems in remarkably high tropospheric altitudes

  • Before the layer arrival (30–31 March), air masses originated from central Eurasia (4–7 km, Figure 4b)

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Summary

Introduction

As anthropogenic climate change drives major modifications in the Arctic environment, Arctic aerosol and its related feedback mechanisms are inextricably affected. Aerosol is involved in aerosol–cloud and aerosol–radiation interactions, which highly depend on the aerosol species, solar zenith angle, and surface albedo [1,2,3]. In the Arctic, the annual mean aerosol radiative forcing at the top-of-atmosphere (TOA) is estimated at −0.12 W m−2 with respect to pre-industrial emissions of anthropogenic aerosol and precursors [3]. The aerosol radiative forcing in the Arctic region still entails high uncertainties [1,2,3]. A better understanding of the aerosol-related physical processes is crucial in the changing Arctic environment, where the most rapid near-surface temperature increase is taking place, known as “Arctic amplification” [5,6]

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