Caractérisation in situ des propriétés optiques et microphysiques des aérosols troposphériques dans l’archipel arctique canadien

• Main Author: Vicente-Luis, Andy
• Other Authors: Hayes, Patrick
• Format: Thesis
• Language: French
• Published: 2021
• Subjects: geo; envir; Arctic; Canada; Canadian Arctic Archipelago; Eureka; Nunavut; Arctic Archipelago; Arctique*; Global warming; Sea ice
• Online Access: http://hdl.handle.net/1866/24156

Global warming in the Canadian Arctic is twice as fast as the global average, accelerating the melting of sea ice and radically disrupting the fauna, the flora, and the communities of the whole region. Arctic warming is caused not only by rising greenhouse gas emissions, but also by the short-lived climate forcing agents such as tropospheric aerosols. However, aerosol radiative forcing in the polar region is less precisely estimated than that of greenhouse gases, notably CO2, and remains highly uncertain. This large uncertainty arises mainly from the high spatiotemporal variability in aerosol chemical and physical properties, in addition to the complexity of the feedback loops observed in the Arctic. Furthermore, datasets on aerosol characteristics and their distribution across the region are very limited, particularly in the Canadian High Arctic. To address this issue, a series of measurements were conducted over a 3-year period (2016-2019) at the Polar Atmospheric Environment Research Laboratory (PEARL, 80N 86W) near Eureka weather station, in Nunavut, Canada. Aerosol size distribution was measured using several instruments including an Optical Particle Counter (OPC), a Scanning Mobility Particle Sizer (SMPS), an Aerodynamic Particle Sizer (APS). Aerosol optical properties were determined by two Photoacoustic Extinctiometers (PAXs) which operate at wavelengths of 405 nm and 870 nm, respectively. Observations made at the PEARL observatory show a strong seasonal variation in the optical and microphysical properties of polar aerosols. In the winter and spring, the Arctic atmosphere is impacted by an anthropogenic haze that results in a sharp increase in aerosol size, number concentration, and optical properties. Arctic haze episodes typically occur in mid-December, when mineral dust events have also been observed, and end in May when formation and growth of new particles begin. Early spring exhibits the highest accumulation-mode aerosol concentrations during the year. The darkest Arctic haze aerosols have been ...