No abstract

[1] During summer of 2004, about 2.7 million hectare of boreal forest burned in Alaska, the largest annual area burned on record, and another 3.1 million hectare burned in Canada. This study explores the impact of emissions from these fires on light absorbing aerosol concentration levels, aerosol optical depths (AOD), and albedo at the Arctic stations Barrow (Alaska), Alert (Canada), Summit (Greenland), and Zeppelin/Ny Å lesund on Spitsbergen (Norway). The Lagrangian particle dispersion model FLEXPART was run backward from these sites to identify periods that were influenced by forest fire pollution plumes. It is shown that the fires led to enhanced values of particle light absorption coefficients (s ap ) at all of these sites. Barrow, about 1000 km away from the fires, was affected by several fire pollution plumes, one leading to spectacularly high 3-hour mean s ap values of up to 32 Mm À1 , more than the highest values measured in Arctic Haze. AOD measurements for a wavelength of 500 nm saturated but were estimated at above 4-5 units, unprecedented in the station records. Fire plumes were transported through the atmospheric column over Summit continuously for 2 months, during which all measured AOD values were enhanced, with maxima up to 0.4-0.5 units. Equivalent black carbon concentrations at the surface at Summit were up to 600 ng m À3 during two major episodes, and Alert saw at least one event with enhanced s ap values. FLEXPART results show that Zeppelin was located in a relatively unaffected part of the Arctic. Nevertheless, there was a 4-day period with daily mean s ap > 0.3 Mm À1 , the strongest episode of the summer half year, and enhanced AOD values. Elevated concentrations of the highly source-specific compound levoglucosan positively confirmed that biomass burning was the source of the aerosols at Zeppelin. In summary, this paper shows that boreal forest fires can lead to elevated concentrations of light absorbing aerosols throughout the entire Arctic. Enhanced AOD values suggest a substantial impact of these plumes on radiation transmission in the Arctic atmosphere. During the passage of the largest fire plume, a pronounced drop of the albedo of the snow was observed at Summit. We suggest that this is due to the deposition of light absorbing particles on the snow, with further potentially important consequences for the Arctic radiation budget.

The Persistent Cold-Air Pool Study (PCAPS) was conducted in Utah's Salt Lake valley from 1 December 2010 to 7 February 2011. The field campaign's primary goal was to improve understanding of the physical processes governing the evolution of multiday cold-air pools (CAPs) that are common in mountain basins during the winter. Meteorological instrumentation deployed throughout the Salt Lake valley provided observations of the processes contributing to the formation, maintenance, and destruction of 10 persistent CAP episodes. The close proximity of PCAPS field sites to residences and the University of Utah campus allowed many undergraduate and graduate students to participate in the study. Ongoing research, supported by the National Science Foundation, is using the PCAPS dataset to examine CAP evolution. Preliminary analyses reveal that variations in CAP thermodynamic structure are attributable to a multitude of physical processes affecting local static stability: for example, synoptic-scale processes impact changes in temperatures and cloudiness aloft while variations in boundary layer forcing modulate the lower levels of CAPs. During episodes of strong winds, complex interactions between the synoptic and mesoscale f lows, local thermodynamic structure, and terrain lead to both partial and complete removal of CAPs. In addition, the strength and duration of CAP events affect the local concentrations of pollutants such as PM2.5.

The Salt Lake Valley experiences severe fine particulate matter pollution episodes in winter during persistent cold-air pools (PCAPs). We employ measurements throughout an entire winter from different elevations to examine the chemical and dynamical processes driving these episodes. Whereas primary pollutants such as NO and CO were enhanced twofold during PCAPs, O concentrations were approximately threefold lower. Atmospheric composition varies strongly with altitude within a PCAP at night with lower NO and higher oxidants (O) and oxidized reactive nitrogen (NO) aloft. We present observations of NO during PCAPs that provide evidence for its role in cold-pool nitrate formation. Our observations suggest that nighttime and early morning chemistry in the upper levels of a PCAP plays an important role in aerosol nitrate formation. Subsequent daytime mixing enhances surface PM by dispersing the aerosol throughout the PCAP. As pollutants accumulate and deplete oxidants, nitrate chemistry becomes less active during the later stages of the pollution episodes. This leads to distinct stages of PM pollution episodes, starting with a period of PM buildup and followed by a period with plateauing concentrations. We discuss the implications of these findings for mitigation strategies.