2 research outputs found
North Pacific SST Forcing on the Central United States “Warming Hole” as Simulated in CMIP5 Coupled Historical and Uncoupled AMIP Experiments
<p>The central United States experienced a cooling trend during the twentieth century, called the “warming hole,” most notably in the last quarter of the century when global warming accelerated. The coupled simulations of the models that participated in the Coupled Model Intercomparison Project, Phases 3 and 5 (CMIP3/5), have been unable to reproduce this abnormal cooling phenomenon satisfactorily. An unrealistic representation of the observed phasing of the Pacific Decadal Oscillation (PDO)—one of the proposed forcing mechanisms for the warming hole—in the models is considered to be one of the main causes of this effect. The CMIP5’s uncoupled Atmospheric Model Intercomparison Project (AMIP) experiment, whose duration approximately coincides with the peak warming hole cooling period, provides an opportunity, when compared with the coupled historical experiment, to examine the role of the variation in Pacific Ocean sea surface temperature (SST) in the warming hole’s formation and also to assess the skill of the models in simulating the teleconnection between Pacific SST and the continental climate in North America. Accordingly, this study compared AMIP and historical runs in the CMIP5 suite thereby isolating the role of SST forcing in the formation of the warming hole and its maintenance mechanisms. It was found that, even when SST forcing in the AMIP run was “perfectly” prescribed in the models, the skill of the models in simulating the warming hole cooling in the central United States showed little improvement over the historical run, in which SST is calculated interactively, even though the AMIP run overestimated the anti-correlation between temperature in the central United States and the PDO index. The fact that better simulation of the PDO phasing in the AMIP run did not translate into an improved summer cooling trend in the central United States suggests that the inability of the coupled CMIP5 models to reproduce the warming hole under the historical run is not mainly a result of the mismatch between simulated and observed PDO phasing, as believed.</p
Real-Time Characterization of Aerosol Particle Composition above the Urban Canopy in Beijing: Insights into the Interactions between the Atmospheric Boundary Layer and Aerosol Chemistry
Despite
extensive efforts into the characterization of air pollution
during the past decade, real-time characterization of aerosol particle
composition above the urban canopy in the megacity Beijing has never
been performed to date. Here we conducted the first simultaneous real-time
measurements of aerosol composition at two different heights at the
same location in urban Beijing from December 19, 2013 to January 2,
2014. The nonrefractory submicron aerosol (NR-PM<sub>1</sub>) species
were measured in situ by a high-resolution aerosol mass spectrometer
at near-ground level and an aerosol chemical speciation monitor at
260 m on a 325 m meteorological tower in Beijing. Secondary aerosol
showed similar temporal variations between ground level and 260 m,
whereas much weaker correlations were found for the primary aerosol.
The diurnal evolution of the ratios and correlations of aerosol species
between 260 m and the ground level further illustrated a complex interaction
between vertical mixing processes and local source emissions on aerosol
chemistry in the atmospheric boundary layer. As a result, the aerosol
compositions at the two heights were substantially different. Organic
aerosol (OA), mainly composed of primary OA (62%), at the ground level
showed a higher contribution to NR-PM<sub>1</sub> (65%) than at 260
m (54%), whereas a higher concentration and contribution (15%) of
nitrate was observed at 260 m, probably due to the favorable gas–particle
partitioning under lower temperature conditions. In addition, two
different boundary layer structures were observed, each interacting
differently with the evolution processes of aerosol chemistry