RESUMO
The atmospheric oxidation of biogenic volatile organic compounds (BVOC) by OH radicals over tropical rainforests impacts local particle production and the lifetime of globally distributed chemically and radiatively active gases. For the pristine Amazon rainforest during the dry season, we empirically determined the diurnal OH radical variability at the forest-atmosphere interface region between 80 and 325 m from 07:00 to 15:00 LT using BVOC measurements. A dynamic time warping approach was applied showing that median averaged mixing times between 80 to 325 m decrease from 105 to 15 min over this time period. The inferred OH concentrations show evidence for an early morning OH peak (07:00-08:00 LT) and an OH maximum (14:00 LT) reaching 2.2 (0.2, 3.8) × 106 molecules cm-3 controlled by the coupling between BVOC emission fluxes, nocturnal NOx accumulation, convective turbulence, air chemistry and photolysis rates. The results were evaluated with a turbulence resolving transport (DALES), a regional scale (WRF-Chem) and a global (EMAC) atmospheric chemistry model.
RESUMO
The development and maintenance of the atmospheric boundary layer (ABL) plays a key role in the distribution of atmospheric constituents, especially in a polluted urban area. In particular, the ABL has a direct impact on the concentration and transformation of pollutants. In this work, in order to analyze the different mechanisms which control the boundary layer growth, we have simulated by means of the non-hydrostatic model MM5 several boundary layer observed in the city of Barcelona (Spain). Sensitivity analysis of the modelled ABL is carried out by using various descriptions of the planetary boundary layer (PBL). Direct and continuous measurements of the boundary layer depth taken by a lidar are used to evaluate the results obtained by the model.