scholarly journals The effects of forest canopy shading and turbulence on boundary layer ozone

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
P. A. Makar ◽  
R. M. Staebler ◽  
A. Akingunola ◽  
J. Zhang ◽  
C. McLinden ◽  
...  
2006 ◽  
Vol 40 (11) ◽  
pp. 1949-1956 ◽  
Author(s):  
Antonio Amoroso ◽  
Harry J. Beine ◽  
Roberto Sparapani ◽  
Marianna Nardino ◽  
Ivo Allegrini

2019 ◽  
Vol 46 (16) ◽  
pp. 10008-10014 ◽  
Author(s):  
Liji M. David ◽  
A. R. Ravishankara

2016 ◽  
Vol 97 (12) ◽  
pp. 2329-2342 ◽  
Author(s):  
Jose D. Fuentes ◽  
Marcelo Chamecki ◽  
Rosa Maria Nascimento dos Santos ◽  
Celso Von Randow ◽  
Paul C. Stoy ◽  
...  

Abstract We describe the salient features of a field study whose goals are to quantify the vertical distribution of plant-emitted hydrocarbons and their contribution to aerosol and cloud condensation nuclei production above a central Amazonian rain forest. Using observing systems deployed on a 50-m meteorological tower, complemented with tethered balloon deployments, the vertical distribution of hydrocarbons and aerosols was determined under different boundary layer thermodynamic states. The rain forest emits sufficient reactive hydrocarbons, such as isoprene and monoterpenes, to provide precursors of secondary organic aerosols and cloud condensation nuclei. Mesoscale convective systems transport ozone from the middle troposphere, enriching the atmospheric boundary layer as well as the forest canopy and surface layer. Through multiple chemical transformations, the ozone-enriched atmospheric surface layer can oxidize rain forest–emitted hydrocarbons. One conclusion derived from the field studies is that the rain forest produces the necessary chemical species and in sufficient amounts to undergo oxidation and generate aerosols that subsequently activate into cloud condensation nuclei.


2006 ◽  
Vol 139 (1-2) ◽  
pp. 40-54 ◽  
Author(s):  
Victoria J. Stokes ◽  
Michael D. Morecroft ◽  
James I.L. Morison
Keyword(s):  

2013 ◽  
Vol 70 ◽  
pp. 123-130 ◽  
Author(s):  
Xiao-Ming Hu ◽  
Petra M. Klein ◽  
Ming Xue ◽  
Fuqing Zhang ◽  
David C. Doughty ◽  
...  

2007 ◽  
Vol 7 (5) ◽  
pp. 1451-1469 ◽  
Author(s):  
S. Morin ◽  
J. Savarino ◽  
S. Bekki ◽  
S. Gong ◽  
J. W. Bottenheim

Abstract. We report the first measurements of the oxygen isotope anomaly of atmospheric inorganic nitrate from the Arctic. Nitrate samples and complementary data were collected at Alert, Nunavut, Canada (82°30 ' N, 62°19 ' W) in spring 2004. Covering the polar sunrise period, characterized by the occurrence of severe boundary layer ozone depletion events (ODEs), our data show a significant correlation between the variations of atmospheric ozone (O3) mixing ratios and Δ17O of nitrate (Δ17O(NO−3)). This relationship can be expressed as: Δ17O(NO−3)/‰, =(0.15±0.03)×O3/(nmol mol–1)+(29.7±0.7), with R2=0.70(n=12), for Δ17O(NO−3) ranging between 29 and 35 ‰. We derive mass-balance equations from chemical reactions operating in the Arctic boundary layer, that describe the evolution of Δ17O(NO−3) as a function of the concentrations of reactive species and their isotopic characteristics. Changes in the relative importance of O3, RO2 and BrO in the oxidation of NO during ODEs, and the large isotope anomalies of O3 and BrO, are the driving force for the variability in the measured Δ17O(NO−3) . BrONO2 hydrolysis is found to be a dominant source of nitrate in the Arctic boundary layer, in agreement with recent modeling studies.


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