Repository hosted by TU Delft Library

Home · Contact · About · Disclaimer ·
 

Exchange of ozone and nitrogen oxides between the atmosphere and coniferous forest

Publication files not online:

Author: Duyzer, J.H. · Weststrate, J.H. · Walton, S
Type:article
Date:1995
Publisher: Kluwer Academic Publishers
Place: Dordrecht, Netherlands
Institution: Instituut voor Milieuwetenschappen TNO
Source:Proceedings of the 1995 5th International Conference on Acidic Deposition: Science & Policy, ACID REIGN'95. Part 3, 26 June 1995 through 30 June 1995, Goteborg, Swed, Conference code: 44450, 4, 85, 2065-2070
Identifier: 233134
doi: DOI:10.1007/BF01186138
Keywords: Agriculture · Air pollution · Atmospheric humidity · Calculations · Chemical reactions · Forestry · Geographical regions · Mathematical models · Nitrogen oxides · Ozone · Particulate emissions · Canopy resistance · Coniferous forest · Deposition flux · Dry deposition · Eddy correlation · Netherlands · Soil emission · Atmospheric chemistry

Abstract

The deposition flux of O3 to a Douglas fir forest in the Netherlands was monitored by eddy correlation during nine months. At the same time the concentration gradients of NO, NO2 and O3 were determined over the forest. The canopy resistance to O3 uptake was calculated from the measurements ant it compared well with model estimates. The sensitivity of the stomatal resistance to humidity calculated in the model was adapted to improve the comparison. A multi-layered model of canopy exchange which included the influence of chemical reactions between NO and O3 and soil emissions was used to interpret the results for NO2. The observed fluxes of NO2 away from the surface into the atmosphere were probably caused by soil emissions of NO. The soil-emitted NO was converted to NO2 in the trunk space and vented into the atmosphere. The model showed that the NO2 flux above the canopy was either away or towards the canopy depending on the strength of the soil emission and the amount of NO2 taken up in the canopy. A 'canopy compensation' point for NO2 could be established above which deposition was the main process and below which emission was observed. The model calculations supported the observations which indicated a compensation point of approximately 10 ppb NO2.