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NH3 and NO2 fluxes between beech trees and the atmosphere – correlation with climatic and physiological parameters

Published online by Cambridge University Press:  23 October 2000

ARTHUR GESSLER
Affiliation:
Albert-Ludwigs-Universität Freiburg, Institut für Forstbotanik und Baumphysiologie, Professur für Baumphysiologie, Am Flughafen 17, D-79110 Freiburg i. Br., Germany
MICHAEL RIENKS
Affiliation:
Albert-Ludwigs-Universität Freiburg, Institut für Forstbotanik und Baumphysiologie, Professur für Baumphysiologie, Am Flughafen 17, D-79110 Freiburg i. Br., Germany
HEINZ RENNENBERG
Affiliation:
Albert-Ludwigs-Universität Freiburg, Institut für Forstbotanik und Baumphysiologie, Professur für Baumphysiologie, Am Flughafen 17, D-79110 Freiburg i. Br., Germany
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Abstract

The dynamic-chamber technique was used to investigate the correlation between NH3 and NO2 fluxes and different climatic and physiological parameters: air temperature; relative air humidity; photosynthetic photon fluence rate; NH3 and NO2 concentrations; transpiration rate; leaf conductance for water vapour; and photosynthetic activity. The experiments were performed with twigs from the sun crown of mature beech trees (Fagus sylvatica) at a field site (Höglwald, Germany), and with 12-wk-old beech seedlings under controlled conditions. Both sets of experiments showed that NO2 and NH3 fluxes depended linearly on NO2 and NH3 concentration, respectively, in the concentration ranges representative for the field site studied, and on water-vapour conductance as a measure for stomatal aperture. The NO2 compensation point determined in the field studies (the atmospheric NO2 concentration with no net NO2 flux) was 1.8–1.9 nmol mol−1. The NH3 compensation point varied between 3.3 and 3.5 nmol mol−1 in the field experiments, and was 3.0 nmol mol−1 in the experiments under controlled conditions. The climatic factors T and PPFR were found to influence both NO2 and NH3 fluxes indirectly, by changing stomatal conductance. Whilst NO2 flux showed a response to changing relative humidity that could be explained by altered stomatal conductance, increased NH3 flux with increasing relative humidity (>50%) depended on other factors. The exchange of NO2 between above-ground parts of beech trees and the atmosphere could be explained exclusively by uptake or emission of NO2 through the stomata, as indicated by the quotient between measured and predicted NO2 conductance of approx. 1 under all environmental conditions examined. Neither internal mesophyll resistances nor additional sinks could be observed for adult trees or for beech seedlings. By contrast, the patterns of NH3 flux could not be explained by an exclusive exchange of NH3 through the stomata. Deposition into additional sinks on the leaf surface, as indicated by an increase in the quotient between measured and predicted NH3 conductance, gained importance in high air humidity, when the stomata were closed or nearly closed and/or when atmospheric NH3 concentrations were high. Although patterns of NH3 gas exchange did not differ between different months or years at high NH3 concentrations (c. 140 nmol mol−1), it must be assumed that emission or deposition fluxes at low ambient NH3 concentration (0.8 and 4.5 nmol mol−1) might vary significantly with time because of variation in the NH3 compensation point.

Type
Research article
Copyright
© Trustees of the New Phytologist 2000

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